U.S. patent application number 13/742520 was filed with the patent office on 2013-05-23 for nasal interface device.
This patent application is currently assigned to THE PERIODIC BREATHING FOUNDATION. The applicant listed for this patent is THE PERIODIC BREATHING FOUNDATION. Invention is credited to Robert W. Daly.
Application Number | 20130125895 13/742520 |
Document ID | / |
Family ID | 38474267 |
Filed Date | 2013-05-23 |
United States Patent
Application |
20130125895 |
Kind Code |
A1 |
Daly; Robert W. |
May 23, 2013 |
NASAL INTERFACE DEVICE
Abstract
A nasal interface device and a method of use are disclosed. The
device includes a facial adaptor configured to be secured to the
nose of a user and having two nostril pads having open channels
configured to be inserted into nostrils of the use and a
piercing/swivel adaptor configured to interact with the facial
adaptor through the two nostril prongs. The piercing/swivel adaptor
is further configured to be coupled to an airway tube, the airway
tube is configured to supply air/gas to the user.
Inventors: |
Daly; Robert W.;
(Providence, RI) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
THE PERIODIC BREATHING FOUNDATION; |
Providence |
RI |
US |
|
|
Assignee: |
THE PERIODIC BREATHING
FOUNDATION
Providence
RI
|
Family ID: |
38474267 |
Appl. No.: |
13/742520 |
Filed: |
January 16, 2013 |
Related U.S. Patent Documents
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
|
|
11787854 |
Apr 17, 2007 |
8074646 |
|
|
13742520 |
|
|
|
|
11405948 |
Apr 17, 2006 |
7900626 |
|
|
11787854 |
|
|
|
|
12383316 |
Mar 23, 2009 |
8381732 |
|
|
11405948 |
|
|
|
|
61070303 |
Mar 21, 2008 |
|
|
|
Current U.S.
Class: |
128/205.25 |
Current CPC
Class: |
A61M 16/0875 20130101;
A61M 2016/0027 20130101; A61B 5/4836 20130101; A61M 16/0066
20130101; A61M 16/0069 20140204; A61M 16/0666 20130101; A61M 16/04
20130101; A61M 16/12 20130101; A61M 16/0694 20140204; Y10S 128/914
20130101; A61M 16/024 20170801; A61M 2016/0036 20130101; A61M
16/202 20140204; A61M 2230/202 20130101; A61M 16/20 20130101; A61M
16/0683 20130101; A61M 2230/432 20130101; A61M 2230/432 20130101;
A61M 16/0057 20130101; A61M 16/08 20130101; A61M 16/0633 20140204;
Y10S 128/911 20130101; A61M 16/0045 20130101; A61M 16/0605
20140204; A61B 5/0836 20130101; A61M 16/209 20140204; A61M 2016/103
20130101; A61M 16/0003 20140204; A61M 16/06 20130101; A61M 2230/005
20130101 |
Class at
Publication: |
128/205.25 |
International
Class: |
A61M 16/06 20060101
A61M016/06; A61M 16/00 20060101 A61M016/00 |
Claims
1. A method of using a nasal interface device for supplying air/gas
to a user, comprising: securing a facial adaptor to the nose of the
user, wherein the facial adaptor includes a nostril pad configured
to be inserted into a nostril of the nose of the user, said nostril
pad is configured to substantially conform to an interior geometry
of the nostril upon insertion of the pad into the nostril and
includes an open channel protruding through the nostril pad;
wherein a nostril tube is configured to be placed through said open
channel in order to supply air/gas to the user.
2. The method according to claim 1, further comprising: inserting a
piercing/swivel adaptor into the nostrils of the user through the
nostril pads of the facial adaptor; and coupling an airway tube to
the piercing/swivel adaptor, wherein the airway tube is configured
to supply air/gas to the user.
3. The method according to claim 2, further comprising: attaching
the facial adaptor to the nose of the user using a friction clamp,
wherein the friction clamp is configured to be coupled to at least
one or both of a bridge of the nose and/or one or both sides of the
nose.
4. The method according to claim 3, wherein the facial adaptor
comprises: a first portion configured to be secured to the bridge
of the user's nose; a second portion coupled to the first portion
via a bendable connection and configured to cover the nostrils of
the user's nose; and a third portion coupled to the second portion
via another bendable connection and configured to be secured by
friction on the sides of the user's nose, the second portion is
configured to be coupled to said nostril pad.
5. The method according to claim 2, wherein the piercing/swivel
adaptor includes: a housing having an interior surface and an
exterior surface, the nostril tube configured to protrude away from
the interior surface of the housing; a connector tube configured to
protrude away from the exterior surface of the housing, the nostril
tube is configured to be located on an opposite side of the housing
as the connector tube; the connector tube further includes a swivel
element configured to allow connection of the airway tube; the
nostril tube and the connector tubes are configured to be connected
to each other via an airway passage disposed inside the housing of
the piercing/swivel adaptor.
