U.S. patent application number 16/703074 was filed with the patent office on 2020-06-11 for systems and methods for the treatment of eye conditions.
The applicant listed for this patent is Alcon Inc.. Invention is credited to Michael Burk, David Eshbaugh, Brian S. Kelleher, Mark Petersen, John Slate, Dan Vance.
Application Number | 20200179168 16/703074 |
Document ID | / |
Family ID | 70050159 |
Filed Date | 2020-06-11 |
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United States Patent
Application |
20200179168 |
Kind Code |
A1 |
Kelleher; Brian S. ; et
al. |
June 11, 2020 |
SYSTEMS AND METHODS FOR THE TREATMENT OF EYE CONDITIONS
Abstract
Systems, methods, and devices used to treat eyelids, meibomian
glands, ducts, and surrounding tissue are described herein. In some
embodiments, an eye treatment device is disclosed, which includes a
scleral shield positionable proximate an inner surface of an
eyelid, the scleral shield being made of, or coated with, an
energy-absorbing material activated by a light energy, and an
energy transducer positionable outside of the eyelid, the energy
transducer configured to provide light energy at one or more
wavelengths, including a first wavelength selected to heat the
energy-absorbing material. Wherein, when the eyelid is positioned
between the energy transducer and the scleral shield, the light
energy from the energy transducer and the heated energy-absorbing
material of the scleral shield conductively heats a target tissue
region sufficiently to melt meibum within meibomian glands located
within or adjacent to the target tissue region.
Inventors: |
Kelleher; Brian S.; (San
Diego, CA) ; Slate; John; (Encinitas, CA) ;
Burk; Michael; (San Marcos, CA) ; Petersen; Mark;
(San Diego, CA) ; Eshbaugh; David; (Valley Center,
CA) ; Vance; Dan; (Valley Center, CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Alcon Inc. |
Fribourg |
|
CH |
|
|
Family ID: |
70050159 |
Appl. No.: |
16/703074 |
Filed: |
December 4, 2019 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
62776333 |
Dec 6, 2018 |
|
|
|
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61N 5/0613 20130101;
A61N 5/0625 20130101; A61F 9/00718 20130101; A61F 9/009 20130101;
A61F 2009/00844 20130101; A61F 2009/00861 20130101; A61F 2007/0088
20130101; A61N 5/0624 20130101; A61F 9/0079 20130101; A61F
2007/0004 20130101; A61F 9/00709 20130101 |
International
Class: |
A61F 9/007 20060101
A61F009/007; A61F 9/009 20060101 A61F009/009 |
Claims
1. A device for treating a mammalian eye having an eyelid,
comprising: an energy transducer having a device that emits light
energy at multiple wavelengths, including a first wavelength
selected to pass through eyelid and a second wavelength selected to
be absorbed by the eyelid for warming; a frontplate positionable
proximate an outer surface of the eyelid, the frontplate being made
of a clear material that passes the wavelengths of light emitted by
the energy transducer, the frontplate further comprising sensors
configured to provide information regarding a position of the
eyelid relative to the frontplate; a backplate positionable
proximate an inner surface of the eyelid, the backplate being made
of or coated with an energy-reflecting material configured to
receive the first wavelength of light energy transmitted through
the eyelid and reflect it back to the eyelid, the backplate further
comprising sensors configured to provide information regarding a
position of the eyelid relative to the frontplate; and wherein when
the eyelid is positioned between the frontplate and backplate and
the light energy from the energy transducer heats a target tissue
region sufficiently to melt meibum within meibomian glands located
within or adjacent to the target tissue region.
2. The device of claim 1, further comprising an actuator coupled to
the frontplate and backplate configured to cause relative movement
between the frontplate and backplate to squeeze the eyelid to
express the meibomian glands.
3. The device of claim 2, wherein the actuator is further
configured to control the amount of light energy emitted from the
energy transducer at the second wavelength, thereby controlling the
heating of the target tissue.
4. The device of claim 1, wherein the energy transducer is further
configured to provide light energy at a third wavelength selected
to treat bacteria.
5. The device of claim 1, further comprising a visualization device
for viewing the eyelid during treatment.
6. The device of claim 1, wherein the energy transducer comprises
at least one of an LED, laser, incandescent lamp, xenon lamp,
halogen lamp, luminescent lamp, high-intensity discharge lamp, and
gas discharge lamp.
7. The device of claim 1, further comprising one or more components
selected from the group consisting of: a display or dashboard
configured to display the device status; a temperature measurement
device configured to measure various temperatures of the eyelid,
including inner and/or outer eyelid surface temperatures; a
datalogger; a voice recorder; a battery configured to power the
device components; battery charging means; a controller; printed
circuit board; and communication circuitry between shield and
energy transducer.
8. A method for treating an eye condition in a mammal, comprising:
positioning a shield proximate an inner surface of an eyelid, the
shield being made of, or coated with, an energy-absorbing material,
the shield further comprising sensors configured to provide
information regarding a position of the eyelid relative to the
shield; positioning an energy transducer outside of an eyelid of
the mammal, the energy transducer configured to provide light
energy at one or more wavelengths; positioning an energy
transmission surface outside the eyelid, the energy transmission
surface comprising sensors configured to provide information
regarding a position of the eyelid relative to the energy
transmission surface; causing relative movement between the energy
transmission surface and the shield so as to modify a spaced
relationship between the energy transmission surface and the
shield; directing light energy from the energy transducer toward
the shield at a first wavelength selected to heat the
energy-absorbing material; and heating the energy-absorbing
material with the light energy to heat a target tissue region
sufficiently to melt meibum within meibomian glands located within
or adjacent to the target tissue region.
9. The method of claim 8, further comprising directing light energy
from the energy transducer toward an outer surface of the eyelid at
a second wavelength selected to heat a target tissue region within
the eyelid.
10. The method of claim 8, further comprising directing light
energy from the energy transducer toward the eye at a third
wavelength selected to treat bacteria.
11. The method of claim 8, further comprising compressing the
eyelid between the energy transmission surface and the shield.
12. The method of claim 11, further comprising focusing the
compression on a sty or a pimple to treat a hordeolum.
13. The method of claim 11, further comprising focusing the
compression on an occluded gland to treat a chalazion.
14. The method of claim 8, wherein a safety feature electrically
coupled to the energy transducer prevents or interrupts the light
energy from occurring if the shield and associated assembly are not
properly attached to, and aligned with, the device.
15. The device of claim 3, wherein the actuator is at least one of
a lever, a button, a wheel, a slider, and a switch.
16. The device of claim 3, wherein the relative movement between
the energy transmission surface and the shield comprises movement
of the energy transmission surface relative to the shield.
17. The device of claim 3, wherein the relative movement between
the energy transmission surface and the shield comprises a sliding
movement of the energy transmission surface relative to the
shield.
18. The method of claim 8, wherein causing relative movement
between the energy transmission surface and the shield comprises
actuating an actuator coupled to the energy transmission
surface.
19. The method of claim 18, wherein actuating an actuator comprises
pressing a button.
20. The method of claim 8, wherein causing relative movement
between the energy transmission surface and the shield comprises
causing the energy transmission surface to slide relative to the
shield.
21. The method of claim 8 wherein the position of the eyelid
relative to the positions of the shield and the energy transducing
surface must be within a predetermined range for the energy
transducer to emit light energy.
Description
CROSS-REFERENCES TO RELATED APPLICATIONS
[0001] This application claims the benefit of U.S. Provisional
Application No. 62/776,333, filed Dec. 6, 2018, which is
incorporated herein by reference. Priority of the aforementioned
filing date is claimed.
BACKGROUND
[0002] The present disclosure relates to medical devices and
methods of using the same. More particularly, the disclosure
relates to systems, methods, and apparatus used to diagnose and
treat conditions of the eye such as meibomian gland dysfunction and
blepharitis, typically involving eyelids, meibomian glands, ducts,
orifices, and surrounding tissue.
[0003] Meibomian gland dysfunction (MGD) is thought to be the most
common cause of evaporative dry eye disease, with studies showing a
prevalence ranging from 20% to 60% in the general population. MGD
is associated with a failure of meibomian glands to produce an
adequate quantity of normal secretions (called meibum). Meibum is a
lipid-rich essential component of a healthy tear film. When
sufficient meibum is not present in the tear film, the film readily
evaporates, leading to evaporative dry eye disease. In some
patients, the viscosity and melting point of the meibum may
elevate, resulting in thickened meibum that does not flow easily
out of the glands. Further, the channel or duct within the
meibomian gland may become hyperkeratinized, leading to excessive
cellular debris and contributing to the clogging of the gland over
time. Once the glands become chronically clogged (inspissated),
they may atrophy, and no longer be able to produce or secrete
meibum.
[0004] Blepharitis is a common chronic inflammatory condition
involving the eyelid and eyelid margin, and is often associated
with MGD. Studies show a prevalence of blepharitis in the general
population ranging from 12% to 47%, with higher prevalence amongst
older individuals. In addition to certain causative factors
relating to MGD, blepharitis may be caused in part by an abundance
of certain bacteria in and around the eye and eyelid. By-products
of the bacteria are thought to be irritating to the eye, leading to
further inflammation and discomfort to the patient. In addition,
several types of common mites may play a role in adding to the
inflammation of the meibomian glands or sebaceous glands in and
around the eyes. The inflammation caused by these factors can lead
to further constriction of the meibomian gland ducts, limiting the
flow of meibum from the glands and aggravating the condition.
[0005] Diagnosis of meibomian gland dysfunction can be done in many
ways. Typical approaches include measurement of tear break-up time
(TBUT), staining of various ocular surfaces, and examination of the
meibomian glands and their secretions. One common technique used to
examine the glands themselves is to evert the eyelid and to place a
light source under the everted lid (on the outer surface of the
lid) while examining the "transilluminated" image of the glands
created by passing light through the lid. The image may be observed
by an unaided eye, through a biomicroscope, or with a camera.
Healthy glands appear as long, relatively straight forms, while
dysfunctional glands may appear tortuous and swollen, and atrophied
glands show a lack of continuity between the gland mass and the
duct or orifice. In certain cases, infrared light is projected onto
or through the everted lid, and an IR-sensitive camera is used to
view the meibomian glands. The disadvantage of these
transillumination techniques is that they require the lid to be
everted, which is uncomfortable for most patients, and which can be
difficult for the clinician to perform on some eyelids.
[0006] Another common technique for diagnosing MGD is to apply
pressure to the eyelid while observing the meibomian gland ducts or
orifices along the lid margin, usually with a magnifying means such
as a biomicroscope. Healthy glands produce a clear oily secretion
in response to the applied pressure. Glands that are partially
dysfunctional produce less oil and/or cloudy oil. Glands that are
more severely dysfunctional (inspissated) produce a paste-like
secretion, which can only be squeezed out when more significant
pressure is applied to the lid. Glands that are completely
atrophied or that have had their orifices occluded do not produce
any oil, even under high pressure.
[0007] MGD and blepharitis are chronic conditions with limited
effective treatment. One of the most commonly recommended
treatments is the application of a hot compress and massage (using
the compress or fingertips) to the eyelid region. The intended goal
of hot compress treatment is to heat up inspissated meibomian
glands where thickened meibum resides, causing the meibum to soften
and thereby more easily be expressed through the ducts. This
process is thought to unclog the ducts and thereby allow the ducts
to resume normal secretions and maintain a healthier tear film.
Patients are generally instructed to apply a hot washcloth or other
hot compress to the eyelid for five to ten minutes, multiple times
daily. However, the efficacy of such an approach may be
limited.
[0008] In-office treatment of MGD is often limited to squeezing the
affected eyelids in order to express meibum from clogged or
inspissated glands. Most clinicians use their fingertip or a cotton
swab to apply pressure to the outer lid surface, but sometimes they
also use a swab or a flat metal device (sometimes called a Mastrota
paddle) on the inner lid while pushing against the outer lid in
order to squeeze meibum out. All of these techniques are cumbersome
for clinicians and painful for most patients.
[0009] Another in-office treatment uses intense pulsed light (IPL)
around the eyes and eyelids. Such treatments are said to produce an
improvement in dry eye symptoms over multiple sessions, but the
mechanism is not understood and the equipment is expensive.
[0010] Still another in-office treatment is the TearScience
LipiFlow.RTM. system, wherein heating elements are placed
underneath the eyelids and an automated external controller
maintains the heating elements at a target temperature while
applying a predetermined pattern of compression against the outer
lids by way of inflatable bladders. This system is expensive and
does not allow the clinician to control the treatment such to
visually monitor the eyelid margin and meibomian gland ducts and to
vary the level of heating and compression during the procedure in a
manner that optimizes the treatment outcome. Such clinician control
over the treatment may be important and is not present in the
TearScience system.
[0011] Patients may also use saline drops or artificial tears to
reduce the discomfort associated with dry eye; however, this
approach fails to treat the dysfunctional meibomian glands and
underlying inflammation. Additionally or alternatively, antibiotics
may be prescribed to reduce the bacterial load in and around the
eyelid. Topical and oral antibiotics are available, including oral
tetracycline derivatives, which reduce certain bacteria and provide
a mild anti-inflammatory effect; however, the administration of
antibiotics may cause side effects or adverse allergic reactions,
and the approach is often insufficient to provide significant
long-term relief of blepharitis and MGD. Corticosteroids may be
prescribed to reduce the inflammation; however, prolonged use of
such steroids increases the risk of detrimental cortical lens
changes, intraocular pressure spikes, and infection due to
immunosuppression.
[0012] A need therefore exists for improved methods and devices to
diagnose and treat meibomian gland dysfunction and blepharitis.
SUMMARY
[0013] Embodiments described herein may meet one or more of the
needs identified above and may overcome one or more of the
shortcomings of current MGD and blepharitis treatment methods.
Various implementations of systems, methods, and devices within the
scope of the appended claims each have several aspects, no single
one of which is solely responsible for the desirable attributes
described herein. Without limiting the scope of the appended
claims, some prominent features are described herein.
[0014] The present application relates generally to treatment
systems, methods, and devices used to treat eyelids, meibomian
glands, ducts, and surrounding tissue. Details of one or more
implementations of the subject matter described in this
specification are set forth in the accompanying drawings and the
description below. Other features, embodiments, and advantages will
become apparent from the description, the drawings, and the
claims.
[0015] In an aspect, a device for treating a mammalian eye having
an eyelid is provided, the device including: an energy transducer
having a device that emits light energy at multiple wavelengths,
including a first wavelength selected to pass through eyelid and a
second wavelength selected to be absorbed by the eyelid for
warming; a frontplate positionable proximate an outer surface of
the eyelid, the frontplate being made of a clear material that
passes the wavelengths of light emitted by the energy transducer,
the frontplate further including sensors configured to provide
information regarding a position of the eyelid relative to the
frontplate; a backplate positionable proximate an inner surface of
the eyelid, the backplate being made of or coated with an
energy-reflecting material configured to receive the first
wavelength of light energy transmitted through the eyelid and
reflect it back to the eyelid, the backplate further including
sensors configured to provide information regarding a position of
the eyelid relative to the frontplate; and wherein when the eyelid
is positioned between the frontplate and backplate and the light
energy from the energy transducer heats a target tissue region
sufficiently to melt meibum within meibomian glands located within
or adjacent to the target tissue region.
[0016] In embodiments, the device further includes an actuator
coupled to the frontplate and backplate configured to cause
relative movement between the frontplate and backplate to squeeze
the eyelid to express the meibomian glands. In embodiments, the
actuator is further configured to control the amount of light
energy emitted from the energy transducer at the second wavelength,
thereby controlling the heating of the target tissue. In
embodiments, the actuator is at least one of a lever, a button, a
wheel, a slider, and a switch.
[0017] In embodiments, the energy transducer is further configured
to provide light energy at a third wavelength selected to treat
bacteria. In embodiments, the energy transducer includes at least
one of an LED, laser, incandescent lamp, xenon lamp, halogen lamp,
luminescent lamp, high-intensity discharge lamp, and gas discharge
lamp.
[0018] In embodiments, the device further includes a visualization
device for viewing the eyelid during treatment. In embodiments, the
device further includes one or more components selected from the
group consisting of: a display or dashboard configured to display
the device status; a temperature measurement device configured to
measure various temperatures of the eyelid, including inner and/or
outer eyelid surface temperatures; a datalogger; a voice recorder;
a battery configured to power the device components; battery
charging means; a controller; printed circuit board; and
communication circuitry between shield and energy transducer.
[0019] In another interrelated aspect, a method for treating an eye
condition in a mammal is provided, the method including:
positioning a shield proximate an inner surface of an eyelid, the
shield being made of, or coated with, an energy-absorbing material,
the shield further including sensors configured to provide
information regarding a position of the eyelid relative to the
shield; positioning an energy transducer outside of an eyelid of
the mammal, the energy transducer configured to provide light
energy at one or more wavelengths; positioning an energy
transmission surface outside the eyelid, the energy transmission
surface including sensors configured to provide information
regarding a position of the eyelid relative to the energy
transmission surface; causing relative movement between the energy
transmission surface and the shield so as to modify a spaced
relationship between the energy transmission surface and the
shield; directing light energy from the energy transducer toward
the shield at a first wavelength selected to heat the
energy-absorbing material; and heating the energy-absorbing
material with the light energy to heat a target tissue region
sufficiently to melt meibum within meibomian glands located within
or adjacent to the target tissue region.
[0020] In embodiments, the method further includes directing light
energy from the energy transducer toward an outer surface of the
eyelid at a second wavelength selected to heat a target tissue
region within the eyelid. In embodiments, the method further
includes directing light energy from the energy transducer toward
the eye at a third wavelength selected to treat bacteria.
[0021] In embodiments, the method further includes compressing the
eyelid between the energy transmission surface and the shield. In
embodiments, the method further includes focusing the compression
on a sty or a pimple to treat a hordeolum. In embodiments, the
method further includes focusing the compression on an occluded
gland to treat a chalazion.
[0022] In embodiments, a safety feature electrically coupled to the
energy transducer prevents or interrupts the light energy from
occurring if the shield and associated assembly are not properly
attached to, and aligned with, the device.
[0023] In embodiments, the relative movement between the energy
transmission surface and the shield includes movement of the energy
transmission surface relative to the shield. In embodiments, the
relative movement between the energy transmission surface and the
shield includes a sliding movement of the energy transmission
surface relative to the shield. In embodiments, causing relative
movement between the energy transmission surface and the shield
includes actuating an actuator coupled to the energy transmission
surface. In embodiments, actuating an actuator includes pressing a
button. In embodiments, causing relative movement between the
energy transmission surface and the shield includes causing the
energy transmission surface to slide relative to the shield.
[0024] In embodiments, the position of the eyelid relative to the
positions of the shield and the energy transducing surface must be
within a predetermined range for the energy transducer to emit
light energy.
BRIEF DESCRIPTION OF THE DRAWINGS
[0025] The above-mentioned aspects, as well as other features,
aspects, and advantages of the present technology will now be
described in connection with various embodiments, with reference to
the accompanying drawings. The illustrated embodiments, however,
are merely examples and are not intended to be limiting. Throughout
the drawings, similar symbols typically identify similar
components, unless context dictates otherwise. Note that the
relative dimensions of the following figures may not be drawn to
scale.
[0026] FIG. 1A is a cross-sectional diagram of a mammalian eye
system 10.
[0027] FIG. 1B is a view of the underside surfaces of the upper and
lower eyelids showing meibomian glands with healthy, clogged and
atrophied glands.
[0028] FIG. 2A is a schematic block diagram of one embodiment of an
eye treatment device according to some embodiments.
[0029] FIG. 2B is a schematic block diagram of another embodiment
of an eye treatment device.
[0030] FIG. 2C is a schematic block diagram of another embodiment
of an eye treatment device having a scleral shield.
[0031] FIG. 2D is a schematic block diagram of another embodiment
of an ophthalmic device having a scleral shield with imaging
elements.
[0032] FIG. 2E is a close-up cross-sectional view of a portion of
the embodiment of FIG. 2D.
[0033] FIG. 2F is a front view of the embodiment shown in FIG.
2E.
[0034] FIG. 2G is a schematic block diagram of another embodiment
of an ophthalmic device similar to FIG. 2D.
[0035] FIG. 2H is a schematic block diagram of another embodiment
of an ophthalmic device similar to FIG. 2C.
[0036] FIG. 3A is a schematic block diagram of an embodiment of an
eye diagnostic and treatment device.
[0037] FIG. 3B is an enlarged view of one embodiment of a scleral
shield shown in FIG. 3A.
[0038] FIG. 4A is a schematic side plan view of one embodiment of
an eye treatment device.
[0039] FIG. 4B is a schematic front plan view of the energy
transducer and waveguide modules included in the eye treatment
device embodiment of FIG. 4A.
[0040] FIG. 4C is a schematic side plan view of the eye treatment
device embodiment of FIG. 4A shown in use.
[0041] FIG. 4D is a schematic side plan view of another embodiment
of an eye treatment device.
[0042] FIG. 4E is a perspective view of the optical elements in
another embodiment of an eye treatment device.
[0043] FIGS. 4F-H are front, side and cross-section views of the
prism element from FIG. 4E. FIGS. 4I-L are front, cross-section,
side and perspective views of the shaping lens element of FIG.
4E.
[0044] FIGS. 4M and 4N are theoretical graphical representations of
the irradiance patterns produced by the optical elements of 4E.
[0045] FIG. 5A is a schematic side plan view of a further
embodiment of an eye treatment device.
[0046] FIG. 5B is a schematic front plan view of the eye treatment
device embodiment of FIG. 5A.
[0047] FIGS. 5C-F are side, top, front and perspective views of
portions of another device embodiment.
[0048] FIGS. 5G and 5H are theoretical graphical representations of
the irradiance patterns produced by the optical elements of
5C-F.
[0049] FIG. 6 is a schematic side plan view of an embodiment of an
eye treatment system, which includes an eye treatment device and a
scleral shield.
[0050] FIGS. 7A-7H are schematic front plan and side views of
various embodiments of a scleral shield.
[0051] FIG. 8 is a schematic side plan view of another embodiment
of an eye treatment device.
[0052] FIG. 9 is a schematic side plan view of another embodiment
of an eye treatment device including one or more cooling
mechanisms.
[0053] FIG. 10 is a schematic side plan view of another embodiment
of an eye treatment device including one or more safety
sensors.
[0054] FIG. 11A is a schematic side plan view of another embodiment
of an eye treatment device.
[0055] FIG. 11B is a schematic side plan view of another embodiment
of an eye treatment device.
[0056] FIG. 12 is a schematic side plan view of another embodiment
of an eye treatment device including vibrational means.
[0057] FIG. 13 is a schematic diagram of one embodiment of an eye
treatment system in use by an individual.
[0058] FIG. 14A is a schematic side plan view of an embodiment of
an eye treatment system.
[0059] FIG. 14B is a schematic front plan view of a portion of the
eye treatment system embodiment of FIG. 14A.
[0060] FIG. 15A is a schematic side view of an embodiment of an eye
treatment instrument system.
[0061] FIG. 15B is a front sectional view taken along A-A of the
embodiment shown in FIG. 15A.
[0062] FIG. 15C is a front view of the embodiment shown in FIG.
15A.
[0063] FIG. 15D is a side sectional view taken along B-B of the
embodiment of FIG. 15A.
[0064] FIGS. 16A-O show unique configurations of the energy
transmission surfaces, the scleral shields and support arms of the
system, which define an aperture that allows viewing of one or both
eyelid margins during the application of heat and compression to
the portion of the eyelid being treated.
[0065] FIGS. 17A-C show an embodiment of an energy transducer
module in combination with an energy waveguide module and energy
transmission surface.
[0066] FIG. 17D shows a graphical representation of the irradiance
distribution of infrared light through an eyelid for the embodiment
of FIGS. 17A-C.
[0067] FIGS. 17E-F depict an element of an energy transmission
surface having a certain coating.
[0068] FIG. 17G is a graphical representation of the irradiance
distribution of infrared light through an eyelid for an embodiment
having a certain coating on a portion of the energy transmission
surface.
[0069] FIG. 17H shows the irradiance distribution of lime light on
the outer surface of an eyelid for an embodiment having a certain
coating on a portion of the energy transmission surface.
[0070] FIGS. 18A and 18B are front and side views of another
embodiment of an eye treatment device.
[0071] FIG. 19 is a view showing one embodiment of the frontplate
of the disposable.
[0072] FIG. 20 shows one embodiment of the eye treatment device
display showing details of the melt time.
[0073] FIGS. 21A and 21B are views showing one embodiment of the
eye treatment device having a movable light pipe.
[0074] FIG. 22 shows more features of the disposable including the
frontplate design elements.
[0075] FIG. 23 is an exploded view of the disposable of FIG.
22.
[0076] FIG. 24 shows more features of the disposable including the
thermal isolation of the backplate sensors.
[0077] FIG. 25 shows a graph of pulsing or interleaving the light
source and camera.
[0078] FIGS. 26A and 26B show embodiments of a camera used to view
and/or to photograph the surface of the eyelid and the margin to
detect blocked meibomian glands.
[0079] FIG. 27 shows another embodiment of backplate having a
heating portion to warm the eyelid.
[0080] FIGS. 28A and 28B are front and side views of another
embodiment of an eye treatment device in which the disposable may
be rotated between treatment of the top and bottom eyelids
DETAILED DESCRIPTION
[0081] In the following detailed description, reference is made to
the accompanying drawings, which form a part of the present
disclosure. In the drawings, similar symbols typically identify
similar components, unless context dictates otherwise. The
illustrative embodiments described in the detailed description,
drawings, and claims are not meant to be limiting. Other
embodiments may be utilized, and other changes may be made, without
departing from the spirit or scope of the subject matter presented
herein. It will be readily understood that the aspects of the
present disclosure, as generally described herein, and illustrated
in the Figures, can be arranged, substituted, combined, and
designed in a wide variety of different configurations, all of
which are explicitly contemplated and form part of this
disclosure.
[0082] The terminology used herein is for the purpose of describing
particular embodiments only and is not intended to be limiting of
the disclosure. It will be understood by those within the art that
if a specific number of a claim element is intended, such intent
will be explicitly recited in the claim, and in the absence of such
recitation, no such intent is present. For example, as used herein,
the singular forms "a", "an" and "the" are intended to include the
plural forms as well, unless the context clearly indicates
otherwise. As used herein, the term "and/or" includes any and all
combinations of one or more of the associated listed items. It will
be further understood that the terms "comprises," "comprising,"
"have," "having," "includes," and "including," when used in this
specification, specify the presence of stated features, integers,
steps, operations, elements, and/or components, but do not preclude
the presence or addition of one or more other features, integers,
steps, operations, elements, components, and/or groups thereof.
Expressions such as "at least one of," when preceding a list of
elements, modify the entire list of elements and do not modify the
individual elements of the list.
[0083] To assist in the description of the devices and methods
described herein, some relational and directional terms are used.
"Connected" and "coupled," and variations thereof, as used herein
include direct connections, such as being contiguously formed with,
or glued, or otherwise attached directly to, on, within, etc.
another element, as well as indirect connections where one or more
elements are disposed between the connected elements. "Connected"
and "coupled" may refer to a permanent or non-permanent (i.e.,
removable) connection.
[0084] "Secured" and variations thereof as used herein include
methods by which an element is directly secured to another element,
such as being glued, screwed, or otherwise fastened directly to,
on, within, etc. another element, as well as indirect means of
securing two elements together where one or more elements are
disposed between the secured elements.
[0085] "Proximal" and "distal" are relational terms used herein to
describe position from the perspective of a medical professional
treating a patient. For example, as compared to "distal," the term
"proximal" refers to a position that is located more closely to the
medical professional, while the distal end is located more closely
to the patient during treatment. For example, the distal ends of
the devices disclosed herein oppose the proximal ends of the same
devices, and the distal end of a device often includes, for
example, the end configured for placement against the eyelid of a
patient.
[0086] "Transducer" is a term used herein to describe an element
which receives one form of energy and transforms it into another.
For example, a light source may receive electrical energy and
produce light energy. Likewise, an ultrasonic transducer may
receive electrical energy and produce ultrasonic energy.
[0087] "Light" as used herein refers not only to energy in the
visible light spectrum, but also to energy in the infrared and
ultraviolet portions of the electromagnetic energy spectrum.
[0088] "Waveguide" as used herein refers to any means of
influencing the propagation, distribution or trajectory of
electromagnetic energy such as light, ultrasonic energy and radio
frequency energy. As defined herein, an optical elements such as
diffractors, refractors, diffusers and the like are included in
this broad definition of a waveguide.
