U.S. patent application number 13/172169 was filed with the patent office on 2011-10-27 for hypobaric chamber treatment system.
This patent application is currently assigned to BLUESKY MEDICAL GROUP, INC.. Invention is credited to Richard Scott Weston.
Application Number | 20110264063 13/172169 |
Document ID | / |
Family ID | 35376154 |
Filed Date | 2011-10-27 |
United States Patent
Application |
20110264063 |
Kind Code |
A1 |
Weston; Richard Scott |
October 27, 2011 |
HYPOBARIC CHAMBER TREATMENT SYSTEM
Abstract
A reduced pressure treatment appliance is provided for enclosing
and providing reduced pressure treatment to an object or a portion
of an object. In some embodiments, the reduced pressure treatment
appliance may be used to treat wounds and other conditions, such as
lymphedema, varicose veins, venous insufficiency and stasis, and
other infirmities. In other embodiments, the appliance may be used
to provide reduced pressure (or vacuum) treatment for non-medical
purposes. In some embodiments, the appliance comprises a flexible
chamber and a collapsible frame that may be collapsed while the
appliance is not in use. In yet other embodiments, the appliance
also includes a vacuum system to supply reduced pressure to the
volume within the chamber, a pressurized fluid system to inflate
the collapsible frame, a drainage system to remove fluids from the
appliance, and a treatment port and a forced entry treatment system
to introduce fluids and other treatment instrumentalities into the
volume within the chamber. In still other embodiments, the chamber
is designed for use with distal extremital portions of a body. In
further embodiments, the appliance also comprises a semi-permeable
liner positioned between the chamber and the portion of a body to
be treated. Finally, methods are provided for using various
embodiments of the appliance.
Inventors: |
Weston; Richard Scott;
(Encinitas, CA) |
Assignee: |
BLUESKY MEDICAL GROUP, INC.
Memphis
TN
|
Family ID: |
35376154 |
Appl. No.: |
13/172169 |
Filed: |
June 29, 2011 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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11132549 |
May 19, 2005 |
7998125 |
|
|
13172169 |
|
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|
60573653 |
May 21, 2004 |
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Current U.S.
Class: |
604/319 |
Current CPC
Class: |
A61H 2201/0157 20130101;
A61G 10/023 20130101; A61H 2201/5092 20130101; A61H 2201/0242
20130101; A61H 2201/0103 20130101; A61H 2201/5061 20130101; A61H
9/0021 20130101; A61H 2201/0207 20130101; A61H 2033/145 20130101;
A61H 2201/0214 20130101; A61H 2201/1642 20130101; A61H 2201/5082
20130101; A61H 2205/065 20130101; A61H 9/0092 20130101; A61H
2201/1638 20130101; A61H 2205/12 20130101; A61H 9/0057 20130101;
A61M 1/008 20130101; A61H 2205/067 20130101; A61H 9/0078 20130101;
A61H 2201/0161 20130101 |
Class at
Publication: |
604/319 |
International
Class: |
A61M 1/00 20060101
A61M001/00 |
Claims
1. An appliance for administering reduced pressure treatment to a
digit of a distal extremital portion of a body, the appliance
comprising: a rigid or semi-rigid chamber extending between an
opening at a proximal end and a substantially closed distal end,
the chamber having a substantially cylindrical shape with a
circular cross-section along its length, wherein the rigid or
semi-rigid chamber is sized to enclose at least a portion of a
digit of the distal extremital portion of the body and adapted to
maintain reduced pressure within the volume of the rigid or
semi-rigid chamber; a sealing mechanism at the proximal end of the
chamber, the sealing mechanism comprising a flexible sleeve
configured to receive at least a portion of the digit therethrough
to seal the opening so that reduced pressure may be maintained
within the volume of the rigid or semi-rigid chamber; and a reduced
pressure supply mechanism that operably connects the rigid or
semi-rigid chamber to a reduced pressure supply source via a port
on the chamber, the reduced pressure supply source configured to
provide a supply of reduced pressure to the rigid or semi-rigid
chamber so that the volume within the rigid or semi-rigid chamber
is supplied with reduced pressure by the reduced pressure supply
source and wound exudate is removed from the chamber.
2. The appliance of claim 1, wherein the appliance further
comprises an ancillary treatment system operably attached to the
rigid or semi-rigid chamber, the ancillary treatment system
configured to introduce fluids into the volume within the rigid or
semi-rigid chamber.
3. The appliance of claim 2, wherein the ancillary treatment system
is configured to introduce air or gas into the chamber.
4. The appliance of claim 3, wherein the air or gas is heated or
cooled in an amount sufficient to raise or lower the temperature of
the digit of the distal extremital portion of the body.
5. The appliance of claim 1, wherein the reduced pressure supply
source is a vacuum pump.
6. The appliance of claim 1, wherein the reduced pressure supply
source is a suction bulb system.
7. The appliance of claim 1, wherein the digit of the distal
extremital portion is a human finger.
8. The appliance of claim 1, wherein the digit of the distal
extremital portion is a human toe.
9. The appliance of claim 1, further comprising a fluid impermeable
or semi-permeable liner operably disposed between the chamber and
the portion of the body positioned within the chamber.
10. The appliance of claim 9, further comprising a sealing
mechanism to seal the fluid impermeable or semi-permeable liner and
the portion of the body positioned within the chamber so that
reduced pressure may be maintained within the volume of the chamber
and the volume of the liner.
11. The appliance of claim 1, wherein the flexible sleeve is
conical or frustoconical in shape.
12. The appliance of claim 1, wherein the flexible sleeve comprises
a stretchable material.
13. A method of administering reduced pressure treatment to a digit
of a distal extremital portion of a body, the method comprising:
positioning the digit to be treated within an appliance, the
appliance comprising: a rigid or semi-rigid chamber having an
opening, wherein the chamber is sized to at least partially enclose
the digit to be treated, configured to support the chamber away
from the digit to be treated while the appliance is in use, and
adapted to maintain reduced pressure within the volume of the
chamber; a sealing mechanism to seal the opening so that reduced
pressure may be maintained within the volume of the chamber; and a
reduced pressure supply mechanism to operably connect the chamber
to a reduced pressure supply source that provides a supply of
reduced pressure to the chamber, so that the volume within the
chamber is supplied with reduced pressure by the reduced pressure
supply source; sealing the opening of the chamber about the digit
using the sealing mechanism, so that reduced pressure may be
maintained in the volume within the chamber; operably connecting
the chamber with the reduced pressure supply source using the
reduced pressure supply mechanism so that reduced pressure is
supplied to the volume within the chamber; evacuating wound exudate
from the chamber using the reduced pressure supply source; and
maintaining the reduced pressure in the volume within the chamber
until the digit being treated has progressed toward a selected
stage of treatment.
14. The method of claim 13, further comprising collecting wound
exudate in a container disposed between the chamber and the reduced
pressure supply source.
15. The method of claim 13, further comprising the step of applying
ancillary treatment to the digit, the ancillary treatment
comprising a system configured to introduce fluids into the volume
of the chamber.
16. The method of claim 15, wherein the ancillary treatment
comprises introducing air or gas into the volume of the
chamber.
17. The method of claim 16, further comprising the step of heating
or cooling the air or gas introduced into the volume of the
chamber.
18. The method of claim 13, further comprising the step of removing
the digit from the appliance after the selected stage of treatment
has been reached.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a divisional application of U.S. patent
application Ser. No. 11/132,549, filed on May 19, 2005, which
claims the benefit of U.S. provisional application No. 60/573,653,
filed on May 21, 2004. Both applications are hereby incorporated in
their entirety by reference herein.
BACKGROUND OF THE INVENTION
[0002] The present invention generally relates to administration of
reduced pressure to objects or portions of objects that require the
application of reduced pressure as a part of treatment of such
objects or portions of objects. For example, in some embodiments,
the present invention comprises an improved apparatus and method
for treating wounds and other infirmities and conditions on a
portion of a patient's body by applying reduced pressure to the
portion of the body for which treatment is desired. In this
context, the terms "wound," "infirmity," "condition" and "body" are
to be interpreted broadly, to include any body part of a patient
that may be treated using reduced pressure. As another example, in
other embodiments, the present invention comprises an improved
apparatus and method for reduced pressure treatment related to
industrial-type processes, such as degassing materials and insect
control.
[0003] The treatment of open or chronic wounds that are too large
to spontaneously close or otherwise fail to heal by means of
applying reduced pressure to the site of the wound is well known in
the art. Examples of such treatment systems are disclosed in U.S.
patent application Ser. No. 10/652,100 (filed on Aug. 28, 2003),
Ser. No. 11/026,733 (filed on Dec. 30, 2004), Ser. No. 11/064,813
(filed on Feb. 24, 2005), Ser. No. 11/095,859 (filed by the present
inventor with others on Mar. 31, 2005) Ser. No. 11/098,265 (filed
on Apr. 4, 2005), and Ser. No. 11/098,203 (filed on Apr. 4, 2005),
which were filed by the present inventor with the U.S. Patent and
Trademark Office. The disclosures of these U.S. patent applications
are incorporated herein by reference.
[0004] Reduced pressure wound treatment systems currently known in
the art commonly involve placing a cover that is impermeable to
liquids over the wound, using various means to seal the cover to
the tissue of the patient surrounding the wound, and connecting a
source of reduced pressure (such as a vacuum pump) to the cover in
a manner so that an area of reduced pressure is created under the
cover in the area of the wound. There are, however, certain
instances where it is advantageous to have a wound treatment system
that covers the entire portion of the body of the patient in the
area of the wound, rather than merely the surface of the body
immediately surrounding the wound. For example, certain types of
burns that are treatable by reduced pressure may require treating a
relatively large area of the patient's body with reduced pressure.
In these cases, a device that covers the entire portion of the body
to be treated would be advantageous. In addition, it is possible to
treat and alleviate certain other infirmities using reduced
pressure. Such infirmities may include lymphedema, venous
insufficiency and stasis, and varicose veins. In the case of
lymphedema, the patient suffers from an abnormal interstitial
accumulation of tissue fluid. The mechanism for this accumulation
is impairment of normal fluid uptake by the lymphatic vessels or
excessive production of tissue fluid, which is caused by venous
obstruction that increases capillary blood pressure. Common causes
of lymphedema include neoplastic obstruction of lymphatic flow,
postoperative interference with lymphatic flow, infectious blockade
of lymphatics, and radiation damage to lymphatics. In the case of
venous insufficiency and stasis, blood circulation through the
venous system is inadequate. This condition may be caused by
congestion or by failure of the valves that regulate the flow of
blood in the veins to operate normally. In the case of varicose
veins, the veins become enlarged and dilated, which may lead to
venous insufficiency and stasis. It is well known in the art that
application of pressure to the portions of the body of the patient
affected by these infirmities may provide relief from some of the
symptoms of the infirmities. A device that is capable of enclosing
and providing reduced pressure treatment to an entire portion of a
patient's body affected by such infirmities would be advantageous
because it would be capable of providing this required application
of pressure.
[0005] There are devices extant in the art that may provide this
reduced pressure treatment to the entire portion of a patient's
body. An example of this type of device is disclosed in U.S. patent
application Ser. No. 11/075,020, entitled "Enclosure-Based Reduced
Pressure Treatment System," which was filed by the present inventor
(among others) with the U.S. Patent and Trademark Office on Mar. 8,
2005. The disclosure of this U.S. patent application is also
incorporated herein by reference. Such devices, however, are
positioned immediately adjacent to the tissue of the patient. In
some cases, this may cause irritation of the skin or other tissue
of the patient. In other cases, this may cause pain or discomfort
for the patient. Other devices may provide reduced pressure
treatment to the entire portion of a patient's body without
contacting tissue in the area of the patient to be treated, but the
devices may be heavy due to the nature of their construction. In
addition, such devices may be large and unwieldy, so that they
occupy a substantial amount of space when not in use. This may
result in the devices taking up excessive amounts of storage space.
In both cases, these characteristics may also prevent the devices
from being portable. In yet other cases, the devices may be used in
circumstances where it is not necessary to avoid contact with
patient tissue, but the devices may become contaminated by exudate
aspirated from the wound while in use.
[0006] Therefore, there is a need for a reduced pressure treatment
system capable of enclosing the entire portion of a patient's body
to be treated for a wound or other infirmity in a manner so that
the system does not contact certain portions of the body of the
patient. This includes the case of distal extremities, such as
fingers and toes. There is also a need for such system to evenly
distribute pressure on the surface of the portion of the body to be
treated in certain instances. There is also a need for a reduced
pressure treatment system that is lightweight. In addition, there
is a need for a reduced pressure treatment system that is
collapsible, so that it may be collapsed when not in use, requiring
less storage space. Further, there is a need for a reduced pressure
treatment system enclosing a portion of the body that provides for
efficient removal of any fluid aspirated from the portion of the
body being treated. There is also a need for a reduced pressure
treatment system that is relatively inexpensive, while meeting the
needs described above. Finally, there is a need for a reduced
pressure treatment system that meets all or some of the needs
described above, but where the system may be used in reduced
pressure applications other than medical treatment.