6. The method according to claim 5, further comprising: inserting
the nostril tube into the open channel of the nostril pad.
7. The method according to claim 6, wherein upon insertion of the
nostril tubes into the open channels, the piercing/swivel adaptor
is configured to create an airway passage between the nose of the
user and the airway tube when the airway tube is coupled to the
swivel element of the piercing/swivel adaptor.
8. The method according to claim 7, wherein the swivel element
allows rotation of the airway tube when the airway tube is coupled
to the swivel element.
9. The method according to claim 4, wherein the facial adaptor is
manufactured from any biocompatible elastomeric material having a
Shore A hardness rating in range of approximately Shore A 00 to
approximately Shore A 60.
10. The method according to claim 1, wherein the nostril pads are
manufactured from an elastomeric material.
11. The method according to claim 3, wherein the facial adaptor
further comprises two nostril pads, wherein each nostril pad
includes a respective open channel.
12. The method according to claim 11, wherein the piercing/swivel
adaptor further comprises two nostril tubes configured to be
inserted into each respective open channel in the nostril pads.
13. A nasal interface device, comprising: a facial adaptor
configured to be secured to the nose of a user and having two
nostril pads configured to be inserted into nostrils of the user; a
piercing/swivel adaptor configured to interact with said facial
adaptor through said two nostril pads; wherein said piercing/swivel
adaptor is further configured to be coupled to an airway tube, said
airway tube is configured to supply air/gas to the user.
14. A method of using a nasal interface device, comprising:
securing a facial adaptor to the nose of the user, wherein the
facial adaptor includes nostril pads configured to be inserted into
nostrils of the user; inserting a piercing/swivel adaptor into the
nostrils of the user through the nostril pads of the facial
adaptor; and coupling an airway tube to the piercing/swivel
adaptor, wherein the airway tube is configured to supply air/gas to
the user.
15. A system for controlling breathing of a patient, comprising: a
nasal interface device, having a facial adaptor configured to be
secured to the nose of a user and having two nostril pads
configured to be inserted into nostrils of the user; a
piercing/swivel adaptor configured to interact with said facial
adaptor through said two nostril pads; wherein said piercing/swivel
adaptor is further configured to be coupled to an airway tube, said
airway tube is configured to supply air/gas to the user.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] The present application claims priority to U.S. patent
application Ser. No. 12/383,316, filed Mar. 23, 2009 which claims
priority from U.S. Patent Provisional Patent Application No.
61/070,303 to Daly, filed Mar. 21, 2008, and entitled "Nasal
Interface Device", and incorporates its disclosure herein by
reference in its entirety.
[0002] The present application also relates to U.S. patent
application Ser. No. 11/405,948, filed on Apr. 17, 2006, U.S.
patent application Ser. No. 11/787,854, filed on Apr. 17, 2007, and
International Patent Application No. PCT/US2007/009454, filed on
Apr. 17, 2007, the disclosures of which are incorporated herein by
reference in their entireties.
BACKGROUND OF THE INVENTION
[0003] 1. Field of the Invention
[0004] The present invention relates generally to treatment of
breathing disorders. In particular, the present invention relates
to a nasal interface device that is relatively small, lightweight,
easy to use, and can be connectable to a breathing apparatus.
[0005] 2. Background of the Invention
[0006] Sleep-disordered breathing ("SDB") includes all syndromes
that pose breathing difficulties during sleep. These include
obstructive sleep apnea ("OSA"), mixed sleep apnea ("MSA"), central
sleep apnea ("CSA"), Cheyne-Stokes respiration ("CSR"), and others.
Some form of SDB occurs in approximately 3-5% of the U.S.
population.
[0007] Anatomical problems such as obesity or an abnormally narrow
upper airway are known to cause obstructive forms of SDB, in which
the airway is vulnerable to collapse as a result of fluid dynamic
stresses imposed by breathing. These stresses produce collapse
during sleep, especially during rapid-eye-movement ("REM") sleep,
when there is a reduction in the tone of muscles holding the airway
open. An appropriate interface is required in order to deliver
continuous positive airway pressure ("CPAP") therapy, during which
air pressure in the range of 4-25 cm H.sub.2O is delivered from a
pressure generator, via delivery hosing, and through the interface
in order to pressurize the airway so that it will resist such
collapse. Various types of interfaces are known, including nasal
masks covering and creating a seal with the skin surrounding the
nose, oro-nasal masks covering and creating a seal with the skin
surrounding the nose and mouth, and "nasal pillow" devices which
directly engage the nares of the nose by inserting soft, expandable
elastomer tubes just inside the entrance to the nostrils. Small
leaks are acceptable in such devices, which in any ease usually
incorporate an exhalation orifice producing a fixed leak in the
range of 30-50 liters per minute to provide bias flow for the
pressure generator and to prevent rebreathing of exhaled gases.