[0089] "Optical path length" is used herein to describe the length
of the path (for example, within a tissue section) through which
energy travels.
[0090] Embodiments disclosed herein relate to ophthalmic devices,
systems, and methods. The devices, systems, and methods disclosed
herein can be used to treat meibomian glands, ducts, orifices, and
surrounding tissue and are particularly directed to the treatment
of MGD, blepharitis and conditions having a physiological
relationship with MGD and blepharitis, such as evaporative dry eye
disease. FIG. 1A is a cross-sectional diagram of a mammalian eye
system 10, which includes an eyeball 20 and surrounding eyelid
anatomy. As recited within this disclosure and as identified in
FIG. 1A, the "central ocular axis" 30 of the eye is the central
axis running through the center of the cornea 22, iris 24, pupil
25, lens 26, and vitreous body 28 of the eyeball 20. Eye system 10
includes an upper eyelid 12, a lower eyelid 14, and eyelashes 16.
Within the tissue of each eyelid 12, 14, there are meibomian glands
18 each having an orifice or duct 19. In healthy eye systems 10,
the meibomian glands 18 secrete out of ducts 19 a substance called
meibum, comprised primarily of lipids and proteins. The meibum
forms part of the tear film that covers the surface of the eyeball
20.
[0091] FIG. 1B is a view of the inner eyelid showing meibomian
glands with healthy, clogged and atrophied glands. Chronic blocking
of the glands is associated with MGD and some forms of blepharitis,
and may lead to capping of the ducts and/or atrophy of the glands.
Inflammation associated with MGD or blepharitis may in turn cause a
further constriction of gland ducts 19, leading to a reduction of
meibomian gland secretion, and accordingly, a decreased amount of
lipids in the tear film. Tear film with reduced lipid content may
evaporate quickly and lead to evaporative dry eye. A reduced tear
film may also be associated with increased levels of bacteria in
and around the eye. Such bacteria can aggravate the inflammation by
themselves or by certain by-products which are irritating to the
eye. It is believed that by periodically clearing our chronically
blocked glands, the glands can be spared from becoming permanently
atrophied.
[0092] Another factor thought to contribute to blepharitis is the
presence of Demodex folliculorum and Demodex brevis mites, which
are commonly found on most humans, reported in higher quantities on
individuals suffering from blepharitis. The mites may live in the
hair follicles of the eyelashes and eyebrows and in meibomian
glands and sebaceous glands. Their presence alone may lead to
inflammation in certain individuals, but it is also thought that
such mites may harbor certain bacteria which can be released into
the eyelid region during their lifecycle, leading to further
inflammation.
[0093] FIG. 2A is a schematic block diagram of an eye treatment
device 100 according to various embodiments. As shown in FIG. 2A,
the depicted eye treatment device 100 includes a power source
module 110, an energy transducer module 120, an energy waveguide
module 130, and an energy transmission surface 140 (also referred
to as a compression element). In some embodiments, the energy
waveguide module 130 may be optional. In other embodiments, the
energy transducer module 120 and energy waveguide module 130 may be
combined in a single unit.
[0094] The power source module 110 of various embodiments provides
energy to the energy transducer module 120. The power source module
110 may include any structure configured for delivering power to
one or more other components of the eye treatment device 100. In
some embodiments, the power source module 110 includes a disposable
battery, a rechargeable battery, a solar cell, a power transforming
module such as a power supply or power converter, or a power
transfer mechanism such as a cord, outlet, or plug configured to
receive alternating current or direct current from an external
source.
[0095] The energy transducer module 120 may include one or more
energy transducers configured to emit one or more forms or type of
energy. For example, as described in more detail below, in some
embodiments, the energy transducers emit photonic, acoustic, radio
frequency, electrical, magnetic, electromagnetic, vibrational,
infrared or ultrasonic energy. In some embodiments, the energy
transducer module 120 generates multiple types of energy
simultaneously or in a predetermined order.
[0096] The energy waveguide module 130 includes one or more
structures configured to control or focus the direction of energy
emission from the energy transducers. For example, the energy
waveguide module 130 may include one or more reflectors,
refractors, diffractors, or diffusers (described in more detail
below) configured to focus photonic energy toward a desired region,
or other structures for configuring and directing the energy
emission, such as ultrasonic horns or fiber optics.
[0097] The eye treatment device 100 of FIG. 2A may further
advantageously include an energy transmission surface 140
configured to further direct energy generated by the energy
transducer module 120 toward a desired region. For example, the
energy transmission surface 140 may include one or more lenses
configured to focus energy generated by the energy transducer
module 120.
[0098] In some embodiments, the energy waveguide module 130 and the
energy transmission surface 140 may also prevent or limit the
transmission of energy generated by the energy transducer module
120 to particular regions of the eye. The energy transmission
surface 140 may include regions that are substantially opaque or
non-transmissive to the energy produced by the energy transducer
module 120 and regions that are translucent or transmissive to the
energy produced by the energy transducer module 120. The modules of
the eye treatment device 100 are described in further detail below
in relation to other embodiments of the disclosure and may include
other components.
[0099] FIG. 2B is a schematic block diagram of an eye treatment
device 100 according to various embodiments. FIG. 2B is similar to
FIG. 2A and includes a power source module 110, an energy
transducer module 120, an optional energy waveguide module 130, and
an energy transmission surface 140. The energy transmission surface
140 may be substantially solid, or it may include elements that are
spaced apart from other parts of the energy transmission surface
140 or eye treatment device 100. For example, energy transmission
surface 140 may include an extension element that is positioned at
a certain distance from the solid portion of energy transmission
surface 140. For example, in FIG. 2B, extension element 143 is
depicted as a mesh-like structure spaced apart from the main
portion of energy transmission surface 140 (if any). Extension
element 143 may comprise a surface that is at least partially
transparent to the desired energy generated by energy transducer
module 120, while keeping a gap between the main portion of the
energy transmission surface 140 (if any) or the energy waveguide
(if any) or the energy transducer module and the eyelid surface 12,
14. The gap created by extension element 143 may be beneficial in
providing a path for forced-air cooling of the eyelid, for example.
Additionally, pressing extension element 143 against the eyelid
surface may reduce the optical path length for heating the eyelid
12, 14 and/or targeted components within the eyelid. Reducing the
optical path length may be advantageous for heating tissue due to
improvements in radiant throughput, decreased scattering,
refractive index matching, and increased fluence. Extension element
143 may be made of a low thermal mass material, like a thin-wire or
plastic mesh or perforated thin metal or plastic surface, and may
be structured to conform to the shape of the eyelid while applying
pressure to the surface of the eyelid. In one embodiment, extension
element 143 may be structured so that when it is pressed against
both the upper and lower eyelids, it can distribute the applied
pressure either uniformly or non-uniformly across the combined
upper and lower outer eyelid surfaces. For example, in one
embodiment, extension element 143 may apply less pressure to the
central ocular axis 30 and more pressure elsewhere, which may be
desirable in cases where pressure applied repeatedly to the eyelids
over the central ocular axis may be thought to increase the
possibility of developing a complication such as keratoconus. In
other embodiment, extension element 143 may be actively heated or
cooled.
[0100] FIG. 2C is a schematic block diagram of another embodiment
of an eye treatment device 100 having a power source module 110, an
energy transducer module 120, an optional energy waveguide module
130, an energy transmission surface 140 and scleral shield 300
(also referred to as a backplate). In this embodiment, one or more
eyelids 12, 14 are positioned between the energy transmission
surface 140 and scleral shield 300.
[0101] The energy transducer module 120 may include one or more
energy transducers configured to emit one or more forms or type of
energy. For example, as described in more detail below, in some
embodiments, the energy transducers emit photonic, acoustic, radio
frequency, electrical, magnetic, electromagnetic, vibrational,
infrared or ultrasonic energy. In some embodiments, the energy
transducer module 120 generates multiple types of energy
simultaneously or in a predetermined order. An optional energy
waveguide module may be included to control or focus the direction
of energy emission from the energy transducers, as described
above.
[0102] The eye treatment device 100 of FIG. 2C may further
advantageously include an energy transmission surface 140
configured to further direct energy generated by the energy
transducer module 120 toward a desired region. The energy
transmission surface 140 may include one or more lenses configured
to focus energy generated by the energy transducer module 120. The
energy transmission surface 140 (and/or extension element 143 shown
in FIG. 2B) may be movable along a movement path 145 in order to
adjust certain energy transmission properties (such as focus)
and/or to contact the surface of the eyelid 12, 14 and/or to apply
pressure to the eyelid 12, 14. By applying pressure to the eyelid
12, 14 while keeping scleral shield 300 in a fixed spatial
relationship relative to other parts of eye treatment device 100,
the eyelid 12, 14 may be compressed, thereby reducing the optical
path length for heating the eyelid 12, 14 and/or targeted
components within the eyelid. Reducing the optical path length is
advantageous for heating tissue due to improvements in radiant
throughput, decreased scattering, refractive index matching, and
increased fluence. The eyelid may be compressed by the backplate
300 compressing or pushing the eyelid against the compression
element. Or the eyelid may be compressed by the compression element
compressing or pushing the eyelid against the backplate 300.
[0103] In some embodiments, the energy transducer module 120 may
generate multiple types of energy simultaneously, such as photonic,
acoustic, radio frequency, electrical, magnetic, electromagnetic,
vibrational, infrared or ultrasonic energy. For example, a first
energy may heat the outer surface of the eyelid while a second
energy may penetrate more deeply into the eyelid tissue and/or
interact with the scleral shield in modes described in further
detail below.
[0104] FIG. 2D is a schematic block diagram of another embodiment
of an eye treatment device 100 having a power source module 110, an
energy transducer module 120, an optional energy waveguide module
130, an energy transmission surface 140 and scleral shield 300,
similar to FIG. 2C. In some embodiments, the scleral shield 300 may
further include an image translator 155 integrated into scleral
shield 300. FIG. 2E shows a close-up cross-sectional view of image
translator 155 embedded in scleral shield 300, with eyelid 14
positioned adjacent to image translator 155. In the embodiment
shown, image translator 155 is reflective. Illumination energy 170,
which may be visible or infrared light, for example, is passed
through eyelid 14 and therefore through meibomian glands 18, and
then along optical path 175 through energy transmissive material
185 as it reflects off of reflective surfaces 180, eventually
exiting image translator 155 above the eyelid margin 14a. It will
be appreciated that the resulting image appearing out of image
translator 155 will be a shadow image, or transilluminated image,
of that portion of eyelid 14 that is adjacent to image translator
155 and which is illuminated by illumination energy 170. In this
manner, image translator 155 allows viewing of a transilluminated
image 190 of the inner side of the eyelid 14 under direct
visualization or with the aid of a magnifying element or camera,
shown collectively as a visualization device or visualization means
160, without having to evert the eyelid. FIG. 2F is a front view of
the same embodiment shown in FIG. 2E, showing transilluminated
images 190 of the meibomian glands.
[0105] Image translator 155 may comprise a set of mirrored surfaces
or a prism having reflective surfaces. Alternatively, image
translator may comprise a light-bending element such as a light
pipe, a fiberoptic bundle, an image sensor, or some combination
thereof. It will be appreciated that various desirable optical
properties may be incorporated into image translator 155, such as
image projection, angulation or magnification. Such properties may
be achieved, for example, by curving the reflective surfaces 180,
by shaping the surfaces of transmissive material 185 and/or by
varying the index of refraction, by varying the density and
distribution of fiber elements in a bundle, or by some combination
thereof. In embodiments where image translator 155 includes an
image sensor, such sensor may be of a CCD-type, CMOS type,
luminescent concentrator (such as has been fabricated at Johannes
Kepler University, Linz, Austria), or any type of sensor that can
capture the transillumination data and translate it into either
visual, optical or electrical information.
[0106] In some embodiments, visualization of eyelid margin 14a
during diagnosis and treatment of eyelid 14 provides a significant
benefit. For example, as described above, positioning eyelid 14
between the energy transmission surface 140 and scleral shield 300
having image translator 155 allows visualization of the
transilluminated image of the eyelid and meibomian glands. As shown
in FIG. 1B, the morphology of healthy, clogged and atrophied glands
is distinct enough to allow diagnosis of the status of each gland
by viewing a transilluminated image of the glands. Referring back
to FIG. 2D, gland status may be also be evaluated without
transillumination by observing eyelid margin 14a while moving
energy transmission surface 140 along movement path 145 to press
against eyelid 14. As the eyelid 14 is compressed, eyelid margin
14a is observed and gland status is assessed by the quality and
quantity of secretions from ducts 19, as discussed previously.
[0107] If treatment is desired after diagnosis, eye treatment
device 100 may be repositioned along eyelid 14 so that the
preponderance of diseased glands are positioned between energy
transmission surface 140 and scleral shield 300. Once ideally
positioned, energy transmission surface 140 may be moved along
movement path 145 to contact the surface of the eyelid 12, 14
and/or to continue to move toward the scleral shield 300 and apply
pressure to the eyelid 12, 14.
[0108] Referring again to FIG. 2D, an optional coupling medium 195
may be positioned between the eyelid 12, 14 and the energy
transmission surface 140. Coupling medium 195 may be a fluid, gel,
cream or the like, and may contain an agent such as glycerol, which
can increase the efficiency of light transmission into the eyelid
and target tissue by reducing light scattering and increasing light
transmittance by reducing the refractive mismatch between the
eyelid 12, 14 and the energy transmission surface 140. It may also
assist in reducing scattering by hydrating portions of the eyelid
skin surface such as the stratum corneum.
[0109] FIG. 2G is a schematic block diagram of another embodiment
of an eye treatment device 100 having a power source module 110, an
energy transducer module 120, an optional energy waveguide module
130, an energy transmission surface 140, and image translator 155
integrated into scleral shield 300. The image translator 155 allows
at least a portion of the energy from the energy transmission
surface 140 to be redirected toward the inner side of the eyelid
14. For example, the eyelid 14 may be positioned between the energy
transmission surface 140 and scleral shield 300 which includes the
image translator 155. The energy transmission surface 140 directs
energy toward at least one of the outer side of the eyelid and the
image translator 155. The image translator 155 is able to redirect
energy from the energy transmission surface 140 toward the inner
side of the eyelid. The benefit of directing energy via the image
translator 155 to the inner surface of the eyelid is that it can
provide an efficient mode of delivering energy, and thus heat, to
at least the portion of the inner surface adjacent to the eyelid
margin. By combining this mode of heating (via image translator
155) with the mode of heating whereby the energy is directed
through the eyelid, overall heating efficiency of the inner eyelid
surface may be optimized, and preferential additional heating of
the inner surface adjacent to the lid margin may be achieved, since
that is the zone where significant clogging and blockage may occur.
An additional temperature sensor may be positioned near the inner
eyelid surface tissue adjacent to the lid margin, where the
preferential additional heating may occur (described and depicted
below with reference to FIG. 3A).
[0110] FIG. 2H is a schematic block diagram of another embodiment
of an eye treatment device 100 having a power source module 110, an
energy transducer module 120, an optional energy waveguide module
130, an energy transmission surface 140 and scleral shield 300,
similar to FIG. 2C. In some embodiments, the scleral shield 300 may
further include an energy conversion coating 194 capable of being
activated by certain types of energy passing through the eyelid. In
one embodiment, the energy conversion coating 194 is able to
convert the direction of energy back toward the inner side of the
eyelid, using the same form of energy that originally passed
through the eyelid. In another embodiment, the energy conversion
coating 194 may alter the type of energy and direct or emit the
altered energy in a preferred direction. In one embodiment, the
coating is a phosphorescent. By way of example, the energy
transmitted through the eyelid may be visible or infrared light of
a wavelength that passes readily through the tissue with little
absorption, and once that energy reaches energy conversion coating
194, the phosphorescent material emits light energy of a different
wavelength that is more readily absorbed by the tissue adjacent to
the coating, which, in the preferred embodiment, would be the inner
surface of the eyelid, containing the meibomian glands. In another
embodiment, a certain form of energy absorbed by the coating
triggers an exothermic chemical reaction that may heat the inner
surface of the eyelid. Some embodiments of FIGS. 2A-2H may also
include one or more of the following: a scleral shield with support
arms, a reflective imager integrated into scleral shield, a display
of various temperatures, a consumable portion, a connector and
circuitry for communication between device and the consumable in
order to identify the consumable and prevent reuse, a data logger,
a voice recorder and a camera with recording and/or transmission
capability activated by certain types of energy passing through the
eyelid. In one embodiment, the energy conversion coating 194 is
able to convert the direction of energy back toward the inner side
of the eyelid, using the same form of energy that originally passed
through the eyelid. In another embodiment, the energy conversion
coating 194 may alter the type of energy and direct or emit the
altered energy in a preferred direction. In one embodiment, the
coating is a phosphorescent material that is activated by the
energy transmitting through the eyelid from the energy transmission
surface 140. By way of example, the energy transmitted through the
eyelid may be visible or infrared light of a wavelength that passes
readily through the tissue with little absorption, and once that
energy reaches energy conversion coating 194, the phosphorescent
material emits light energy of a different wavelength that is more
readily absorbed by the tissue adjacent to the coating, which, in
the preferred embodiment, would be the inner surface of the eyelid,
containing the meibomian glands. In another embodiment, a certain
form of energy absorbed by the coating triggers an exothermic
chemical reaction that may heat the inner surface of the
eyelid.
[0111] FIG. 3A is a schematic side plan view of one embodiment of
an eye treatment device 200. The eye treatment device 200 shown in
FIG. 3A is shown to be positioned relative to an eyeball 20 for
treatment of the eyelid 14 for MGD, blepharitis and other medical
conditions. In some embodiments, the eye treatment device 200 is
configured to heat the inner and/or outer surfaces of the eyelid
while compressing the eyelid. As the heat from the eye treatment
device 200 is transmitted to the eye system 10, particularly to the
treatment tissue such as the meibomian glands, the heat can soften
the meibum and thereby allow the meibum to be more readily
expressed during massage or eye exercises. The eye treatment device
200 can include configurations of the modules depicted in FIGS.
2A-2H, along with additional components useful in operation of the
eye treatment device 200.
[0112] The eye treatment device 200 can include a housing 202
coupled with a removable or consumable portion 260, which may be
coupled to housing 202 u engagement means 186, which can be pins,
alignment guides, slide locks, and the like. Housing 202 may
include a power source module 110, an optional controller 212, an
energy transducer module 120, and an energy transmission surface
140 in a slidable relationship along movement path 145 with energy
transducer module 120. Alternatively, energy transmission surface
140 may linked with, or part of, energy transducer module 120, and
optionally thermal management structure 220, and together they may
be in a slidable relationship with respect to housing 202 or other
parts of eye treatment device 200. Movement of energy transmission
surface 140 and linked parts may be done using actuator 182, for
example. The energy transducer module 120 of some embodiments, such
as is shown in FIG. 3A, may include an LED device formed of one or
more of an LED emitter 207, an LED lens 208, a thermal management
structure 220, and an energy transducer module driver 209. The
housing 202 may further include visualization means 160 for
enhanced monitoring of the eyelid margin during diagnosis and
treatment, a display or dashboard 218 showing various temperatures
of the eyelid, such as inner and/or outer surface temperatures, a
datalogger 214, voice recorder 213, and circuitry 226 a for
communication between device and consumable circuitry 226 b in
order to identify the type of consumable, ensure that the
consumable is in proper alignment and/or prevent reuse of the
consumable. The consumable portion 260 may include a scleral shield
300 that can be positioned between the eyelid 12, 14 and eyeball 20
to cover sensitive anatomy of the eye system 10 (such shown in FIG.
1). For example, the scleral shield may be positioned over the
sclera 21 and cornea 22 and may also provide protection to other
internal anatomy of the eye such as the iris 24, pupil 25, lens 26,
and other light sensitive anatomy of the eye system 10. Use of the
scleral shield 300 can increase safety and reduce the potential of
harmful light emissions from the energy transducer module 120
reaching and damaging sensitive eye anatomy. The scleral shield 300
may be formed from an energy absorbing material and/or may have an
energy absorbing front face 302. In either case, energy transmitted
through the eyelid which is absorbed by the scleral shield 300 or
energy absorbing front face 302 may heat the shield or front
surface, respectively, and thereby provide warmth to the inner
surface of the eyelid. The back surface and edges of scleral shield
300 are preferably made from a material and process that ensures a
smooth, burr-free finish that cannot cause injury, or reduces the
likelihood of injury, to the cornea or other sensitive eye
structures. In one preferred embodiment, the back surface and edges
are covered with an expanded Teflon.RTM. (ePTFE) material. The
scleral shield 300 may also incorporate one or more temperature
sensors 310 in order to monitor temperature, as well as force or
pressure sensors 221 to monitor the amount of force or pressure
applied on the eyelid. Electrical conductors such as wires 420 may
connect sensors 310 and 221 to circuitry in the housing 202. FIG.
3B shows one embodiment of a scleral shield 300 further including
an image translator 155 which, as described previously, enables
viewing of the inner side of the eyelid 14 and the meibomian glands
behind the eyelid. In some embodiments, the scleral shield 300 may
further include a data transmission means and/or an embedded power
source, both discussed in more detail below as data transmission
means 320 and embedded power source 330, such as in FIG. 7A. By way
of further clarification, scleral shield 300 may be coupled to
housing 202 in various manners such as with one or more wires 420,
such wires having insulation with sufficient mechanical strength to
serve as support arms 262. In addition, some embodiments may have
circuitry 226 a and 226 b for communication between the device and
the consumable.
[0113] In some embodiments, a lens 208 may be used, such as an LED
lens over the LED emitter 207. In some embodiments, the LED lens
208 may be a specially shaped lens used to control the direction
and intensity of the LED emitter 207 to the desired treatment
tissue and/or the scleral shield 300. In some embodiments, the
energy transmission surface 140 may act as a lens or used in
combination with a lens, to focus and direct the energy from the
energy transducer module 120 or LED emitter 207 to the desired
treatment areas.
[0114] Each of these components, either alone, or in combination
with other components any of the embodiments described herein.
[0115] The eye treatment device 200 can include a power source
module 110 for providing power to the various components of the eye
treatment device 200 and may be electrically coupled to some or all
of the components. In some embodiments, the power source module 110
is battery operated using either regular or rechargeable batteries
that may be coupled to a recharging system. In other embodiments,
the power source module 110 may be coupled to an external power
source, such as an electrical outlet or external battery supply. In
some embodiments, the power source module 110 may be electrically
coupled with the controller 212 to receive instructions from the
controller 212 to provide electrical energy to the various
components of the eye treatment device 200.
[0116] In certain embodiments having a controller 212, the
controller 212 can receive input instructions from a user (for
example, through a user interface device 270, such as a button,
switch, touch screen, voice commands, from another module or
device, such as a smartphone) to emit light from the LED emitter
207. Upon receipt of the user input instructions, the controller
212 can instruct the power source module 110 to deliver energy to
or from the energy transducer module driver 209 which enables LED
emitter 207 to convert the electrical energy from the power source
module 110 into another form of electromagnetic energy (such as
light). In this manner, the energy transducer module driver 209 and
the LED emitter 207 can act as a transducer of the electrical
energy received from the power source module 110.
[0117] The energy transducer module driver 209 can comprise any
LED-powering and controlling circuitry, whether configured as an
actual printed circuit board, an integrated circuit, or discrete
components. In some embodiments, it serves the function of an LED
driver, providing a controlled current, voltage or power level
through the LED emitter 207 within the LED specifications to
provide a desired illumination intensity therefrom. Optionally, the
LED printed circuit board can include a pulse-width modulation
function, PID circuit, or similar scheme in order to modulate the
effective intensity of the emissions over time to achieve a desired
heating of a target region of the eyelid.
[0118] The LED emitter 207 is a part of one type of energy
transducer module 120 that can be configured to emit light of the
appropriate wavelength necessary for the desired treatment. The
treatments may include one or more of the following: diagnosing the
eyelids 12, 14 by the illuminating the inner and/or outer surfaces,
eyelid margins, and/or the meibomian glands behind the eyelids;
heating the target tissue region of the eye system 10 (e.g., the
meibomian gland behind the eyelids 12, 14); and antibacterial
treatment to kill bacteria in the eye system 10. Note that the
descriptions of the various devices herein (including the eye
treatment device 200) are exemplary, and not limiting. Thus, for
example, while this detailed description mentions particular
elements and circuitry having particular functions, this does not
limit the disclosure to those particular embodiments. For example,
while LEDs are mentioned, other light sources, such as
incandescent, xenon, halogen, high-intensity discharge, cold
cathode tube, fluorescent, laser and other light sources or energy
sources can be used. Similarly, while a controller 212 and energy
transducer module driver 209 are mentioned, it will be understood
that the controller could be integrated with driver circuitry for
the light source or circuitry for a solid-state or other power
supply, or other configurations could be used to provide the
desired result. Further, some or all of the functions described as
being handled by, or controlled by, controller 212, may be
implemented using discrete logic or analog circuitry, or a
combination thereof. Moreover, although the various embodiments
such as eye treatment device 200 are illustrated schematically,
they can be produced in a variety of handheld or stationary
configurations with optional gripping surfaces, manipulation and
control structures, and the like. Furthermore, the devices
described herein can be designed for use in a plurality of
settings, including in-home use and use within an eye care
professional's office, a health clinic, or other healthcare
facility.
[0119] In some embodiments, the energy transducer module 120 can
instead be, for example, a broad-spectrum lamp, such as an
incandescent, xenon, or halogen lamp. Such broad-spectrum lamps can
be used in conjunction with one or more color filters to remove
specific wavelengths not necessary for the treatment of the eye
condition, or to remove specific wavelengths that may be harmful to
the treatment tissue in the target region (e.g., meibomian glands
18) of the eye system 10 during application of energy from the
energy transducer module 120 to the treatment tissue.
[0120] In some embodiments, the energy emitted from the power
source module 110 can be converted into visible light and can be
emitted by the LED emitter 207. For some embodiments, it is
desirable to use light with a wavelength selected to: a) penetrate
the eyelid to the depth of the meibomian gland (e.g., typically
about 1-2 mm in certain individuals) or other adjacent target
tissue in the eyelid, and be absorbed there, b) minimize the amount
of light that penetrates beyond the eyelid tissue, and c) minimize
the amount of heating that occurs at the surface of the eyelid. For
example, in some embodiments, the LED emitter 207 can emit light
having a wavelength in the range of about 400-700 nm. In some
embodiments, the LED emitter 207 can emit light that is
substantially a single color selected for optimal treatment of the
meibomian glands 18 in the eye system 10. In some embodiments, the
LED emitter 207 can emit light in a range of wavelengths, the
wavelength being selectable based on the treatment requirements of
the patient, or based on the intended purpose of the particular
step in a multi-step treatment regimen.
[0121] In some embodiments, an illumination source emitting
wavelengths in the range of 500-600 nm is chosen. In selecting
wavelengths in the range of 500-600 nm, a plurality of
considerations may be taken into account. For example, this range
may be selected to achieve the highest absorption of light rays in
tissue. Light energy incident on mammalian skin is reflected,
transmitted, or absorbed. Reflection is a function of skin
properties, wavelength, and angle of incidence. Light rays that
reach the skin surface orthogonal to the plane of the surface are
reflected less than those that reach the skin at an oblique angle.
Transmission of light through the skin is a function of internal
scattering, wavelength, and absorption. Internal scattering is a
function of the chemical and physical properties of the skin and
underlying tissues. Eyelid thickness, density of keratinocytes,
collagen, and fat may play a role. Absorption is primarily a
function of the concentration and distribution of certain molecules
called chromophores which tend to selectively absorb certain
wavelengths of light. In human skin, the primary chromophores that
absorb light in the visible spectrum are oxyhemoglobin,
deoxyhemoglobin, various melanins, and to some extent, water. Water
does not significantly absorb wavelengths of light until the deep
red and infrared part of the spectrum. Melanins tend to have a
fairly high degree of absorption of the visible spectrum, tapering
off gradually as wavelength increases. Two absorption peaks for
oxyhemoglobin are seen at around 532 nm and 577 nm. Deoxyhemoglobin
peaks around 550 nm.
[0122] In various embodiments, engineering constraints also affect
wavelength selection. The wavelength selected is one that can be
emitted by a device, which can be readily produced in a practical
configuration, with a wattage and physical package appropriate for
a device that delivers light energy to the eyelid. In the case of
very high power LEDs, there are presently limited choices, although
future improvements are likely. For example, LED Engin Inc. (San
Jose, Calif.) produces green LEDs in a 10 W version, such as
LZ4-00G108, having a nominal center/peak wavelength of around 523
nm. Limited quantities are also available with peak wavelengths of
about 527 and 532 nm.