SUMMARY OF THE INVENTION
[0007] The present invention is directed to a reduced pressure
treatment appliance and methods that satisfy the needs described
above. As described in greater detail below, they have many
advantages over existing reduced pressure treatment apparatus and
methods when used for their intended purpose, as well as novel
features that result in a new reduced pressure treatment appliance
and methods that are not anticipated, rendered obvious, suggested,
or even implied by any of the prior art apparatus or methods,
either alone or in any combination thereof
[0008] In accordance with the present invention, an appliance is
provided for treating a portion of a body by applying reduced
pressure (i.e., pressure that is below ambient atmospheric
pressure) to the portion of the body to be treated in a controlled
manner for a selected time period in a manner that overcomes the
disadvantages of currently existing apparatus. For example, the
application of reduced pressure to a wound provides such benefits
as faster healing, increased formation of granulation tissue,
closure of chronic open wounds, reduction of bacterial density
within wounds, inhibition of burn penetration, and enhancement of
flap and graft attachment. Wounds that have exhibited positive
response to treatment by the application of negative pressure
include infected open wounds, decubitus ulcers, dehisced incisions,
partial thickness burns, and various lesions to which flaps or
grafts have been attached. In addition, applying reduced pressure
to portions of the body affected by lymphedema, venous
insufficiency and stasis, varicose veins, and other conditions
provides benefits such as increasing the circulation of lymph
through the lymphatic system, increasing the circulation of blood
through the venous system, faster healing of such conditions, and
relief from the symptoms of such conditions. Further, the appliance
may also be used in other types of applications requiring the
administration of reduced pressure to an object or a portion of an
object.
[0009] In a first version of the present invention, an appliance
for administering reduced pressure treatment to an object or a
portion of an object is comprised of a flexible chamber having an
opening, a collapsible frame, sealing means (which are described in
more detail below) to seal the opening, and reduced pressure supply
means (which are also described in more detail below). The flexible
chamber is generally sized to enclose the object or the portion of
the object to be treated and adapted to maintain reduced pressure
within the volume of the flexible chamber. The collapsible frame
supports the flexible chamber away from the object or the portion
of the object to be treated while the appliance is in use. The
sealing means (which are described in more detail below) seal the
opening so that reduced pressure may be maintained within the
volume of the flexible chamber. The reduced pressure supply means
operably connect the flexible chamber to a reduced pressure supply
source that provides a supply of reduced pressure to the flexible
chamber, so that the volume within the flexible chamber is supplied
with reduced pressure by the reduced pressure supply source.
[0010] In this first version of the present invention, the flexible
chamber and the collapsible frame may be collapsed to a smaller
size when the appliance is not in use. In some embodiments of this
first version of the invention, the collapsible frame is further
comprised of at least one inflatable member, wherein the at least
one inflatable member is inflated with a pressurized fluid when the
appliance is in use and may be deflated when the appliance is not
in use. In these embodiments, the appliance is further comprised of
a pressurized fluid supply source and pressurized fluid supply
means to operably connect the collapsible frame to the pressurized
fluid supply source, so that the at least one inflatable member is
supplied with the pressurized fluid by the pressurized-fluid supply
source. In some embodiments, the collapsible frame is comprised of
at least two inflatable members and the at least two inflatable
members are operably connected together so that the pressurized
fluid may flow between them. In other embodiments, the collapsible
frame is comprised of a plurality of rigid or semi-rigid frame
members and frame member connecting means to connect the plurality
of rigid or semi-rigid frame members together, so that the
plurality of rigid or semi-rigid frame members may be collapsed
when the appliance is not in use. In yet other embodiments, the
flexible chamber is comprised of a flexible or semi-flexible
polymer material.
[0011] In some embodiments of this first version of the present
invention, the appliance administers reduced pressure treatment to
a portion of a body and is comprised of a treatment device, a
pressurized fluid system, and a vacuum system. In these
embodiments, the treatment device is further comprised of a
flexible chamber having an opening, a collapsible frame, and
sealing means (described in more detail below) to seal the opening
so that reduced pressure may be maintained within the volume of the
flexible chamber. The flexible chamber is generally sized to
enclose the portion of the body to be treated and adapted to
maintain reduced pressure within the volume of the flexible
chamber. The collapsible frame is comprised of at least one
inflatable member, wherein the at least one inflatable member is
inflated with a pressurized fluid when the appliance is in use and
may be deflated when the appliance is not in use. In these
embodiments, the collapsible frame supports the flexible chamber
away from the portion of the body to be treated while the appliance
is in use and the flexible chamber and the collapsible frame may be
collapsed to a smaller size when the appliance is not in use. The
pressurized fluid system is comprised of a pressurized fluid supply
source and pressurized fluid supply means to operably connect the
collapsible frame to the pressurized fluid supply source, so that
the at least one inflatable member of the collapsible frame is
supplied with pressurized fluid by the pressurized fluid supply
source. The vacuum system is comprised of a reduced pressure supply
source and reduced pressure supply means to operably connect the
flexible chamber to the reduced pressure supply source, so that the
reduced pressure supply source provides a supply of reduced
pressure to the volume within the flexible chamber. In some
embodiments, the pressurized fluid is compressed air and the
pressurized fluid supply source is an air compressor. In other
embodiments, the sealing means is comprised of a flexible sleeve.
In yet other embodiments, the reduced pressure supply source may be
comprised of a vacuum pump and the reduced pressure supply means
may be comprised of flexible tubing. In yet other embodiments, the
vacuum source may be further comprised of a suction bulb system,
which is described in more detail below. In some embodiments, the
reduced pressure within the volume of the flexible chamber in the
area of the portion of the body to be treated is in the range from
approximately 20 mm of Hg below atmospheric pressure to
approximately 125 mm of Hg below atmospheric pressure. In other
embodiments, the reduced pressure may be applied in a cyclic
nature, the cyclic nature providing alternating time periods of
application of reduced pressure and without application of reduced
pressure. In still other embodiments, the treatment device further
comprises a treatment port operably attached to the flexible
chamber. The treatment port permits fluids and other
instrumentalities to be introduced into the volume within the
flexible chamber. In further embodiments, the treatment device
further comprises a forced entry treatment system operably
connected to the flexible chamber for introducing ancillary fluids
into the volume within the flexible chamber.
[0012] In other embodiments of this first version of the invention,
the appliance administers reduced pressure treatment to a portion
of a body and is comprised of a treatment device, which is also
comprised of flexible chamber and collapsible frame substantially
the same as described above. The appliance also comprises a vacuum
system, which is substantially the same as described above, and a
drainage system, which is described in more detail below. The
drainage system is operably disposed between the flexible chamber
and the portion of the body to be treated. In some of these
embodiments, the drainage system further comprises an overlay,
which is sized to be placed over and enclose a part of the portion
of the body to be treated, and overlay sealing means to operably
seal the overlay to the body. In some of these embodiments, the
overlay is comprised of a semi-permeable material, so that reduced
pressure may be maintained in the volume under the overlay at said
part of the body. In other embodiments, the drainage system further
comprises draining means extending from the volume under the
overlay at said part of the body to an area outside the volume of
the flexible chamber so that exudate aspirated from said part of
the body may be drained from said part of the body to such outside
area. In some of these embodiments, the area outside the volume of
the flexible chamber is the reduced pressure supply source, so that
the draining means is in fluid communication with the reduced
pressure supply source and reduced pressure is supplied by the
draining means to the volume under the overlay at said part of the
body. In other embodiments, the draining means is further comprised
of a collection system that is operably positioned between the
overlay and the reduced pressure supply source. The collection
system comprises a container to receive and hold fluid aspirated
from said part of the body. The collection system may also further
comprise pressure halting means to halt the application of reduced
pressure to the volume under the overlay at said part of the body
when the fluid in the container exceeds a predetermined amount. The
drainage system may also further comprise wound packing means
disposed between the overlay and said part of the body.
[0013] In other embodiments of this first version of the present
invention, the appliance administers reduced pressure treatment to
a portion of a body and is comprised of a treatment device and a
vacuum system. In these embodiments, the treatment device is
further comprised of a flexible chamber having an opening, a
collapsible frame, and sealing means (described in more detail
below) to seal the opening so that reduced pressure may be
maintained within the volume of the flexible chamber. The flexible
chamber is generally sized to enclose the portion of the body to be
treated and adapted to maintain reduced pressure within the volume
of the flexible chamber. The collapsible frame, however, is
comprised of a plurality of rigid or semi-rigid frame members and
frame member connecting means to connect the plurality of rigid or
semi-rigid frame members together. The collapsible frame supports
the flexible chamber away from the portion of the body to be
treated while the appliance is in use and the flexible chamber and
the collapsible frame may be collapsed to a smaller size when the
appliance is not in use. The vacuum system and other features,
characteristics and operation of this appliance is substantially
the same as described above.
[0014] The present invention also includes a method of
administering reduced pressure treatment to an object or a portion
of an object using the embodiments of the first version of the
invention described above. Generally, the method comprises the
steps of: (1) providing an appliance for administering reduced
pressure to the object or portion of the object, as described
above; (2) positioning the appliance for use, so that the flexible
chamber and collapsible frame are in an extended state; (3)
positioning the object or portion of the object to be treated
relative to the appliance so that the object or portion of the
object to be treated is positioned within the volume of the
flexible chamber; (4) sealing the opening of the flexible chamber
using the sealing means, so that reduced pressure may be maintained
in the volume within the flexible chamber; (5) operably connecting
the flexible chamber with the reduced pressure supply source using
the reduced pressure supply means so that reduced pressure is
supplied to the volume within the flexible chamber; and (6)
maintaining the reduced pressure in the volume within the flexible
chamber until the object or portion of the object being treated has
progressed toward a selected stage of treatment. In other
embodiments, the method further comprises the steps of removing the
object or portion of the object to be treated from the appliance
after the selected stage of treatment has been reached and
collapsing the appliance. Where the collapsible frame is further
comprised of at least one inflatable member, the step of
positioning the appliance for use, so that the flexible chamber and
collapsible frame are in an extended state, is further comprised of
inflating the at least one inflatable member with the pressurized
fluid using the pressurized fluid supply source and pressurized
fluid supply means. Where the collapsible frame is further
comprised of a plurality of rigid or semi-rigid frame members and
frame member connecting means to connect the plurality of rigid or
semi-rigid frame members together, the step of positioning the
appliance for use, so that the flexible chamber and collapsible
frame are in an extended state, is further comprised of the step of
extending the plurality of rigid or semi-rigid frame members.
[0015] In a second version of the present invention, an appliance
for administering reduced pressure treatment to a distal extremital
portion of a body, such as a finger or toe, is comprised of a rigid
or semi-rigid chamber having an opening, sealing means (described
in more detail below) to seal the opening so that reduced pressure
may be maintained within the volume of the rigid or semi-rigid
chamber, and reduced pressure supply means. The rigid or semi-rigid
chamber is generally sized to enclose the distal extremital portion
of the body and adapted to maintain reduced pressure within the
volume of the rigid or semi-rigid chamber. The reduced pressure
supply means operably connects the rigid or semi-rigid chamber to a
reduced pressure supply source that provides a supply of reduced
pressure to the rigid or semi-rigid chamber, so that the volume
within the rigid or semi-rigid chamber is supplied with reduced
pressure by the reduced pressure supply source. In some of these
embodiments, the sealing means may be comprised of a flexible
sleeve. In other embodiments, the appliance may further comprise an
ancillary treatment system operably attached to the rigid or
semi-rigid chamber. The ancillary treatment system permits fluids
and other instrumentalities and treatment means to be introduced
into the volume within the rigid or semi-rigid chamber. The
appliance may also be further comprised of the reduced pressure
supply source, which may be comprised of a vacuum pump or a suction
bulb system, which is described in more detail below.
[0016] In a third version of the present invention, the appliance
administers reduced pressure treatment to a portion of a body and
comprises a chamber, a semi-permeable liner, sealing means (which
are described in more detail below), and reduced pressure supply
means (which are also described in more detail below). The chamber
has an opening, is sized to enclose the portion of the body to be
treated, is adapted to maintain reduced pressure within the volume
thereof, and is supported away from the portion of the body to be
treated when the appliance is in use. The semi-permeable liner is
disposed between the chamber and the portion of the body positioned
within the chamber. The sealing means is used to seal the opening
and to seal the semi-permeable liner to the body, so that reduced
pressure may be maintained within the volume of the chamber and the
volume of the semi-permeable liner. The reduced pressure supply
means operably connects the chamber to a reduced pressure supply
source that provides a supply of reduced pressure to the chamber,
so that the volume within the chamber is supplied with reduced
pressure by the reduced pressure supply source. In some
embodiments, the chamber is comprised of a rigid or semi-rigid
material. In other embodiments, the chamber is comprised of a
flexible chamber and a collapsible frame, as described above. In
other embodiments, the appliance further comprises a drainage
system operably disposed between the semi-permeable liner and the
portion of the body to be treated. In yet other embodiments, the
sealing means are comprised of a flexible sleeve that extends from
the portion of the chamber approximately adjacent to the opening to
a portion of the semi-permeable liner.
[0017] In other embodiments of this third version of the present
invention, the appliance is comprised of a treatment device and a
vacuum system. The treatment device is further comprised of a
chamber having an opening, sealing means (described in more detail
below) to seal the opening so that reduced pressure may be
maintained within the volume of the chamber, a semi-permeable
liner, and liner sealing means (also described in more detail
below). The chamber is generally sized to enclose the portion of
the body to be treated and is supported away from the portion of
the body to be treated when the appliance is in use. The
semi-permeable liner is operably disposed between the chamber and
the portion of the body positioned within the chamber. The liner
sealing means is used to seal the semi-permeable liner to the
chamber and around a portion of the body so that reduced pressure
may be maintained in the volume within the chamber and the volume
within the semi-permeable liner. The vacuum system has
substantially the same structure, features, characteristics and
operation as the embodiments of the vacuum systems described above.