[0008] Neurological difficulties in controlling levels of blood
gases, such as carbon dioxide ("CO.sub.2") and oxygen ("O.sub.2"),
are increasingly being recognized as important contributors to
other forms of SDB. This is especially true of the "central"
syndromes, MSA, CSA and CSR, which may account for as much as 20%
of all SDB. Changes in the neurological system that control blood
gases often produce cyclic fluctuations in blood gases, and thus,
unsteady respiratory patterns that cause arousals from sleep. These
changes are accompanied by spikes in blood pressure and release of
stress hormones that can cause long-term damage to a number of
organ systems. Additionally, some SDB syndromes involve not only
fluctuations in levels of blood gases, but also abnormal average
levels of blood gases. For example, low levels of dissolved
CO.sub.2 in arterial blood are frequently encountered in CSR,
making the blood alkaline and posing a clinical problem. Therapies
directed towards the central SDB syndromes may Involve modulation
of breathing gases or control of exhalation of carbon dioxide.
These therapies are able to stabilize respiration and establish
appropriate blood gas levels by restoring normal control of blood
gases. When such therapies are in use substantially leak-proof
interfaces are required in order to permit careful control of the
gases being exchanged between the therapy devices and the user.
Leaks as small as one liter per minute, which would equate to the
amount of flow that would pass through a hole as small as 1
millimeter in diameter, may negate the effects of the therapy.
Thus, many conventional interface designs currently in use for
delivery of CPAP therapy would not be suitable for use in treatment
of the central SDB syndromes, and a much more secure interface
design is needed for optimum therapy.
[0009] Respiratory interfaces typically provide gaseous
substance(s) to a user in a variety of applications, including
treatment of the above referenced illnesses, anesthesiology, and
assistance in breathing.
[0010] Many respiratory therapies attempt to manage precisely the
inhaled, mixed and exhaled gases for a user. This may be achieved
through a tight seal between the interface and facial contours of
the user. A tight seal may be necessary not only in order to
provide precise control of gases exchanged with the user, but also
to prevent escape of inhalational agents into ambient air where
they may affect clinical personnel. For example, when a respiratory
interface is utilized in treating complex sleep apnea, a closed
system is required to control the amount of carbon dioxide that is
exhaled by the user.
[0011] in the past, a tight seal has usually been achieved through
the use of straps and harnesses to pull the interface tightly
against the user's face. Since facial geometries vary, the amount
of pressure applied to the skin by the interface will vary from
place to place on the face, creating "hot spots" where pressure may
be quite high. In some instances, the pressure may be high enough
to prevent effective blood perfusion at the hot spots, causing
long-term skin breakdown and damage to the face of the user.
Therefore, it may be desirable to have an interface that conforms
to a users face and puts little or no positive pressure on the
user's face while providing a sufficient seal.
[0012] The hoses and tubes associated with many respiratory
therapies apply various torque forces to the interface, making
desirable for the interface to be sufficiently rigid or stiff to
provide a stable physical platform to resist such forces, and to
provide the user with the perception of security and stability of
the interface and seal when in use. In the case of respiratory
interfaces that create a seal by engaging the nares of the nose
with nasal pillows, it is essential that interface provide a
geometrically stable platform to hold the nasal pillows securely in
relationship to the nose, otherwise there is a risk that torque
forces will cause one or both of the nasal pillows to disengage
from the nare, creating a large air leak.
[0013] A competing concern to the rigidity of an interface is its
ability to conform to user's individual facial features while
providing comfort to the user. Compliance with continuous positive
airway pressure therapy is reported to be less than 50% after one
year, primarily as a result of interface discomfort. The ability of
an interface to conform a user's thee comfortably is generally
provided by a cushion. However, the cushion also serves to
distribute forces applied to the interface such as pulling caused
by the attached hoses and tubing, thereby limiting the degree of
conformity with the face and the degree of comfort.
[0014] Further, conventional CPAP masks an other interface devices
are bulky, heavy, and are difficult operate. Thus, there is a need
for a light-weight nasal interface device that can provide
air-tight connection to a breathing apparatus and allow flexibility
of movement to its user.
SUMMARY OF THE INVENTION
[0015] A nasal interface device and a method of use are disclosed.