[0123] Various embodiments emit wavelengths within the 500-700 nm
portion of the visible spectrum in order to produce the desired
tissue heating effect without excessive transmission through the
eyelid (and subsequent unwanted heating of structures beyond the
eyelid), and without excessive surface heating. Furthermore,
emitting wavelengths within this portion of the visible light
spectrum avoids the undesired portion of the electromagnetic
spectrum for embodiments that do not incorporate a scleral shield,
including ultraviolet, infrared, and blue.
[0124] In some embodiments, longer wavelengths of light are used
penetrate deeper into the tissue. For example, `red` and
near-infrared (NIR) at wavelengths between 700-1000 nm pass more
readily through the eyelid, penetrating more deeply than the
wavelength ranges described above. There is an "optical window" of
human tissue around 800-900 nm, where energy passes most
efficiently through tissue and eyelids due to the fact that
chromophore absorption is at its lowest level. For the application
of light therapy to the eyelids without the use of a scleral
shield, the use of NIR would likely not be used due to excessive
light energy passing through the eyelid directly to the eye,
possibly affecting sensitive tissues of the eye. When using the
scleral shield to protect the eye, however, NIR may be used
advantageously to pass through the eyelid. For example, NIR at 850
nm may pass through the eyelid and be absorbed by the scleral
shield, which, in turn, can warm adjacent tissue on the inner
surface of the eyelid. For completeness of discussion, it should be
noted that certain wavelengths of short-wavelength and
mid-wavelength infrared (sometimes referred to as IR-B and IR-C)
have higher levels of absorption by water than the highest combined
absorption of the other chromophores discussed above. In
particular, a wavelength of 3,000 nm has been shown to have such
higher absorption. As such, there may be embodiments that use this
wavelength or others within the band safely, with or without a
scleral shield. Note that there are also other "optical windows"
(in addition to the window mentioned at 800-900 nm) at these higher
wavelengths, which may be advantageous to utilize in some
embodiments.
[0125] In some embodiments, an illumination source emitting blue or
violet light in the range of 400-450 nm may be used to reduce
and/or eliminate bacteria in the eye system 10. It is known that
exposure to visible light, more specifically, blue or violet light
wavelengths, causes inactivation of certain bacterial species.
Common bacteria include S. aureus, S. epidermidis, B. oleronius,
and P. acnes. In selecting wavelengths in the range of 400-450 nm,
a plurality of considerations may be taken into account. For
example, it is important that the emitting source (LED) does not
emit a significant amount of energy below about 400 nm, which is in
the UVA spectrum and can be associated with skin cancer.
[0126] In another embodiment, one or more wavelengths of light may
be chosen which are preferentially absorbed by the exoskeletons,
internal structures or eggs of the Demodex mites, in order to kill,
inactivate or interrupt reproductive processes.
[0127] In some embodiments, an illumination source may be used to
characterize the tear film thickness and stability. For example,
the energy transducer module could have a cobalt blue source, and
the visualization means 160 (viewing lens, for example) could have
a yellow Wrattan filter, and the patient could be given fluorescein
eye drops, whereby the clinician could measure the tear break-up
time by viewing the surface of the eye through the Wrattan filter.
Alternatively, various wavelengths of photonic energy could be
shined onto or across the surface of the eye, with or without
indicator eye drops, and either through direct visual observation
or image capture and processing, the stability and/or thickness of
the tear film and/or lipid layer may be determined.
[0128] In another embodiment utilizing LEDs as an illumination
source, the LED emitter 207 can include one or more multi-spectral
LEDs or multiple LEDs to emit light of differing or the same
wavelength from each LED. In some embodiments, each LED of the LED
emitter 207 is configured to emit light of a different wavelength.
The LED emitter 207 can emit the light from each differently
colored LED either consecutively or simultaneously. For example, in
some embodiments, the LED emitter 207 can include a red, green,
blue (RGB) LED system, or other multi-spectral LED system, to emit
light of various wavelengths in the visible light spectrum and IR
spectrum. In some embodiments, the LEDs of the LED emitter 207 can
be configured to operate simultaneously to emit white light.
Alternatively, in some embodiments, the user can select the
wavelength of light to be emitted from the multi-spectral LEDs.
Further, an LED with using a special phosphorescent coating may be
fabricated in order to produce the most efficient output spectrum
relative to input power.
[0129] In some embodiments, the LED emitter 207 can include a
high-intensity LED array. The high-intensity LED array, as part of
the LED emitter 207, can, in some embodiments, operate at an input
power rating of about 0.5-75 W, but preferably in a range of 1-10
W. To help keep the temperature of energy transducer module 120
within functional limits, thermal management structure 220 (such as
a heat sink other substantial thermal mass) may be thermally linked
to LED emitter 207. In a specific embodiment, the high-intensity
LED array may emit light having a wavelength of between about
500-600 nm.
[0130] The energy transducer module 120 can, in some embodiments,
provide electromagnetic energy to the treatment tissue in the form
of infrared energy, such as in the NIR band described above. For
example, the LED emitter 207 can be a commercially available LED
such as LZ4-00R408, which emits 850 nm NIR and is manufactured by
LED Engin, Inc. (San Jose). Additionally, the energy transducer
module 120 can be another source of infrared energy instead of an
LED light source, such as, for example, an incandescent, xenon,
halogen, cold incandescent, or halogen broad spectrum lamp
configured to emit infrared energy to the treatment tissue
site.
[0131] The eye treatment device 200 may include a reflector (such
as reflector 210 in other embodiments below), which may act as a
waveguide to direct the electromagnetic energy (e.g., light)
emitted from the energy transducer module 120. The reflector can be
configured to direct electromagnetic energy evenly from the point
source, such as, for example, the LED emitter 207, through the
energy transmission surface 140, to the target treatment site of
the patient.
[0132] The energy transducer module 120 can include an LED lens 208
that can be used in conjunction with the LED emitter 207 or other
electromagnetic energy source to direct the energy to the eyelid at
a desired angle or in a desired pattern, at a desired
intensity.
[0133] Shown in FIG. 3A is an energy transmission surface 140
forming part of the eye treatment device 200. The energy
transmission surface 140 has a slidable relationship along movement
path 145 relative to the energy transducer module 120. The energy
transmission surface 140 can be positioned in the housing 202 at a
location distal to the energy transducer module 120, and positioned
in between the energy transducer module 120 and the tissue
treatment site of the eye system 10. Positioned in this manner, the
energy transmission surface 140 can pass, or receive and transmit,
the electromagnetic energy transmitted from the energy transducer
module 120. In some embodiments, the energy transmission surface
can be a concave shape (relative to the eye treatment device 200),
such that the energy transmission surface 140 corresponds to the
shape of the eyelids 12, 14 when closed. The energy transmission
surface 140 may be shaped such that any electromagnetic energy
emanating from the energy transducer module 120 must pass through
the energy transmission surface 140.
[0134] In some embodiments, the energy transmission surface 140 is
positioned adjacent to the eyelids 12, 14, and does not physically
contact the eyelids 12, 14, but instead transfers heat to the
treatment tissue radiantly. The energy transmission surface 140 can
be substantially transparent to the desired electromagnetic energy
transmitted by the energy transducer module 120 to allow for the
transmission of energy from the energy transducer module 120
without significantly hindering the desired energy type or
wavelength from reaching the treatment tissue. In some embodiments,
the energy transmission surface 140 can be made of an optical
plastic, sapphire, glass, calcium fluoride, or fiberglass. It can
have an easy to clean outside surface and can be scratch resistant.
Optionally, a temperature sensor 310 may be positioned on, in or
adjacent to energy transmission surface 140 to provide temperature
feedback for the energy transmission surface 140 and/or the outer
surface of the eyelid.
[0135] In some embodiments, the energy transmission surface 140 can
be configured to operate in conjunction with the energy transducer
module 120 to filter unwanted wavelengths from reaching the
treatment tissue or other portions of the eye system 10. For
example, in some embodiments, the illumination source may transmit
electromagnetic energy in both the IR and visible light spectra.
The energy transmission surface 140 can be used to allow passage
of, for example, the energy from the visible light spectrum, but
filter out the energy from the IR spectrum. Likewise, if it is
desired that only energy from one color reaches the treatment
tissue, the energy transmission surface 140 can be used as a
bandpass filter or be used with a filter to restrict passage of
energy of wavelengths other than the color desired.
[0136] In some embodiments, the energy transmission surface 140 can
be configured to come in physical contact with the eyelids 12, 14.
As discussed above, in some embodiments the energy transmission
surface 140 may be in a slidable relationship along movement path
145 with the energy transducer module 120. This allows the energy
transducer module 120 to be in a fixed relationship with the eyelid
while the energy transmission surface 140 may be moved forward into
contact with the eyelids 12, 14. Alternative approaches to reducing
the space between the outer surface of the eyelids 12, 14 and the
energy transmission surface 140 are possible. For example, the
energy transducer module 120 and energy transmission surface 140
may move together toward the eyelids, with the scleral shield 300
remaining in a relatively fixed position, or the scleral shield 300
may move relative to the other parts of the device. In any case,
movement is preferably done manually by the clinician in order to
allow the clinician some measure of tactile feedback. In certain
embodiments, the eye treatment device 200 may include an actuator
182 such as a lever, button, wheel, slider or switch to move the
energy transmission surface 140.
[0137] In some embodiments, at least a portion of energy
transmission surface 140 may be configured as a single-use cover
element or outer eyelid pad 147, as shown in FIG. 3A. Preferably,
such outer eyelid pad 147 is incorporated into the consumable
portion 260 of the device, wherein the outer eyelid pad 147 is
automatically aligned and loaded onto energy transmission surface
140 as the consumable portion is attached to the housing 202.
[0138] In some embodiments, the energy transmission surface 140 may
be heated to conductively transfer heat to the treatment tissue. In
other embodiments, most of the tissue heating occurs as a result of
radiant heating from the energy transducer module 120 to the tissue
and/or the scleral shield 300, wherein substantially all of the
desired electromagnetic energy passes through energy transmission
surface 140, with little or no heating of the energy transmission
surface 140. In still other embodiments, tissue heating may be done
as a result of a combination of conductive heating caused by
pre-heating or active heating of energy transmission surface 140
and radiant heating of tissue and/or the scleral shield. The energy
transmission surface 140 may incorporate an energy-absorbing layer
or pattern that may be pre-heated by light energy or other means,
for example up to 42 degrees Celsius, prior to contact with the
outer surface of the eyelid. Or, energy transmission surface may be
made from a thermally-conductive material and may be heated by a
heater that is thermally linked to energy transmission surface 140.
In the case where energy transmission surface 140 is made from a
thermally-conductive material, the material may be transmissive to
an energy source (such as light) coming from energy transducer
module 120, or it may be solid, opaque or otherwise not
transmissive to another form of energy other than conductive
heating. In the case where energy transmission surface 140 is
opaque or non-transmissive, it may be made from a conductive metal
such as copper or aluminum, in which case energy transmission
surface 140 may be heated by an energy transducer module 120
comprising any means of heating a thermal mass (such as a resistive
heater), and then pushed against the eyelid to conductively heat
the eyelids. In the case where energy transmission surface 140 is
transmissive to another form of energy as well as thermally
conductive, it may be fabricated from materials such as sapphire,
calcium fluoride, diamond, graphene and the like. In one preferred
embodiment, up to three modes of heating may occur simultaneously:
i) the inner surface of the eyelid is warmed using red or infrared
light transmitted to an energy-absorbing scleral shield 300, ii)
eyelid tissue is heated radiantly by visible light (e.g., green)
which is absorbed by chromophores, and iii) eyelid tissue is heated
conductively by bringing a pre-heated energy transmission surface
140 into contact with the outer surface of the eyelid. It will be
appreciated that a significant advantage of using the light-based
heating techniques described herein, and specifically infrared
heating of an energy-absorbing surface, alone or in combination
with the other two modes of heating (visible light heating of
chromophores and conductive heating of the tissue), heating of the
target tissue may be accomplished significantly faster than with
any conventional method of conductive heating of the outer or inner
eyelid surfaces. Specifically, with these combined modes, the
meibomian gland tissue may be brought up to a temperature of, for
example, about 40-42 degrees Celsius, in less than one minute.
Specifically, in some cases, the meibomian gland tissue may be
brought to about 40-42 degrees Celsius within 10, 15, 20, 25, 30 or
45 seconds.
[0139] As shown in FIG. 3A, a visualization device or means 160 may
be used to view the eyeball 20. In some embodiments, the
visualization means 160 may be part of eye treatment device 200. In
other embodiments, the visualization means 160 may be a separate
component. The visualization means 160 may include, for example, a
magnifier, a camera, microscope, a slit lamp instrument, or other
suitable visualization instrument.
[0140] In some embodiments, the scleral shield 300 may further
include an image translator 155 that allows viewing of a
transilluminated image of a portion of the eyelid and the meibomian
glands. As described previously, the image translator may include,
for example, one or more reflective surfaces, mirrors, light pipes,
prisms, fiber bundles, image sensors or other suitable image
translation means. As shown in FIG. 3A, the image translator 155 is
integrated into scleral shield 300, but in other embodiments, the
image translator 155 may be a separate component.
[0141] In some embodiments, an additional shielding element 258 may
be used to prevent unwanted photonic energy (such as IR or
blue/violet light) from reflecting off the transillumination
element back to the clinician. For example, the shielding element
258 may be a thin, opaque shield or filter (blocking at least
visible blue and IR light energy) that swings, flips, or slides (as
indicated in FIG. 3A) into position over the image translator 155
and possibly also the energy transducer module 120 or energy
transmission surface 140 during the heating and blue/violet light
treatment modes, to protect the clinician. Alternatively, a portion
of image translator 155 and/or visualization means may include a
selective optical filter or photochromic element, such that during
low-level illumination of the eyelid for purposes of evaluating
transilluminated images of the meibomian glands, the photochromic
element passes substantially all of the light, whereas during the
heating mode where infrared energy or high-level visible light may
be used, some or all of that energy may be attenuated, thereby
shielding the clinician from harm.
[0142] By way of further clarification, several classes of
embodiments will now be described. In one class of embodiments,
devices are intended for self-administered use by individuals,
typically in a home-use environment. For this class, scleral
shields are not necessarily practical to use, and therefore, there
can be a higher risk of unwanted forms of energy (such as certain
wavelengths of light or infrared energy) penetrating the eyelids
and reaching sensitive anatomy of the eye. As such, this class of
embodiments may sometimes be limited to the use of safer forms of
energy such as visible light in the range of 450-700 nm. In another
class of embodiments, devices are intended for use by eye care
professionals in a controlled office environment, where a treatment
system having a scleral shield component can more likely be safely
utilized. In this class, the scleral shield can be designed with
shapes and materials to increase the likelihood that little or no
damaging energy reaches sensitive eye structures.
[0143] IN-OFFICE DEVICE--Embodiments of the in-office device may
include one or more of the following: diagnosing the meibomian
glands; treating the meibomian glands; and antimicrobial treatment
of the eye system. In one set of preferred embodiments, diagnosing
the meibomian glands is carried out two ways. First, using visible
or IR illumination from the energy transducer module which is
directed toward the outer surface of the eyelid in order to view
and evaluate the meibomian glands using the image translator, with
or without the visualization means. Second, by slight compression
of the eyelid while observing the eyelid margins to note the
quantity and quality of oily secretions from the meibomian gland
ducts. For treatment, in one set of embodiments, the eyelid is
heated and compressed. Near infrared (NIR) energy from the energy
transducer module at approximately around 800-900 nm is transmitted
through the eyelid to the scleral shield, which then heats up and
consequently warms the inner surface of the eyelid. Additionally,
visible light from the energy transducer module in the range of
about 500-600 nm (green light) is directed at the outer surface of
the eyelid which heats the tissue by means of chromophore
absorption. The energy transmission surface is then moved toward
the eyelid by the clinician via direct or indirect manual control,
in order to compress the eyelid between the energy transmission
surface and scleral shield. Optionally, the energy transmission
surface may be pre-warmed and/or actively warmed during the
treatment to provide some conductive heating of the outer eyelid.
The temperature of the inner and/or outer eyelid surface may be
measured and displayed for the clinician. The clinician applies
heating energy and compressive force while visually monitoring the
eyelid margin to optimize the expression of meibum from clogged
meibomian glands. Finally, the energy transducer module may produce
blue/violet light in the range of about 400-450 nm to reduce and/or
eliminate bacteria in the eye system 10.
[0144] HOME-USE DEVICE--Embodiments of the in-home device use
visible light transmitted through the energy transmission surface
from the energy transducer module aimed at the outer surface of the
eyelid to heat the tissue by means of chromophore absorption. In
certain preferred embodiments, the visible light may be
high-intensity broad spectrum (e.g., white) LED light passing
through certain filters, or it may be a green, greenish-yellow, or
greenish-white LED (500-600 nm) with no filters. In some
embodiments, the energy transmission surface is transparent to
visible light and is thermally conductive, allowing warming (e.g.
to 42 degrees Celsius) prior to or during compression of the
surface against the eyelid (see FIG. 2A). In some embodiments, the
energy transmission surface may have an extension element 143 (such
as in FIG. 2B and described previously) that allows most of the
light energy to pass through it, while keeping a gap between the
energy transducer module and the eyelid surface 12, 14 (to enable
passive or active air cooling of the eyelid, for example). The
energy transmission surface may conform to the shape of the eyelid
and apply pressure to the surface of the eyelid to shorten the
optical path length of radiant energy. In some embodiments eyecups
are utilized to prevent light from escaping from the immediate
treatment area and to keep at least a portion of the device at a
predetermined distance from the eyelids or periocular region.
[0145] FIGS. 4A-4C are representative of another embodiment of an
eye treatment device. FIG. 4A is a schematic side plan view of an
eye treatment device 200. The eye treatment device 200 shown in
FIG. 4A is positioned adjacent to an eyeball 20 for treatment of
the eyeball for MGD, blepharitis and other medical conditions. For
simplicity, sensitive eye structures such as the cornea, iris,
pupil lens, and adjacent elements are depicted in FIGS. 4A-D, 5A-B,
6, 11A-B, 12, 13 and 15A as a single element called anterior eye
structures 27. The eye treatment device 200 can include
configurations of the modules depicted in FIGS. 2 and 3, along with
additional components useful in operation of the eye treatment
device 200. The eye treatment device 200 can include a power source
module 110, a controller 212, an energy transducer module 120, an
energy waveguide in the form of reflector 210, and an energy
transmission surface 140. The energy transducer module 120 of some
embodiments may include an LED device formed of one or more of an
LED emitter 207, an LED lens 208, and an energy transducer module
driver 209. Each of these components, either alone, or in
combination with other components (either shown herein or not
disclosed) can correspond or be part of the modules described in
relation to FIGS. 2A-2H. The components of the eye treatment device
200 can be contained in a housing 202. Some of the embodiments of
the eye treatment device 200 may also include a consumable portion
260 and/or a scleral shield 300, such as shown in FIGS. 3 and
6.
[0146] The energy transducer module driver 209 can comprise any
LED-powering and controlling circuitry, whether configured as an
actual printed circuit board, an integrated circuit, or discrete
components. In some embodiments, it serves the function of an LED
driver, providing a controlled current, voltage or power level
through the LED emitter 207 within the LED specifications to
provide a desired illumination intensity therefrom. Optionally, the
LED printed circuit board can include a pulse-width modulation
function, PID circuit, or similar scheme in order to modulate the
effective intensity of the emissions over time to achieve a desired
heating of a target region of the eyelid.
[0147] The energy transmission surface 140 can be positioned
relative to the housing 202 at a location distal to the energy
transducer module 120, and positioned in between the energy
transducer module 120 and the tissue treatment site of the eye
system 10. Positioned in this manner, the energy transmission
surface 140 can pass, or receive and transmit, the electromagnetic
energy transmitted from the energy transducer module 120. The
energy transmission surface can be a concave shape, such that the
energy transmission surface 140 corresponds to the shape of the
eyelids 12, 14 when closed and covering the eyeball 20. The energy
transmission surface 140 may be an integral part of housing 202 and
may substantially seal the distal end of the eye treatment device
200. Additionally, energy transmission surface 140 may move
independently, or with energy transducer module 120, relative to
housing 202. A sealing element such as a bellows, gasket, o-ring or
similar sealing means may be used to prevent contamination of the
interface between the movable elements and the housing.
[0148] In some embodiments, the energy transmission surface 140 is
positioned adjacent to the eyelids 12, 14, and does not physically
contact the eyelids 12, 14, but instead transfers heat to the
treatment tissue radiantly. The energy transmission surface 140 can
be substantially transparent to the desired electromagnetic energy
transmitted by the energy transducer module 120 to allow for the
transmission of the thermal energy from the energy transducer
module 120 without significantly hindering the desired energy type
or wavelength from reaching the treatment tissue. In some
embodiments, the energy transmission surface 140 can be made of an
optical plastic, sapphire, glass, calcium fluoride, or fiberglass.
It can have an easy to clean outside surface and can be scratch
resistant. In some embodiments, the energy transmission surface 140
can be configured to operate in conjunction with the energy
transducer module 120 to filter unwanted wavelengths from reaching
the treatment tissue or other portions of the eye system 10. For
example, in some embodiments, the illumination source may transmit
electromagnetic energy in both the IR and visible light spectra.
The energy transmission surface 140 can be used to allow passage
of, for example, the energy from the visible light spectrum, but
filter out the energy from the IR spectrum. Likewise, if it is
desired that only energy from one color reach the treatment tissue,
the energy transmission surface 140 can be used as a bandpass
filter or be used with a filter to restrict passage of energy of
wavelengths other than the color desired. Alternatively, as
described previously, energy transmission surface 140 may include a
single-use outer eyelid pad 147. Such outer eyelid pad 147 may be
transparent to all relevant wavelengths of light or other forms of
energy, or it may have desirable filtering properties, and it may
additional include a temperature or pressure sensor.
[0149] In some embodiments, the energy transmission surface 140 can
be configured to come in physical contact with the eyelids 12, 14
and may conductively transfer heat to the treatment tissue (or
facilitate cooling of the eyelid, as described below). In other
embodiments, a preponderance of tissue heating occurs as a result
of radiant heating from the energy transducer module 120, wherein
substantially all of the desired electromagnetic energy passes
through energy transmission surface 140 and is absorbed by the
tissue, thereby causing heating of the tissue and little or no
heating of the energy transmission surface 140. It will be
appreciated that the device may be configured without an energy
transmission surface 140. However, the energy transmission surface
140 provides certain benefits such as ease of cleaning of the
primary patient contact surface, as well as the potential for the
energy transmission surface 140 to assist in keeping the outer
surface of the eyelid within a desired temperature range, and to
provide a convenient location for certain safety sensors. In
embodiments where a single-use outer eyelid pad 147 is used as part
or all of the energy transmission surface 140, the outer eyelid pad
147 may contain a temperature sensor, but preferably a non-contact
temperature sensor is utilized instead, such as a thermopile or
pyroelectric sensor, positioned proximal (relative to the housing)
to the outer eyelid pad 147. In such embodiments, the outer eyelid
pad 147 is preferably transparent to the wavelengths of infrared
that the non-contact temperature sensors are designed to sense.
[0150] FIG. 4B is a schematic front plan view of the energy
transducer module 120 of the eye treatment device 200. As shown in
FIG. 4B, the LED emitter 207 can be arranged as an array of
individual LEDs. As represented, the LED emitter 207 is arranged in
a 3.times.3 array of LEDs (such as in the LZ9 configuration offered
by LED Engine, Inc.), though the LED emitter 207 is not limited to
this arrangement and can include arrays of varying numbers of LEDs
arranged in varying arrays of columns and rows; and some
embodiments may include a single LED or other type of illumination
source. The reflector 210 may partially or fully surround the LED
emitter 207, such that it can direct the emission of light from the
LED emitter 207 in a desired manner. The LED lens 208 can be
positioned over the LED emitter 207 and positioned within the
internal diameter of the reflector 210.
[0151] FIG. 4C is a schematic side plan view of one embodiment of
an eye treatment device 200, wherein the device is operational and
transmitting light 211 to the eye system 10 and the treatment
tissue. In FIG. 4C, the light 211 is emitted from the energy
transducer module 120. Some portion of the light 211 may initially
be radiated at an angle such that light, without correction, would
not reach the energy transmission surface 140 for passage to the
treatment tissue. As shown, the reflector 210 may reflect or guide
the angled light towards the energy transmission surface 140,
thereby improving the efficiency of heating the target tissue.
Portions of the light 211 may also be transmitted directly from the
energy transducer module 120 to the energy transmission surface
140.
[0152] FIG. 4D is a schematic side plan view of another embodiment
of an eye treatment device 200. In this embodiment, the
transmission of the light 211 may be administered without the aid
of a reflector 210, if, for example, other components of the eye
treatment device 200 can be used to control the direction and
intensity of the light 211 such as a specially shaped lens, an
additional lens element, a light pipe, a total internal reflective
(TIR) element, a refractive element, a diffractive element, a
mirror element, a diffuser, and the like, or a combination thereof.
It may be desirable in this manner to control the focus and the
intensity of the light energy so that the light energy penetrates
deeply into, but not significantly beyond, the target tissue in the
eyelids 12, 14, such as the meibomian glands. In some embodiments,
the energy transmission surface 140, acting as a lens or with a
lens, may be used to focus and direct the light 211 to the desired
treatment tissue and away from the central ocular axis, to avoid
the anterior eye structures 27 of the eyeball 20 and other
sensitive anatomy of the eye such as the retina. It will be
appreciated that the region along which the upper eyelid 12 and
lower eyelid 14 meet may vary from one individual to another; in
most individuals the region is generally below the central ocular
axis. However, for purposes of demonstrating how certain
embodiments can mitigate the risk of excessive light 211
penetrating the eyelids at the central ocular axis, the worst-case
situation of having the eyelids meet at the central ocular axis is
shown. It will be further appreciated that at least some of the
risk associated with excessive rays penetrating the eyelids and
reaching sensitive tissues may be mitigated by having the
individual being treated move his/her eyeball off-axis, such that
most of the rays penetrating the eyelids only reach the sclera,
which is generally less sensitive.
[0153] FIG. 4E shows a particular embodiment comprising additional
optical elements to improve the distribution of light energy across
the eyelid surface, while minimizing the amount of light passing
directly through the central ocular axis. Energy transducer module
120 comprises an LED such as an LZ9 from LED Engin Inc., a prism
280, a shaping lens 282, and face glass 284 (serving a similar
function as energy transmission surface 140 in other embodiment
disclosed herein). Eyelids 12, 14 and eyeball 20 are also shown in
relation to the optical elements. In this particular design, the
prism is a glass element with 6 polished surfaces and one half ball
concave surface with radius 3.5 mm to accommodate the LED. There is
no coating on the prism surfaces. Entrance and exit surfaces can
have anti-reflection coating (optional) which increases the
efficiency by about 5-6%. FIGS. 4F-H show exemplary details of the
shape and dimensions of prism 280. The material may be BK7, and the
surfaces are preferably polished. FIG. 4F is a front view, FIG. 4G
is a side view, and FIG. 4H is a section view through section A-A.
FIGS. 4I-L show exemplary details of the shape and dimensions of
shaping lens 282. FIG. 4I is a front view, FIG. 4J is a section
view through section A-A, FIG. 4K is a side view, and FIG. 4L is a
perspective view. FIGS. 4M and 4N show the theoretical optical
performance of the system described in FIGS. 4E-L above. FIG. 4M
shows the light distribution, measured as irradiance in Watts per
square millimeter, on the surface of the eyelids, wherein the light
distribution is shown to be fairly uniform (as opposed to shining
the LED of energy transducer module 120 directly at the eyelids or
through a plain glass energy transmission surface, in which case
most of the light would be projected in the middle of the lid and
very little would reach the edges). The total calculated flux is
0.86 Watt, the maximum irradiance is 2.2 milliwatts per square
millimeter and the uniformity is estimated at about 80%. FIG. 4N
shows the amount of irradiance reaching the eye (i.e., passing
through the eyelid tissue). The total calculated flux is 0.019
Watts, and the maximum irradiance is 0.18 milliwatt per square
millimeter.