In other embodiments, the treatment device may also comprise a
treatment port operably attached to the chamber or a forced entry
treatment system operably connected to the chamber.
[0018] In its various versions and embodiments, the present
invention therefore meets the needs discussed above in the
Background section. For example, the appliance of the present
invention represents a reduced pressure treatment system capable of
enclosing the entire portion of a patient's body to be treated for
a wound or other infirmity in a manner so that the system does not
contact certain portions of the body of the patient. This is also
true in the case of distal extremities, such as fingers and toes.
The appliance also provides for evenly distributed pressure on the
surface of the portion of the body to be treated in certain
instances. The appliance may also be constructed of lightweight
materials. In some embodiments, the appliance is also collapsible,
so that it may be collapsed when not in use, requiring less storage
space. The appliance also has features that separately enclose a
portion of the body, providing for efficient removal of any fluid
aspirated from the portion of the body being treated. The appliance
should also be relatively inexpensive to produce, while meeting the
needs described above. Finally, in various embodiments, the
appliance meets all or some of the needs described above and may be
used in reduced pressure applications other than medical
treatment.
[0019] There has thus been outlined, rather broadly, the more
primary features of the present invention. There are additional
features that are also included in the various embodiments of the
invention that are described hereinafter and that form the subject
matter of the claims appended hereto. In this respect, it is to be
understood that the invention is not limited in its application to
the details of construction and to the arrangements of the
components set forth in the following description or illustrated in
the following drawings. This invention may be embodied in the form
illustrated in the accompanying drawings, but the drawings are
illustrative only and changes may be made in the specific
construction illustrated and described within the scope of the
appended claims. The invention is capable of other embodiments and
of being practiced and carried out in various ways. Also, it is to
be understood that the phraseology and terminology employed herein
are for the purpose of the description and should not be regarded
as limiting.
BRIEF DESCRIPTION OF THE DRAWINGS
[0020] The foregoing summary, as well as the following detailed
description of the preferred embodiments of the present invention,
will be better understood when read in conjunction with the
appended drawings, in which:
[0021] FIG. 1 is a view of an embodiment of an appliance comprising
the present invention, in which an embodiment of a treatment
device, shown in partially broken-away perspective view, encloses
the lower arm portion of a patient, and in which embodiments of a
vacuum system, a pressurized fluid system, and a forced entry
treatment system, depicted generally and shown partially in
schematic elevation view, provide reduced pressure, pressurized
fluid, and various treatment means, respectively, to the treatment
device;
[0022] FIG. 2 is an enlarged view of an embodiment of the
collection system of the vacuum system illustrated in FIG. 1.
[0023] FIG. 3 is a view of an appliance comprising the present
invention, in which an embodiment of a treatment device, shown in
perspective view, encloses the lower arm portion of a patient, and
in which an embodiment of a vacuum system, depicted generally and
shown partially in schematic elevation view, provides reduced
pressure to the treatment device;
[0024] FIG. 4 is a perspective view of the collapsible frame
portion of the embodiment of the treatment device illustrated in
FIG. 2, without the flexible chamber covering the collapsible frame
portion;
[0025] FIG. 5 is an enlarged elevation view of a joint comprising
the embodiment of the collapsible frame portion illustrated in FIG.
4;
[0026] FIG. 6 is a perspective view of the flexible chamber portion
of the embodiment of the treatment device illustrated in FIG. 3,
without the collapsible frame portion;
[0027] FIG. 7 is a view of an embodiment of an appliance comprising
the present invention, in which an embodiment of a treatment
device, shown in perspective view, encloses a portion of the finger
of a patient, and in which embodiments of a vacuum system and an
ancillary treatment system, depicted generally and shown partially
in schematic elevation view, provide reduced pressure and various
treatment means, respectively, to the treatment device;
[0028] FIG. 8 is a perspective view of an embodiment of a suction
bulb system that may be used as a source of reduced pressure or
fluid collection or both, and a supplemental vacuum system,
depicted generally and shown in schematic elevation view; and
[0029] FIG. 9 is a view of an embodiment of an appliance comprising
the present invention, in which an embodiment of a treatment
device, shown in partially broken-away perspective view, encloses
the lower leg portion of a patient, and in which embodiments of a
vacuum system and a forced entry treatment system, depicted
generally and shown in schematic elevation view, provide reduced
pressure and various treatment means, respectively, to the
treatment device.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
[0030] In accordance with the present invention, an appliance and
methods for using the appliance are provided for administering
reduced pressure to all or a portion of an object. The description
of the present invention set forth herein is directed primarily
toward use of the appliance and methods for treatment of wounds and
other infirmities and conditions on a portion of a patient's body.
In these cases, an appliance is provided for treating a portion of
the body of a patient by applying reduced pressure (i.e., pressure
that is below ambient atmospheric pressure) to the portion of the
body to be treated in a controlled manner for a selected time
period in a manner that overcomes the disadvantages of currently
existing apparatus. It is to be noted, however, that the appliance
and methods may be used to provide reduced pressure treatment for
other objects and purposes. For example, in some embodiments, the
present invention may be used for reduced pressure treatment
related to industrial-type processes, such as degassing materials
and insect control. Such uses are encompassed within the scope of
the present invention to the extent they are included within the
scope of the appended claims.
[0031] An embodiment of an appliance 10 of a first version of the
invention is illustrated in FIG. 1. In this embodiment, the
appliance 10 is generally comprised of a treatment device 20, a
vacuum system (illustrated schematically in part and generally
designated 30), a pressurized fluid system (illustrated
schematically in part and generally designated 40), a drainage
system 50, and a forced entry treatment system (illustrated
schematically in part and generally designated 60). The treatment
device 20 is generally comprised of a flexible chamber 21 and a
collapsible frame 22, which is generally comprised of a plurality
of inflatable members 22a, 22b that are interconnected in a manner
so that fluid may flow between them. The flexible chamber 21 has an
opening 23 at one end, which is sealed using sealing means that are
described in more detail below. In the illustrated embodiment, the
lower arm portion 12 of a patient extends through the opening 23 so
that the lower arm portion 12 may be treated with reduced pressure
by the appliance 10. The vacuum system 30, which is described in
more detail below, is generally comprised of a reduced pressure
supply source, generally designated 31, and reduced pressure supply
means 32 that operably connect the reduced pressure supply source
31 to the flexible chamber 21 so that reduced pressure is supplied
to the volume within the flexible chamber 21 at the portion of the
body 12 to be treated, as described in more detail below. The
reduced pressure supply source may also provide a supply of reduced
pressure to the drainage system 50, as described in more detail
below. The pressurized fluid system 40, which is described in more
detail below, is generally comprised of a pressurized fluid supply
source, generally designated 41, and pressurized fluid supply means
42 that operably connect the pressurized fluid supply source 41 to
the collapsible frame 22 so that pressurized fluid is supplied to
the inflatable members 22a, 22b comprising the collapsible frame
22, as described in more detail below. The forced entry treatment
system 60 is used to provide various treatments to the portion of
the body 12 within the volume of the flexible chamber 21, as
described in more detail below. The drainage system 50 may
generally be used to remove exudate aspirated from the portion of
the body 12 to be treated, as described in more detail below.
[0032] In the embodiment of the appliance 10 illustrated in FIG. 1,
the treatment device 20 is comprised of the flexible chamber 21 and
the collapsible frame 22. The flexible chamber 21 may be of almost
any size, and is generally sized to enclose the object or the
portion of the object (the lower arm portion 12 in FIG. 1) to be
treated. In addition, the flexible chamber 21 may be of almost any
shape. Thus, even though the flexible chamber 21 of the appliance
10 of FIG. 1 is generally cylindrical, the flexible chamber 21 may
be of other shapes in other embodiments of the present invention.
For example, the flexible chamber 21 may also be cubical,
spherical, spheroidal, hexahedral, polyhedral, or have arcuate or
linear shaped portions, or may be comprised of any combination of
any such shapes, in other embodiments. The preferred size and shape
of the flexible chamber 21 is thus dependent upon the size and
shape of the object or portion of the object to be treated, the
magnitude of reduced pressure to be maintained within the volume of
the flexible chamber 21, the nature of the reduced pressure
treatment desired, and the preference of the user of the appliance
10. The flexible chamber 21 is also adapted to maintain reduced
pressure within its interior volume. Thus, the flexible chamber 21
may be constructed of almost any flexible or semi-flexible, opaque
or transparent, fluid-impermeable material that is currently known
in the art or that may be developed in the art in the future, as
long as the flexible chamber 21 is able to generally maintain its
shape while reduced pressure is present in the interior volume of
the flexible chamber 21 and the flexible chamber 21 is supported by
the collapsible frame 22. For example, the flexible chamber 21 may
be constructed of rubber (including neoprene), silicone,
polyurethane, other plastics, or other flexible or semi-flexible
polymers (such as that sold under the trademark KRATON) or
combinations of any such materials. In cases where the treatment
device 20 is used in medical applications, the material comprising
the flexible chamber 21 is typically also of medical grade, so that
it is suitable for purposes of wound treatment (e.g., can be
sterilized and does not absorb significant amounts of fluids, such
as wound exudate). Preferably, the flexible chamber 21 is comprised
of silicone or a silicone blend. It is to be noted that in various
embodiments, the flexible chamber 21 may be constructed in whole or
in part of gas-permeable materials, allowing limited amounts of air
to penetrate the flexible chamber 21 so that the portion 12 of the
body within the flexible chamber 21 can "breathe." In some
embodiments, all portions of the flexible chamber 21 may be
constructed of one type of material, such as silicone, while in
other embodiments different portions of the flexible chamber 21 may
be constructed of different materials, such as where one portion is
constructed of rubber and another portion is constructed of
silicone. This may be the case where it is desired that some
portions of the flexible chamber 21 have greater strength and other
portions of the flexible chamber 21 have greater flexibility.
Likewise, some portions of the flexible chamber 21 may be comprised
of a transparent material (to provide a viewing "window") and some
portions of the flexible chamber 21 may be comprised of an opaque
material. In addition, the thickness of the material comprising the
flexible chamber 21 must be great enough so that the flexible
chamber 21 is generally able to retain its shape when reduced
pressure is present within its interior volume, while allowing the
flexible chamber 21 to collapse when it is not in use. By
"collapse," it is generally meant that the flexible chamber 21 may
be generally flattened and folded, such as may be the case when it
is necessary or desirable to store the flexible chamber 21 when it
is not in use. It is also to be noted that in various embodiments,
the thickness of various portions of the flexible chamber 21 may
vary. This may also be the case where it is desired that some
portions of the flexible chamber 21 have greater strength and other
portions of the flexible chamber 21 have greater flexibility. The
preferred thickness of the flexible chamber 21 is generally
dependent upon the material of which the flexible chamber 21 is
constructed, the size and shape of the flexible chamber 21, the
level of reduced pressure anticipated within the volume of the
flexible chamber 21, and the nature of the reduced pressure
treatment desired.
[0033] In the illustrated embodiment, the flexible chamber 21 of
the appliance 10 has an opening 23 at one end thereof that is
approximately circular in shape. The opening 23 may be of almost
any size or shape, as long as it does not interfere with the
operation of the flexible chamber 21 and permits the object or
portion of the object to be treated (the lower arm portion 12 in
FIG. 1) to be positioned within the volume of the flexible chamber
21. In cases where only a portion of the object is to be treated in
the flexible chamber 21, the opening 23 is generally of a size and
shape to permit the sealing means to seal around the portion of the
object that is approximately adjacent to the object. For example,
as illustrated in FIG. 1, the opening 23 is sized and shaped to fit
snugly against the portion of the lower arm 13 that is
approximately adjacent to the opening 23. In this embodiment, the
sealing means is comprised of a flexible sleeve 24 that is somewhat
conical in shape, having an approximately cylindrical end portion
24a that is positioned approximately adjacent to the portion 13 of
the arm disposed within the cylindrical end portion 24a. The
flexible sleeve 24 may generally be comprised of flexible materials
similar to those used to construct the flexible chamber 21.
Although it is not necessary that the flexible sleeve 24 be
comprised of the same material as the flexible chamber 21, it is
preferred that such be the case. To assist in positioning the lower
arm portions within the flexible chamber 21 and the cylindrical end
portion 24a, the flexible sleeve 24 also has a gas-tight zipper
24b. Such gas-tight zippers 24b are well known in the relevant art.