In some embodiments, the device includes a facial adaptor
configured to be secured to the nose of a user and incorporating
pads configured to be secured inside the nostrils of a user and
further configured to extend into the interior of one or both
nostrils of the user (for illustrative purposes and ease of
description only, also referred to as "nostril pads"). Each nostril
pad is configured to be manufactured from a soft, elastomeric
material. In some embodiments, the pad is configured to conform to
the interior geometry of the user's nostril and to substantially
follow the typical interior architecture of the nostril, especially
the inner curvature of the nostril, wherein the inner circumference
of the nostril at approximately 2-3 millimeters inside the nostril
is substantially greater than the inner circumference at the
opening of the nostril. In some embodiments, the nostril pads
further include pilot holes disposed in each nostril pad. Each
pilot hole is configured to be pierced using an appropriately-sized
tube or a "nostril prong" by placing the nostril prong through the
pilot hole after the nostril pad is inserted into the nostril. Upon
insertion into the user's nostril, the nostril prongs provide a
breathing passage through which air could be inhaled and exhaled
without excessive resistance by the user. In some embodiments, the
nostril prongs can be configured to be coupled to a piercing/swivel
adaptor configured to interact with a facial adaptor via the two
nostril prongs. Insertion of the nostril prongs into the pilot
holes in the facial adaptor would expand the soft nostril pads,
causing them to flare out and form a tight seal with the inner wall
of the nostril, thereby "locking" the facial adaptor into the nose
and providing an airtight seat due to the larger diameter of the
inside of the nostril relative to the opening of the nostril. The
piercing/swivel adaptor is further configured to be coupled to an
airway tube, the airway tube is configured to supply air/gas to the
user.
[0016] In some embodiments, the present invention relates to a
method of applying a nasal interface device to a nose of a user.
The method includes securing a facial adaptor to the nose of the
user, wherein the facial adaptor includes soft elastomeric nasal
pads with pilot holes. The nasal pads are configured to he inserted
into the nostrils of the user The method further includes inserting
a piercing/swivel adaptor incorporating tubular nostril prongs
through the pilot holes in order to lock the facial adaptor inside
the nostrils and to establish an air channel, and coupling an
airway tube to the piercing/swivel adaptor, wherein the airway tube
is configured to supply air/gas to the user.
[0017] In some embodiments, the present invention relates to a
nasal interface device having a facial adaptor configured to be
secured to the nose of a user and having a nostril pad configured
to be inserted into a nostril of the user. The nostril pad is
configured to substantially conform to an interior geometry of the
nostril upon insertion of the pad into the nostril and includes an
open channel protruding through the nostril pad. A nostril tube is
configured to be placed through the open channel in order to supply
air/gas to the user.
[0018] In some embodiments, the present invention relates to a
method of using a nasal interface device for supplying air/gas to a
user. The method includes securing a facial adaptor to the nose of
the user, wherein the facial adaptor includes a nostril pad
configured to be inserted into a nostril of the nose of the user,
the nostril pad is configured to substantially conform to an
interior geometry of the nostril upon insertion of the pad into the
nostril and includes an open channel protruding through the nostril
pad. A nostril tube is configured to be placed through the open
channel in order to supply air/gas to the user.
[0019] In some embodiments, the present invention relates to a
nasal interface device having a facial adaptor configured to he
secured to the nose of a user and having two nostril pads
configured to he inserted into nostrils of the user, and a
piercing/swivel adaptor configured to interact with the facial
adaptor through the two nostril pads. The piercing/swivel adaptor
is further configured to be coupled to an airway tube, the airway
tube is configured to supply air/gas to the user.
[0020] In some embodiments, the present invention relates to a
method of using a nasal interface device. The method includes
securing a facial adaptor to the nose of the user, wherein the
facial adaptor includes nostril pads configured to be inserted into
nostrils of the user, inserting a piercing/swivel adaptor into the
nostrils of the user through the nostril pads of the facial
adaptor, and coupling an airway tube to the piercing/swivel
adaptor, wherein the airway tube is configured to supply air/gas to
the user.
[0021] In some embodiments, the present invention relates to a
system for controlling breathing of a patient. The system includes
a nasal interface device. The device includes a facial adaptor
configured to be secured to the nose of a user and having two
nostril pads configured to be inserted into nostrils of the user, a
piercing/swivel adaptor configured to interact with the facial
adaptor through the two nostril pads. The piercing/swivel adaptor
is further configured to be coupled to an airway tube, the airway
tube is configured to supply air/gas to the user.
[0022] Further features and advantages of the invention, as well as
structure and operation of various embodiments of the invention,
are disclosed in detail below will reference to the accompanying
drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
[0023] The present invention is described with reference to the
accompanying drawings. In the drawings, like reference numbers
indicate identical or functionally similar element Additionally,
the left-most digit(s) of a reference number identifies the drawing
in which the reference number first appears.
[0024] FIG. 1 illustrates an exemplary nasal interface device,
according to some embodiments of the present invention.
[0025] FIG. 2 is a side view from beneath the nose of the nasal
interface device shown FIG. 1.