[0154] FIGS. 5A and 5B are representative of one embodiment of an
eye treatment device 200. FIG. 5A is a schematic side plan view of
the eye treatment device 200 and FIG. 5B is a schematic front plan
view of the eye treatment device 200. The embodiment of the eye
treatment device 200 may contain components similar to those shown
in FIGS. 4A-4C, including the power source module 110 and the
controller 212, though such components are not shown in FIGS. 5A
and 5B. FIG. 5A provides a different configuration for the energy
transducer module 120 in order to focus and control the direction
of the light 211. In some embodiments, the eye treatment device 200
can include multiple energy transducer modules 120, such that at
least one energy transducer module 120a can be positioned in an
upper region of the eye treatment device 200 to provide
electromagnetic energy (e.g., light 211) to the target tissue
within the upper eyelid 12 and at least one energy transducer
module 120b can be positioned in a lower region of the eye
treatment device 200 to provide electromagnetic energy (e.g., light
211) to the target tissue residing in the lower eyelid 14. Having
separate energy transducer modules 120a, 120b positioned separately
in the eye treatment device 200, allows the eye treatment device
200 to direct light energy directly toward the target tissue within
the upper eyelid 12 and the lower eyelid 14 and reduces the amount
of light that may be directed towards sensitive anterior eye
structures 27 along the central ocular axis 30.
[0155] As shown in FIG. 5A, use of the eye treatment device 200 for
treatment of an eye condition such as MGD and blepharitis, can
include positioning the energy transmission surface 140 of the eye
treatment device 200 adjacent to, or in contact with, the closed
upper and lower eyelids 12, 14 of a patient. With the eye treatment
device 200 positioned in this way, the upper energy transducer
module 120a can be positioned above the central ocular axis 30 to
provide electromagnetic energy in the form of light 211 to the
meibomian glands 18 within the upper eyelid 12, and the lower
energy transducer modules 120 b can be positioned below the central
ocular axis 30 to provide electromagnetic energy in the form of
light 211 to the meibomian glands 18 within the lower eyelid 14.
The eye treatment device 200 can also include a reflector 210
positioned behind the upper and lower energy transducer modules 120
to reflect back any light to the treatment tissue.
[0156] As depicted in FIG. 5A, the upper and lower energy
transducer modules 120 can be tilted at an angle, each having a
central optical axis directed substantially at an oblique angle to
the surface of each eyelid, such that the majority of light energy
passing into each eyelid is absorbed before reaching the sensitive
anterior eye structures 27 of the eyeball 20. In some embodiments,
the upper and lower energy transducer modules 120 can have other
directional orientations. For example, in some embodiments, the
upper and lower energy transducer modules 120 can be positioned
such that each central optical axis of the illumination sources is
substantially horizontal. As such, the light 211 transmitted from
the energy transducer modules 120 configured in this way can travel
horizontally from the energy transducer modules 120 to the energy
transmission surface 140 and may then be refracted, diffracted, or
reflected at an angle toward the treatment tissue, in a manner that
maximizes penetration, absorption and heating in the targeted
regions of the eyelids while minimizing the proportion of light
that reaches the sensitive anterior eye structures 27.
[0157] The eye treatment device 200 of the embodiments shown in
FIGS. 5A and 5B can include more than one energy transducer module
120 in each of the upper and lower regions of the eye treatment
device 200. For example, as shown in FIG. 5B, the eye treatment
device 200 can include three separate energy transducer modules
120a-c in the upper region and three separate energy transducer
modules 120 d-f in the lower region. Other numbers of energy
transducer modules 120 are contemplated, such as, for example 2, 4,
5, 6, 7, 8, 9, 10, etc. energy transducer modules 120 in each of
the upper and lower regions of the eye treatment device 200.
Positioning multiple energy transducer modules 120 laterally in the
upper and lower regions of the eye treatment device 200 allows for
improved coverage and distribution of the electromagnetic energy
across the width (side-to-side) of the upper and lower eyelids 12,
14 to better reach the full width of the target tissue (e.g., the
meibomian glands within the eyelids 12, 14). Also as shown in FIG.
5B, the upper and lower energy transducer modules 120a-c, 206d-f
can be arranged in an arc pattern to follow the upper and lower
contours of the eyeball.
[0158] It is also contemplated, though not depicted in FIG. 5B,
that the upper and lower illumination regions of the eye treatment
device 200 can be fitted with more than one row of energy
transducer modules 120. For example, in FIG. 5B one or more
additional energy transducer modules 120 could be positioned above
or below each of the energy transducer modules 120a-c. Including
additional rows of energy transducer modules 120a-c can provide
additional vertical coverage and distribution of the
electromagnetic energy directed to the target treatment tissue. It
is additionally contemplated, though not depicted, that the eye
treatment device 200 may include two sets of energy transducer
modules 120, reflectors 210, and energy transmission surfaces 204
within a housing, configured like binoculars, to be positioned
adjacent to, or against, both of a patient's eyes simultaneously.
Devices of such embodiments may speed up the treatment time, as
both eyes can be treated at the same time.
[0159] FIGS. 5C-F show side, top, front and perspective views,
respectively, of an 8-LED configuration, similar to that depicted
in FIGS. 5A-B (only with eight LEDs 120a, 120b instead of six). The
eight LEDs 120a, 120b may be of an LZ1 type from LED Engin, Inc.,
and are shown arranged on a spherically curved surface, which may
be a circuit board or an energy transducer module driver 209,
positioned behind face glass 284 whose shape matches the curvature
of eyelids 12, 14 adjacent to eyeball 20. FIG. 5G shows the
calculated irradiance pattern onto eyelids 12, 14, with a total
flux of 2.7 Watts and a maximum irradiance of 10.7 milliwatts per
square millimeter. FIG. 5H shows the calculated irradiance passing
through the eyelids, with a total flux of 0.07 Watts and a maximum
irradiance of 0.6 milliwatts per square millimeter. It will be
appreciated that the pattern of irradiance in FIGS. 5G and 5H are
less uniform than the patterns shown in FIGS. 4N and 4P. The
trade-off between the two designs is compactness of the device
versus uniformity. The designs of FIGS. 4E-L include a rather large
prism, while the designs of FIGS. C-F do not include any optical
elements other than the LEDs and lenses and the face glass. Those
skilled in the art may combine the two approaches, for example, by
adding one or more prisms 280, shaping lenses 282, or other
elements such as diffusers, gratings and the like, to the designs
of FIGS. 5C-F, in order to optimize the uniformity of light
distribution while keeping the size of the device as compact as
possible.
[0160] FIG. 6 is a schematic side plan view of an eye treatment
device 200, such as the eye treatment device 200 depicted in FIG.
5A. Also shown in FIG. 6 is a scleral shield 300, which, in
conjunction with the eye treatment device 200, can provide a system
of treating the target tissue with increased safety and efficacy.
The scleral shield 300 can be positioned under eyelids 12, 14 and
adjacent to the patient's eyeball 20 to cover sensitive anterior
eye structures 27. For example, the scleral shield may be
positioned (referring to FIG. 1) over the sclera 21 and cornea 22
and may also provide protection to other internal anatomy of the
eye such as the iris 24, pupil 25, lens 26, and other light
sensitive anatomy of the eye system 10.
[0161] Referring back to FIG. 6, the scleral shield 300 may be of
similar disc shape as a contact lens, or it may be substantially
larger to cover the entire cornea and optionally at least some of
the sclera (as in the case of a conventional corneal shield), or it
may have a partial disc or paddle shape, similar to the under-lid
portion of a Mastrota paddle. Shield 300 may be positioned in the
eye prior to treatment with the eye treatment device 200, or it may
be integral with eye treatment device 200, and therefore placed in
the eye or under the lid during the treatment. In addition to
providing basic safety benefits, the scleral shield 300 can also
allow for increased efficacy of the eye treatment device 200. For
example, in some circumstances, the intensity of the energy
emanating from the energy transducer modules 120 must be modulated
to prevent injury to the sensitive eye anatomy; however, when the
eye anatomy is protected by the use of the scleral shield 300, the
intensity of the electromagnetic energy directed from the energy
transducer modules 120 can be increased. As shown in FIGS. 7E-7G,
the scleral shield 300 may include a top curved portion 264 of the
shield that prevents scattered photonic energy from reaching the
cornea, lens, iris and pupil. Though the scleral shield 300 is
shown in FIG. 6 to be used in the conjunction with the embodiment
of the eye treatment device 200 described in relation to FIGS. 5A
and 5B, it will be appreciated by the skilled artisan that the
scleral shield 300 can be used in conjunction with any of the
embodiments of the eye treatment device 200 disclosed herein to
create a system for safe and efficacious treatment of eye
disorders.
[0162] It will be further appreciated that the scleral shield 300
may include features which provide even more benefits to the
device. For example, the scleral shield 300 of some embodiments is
configured to reflect energy away from the eyeball and toward the
inner eyelids, providing heating to the inner eyelids. In some
embodiments, the scleral shield 300 may also include an image
translator 155, as discussed above. The image translator 155 allows
viewing of the inner side of the eyelid 14 and transillumination of
the meibomian glands from behind the eyelid. In some embodiments,
the scleral shield 300 may be made of an energy-absorbing material
or have an energy transmission surface on a front face 302 for
heating the meibomian glands from behind the eyelid during
treatment. The energy-absorbing material may be a visible light or
IR-absorbing material or surface made of black plastic or coated
with a black substance, either of which may contain carbon black
(e.g. 5% or more) or other material which absorbs light energy such
as red light and NIR.
[0163] Additionally, as shown in the schematic front plan views of
the scleral shield 300 in FIGS. 7A-7H, the shield 300 may
incorporate one or more temperature sensors 310 on the front or
back surfaces of the shield 300. The shield 300 may also include
data transmission means 320, so that temperature data may be sent
to the eye treatment device 200 in order to monitor or modulate the
treatment session, so that the inner surfaces of the eyelids may
reach a target temperature without exceeding a predetermined
threshold, along with ensuring that the sensitive tissues of the
eye do not exceed another predetermined threshold. In some
embodiments, such as the embodiment of FIG. 7A, the shield 300 has
an embedded power source 330, an array of temperature sensors 310,
and a data transmission means 320, which transmits data wirelessly,
such as by RF, to an external interrogator 400 (which may be
incorporated into the eye treatment device 200). In some
embodiments, the data transmission means 320 includes an antenna
embedded in the shield 300. In another embodiment, such as the
embodiment depicted in FIG. 7B, the shield 300 may be passive
(without a power source 330) and configured to be interrogated by
an external interrogator 400 (which may be incorporated into the
eye treatment device 200) using RF. For example, the external
interrogator 400 shown schematically in FIG. 7B may be configured
to provide power to circuitry in the shield 300 adequate to measure
the temperature(s); the interrogator 400 may also provide power to
a transmitter to send the temperature data back to the interrogator
400. In yet another embodiment, such as the embodiment of FIG. 7C,
the shield 300 may be fully passive and contain one or more
temperature sensors 310 in resonant circuits whose points of
resonance will be modulated by changes (such as resistance) in the
temperature sensors 310, and whose points of resonance can be
detected by sweeping an external RF field, for example using the
external RF sweeper 410 depicted schematically in FIG. 7C, and
monitoring the impedance or other characteristic of the field. In a
further embodiment, such as the embodiment of FIG. 7D, the shield
300 may be physically linked to an external device such as an
interrogator or eye treatment device 200 (e.g. of FIG. 3A) via a
wire or wire array 420 extending from the shield 300 to an external
device, wherein such external device may provide power to the
active elements in the shield 300 and send and receive data to and
from the shield 300. Wire or wire array 420 may comprise
conventional stranded or solid wire conductors with thin-wall
insulation, or they may be embedded in more substantial structural
insulation.
[0164] FIGS. 7E and 7E are schematic side and front plan views of
the shield 300 having a temperature sensor 310 in the middle and
one wire 420 coming out of each side of the shield. The upper
curved portion of the shield 264 is used to protect the patient's
cornea, lens, iris and pupil from the light or IR energy. The
temperature data from the temperature sensor 310 may be sent to the
eye treatment device 200 via the wires 420 in order to monitor or
modulate the treatment session, ensuring that the inner surfaces of
the eyelids reach a desired temperature range without exceeding a
predetermined threshold, along with ensuring that the sensitive
tissues of the eye do not exceed another predetermined
threshold.
[0165] FIGS. 7G and 7H are schematic side and front plan views of
the shield 300 having a temperature sensor 310 in the middle and
one wire 420 coming out of each side of the shield. In these
embodiments, scleral shield 300 may be coupled to the housing 202
with one or more support arms 262, with the wires being positioned
on or within the arms, and, in certain embodiments, with the
structural portion of support arms 262 made from insulating
materials surrounding or otherwise channeling the conductive
portions of wire or wire array 420.
[0166] FIG. 8 depicts a side view of another embodiment of an eye
treatment device 200. In some embodiments, such as the presently
depicted embodiment, the eye treatment device 200 is configured to
apply energy to one eyelid at a time in order to further protect
the tissue of the eye from harm or discomfort. In such a
configuration, the energy transducer module 120 within the housing
202 is sized to target the meibomian gland and surrounding tissue
of one eyelid, for example, the upper eyelid 12 of FIG. 1 or the
lower eyelid 14 of FIG. 1 and the energy transmission surface 140
is in a slidable relationship along movement path 145 with the
energy transducer module 120. In such embodiments, the energy
transmission surface 140 is also sized for placement along one
eyelid at a time. In use, a patient using such an eye treatment
device 200 may be instructed to open an eye widely, thus ensuring
that the eyelid is relatively far away from the sensitive anterior
eye structures and the central ocular axis.
[0167] In some embodiments, the eye treatment device 200 includes
one or more features to help ensure the eye treatment device 200 is
safely and properly placed against the eyelid. For example, in some
embodiments, the eye treatment device 200 includes a pupil
alignment guide 242. The pupil alignment guide 242 may be, for
example, a mirror with a circle, X, bull's-eye, or other target
mark. In use, a patient may be able to properly position their eye
by looking into the pupil alignment guide 242, observing the
reflection of their pupil in the mirror, and aligning the pupil
with the target mark. Additionally or alternatively, in some
embodiments, the eye treatment device 200 includes a display 244,
which may be a screen, a digital display, or other optical display.
The display may present, for example, an image for the patient to
stare at during use, a timer counting down the remaining treatment
time, and/or reminder messages such as "Look Up" (explained below).
The display 244 may also include a visualization means 160 for
enhanced monitoring of eyelid margin during diagnosis and
treatment.
[0168] The eye treatment device 200 of FIG. 8 may include any or
all of the features described in relation to other embodiments
presented herein. For example, in the depicted embodiment, the
energy transducer module 120 is an infrared LED array. However, in
other embodiments, including other embodiments configured to apply
energy to one eyelid at a time, the energy transducer module 120
may include an LED emitting light in the visible light spectrum, a
laser, an incandescent lamp, a xenon lamp, a halogen lamp, a
luminescent lamp, a high-intensity discharge lamp, or a gas
discharge lamp. The eye treatment device 200 may further include a
scleral shield 300 made of an energy-absorbing material or have an
energy-absorbing or energy transmission surface on a front face 302
for absorbing or transmitting heat and warming the inner surface of
the eyelid during treatment. The scleral shield 300 may also
incorporate one or more temperature sensors 310 in order to monitor
the treatment session, ensuring that the inner surfaces of the
eyelids reach a desired temperature and/or do not exceed a
predetermined threshold. The scleral shield 300 may further include
an image translator 155 integrated into the scleral shield,
allowing viewing of the meibomian glands behind the eyelid. The eye
treatment device 200 of FIG. 8 preferably also includes a power
source module 110 and optionally a controller 212, along with other
components as described in relation to various embodiments
presented herein. Additionally, the eye treatment device 200 of
FIG. 8 includes a reflector 210. In the depicted embodiment, the
reflector 210 is formed of a barrel and backplate, which together
surround the energy transducer module 120 in all but a distal
direction.
[0169] The eye treatment device 200 of various embodiments also
includes one or more thermal management structures configured to
cool at least a portion of the device. In some embodiments, the
thermal management structures are provided to manage the heat of
the energy transducer module 120 and prevent the eye treatment
device 200 from overheating. Additionally or alternatively, in some
embodiments, the thermal management structures are provided to cool
a surface of the eyelid to limit discomfort and avoid injury to the
eyelid tissue during treatment. In FIG. 8, for example, the eye
treatment device 200 includes a thermal management structure 220
(shown as a finned heat sink), a thermoelectric (Peltier) module
224, and one or more thermally conductive surfaces that are
passively or actively cooled. In some embodiments, a passive heat
sink may be provided as an adequate thermal management structure
220 to dissipate heat from the energy transducer module 120 into
the surrounding environment without the need for a thermoelectric
module 224. Some embodiments include a thermoelectric module 224 or
other type of cooler (such as a compact vapor-compression cooler)
designed to cool the energy transducer module 120 by transferring
heat directionally away from the energy transmission surface 140.
In FIG. 8, the thermoelectric module 224 and thermal management
structure 220 are coupled such that the thermoelectric module 224
pumps heat away from the energy transducer module 120 towards
thermal management structure 220 for dissipation. Additionally or
alternatively, some embodiments include one or more thermally
conductive surfaces. For example, in FIG. 8, the barrel and
backplate of the reflector 210 are thermally conductive and coupled
to both the energy transmission surface 140 and the thermoelectric
module 224. Moreover, the energy transmission surface 140 is
thermally conductive. As a result, heat from the surface of the
eyelid and the energy transmission surface 140 can be pulled
towards the thermoelectric module 224 to help maintain a
comfortable temperature against the eyelid. Actively cooling the
energy transmission surface 140 may occur not only during the heat
treatment period, but before, after or intermittently, as a means
of cooling the eyelids. Such a feature may not only provide relief
from the burning and itching sensation that often accompanies MGD
and blepharitis, but may also provide reduction of inflammation of
the eyelids.
[0170] In some embodiments, the eye treatment device 200 includes a
non-contact temperature sensor 232 to be used, for example, in
conjunction with one or more thermal management structures. The
non-contact temperature sensor 232 may be a remote reading IR
thermometer or other suitable temperature sensor. The non-contact
temperature sensor 232 can be focused on a region of the eye of
particular interest. For example, in FIG. 8, the non-contact
temperature sensor 232 is focused on a bottom edge of the cornea,
and thus, provides a reading of the temperature at the cornea's
edge. The non-contact temperature sensor 232 may be operatively
coupled to a controller 212 such that, in some embodiments, the
controller 212 modulates or shuts down the energy transducer module
120 or activates one or more thermal management structures in
response to receiving an elevated temperature reading from the
non-contact temperature sensor 232. In some embodiments, while heat
is being applied to the lower eyelid (for example), the display 244
may instruct the patient to "Look Up" in order to allow the
non-contact temperature sensor 232 to measure the temperature of
the eye (sclera) at a location that is directly behind the portion
of the eyelid being heated. In this manner, the eye treatment
device 200 can continue to heat the eyelid while periodically
ensuring that the eyeball is not being overheated. It will be
appreciated that the device configuration shown in FIG. 8 may
easily be adapted for treating the upper eyelid, for example by
reversing the orientation of the energy delivery elements while
keeping the display 244 and alignment elements in their upright
(readable) orientation.
[0171] FIG. 9 depicts a side view of another embodiment of an eye
treatment device 200 having one or more thermal management
structures 220. Any of the thermal management structures 220
described with reference to FIG. 8 or 9 are suitable for use, and
expressly contemplated for use, with any of the eye treatment
device 200 embodiments described herein. The thermal management
structure 220 may include any suitable structure configured to
remove heat from the energy transducer module 120 so that the
energy transducer module 120 remains within a desired temperature
range to maintain efficiency of the energy transducer module 120.
In some embodiments, the thermal management structure 220 is
disposed at least partially within the housing 202 of the eye
treatment device 200, along with the power source module 110 and
other internal components. In some embodiments, one or more of the
following thermal management structures 220 are provided within the
housing 202: a heat sink (e.g., the finned heat sink embodiment of
thermal management structure 220 shown in FIG. 8), a thermoelectric
(Peltier) module (e.g., the thermoelectric module 224 of FIG. 8), a
compact vapor-compression module, and a fan. In some embodiments,
the thermal management structures 220 direct and distribute the
heat in a manner that keeps the housing 202 cool to the touch.
[0172] Additionally, in some embodiments, the eye treatment device
200 includes a surface cooling system designed to prevent the
eyelid surface from heating to the point of discomfort or injury
while the target tissue below the surface is being heated. A
surface cooling system is not needed in all embodiments; for
example, in some embodiments, the selected energy transducer module
120 is configured to emit light energy at a wavelength that is
absorbed into a target tissue region within the eyelid or an
energy-absorbing portion of a scleral shield with minimal heating
of an eyelid's surface tissue. In embodiments in which a surface
cooling system is present, the surface cooling system may be
configured to cool the surface of a patient's eyelid to or below
body temperature or to a temperature below the target tissue
temperature or below a threshold of discomfort before, during, or
after delivery of energy to the target tissue region. The surface
cooling system may include any suitable structure configured to
cool a surface of the eyelid and/or cool the energy transmission
surface 140. For example, in some embodiments, the surface cooling
system includes an active cooling element, such as a fan. In some
such embodiments, the energy transmission surface 140 is shaped
such that an air gap exists between the energy transmission surface
140 and at least a portion of the eyelid. FIG. 2B depicts an
embodiment appropriately structured for this purpose. In such
embodiments, air may be blown within the air gap across the surface
of the eyelid. In other embodiments, the energy transmission
surface 140 may have one or more holes or channels extending
through or along the energy transmission surface 140, through which
air can be blown. In some embodiments, air is cooled before being
blown across the surface of the eyelid. The air may be cooled, for
example, using a thermoelectric cooler, compressor, ice, or other
chilling element.
[0173] In other embodiments, an evaporative agent such as water or
alcohol may be applied to the energy transmission surface 140, such
that a surface of the eyelid then comes into contact with the
evaporative agent. Additionally or alternatively, an evaporative
agent may be applied to the surface of the eyelid before, during,
or directly after treatment with the eye treatment device 200. As
evaporation occurs on the surface of the eyelid as a consequence of
the evaporative agent, a cooling and relieving sensation may be
experienced by the patient. In still other embodiments, the eye
treatment device 200 may include a cooling bladder positioned
between the energy transmission surface 140 and the surface of the
eyelid. The bladder may be filled with a cool water or gel and
provide a cooling and relieving sensation to the patient when the
bladder is in contact with the surface of the eyelid. As another
non-limiting example, the surface cooling system may include the
energy transmission surface 140 itself. In some such embodiments,
the energy transmission surface 140 may be formed from an
energy-absorbing material, such as, for example, diamond, sapphire,
calcium fluoride, or graphene, and thermally linked to a larger
thermal mass. Such large thermal masses take a long time to heat,
and thus, may not heat up significantly during a treatment period.
The large thermal mass may, therefore, sink heat away from the
energy transmission surface 140 during a treatment period. In
addition, the large thermal mass may be cooled prior to, or during,
the treatment period, and may also be formed from the same
materials, and as part of, the energy transmission surface 140, or
it may be formed as a separate element out of materials such as
copper, aluminum, or other energy-absorbing or conducting
material.
[0174] In addition to the thermal management structures 220 and
surface cooling systems described above, at least some eye
treatment devices 200 include one or more safety sensors 230, for
example, to monitor parameters of the eye treatment device 200 or
to ensure patient safety. FIG. 10 provides one example of an eye
treatment device 200 having one or more safety sensors 230. Any of
the safety sensors 230 and related controllers 212 described with
reference to FIG. 10 are expressly contemplated for use with any of
the eye treatment device 200 embodiments described herein. Any
particular eye treatment device 200 may include one or more types
of safety sensors 230. A first set of safety sensors 230 provided
in FIG. 10 are configured to sense temperature. Such safety sensors
230 include a non-contact temperature sensor 232 and a thermocouple
or thermistor 234. The non-contact temperature sensor 232 may be a
remote reading IR thermometer (such as a thermopile or pyroelectric
or microbolometer) or other suitable non-contact sensor. The
non-contact temperature sensor 232 may be designed to gather
temperature data from the full field of illumination, such as
during a treatment period, to monitor the surface temperature of
one or more eyelids, or it may be designed to focus on a particular
region and provide a temperature reading of that region. For
example, the non-contact temperature sensor 232 may be positioned
and configured to provide a temperature reading of a portion of the
cornea, sclera, or other region of the eye, to ensure such tissue
is not overheated and damaged, as is depicted in FIG. 8, for
example.
[0175] Additionally or alternatively, some embodiments include a
thermocouple or thermistor 234 (or RTD) positioned on or near the
energy transducer module 120. Such a placement allows the
thermocouple or thermistor 234 to detect the temperature of the
energy transducer module 120 so that the temperature of the energy
transducer module 120 can be monitored. If the energy transducer
module 120 runs too hot, it can become inefficient and/or damaged.
Additionally or alternatively, a thermocouple or thermistor 234 may
be disposed on, within, or adjacent to the energy transmission
surface 140. Such a placement allows the thermocouple or thermistor
234 to detect the temperature of the energy transmission surface
140 and/or the surface of an eyelid. Monitoring the temperature of
such surfaces may help to ensure that a patient does not experience
significant discomfort or injury from use of the eye treatment
device 200. In certain embodiments, the various temperature sensors
232, 234 are operatively coupled to a controller 212, which may be
programmed to modulate the output of the energy transducer module
120 or one or more thermal management structures or surface cooling
systems, in order to bring or hold the temperature to within a
predetermined target range. Also, if the temperature inputs from
the temperature sensors 232, 234 are above the predetermined range,
the controller 212 may turn off the output from the energy
transducer module 120. Additionally or alternatively, temperature
sensors 232, 234 may be coupled with the scleral shield 300 (not
shown in this figure) to monitor the temperature of the inner
surface of the eyelid and/or surface of the eye. Additionally, a
pressure sensor or sensors 221 may be disposed on, within, or
adjacent to the scleral shield 300 and/or the energy transmission
surface 140 to monitor the pressure or force applied by the user on
the eyelid.
[0176] A second set of safety sensors 230 present in FIG. 10 are
provided to sense the position of the eye treatment device 200
relative to the eyelid of a patient. A light sensor 236 present in,
on, or near the energy transmission surface 140 is configured to
detect light. In various configurations of the eye treatment device
200, when the energy transmission surface 140 is properly placed
adjacent to one or two eyelids, depending upon the configuration,
it should significantly reduce the amount of ambient light that can
reach the light sensor 236. In some embodiments, if light is
detected in, on, or near the energy transmission surface 140 above
a threshold range, it is an indication that the energy transmission
surface 140 is not properly placed. Similarly, contact sensors 238
may be present in or on the energy transmission surface 140. Each
contact sensor 238 may be configured to detect changes in
capacitance, such as, for example, the change in capacitance that
occurs when a contact sensor 238 is near human skin. Alternatively,
contact sensors 238 may comprise electrodes that apply a small DC
or AC microcurrent and which sense changes in impedance a result of
contact with skin. Or, contact sensors 238 may comprise
microswitches or force or pressure sensors, all of which produce a
change in signal characteristics when energy transmission surface
140 is against skin. Thus, sensors 238 can be used to help
determine the placement of the eye treatment device 200. If the eye
treatment device 200 is properly placed against a closed eye, an
upper contact sensor 238 and a lower contact sensor 238 should each
come into contact with the skin of an eyelid and sense a change in
capacitance (or impedance, switch status, force, pressure, etc.).
In various embodiments, the light sensor 236 and/or contact sensors
238 are operatively coupled to a controller 212. In some such
embodiments, the controller 212 is programmed to prevent activation
of the energy transducer module 120 until the controller 212
detects, through signals from the sensors 236, 238 that the eye
treatment device 200 is properly placed adjacent to a closed eye.
Additionally, in some embodiments, the controller 212 is programmed
to shut off the energy transducer module 120 if signals received
from the sensors 236, 238 indicate that the eye treatment device
200 is no longer placed properly against a closed eye.
Additionally, or alternatively, thermocouples or thermistors 234
on, in or adjacent to energy transmission surface may be used to
indicate when the device is properly positioned adjacent to a
patient's eye. For example, the thermocouples or thermistors 234
may register room temperature prior to placement of the device
adjacent to the eye, and as the energy transmission surface 140
comes into contact with the eyelid skin (in embodiments where
direct contact is desired), the thermocouples or thermistors 234
will register a value closer to body temperature, and therefore,
confirm proper positioning. Further, if multiple thermocouples are
used in embodiments which treat both the upper and lower eyelid,
the data from the thermocouples or thermistors 234 may be used to
determine if the eye is open or closed. A reflective or color
sensor 237 may also be incorporated into the device in order to
confirm that the eye is closed. Such a sensor 237 can either
determine the color of a region of the optical field in front of
the sensor 237, or it can determine the degree of reflection of the
surface in front of the reflective or color sensor 237. In either
case, the sensor 237 provides data indicating whether or not there
is tissue that appears to be eyelid skin (e.g., flesh colored and
not wet or shiny) or eye tissue (white or iris colored, and wet and
shiny).