Other means for accomplishing the same purpose, which may be used
with other embodiments of the present invention, comprise
overlapping folds or flaps in the cylindrical end portion 24a
(which may be held in place by hook and loop fasteners (such as
VELCRO), other clamps or fasteners, or the reduced pressure within
the flexible chamber 21), stretchable material that allows the
opening 23 to be stretched to a greater diameter and then return to
its original shape, or any combination of the same. It is to be
noted that the flexible sleeve 24 may also be oriented in a
direction different from that illustrated in FIG. 1. For example,
the flexible sleeve 24 may extend into the flexible chamber 21,
rather than away from the interior of the flexible chamber 21. In
yet other embodiments where only a portion of an object is to be
treated, the sealing means may be comprised of a means other than a
flexible sleeve 24. For example, the opening 23 may be within the
plane of the end 21a of the flexible chamber 21, and the perimeter
of the opening 23 may have an inflatable cuff similar to that for
the inflatable members 22a, 22b comprising the collapsible frame
22. In these embodiments, the portion of the object to be treated
is positioned through the opening 23 into the interior volume of
the flexible chamber 21. The inflatable cuff of this type of
sealing means is then inflated using pressurized fluid from the
pressurized fluid system 40 (or some other source, such as a
bellows) until it fits snugly against the portion of the object
(such as the lower arm portion 13 in FIG. 1) approximately adjacent
to the inflatable member so that a gas-tight seal is made at that
location. An example of this type of means and seal is disclosed in
U.S. Pat. No. 5,425,742, the disclosure of which is incorporated
herein by reference. In embodiments in which the entire object is
placed within the interior volume of the flexible chamber 21 for
treatment, the opening 23 is generally of a size and shape that
allows the object to be placed into and removed from the flexible
chamber 21. In these embodiments, the sealing means is generally
used to seal the opening 23 closed in a manner that does not
involve a seal against a portion of the object. For example, as
illustrated and described in more detail below in connection with
FIG. 6, the sealing means may be a chamber end cap portion 121c
that is removably attached to a chamber body portion 121b in a
manner so that the entire opening is sealed closed. In other
embodiments where the object is placed entirely within the flexible
chamber 21, the sealing means may also be any type of entry means
that may be sealed in a gas-tight manner. Examples include caps,
hatches, portals, and doors having seals similar to those disclosed
in U.S. patent application Ser. No. 11/098,203, which was filed by
the present inventor with the U.S. Patent and Trademark Office on
Apr. 4, 2005, the disclosure of which is hereby incorporated by
reference.
[0034] In the embodiment of the appliance 10 illustrated in FIG. 1,
the collapsible frame 22 is comprised of generally circumferential
inflatable members 22a and generally longitudinal inflatable
members 22b. The circumferential inflatable members 22a generally
extend around the exterior circumferential surface of the
cylindrically-shaped flexible chamber 21. The longitudinal
inflatable members 22b are generally disposed on the exterior
surface along the longitudinal axis of the cylindrically-shaped
flexible chamber 21. The circumferential inflatable members 22a and
the longitudinal inflatable members 22b are in fluid communication
with one another at the points where they intersect, so that fluid
is permitted to flow between them. In the illustrated embodiment,
the circumferential inflatable members 22a and the longitudinal
inflatable members 22b are attached to the flexible chamber 21. The
collapsible frame 22 is connected to the pressurized fluid system
40, which provides pressurized fluid to the collapsible frame 22,
as described in more detail below. When the collapsible frame 22 is
inflated with pressurized fluid, the collapsible frame 22 becomes
rigid, so that it can support the flexible chamber 21 away from the
object or the portion of the object to be treated (the lower arm
portion 12 in FIG. 1) while the appliance 10 is in use. In other
embodiments, the inflatable members 22a, 22b of the collapsible
frame 22 may have almost any combination of shapes, orientations,
configurations and sizes, as long as the inflatable members 22a,
22b are capable of supporting the flexible chamber 21 away from the
object or portion of the object to be treated (the lower arm
portion 12 in FIG. 1) while the appliance 10 is in use. For
example, the collapsible frame 22 may consist of inflatable members
22a, 22b that are positioned around the circumference of the
flexible chamber 21, but are also displaced somewhat along the
longitudinal axis of the flexible chamber 21 in different
directions so that they cross, giving rise to a series of
"X-shaped" patterns. In addition, the shape of the inflatable
members 22a, 22b themselves may vary. Thus, instead of having the
approximately semicircular cross-section illustrated in FIG. 1, the
inflatable members 22a, 22b may have a different shape or
combination of shapes. For example, the inflatable members 22a, 22b
(or any of them) may have an approximately circular, elliptical,
square, rectangular, triangular, polygonal or other arcuate or
liner cross-sectional shape or a cross-section having any
combination of such shapes. Further, the size of each of the
inflatable members 22a, 22b relative to each other and to the
flexible chamber 21 may also vary. For example, the circumferential
inflatable members 22a may have an interior cross-sectional radius
of 1/2 inch and the longitudinal inflatable members 22b may have an
interior cross-sectional radius of one inch. The collapsible frame
22 is designed to collapse in a manner similar to the flexible
chamber 21, as described in more detail above. In order to
collapse, the collapsible frame 22 of the illustrated embodiment is
constructed of flexible or semi-flexible materials, which may be
similar to those used to construct the flexible chamber 21.
Although the flexible chamber 21 and the collapsible frame 22 need
not be constructed of the same material, the flexible chamber 21
and the collapsible frame 22 are preferably constructed of the same
material, as illustrated in FIG. 1. In addition, the material used
to construct the inflatable members 22a, 22b has a thickness great
enough to contain the pressurized fluid at a pressure adequate to
support the flexible chamber 21 away from the portion 12 of the
body to be treated while the appliance 10 is in use, but is thin
enough to generally flatten and fold when the appliance 10 is not
in use. The preferred material and thickness for the inflatable
members 22a, 22b is generally dependent upon the size and shape of
the flexible chamber 21, the size and shape of the inflatable
members 22a, 22b, the pressure of the pressurized fluid used to
inflate the inflatable members 22a, 22b, and the level of reduced
pressure in the volume of the flexible chamber 21. As illustrated
in FIG. 1, the collapsible frame 22 may be positioned on the outer
surface of the flexible chamber 21. In yet other embodiments, the
collapsible frame 22 may be embedded within the wall of the
flexible chamber 21. In still other embodiments, the collapsible
frame 22 may be positioned inside the flexible chamber 21. In all
such embodiments, the collapsible frame 22 may be permanently or
removably attached to the flexible chamber 21 using any suitable
means. Examples of such means include hook and loop fasteners (such
as VELCRO), welding, fusing, adhesives, adhesive tapes, glues,
epoxies, clamps, clasps, and other fasteners and combinations of
such means. In other cases, the collapsible frame 22 and the
flexible chamber 21 may be fabricated as a single piece. In
embodiments where the collapsible frame 22 is positioned inside the
volume of the flexible chamber 21, the collapsible frame 22 may not
be permanently or removably attached to the flexible chamber 21,
but may instead merely rest upon the surface of the flexible
chamber 21. In other embodiments of this first version of the
invention, as illustrated and described below in connection with
FIG. 3 through FIG. 6, the collapsible frame 122 may utilize a
plurality of rigid or semi-rigid frame members 122a, 122b, 122c,
rather than inflatable members 22a, 22b.
[0035] In some embodiments of this first version of the present
invention, as illustrated in FIG. 1, the treatment device 20
further comprises a vacuum port 25. The vacuum port 25 is adapted
to be of a size and shape so that the reduced pressure supply means
32 may be operably connected to the flexible chamber 21 by means of
the vacuum port 25. When the vacuum port 25 is operably connected
to the reduced pressure supply means 32, reduced pressure may be
supplied to the volume within the flexible chamber 21. Although the
vacuum port 25 is positioned at a location approximately at the top
of one end of the flexible chamber 21 (as viewed during use) in the
embodiment illustrated in FIG. 1, the vacuum port 25 may be located
at other locations on the flexible chamber 21 in other embodiments,
as long as the vacuum port 25 does not adversely affect the ability
of the opening 23 of the flexible chamber 21 to make an operable
seal with the portion 13 of the body adjacent to the opening 23, as
described in more detail above, or otherwise adversely affect the
operation of the flexible chamber 21. For example, the vacuum port
25 may be located near the bottom of the flexible chamber 21 (as
viewed during use) so that any fluids accumulating in the flexible
chamber 32 may be extracted through the reduced pressure supply
means 32. Although the vacuum port 25 may be constructed of a
material different from the material comprising the flexible
chamber 21 in various embodiments of the invention, the vacuum port
25 is preferably constructed from the same material comprising the
flexible chamber 21. In the embodiment of the treatment device 20
illustrated in FIG. 1, the vacuum port 25 is generally cylindrical
in shape and is further comprised of an approximately cylindrical
channel 25a that extends from the top of the vacuum port 25 to the
bottom of the vacuum port 25. The vacuum port 25 of this embodiment
is thus able to receive a vacuum system 30 or reduced pressure
supply means 32, which are described in more detail below, adapted
to be connected to this shape of vacuum port 25 and channel 25a. In
other embodiments of this first version of the invention, the
vacuum port 25 or the channel 25a, or both, may have different
shapes and configurations as may be desired to adapt and connect
the vacuum port 25 and the channel 25a to the vacuum system 30 or
reduced pressure supply means 32, which are described in more
detail below. In some of the embodiments comprising a vacuum port
25, the treatment device 20 may be further comprised of flow
control means (not illustrated) that are operably connected to the
vacuum port 25. The flow control means permit fluids to flow from
the volume within the flexible chamber 21 through the vacuum port
25 to a volume (such as the reduced pressure supply means 32)
outside the flexible chamber 21, but not in the opposite direction.
In some of these embodiments, the flow control means may be a
one-way valve that is located within the channel 25a in the vacuum
port 25. Such valves are well known in the relevant art. In other
embodiments of this first version of the present invention, a means
of connecting the flexible chamber 21 to the reduced pressure
supply means 32 (described in more detail below) may be located on
the flexible chamber 21 in lieu of or in conjunction with the
vacuum port 25. For example, in some embodiments, the vacuum port
25 may be combined with a variable descending diameter adapter
(commonly referred to as a "Christmas tree" adapter).
[0036] In the embodiment of the first version of the present
invention illustrated in FIG. 1, the reduced pressure supply source
31 of the vacuum system 30, which produces a source of reduced
pressure or suction that is supplied to the flexible chamber 21, is
comprised of a vacuum pump 33, a control device 34, and a filter
35. Although the preferred means of producing the reduced pressure
or suction is a vacuum pump 33 in this embodiment, in other
embodiments of this first version of the invention other means may
be used, such as an outlet port of a centralized hospital vacuum
system or a suction bulb system, which is described in more detail
below. In the illustrated embodiment, predetermined amounts of
suction or reduced pressure are produced by the vacuum pump 33. The
vacuum pump 33 is preferably controlled by a control device 34,
such as a switch or a timer that may be set to provide cyclic
on/off operation of the vacuum pump 33 according to user-selected
intervals. Alternatively, the vacuum pump 33 may be operated
continuously without the use of a cyclical timer. In addition, in
some embodiments the control device 34 may provide for separate
control of the level of reduced pressure applied to the volume
within the flexible chamber 21 at the portion 12 of the body to be
treated and the flow rate of any fluid that may be extracted from
the volume within the flexible chamber 21. In these embodiments,
relatively low levels of reduced pressure may be maintained at the
portion 12 of the body to be treated within the treatment device
20, while still providing for the removal of a relatively large
volume of exudate from the portion 12 of the body to be treated. A
filter 35, such as a micropore filter, is preferably attached to
the inlet of the vacuum pump 33 to prevent potentially pathogenic
microbes or aerosols from contaminating, and then being vented to
atmosphere by, the vacuum pump 33. In other embodiments, the filter
35 may also be a hydrophobic filter that prevents any exudate from
contaminating, and then being vented to atmosphere by, the vacuum
pump 33. It is to be noted that in other embodiments of the
invention, the reduced pressure supply source 31 may not have a
filter 35 or a control 34 or any combination of the same.
[0037] In other embodiments of this first version of the invention,
the reduced pressure supply source 31 of the vacuum system 30, may
be comprised of a small, portable vacuum pump 33. In some of these
embodiments, a filter 35 or a power source (not illustrated), or
both, may also be contained within the housing for the portable
vacuum pump 33. In these embodiments, the portable vacuum pump 33
is preferably controlled by a control device 34 that is also
located within the housing for the portable vacuum pump 33, which
may provide substantially the same functions as the control device
34 described above. Except for its smaller size, the portable
vacuum pump 33 may operate in substantially the same manner as the
vacuum pump 33 described above. Also, in these embodiments, the
filter 35 may have the same structure, features, characteristics
and operation, and provide substantially the same functions, as the
filter 35 described above. In some of these embodiments, the filter
35 may be rigidly connected to the portable vacuum pump 33. The
power source may be any source of energy currently known in the
relevant art or that may be developed in the relevant art in the
future that may be used to power the portable vacuum pump 33. For
example, in some embodiments, the power source may be a fuel cell,
battery or a standard wall electrical outlet.
[0038] In the embodiment of the first version of the invention
illustrated in FIG. 1, the reduced pressure supply means 32 of the
vacuum system 30, which are used to connect the reduced pressure
supply source 31 to the flexible chamber 21 so that reduced
pressure is supplied to the volume within the flexible chamber 21
at the portion 12 of the body to be treated is comprised of at
least one tubing member 32. In this embodiment, the at least one
tubing member 32 is sufficiently flexible to permit movement of the
at least one tubing member 32, but is sufficiently rigid to resist
constriction when reduced pressure is supplied to the flexible
chamber 21 or when the location of the portion 12 of the body to be
treated is such that the patient must sit or lie upon the at least
one tubing member 32 or the treatment device 20 must rest upon the
at least one tubing member 32. In the embodiment illustrated in
FIG. 1, the at least one tubing member 32 is connected to the
flexible chamber 21 by inserting one end of the at least one tubing
member 32 into the channel 25a of the vacuum port 25. In this
embodiment, the at least one tubing member 32 is held in place in
the channel 25a by means of an adhesive. It is to be noted that in
other embodiments of this first version of the invention, the at
least one tubing member 32 may be connected to the vacuum port 25
using any suitable means currently known in the art or developed in
the art in the future. Examples include variable descending
diameter adapters (commonly referred to as "Christmas tree"
adapters), luer lock fittings and adapters, clamps, and
combinations of such means. Alternatively, the vacuum port 25 and
the at least one tubing member 32 may be fabricated as a single
piece. Similar means may be used to connect the other end of the at
least one tubing member 32 to the vacuum pump 33 or other reduced
pressure supply source 31 providing the reduced pressure.