[0026] FIGS. 3-4 illustrate various views of an exemplary facial
adaptor of the nasal interface device shown in FIG. 1 according to
some embodiments of the present invention.
[0027] FIGS. 5-8 illustrate various views of the facial adaptor
shown in FIGS. 3-4 being applied to the nose of the user.
[0028] FIGS. 9a-e illustrate in exemplary piercing/swivel adaptor
of the nasal interface device show in FIG. 1, according to some
embodiments of the present invention.
[0029] FIGS. 10-11 illustrate various views of the piercing/swivel
adaptor shown in FIGS. 9a-c being applied to the nose of the
user.
DETAILED DESCRIPTION OF THE INVENTION
[0030] In some embodiments, the present invention relates to a
respiratory interface device that can be attached to the face of a
user (or a patient) order to allow the user to breathe through the
device, where the device can be coupled to a breathing apparatus
providing positive air pressure to the user.
[0031] FIG. 1 illustrates an exemplary nasal interface apparatus
100, according to some embodiments of the present invention. The
nasal interface device 100 includes a facial adaptor 102 and a
swivel/piercing element 104. The nasal interface device 100 is
configured to be coupled to a swivel 106. The tubing 106 can be
further coupled to a system for controlling breathing of a patient
(not shown in FIG. 1), such as those described in the
co-owned/co-pending U.S. patent application Ser. No. 11/405,948,
filed on Apr. 17, 2006, U.S. patent application Ser. No.
11/787,854, filed on Apr. 17, 2007, and International Patent
Application No. PCT/US2007/009454, filed on Apr. 17, 2007, the
disclosures of which are incorporated herein by reference in their
entireties.
[0032] FIG. 2 is a side view of the nasal interface apparatus 100
shown in FIG. 1. FIG. 2 further illustrates that the
swivel/piercing element 104 allows the tubing 106 to rotate as the
user moves his/her head the user rolls to the side on his/her bed
during sleep). In some embodiments, the tubing 106 is configured to
be coupled to the system for controlling breathing (not shown in
FIGS. 1 and 2) that can he discretely disposed above the user's
head or away from sight to sustain an aesthetic appearance of the
room and prevent formation of the tubing clutter around the
user.
[0033] FIGS. 3-4 illustrate exemplary facial adaptor 102, according
to some embodiments of the present invention. The facial adaptor
102 is configured to be coupled to the user's nose at various
locations on the nose, as illustrated in FIGS. 5-8. The facial
adaptor 102 includes nose attachment portions 304 and 308. The
first portion 304 is configured to be attached to the bridge of the
user's nose. The first portion 304 includes a strip 314 and side
flaps 306a and 306b. The strip 314 includes a proximate end 322 and
a distal end 324. The side 306 are configured to be coupled at or
substantially adjacent to the distal end 324 of the strip 314. The
strip 314 is figured to be bendably coupled to the second portion
308 of the facial adaptor 102 at the bendable connection 326.
[0034] The side flaps 306 of the strip 314 are configured to bend
around the axis strip 314. The side flaps 306 are configured to
have a curved shape. The width, length, and height of the side
flaps 306 are configured to accommodate the height of the bridge of
the user's nose. The length of the strip 314 can be configured to
accommodate length of bridge the user's nose. Thus, the present
invention can be manufactured in way to accommodate child and adult
users having varying facial parameters.
[0035] In some embodiments, the strip 314 and the side flaps 306
can be configured to include various means of attachment (shown in
FIGS. 3-4) to allow further securing of the strip 314 and the flaps
306 to the nose of the use. In some embodiments, the strip 314 and
the flaps 306 can be configured to form a friction clamp, whereby
upon placement of the snip 314 and the flaps 306 on the bridge of
the nose, the flaps 306 are bent toward the nose in a pinching-type
motion, thus, gently squeezing the nose and preventing slippage of
the facial adaptor 102 from the nose. In some embodiments, the
flaps 306 can include various materials that can be configured to
retain a certain shape once they are bent into a particular
configuration and/or subject to a certain temperatures. In some
embodiments, the flaps 306 can be configured to include any other
means for attaching the flaps to the nose of the user, including
but not limited to, adhesives, glue, friction devices, straps, or
any other suitable devices. In some embodiments, the strip 314 is
configured to be placed over the top of the bridge of the user's
nose (or over the skin covering cartilage of the septum). The strip
314 is attached to the bridge of the user's nose in a way so that
the proximate end 322 of the strip 314 is configured to coincide
with the tip of the user's nose. Such attachment allows bending of
the facial adaptor 102 at the bendable connection 326. Such
attachment further allows the user to bend second portion 308 in a
downward direction toward nasal airways of the user. Once the strip
314 is placed on the bridge of the user's nose, the side flaps 306
are forced in a downward direction toward the skin of the nose and
are further attached to the nose as discussed above. As can be
understood by one having ordinary skill in the art, the facial
adaptor 102 can be manufactured from materials that can be
configured to allow the adaptor 102 to retain a certain shape upon
bending or twisting the adaptor 102 in a particular way.