[0177] In some embodiments, contact sensor 238 comprises a
microswitch embedded behind a flexible, sealed surface. In other
embodiments, contact sensor 238 comprises a sensor which provides
an indication of the amount of force or pressure applied by energy
transmission surface 140 against the eyelid. Such an indication may
be useful in order to avoid applying excessive force during a
treatment, or to apply force within a certain range during initial
diagnosis when the eyelid is meant to be slightly compressed to
enable assessment of meibomian gland secretions. It will be
appreciated that the force of the energy transmission surface 140
against the eyelid or eyelids applied by the clinician can be
either regulated or not regulated. Further, the in-office device
the force may be applied with a rolling or angular component to
assist in moving the meibum out of the meibomian glands and ducts.
In some embodiments, the energy transmission surface and/or scleral
shield may have a curved or angular shape surfaces, or may have a
rocking elements, such that when the energy transmission surface
compresses the eyelid against the shield, there is initially more
compression in the lower region of the meibomian glands that
gradually transfer to the upper region as compression increases,
moving meibum from the lower region to the upper region and then
out of the meibomian gland ducts.
[0178] FIGS. 11A and 11B depict side views of additional
embodiments of an eye treatment device 200 having energy transducer
205 configured to convert electrical energy from the power source
module 110 into ultrasonic energy. The ultrasonic energy transducer
205 may be formed from any suitable material, such as a
piezoelectric ceramic, polymer, or composite. In the various
embodiments described above, an ultrasonic energy transducer 205
may be used in combination with the light energy transducer module
120.
[0179] In FIG. 11A, the eye treatment device 200 includes a flat
piezo ultrasonic energy transducer 205 configured to emit unfocused
ultrasound waves. While the direction of the waves is unfocused,
the wavelength of the ultrasonic energy can still be manipulated so
as to target particular regions of a tissue. With ultrasonic
energy, the longer the wavelength, the deeper the penetration.
Accordingly, in some embodiments, short, high-frequency waves of
20-100 MHz, 50-100 MHz, or any sub-range or individual value
therebetween are emitted. Ultrasonic waves of such frequencies may
penetrate the tissue of the eyelid 1-3 mm. Advantageously, at such
penetration depths, the meibomian glands and other surrounding
target tissue can be heated without significant heating within the
eye. In other embodiments, a wavelength of greater than 100 MHz may
be emitted from the ultrasonic energy transducer 205.
[0180] The eye treatment device 200 of FIG. 11B includes one or
more curved piezo ultrasonic energy transducers 205 configured to
produce focused ultrasound waves. In some embodiments, the
ultrasound waves are directionally focused to selectively heat a
target tissue region sufficiently to melt meibum within meibomian
glands located within or adjacent to the target tissue region. In
some such embodiments, the ultrasound waves are targeted and
directed through the use of a shaped or curved transducer having a
focal point. FIG. 11B depicts one such embodiment. In other
embodiments, the ultrasound waves are targeted and directed using a
shaped array of individual ultrasonic elements. There may be more
than one array of ultrasonic elements; for example, one array may
be directed at the lower eyelid, and another array may be directed
at the upper eyelid. It will be appreciated that in order to
efficiently transmit ultrasonic energy into the target tissue, the
energy transmission surface 140 must be made from an appropriate
material. For lower-frequency ultrasonic waves, traditional
materials such as silicone or other polymers and elastomers may be
utilized. In certain embodiments, it may be desirable to cool the
surface of the eyelid as the ultrasonic energy is applied, to
prevent exceeding a predetermined threshold. In such cases, the
energy transmission surface 140 may be made from a material that
not only can pass the ultrasonic energy, but which is also
thermally conductive (so that the cooling techniques described
previously herein may be applied). Examples of materials that can
pass higher-frequency ultrasonic energy as well as provide adequate
thermal conductivity include diamond or graphene.
[0181] It will be appreciated that, in addition to providing tissue
heating effects, the ultrasonic waves may disturb, disrupt, or even
kill the Demodex mites mentioned previously. As such, it may be
beneficial to combine energy modalities such as light and
ultrasound in order to achieve the best overall treatment for MGD,
blepharitis and related maladies.
[0182] In addition to heating a target tissue region, the eye
treatment device 200 of certain embodiments may also be configured
to send vibrational energy into an area that includes the target
tissue region. FIG. 12 provides one example of an eye treatment
device 200 configured to produce vibrational energy. The vibratory
mechanism 250 embodiments described in relation to FIG. 12 are
expressly contemplated for use with any of the eye treatment device
200 embodiments described herein. The eye treatment device 200 of
FIG. 12 includes a vibratory mechanism 250 within a portion of the
housing 202. Any suitable vibratory mechanism 250 may be used. In
various embodiments, the vibratory mechanism 250 is configured to
generate a specific vibratory pattern. For example, when held
against the eyelid of a patient, an eye treatment device 200 having
a vibratory mechanism 250 may vibrate forward and backward along an
axis parallel with the central ocular axis 30. In other
embodiments, the eye treatment device 200 may vibrate side-to-side
or up-and-down in directions orthogonal to the central ocular axis
30. In still other embodiments, the eye treatment device 200 may
vibrate in a circular pattern, for example, a circular pattern
orthogonal to the central ocular axis 30. In some embodiments, the
eye treatment device 200 may include multiple settings such that a
plurality of vibration patterns can be selected. The vibratory
pattern may be applied to an eyelid before, during, or after the
delivery of heat to the target tissue region.
[0183] In some embodiments, the frequency of vibration is between
about 1 Hz and about 20 KHz, but may extend into the ultrasonic
frequency range up to 20 MHz, and may include any sub-range or
individual value therebetween. Vibrations within the frequency
range may help aid in expressing meibum, which has thickened or is
blocked within the meibomian glands. In addition, the vibration
pattern may disturb or disrupt the Demodex mites, thereby reducing
their proliferation. It will be appreciated that combinations of
vibration and/or ultrasonic energy application may be employed to
generate the most effective overall treatment including tissue and
meibum heating, meibum vibration and expression, and mite
disruption.
[0184] As further depicted in FIG. 12, in some embodiments, the
vibratory mechanism 250 is positioned in a distal portion 203 of
the housing 202. In some such embodiments, a vibratory isolation
element 252 is positioned between the distal portion 203 of the
housing 202 and a proximal portion 201 of the housing 202 such that
the force of the vibrations is damped in the proximal portion 201.
In some embodiments, a handle or hand gripping portion of the eye
treatment device 200 is located in the proximal portion 201; thus,
the vibratory isolation element 252 helps limit vibrations of a
user's hand during use. In other embodiments, no isolation element
252 is present. In still other embodiments, the vibratory mechanism
250 is disposed within the proximal portion 201 of the housing 202,
with a translational linkage between the vibratory mechanism 250
and the distal portion 203.
[0185] It should be emphasized that the foregoing specific
embodiments are exemplary, and that this disclosure encompasses a
large number of variants beyond those particular embodiments. Some
of these will now be described in greater detail.
[0186] When the energy transducer module 120 is an LED emitter 207,
some embodiments includes the use of one or more LEDs, preferably
having high intensity. For example, one or more LEDs having a
combined power output of at least 10 watts, preferably at least
about 15 watts, or even 20 watts or more of combined power output.
The combined intensity of those LEDs can advantageously be at least
about 20, 30, 40, 50, 75, 100, 150, 200, 250, 300, 400, 500, 1000,
2000 or more lumens. When directed to the eyelid, the continuous
intensity of the applied luminous energy can preferably be between
about 0.02 and 2 Watts/square-centimeter.
[0187] In some embodiments, the LEDs can be green LEDs. Green is
advantageous in that it penetrates and heats tissue to the depth of
about 0.5-2 mm, beyond which it is significantly attenuated. This
allows the light energy to penetrate to the treatment area
encompassing tissue at or adjacent to the meibomian glands, with
limited light transmitted to the eye. Some preferred wavelengths
for the light can be 495-570 nm, 500-600 nm, and more preferably
about 510-540 nm or 520-530 nm. In some embodiments, an infrared
radiation source can be 700-1000 nm, preferably in the "optical
window" of human tissue around 800-900 nm, and more preferably
about 850 nm. Longer wavelengths would work also, potentially
taking advantage of more absorption by water in tissue as the
wavelength increases. For example, 3,000 nm infrared may be able to
provide ideal heating of the eyelid tissue with minimal penetration
and heating of the eyeball and sensitive structures. In other
embodiments, the LEDs can be blue, yellow, red, white, or a
combination of any of the foregoing.
[0188] The energy transducer module 120 can alternatively comprise
a broad or narrow spectrum lamp, such as an incandescent lamp, a
xenon lamp, halogen lamp, a cold cathode tube, a fluorescent tube,
and the like. The illumination source may further comprise a
spectral limiting element to reduce the intensity of or
substantially eliminate certain undesired wavelengths from the
spectrum of the lamp. Those spectral limiting elements can include
colored filters, dichroic filters, IR cutoff filters, gratings,
bandpass filters, spectral separating elements such as prisms or
gratings, and the like. Infrared lamps or heating elements can also
be used. The primary wavelengths allowed to reach the eyelid can be
selected as discussed above for LEDs, or can be limited primarily
to infrared radiation.
[0189] The energy emitted by the illumination source and delivered
to the patient is preferably continuous in delivery (with
pulse-width or other form of modulation, if desired), as opposed to
low duty cycle, high-intensity pulsed light (such as IPL). The
treatment period is preferably for multiple seconds or minutes,
e.g., 5, 7, 10, 12, 15, 18, 20, 15, 30, 40, 45, 50, 60 seconds, or
1, 1.5, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, or even 30 minutes or
more.
[0190] In some embodiments, visible light delivery from the energy
transducer module 120 can be facilitated by, or replaced with, an
alternative energy transducer functioning as a heating modality.
These can include, for example, an ultrasound transducer or a radio
frequency emitter. When an ultrasound transducer is used, it can be
either focused or unfocused. High frequencies are preferred, to
limit the depth of heating, to concentrate heating on the target
tissue area comprising or adjacent to the meibomian gland, and to
reduce or eliminate effects on the eyeball or other tissue in the
region. Preferred frequencies are 50-100 MHz or greater than 100
MHz to 250 MHz. Focused ultrasound, for example, using multiple
transducers, including phase-managed arrays to facilitate
directional focus, or shaped transducers having a limited focal
area, are particularly preferred. As with the light energy,
relatively continuous delivery can be used, as can pulsed
delivery.
[0191] When a radio frequency emitter is used, frequencies known to
provide localized heating are preferred. Frequencies used for
electrosurgery, such as 300 KHz-4 MHz can be advantageously used.
In one such embodiment, bipolar electrodes are provided in or on
the energy transmission surface 140 to contact the eyelid and
permit control of location and depth of heating.
[0192] Alternatively, higher frequency radio waves, in the 5 MHz to
10 MHz range, can be used due to their higher attenuation rate in
tissue, thus allowing careful selection of penetration depth and
limitation of heating to the desired region of tissue. For example,
frequencies above about 245 MHz penetrate human skin and tissue to
a depth of about 1-3 mm, which matches the typical distance between
the exterior of the eyelid and the target tissue (i.e., the
meibomian glands and adjacent tissue).
[0193] The energy waveguide module 130 is designed to transmit
energy from a transducer or generator to the energy transmission
surface 140 and thence into the target tissue. For example, when
creating light energy from a small source such as a LED or small
lamp, the energy waveguide module 130 can direct even illumination
from the source to the target tissue zones. In some embodiments, it
may be desirable to include a waveguide structure to direct light
toward the eyelid and the target tissue without directing it along
the central ocular axis of the eye. This can then reduce the amount
of light penetrating into the cornea and into the eye, while still
directing the light to the eyelid, albeit at a more tangential
angle. Suitable structures for accomplishing this purpose include
light pipe arrays, refractive elements, reflective elements,
diffractive elements, total internal reflection elements (TIRs),
and diffusers. For example, fiber optics, mirrors, lenses, prisms,
and the like can be used to direct light and change its angle of
incidence onto a target surface (to avoid central ocular axis, for
example). In some embodiments, it may be desirable to direct light
toward the scleral shield 300 and image translator 155 to view the
inner side of the eyelid 14 and/or heat the meibomian glands behind
the eyelid, as described above.
[0194] In another embodiment, the energy waveguide module 130 is an
ultrasonic waveguide having surfaces that reflect ultrasonic energy
to direct and/or focus it onto a desired region, e.g., the target
tissue region. Similarly, a microwave or other RF waveguide of
known design can be used to direct RF energy to the desired
region.
[0195] The energy transmission surface 140 is interposed between
the interior of the eye treatment device 200 and the patient,
providing a barrier therebetween. It can be envisioned in some
embodiments as a window through which the energy is delivered to
the patient. It can be configured to directly contact the eyelid of
the patient, or to be spaced a small distance from the eyelid, such
as between 0.5 mm and 12 mm from the eyelid during treatment.
Preferably, the exterior surface of the energy transmission surface
is smooth and easily cleaned. In some embodiments, a single-use
outer eyelid pad 147 may be placed over energy transmission surface
140 in order to prevent cross-contamination between patients. The
outer eyelid pad 147 may be fabricated from any suitable material
such as glass, pyrex, quartz, mica, or polymers such as
polycarbonate or other optically transparent materials can be used,
or a combination thereof, in order to obtain the desired structural
and optical properties. In some embodiments, the energy
transmission surface 140 may be in a slidable relationship along
movement path 145 with respect to either the energy transducer
module 120 or scleral shield 300 or housing 202, so as to ensure
energy transmission surface 140 can be pressed up against the
eyelid or eyelids to: a) minimize photonic energy leakage during
treatment and imaging, and b) if desired, apply a compressive force
to the eyelid during evaluation or expression of meibomian
glands.
[0196] When using light energy to heat the target tissue region,
the energy transmission surface 140 is advantageously transparent
to visible or infrared light as desired. In some embodiments, it is
transparent to the peak or desired wavelengths used for treatment,
such as visible light or green light, but blocks infrared light,
thus reducing IR heating of the eyelid. Glass, pyrex, quartz, mica,
or polymers such as polycarbonate or other optically transparent
materials can be used.
[0197] When heating the target tissue region with ultrasound or RF,
transparency to visible light is not necessary; instead, an
ultrasound-transparent or RF-transparent material can be used. In
some embodiments, it is desirable that the materials be thermally
conductive, to facilitate cooling of the eyelid by cooling the
energy transmission surface 140. Diamond, sapphire, and graphene
are suitable thermally-conductive materials. In another embodiment,
either the entire energy transmission surface 140 or at least a
window thereof is transparent to safety sensors disclosed herein.
For example, where a non-contact infrared temperature sensor is
used to sense the temperature of the exterior of the eyelid, an
IR-transmissive material is advantageously used for all or at least
the relevant region or regions of the energy transmission surface
140.
[0198] When applying heating energy to the eyelid from the eye
treatment device 200, some embodiments includes surface-cooling the
eyelid by cooling the energy transmission surface 140. If the
exterior of the eyelid is cooled while irradiating the target
tissue region with light, ultrasound, or RF energy, patient comfort
can be enhanced while maximizing efficacy through optimal heating
of the target tissue. The energy transmission surface 140 can be
cooled by: airflow across the interior of the energy transmission
surface 140; application of an evaporative agent to the inside of
the energy transmission surface 140, such as a refrigerant or
water; circulating a cooling fluid through channels in or on the
energy transmission surface 140; or contacting the energy
transmission surface with a thermoelectric (Peltier junction) or a
heat sink linked to a cooling modality. Alternatively, the energy
transmission surface 140 can have a sufficiently large thermal mass
(or be in contact with such a thermal mass) so as to remove
sufficient heat from the eyelid during the treatment of the patient
to maintain the eyelid within a desired temperature range. The
thermal mass can be pre-cooled or simply begin at ambient
temperature before the treatment. Other methods of cooling the
energy transmission surface 140 and/or the eyelid include
incorporating a reservoir between the energy transmission surface
and the skin of the eyelid, such as a water-filled bladder. The
bladder can be pre-cooled or actively cooled during the procedure,
such as by circulation of cool water therethrough or through using
a chilling element such as a thermoelectric device, a compressor, a
refrigerant, or other chilling element.
[0199] In another embodiment, the energy transmission surface 140
is spaced a small distance from the eyelid to allow passage of a
cooling fluid, such as relatively cool air, mist, water, and the
like between the energy transmission surface 140 and the eyelid.
For example, cool air can be induced to flow transversely across
the surface of the eyelid and the energy transmission surface 140,
or the energy transmission surface 140 can include holes or
channels to direct the cooling fluid onto the eyelid. The cooling
fluid can be ambient temperature or can be pre-cooled, such as
through refrigeration, ice, and the like.
[0200] When a vibratory mechanism 250 is used, it can comprise, for
example, a reciprocating element such as an electromechanical
solenoid or the like, a rotating eccentric weight, such as an
eccentric weight coupled to a motor shaft, or a rotating cam.
Preferably, the vibratory mechanism is vibrationally coupled to the
eyelid but vibrationally isolated from other patient or clinician
contact points, such as the proximal end of the eye treatment
device 200, including any handle region that a patient or clinician
might hold.
[0201] Patient safety and comfort are important considerations in
the present device and method. Safety sensors and warnings can thus
advantageously be incorporated into the device. These include
sensors for preventing overheating of the skin, sensors for
preventing undesired activation of the device, and sensors
monitoring the delivery of energy to the patient. In some
embodiments, a safety sensor may be utilized to make sure that a
consumable portion 260 having a protective scleral shield 300 is in
the correct position prior to turning on an energy transducer
module 120, thus preventing damage to the eye system 10.
[0202] As illustrated in FIG. 10, a safety warning apparatus 240
can be incorporated into the device to let the patient know of an
unsafe condition, as sensed by any of the sensors described herein.
This can include a flashing light, a flashing warning, a sound
warning beep, a picture, a vibration pattern, or words indicative
of the potential for or existence of an unsafe condition.
[0203] Again with reference to FIG. 10, a first set of safety
sensors 232, 234, is preferably located on, in, in back of, or
otherwise in the vicinity of the energy transmission surface 140.
Both sensors are configured to detect heating of the outer eyelid
surface and to prevent overheating thereof. Sensor 232 is
preferably a non-contact sensor such as a pyroelectric sensor (for
example, IRA-E700ST0 from Murata) or a thermopile (such as
ST25T0-18 from Dexter Research, Dexter, Mich.) or a conventional
temperature monitoring device such as a thermocouple, a thermistor,
a fiberoptic thermal sensor, or a digital temperature sensor (such
as a Dallas Semiconductor DS-18620). In addition to temperature
sensors 232 and 234, temperature sensors 310 may be mounted on the
front or back surfaces of scleral shield 300, as shown in FIGS. 3,
7A-H and 8, to monitor the inner eyelid surface temperature and
eyeball temperature, respectively. A threshold temperature may be
programmed into the eye treatment device 200, such as 40.degree.
C., 45.degree. C. or 50.degree. C. In some embodiments, when the
threshold temperature is reached or exceeded, the safety sensor may
be configured to shut off the eye treatment device 200 and/or via
safety warning apparatus 240 to signal the user or clinician to
stop treatment using lights, beeps or other notification means. In
some embodiments, when the threshold temperature at any particular
location is reached or exceeded, the controller 212 (or discrete
circuitry independent of any controller) may be used to prevent
heating of the eyelid beyond this threshold temperature. This can
be accomplished, for example, by shutting off the eye treatment
device 200, by reducing the energy being delivered (such as
reducing intensity of the light, pulse-width modulation of the
LEDs, reducing power input for ultrasound or RF energy, etc.), or
by activating cooling measures to reduce eyelid temperature.
[0204] A second type of safety sensor is also illustrated in FIG.
10. This may include a single sensor or a plurality of sensors. The
purpose of the second type of safety sensor is to ensure that the
eye treatment device 200 is properly positioned against the eyelid
prior to activation of the treatment. The second type of safety
sensor can include one or more of the following sensors. One sensor
can be a light sensor 236. When the device is positioned against
the eyelid, ambient light is blocked. Thus, the absence of such
light can be detected. Alternatively, a reflective optocoupler-type
device can be used in which a light source is directed distally and
is coupled with a sensor also aimed distally. This allows the
presence of the patient to be detected, together with an
approximation of the distance to the patient. Depending on the
distance between the light source and the optocoupler-type device,
light detection is either maximized or eliminated when the eye
treatment device 200 is properly positioned. Another
light-detection scheme is to provide a light sensor 236 facing
distally toward the patient but outside of the path of the
treatment light. When the eye treatment device 200 is spaced from
the eyelid, reflected treatment light can reach the sensor 236, but
when properly positioned, most such light is blocked from the
sensor 236. The light sensor approach can be coupled with data from
one of the temperature sensors to simultaneously detect light and
skin temperature as an indication of the positioning of the device.
In any of the light detection embodiments, an ambient light sensor
236 can be incorporated into the eye treatment device 200 to
measure ambient light levels to facilitate the optical detection of
proximity to the eyelid. Similarly, when using a temperature sensor
in conjunction with the second type of sensor, an ambient light
sensor 236 can facilitate determining when the eye treatment device
200 is against the skin, particularly in a high temperature
environment. Other distance or contact detection elements, such as
an ultrasonic range-finding module, can also be used. In some
embodiments, thermocouples or thermistors 234 on, in or adjacent to
the energy transmission surface may be used to indicate when the
device is properly positioned adjacent to a patient's eye. For
example, the thermocouples or thermistors 234 may register room
temperature prior to placement of the device adjacent to the eye,
and as the energy transmission surface 140 comes in proximity to
the eyelid skin, the thermocouples or thermistors 234 will register
a value closer to body temperature, and therefore, confirm proper
positioning. A reflective or color sensor 237 may also be
incorporated into the device to confirm that the eye is closed. As
described above, such sensors 237 can provide data indicating
whether or not there is tissue that appears to be eyelid skin
(e.g., flesh colored and not wet or shiny) or eye tissue (white or
iris colored, and wet and shiny).
[0205] In another embodiment, the second type of sensor can be a
touch sensor, detecting when the eye treatment device 200 is
touching the face. The touch sensor can be a resistive sensor,
utilizing two electrodes and sensing a microcurrent through the
skin, or a conventional resistive touch sensor. Alternatively, a
capacitive sensor can be used to detect when the eye treatment
device 200 is touching the skin. This can be either a single sensor
or, for a better signal, a plurality of sensors wherein all or a
subset of them must be activated to allow the treatment to proceed.
Finally, the touch sensor can comprise an electrical switch (such
as a microswitch) or a strain gauge that is activated when the
device is pressed against the skin. For example, the microswitch
can be embedded behind a flexible, sealed surface, or it can be
activated when sufficient pressure is applied to allow a first part
of the eye treatment device 200 to move with respect to a second
part of the eye treatment device 200.
[0206] A third type of safety sensor may also be used in the eye
treatment device 200 to monitor the energy delivery transducers to
assure proper operation within predetermined parameters. Again,
this may be a single sensor or combination of sensors, including
one or more of the following. In some embodiments, the safety
sensor can measure current and/or voltage applied to a transducer,
as shown in FIG. 10 as transducer monitor 246. Thus, when the
transducer is one or more LED emitter 207, the drive current or
forward voltage of the LEDs can be monitored, where deviation from
pre-established parameters can indicate failure of an LED or LED
driver or unsafe operating conditions. The voltage across an RF or
ultrasound transducer can similarly be monitored by transducer
monitor 246, as can the current supplied thereto. In another
embodiment, a thermal sensor such as thermocouple or thermistor 234
shown adjacent to energy transducer module 120 in FIG. 10 may be
configured to monitor the internal or external temperature of a
transducer element, wherein overheating can indicate unsafe
operation or failure of an element, and lack of heating may also be
indicative of an operational failure.
[0207] In some embodiments, the controller 212 may be a manual, or
open-loop system, with autonomous discrete analog and digital
circuitry for manual operation without any automatic control. The
manual operation may include turning the eye treatment device 200
on and off, and receiving safety and feedback information. In this
case, the eye treatment device 200 is operated manually without a
controller by the user or clinician turning the eye treatment
device 200 on and assessing desired treatment of the eyelid using
the feedback and adjusting the process in response to the
assessment. The feedback features may signal the user or clinician
of the status, such as on/off, lights or beeps, temperature data,
pressure data, safety data, or other data that could help the user
or clinician assess the process. In some embodiments, the
controller 212 may include direct-acting threshold detectors and
shut-off circuits for safety. In some embodiments, the controller
212 may include a processor or centralized controller configured to
monitor the process with feedback features and some portion of the
feedback is returned to the controller for safety, such as turning
the system off in an unsafe condition.
[0208] The controller 212 functional block encompasses and performs
both operational functions, to direct the intended operation, and
safety functions, and to interface with the various safety sensors
230. It can be a single processor controlling all functions, i.e.,
one controller 212 as illustrated in FIGS. 3 and 4A, or can
comprise two or more controllers, such as a primary controller with
a secondary safety controller acting as a watchdog on the first
controller, as is well-known to those skilled in the art.
Specifically, the secondary safety controller may be designed to
monitor the functionality of the primary controller--if one or more
parameters indicate the primary controller 212 may not be
functioning properly, the secondary safety controller is configured
to power down the energy transducer and/or the entire eye treatment
device 200. The functions associated with controller 212 can be
accomplished with a controller such as a microprocessor or
microcontroller with associated software, but certain embodiments
may preferably operate without a controller, and instead utilize
one or more of a programmable gate array, a logic array, analog
circuitry, digital circuit elements, or any combination of the
foregoing.
[0209] In one simple embodiment, the secondary safety controller
comprises an array of analog or digital circuit elements without a
processor. For example, optical, temperature, and/or pressure
switches either hard wired together or with logic circuitry, op
amps, and/or relays are configured to allow initial or continued
operation of the device only if the sensors are in a predetermined
state. In an alternative embodiment illustrating full processor
control, all sensors are monitored through digital or ADC inputs to
one or more programmed processors to perform the functions of a
second safety controller and to either prevent operation outside of
predetermined parameters or to modulate the operation of active
elements in the eye treatment device 200 to stay within those
parameters.
[0210] In addition to safety functions, the controller 212 may
direct the normal operation of the eye treatment device 200. For
example, it can interface with the user through a user interface
270 which may include control buttons, rotary encoders, touch
screens, voice commands, or any other conventional user interface.
It can control a power manager, direct or interrupt current flow to
the energy transducer and modulate its output, initiate or stop
operation of the vibration apparatus, initiate or disable a safety
warning, initiate, modulate, or stop operation of the surface
cooling apparatus, and monitor and modulate cooling of the energy
transducer through the thermal manager. The controller 212, or the
discrete circuit substitute, may be operationally linked to some or
all of these systems within the eye treatment device 200. In
addition, it can include a timer function to automatically shut off
the energy transducer and thus interrupt delivery of heating or
vibrational energy to the eyelid after a predetermined period of
operation, or in response to signals from the first, second, or
third type of safety sensors.
[0211] The power source module 110 is designed to facilitate supply
of power to the eye treatment device 200. It can include external
power interfaces, such as cords or cables interconnecting with an
external power source. In a preferred embodiment, the power manager
includes an internal power supply. In some embodiments, the power
manager includes a rechargeable battery or battery pack. This could
include nickel-metal hydride batteries, lithium ion or lithium
polymer batteries, nickel cadmium batteries, or any other suitable
rechargeable or non-rechargeable batteries. The batteries
preferably provide a high current capacity, such as 1-5 amps,
preferably at least 3 amps surge current, with the ability to
deliver such high current for 1, 2, 3, 4, 5, or more minutes. In
some embodiments, the internal batteries deliver 3, 4, 5, 6, 7, 8,
9, 10, or 12 volts or more. The capacity of the batteries is
dictated by the design load, and may be, for example, a battery
pack having at least a 200, 300, 400, 500, 1000, 2000, 2500 mA-hour
capacity or more. The desired voltage can be accomplished by
connecting lower voltage batteries in series to achieve the desired
voltage, or through use of a DC:DC converter to step up a lower
voltage to the desired voltage. In some embodiments, the batteries
supply a voltage lower than that required by the energy transducer
power supply, and the voltage is stepped up for the energy
transducer while a lower voltage, e.g., 5V or 3.3V, is supplied to
the controller 212 or alternative discrete circuitry.