[0039] In the embodiment illustrated in FIG. 1, the reduced
pressure supply means 32 further comprise a fluid collection
system, generally designated 36, that is interconnected between the
suction pump 33 and the flexible chamber 21 to remove and collect
any exudate that may be aspirated from the portion 12 of the body
to be treated and collected within the flexible chamber 21. The
reduced pressure in the flexible chamber 21 may function to
actively draw fluid or exudate from the portion 12 of the body to
be treated. It may be advantageous in some circumstances to locate
the vacuum port 25 near the bottom of the flexible chamber 21 (as
viewed while the flexible chamber 21 is in use) in order to drain
this exudate so that it does not collect and fill the flexible
chamber 21. In such cases, collection of exudate in a fluid
collection system 36 intermediate the vacuum pump 33 and the
flexible chamber 21 is desirable to prevent clogging of the vacuum
pump 33. In the illustrated embodiment, the fluid collection system
36 is comprised of a fluid-impermeable collection container 37 and
a shutoff mechanism 38, which are described in more detail below in
connection with FIG. 2. The container 37 may be of any size and
shape capable of intercepting and retaining a predetermined amount
of exudate. Many examples of such containers are available in the
relevant art. Referring to FIG. 2, which is an enlarged elevational
cross-sectional view of the preferred embodiment of the container
37, the container 37 includes a first port 37a at the top opening
of the container 37 for sealed connection to tubing member 32a,
where the other end of the tubing member 32a is connected to the
flexible chamber 21. The first port 37a enables suction to be
applied to the flexible chamber 21 through the tubing 32a and also
enables exudate from the portion 12 of the body enclosed by the
flexible chamber 21 to be drained into the container 37. The
container 37 provides a means for containing and temporarily
storing the collected exudate. A second port 37b is also provided
on the top of the container 37 to enable the application of suction
from the vacuum pump 33. The second port 37b of the collection
system 36 is connected to the vacuum pump 33 by tubing member 32b.
The collection system 36 is sealed generally gas-tight to enable
the vacuum pump 33 to supply suction to the flexible chamber 21
through the collection system 36.
[0040] The embodiment of the collection system 36 illustrated in
FIG. 2 also includes a shutoff mechanism 38 for halting or
inhibiting the supply of reduced pressure to the flexible chamber
21 in the event that the exudate aspirated from the portion 12 of
the body to be treated exceeds a predetermined quantity.
Interrupting the application of suction to the flexible chamber 21
may be desirable in some circumstances to prevent exsanguination in
the unlikely event a blood 10 vessel ruptures within the portion 12
of the body to be treated during treatment. If, for example, a
blood vessel ruptures within such portion 12, a shut-off mechanism
would be useful to prevent the vacuum system 30 from aspirating any
significant quantity of blood from the patient. In the preferred
embodiment of the shutoff mechanism 38, as illustrated in FIG. 2,
the shutoff mechanism 38 is a float valve assembly in the form of a
ball 38a which is held and suspended within a cage 38b positioned
below a valve seat 38c disposed within the opening at the top of
the container below the second port 37b that will float upon the
exudate and will be lifted against the valve seat 38c as the
container 37 fills with exudate. When the ball 38a is firmly seated
against the valve seat 38c, the float valve blocks the second port
37b and thereby shuts off the source of suction from the reduced
pressure supply source 31. In other embodiments of the collection
system 36, other types of mechanisms may also be employed to detect
the liquid level within the container 37 in order to arrest
operation of the vacuum system 30. In addition, in various
embodiments of this first version of the invention, the shutoff
mechanism 38 may be comprised of any means that enables the vacuum
system 30 to halt the supply of reduced pressure to the flexible
chamber 21 at any time that the volume of exudate from the portion
12 of the body to be treated exceeds a predetermined amount. Such
means may include mechanical switches, electrical switches operably
connected to the vacuum system controller 34, optical, thermal or
weight sensors operably connected to the vacuum system controller
34, and any other means that are currently known in the relevant
art or that may be developed in the art in the future. Such means
may be located in the container 37 or in the flexible chamber 21 in
various embodiments.
[0041] In some embodiments of this first version of the present
invention, as illustrated in FIG. 1, the treatment device 20
further comprises a pressurized fluid port 26. The pressurized
fluid port 26 is adapted to be of a size and shape so that the
pressurized fluid supply means 42 may be operably connected to the
collapsible frame 22 by means of the pressurized fluid port 26.
When the pressurized fluid port 26 is operably connected to the
pressurized fluid supply means 42, pressurized fluid may be
supplied to the volume within the inflatable members 22a, 22b of
the collapsible frame 22. Although the pressurized fluid port 26 is
positioned at a location approximately at the top of the
circumferential inflatable member 22a at one end of the collapsible
frame 22 in the embodiment illustrated in FIG. 1, the pressurized
fluid port 26 may be located at other locations on the collapsible
frame 22 in other embodiments, as long as the pressurized fluid
port 26 does not adversely affect the operation of the collapsible
frame 22. In addition, there may be multiple pressurized fluid
ports 26, which may be located at multiple locations on the
collapsible frame 22. Although the pressurized fluid port 26 may be
constructed of a material different from the material comprising
the collapsible frame 22 in various embodiments of the invention,
the pressurized fluid port 26 is preferably constructed from the
same material comprising the collapsible frame 22. In the various
embodiments of the first version of the invention that utilize an
inflatable collapsible frame 22, such as is illustrated in
[0042] FIG. 1, the pressurized fluid port 26 and the pressurized
fluid supply means 42 may generally have substantially the same
structure, features, characteristics, and operation as the various
embodiments of the vacuum port 25 and reduced pressure supply means
32, respectively, illustrated and described above in connection
with FIG. 1, as long as the pressurized fluid port 26 and the
pressurized fluid supply means 42 are adapted to cooperate in the
supply of pressurized fluid from the pressurized fluid supply
source 41 to the collapsible frame 22. In some of the embodiments
comprising a pressurized fluid port 26, the treatment device 20 may
be further comprised of flow control means that are operably
connected to the pressurized fluid port 26. The flow control means
regulate the flow of pressurized fluids to and from the collapsible
frame 22 through the pressurized fluid port 26. In some of these
embodiments, the flow control means may be a valve that is
incorporated as a part of the pressurized fluid port 26 or the
pressurized fluid supply means 42. Such valves are well known in
the relevant art. In other embodiments of this first version of the
present invention, a means of connecting the collapsible frame 22
to the pressurized fluid supply means 42 (described in more detail
below) may be located on the collapsible frame 22 in lieu of or in
conjunction with the pressurized fluid port 26. For example, in
some embodiments, the pressurized fluid port 26 may be combined
with a variable descending diameter adapter (commonly referred to
as a "Christmas tree" adapter).
[0043] In the embodiment of the first version of the present
invention illustrated in FIG. 1, the pressurized fluid supply
source 41 of the pressurized fluid system 40, which produces a
source of pressurized air that is supplied to the collapsible frame
22, is comprised of an air compressor 43, a control device 44, and
a filter 45. Although the preferred pressurized fluid is compressed
air and the preferred means of producing the compressed air is an
air compressor 43 in this embodiment, in other embodiments of this
first version of the invention other pressurized liquids and gases,
such as carbon dioxide or water, may be used instead. In addition,
other pressurized fluid supply means may be used instead. For
example, it may be possible to use containers of compressed fluid
(such as tanks and cartridges containing compressed air or carbon
dioxide), pumps (such as may be used to pressurized water), an
outlet port of a centralized hospital compressed gas system, or a
bellows-type system. In the illustrated embodiment, predetermined
amounts of pressurized fluid are produced by the air compressor 43.
The air compressor 43 is preferably controlled by a control device
44, such as a switch or a timer that may be set to provide cyclic
on/off operation of the air compressor 43 according to
user-selected intervals. Alternatively, the air compressor 43 may
be operated continuously without the use of a cyclical timer. In
addition, in some embodiments the control device 44 may provide for
separate control of the level of pressurized fluid applied to the
volume within the inflatable members 22a, 22b of the collapsible
frame 22. For example, the control device 44 may also be operably
connected to a pressure sensor located on or within the collapsible
frame 22, so that the control device 44 halts operation of the air
compressor 43 when the pressure within the collapsible frame 22
reaches a predetermined level and turns the air compressor 43 on
when the pressure within the collapsible frame 22 falls below a
predetermined level. A filter 45, such as a micropore filter, is
preferably attached to the outlet of the air compressor 43 to
prevent contaminants from being transferred from the air compressor
43 to the interior volume of the collapsible frame 22. In other
embodiments, the filter 45 may also be a hydrophobic filter that
prevents any moisture from being transferred from the air
compressor 43 to the interior volume of the collapsible frame 22.
It is to be noted that in other embodiments of the invention, the
pressurized fluid supply source 41 may not have a filter 45 or a
control 44 or any combination of the same. In other embodiments of
this first version of the invention, the pressurized fluid supply
source 41 of the pressurized fluid system 40 may be comprised of a
small, portable air compressor 43 or container of compressed fluid,
which may also contain a filter 45 or a control device 44 or both
within the same housing for the air compressor 43 or container.
Except for its smaller size, the portable air compressor 43, and
the filter 45 and controller 44, if any, may operate in
substantially the same manner as the air compressor 43, filter 45,
and controller 44, respectively, described above. The air
compressor 43 may also comprise a power source, such as a fuel
cell, battery or a standard wall electrical outlet. In other
embodiments, the air compressor 43 and the vacuum pump 33 may
operate as an integrated unit contained in a single enclosure. In
some of these embodiments, the air compressor 43 and the vacuum
pump 33 may be driven by the same mechanical source (such as an
electric motor).
[0044] In the embodiment of the first version of the invention
illustrated in FIG. 1, the pressurized fluid supply means 42 of the
pressurized fluid system 40, which are used to connect the
pressurized fluid supply source 41 to the collapsible frame 22 so
that pressurized fluid is supplied to the volume within the
inflatable members 22a, 22b of the collapsible frame 22 is
comprised of at least one tubing member 42. In this embodiment, the
at least one tubing member 42 is sufficiently flexible to permit
movement of the at least one tubing member 42, but is sufficiently
rigid to resist expansion when pressurized fluid is supplied to the
collapsible frame 22 and is sufficiently rigid to resist
constriction when the location of the portion 12 of the body to be
treated is such that the patient must sit or lie upon the at least
one tubing member 42 or the treatment device 20 must rest upon the
at least one tubing member 42. In the embodiment illustrated in
FIG. 1, the at least one tubing member 42 is connected to the
collapsible frame 22 by inserting one end of the at least one
tubing member 42 into a channel 26a in the pressurized fluid port
26. In this embodiment, the at least one tubing member 42 is held
in place in the channel 26a by means of an adhesive. It is to be
noted that in other embodiments of this first version of the
invention, the at least one tubing member 42 may be connected to
the pressurized fluid port 26 using any suitable means currently
known in the relevant art or developed in the relevant art in the
future. Examples include variable descending diameter adapters
(commonly referred to as "Christmas tree" adapters), luer lock
fittings and adapters, clamps, and combinations of such means.
Alternatively, the pressurized fluid port 26 and the at least one
tubing member 42 may be fabricated as a single piece. Similar means
or other means, which are currently known in the relevant art or
may be developed in the relevant art in the future, may be used to
connect the other end of the at least one tubing member 42 to the
air compressor 43 or other reduced pressure supply source 41
providing the reduced pressure.
[0045] In the embodiment of the first version of the present
invention illustrated in FIG. 1, the appliance 10 is also comprised
of a drainage system 50. In the illustrated embodiment, the
drainage system 50 is further comprised of an overlay 51, wound
packing means 52, and draining means 53. The overlay 51, which is
described in more detail below, may generally be used to cover a
wound 14 and collect any exudate aspirated from the wound 14. This
may be desirable to prevent contamination of the flexible chamber
21 in cases where the portion of the body to be treated 12 has a
wound 14 that is expected to aspirate significant quantities of
exudate during the treatment process. The wound packing means 52,
which is also described in more detail below, may be placed into or
over the wound 14 to assist in healing of the wound 14. The
draining means 53, which are also described in more detail below,
may be used to remove exudate aspirated by the wound 14 from the
overlay 51 and the treatment device 20. It is to be noted that the
drainage system 50 need not be used in every embodiment of the
present invention. It is also to be noted that in some embodiments,
only the overlay 51 and draining means 53 may be used, while in
other embodiments only the overlay 51 and wound packing means 52
may be used. In still other embodiments, only the wound packing
means 52 and draining means 53 may be utilized.
[0046] The overlay 51, which is constructed of a semi-permeable or
impermeable material, is generally adapted to be of a size and
shape to cover the wound 14. Overlays 51 that may be used for this
purpose are well known in the art. Examples of such overlays are
generally disclosed in U.S. patent application Ser. No. 10/652,100
(filed on Aug. 28, 2003), Ser. No. 11/026,733 (filed on Dec. 30,
2004), Ser. No. 11/064,813 (filed on Feb. 24, 2005), Ser. No.
11/095,859 (filed by the present inventor with others on Mar. 31,
2005) Ser. No. 11/098,265 (filed on Apr. 4, 2005), and Ser. No.