[0036] The second portion 308 is configured to cover a bottom
portion of the user's nose underneath the tip of the nose. In some
embodiments, the second portion 308 can be shaped substantially
similar to the bottom portion of the user's nose. In some
embodiments, the second portion 308 has a substantially triangular
shape. The second portion 308 has a substantially flat interior
surface 332 that is configured to interact with the bottom portion
of the nose. In some embodiments, the interior surface 332 is
configured to cover the bottom edges of the user's nostrils upon
adaptor 102 being installed on the user's nose. In some
embodiments, the interior surface 332 can include glue, adhesives,
friction-type devices, straps or any other types of mechanisms that
are configured to further secure the facial adaptor 102 to the nose
of the user. The second portion 308 further includes nostril pads,
protrusions, or otherwise extensions (winch will be referred to as
"pads" in the following description) 312a and 312b. In some
embodiments, the nostril pads 312 are configured to have
substantially teardrop shape and protrude substantially vertically
away from the interior surface 332. In some embodiments, the
nostril pads 312 can be configured to protrude at an angle with
regard to the interior surface 332. Further, the nostril pads 312
can be configured to have any desired shape. In some embodiments,
the nostril pads 312 can be configured to create a substantially
hermetic fit inside user's nostrils. As such, no air/gas can escape
from the nostrils while the user is using the above device. As can
be understood by one skilled in the art, the sizes of the nostril
pads 312 can differ in order to accommodate varying size nostrils
(e.g., children and adults). As can be further understood by one
skilled in the art, the pads 312 can have any desired shape,
including teardrop, cylindrical, oval, or any other suitable
shape.
[0037] In some embodiments, the nostril pads 312 can be configured
to have a greater diameter (or otherwise be larger) at the end
distal from the interior surface 332 than the diameter of the
nostril pads at the end proximate to the interior surface 332. This
allows for the nostril pads to better conform to the interior
geometry of the user's nose, whereby the diameter of a nostril may
be greater at a point distal from the opening of the nostril than
the diameter of the nostril at its opening.
[0038] In some embodiments, the nostril pads 312 include pilot
holes 342 (a, b), respectively, formed along the axis of the
nostril pads 312. The pilot holes 342 create open or pilot channels
and allow insertion of tubes or nostril prongs disposed on the
swivel/piercing element 104 (as shown and discussed below with
regard to FIGS. 9a-c).
[0039] Side flaps 310(a) and 310(b) are coupled to the second
portion 308 via bendable connections 344. As illustrated in FIG. 4,
side flaps 310 are configured to fit immediately adjacent to the
sides of the bottom of the nose of the user, e.g., along the side
of the nose where the nose meets the face. Once the user places the
facial adaptor 102 on the nose, the flaps 310 are configured to be
bent up from the interior surface 332 of the adaptor 102 and be
placed on the side of the user's nose in such a manner as to
provide a clamping action that further secures adaptor 102 to the
bottom portion of the nose. In some embodiments, the interior
surface of side flaps 310 can be configured to include various
means of attachment, including but not limited to, friction-type
mechanisms and clamps, adhesives, glues, straps and any other
suitable devices that that allow side flaps 310 to attach to the
side of the nose.
[0040] In some embodiments, the facial adaptor 102 can he
configured to be formed from a suitable biomedically compatible
grade of soft elastomer such as polyurethane plastic. As can be
understood by one skilled in the art, the facial adaptor 102 can be
formed from any suitable material. Further, the facial adaptor 102
(with the exception of the nostril pads 312) can have a thickness
on the order of 3-5 millimeters. In some embodiments, a
friction-type mechanism, a glue, a thin-film adhesive, or any other
suitable attachment means can be applied to the above-described
parts of the facial adaptor 102. In some embodiments, the
attachment means can be configured to create a non-permanent
attachment to the skin of the user, thus, allowing the user to
temporarily apply the facial adaptor 102 to user's face and remove
it as necessary. Further, the attachment means can be such that
same facial adaptor 102 can be removed from the user's face and
then re-applied, e.g., the facial adaptor can use a repositionable
attachment means that allows the user to remove and reapply the
adaptor. In some embodiments, the facial adaptor 102 can be a
single or as multi-use device. In some exemplary embodiments, the
weight of the facial adaptor 102 can be on order of 2 to 7 grams
("g").