[0212] In one preferred embodiment, the energy transducer may be a
high-power LED similar to one made by LED Engin, Inc.;
specifically, the energy transducer may be an LZ9 configured with
nine green emitters in a non-standard configuration arranged as
three sets of three series emitters in parallel, requiring
approximately 12-14V forward voltage and up to 2.4 amps for maximum
illumination. In this embodiment, three RCR123 LiFePO4 cells or
similar may be utilized in series, having a capacity of 750
mA-hours and providing a starting voltage of 7.2V. A DC-DC
converter circuit is included which boosts the voltage by
approximately two times in order to provide the voltage needed to
drive the LED.
[0213] Power management functions can include a charger, battery
status monitor, and/or temperature monitor. These functions can be
performed by separate circuitry or incorporated in whole or in part
into the controller 212. In some embodiments, power management
includes a battery charger powered through inductive coupling to an
external power supply, which can allow the eye treatment device 200
to be sealed, allowing easy cleaning and preventing ingress of
moisture or dirt. In some embodiments, the inductive coupling may
use a recharging cradle or electrically-isolated mains power
connection. The inductive coupling may include two induction coils
in close proximity (one in the cradle and one in the device) or two
coils tuned to resonate at the same frequency (resonant inductive
coupling or electrodynamic induction).
[0214] Thermal management is also a critical element of many
preferred embodiments, including, in some cases, heat removal from
the energy transducer, such as an LED or LED array. In the case of
LEDs, it is important to maintain the junction temperature below a
predetermined threshold, such as 135 degrees Celsius. Other
transducers similarly have maximum allowable component
temperatures, and proper thermal management helps maintain those
components within allowable temperatures. For example, heat sinks
thermally coupled to the energy transducer elements, fans,
radiators, cooling fluids, and the like may be utilized. In a
preferred embodiment, the eye treatment device 200 is sealed and a
thermal management structure 220 such as shown in FIG. 9 directs
excess heat to an external surface of the eye treatment device 200.
This allows for a sealed device without ventilation openings. In
other embodiments, a cooling fluid is directed from the thermal
manager inside the device to remove heat from the device, such as
through forced air cooling (as shown or FIG. 8), or a liquid-cooled
radiator.
[0215] In a further aspect of the technology, the eye treatment
device 200 may include elements useful in calibrating the device so
that it provides the desired amount of heating to target tissue
over a wide range of eyelid thicknesses. This is important because
without such calibration, the amount of heating that occurs at the
target tissue region (e.g., the meibomian glands and adjacent
tissue) can vary unless the temperature near the target tissue
region is measured during the treatment. As discussed previously,
monitoring of the target tissue region may be accomplished by use
of a scleral shield, or the like, equipped with temperature
sensors. However, it may be inconvenient for users of the device to
insert scleral shields each time they use the device. Therefore, it
may be useful to calibrate each device to an individual's specific
anatomy. To accomplish that, the device may be calibrated by using
a scleral shield initially, preferably in the setting of an eye
care professional's office, and in conjunction with an external
monitor and calibrator.
[0216] For example, with reference to FIG. 13, as the eye treatment
device 200 applies energy to the eyelid(s), the scleral shield 300
transmits temperature data (either through a wired or wireless
connection) to an external monitor and calibrator 500. The external
monitor and calibrator 500 tracks the rate of temperature rise over
time, and thereby characterizes the heating profile of the
patient's eyelid(s). With that data, the external monitor and
calibrator 500 can then program the eye treatment device 200 to
heat the target tissue to the desired temperature range. In a
simple embodiment, the external monitor and calibrator 500 turns on
the energy transducer, measures the amount of time needed for the
target tissue to reach the desired temperature, and then turns off
the energy transducer and programs the eye treatment device 200 to
apply energy for that same amount of time. Alternatively, the eye
treatment device 200 may be programmed to provide increased or
decreased amounts of energy in order to heat the target tissue to
the desired temperature within a preferred period of time. In most
individuals, eyelid thickness is similar from upper eyelid to lower
eyelid and from the right eye to the left eye, however, it will be
appreciated that the external monitor and calibrator may separately
measure and separately program the device to apply specific amounts
of energy to each individual eyelid in order to ensure proper
heating of each one. It will be further appreciated that there may
be variances in the performance of the components used to implement
the energy transducer and related circuitry, and that, without
proper calibration, one device might produce more or less energy
than another. One solution to this is for the factory to measure
the actual energy output for a given command level from the
controller, and to incorporate a calibration table within the
controller, such that every eye treatment device 200 puts out an
equal amount of energy for a given command level. Alternatively,
and additionally, with the external monitor and calibrator 500,
such variances can also be compensated for by the procedure
described above, wherein the ultimate goal of the eye treatment
device 200 is to heat target tissue to a desired temperature, and
each eye treatment device 200 is programmed to do so (regardless of
component variances) on each specific patient (and optionally on
each specific eyelid).
[0217] Referring now to FIGS. 14A and 14B, in one embodiment of the
scleral shield 300, there is an array of temperature transducers
310 embedded in the shield. For this application, where the shield
is not actually being used to shield the eye from the energy, but
instead to measure temperatures, the shield 300 may be made of
materials that are substantially transparent to the energy emitted
from the energy transducer. By way of specific example, if the
energy transducer is a light source, the shield 300 may be made of
a clear material that passes the wavelength(s) of light emitted by
the energy transducer. Preferably, the shield 300 is also as thin
as possible and supple, with no sharp features, so that it can
comfortably be placed under the eyelids with minimal discomfort to
the patient and so it has a minimal effect on the heating of the
tissue. In the embodiments shown in FIGS. 14A and 14B, an example
is shown wherein there is an array of six temperature sensors 310
on a front face 302 of the shield 300, and an array of sensors on
the back face 304. This configuration allows the front-facing
sensors 312 to more directly measure the temperature of the tissue
on the inside surface of the eyelids, where the meibomian glands
are located, while the back-facing sensors 314 more directly
measure the temperature of the surface of the eye, along the
midline of the central ocular axis, where the most sensitive eye
tissues are nominally located. The temperature sensors may be
discrete elements (such as thermocouples made from very fine wire,
or miniature thermistors) embedded in the shield 300, or they may
be thermocouples formed by depositing thin films of appropriate
metals onto intermediate layers of the shield 300. In some
embodiments, the preferred types of materials for the shield 300
are soft, flexible, biocompatible materials such as silicone,
polyurethane, and various hydrogels similar to those used in
contact lenses.
[0218] While the above embodiments describe the configuration
having and external monitor and calibrator 500, it will be
appreciated that the eye treatment device 200 itself can have the
same capability built into it, in which case the scleral shield 300
communicates temperature data directly to the eye treatment device
200, and the eye treatment device 200 programs itself to provide
the correct treatment profile for that particular patient (and
optionally for individual eyes and eyelids). In such embodiments,
the eye treatment device 200 has a sophisticated user interface 270
allowing the clinician to command the eye treatment device 200 to
perform a calibration sequence, and optionally instruct the eye
treatment device 200 as to which eye and/or eyelid is being
calibrated. It is appreciated that if the eye treatment device 200
is calibrated to provide individually calibrated treatment to each
eye or eyelid, the eye treatment device 200 needs to be able to
indicate (via a series of lights or an alphanumeric or graphical
display) to the patient which eye or eyelid is to be treated
next.
[0219] Alternatively or additionally, a calibration element may be
used to measure the energy output of the eye treatment device 200.
For embodiments where the energy transducer is a light source, the
calibration element may be a light meter to measure, for example,
luminous flux, lumens or radiant flux. For embodiments where the
energy source is an ultrasonic transducer, the calibration element
may be an ultrasonic energy meter. The calibration element may be
used to determine if the eye treatment device 200 is operating
within acceptable limits or not, and may also provide data to allow
adjustment of certain parameters (such as energy level or treatment
time) to bring the eye treatment device 200 back into the desired
performance range. It will be appreciated that the calibration
element may also communicate directly with the eye treatment device
200 or indirectly (e.g., through a PC) with the eye treatment
device 200 in order to reprogram the eye treatment device 200 with
updated calibration data to keep the device operating within an
acceptable performance range.
[0220] In some embodiments, the eye treatment device 200 may
further include a temperature display feature or dashboard 218 for
the in-office device, which could include inner lid and outer lid
temperatures. The temperature display feature may display absolute
temperatures, or just relative temperatures versus a maximum. For
example, the temperatures may be displayed in a bar graph format or
with one or more lights.
[0221] In some embodiments, the eye treatment device 200 may
further include a datalogger 214 configured to record aspects of
the treatment, (e.g., time, date, usage parameters, temps, photos,
videos, etc.). In some embodiments, the eye treatment device 200
may further include a voice recorder 213 so clinicians can record
verbal observations of how many MGs are healthy, clogged,
atrophied, etc., along with time, date and patient name. This
allows the clinician to carry out the procedure without the need to
take manual notes and/or without the need to have an assistant
present. In some embodiments, the eye treatment device 200 may
further include a communication means configured to couple with an
external PC, tablet or smartphone for downloading data, voice
recordings, camera images or video clips.
[0222] FIGS. 15A-15D show another embodiment of an eye treatment
device 200 positioned relative to an eyeball 20 for treatment of
the eyelid 14 for MGD, blepharitis and other medical conditions. In
some embodiments, the eye treatment device 200 is configured to
heat the inner and/or outer surfaces of the eyelid while
compressing the eyelid, similar to the embodiment of FIG. 3A. As
the heat from the eye treatment device 200 is transmitted to the
eye system 10, particularly to the treatment tissue such as the
meibomian glands 18, the heat can soften the meibum and thereby
allow the meibum to be more readily expressed during massage or eye
exercises. The eye treatment device 200 can include configurations
of the modules depicted in FIGS. 2A-2H and FIG. 3A, along with
additional components useful in operation of the eye treatment
device 200.
[0223] The eye treatment device 200 can include a housing 202
having a proximal portion 201 and a distal portion 203 coupled with
a removable or consumable portion 260. The housing 202 may include
a power source module 110, a controller 212, an energy transducer
module 120, and an energy transmission surface 140. The energy
transducer module 120 of some embodiments may include an LED device
formed of one or more of an LED emitter 207, a thermal management
structure 220, and an energy transducer module driver 209. The
energy transmission surface 140 and LED emitter 207 are positioned
near a distal portion 203 of the housing 202 and are in a slidable
relationship along movement path 145 with energy transducer module
120 using actuator 182, which allows for the energy transmission
surface 140 to move with the LED emitter 207 simultaneously.
[0224] The housing 202 may further include visualization means 160
for enhanced monitoring of the eyelid margin during diagnosis and
treatment, a display or dashboard 218 showing various temperatures
of the eyelid, such as inner and/or outer surface temperatures, a
datalogger 214, and/or voice recorder 213, and circuitry for
communication between device and consumable circuitry in order to
identify the type of consumable, ensure that the consumable is in
proper alignment and/or prevent reuse of the consumable.
[0225] The consumable portion 260 may include a scleral shield 300,
as discussed above, that can be positioned between the eyelid 12,
14 and eyeball 20 to cover sensitive anatomy of the eye system 10
(such shown in FIG. 1). The scleral shield 300 may be coupled to
the housing 202 with one or more support arms 262, with the wires
being positioned on or within the arms, and, in certain
embodiments, with the structural portion of support arms 262 made
from insulating materials surrounding or otherwise channeling the
conductive portions of wire or wire array 420.
[0226] The eye treatment device 200 can include a power source
module 110 for providing power to the various components of the eye
treatment device 200 and may be electrically coupled to some or all
of the components. In certain embodiments having a controller 212,
the controller 212 can receive input instructions from a user (for
example, through a user interface device 270, such as a button,
switch, touch screen, voice commands, from another module or
device, such as a smartphone) to emit light from the LED emitter
207.
[0227] The LED emitter 207 is a part of one type of energy
transducer module 120 that can be configured to emit light of the
appropriate wavelength necessary for the desired treatment. The
treatments may include one or more of the following: diagnosing the
eyelids 12, 14 by the illuminating the inner and/or outer surfaces,
eyelid margins, and/or the meibomian glands behind the eyelids;
heating the target tissue region of the eye system 10 (e.g., the
meibomian gland behind the eyelids 12, 14); and antibacterial
treatment to kill bacteria in the eye system 10.
[0228] In some embodiments, an additional shielding element 258 may
be used to prevent unwanted photonic energy (such as IR or
blue/violet light) from reflecting off the transillumination
element back to the clinician.
[0229] A feature of many of the embodiments disclosed herein is the
ability of the clinician to view the eyelid margin during the
application of heat and compression. By viewing the margin, the
clinician can see what contents, if any, are being expressed from
the meibomian ducts, and thereby adjust the amount of heating and
compression applied to the eyelid being treated in order to
optimally unclog blocked meibomian glands. By way of example, a
clinician may observe at the start of a treatment that certain
meibomian glands in the portion of the eyelid being treated have a
clear oily discharge, which signals normal glands. In contrast,
some glands may secrete a cloudy oily discharge, or small amounts
of thick, toothpaste-like lipid, both of which signal a
dysfunctional gland. As the clinician applies heat and compression
to the portion of the eyelid being treated, further observation of
the dysfunctional glands can show that the cloudy or thick
secretions change to clear, and the amount of discharge may
suddenly increase, indication that the gland or glands have been
unclogged. At such point, the clinician may reduce the heat and
compression applied to that region, since the treatment has
successfully unclogged the blocked glands. Without this continuous
visual feedback, the clinician would be relegated to applying a
standard treatment regimen, which may either be under- or
over-aggressive for the particular clogged gland(s) in a given
patient.
[0230] By way of reference, at least FIGS. 2D, 2E, 2F, 2G, 2H, 3A,
3B, 15A, 15B and 15D each show example of embodiments wherein the
eyelid margin is exposed for a clinician to visually monitor during
treatment. The clinician would be positioned in front of the eye
being treated.
[0231] Referring now to FIG. 16A, a side cross-sectional view is
shown of an energy transmission surface 140, an eyelid 14 with an
eyelid margin 14a, a scleral shield 300, and a visualization means
160 with optical path 175. This embodiment is the same as is shown
in FIG. 2E, except without image translator 155. In the embodiment
of FIG. 16A, the visualization means is directly focused on eyelid
margin 14a, and more specifically on meibomian ducts 19.
[0232] FIG. 16B is a front perspective view of the same embodiment
of FIG. 16A, showing an example where eyelid 14 is compressed
between energy transmission surface 140 and scleral shield 300,
while eyelid margin 14a is viewable from the front by a clinician.
This embodiment is the same as shown in FIG. 2F without image
translator 155.
[0233] FIG. 16C is a similar embodiment as shown in FIG. 16A, with
the addition of support arm 262. Support arm 262 is the same as
shown in FIGS. 3A, 3B, 7H, 7G, and 15B.
[0234] FIG. 16D is a front perspective of the embodiment shown in
FIG. 16C, showing a pair of support arms 262 coupled to scleral
shield 300. Eyelid margin 14a is exposed, and is adjacent to the
bottom edges of support arms 262, by way of example but not
limitation. FIG. 16E is the same as FIG. 16D but with aperture 440
for viewing the eyelid margin 14a highlighted by the bold dotted
rectangle. FIG. 16F is a top view of the embodiment of FIGS. 16D
and 16E, showing energy transmission surface 140 compressing the
eyelid against scleral shield 300, with eyelid margin 14 exposed
for visual monitoring. FIG. 16G is the same as FIG. 16F but with
aperture 440 for viewing the eyelid margin 14a highlighted by the
bold dotted rectangle. In an embodiment, the distance between the
arms is between 0.2 inches and 1.2 inches. In an embodiment, a
distance between a line defined by the points of attachment between
the two arms and the backplate and a line defined by the points of
attachment between the two arms and compression element is at least
0.04 inches.
[0235] FIG. 16H is a more detailed side cross-sectional view of the
embodiment of FIG. 16C, further defining the boundaries of aperture
440 in certain preferred embodiments. In the figure, Line 1
indicates the lower (horizontal) boundary of the aperture, and Line
2 defines the upper (vertical) boundary. Angle 1 is the angle
between Lines 1 and 2, and is theoretically about 90 degrees,
although variations in the anatomy of cheekbone and eyebrow
structure may result in variations in these boundaries. FIG. 16I is
a more detailed depiction of the embodiment of FIG. 16H, wherein
the preferred lower boundary of aperture 440 is shown as Line 4 and
the preferred upper boundary of aperture 440 is shown as Line 6.
Angle 2 is the angle between horizontal Line 3 and Line 4, and is
preferably between about 5 and about 20 degrees, while Angle 4 is
between Lines 3 and 6, and is preferably between about 60 and 80
degrees. Angle 3 is the angle between Line 3 and Line 5 and is a
preferred angle of viewing of eyelid margin 14a through aperture
440, and is preferably between about 25 and 50 degrees.
[0236] FIG. 16J depicts an embodiment similar to 16H, except energy
transmission surface 140 is shorter than that shown in FIG. 16H,
thereby exposing more of the upper part of eyelid 14 adjacent to
eyelid margin 14a. In this embodiment, aperture 440 is larger,
although the outer boundaries defined by lines 7 and 8 are parallel
to those defined by Lines 1 and 2 in FIG. 16H, and Angle 5 between
them is therefore also about 90 degrees.
[0237] FIG. 16K is similar to the embodiment shown in 16J, except
scleral shield 300 extends behind both the upper and lower eyelid,
and there are portions of energy transmission surface 140 that are
adjacent to upper eyelid 12 as well as lower eyelid 14. In this
embodiment, both the upper and lower eyelids are being heated and
compressed instead of just the lower eyelid. As shown, support arm
262 is linked to scleral shield 300, and energy transmission
surfaces 140 are configured so as to allow viewing of both the
upper and lower eyelid margins through aperture 440. Lines 9 and 10
depict the approximate lower and upper limits of aperture 440,
thereby defining Angle 6, which is preferably between about 10 and
150 degrees, and more preferably between about 20 and 120 degrees.
It will be appreciated that many modifications to the embodiments
herein disclosed are possible, some of which may alter the optical
path and thereby change the angles associated with the aperture.
For example, an image translator such as that shown in FIG. 2E may
be employed, as may other means of reflecting, guiding or
translating the image of the eyelid margin through an aperture to a
clinician. Alternatively, the aperture may be an optically
transmissive window through a structural element. For example, in
FIG. 16K, energy transmission surface 140 may completely cover both
the portions of the upper and lower eyelids being treated, and
instead of there being an opening near the eyelid margin, at least
a segment of energy transmission surface 140 may be transparent
enough for a clinician to view the eyelid margin. Further, there
could be an image sensor, fiberoptic bundle or light pipe mounted
adjacent to, or directed at, the eyelid margin, and the image of
the eyelid margin could be transmitted electronically or optically
to a point outside the energy transmission surface 140. All of
these alternate embodiments, and others apparent to those skilled
in the art, are included within the scope of this disclosure.
[0238] FIG. 16L shows the embodiment of FIG. 16K in a front
perspective view. As shown, dual support arms 262 are linked to
scleral shield 300, and dual energy transmission surfaces 140 are
shown adjacent to the upper eyelid 12 and lower eyelid 14. As
shown, the upper and lower eyelid margins, 12a and 14a,
respectively, are visible, and meibomian ducts 19 are visible as
well. FIG. 16M is the same as FIG. 16L, with aperture 440 generally
defined by the bold dotted rectangle shown.
[0239] FIG. 16N is similar to the embodiment of FIG. 16L, but with
a single support arm 262. FIG. 16O is the same as the embodiment of
FIG. 16N but highlighting the two apertures 440 defined by the gaps
between the upper and lower energy transmission surfaces 140, and
to the right and left of central support arm 262. Other
combinations of single or multiple support arms or other structures
having single or multiple apertures may be contemplated by those
skilled in the art.
[0240] It will be appreciated that FIGS. 16A-16O show the unique
configuration of the energy transmission surfaces 140, the scleral
shields 300 and support arms 262, which define an aperture 440 that
allows viewing of one or both eyelid margins during the application
of heat and compression to the portion of the eyelid being treated.
Many other configurations are possible and only a few exemplary
embodiments have been described herein to demonstrate the
innovative concept.
[0241] Referring now to FIG. 17A, an assembly is shown similar to
portions of the embodiment shown in FIG. 3A. Energy transducer
module 120 is positioned adjacent to the proximal end of energy
waveguide module 130. The distal end of energy waveguide module 130
is adjacent to energy transmission surface 140, made up of face
glass 284 (shown in FIG. 17C) and single-use cover element parts
147a and 147b. Part 147b abuts eyelid 14. FIG. 17B is a front view
of energy transducer module 120, consisting of two infrared LEDs
120a and four lime emitting LEDs 120b, all mounted on a substrate.
FIG. 17C is an exploded view of the same components described in
FIGS. 17A-B, including a call-out 130a for the inside surface of
energy waveguide module 130. In some embodiments, energy waveguide
module 130 may be in a fixed relationship with energy transducer
module 120, while in other embodiments, energy waveguide module 130
may slide with respect to energy transducer module 120, and in
others energy transducer module 120 may slide with respect to 130.
In a preferred embodiment, energy transducer module 120 is fixed
and energy waveguide module 130 slides back and forth around energy
transducer module 120. In such a preferred embodiment, when energy
waveguide module 130 is fully advanced, it pushes energy
transmission surface 140 against eyelid 14 (or 12, when treating an
upper eyelid).
[0242] In order to maximize the efficiency of transmitting light
energy from energy transducer module 120 to energy transmission
surface 140, the inner surface of energy waveguide module 130 may
be coated or lined with a material that is highly reflective to the
wavelengths emitted by energy transducer module 120. By way of
example, the inner surface of energy waveguide module 130 may be
coated with a protected silver material, or it may be lined with
films such as WRF-150 from Fusion Optix, or ESR film from 3M, all
of which are designed to provide >97% reflection of the
wavelengths between 500 nm and 900 nm.
[0243] In certain embodiments, single-use cover element part 147a
may be fabricated from a plastic or glass material that transmits
light energy in the 500-880 nm range. Acrylic is one example of an
acceptable material for single-use cover element part 147a.
Single-use cover element art 147b is preferably a low durometer
material such as silicone in order to provide a soft surface to
press against the surface of the eyelid. Since most silicones are
not fully transparent to infrared energy, it is preferable to keep
the thickness of single-use cover element 147b in the range of
about 0.02-0.06 inches in order to minimize energy loss.
[0244] FIG. 17D shows the distribution of infrared energy
transmitted through eyelid 14 when module is fully advanced (with
its distal end about 0.5 inches from the highest point on the
infrared LED lens). Referring to the graph shown in the upper left,
the darker regions are the areas of highest irradiance (Watts per
square millimeter), while the lighter regions are the lowest
irradiance. As shown, the highest irradiance occurs near the
middle, and the irradiance drops off sharply toward the edges. The
asymmetrical distribution across the X axis is not ideal, since it
is desirable to heat the eyelid tissue evenly across from one edge
to the other. In the Y-axis direction, some asymmetry is desirable,
since most of the blockages that occur in a meibomian gland are
near the orifice or duct. In the case where a lower eyelid is being
treated, and the top edge of the energy transmission surface 140 is
aligned with the top edge of the lower eyelid, it would be
preferable to have the irradiance profile (and therefore the tissue
heating profile) be biased toward the top edge, while also warming
the overall eyelid.
[0245] In order to improve the distribution of irradiance of the
infrared light, a partially reflective coating 196 may be applied
to a surface of part single-use cover element part 147a, as shown
in FIG. 17E. In one embodiment, this coating is an apodization
coating which transmits about 33% and reflects about 67% of the
energy in the 820-880 nm range. FIG. 17F shows a more detailed view
of the coating pattern, with two zones 196 a and 196 b shown. FIG.
17G shows the resulting distribution of irradiance through the
eyelid when the apodization coating is utilized. As shown, the
highest irradiance zone is much wider and is skewed toward the top
edge, and there is much less drop-off in irradiance toward the
right and left ends along the top edge. As such, there will be
preferential heating of tissue along the upper half of the eyelid
(in the case of treating a lower eyelid), and the heating from left
to right across the eyelid is more uniform.
[0246] If the apodization coating 196 is also reflective of
wavelengths in the lime region (500-600 nm), then very little lime
light will reach the desired parts of the eyelid, and there will
therefore be less heating of the eyelid tissue through chromophore
absorption of the lime light energy. To address this, in one
embodiment, it is preferable for coating region 196 a to be
partially reflective only for infrared only (67% reflective, 33%
transmissive for 820-880 nm; >90% transmissive for lime 500-600
nm), and for coating region 196 b to be partially reflective (67%
reflective, 33% transmissive) to both infrared (820-880 nm) and
lime (500-600 nm).
[0247] FIG. 17H shows a lime irradiance distribution plot on the
surface of the eyelid for an embodiment having an apodization
coating as described above (zone 196 a transmits lime and partially
reflects infrared, and zone 196 b partially reflects both). As can
be seen, the irradiance pattern is preferentially skewed to the
upper half of the eyelid and is well distributed from the right to
left end, without significant drop-off in irradiance.
[0248] It will be appreciated that the examples of coating types
and deposition patterns disclosed herein are simple examples of
demonstration and that alternate configurations may result in more
even distribution of irradiance in the desired spectra. For
example, another method of shaping the heating pattern of the
eyelid is to modify the deposition pattern or properties of the
energy absorbing surface 302 of scleral shield 300 (as shown in
FIG. 3B). For example, in order to even out the heating of the
scleral shield if the irradiance pattern is as shown in FIG. 17D,
the right and left portions of the surface of scleral shield 300
may be more densely coated with energy-absorbing material than the
central portions of scleral shield 300. Further, in order to skew
the heating toward the upper portion of the eyelid, the upper
portion of the surface of the scleral shield could be more densely
coated with energy-absorbing material. Combinations of coatings on
elements within the energy transmission path as well as alterations
of the energy reflecting and absorbing properties of the surface of
the scleral shield are all included within the scope of the
disclosure.
[0249] FIGS. 18A and 18B show another embodiment of an eye
treatment device 200. In some embodiments, the eye treatment device
200 may be configured for use by an Eye Care Professional (ECP).
For example, the eye treatment device 200 can allow an ECP to apply
localized heat and pressure to the eyelids 12, 14 (not shown in
FIGS. 18A-18B). In some embodiments, the system can include a
handheld instrument 1800 configured to be coupled to a sterile
disposable component 260 positioned behind the eyelids 12, 14. For
example, the sterile disposable component 260 may be single-use,
removable, or consumable. In some embodiments, the sterile
disposable component 260 can be releasably attached to the handheld
instrument 1800, and the handheld instrument 1800 can include a
disposable release button 1805. In some embodiments, the handheld
instrument 1800 also includes a power button 1807. In some
embodiments, the eye treatment device 200 device can allow an ECP
to view the eyelid margin through a visualization device or
visualization means 160, such as an integrated camera. The eye
treatment device 200 can then warm the eyelid tissue to a target
temperature range, such as to melt the meibum blocking the
orifices. In embodiments, the target temperature range is about
40.degree. C. to about 42.degree. C. The eye treatment device 200
can further apply compression to the eyelids 12, 14, such as to
express the melted meibum through the orifices. In some
embodiments, the amount of heat and pressure applied is under
direct control of the ECP at all times, and the ECP may monitor the
response of the glands and the comfort of the patient during
treatment.
[0250] As shown in FIGS. 18A-18B, the eye treatment device 200 can
include an electronic handheld instrument 1800. The handheld
instrument 1800 can be used together with the sterile disposable
component 260, for example, to apply heat and pressure to the
eyelids 12, 14. The eye treatment device 200 can have the
approximate dimensions of 8'' (L).times.11/2'' (W).times.21/4''
(H). The eye treatment device 200 may have other dimensions without
departing from the scope of the present disclosure. In some
embodiments, the sterile disposable component 260 can be secured to
the handheld instrument 1800 by at least two latches 1801. The at
least two latches 1801 may grasp at least one attachment tab 2203
(not shown). The sterile disposable component 260 may be released
from the handheld instrument 1800 by pressing the disposable
release button 1805. The eye treatment device 200 can include
electronic circuits that read temperature sensors 310 in the inner
eyelid pad 300 and the outer eyelid pad 147. The electronic
circuits can be used to measure temperatures representative of
inner and outer eyelid temperature. Warming can be accomplished
using light energy emitted from LEDs in the handheld instrument
1800 A mechanism in the handheld instrument 1800 can allow the
operator to apply pressure to the eyelid by controlling the
movement of the outer eyelid pad 147 using finger pressure applied
to a compression control button 1822. In some embodiments, the eye
treatment device 200 can also include a graphic screen or display
244 configured to display information used to operate the handheld
instrument 1800 such as during a treatment. In some embodiments,
the eye treatment device 200 can include a visualization device or
visualization means 160, configured to allows the operator to view
the eyelid margin during treatment.