11/098,203 (filed on Apr. 4, 2005), which were filed by the present
inventor with the U.S. Patent and Trademark Office. The disclosures
of these U.S. patent applications are incorporated herein by
reference. The overlay 51 may be comprised of rigid, semi-rigid, or
flexible materials or combinations of such materials. Where the
overlay 51 is constructed of a semi-permeable material, the reduced
pressure within the flexible chamber 21 is also applied to the
wound 14 under the overlay 51, but exudate aspirated from the wound
14 is generally not able to pass through the overlay 51 to the
interior volume of the flexible chamber 21. Where the overlay 51 is
constructed of a fluid (liquid and gas) impermeable material, the
reduced pressure within the flexible chamber 21 is not generally
applied to the wound 14 under the overlay 51, and exudate aspirated
from the wound 14 is generally not able to pass through the overlay
51 to the interior volume of the flexible chamber 21. In such
cases, it may be possible to provide reduced pressure treatment to
some parts of the portion 12 of the body within the volume of the
flexible chamber 21, but not others, such as the wound 14 covered
by a rigid, fluid-impermeable overlay 51. The overlay 51 may be
removably attached to the tissue of the patient surrounding the
wound 14 using any suitable means currently known in the relevant
art or that may be developed in the relevant art in the future,
such as adhesives, adhesive tapes, reduced pressure, means
disclosed in any of the U.S. patent applications referenced above
in this paragraph, or other means or combinations of any such
means. It is to be noted that the overlay 51 may be used in other
embodiments of the present invention with or without drainage means
53 or wound packing means 52.
[0047] In some embodiments of this first version of the invention,
the drainage system 50 further comprises tissue protection means
(not illustrated) to protect and strengthen the surface tissue
surrounding the wound 14 that is adjacent to the overlay 51. The
tissue protection means protects such tissue by preventing abrasion
and maceration of the tissue. Preferably, the tissue protection
means is a hydrocolloid material, such as COLOPAST Hydrocolloid
2655, anhydrous lanoline, or any combination of such hydrocolloid
materials. More preferably, the tissue protection means is COLOPAST
Hydrocolloid 2655. The tissue protection means may be applied to
the body tissue to be protected, or it may be applied to the
surface of the overlay 51 that is to be in contact with the body
tissue, or both, prior to placing the overlay 51 over the wound 14.
It is to be noted that application of the tissue protection means
to the body tissue that is adjacent to the overlay 51 surrounding
the wound 14 may only entail application of the tissue protection
means to the parts of the body tissue adjacent to the overlay 51
that require such protection.
[0048] In the embodiment of the first version of the invention
illustrated in FIG. 1, the drainage system 50 is further comprised
of wound packing means 52, which is placed in the area of the wound
14 under the overlay 51. In this embodiment, the overlay 51 may be
used to hold the wound packing means 52 in place. It is to be noted
that the wound packing means 52 may be used with other embodiments
of the present invention with or without drainage means 53 or an
overlay 51. In the illustrated embodiment, the overlay 51 is placed
over the wound 14 and the wound packing means 52 when the overlay
51 is positioned on the surface of the body at the site of the
wound 14. In some embodiments of this first version of the
invention, the wound packing means 52 may be placed within the
wound 14 to prevent overgrowth of the tissue in the area of the
wound 14. For example, and preferably in these cases, the wound
packing means 52 may be comprised of absorbent dressings,
antiseptic dressings, nonadherent dressings, water dressings, or
combinations of such dressings. More preferably, the wound packing
means 52 may be comprised of gauze or cotton or any combination of
gauze and cotton. In still other embodiments of this first version
of the invention, the wound packing means 52 may be comprised of an
absorbable matrix adapted to encourage growth of the tissue in the
area of the wound 14 into the matrix. In these embodiments, the
absorbable matrix (as wound packing means 52) is constructed of an
absorbable material that is absorbed into the epithelial and
subcutaneous tissue in the wound 14 as the wound 14 heals. The
matrix (as wound packing means 52) may vary in thickness and
rigidity, and it may be desirable to use a spongy absorbable
material for the patient's comfort. The matrix (as wound packing
means 52) may also be perforated and constructed in a sponge-type
or foam-type structure to enhance fluid flow and to reduce the
weight of the matrix. Because of the absorbable nature of the
absorbable matrix (as wound packing means 52), the matrix should
require less frequent changing than other dressing types during the
treatment process. In other circumstances, the matrix (as wound
packing means 52) may not need to be changed at all during the
treatment process. In some embodiments of this first version of the
invention, the absorbable matrix (as wound packing means 52) may be
comprised of collagens or other absorbable materials or
combinations of all such materials. U.S. patent application Ser.
No. 10/652,100, which was filed by the present inventor with the
U.S. Patent and Trademark Office on Aug. 28, 2003, and is hereby
incorporated by reference, also discloses various embodiments of an
absorbable matrix that may be utilized with various embodiments of
this first version of the present invention. It is to be noted that
wound packing means 52 may also be utilized in other versions of
the invention.
[0049] In the embodiment of the first version of the invention
illustrated in FIG. 1, the drainage system 50 of the appliance 10
is also comprised of draining means 53. In this embodiment, the
draining means 53 are further comprised of a bottom drain portion
53a extending into the area of the wound 14 under the overlay 51
from a top drain portion 53b positioned outside the volume under
the overlay 51 at the area of the wound 14. In the illustrated
embodiment, the top drain portion 53b is operably connected to the
reduced pressure supply source 31 so that the draining means 53 are
in fluid communication with the reduced pressure supply source 31
and reduced pressure is supplied to the volume under the overlay 51
in the area of the wound 14 by the draining means 53. It is to be
noted that the reduced pressure supply source 31 may include
another filter 35', which may have substantially the same
structure, features, characteristics and operation as filter 35. In
this embodiment, valves 54a, 54b are operably positioned in the top
drain portion 53b to regulate flow of reduced pressure and exudate
within the drainage system 50. In addition, a collection system 56
is operably positioned within the drainage system 50. In various
embodiments, the collection system 56 may have substantially the
same structure, features, characteristics and operation as various
embodiments of the collection system 36 that is part of the vacuum
system 30. It is to be noted, however, that the collection system
56 need not be present in all embodiments of the present invention.
Thus, when valve 54a is closed and valve 54b is open, any exudate
aspirated from the wound 14 is collected by the draining means 53
from the volume under the overlay 51 and flows into the collection
system 56. In embodiments without a collection system 56, the
exudate may flow to any other receptacle or means for disposing of
the exudate. In these cases, there is no source providing reduced
pressure to the volume under the overlay 51 at the site of the
wound 14. When valve 54a is open and valve 54b is closed, any
exudate aspirated from the wound 14 is also collected by the
draining means 53 from the volume under the overlay 51 and flows
into the collection system 56. In this case, however, reduced
pressure is supplied by the reduced pressure supply source 31
through the draining means 53 to the volume under the overlay 51 at
the site of the wound 14. This reduced pressure may act to draw
exudate aspirated from the wound 14 into the draining means 53 (and
thus into the collection system 56). It is to be noted that in
other embodiments the drainage system 50 may not have any valves
54a, 54b, so that the draining means 53 is connected directly to
the reduced pressure supply source 31. In yet other embodiments,
the draining means 53 may not be connected to the reduced pressure
supply source 31 at all, so that exudate collected from the volume
under the overlay 51 may flow directly to a receptacle (such as the
collection system 56) or other means for disposing of the exudate.
In the latter cases, there is no source providing reduced pressure
to the volume under the overlay 51 at the site of the wound 14.
[0050] In the illustrated embodiment, the top drain portion 53b
passes through and is attached to a drainage port 27 located on the
flexible chamber 21. The drainage port 27 may generally have
substantially the same structure, features, characteristics and
operation as the vacuum port 25 described above. In addition, the
drainage port 27 may be positioned on the flexible chamber 21 in
substantially the same manner as the vacuum port 25, as described
above. In this embodiment, the top drain portion 53b may be
comprised of two portions, where one portion is attached to the
opening of the drainage port 27 that is inside the flexible chamber
21 and the other portion is attached to the opening of the drainage
port 27 that is outside the flexible chamber 21. In some
embodiments, the top drain portion 53b may be permanently or
removably attached to the interior surface of the opening of the
drainage port 27 using any suitable means, such as an adhesive, or
by the top drain portion 53b having a shape adapted so that all or
a portion of it fits tightly against all or a portion of the
interior surface of the opening in the drainage port 27. The
suction drain system disclosed in U.S. patent application Ser. No.
11/026,733, entitled "Improved Reduced Pressure Wound Treatment
Appliance," which was filed by the present inventor with the U.S.
Patent and Trademark Office on Dec. 30, 2004, may also be used in
conjunction with the present invention. The disclosure of this U.S.
patent application is incorporated herein by reference. In yet
other embodiments, the top drain portion 53b may pass through the
opening 23 in the flexible chamber 21 in a manner so that the
sealing means (the flexible sleeve 24) provides a gas-tight seal
with the top drain portion 53b as well as the portion 13 of the
body adjacent to the flexible sleeve 24. In yet other embodiments,
the drainage port 27 may be comprised of a different connecting
means, such as a variable descending diameter adapter (commonly
referred to as a "Christmas tree" adapter), clamp, fastening
collar, luer lock fitting and adapter, or other fastener or
combination thereof In yet other embodiments, the top drain portion
53b may be fused or welded to the drainage port 27 or another
portion of the flexible chamber 21. In still other embodiments, the
top drain portion 53b may be fabricated as a part of the flexible
chamber 21. In each case, the top drain portion 53b may pass
through the flexible chamber 21 at any point that is convenient, as
long as the operation of the treatment device 20 is not adversely
affected.
[0051] In the embodiment illustrated in FIG. 1, the top drain
portion 53b and the bottom drain portion 53a of the draining means
53 are comprised of polymer tubing that is flexible enough to allow
the tubing to easily bend, but rigid enough to prevent the tubing
from collapsing during use. In other embodiments, portions of the
top drain portion 53b and the bottom drain portion 53a of the
draining means 53 may be comprised of other materials, such as
flexible or semi-rigid polymers, plastics, rubber, silicone, or
combinations of such materials. In yet other embodiments, the
draining means 53 may have different cross-sectional shapes, such
as elliptical, square, rectangular, pentagonal, hexagonal, or other
shapes. In still other embodiments, the bottom drain portion 53a of
the draining means 53 may be further comprised of wound suction
means (not illustrated) that may be used to remove debris, exudate
and other matter from the wound 14. For example, the wound suction
means may be comprised of a distal end portion (not illustrated) of
the tubing comprising the bottom drain portion 53a having a
plurality of perforations in the surface of the distal end portion.
The suction drain system disclosed in U.S. patent application Ser.
No. 11/026,733, entitled "Improved Reduced Pressure Wound Treatment
Appliance," which was filed by the present inventor with the U.S.
Patent and Trademark Office on Dec. 30, 2004, discloses examples of
this type of wound suction means. The disclosure of this U.S.
patent application is incorporated herein by reference. In the
illustrated embodiment, the bottom drain portion 53a of the
draining means 53 extends into the interior volume of the wound
packing means 52. In this embodiment, the wound packing means 52
and the draining means 53 may be fabricated by snaking the distal
end portion of the bottom drain portion 53a of the draining means
53 through an internal passageway in the wound packing means 52,
such as by pulling the distal end portion of the draining means 53
through the passageway using forceps. Alternatively, the wound
packing means 52 and the draining means 53 may be manufactured as a
single piece in sterile conditions and then be stored in an aseptic
package until ready for use. In other embodiments, the distal end
portion of the draining means 53 may be placed adjacent or close to
the wound packing means 52 in the area of the wound 14. The
preferred means of placement of the draining means 53 relative to
the wound packing means 52 is dependent upon the type of wound 14,
the type of wound packing means 52, and the type of treatment
desired.
[0052] In the embodiment of the present invention illustrated in
FIG. 1, the treatment device 20 is further comprised of a treatment
port 28. The treatment port 28 allows for access to the volume
within the flexible chamber 21 for purposes of attending to the
object or portion of the object (the portion 12 of the lower arm in
FIG. 1) within the volume of the flexible chamber 21. For example,
the treatment port 28 may be used to provide treatment to the lower
arm portion 12 by injecting medical gases, as well as treatment
devices and related electrical, hydraulic and other supply lines
into the volume of the flexible chamber 21. The treatment port 28
may be of almost any size and shape, as long as it does not
adversely interfere with the operation of the appliance 10. Thus,
in some embodiments, the treatment port 28 may have substantially
the same structure, features, characteristics and operation as the
vacuum port 25, the pressurized fluid port 26, or the drainage port
27 described in more detail above, or any other type of gas-tight
port currently known in the relevant art or developed in the
relevant art in the future. In such embodiments, supply lines may
be used in connection with the treatment port 28 in substantially
the same manner that the reduced pressure supply means 32 is used
with the vacuum port 25, the pressurized fluid supply means 42 is
used with the pressurized fluid port 26, or the draining means 53
is used with the drainage port 27, or any combination thereof In
other embodiments, the treatment port 28 may be larger, as
illustrated in FIG. 1. In addition, the treatment port 28 may be
located at almost any position on the flexible chamber 21, as long
as it does not adversely interfere with the operation of the
appliance 10. Further, the treatment port 28 may have almost any
structure that allows it to remain gas-tight while the appliance 10
is in use. For example, as illustrated in FIG. 1, the treatment
port 28 is comprised of a port body 28a that is attached to the
flexible chamber 21 and a port cap 28b, which is removably attached
to the port body 28a. Any means suitable to produce a gas-tight
seal may be used to removably attach the port cap 28b to the port
body 28a. For example, an o-ring/groove seal may be used. Other
suitable means are disclosed in U.S. patent application Ser. No.