[0041] The nostril pads 312 can be manufactured from a soft
elastomeric material, such as medical grade polyurethane or any
other suitable material. The elastomeric material can be configured
to have a varying hardness coefficient that determines how
flexible/hard this material can be. The hardness coefficient can be
measured using a Shore-A scale having values between A 00,
corresponding to the softest material, and A 100, corresponding to
the hardest material. As can be understood by one skilled in the
art, the nostril pads 312 can have a hardness coefficient in the
range of approximately A 00 to approximately A 60. In some
embodiments, the nostril pads 312 can be injection molded and
attached (by any methods, including gluing, stapling, welding,
thermo-gluing, or any other methods) to the interior surface 312 of
the second portion 308. In some embodiments, the entire facial
adaptor 102 can be manufactured from a single material, such as
polyethylene, polyurethane, polyester, and an other plastic
polymers.
[0042] The nostril pads 312 are configured to be disposed
substantially in the center of the second portion 308 of the facial
adaptor 102 and further match the location of user's nostrils so
that upon insertion of the nostril pads 312 into the user's
nostrils, the nostril pads 312 are comfortably disposed inside
user's nostrils. In some embodiments, the nostril pads 312 can be
disposed at an angle with regard to each other, as illustrated in
FIGS. 3-4. With just the nostril pads 312. (i.e., without the
breathing tubes or nostril prongs) being inserted into the user's
nostrils, the user may be able to breathe through the nose.
However, upon insertion, of the breathing tubes, the nostril pads
312 expand inside the nostrils to provide a hermetic seal and, as
stated above, do not allow leaking of air/gas between the interior
walls of the nostrils and the pads.
[0043] In some embodiments, the nostril pads 312 can be used
independently of the rest of adaptor 102 and configured to be
individually inserted by the user into each nostril. In some
embodiments, the nostril pads 312 can include a connector that
connects the two pads 312. The connector allows the pads to be
inserted into both nostrils simultaneously.
[0044] In order to put the facial adaptor 102 on the face, the user
may perform the following steps. As discussed below, these steps
may not necessarily be performed in the order that they are
described. As can be understood by one skilled in the art, the
steps can be performed in any order. In some embodiments, the user
may first align the proximate end 322 of the first portion 304 with
the tip of the user's nose and then apply the strip 314 along with
wingtips 306 to the bridge and sides of the user's nose. Upon
applying the strip 314 to the bridge of the user's nose, the
wingtips 306 are bent in a downward direction and are applied to
the sides of the user's nose. Then, the second portion 308 is bent
in a downward direction toward the user's nostrils in order to
cover the nose's airways. The nostril pads 312 are inserted into
the nostrils. The side flaps 310 are then bent in an upward
direction along the sloe of the user's nose. FIGS. 5-8 illustrate
the facial adaptor 102 being placed over the user's nose.
[0045] In some embodiments, the facial adaptor 102 can be packaged
by a manufacturer in a single-use sealed tray. The user would
remove the adaptor 102 from the tray, (in embodiments using
adhesives, the user also removes the adhesive liner coveting the
adhesive on the facial adaptor 102), then insert the nostril pads
312 into the user's nostrils, and then apply other portions of the
facial adaptor 102 to the user's face (i.e., the first portion 304
is applied to the bridge of the user's nose and the side flaps 310
to the side of the user's nose).
[0046] In some embodiments, the strip 314 of the first portion 304
can be stiffened with laminated elastomer/PET structures. The
bendable connections 326 and 344 as well as those. between wingtips
306 and the strip 314 can be configured to be molded-in ridges that
allow bending of the appropriate components of the facial adaptor
102. Further, the wingtips 306 as well as side flaps 310 can be
configured to provide, some squeezing three to the user's nose,
when the facial adaptor 102 is applied to the nose, in order to
further secure the adaptor 102 to the nose.
[0047] FIGS. 9a-c illustrate an exemplary swivel/piercing element
104, according to some embodiments of the present invention. The
swivel/piercing element 104 includes a housing 902, nostril prongs
or tubes 906(a, b), a connector tube 904, and a swivel adaptor 922.
The housing 902 further includes an interior surface 912 and an
exterior surface 914. The interior surface 912 is configured to
interact with the facial adaptor 102 (not shown in FIGS. 9a-c). The
exterior surface 914 is facing away from the user's nostrils. In
some embodiments, the shape and size of the housing 902 is
configured to conform to the shape and size of the second portion
308 of the facial adaptor 102 (now shown in FIGS. 9a-e) and can
have a substantially triangular shape, as illustrated in FIGS. 9b
and 9c. As can be understood by one skilled in the art, the element
104 can have any other desired shape and size.