[0251] Eyelid temperature can be measured using sensors 310 in the
sterile disposable component 260, including two sensors in the
outer eyelid pad 147 and two sensors in the inner eyelid pad 300.
For example these sensors can be mounted on a flexible printed
circuit board (PCB) that may also have an array of contact pads.
When the sterile disposable component 260 is attached to the
handheld instrument 1800, spring loaded pins mounted below a shroud
2100 (not shown) can make an electrical connection to the outer
eyelid pads 140 and the inner eyelid pads 300 in the sterile
disposable component 260. In some embodiments, electronic circuitry
in the handheld instrument 1800 can read the sensors and determine
temperatures rapidly, for example more than 20 times a second. The
accuracy of the temperature measurement system can be .+-.1.degree.
C. In some embodiments, the electronic circuitry performs self-test
checks to ensure the sensors are operating properly. For example,
if the electronic circuitry detects a failure, an error code may be
displayed and the heat source may be disabled.
[0252] In some embodiments of the eye treatment device 200,
pressure applied to the eyelid can be controlled by the ECP, such
as by the ECP depressing the compression control button 1822 using
their thumb or finger. This depression of the compression control
button 1822 can cause the outer eyelid pad 147 to move towards the
opposing inner eyelid pad 300. In some embodiments, when the
sterile disposable component 260 is attached to the handheld
instrument 1800 the outer eyelid pad 147 automatically attaches to
the front of the shroud 2100. The shroud 2100 may be a component
that may be movable, and which encloses the warming LEDs and guides
light towards the eyelid. In some embodiments, the compression
control button 1822 is connected to the shroud 2100, thereby
enabling the clinician to advance the outer eyelid pad 147 using
thumb or finger force. For example, the force applied can be
measured by a sensor mounted in the mechanism of the compression
control button 1822, and can be displayed on the display screen 244
as a relative number from 1 to 9. The displayed value may be a
relative reference for the clinician. The actual force applied
should be determined by clinical judgment, taking into
consideration the condition and response of the eyelid being
treated as well as patient sensitivity.
[0253] In some embodiments, the eyelid tissue can be warmed by
light energy produced by LEDs in the handheld instrument 1800 and
transmitted through the clear outer eyelid pad 300. The LEDs can be
located behind a clear window on an open end of the shroud 2100.
For example, two wavelengths of light can be used: lime-green and
near-infrared. Chromophores in the eyelid can absorb the light
energy and thereby heat the surrounding tissue.
[0254] In some embodiments, the top surface of the compression
control button 1822 has a heater control switch 1802 that can be
slid forward by the operator's thumb or forefinger, thereby turning
on the warming LEDs. This heater control switch 1802 can have a
spring-return feature, such that when it is released, or when the
operator's thumb or forefinger is relaxed, the heater control
switch 1802 returns to its normal "off" position.
[0255] In some embodiments, the eye treatment device 200 may be
designed to protect the eye against unintended exposure to the
light. For example, the inner eyelid pad 300 and an eye shield can
block light 211 from directly shining into the eye during a
treatment. In some embodiments, the handheld instrument 1800 can
disable the warming of the LEDs if a valid sterile disposable
component 260 is not attached to the handheld instrument 1800, or
if the outer eyelid pad 147 is more than 6 mm from the inner eyelid
pad 300.
[0256] FIG. 19 shows an example of a frontplate or force pad used
as the outer eyelid pad 147, which may be interposed between the
eye treatment device 200 and the eyelids 12, 14 of the patient,
such as to provide a barrier therebetween. In some embodiments, the
outer eyelid pad 147 can be a transparent outer eyelid pad 147 that
may act as a window through which the energy can be delivered to
the eyelids 12, 14. For example, the transparent outer eyelid pad
147 may be fabricated from any suitable material such as glass,
pyrex, quartz, mica, or polymers such as polycarbonate or other
optically transparent materials, or a combination thereof, in order
to obtain the desired structural and optical properties. In
embodiments, the outer eyelid pad 147 can be configured to directly
contact the eyelids 12, 14 of the patient. In other embodiments,
the outer eyelid pad 147 can be configured to be spaced a small
distance from the eyelids 12, 14, such as for example between 0.5
mm and 12 mm from the eyelid, during a treatment. Preferably, the
exterior surface of the outer eyelid pad 147 is configured to be
smooth and easily cleaned. For example the transparent outer eyelid
pad 147 may be in a slidable relationship along movement path 145
with respect to either the energy transducer module 120 or scleral
shield 300 or housing 202, so as to ensure the transparent outer
eyelid pad 147 can be pressed up against the eyelids 12, 14. The
pressure of the transparent outer eyelid pad 147 against the
eyelids 12, 14 can serve to minimize photonic energy leakage during
treatment and/or imaging, and if desired, to apply a compressive
force to the eyelids 12, 14 during evaluation and/or expression of
meibomian glands.
[0257] FIG. 19 shows an embodiment of an outer eyelid pad 147 that
includes a set of temperature sensors 310 positioned toward the
outer eyelid. In some embodiments, the set of temperature sensors
310 may be discrete elements (such as thermocouples made from very
fine wire, miniature thermistors, etc.) embedded or positioned in
the outer eyelid pad 147. Additionally and/or alternatively, the
set of temperature sensors 310 may be thermocouples formed by
depositing a thin film or films of appropriate metals onto
intermediate layers of the outer eyelid pad 147. In some
embodiments, the preferred types of materials for the outer eyelid
pad 147 are soft, flexible, biocompatible materials such as
silicone, polyurethane, and various hydrogels similar to those used
in contact lenses.
[0258] In embodiments, the outer eyelid pad 147 may also include a
plurality of bumps on the eyelid-facing surface, such as to create
an airspace for the set of temperature sensors 310.
[0259] The set of temperature sensors 310 may be configured to
sense the position of the eye treatment device 200 relative to the
eyelids 12, 14 of a patient. The set of temperature sensors 310 may
be temperature sensors that measure room temperature prior to
placement of the eyelid in the device. As the set of temperature
sensors 310 is positioned near the eyelid skin, the set of
temperature sensors 310 will register a value closer to body
temperature and therefore confirm proper positioning. If the set of
temperature sensors 310 does not match, such as one sensor showing
room temperature and the other sensor showing eyelid temperature,
it may be an indication that the eyelid is not properly positioned
in the eye treatment device 200 for treatment.
[0260] FIG. 19 shows an embodiment of a frontplate or outer eyelid
pad 147 having sensors 310 designed the measure the eyelid
temperature. When infrared light waves hit the skin, part of the
light is reflected back toward the sensors 310 and may heat the
sensors 310. This may cause the reading of the eyelid temperature
to be incorrect. In some embodiments, to prevent unwanted photonic
heating of the sensors 310, a reflective and/or white paint may be
used to over the sensors 310.
[0261] Referring again to FIG. 19, when infrared light waves hit
the skin, they are absorbed and the energy from the light is
transferred into heat thereby warming the skin. In general, darker
skin colors absorb more infrared light than lighter skin colors,
which therefore means that darker skin becomes hotter faster as it
is transforming more light into heat.
[0262] Using this knowledge, the eye treatment device 200 may be
able to detect differences in skin pigmentation and adjust the
treatment accordingly. For example, the eye treatment device 200
can have sensors 310 on the frontplate and stationary backplate to
measure the inner eyelid surface temperature and the outer eyelid
surface temperature during heating. If the outer eyelid surface
warms quickly, it might be an indication of darker skin color,
conversely if the outer skin surface warms slowly, it might
indicate a lighter skin color.
[0263] In some embodiments, to compensate for this difference in
warming rates for different levels of skin pigmentation, the eye
treatment device 200 may adjust the light such that the inner and
outer skin warm at the same rate. For example, the frequency of the
light may be adjusted for the slow-warming surface, such as to
increase the warming speed so that the inner and outer eyelids warm
at the same rate. If the inner eyelid skin needs more warming, the
eye treatment device 200 may turn up the green light and turn down
the infrared light. In other embodiment, the light used may be
multiple wavelengths to adjust between the plates and keep the
warming the same.
[0264] Some embodiments of the eye treatment device 200 can include
a first set of sensors that may be positioned on the surface of the
transparent outer eyelid pad 147 and facing the outer eyelid to
monitor the temperature of the outer eyelid surface, and a second
set of sensors that may be coupled with the scleral shield 300 on
the surface facing the inner eyelid to monitor the temperature of
the eyelid surface. Such a placement can allow the thermocouples or
thermistors to detect the temperature of the outer and/or inner
surfaces of an eyelid. For example, the first set of sensors and
the second set of sensors can be coupled to a controller 212, and
the sensors can be configured to detect the temperature of the
outer eyelid surface and/or inner eyelid surface and relay the
temperature information to the controller 212. Monitoring the
temperatures of such surfaces may help to ensure that a patient
does not experience significant discomfort or injury from use of
the eye treatment device 200.
[0265] In some embodiments, the first set of sensors and the second
set of sensors may be safety sensors. The first set of sensors and
the second set of sensors may preferably be non-contact sensors
such as pyroelectric sensors (for example, IRA-E700ST0 from Murata)
or thermopiles (for example, ST25T0-18 from Dexter Research,
Dexter, Mich.) or conventional temperature monitoring devices such
as a thermocouple, a thermistor, a fiberoptic thermal sensor, or a
digital temperature sensor (such as a Dallas Semiconductor
DS-18B20). In some embodiments, the first set of sensors and the
second set of sensors may be discrete elements (such as, for
example, thermocouples made from very fine wire, or miniature
thermistors, etc.) embedded in the outer eyelid pad 147 (such as,
for example, within a pocket) and/or the scleral shield 300. In
some embodiments, the first set of sensors and the second set of
sensors may be formed by depositing thin films of appropriate
metals onto surface layers and/or intermediate layers of the outer
eyelid pad 147 and/or the scleral shield 300.
[0266] In some embodiments, the eye treatment device 200 can
include a current sense circuit to monitor LED function. The
current sense circuit may be a circuit that is configured to sense
current passing through the current sense circuit to the LED. For
example, the current sense circuit may be configured to detect
fault conditions such as a short circuit or open circuit in the
current path, which may be due to connection problems and/or
problems with the LED. In such current sense circuits, it is
important to not only detect a condition, but also to ensure the
safe operation of the detection circuitry itself. If a fault is
detected, the system may shut-off the fault circuits and/or shut
off the eye treatment device 200. In such instances, error codes
may be displayed in the screen, to alert the user or clinician to
the fault status.
[0267] In some embodiments, after temperature of the eyelids 12, 14
reaches a target temperature range, such as a treatment
temperature, it may desirable for the user or clinician to know how
long the eyelid stays within the target temperature range. For
example, the target temperature range can be between a minimum
temperature required to treat the eye condition and a maximum
temperature above which discomfort or thermal damage to the eye or
eyelid may occur. In some such embodiments, the target temperature
range is between about 40 and about 80 degrees Celsius. In some
embodiments, the target temperature range is between 50 degrees
Celsius and 80 degrees Celsius. In some embodiments, the target
temperature range is between 60 degrees Celsius and 80 degrees
Celsius. In some embodiments, the target temperature range is
between 70 degrees Celsius and 80 degrees Celsius. In some
embodiments, the target temperature range is between 40 degrees
Celsius and 70 degrees Celsius. In some embodiments, the target
temperature range is between 40 degrees Celsius and 60 degrees
Celsius. In some embodiments, the target temperature range is
between 40 degrees Celsius and 50 degrees Celsius. In some
embodiments, the target temperature range is between 40 degrees
Celsius and 45 degrees Celsius.
[0268] As shown in FIG. 20, the eye treatment device 200 can
include a melt time indicator, configured to count the time the
eyelids 12, 14 are within the target temperature range. The melt
time may be shown on the display 244 of the handheld device 1800.
For example, the timer can start a counter once the eyelid
temperature reaches a minimum temperature and can continue counting
until the eyelid temperature falls below a minimum temperature. In
some embodiments, the timer may use the actual measured temperature
at a measurement time, while in other embodiments, the timer may
use a preset time period.
[0269] FIG. 20 shows an embodiment of a dashboard 218 of the
display screen 244, configured to display the status of the eye
treatment device 200. For example, the dashboard 218 can include a
temperature measurement device or means configured to measure
various temperatures of the eyelid, such as inner and/or outer
surface temperatures, a datalogger 214, a voice recorder 213, a
battery configured to power the components of the dashboard, a
battery charging means, a controller, printed circuit board, and/or
communication circuitry between the scleral shield 300 and the
energy transducer 205.
[0270] In some embodiments, the eye treatment device 200 may
further include a display screen 244 configured to display the
inner eyelid and outer eyelid temperatures. For example. the
temperature display feature may display absolute temperatures, or
may display relative temperatures versus a maximum. For example,
the temperatures may be displayed in a bar graph format, or with
one or more lights, etc.
[0271] In some embodiments, during use of the eye treatment device
200, the temperature of the inner and/or outer eyelid surface can
be measured and displayed on the display screen 244 for the
clinician. For example, the clinician can apply heating energy to
the eyelid, and when the eyelid temperature reaches the treatment
temperature, the clinician can apply a compressive force while
visually monitoring the eyelid margin, such as to optimize the
expression of meibum from clogged meibomian glands.
[0272] FIGS. 21A and 21B show another embodiment of an eye
treatment device 200. FIG. 3A is a schematic side plan view of the
embodiment of an eye treatment device 200 of FIGS. 21A-21B, wherein
the eye treatment device 200 is operational and is transmitting
light 211 to the eyeball 20 and the treatment tissue. In some
embodiments, a movable light pipe or shroud 2100 having an internal
reflective surface can be used to reflect or guide the light 211
towards the energy transmission surface 140, thereby improving the
efficiency of the heating of the target tissue. FIG. 21A shows the
shroud 2100 in a retracted position, and FIG. 21B shows the shroud
2100 in an advanced position. For example, the shroud 2100 may be
used when the light 211 that is emitted from the energy transducer
module 120 includes a portion of the light 211 initially radiated
at an angle such that without correction the light 211 would not
reach the energy transmission surface 140 for passage to the
treatment tissue. The movable light pipe or shroud 2100 can be used
to correct this and focus the light 211 toward the treatment
tissue.
[0273] In some embodiments, the movable reflector, light pipe or
shroud 2100 can be a sliding assembly that surrounds the heat
source LEDs and guides light 211 towards the eyelid. For example,
the user or clinician can control movement of the shroud 2100 by
pressing a compression control button 1822 connected to the shroud
2100. In some embodiments, when a sterile disposable component 260
is attached to the handheld instrument 1800, the outer eyelid pad
147 can automatically attach to the front of the shroud 2100. When
the clinician presses the compression control button 1822, the
shroud 2100 and outer eyelid pad 147 can be advanced toward the
eyelid. In some embodiments the outer eyelid pad 147 is positioned
at the eyelid surface for heating the eyelid without compression.
In other embodiments, the eyelid is compressed between the outer
eyelid pad 147 and a stationary backplate. For example, when the
clinician depresses the compression control button 1822 with their
finger or thumb, the shroud 2100 and outer eyelid pad 147 advance
toward the stationary backplate. The amount of heat and pressure
applied may thus be under direct control of the clinician, who can
monitor the response of the glands and the comfort of the
patient.
[0274] In some embodiments, the inner wall surface of the shroud
2100 may be smooth and/or polished, such as to avoid or minimize
light 211 scattering when experiencing reflection from the walls.
For example, the walls can have a mirror-like surface such that
reflection of the light 211 is kept within the shroud 2100, even
when the light 211 hits the side walls. In embodiments, mirrored
surfaces of the walls can be obtained by depositing a reflective
layer or layers using any known means, such as, for example,
silvering, aluminizing or laminating with a mirrored film, or other
types of mirror finishing, to further enhance the ability of the
shroud 2100 to conduct light 211.
[0275] FIGS. 22 and 23 show an embodiment of a front pad of an eye
treatment device. For example, an outer eyelid pad 147 can be
interposed between the light source of the eye treatment device 200
and the patient's outer eyelid. The outer eyelid pad 147 may be
configured to engage the shroud 2100 when the shroud 2100 is
extended for treatment. Because the shroud 2100 may become warm
during treatment, the outer eyelid pad 147 may include a perimeter
frame to engage the walls of the shroud 2100 such as to keep the
outer eyelid pad 147 from warming.
[0276] In some embodiments, the outer eyelid pad 147 may not be
used to shield the eye from heat energy, but may instead be used to
measure temperatures. For example, the outer eyelid pad 147 may be
made of materials that are substantially transparent to the energy
emitted from the energy transducer. By way of specific example, if
the energy transducer is a light source, the outer eyelid pad 147
may be made of a clear material that does not impede the
wavelength(s) of light emitted by the energy transducer.
[0277] FIG. 22 shows embodiments of the sterile disposable
component 260. In embodiments, the sterile disposable component 260
includes the following exemplary components: an inner eyelid pad
300, an outer eyelid pad 147, an eye shield 264, a silicone cover
2201, attachment tabs 2203, a guide 2204, and support arms
2205.
[0278] The inner eyelid pad 300 can be made of plastic that is
configured to be heated by the light-based heat source in the
handheld Instrument 1800. In embodiments, the plastic parts can be
surrounded by a soft, biocompatible silicone cover 2201. In
embodiments, there are two temperature sensors 310 located in the
inner eyelid pad 300 that can measure the temperature of the inner
surface of the eyelid. The inner eyelid pad 300 is also referred as
the backplate.
[0279] The outer eyelid pad 147 can be configured as a clear,
biocompatible silicone pad that is mounted on a plastic frame. In
embodiments, the plastic frame has a minimum thickness of 0.010''
at the location of the temperature sensors 310. In some
embodiments, the outer eyelid pad 147 is in patient contact during
the treatment. When the sterile disposable component 260 is
attached to the handheld instrument 1800, the frame can attach to
the shroud 2100 of the handheld instrument 1800. Light from the
heat source in the handheld Instrument 1800 can shine through the
outer eyelid pad 147 to heat the eyelid tissue. In some
embodiments, there are two temperature sensors 310 located in the
outer eyelid pad 147 that can measure the temperature of the outer
surface of the eyelid.
[0280] The eye shield 264 can block light emitting from the
handheld instrument 1800, and thereby protect portions of the eye
that are not intended to be heated. In embodiments, the inner
eyelid pad 300 and portions of the eye shield 264 can be covered
with a soft, biocompatible silicone component or silicone cover
2201. For example, the silicone cover 2210 can have a minimum
thickness of 0.010'' at the location of the temperature sensors
310. In some embodiments, the silicone cover 2201 is in patient
contact during the treatment.
[0281] The sterile disposable component 260 can be secured to the
handheld instrument 1800 by the attachment tabs 2203. For example,
when the sterile disposable component 260 is attached to the
handheld device 1800, spring-loaded latches can mate with openings
in each of the attachment tabs 2203, thereby securing the sterile
disposable component 260 to the handheld instrument 1800. The guide
2204 can assist in aligning the sterile disposable component 260 to
the handheld instrument 1800. The support arms 2205 can connect the
inner eyelid pad 300 to the main body of the sterile disposable
component 260. These support arms 2205 serve as a guide to the
proper depth to insert the Inner Eyelid Pad 300 behind the
eyelid.
[0282] FIG. 23 is an exploded view of the sterile disposable
component 260, showing an embodiment of the temperature sensors 310
on the outer eyelid pad 147. Any of the pads shown in FIG. 23 can
be formed of multiple pieces, or can be one monolithic piece. In
embodiments, the temperature sensors 310 can be designed to measure
the outside eyelid temperature. During use, light 211 can hit the
rear of the set of temperature sensors 310. If this happens, the
temperature sensors 310 may read the light temperature instead of
the eyelid temperature. To prevent this, the rear of the
temperature sensors 310 may be covered with a material that will
not heat. For example, the rear of the temperature sensors 310 may
be covered with a reflective coating to reflect the light 211 away
from the temperature sensors 310 without heating the rear of the
temperature sensors 310.
[0283] FIG. 23 shows an embodiment of a sterile disposable
component 260 that is designed for single-use and should not be
reused. In some embodiments, in order to keep track of the number
of uses, the sterile disposable component 260 may include an
on-board memory that contains custom treatment parameters. For
example, the custom treatment parameters could include the number
of uses available, such as for a single-use sterile disposable
component 260, and conveys the information to the eye treatment
device 200. Once the eye treatment device 200 is used for
treatment, the custom treatment parameters will not all allow it to
be used again. In some embodiments, once the sterile disposable
component 260 is attached, the use information may also be
displayed on the display 244, so the user knows that the sterile
disposable component 260 may be used for single-use.
[0284] In some embodiments, the sterile disposable component 260
may be designed for multi-use. For example, the on-board memory may
keep track of the number of uses, and once the maximum number of
uses is reached, the eye treatment device 200 will not allow
treatment with the sterile disposable component 260. This
information may displayed on the display 244 when the sterile
disposable component 260 is attached, showing the number of
remaining uses available. Once the eye treatment device 200 is used
for treatment to the maximum number of allowed uses, the custom
treatment parameters will not all allow it to be used again.
[0285] FIGS. 23 and 24 show an embodiment of a stationary backplate
or stationary inner eyelid pad 300. In embodiments, the stationary
inner eyelid pad 300 can be configured to be positioned between the
eyelids 12, 14 and the eyeball 20, such as to cover the sensitive
anatomy of the eye system 10 and prevent light 211 from contacting
the eyeball 20. For example, the stationary inner eyelid pad 300
can include a reflective surface configured to receive the light
211 and reflect the light 211 toward the inner eyelid surface for
warming.
[0286] In some embodiments, the stationary inner eyelid pad 300 can
include a set of temperature sensors 310 positioned toward the
inner eyelid. For example. the set of temperature sensors 310 may
be discrete elements (such as thermocouples made from very fine
wire, miniature thermistors, etc.) embedded or positioned in the
stationary inner eyelid pad 300. In some embodiments, the set of
temperature sensors 310 may be thermocouples, formed by depositing
thin films of appropriate metals onto intermediate layers of the
stationary inner eyelid pad 300.
[0287] In embodiments, to prevent the stationary inner eyelid pad
300 from warming or heating the set of temperature sensors 310, the
energy absorbing surface or reflective surface of the stationary
inner eyelid pad 300 can include sensor windows for the set of
temperature sensors 310 to extend through and thereby contact the
inner eyelid surface directly.
[0288] FIGS. 19 and 24 are views showing details of embodiments of
the frontplate or outer eyelid pad 147, and backplate or inner
eyelid pad 300. In some embodiments, the sets of temperature
sensors 310 are redundant sensors that are collocated for
redundancy and improved accuracy. Each set of temperature sensors
310 can provide a primary and a secondary measure of the eyelid
temperature. The secondary measure of eyelid temperature can be
used in conjunction with primary eyelid temperature measurements
for improved temperature sensing accuracy and reliability.
[0289] In some embodiments, obtaining two or more eyelid
temperature readings facilitates redundancy. One aspect of the
present disclosure includes the step of comparing the primary
eyelid temperature reading and the secondary eyelid temperature
reading, such as to determine whether both sensors of the set of
temperature sensors 310 are operational.
[0290] The set of temperature sensors 310 can be subjected to
mechanical and/or thermal stresses, and one of the set of
temperature sensors 310 may stop working. Having a redundant set of
temperature sensors 310 can allow the system to use the second set
of temperature sensors 310 to provide the temperature information
required to finish the procedure.
[0291] In some embodiments, the sets of inner and outer eyelid
temperature sensors 310 may be redundant temperature sensors 310.
For example, each set of temperature sensors 310 may measure the
inner eyelid surface temperature or outer eyelid surface
temperature. Both of the sets of temperature sensors 310 should
read the same temperature. If the temperature provided by the sets
of temperatures sensors 310 does not match, it might mean that
treatment is not correctly positioned on eyelid, or that there is a
problem and the system should be shut down.
[0292] FIGS. 23 and 24 show an embodiment of a sterile disposable
component 260 that includes an identification (ID) chip. The ID
chip may protect against counterfeit disposables by ensuring that
genuine sterile disposable components 260 are used in treatment.
The ID chip may also provide automated treatment tracking, by
tracking the usage of sterile disposable components 260 and
adherence to disposable guidelines for the maximum number of uses.
Additionally, the ID chip may help to maintain inventory visibility
by managing supplies and inventories in real-time, for direct
purchase and consignment.
[0293] In some embodiments, the eye treatment device 200 may use
authentication methods and/or protocols to determine whether the
sterile disposable component 260 is counterfeit. For example, the
eye treatment device 200 may include a communications protocol
configured to provide the ability to distinguish between an
authorized sterile disposable component 260 and an unauthorized
clone. The communications protocol may be further configured to
allow the eye treatment device 200 to reject the sterile disposable
component 260 if it is determined to be an unauthorized clone. In
some embodiments, the eye treatment device 200 may also include a
mechanism to limit usage and/or count the number of uses of the
sterile disposable component 260, and allow the eye treatment
device 200 to reject the sterile disposable component 260 if it
exceeds the maximum allowed usage and/or number of uses.
[0294] In some embodiments, the sterile disposable component 260
includes an on-board memory that contains custom treatment
parameters, specific to the type of sterile disposable component
260 that is being used. For example, when the sterile disposable
component 260 is attached to the eye treatment device 200, the eye
treatment device 200 can read the treatment parameters and adjust
the treatment to match the custom parameters.
[0295] In some embodiments, different sterile disposable components
260 are used during treatment of the eye. Therefore, the custom
treatment parameters might include light settings for each
different sterile disposable component 260. For example, some of
the sterile disposable components 260 may have different backplate
designs and may therefore require different treatment settings. In
some embodiments, the backplate can include an energy absorbing
portion that warms, and then transfers the heat to the inner
eyelid. In other embodiments, the backplate can have a reflective
surface that reflects the light energy back onto the eyelid for
heating.
[0296] In some embodiments, the sterile disposable component 260
may be used for taking pictures of the eyelid, and the custom
parameters can include a light lock-out feature configured to
ensure that the light does not shine.
[0297] In some embodiments, the sterile disposable component 260
may be used for both treatment and video. For example, the
treatment parameter may include the interleaving of the video clips
and light-based heating such that the video is not washed out.
[0298] FIGS. 19, 22, 23, and 24 are embodiments showing a sterile
disposable component 260 that is a sterile, single-use component
and that includes all of the parts intended to contact the
patient's eyelid. The sterile disposable component 260 is removed
from packaging prior to use and attached to the handheld instrument
1800.
[0299] The handheld instrument 1800 is a hand-held eye treatment
device 200 that allows the ECP to view, heat and compress the
portion of the eyelid that is in contact with the sterile
disposable component 260. The source of heating is optical
radiation produced by lime-green and infrared LEDs in the handheld
instrument 1800.
[0300] In some embodiments, an internal rechargeable lithium ion
battery provides power to operate the handheld instrument 1800. For
example, the battery can be recharged by placing the handheld
instrument 1800 in a separate charging stand that is powered by an
AC Power Supply.
[0301] The main parts of the sterile disposable component 260 are
shown in FIG. 22. In some embodiments, the sterile disposable
component 260 can have the approximate dimensions of 11/2''
(L).times.1'' (W).times.1'' (H). The sterile disposable component
260 may have different dimensions without departing from the scope
of this disclosure. In embodiments, the sterile disposable
component 260 can be a sterile component, used for a single patient
treatment and then disposed of. For example, during a treatment,
the inner eyelid pad 300 can be inserted behind the eyelid in the
fornix, and may be intended to contact the inner mucosal lining
(i.e., the palpebral conjunctiva). The outer eyelid pad 147, which
opposes the inner eyelid pad 300, can contact the skin on the outer
surface of the eyelid. Light 211 produced by the handheld
instrument 1800 can be transmitted through the clear outer eyelid
pad 147 to warm the eyelid tissue. The outer eyelid pad 147 can be
used to apply pressure to the eyelid by moving towards the inner
eyelid pad 300 by means of a mechanism in the handheld instrument
1800. Temperature sensors 310 in the outer eyelid pad 147 and inner
eyelid pad 300 can monitor eyelid temperature during a
treatment.