11/098,203, which was filed by the present inventor with the U.S.
Patent and Trademark Office on Apr. 4, 2005, the disclosure of
which is hereby incorporated by reference. In yet other
embodiments, the treatment port 28 may be relatively large, as
illustrated in FIG. 1, and have additional ports similar to the
vacuum port 25, the pressurized fluid port 26, or the drainage port
27, other types of ports, or any combination thereof positioned on
the port body 28a, the port cap 28b, or both. It is to be noted
that in various embodiments of the present invention, there may be
more than one treatment port 28 or no treatment port 28. In
addition, where there is more than one treatment port 28, the
treatment ports 28 may vary in size and structure. The treatment
port 28 may be constructed of any suitable rigid, semi-rigid or
flexible material or combinations of such materials. For example,
the treatment port 28 may be constructed in whole or in part of
metals, ceramics, glasses, silicone, rubber (including neoprene),
polycarbonate, polyvinyl chloride, polyurethane, or other polymers
or combinations of any such materials.
[0053] In the embodiment of the present invention illustrated in
FIG. 1, the treatment device 20 is further comprised of a forced
entry treatment system 60. In the illustrated embodiment, the
forced entry treatment system 60 is further comprised of a forced
entry supply source, illustrated schematically and generally
designated 61, forced entry supply means 62, and venting means 63.
The forced entry treatment system 60 generally provides for
introducing ancillary fluids into the volume within the flexible
chamber 21. For example, air or other gas that is heated or cooled
may be introduced by the forced entry treatment system 60 into the
volume within the flexible chamber 21 in order to raise or lower,
respectively, the temperature of the object or portion of the
object to be treated (the lower arm portion 12 in FIG. 1). As
another example, ionized gases and dyes may be introduced by the
forced entry treatment system 60 into the volume within the
flexible chamber 21. Thus, the forced entry supply source 61 may be
comprised of any type of equipment that is related to providing the
forced entry treatment. For example, the forced air supply source
61 may be comprised of equipment to heat or cool (or both) gases or
liquids or both and cause such gases or liquids to flow from the
forced entry supply source 61 through the forced entry supply means
62 to the flexible chamber 21. Equipment of this type, such as heat
exchangers, boilers and heating elements, refrigeration coils, and
blowers and pumps are well known in the relevant art. The forced
entry supply means 62 may be comprised of any suitable means
currently known in the relevant art or the may be developed in the
relevant art in the future. For example, the forced entry supply
means 62 may be comprised of one or more tubing members similar to
those used for the reduced pressure supply means 32, the
pressurized fluid supply means 42, or the draining means 53, as
described above. As another example, the forced entry supply means
62 may be comprised of ducts, which are constructed from any
suitable material, such as metals, woods, plastics, or other
polymers or combinations of any such materials. The forced entry
supply means 62 is connected to the flexible chamber 21 by means of
a forced entry port 29, which may be of almost any size and shape,
as long as it does not adversely interfere with the operation of
the appliance 10. Thus, in some embodiments, the forced entry port
29 may have substantially the same structure, features,
characteristics and operation as the vacuum port 25, the
pressurized fluid port 26, or the drainage port 27 described in
more detail above, or any other type of gas-tight port currently
known in the relevant art or developed in the relevant art in the
future. In such embodiments, forced entry supply means 62 may be
used in connection with the forced entry port 29 in substantially
the same manner that the reduced pressure supply means 32 is used
with the vacuum port 25, the pressurized fluid supply means 42 is
used with the pressurized fluid port 26, or the draining means 53
is used with the drainage port 27, or any combination thereof. In
other embodiments, the forced entry port 29 may be larger. In
addition, the forced entry port 29 may be located at almost any
position on the flexible chamber 21, as long as it does not
adversely interfere with the operation of the appliance 10.
Further, the forced entry port 29 may have almost any structure
that allows it to remain gas-tight while the appliance 10 is in
use. It is to be noted that in various embodiments of the present
invention, there may be more than one forced entry port 29 or no
forced entry port 29. In addition, where there is more than one
forced entry port 29, the forced entry ports 29 may vary in size
and structure. The venting means 63 may generally be used to vent
fluids that are introduced into the interior volume of the flexible
chamber 21 by the forced entry supply source 61 and forced entry
supply means 62. In the illustrated embodiment, the venting means
63 is further comprised of a vent member 63a and a valve 63b, which
regulates the flow of fluid from the interior volume of the
flexible chamber 21 through the vent member 63a. The venting means
63 may discharge fluid to the ambient atmosphere or to a suitable
receptacle or return the fluid to the forced entry supply source 61
for processing, recycle or some other purpose. It is to be noted
that in some embodiments, the appliance 10 may not include a forced
entry treatment system 60 or may have more than one forced entry
treatment system 60. In other embodiments, the forced entry
treatment system 60 may not include any venting means 63 or may
have more than one venting means 63.
[0054] The present invention also includes a method of
administering reduced pressure treatment to an object or a portion
of an object using various embodiments of the first version of the
present invention, as described above and illustrated in connection
with FIG. 1 and FIG. 2. Generally, the method comprises the
following steps. First, an appliance 10 for administering reduced
pressure to the object or portion of the object (the lower arm
portion 12 in FIG. 1) is provided. Second, the appliance 10 is
positioned for use, so that the flexible chamber 21 and collapsible
frame 22 are in an extended state. For example, where the
collapsible frame 22 is further comprised of at least one
inflatable member 22a, 22b, and the appliance 10 is further
comprised of a pressurized fluid supply source 41 and pressurized
fluid supply means 42 to operably connect the at least one
inflatable member 22a, 22b to the pressurized fluid supply source
41, the at least one inflatable member 22a, 22b is inflated to the
desired pressure with pressurized fluid using the pressurized fluid
supply source 41 and pressurized fluid supply means 42. Third, the
object or portion of the object to be treated (the lower arm
portion 12 in FIG. 1) is positioned relative to the appliance 10 so
that the object or portion of the object to be treated (the lower
arm portion 12 in FIG. 1) is positioned within the volume of the
flexible chamber 21. In the embodiment illustrated in FIG. 1, the
lower arm portion 12 is inserted through the opening 23 into the
interior volume of the flexible chamber 21. Fourth, the opening 23
of the flexible chamber 21 is sealed using the sealing means (the
flexible sleeve 24 in FIG. 1), so that reduced pressure may be
maintained in the volume within the flexible chamber 21. Fifth, the
flexible chamber 21 is operably connected with the reduced pressure
supply source 31 using the reduced pressure supply means 32 so that
reduced pressure is supplied to the volume within the flexible
chamber 21. It is to be noted that the fifth step may be also
performed before either the second, third or fourth step described
above. In the preferred embodiments of this first version of the
invention involving medical treatment, the reduced pressure
maintained in the volume within the flexible chamber 21 at the
portion 12 of the body to be treated is in the range from
approximately 20 mm of Hg below atmospheric pressure to
approximately 125 mm of Hg below atmospheric pressure. In yet other
embodiments, the reduced pressure is applied to the flexible
chamber 21 in a cyclic nature, the cyclic nature providing
alternating time periods of application of reduced pressure and
non-application of reduced pressure. Sixth, the reduced pressure is
maintained in the volume within the flexible chamber 21 until the
object or portion of the object being treated (the lower arm
portion 12 in FIG. 1) has progressed toward a selected stage of
treatment. Seventh, the object or portion of the object to be
treated (the lower arm portion 12 in FIG. 1) is removed from the
appliance 10 after the selected stage of treatment has been reached
and the reduced pressure within the volume of the flexible chamber
21 has been released. Eighth, the appliance 10 is placed in its
collapsed state. In the embodiment illustrated in FIG. 1, this
involves the deflation of the at least one inflatable member 22a,
22b and folding the collapsible frame 22 and the flexible chamber
21. In embodiments comprising a drainage system 50, the method also
includes the step of positioning the wound packing means 52 (if
any) in the wound 14, positioning the draining means 53 (if any) in
or over the wound 14 (or in the wound packing means 52),
positioning the overlay 51 over the wound 14 (and wound packing
means 52 and draining means 53, if any), and connecting the
draining means 53 to the reduced pressure supply source 31 and the
collection system 56, if desired. In embodiments comprising a
forced entry treatment system 60, the method also includes the step
of positioning the forced 25 entry supply source 61 in proximity to
the treatment device 20, connecting the forced entry supply means
62 to the forced entry supply source 61 and the flexible chamber
21, and operating the forced entry treatment system 60 until the
desired force entry treatment is completed.
[0055] Another embodiment of the first version of the present
invention is illustrated in FIG. 3 through FIG. 6. In this
embodiment, the treatment device 120 is also comprised of a
flexible chamber 121 and a collapsible frame 122, but the
collapsible frame 122 is comprised of a plurality of rigid or
semi-rigid frame members 122a, 122b, 122c and frame member
connecting means, which are described in more detail below. The
frame member connecting means are used to connect the plurality of
rigid or semi-rigid frame members 122a, 122b, 122c together in a
manner so that the plurality of rigid or semi-rigid frame members
122a, 122b, 122c may be extended when the appliance 110 is in use
and collapsed when the appliance 110 is not in use. In the
illustrated embodiment, the flexible chamber 121 is constructed of
a transparent material so that the collapsible frame 122 may be
viewed from outside the flexible chamber 121. Also in the
illustrated embodiment, the flexible chamber 121 and the sealing
means 124 may have substantially the same structure, features,
characteristics and operation as the various embodiments of the
flexible chamber 21 and the sealing means 124, respectively,
described above and illustrated in connection with FIG. 1. In this
embodiment, however, the flexible chamber 121 is generally
comprised of a chamber body portion 121b, a flexible sleeve 124 (as
sealing means) having an opening 123 that is positioned at one end
121a of the chamber body portion 121b, and a chamber end cap
portion 121c that is removably attached to the other end of the
chamber body portion 121b. Generally, the chamber end cap portion
121c is removed from the chamber body portion 121b so that the
collapsible frame 122 may be inserted into the chamber body portion
121b. After the collapsible frame 122 is inserted into the chamber
body portion 121b, the chamber end cap portion 121c is attached to
the chamber body portion 121b by end cap attachment means. The end
cap attachment means may be any suitable means that permits the
chamber end cap portion 121c to be detached from the chamber body
portion 121b and to be re-attached in a manner that provides a
hermetic seal between the chamber end cap portion 121c and the
chamber body portion 121b, so that reduced pressure may be
maintained within the volume of the flexible chamber 121 while the
appliance 110 is in use. For example, the end cap attachment means
may include gas-tight zippers, hook and loop fasteners, or other
fasteners or combinations of such fasteners.
[0056] In the embodiment of the present invention illustrated in
FIG. 3 through FIG. 6, the collapsible frame 122 is generally
comprised of a plurality of rigid or semi-rigid frame members 122b
that extend longitudinally, rigid or semi-rigid frame members 122a
that are approximately circular in shape and positioned at the ends
of the collapsible frame 122, a rigid or semi-rigid frame member
122c that supports the chamber end cap portion 121c, and frame
member connecting means, which are described in more detail below.
In the illustrated embodiment, the plurality of rigid or semi-rigid
frame members 122a, 122b, 122c are comprised of rigid or semi-rigid
materials, so that they are generally capable of maintaining their
shape and supporting the flexible chamber 121 away from the object
or portion of the object to be treated (the lower arm portion 112
in FIG. 3) while reduced pressure is present within the volume
inside the flexible chamber 121. Examples of such materials include
wood, metal, ceramics, plastics and other rigid or semi-rigid
polymers (such as polyvinyl chloride and polycarbonate) and
combinations of such materials. The frame member connecting means
may be comprised of any means suitable for connecting the rigid or
semi-rigid frame members 122a, 122b, 122c together in a manner that
allows the rigid or semi-rigid frame members 122a, 122b, 122c to
pivot, rotate or otherwise move in a manner that permits the rigid
or semi-rigid frame members 122a, 122b, 122c to collapse and to
extend when desired. For example, as illustrated in FIG. 5, the
frame member connecting means may be comprised of a rivet 122d that
is used to join the ends of the rigid or semi-rigid frame members
122b together. The frame member connecting means may also include
additional features to enable the rigid or semi-rigid frame members
122a, 122b, 122c to retain the extended position when desired. For
example, as illustrated in FIG. 5, the rigid or semi-rigid frame
members 122b are also comprised of a tab portion 122e, a raised
portion 122f, and an indented portion 122g. In this embodiment, the
tab portion 122e rests against the surface of the adjoining rigid
or semi-rigid frame member 122b when the rigid or semi-rigid frame
members 122b are fully extended. In addition, the raised portion
122f, which is positioned in the indented portion 122g when the
rigid or semi-rigid frame members 122b are fully extended, acts to
hold the collapsible frame 122 in place in the extended position.
It is to be noted that the frame member connecting means may
comprise other means in other embodiments of the present invention.
For example, the frame member connecting means may include pins,
nut/bolt combinations, dowels, screws, hinges, or other connectors
or combinations of such means.