[0048] The nostril tubes 906 are configured to protrude away from
the interior surface 912. The tubes 906 are configured to be
inserted into the openings or pilot holes 342 created in the
nostril pads 312 (not shown in FIGS. 9a-e). Upon insertion of the
nostril tubes 906, the tubes 906 are configured to push the
elastomeric material of the nostril pads 312 away from the outer
surface of the tubes 906 and toward the interior surfaces of the
user's nostrils. By pushing the elastomeric material in such
manner, the tubes 906 along with the nostril pads 312 are
configured to create an air-tight seal in the nostrils, so that the
only air/gas that is able to travel into the user's nose would go
through the tubes 906 of element 104 and no air/gas can leak
between the nostrils and the nostril pads 312.
[0049] The connector tube 904 is configured to protrude away from
the exterior surface 914 of the housing 902. The tube 904 is
configured to connect to the airway tube 106 not shown in FIGS,
9a-c, but is shown in FIG. 1). To allow such connection, the tube
904 includes a swivel adaptor 922. The swivel adaptor 922 allows
the airway tube 106 to rotate in any desired direction, as
indicated by directional arrows A and B. Such rotation provides
flexibility to the user, for example, when the user is rolling
around in bed, walking around, or any performing any other
activities.
[0050] The housing 902 and the tubes 906 and 904 are further
configured to contain interior connector tubing 910 and 916 that
connects tubes 906 and 904. Such interior connector tubing 910 and
916 provides airways from the user's nostrils through the tips 908,
into the tubes 906, through the housing 902, into the tube 904, and
then into the airway tube 106 (not shown in FIGS. 9a-c). When the
nasal interface apparatus 100 is fully connected, as shown in FIGS.
1 and 2, the air/gas can travel to/from user's nostrils and into
the airway tube 106. Alternatively, the housing 902 can be
substantially hollow, providing an internal connection between the
tubes 906 and 904. In some embodiments, the airway tube 106 can
connected to a CPAP machine, as disclosed in co-owned/co-pending
U.S. patent application Ser. No. 11/405,948, filed on Apr. 17,
2006, U.S. patent application Ser. No. 11/787,854, filed on Apr.
17, 2007, and International Patent Application No,
PCT/US2007/009454, filed on Apr. 17, 2007, the disclosures of which
are incorporated herein by reference in their entireties.
[0051] Referring to FIGS. 9a-c, once the user has attached the
facial adaptor 102 to his/her nose, the element 104 is inserted,
using its tubes 906, through the openings 342 (not shown in FIGS.
9a-c). FIGS. 10-11 illustrate such element 104 being coupled to the
facial adaptor 102. The airway tube 106 can then be coupled to the
swivel adaptor 922, as illustrated in FIGS. 1 and 2. As can be
understood by one skilled in the art, this assembly can be
disconnected at will. In some embodiments, the element 104 can he
manufactured from a light, semi-rigid Teflon material. As can be
understood by one skilled in the art, the element 104 can be
manufactured from any polyester, polyethylene, or any other polymer
materials. The element 104 can be reusable or disposable. The
swivel adaptor 922 can be any conventional swivel mechanism that
allows rotation of the airway tube 106 once it is connected to the
swivel adaptor 922.
[0052] In some embodiments, the thickness of the housing 902 can be
on the order of 6-10 mm. Further, the length of the tubes 906 and
908 can be on the order of between approximately 4 mm to
approximately 7 mm.
[0053] In some embodiments, each nostril pad 312 can be separately
inserted into each respective nostril of the user, where nostril
pads 312 are not attached to any external supporting devices, such
as adaptor 102. In some embodiments, the nostril pads 312 can be
configured to be coupled to a friction damp or any other fixation
device, which can be similar to the pads 306 being coupled to the
first portion 304, that is configured to further secure the nostril
pads 312 to the nose of the user. Additionally, in some
embodiments, each one of the nostril prongs 906 can be configured
to be separately inserted through the pilot holes 342 of the
nostril pads without being coupled to the housing 902, i.e., each
prong 906 can be coupled to a tube, which is further connected to
an airway device. The prongs 906 are configured to create a locking
arrangement inside the user's nostrils once the prongs 906 are
inserted through the pilot holes 342.
[0054] In some embodiments, the present invention can he used in
connection with a system for controlling breathing of a patient.
The exemplary system includes the facial adaptor discussed above
coupled to an airway device for supplying air/gas to the patient
via an airway tube. Such system can be employed anywhere, including
user's home, hospital, clinic, or any other facility. The system
and/or the nasal interface device can he operated by the user
himself/herself or a medical professional (e.g., doctor, nurse,
etc).
[0055] Example embodiments of the methods, circuits, and components
of the present invention have been described herein. As noted
elsewhere, these example embodiments have been described for
illustrative purposes only, and are not limiting. Other embodiments
are possible and are covered by the invention. Such embodiments
will be apparent to persons skilled in the relevant art(s) based on
the teachings contained herein. Thus, the breadth and scope of the
present invention should not be limited by any of the
above-described exemplary embodiments, but should be defined only
in accordance with the following claims and their equivalents.
* * * * *