[0302] The embodiment of the sterile disposable component 260 shown
in FIGS. 19, 23, and 24 may further include drug-eluting front
and/or rear pads that can contact the eyelid and transfer the drug
to the outer and/or inner eyelid surface. The drugs may treat a
number of conditions. For example, the drug-eluting pads may
include one or more of the following: a numbing agent, such as to
block the nerves in the eyelid from feeling pain or discomfort
during treatment; an antibiotic, such as for the treatment of
blepharitis, to decrease inflammation and more quickly diminish
symptoms; and/or a steroid, such as for treatment of inflammatory
skin conditions including atopic dermatitis, psoriasis, seborrhea,
contact dermatitis, and the like. There are some treatment drugs
that may need to additional help to permeate the eyelid skin, such
as via iontophoresis.
[0303] Iontophoresis is a method of non-invasive transdermal drug
delivery to the eyelid skin, based on the transfer of charged
molecules using a low-intensity electric current. In some
embodiments, the eye treatment device 200 may deliver the drugs via
iontophoresis-mediated drug infusion to the eyelid. For example,
the disposable pads can include the drug, and the
iontophoresis-mediated drug infusion can use a weak electrical
current to stimulate drug-carrying ions to pass through the eyelid
skin. The electrical current may be provided by the sterile
disposable component 260 or the handheld instrument 1800. In some
cases, local anesthesia may be required for the eyelid treatment
for patients that fear the pain. For these cases, lidocaine can be
delivered to the eyelid using iontophoresis-mediated drug
infusion.
[0304] In some embodiments, the eye treatment device 200 may be
configured to treat hordeolum and/or chalazion. Chalazia and
hordeola (styes) are sudden-onset, localized swellings of the
eyelid. A chalazion is caused by noninfectious meibomian gland
occlusion, whereas a hordeolum usually is caused by infection. Both
conditions initially cause eyelid hyperemia and edema, swelling,
and pain.
[0305] To treat hordeolum, the inner eyelid pad 300 and/or outer
eyelid pad 147 may include features to focus pressure on the sty or
pimple, to squeeze the eyelid and drain the hordeolum. To treat
chalazion, the inner eyelid pad 300 and/or outer eyelid pad 147 may
have features to focus pressure on the occluded meibomian gland, to
open the gland.
[0306] In some embodiments, the eye treatment device 200 can
include an integrated camera as a visualization means 160. For
example, the integrated camera or integrated visualization means
160 can allow the user to determine how treatment is progressing
either before, during, or after treatment. In some embodiments, the
integrated visualization means 160 may include fixed optics,
adaptive optics, and/or active optics to view different areas of
the eyelid, including the front surface, rear surface and eyelid
margin. For example, adaptive and active optics can be configured
for focusing and/or zooming onto the image or target area. When
viewing the eyelid margins, the integrated visualization means 160
can view the expression of the glands. When viewing the rear of the
eyelid with light shining on the front of the eyelid, the
integrated visualization means 160 may view the internal gland
structure of the eyelid.
[0307] In some embodiments, the integrated visualization means 160
may provide video and/or still images of the eyelid. The integrated
visualization means 160 may further be coupled to electronics, such
as to record and/or transmit images to an external device. In some
embodiments, the integrated visualization means 160 can include the
electronics. In some embodiments, the integrated visualization
means 160 can be coupled to the device controller, with the
controller being capable of storing and/or transmitting the still
images and/or videos.
[0308] The mammalian eyelid is curved, and this curvature is not a
serious detriment to direct visual observation by viewing, due to
the natural ability of the eye to accommodate (refocus) the
curvature. However, when using a photographic camera, the field
curvature induces defocus error, which can be significant. One way
to correct for field curvature is by placing a single thin lens
just in front of the final focus. With the proper choice of
parameters, the thin lens flattens the field while inducing very
low aberrations. In some embodiments, a field flattener may be used
to flatten the curved image. For example, the field flattener can
provide more focus throughout the field.
[0309] In some embodiments, the eye treatment device 200 may have
the capability for an on-board video display. In some embodiments,
the video may be recorded to memory within the device, or the video
may be recorded to a portable drive, such as a microSD. Once the
procedure is complete, the portable drive may be removed and
replaced with a blank one for the next procedure.
[0310] When the integrated visualization means 160 takes a video
during treatment, the light 211 used for heating may wash out the
video or pictures taken. One solution is to interleave the video
and the light-based heating. FIG. 25 shows the pulsing of the light
source and the integrated visualization means 160, for example when
the light is off the camera is on and when the light comes on the
camera turns off. This can allow the video to be taken without
disruption from the light 211.
[0311] In some embodiments, the eye treatment device 200 may
include a special photo disposable, such as for taking photos of
the eyelid before and after treatment. For example, the photo
disposable can be similar to the sterile disposable component 260
but may use a spacer in place of a stationary backplate 300, to
position the eyelid at the proper position. The special photo
disposable does not include a backplate 300 because the light 211
is not turned on and is not shining toward the eye. During use, the
photo disposable may initially be used for photos prior to
treatment. The photo disposable can then be replaced by the sterile
disposable component 260. When treatment is complete, the sterile
disposable component 260 can be removed and replaced by the photo
disposable.
[0312] In some embodiments, the photo disposable may include a
memory having parameters to customize the camera settings. For
example, the photo disposable may be configured to control the type
of light used, depending on the photo settings. For example, one of
the settings may direct the eye treatment device 200 to shine white
light on the eyelid for visualization, while another setting may
include the use of infrared light for photo.
[0313] In some embodiments, the photo disposable may include a
diffractive surface to after the light path. Refraction occurs as
light changes angle traveling through the surface. The diffractive,
surface may narrow the light beam, widen the light beam, or scatter
the light beam. In some embodiments, it may be desirable to
diffract the light into a narrow beam to focus on a desired
treatment area on the eyelid. In some embodiments, it may be
desirable to widen the light beam to widen the treatment area on
the eyelid. In some cases, it may be desirable to diffract the
light for more uniform coverage of the treatment area.
[0314] In some embodiments, the eye treatment device 200 may be
configured to stream video using the integrated visualization means
160. For example, the integrated visualization means 160 and/or the
eye treatment device 200 may include a wireless link to send the
video to an external device, such as an external monitor for
viewing, or to stream the video to another external device, such as
a computer. In some embodiments, metadata may be added to the video
live stream, to relay more treatment information on the monitor.
For example, the metadata may include sensor readings, such as
information relating to inner and/or outer eyelid temperatures,
pressure and/or force applied to the eyelid, light intensity, light
frequencies, etc. Other data may also be included, such as the date
and time, the patient's name or medical record number, clinician's
name, or other information related to the treatment.
[0315] Meibography is a technique that yields information on the
morphological characteristics of meibomian glands by observing
their silhouette via transillumination of the eyelids 12, 14. One
type of meibography is a non-contact infrared meibography technique
that allows for non-contact observation of the structure of the
meibomian gland with no discomfort to the patient. Meibography
incorporates an infrared LED light to capture an image of the
meibomian glands of the upper and lower eyelids. It provides a
detailed picture of meibomian gland structure, including those
glands that have increased tortuosity or have stopped functioning,
resulting in meibomian gland dropout. A non-contact meibography
system may include an integrated visualization means 160, an
external monitor, and/or a recording device. Images may be obtained
using an infrared light source. Such a meibography system can allow
for easy observation of the meibomian gland structures in both the
upper and lower eyelids without causing patient discomfort.
[0316] Transillumination can be used to image the meibomian glands
in one of several ways. In one variation, illuminating light can be
directed at the outer surface of the eyelid at an angle, with
imaging also taking place from the outer surface of the eyelid.
This is referred to as oblique illumination. In a second variation,
light can be directed from behind the eyelid through the eyelid
with imaging taking place through the outer surface of the eyelid.
In a third variation, the surface is illuminated from the front in
a manner such that the light source partially blocks the image
being recorded, with averaging, adding or otherwise combining of
multiple images being used to produce a complete image. In each
instance, the meibomian gland is illuminated in order to visually
examine the gland using light transmitted through the eyelid
tissue. The eyelid can then be imaged using still or moving
photography (visible light, NIR or IR, or other suitable light
wavelength) in a manner similar to that described above.
[0317] One method of viewing the glands is via transillumination of
the lid and observation with the integrated visualization means
160. For example, the light can be positioned on one side of the
eyelid and the silhouette of the meibomian glands can then be
observed on the other side of the eyelid, using the integrated
visualization means 160. This method can provide information about
the morphology and physical characteristics of the meibomian
glands. Some of the information that can be measured may include
the number of glands and the degree of gland dropout, or area of
meibomian gland loss, etc.
[0318] In some embodiments, the eye treatment device 200 may be
used to assess the severity of dry eye by observing the tear film
break-up time. Tear film break-up time is a method for determining
the stability of the tear film and checking for evaporative dry
eye. Tear film break-up time can be helpful in assessing the
stability of the tear film and therefore the severity of meibomian
gland dysfunction. In testing for tear film break-up time,
fluorescein dye is added to the eye and the eyelid is held open.
The tear film is observed using a magnifier while the patient
avoids blinking until tiny dry spots develop, i.e. tear film
break-up. The tear film break-up time is then measured, in some
embodiments, the eye treatment device 200 may have a timing
feature, configured to record a tear film break-up time
measurement, A short tear film break-up time is a sign of a poor
tear film, and a longer tear film break-up time indicates a more
stable tear film. For example, >10 seconds is thought to be a
normal tear film break-up time, 5 to 10 seconds is considered
marginal, and <5 seconds is considered low.
[0319] In some embodiments, the eye treatment device 200 may be
used for skin pigmentation measurement, and may be adjusted to
tailor treatment parameters based on the pigmentation. For example,
the integrated visualization means 160 may view and/or record the
skin as the light is reflected from the skin. Differences in
reflection occurs between different skin types. Using this
knowledge, the eye treatment device 200 may tailor treatment
parameters based on the skin pigmentation indicated by the light
reflection measurement. In general, darker skins colors absorb more
infrared light than lighter skin colors, therefore the skin becomes
hotter faster as more light is transformed into heat. The eye
treatment device 200 may thus be configured to tailor treatment
parameters by adjusting the light frequency based on the
pigmentation measurement.
[0320] The pigmentation of skin is related to the amount of melanin
in the keratinocytes of the epidermis. The various contents of
melanin produce the wide spectrum of human skin color observed.
When light hits the skin, part of the light is reflected by
melanin, and this reflection may be used to detect the pigmentation
level of the skin.
[0321] In some embodiments, the eye treatment device 200 can shine
the light 211 on the skin and the integrated visualization means
160 can view and/or record the skin as the light 211 is reflected
from the skin, Because reflection differences occur between
different skin types or skin pigmentations, the integrated
visualization means 160 can be used to detect pigmentation.
[0322] Spectroscopy is the study of how substances absorb,
transmit, or reflect light. Spectroscopy may be used to detect skin
pigmentation. Because different skin pigmentations have unique
reflectance characteristics, we can determine the skin pigmentation
by analyzing the light reflectance characteristics.
[0323] In some embodiments, the eye treatment device 200 is
configured to detect whether the eyelid is properly captured in the
correct position for treatment. In some embodiments, the detection
of proper eyelid capture may be achieved by visual means, such as
using the magnifier 1804 or integrated visualization means 160. In
some embodiments, the detection of proper eyelid capture may be
done using one or more contact sensors 238. The integrated
visualization means 160 may be used for direct visualization of the
eyelid and may be used to determine whether the eyelid is properly
positioned for the desired treatment or procedure. In addition, the
eye treatment device 200 may include an image recognition feature
that may use the image from the integrated visualization means 160
to determine whether the eyelid is in the proper position. The
contact sensors 238 may be configured to shut off the eye treatment
device 200, and/or the eye treatment device 200 may signal the user
or ECP to stop treatment using lights, beeps or other notification
means. For example, the contact sensors 238 may be configured to
provide information to a user or ECP using signals from one or more
outputs. The outputs may be configured to display light in one or
more colors, or sound in one or more tones. The outputs can be
configured to display different light patterns or sound patterns,
configured to vary the intensity of a light or a sound, configured
to provide light and sound combinations, or otherwise configured to
indicate different statuses or modes of eyelid capture. In
embodiments, the contact sensors 238 may be configured to
communicate eyelid capture information to other medical devices
and/or communication devices.
[0324] FIG. 26A shows an embodiment of an integrated visualization
means 160 used to photograph the surface of the eyelid and the
eyelid margin, to detect blocked meibomian glands. There are
several factors to be considered when assessing the meibomian
glands. These factors include the percentage of partial glands; the
presence of chalazia, and the number of glands present within the
eyelid margin.
[0325] Photographs may be used for meibomian scoring (MG scoring)
which may correspond proportionally to the area of destruction.
Scoring may range from 0 to 3, with 0 indicating that the eyelid
margin has no partial or missing glands, 1 indicating that less
than of the eyelid margin area is involved, 2 indicating that the
area of the eyelid margin involved encompasses between 33% and 66,
or 3 indicating that the involved area encompasses more than 66% of
the eyelid margin. The numerical values obtained for the upper and
lower eyelids are summed together to obtain a score ranging from 0
to 6.
[0326] In some embodiments, the integrated visualization means 160
may also be used during treatment to record the meibum expression
from the glands as they are heated and squeezed by the eye
treatment device 200. The expressed meibum may be graded as
follows: 0 indicates clear meibum expressed easily, 1 indicates
cloudy meibum expressed gently; 2 indicates cloudy meibum that can
be expressed with more than moderate pressure; and 3 indicates that
no meibum can be expressed even with hard pressure. The expressed
meibum material may be used to diagnose other conditions, such as
blepharitis, abnormal lid margin, lid margin irregularity, lid
margin thickening, partial glands, and/or gland dropout, etc.
[0327] In some embodiments, the integrated visualization means 160
may also use IR light to locate the Meibomian glands and determine
whether the glands are filled with material which may have a
different NIR response than the tissue around it. For example,
using a sophisticated High Resolution NIR camera should be
sufficient to differentiate between areas of tissue and areas of
glands. The wavelength and optics used for the NIR camera should be
selected to provide suitable imaging of the meibomian glands, and
can be optimized by experimentation. Additionally, it may be
advantageous to digitally process the resulting images to enhance
the contrast level and/or assign coloration to distinguish between
the NIR responses of the various tissues.
[0328] Image enhancement techniques have been widely used in many
applications of image processing where the subjective quality of
images is important for human interpretation. Contrast is an
important factor in any subjective evaluation of image quality.
Contrast is created by the difference in luminance reflected from
two adjacent surfaces. In other words, contrast is the difference
in visual properties that makes an object distinguishable from
other objects and the background. In visual perception, contrast is
determined by the difference in the color and brightness of the
object with other objects. Many algorithms for accomplishing
contrast enhancement have been developed and applied to problems in
image processing. One is a stretch algorithm that may be used to
increase the image contrast, and may also improve the
lightness.
[0329] When the eyelid is inverted for viewing, it has a curved
surface. When taking a picture of the curved surface, some of the
areas are in focus, while other portions are out of focus. One
option is to physically flatten the curved eyelid surface. Another
option is to use different photographing techniques for curve
surfaces. To physically flatten the eyelid, a clear flat element,
such a glass, may be used. Once the eyelid is inverted, the clear
flat element can be pressed against the eyelid surface to flatten
it for the camera. One method of taking pictures of everted eyelid
curved surfaces is focus stacking. Focus stacking is a digital
image processing technique which combines multiple images taken at
different focus distances, to give a resulting image with a greater
depth of field (DOF) than any of the individual source images. The
starting point for focus stacking is a series of images captured at
different focal depths. In each image, different areas of the
everted eyelid will be in focus. While none of these images has the
sample entirely in focus, they collectively contain all of the data
required to generate an image which has all parts of the eyelid in
focus. In-focus regions of each image may be detected
automatically, for example via edge detection or Fourier analysis,
or may be selected manually. The in-focus patches are then blended
together to generate the final image of the eyelid.
[0330] A common technique of image interpretation as a part of the
medical diagnostic process is visual interpretation. Visual
interpretation makes the process depend on the observer. Human
visual perception of images depends on a small set of image
characteristics: brightness, contrast, sharpness, saturation, and
dynamics. To improve the readability of images and to reduce the
factors influencing information extraction and perception, the
images are enhanced. Image enhancement refers to a technique that
improves or modifies digital images, such that the resulting image
is better suited than the original for a particular application.
During the image enhancement process, one or more attributes of the
image are modified. The set of modified attributes, the
modification method, and the range of possible attribute values are
specific to a given task. One technique for image enhancement is
High Dynamic Range (HDR) imaging. HDR imaging methods compensate
for detail loss by taking multiple pictures at different exposure
levels and stitching them together, to create an image which
presents the greatest number of details in both dark and bright
areas. Another technique for image enhancement is pseudo-color. The
purpose of pseudo-coloring is to harness the perceptual
capabilities of the human visual system in order to extract more
information from an image, for example an image of an eyelid. The
term "pseudo-color" or "false color" is used to differentiate the
process of assigning colors to monochrome images from the process
associated with true color images. The pseudo-color process can
significantly improve the detectability of weak features,
structures, and patterns in an image by providing image details
that otherwise would not be noticed.
[0331] FIG. 26B shows one embodiment of a stationary inner eyelid
pad 300 that avows viewing of the inner side of the eyelid 14 and
transillumination of the meibomian glands from behind the eyelid
14. In some embodiments, the reflective surface of the stationary
inner eyelid pad 300 may also be configured to view the inner
surface of the eyelid 14 with the visualization means 160. In some
embodiments, viewing the inner surface of the eyelid 14 includes
transillumination of the eyelid 14 and meibomian glands. The image
translator 155 allows viewing of the inner side of the eyelid 14
and transillumination of the meibomian glands from behind the
eyelid 14.
[0332] Illumination energy 170, which may be visible or infrared
light, for example, is passed through the eyelid 14 and therefore
through meibomian glands 18 as it reflects off of reflective
surface of the stationary inner eyelid pad 300, eventually exiting
above the eyelid margin 14a, In this manner, the reflective surface
allows viewing of a transilluminated image 190 of the inner side of
the eyelid 14 under direct visualization or with the aid of a
magnifying element or camera, shown collectively as a visualization
device or visualization means 160, without having to evert the
eyelid 14. FIG. 2F is a front view of the embodiment shown in FIG.
26B, showing transilluminated images 190 of the meibomian
glands.
[0333] Some medical devices may carry bacteria which can lead to
infections or cross-contamination. Antibacterial coatings on the
eye treatment devices 200, such as antibiotics or silver particles,
can lower the risk of infections. In some embodiments the eye
treatment device 200 and/or sterile disposable component 260
includes one or more antibacterial coatings to prevent
cross-contamination or the spread of bacteria.
[0334] In some embodiments, the sterile disposable component 260 is
used to treat both eyes of a patent. Between eyes, the sterile
disposable component 260 should be treated with a disinfectant to
prevent cross-contamination between the eyes. Wiping the sterile
disposable component 260 between eyes also cleans any fluids or
eyelid expression from the sterile disposable component 260.
[0335] In some embodiments, the device includes a capacitance
sensor or contact sensor 238, or other proximity sensor, to sense
the position of the eye treatment device 200 relative to the
eyeball 20 or eyelid 14 of a patient. In some embodiments, the
contact sensor 238 may include one or more electrodes configured to
sense a capacitance and/or a change in capacitance as the contact
sensor 238 touches the eyeball 20 or eyelid 14. In some
embodiments, the contact sensor 238 may include microswitches or
force or pressure contact sensors 238, all of which produce a
change in signal characteristics when it touches the eyeball 20 or
skin of the eyelid 14. Thus, contact sensors 238 can be used to
help determine the placement of the eye treatment device 200.
[0336] For treatment of the inner eyelid, the inner eyelid pad 300
should be in contact with the inner eyelid surface. To detect this,
some embodiments of the eye treatment device 200 include a
capacitance sensor or contact sensor 238 to detect if the inner
eyelid pad 300 is touching the inner eyelid or the eyeball. If the
contact sensor 238 detects the eyeball or is too close to the
eyeball, the eye treatment device 200 may signal the user to pull
further outward toward the eyelid. If the contact sensor 238
detects touching the eyelid, the eye treatment device 200 is in the
correct position for treatment.
[0337] In some such embodiments, the controller is programmed to
prevent activation of the eye treatment device 200 until the
controller detects, through signals from the contact sensors 238
that the eye treatment device 200 is properly placed adjacent to an
inner eyelid. Additionally, in some embodiments, the controller is
programmed to shut off the energy if signals received from the
contact sensors 238 indicate that the eye treatment device 200 is
no longer placed properly against the eyelid.
[0338] For insertion of the stationary inner eyelid pad 300 behind
the eyelid, many people pull the eyelashes to lift the eyelid away
from the eyeball for insertion of the inner eyelid pad 300. Many
times, this method pulls out the eyelashes and causes pain.
[0339] In some embodiments, a suction device can be attached to the
outer surface of the eyelid and can pull the eyelid up to make room
for the inner eyelid pad 300. Once the inner eyelid pad 300 is in
place, the suction device can be detached and removed. For example,
lifting the eyelid with the suction device can include: placing a
suction portion of the suction device on the outer eyelid, creating
a suction to engage the outer eyelid skin, pulling the eyelid away
from the eyeball, and once the inner eyelid pad 300 is inserted
behind the eyelid, releasing the suction and removing the suction
device.
[0340] In some embodiments, a pulling device having a curved or
hook tip can be slid behind the eyelid and can pull the eyelid way
from the eyeball to make room for the inner eyelid pad 300. Once
the inner eyelid pad 300 is in place, the pulling device can be
removed.
[0341] In some embodiments, the sterile disposable component 260 or
the inner eyelid pad 300 may have lifting feature, such as a curved
tip, hook, or other similar feature to lift the eyelid away from
the eyeball. The lifting feature could be incorporated in the
design of the inner eyelid pad 300, or may be an add-on part.
Lifting the eyelid with the lifting device can include: sliding a
lifting feature on a distal end of the lifting device behind the
eyelid, lifting the eyelid away from the eyeball, and once the
inner eyelid pad 300 is inserted behind the eyelid, removing the
lifting device.
[0342] In some embodiments, the sterile disposable component 260 or
the inner eyelid pad 300 may include a light source for viewing the
eyelid, for example, for transillumination or meibography. For
transillumination, for example, a light feature on the sterile
disposable component can shine light on one side of the eyelid,
such as the inner eyelid, such that the user is able to view the
glands within the eyelid. In some embodiments, infrared light is
projected onto or through the everted lid, and an IR-sensitive
camera is used to view the meibomian glands. For meibography, the
sterile disposable component 260 can include an infrared LED light
source that shines on the eyelid such that the image is captured on
a camera. The meibography provides a view of all of the meibomian
glands in the eyelid. In some embodiments, the light source emits
blue or violet light in the range of 400-450 nm to reduce and/or
eliminate bacteria.
[0343] FIG. 27 shows one embodiment of a reflective inner eyelid
pad 300 that can be positioned between the eyelid 14 and eyeball 20
to cover sensitive anatomy of the eye system 10 to prevent light
from contacting the eye. The inner eyelid pad 300 is designed to
receive the light energy that is transmitted through the eyelid 14
and reflect it back to the eyelid inner surface for warming.
[0344] The reflective inner eyelid pad 300 may include a set of
temperature sensors 310 positioned toward the inner eyelid. The
sensors may be discrete elements (such as thermocouples made from
very fine wire, or miniature thermistors) embedded or positioned in
the inner eyelid pad 300, or they may be thermocouples formed by
depositing thin films of appropriate metals onto intermediate
layers of the inner eyelid pad 300.
[0345] To prevent the reflective inner eyelid pad 300 from warming
or heating the sensors, the energy reflective surface includes
sensor windows for the sensors to extend through and contact the
inner eyelid surface directly.
[0346] In some embodiments the reflective inner eyelid pad 300 may
act as a mirror to avow viewing of the inner side of the eyelid 14
with the visualization means. and transillumination of the
meibomian glands from behind the eyelid. In some embodiments, the
reflected light from the reflective surface of the inner eyelid pad
300 may be used for transillumination of the eyelid and meibomian
glands.
[0347] FIG. 27 also shows a portion of a sterile disposable
component 260 having an inner eyelid pad 300 that may include an
energy absorbing front face 302 to warm the inner eyelid. The
energy absorbing front face 302 may include a light source for
heating. In some embodiments, the light source can be on the inner
eyelid pad 300 and directed to the inner eyelid to warm the glands.
For example, the light source can emit wavelengths in the range of
about 500 nm to about 600 nm, such as to achieve the highest
absorption of light rays in tissue.
[0348] In some embodiments, the energy absorbing front face 302 can
include a light pipe and/or other refractive elements, configured
to direct the heating light toward the inner eyelid pad 300 and
shine the light on the inner eyelid to heat the meibomian glands
behind the eyelid.
[0349] In some cases, the meibomian glands may be inflamed or
dysfunctional, so it may be desirable to obtain a sample of the
meibum to analyze. For example, the meibomian glands may become
inflamed due to production of meibum with an increased composition
of omega-6 essential fatty acids. Additionally and/or
alternatively, bacteria may be in the meibomian glands and may
cause inflammation. For these cases, the eye treatment device 200
or sterile disposable component 260 can include a sample receiving
portion, configured to obtain a meibum sample as it is being
expressed. For example. the sample receiving part may be a meibum
reservoir in the sterile disposable component 260 that receives the
meibum. In some embodiments, there may be multiple sample receiving
parts, such as one for each eyelid. Once obtained, the meibum
sample can be tested. In embodiments, the testing may include
contacting the meibum with a color sensitive marker that uses color
to indicate the presence of bacteria. If there is bacteria present,
the ECP may prescribe a treatment plan. Additionally and/or
alternatively, a camera may be helpful in obtaining the meibum
sample. For example, the camera can view the meibum as it is
expressed, either taking pictures or video, to document the capture
of the meibum sample.
[0350] Eyes and eyelids come in a variety of sizes, from child to
adult. To accommodate this, the disposable inner eyelid pad 300 may
be made in different sizes. For example, there may be a child size,
a small adult size, a medium adult size, and large adult size.
[0351] FIGS. 28A and 28B illustrate another embodiment of an eye
treatment device 200. In some embodiments, both the eye treatment
device 200 and sterile disposable component 260 can be rotated 180
degrees between treatment of the lower eyelid and upper eyelid.
Along with this, all of the controls on the eye treatment device
200 would also be rotated, such that, when treating the upper
eyelid, the controls are upside down. This may be an issue for some
users. As shown in FIGS. 28A and 28B, one option to avoid this
potential issue is to rotate the sterile disposable component 260
by 180 degrees while the handheld instrument 1800 remains
stationary, such that the eye treatment device 200 is in one
position while the sterile disposable component 260 can be in two
positions.
[0352] In some embodiments, it may be desirable to warm or heat the
meibomian glands without squeezing the eyelid. For example, the eye
treatment device 200 can be designed as a non-contact infrared
heating device, using IR LEDs, and can be configured to heat the
meibomian glands within the eyelid without squeezing the eyelid
[0353] For purposes of summarizing the disclosure, certain aspects,
advantages and features have been described herein. It is to be
understood that not necessarily all such advantages may be achieved
in accordance with any particular embodiment. Thus, the disclosed
devices and methods may be embodied or carried out in a manner that
achieves or optimizes one advantage or group of advantages as
taught herein without necessarily achieving other advantages as may
be taught or suggested herein.
[0354] While this disclosure has been described in connection with
what are presently considered to be practical embodiments, it will
be appreciated by those skilled in the art that various
modifications and changes may be made without departing from the
scope of the present disclosure. It will also be appreciated by
those of skill in the art that parts mixed with one embodiment are
interchangeable with other embodiments; one or more parts from a
depicted embodiment can be included with other depicted embodiments
in any combination. For example, any of the various components
described herein and/or depicted in the Figures may be combined,
interchanged or excluded from other embodiments. With respect to
the use of substantially any plural and/or singular terms herein,
those having skill in the art can translate from the plural to the
singular and/or from the singular to the plural as is appropriate
to the context and/or application. The various singular/plural
permutations may be expressly set forth herein for sake of
clarity.
[0355] While the present disclosure has described certain exemplary
embodiments, it is to be understood that the disclosure is not
limited to the disclosed embodiments, but, on the contrary, is
intended to cover various modifications and equivalent arrangements
included within the scope of the appended claims, and equivalents
thereof.
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