[0057] In the embodiment of the collapsible frame 122 illustrated
in FIG. 3 through FIG. 6, the collapsible frame 122 is
approximately cylindrical in shape when it is fully extended, as
illustrated in FIG. 3. When the collapsible frame 122 is not in use
and sufficient force is exerted on the various rigid or semi-rigid
frame members 122a, 122b, 122c comprising the collapsible frame
122, the collapsible frame 122 collapses in an "accordion" fashion,
as illustrated in FIG. 4, in which the collapsible frame 122 is
shown in a partially collapsed state. It is to be noted that the
collapsible frame 122 may be of almost any shape and size necessary
to adapt to the shape of the flexible chamber 121. In addition, it
is to be noted that the plurality of rigid or semi-rigid frame
members 122a, 122b, 122c comprising the collapsible frame 122 may
be arranged in many different structural patterns and have many
different ways in which to collapse and extend. Further, the frame
member connecting means may include many different means of
connecting the rigid or semi-rigid frame members 122a, 122b, 122c
comprising the collapsible frame 122. All such sizes, shapes,
structural patterns, means of collapse and extension, and
connecting means are encompassed by the present invention, as set
forth in the appended claims. It is also to be noted that all of
the features of the appliance 10 described above and illustrated in
connection with FIG. 1 may also be utilized with the appliance 110
illustrated in FIG. 3 through FIG. 6. For example, the appliance
110 generally comprises a vacuum system 130 having a reduced
pressure supply source 131 and reduced pressure supply means 132,
which may have substantially the same structure, features,
characteristics and operation as the various embodiments of the
vacuum system 30 of appliance 10. Finally, it is to be noted that
in operation of the appliance 110, the step of positioning the
appliance 110 for use further comprises the steps of extending the
rigid or semi-rigid frame members 122a, 122b, 122c comprising the
collapsible frame 122 to their extended state.
[0058] An embodiment of a second version of the present invention
is illustrated in FIG. 7. In this embodiment, an appliance 210 is
disclosed that is generally comprised of a treatment device 220, a
vacuum system 230, and an ancillary treatment system 260. The
treatment device 220 is further comprised of a chamber 221 having
an opening 223 at one end, which is sealed using sealing means that
are described in more detail below. In the illustrated embodiment,
the finger 212 of a patient extends through the opening 223 so that
the finger 212 may be treated with reduced pressure by the
appliance 210. The vacuum system 230 is generally comprised of a
reduced pressure supply source, illustrated schematically and
generally designated 231, and reduced pressure supply means 232
that operably connect the reduced pressure supply source 231 to the
chamber 221 so that reduced pressure is supplied to the volume
within the chamber 221 at the portion of the body (finger 212) to
be treated. In the various embodiments of this second version of
the present invention, the vacuum system 230 may have substantially
the same structure, features, characteristics and operation as the
embodiments of the vacuum system 30 described above and illustrated
in connection with FIG. 1. In other embodiments, the vacuum system
230 may be comprised of a suction bulb system, which is illustrated
in FIG. 8 and described in more detail below. The ancillary
treatment system 260 is generally comprised of a treatment supply
source, illustrated schematically and generally designated 261, and
treatment supply means 262 that operably connect the treatment
supply source 261 to the chamber 221 so that various treatments may
be supplied to the volume within the chamber 221 at the portion of
the body (finger 212) to be treated. In the various embodiments of
this second version of the present invention, the ancillary
treatment system 260 may have substantially the same structure,
features, characteristics and operation as the embodiments of the
treatment port 28 or the forced entry treatment system 60, or both,
described above and illustrated in connection with FIG. 1. It is to
be noted that in some embodiments there may be more than one
ancillary treatment system 260 or more than one treatment supply
means 262, and in other embodiments there may not be any treatment
system 260. The chamber 221 is generally adapted to be of a size
and shape to fit over and enclose all or a portion of a distal
extremity (i.e., finger or toe) of a patient. The chamber 221 is
also generally constructed of a rigid or semi-rigid material that
is rigid enough to generally support the chamber 221 away from the
portion of the distal extremity (finger 212) to be treated by the
appliance 210, although there may be some contact between such
portion 212 and the interior surface of the chamber 221. For
example, the chamber 221 may be constructed of woods, metals,
glasses, ceramics, plastics, or other rigid or semi-rigid polymers
(such as polyvinyl chloride or polycarbonate) or combinations of
such materials. Although the opening 223 of the chamber 221 in the
illustrated embodiment is approximately circular in shape, the
opening 223 may be of almost any size or shape, as long as it does
not interfere with the operation of the chamber 221 and permits the
distal extremity (the finger 212 in FIG. 7) to be treated to be
positioned within the volume of the chamber 221. In the illustrated
embodiment, the sealing means 224 is comprised of a flexible sleeve
224 that has substantially the same structure, features,
characteristics and operation as the embodiments of the flexible
sleeve 24 described above and illustrated in connection with FIG.
1. In other embodiments, the sealing means 224 may be comprised of
substantially the same structure, features, characteristics and
operation as any of the embodiments of the sealing means 24
described above and illustrated in connection with FIG. 1, to the
extent that such sealing means 24 applies to treatment of only a
portion of an object. In addition, the sealing means 224 may be
comprised of the shape of the opening 223 being approximately the
same size and shape as the portion of the body that is adjacent to
the opening 223, wherein the chamber 221 is held against such
adjacent portion of the body using an adhesive, adhesive tape,
lubricating material (such as lanoline), or the reduced pressure
within the chamber 221.
[0059] An embodiment of a suction bulb system that may be used with
embodiments of the present invention is illustrated in FIG. 8. In
this embodiment, the vacuum system 230 is generally comprised of a
suction bulb 271 having an inlet port 272 and an outlet port 273, a
bulb connection tubing member 274, an exhaust tubing member 275, an
exhaust control valve 276, a filter 277, and a supplemental vacuum
system (illustrated schematically and generally designated 230a).
In this embodiment, the suction bulb 271 is a hollow sphere that
may be used to produce a supply of reduced pressure for use with
the treatment device 220. In addition, the suction bulb 271 may
also be used to receive and store fluid aspirated from the distal
extremity 212. The inlet port 272 of the suction bulb 271 is
connected to one end of the bulb connection tubing member 274,
which is also the reduced pressure supply means 232 in this
embodiment. The connection tubing member 274 is connected to the
chamber 221 by a port 225 in a manner so that the interior volume
of the suction bulb 271 is in fluid communication with the volume
within the chamber 221. In this embodiment, the bulb connection
tubing member 274 is sufficiently flexible to permit movement of
the bulb connection tubing member 274, but is sufficiently rigid to
resist constriction when reduced pressure is supplied to the
chamber 221. The outlet port 273 of the suction bulb 271 is
connected to the exhaust tubing member 275. In this embodiment, the
exhaust tubing member 275 is sufficiently flexible to permit
movement of the exhaust tubing member 275, but is sufficiently
rigid to resist constriction when reduced pressure is supplied to
the chamber 221. The inlet port 272 of the suction bulb 271 may be
connected to the bulb connection tubing member 274 and the outlet
port 273 of the suction bulb 271 may be connected to the exhaust
tubing member 275 using any suitable means, such as by welding,
fusing, adhesives, clamps, or any combination of such means. In
addition, in some embodiments, which are the preferred embodiments,
the suction bulb 271, the bulb connection tubing member 274, and
the exhaust tubing member 275 may be fabricated as a single piece.
In the illustrated embodiment, the exhaust control valve 276 and
the filter 277 are operably connected to the exhaust tubing member
275. In this embodiment, the exhaust control valve 276 is used to
regulate the flow of fluids (gases and liquids) to and from the
suction bulb 271 and the supplemental vacuum system 230a. In
embodiments of the invention that do not have a supplemental vacuum
system 230a, the exhaust control valve 276 regulates flow of fluids
to and from the suction bulb 271 and the outside atmosphere.
Generally, the exhaust control valve 276 allows fluids to flow out
of the suction bulb 271 through the outlet port 273, but not to
flow in the reverse direction unless permitted by the user of the
appliance 210. Any type of flow control valve may be used as the
exhaust control valve 276, as long as the valve 276 is capable of
operating in the anticipated environment involving reduced pressure
and exudate. Such valves are well known in the relevant art, such
as sprung and unsprung flapper-type valves and disc-type valves,
operating in conjunction with or without ball, gate and other
similar types of valves. In this embodiment, the filter 277 is
operably attached to the exhaust tubing member 275 between the
outlet port 273 of the suction bulb 271 and the exhaust control
valve 276. The filter 277 prevents potentially pathogenic microbes
or aerosols from contaminating the exhaust control valve 276 (and
supplemental vacuum system 230a), and then being vented to
atmosphere. The filter 277 may be any suitable type of filter, such
as a micropore filter. In other embodiments, the filter 277 may
also be a hydrophobic filter that prevents any exudate from the
portion of the distal extremity (finger 212) from contaminating the
exhaust control valve 276 (and the supplemental vacuum system 230a)
and then being vented to atmosphere. In still other embodiments,
the filter 277 may perform both functions. It is to be noted,
however, that the outlet port 273, the exhaust control valve 276,
the filter 277, or any combination of the exhaust control valve 276
and the filter 277, need not be utilized in connection with the
vacuum system 230 in other embodiments of the invention.
[0060] In some embodiments of the present invention that do not
utilize a supplemental vacuum system 230a, the suction bulb 271 may
be used to produce a supply of reduced pressure in the following
manner. First, the user of the appliance 210 appropriately seals
all of the component parts of the appliance 210 in the manner
described herein. For example, the chamber 221 is placed over and
encloses the portion 212 of the body to be treated, and the opening
223 of the chamber 221 is sealed using the sealing means 224. The
user then opens the exhaust control valve 276 and applies force to
the outside surface of the suction bulb 271, deforming it in a
manner that causes its interior volume to be reduced. When the
suction bulb 271 is deformed, the gas in the interior volume is
expelled to atmosphere through the outlet port 273, the exhaust
tubing member 275, the filter 277, and the exhaust control valve
276. The user then closes the exhaust control valve 276 and
releases the force on the suction bulb 271. The suction bulb 271
then expands, drawing fluid (liquid and gas) from the volume within
the treatment device 220 into the suction bulb 271 through the bulb
connection tubing member 274 and causing the pressure in such
volume to decrease. To release the reduced pressure, the user of
the appliance 210 may open the exhaust control valve 276, allowing
atmospheric air into the interior volume of the suction bulb 271.
The level of reduced pressure may also be regulated by momentarily
opening the exhaust control valve 276.
[0061] The suction bulb 271 may be constructed of almost any
suitable fluid impermeable flexible or semi-rigid material that can
be readily deformed by application of pressure to the outside
surface of the suction bulb 271 by users of the appliance 270 and
still return to its original shape upon release of the pressure.
For example, the suction bulb 271 may be constructed of rubber,
neoprene, silicone, or other flexible or semi-rigid polymers, or
any combination of all such materials. In addition, the suction
bulb 271 may be of almost any shape, such as cubical, ellipsoidal,
or polygonal. The suction bulb 271 may also be of varying size
depending upon the anticipated use of the suction bulb 271, the
size of the treatment device 220, use of a supplemental vacuum
system 230a, the level of reduced pressure desired, and the
preference of the user of the appliance 210. In the embodiment of
the invention illustrated in FIG. 8, the supplemental vacuum system
230a is connected to the exhaust tubing member 275 and is used to
provide a supplemental supply of reduced pressure to the suction
bulb 271 and treatment device 220. In this embodiment, the
supplemental vacuum system 230a may have substantially the same
structure, features, characteristics and operation of the various
embodiments of the vacuum system 30 of the first version of the
invention described above and illustrated in connection with FIG.
1. It is to be noted, however, that the supplemental vacuum system
230a need not be used in connection with the vacuum system 230 in
other embodiments of the invention.
[0062] The present invention also includes a method of
administering reduced pressure treatment to a distal extremity
using various embodiments of the second version of the present
invention, as described above and illustrated in connection with
FIG. 7. Generally, the method comprises the following steps. First,
an appliance 210 for administering reduced pressure to the distal
extremity (the finger 212 in FIG. 7) is provided. Second, the
appliance 210 is placed over the portion of the distal extremity to
be treated (the finger 212 in FIG. 5), so that the chamber 221
encloses the portion of the finger 212 to be treated. Third, the
opening 223 of the chamber 221 is sealed using the sealing means
(the flexible sleeve 224 in FIG. 7), so that reduced pressure may
be maintained in the volume within the chamber 221. Fourth, the
chamber 221 is operably connected with the reduced pressure supply
source 231 using the reduced pressure supply means 232 so that
reduced pressure is supplied to the volume within the chamber 221.
It is to be noted that the fourth step may be also performed before
either the second or third step described above. In the preferred
embodiments of this second version of the invention, the reduced
pressure maintained in the volume within the chamber 221 at the
portion of the distal extremity to be treated (the finger 212 in
FIG. 7) is in the range from approximately 20 mm of Hg below
atmospheric pressure to approximately 125 mm of Hg below
atmospheric pressure. In yet other embodiments, the reduced
pressure is applied to the chamber 221 in a cyclic nature, the
cyclic nature providing alternating time periods of application of
reduced pressure and non-application of reduced pressure. Fifth,
the reduced pressure is maintained in the volume within the chamber
221 until the portion of the distal extremity being treated (the
finger 212 in FIG. 7) has progressed toward a selected stage of
treatment. In embodiments comprising an ancillary treatment system
260, the method also includes the step of positioning the treatment
supply source 261 in proximity to the treatment device 220,
connecting the treatment supply means 262 to the treatment supply
source 261 and the chamber 221, and operating the ancillary
treatment system 260 until the desired treatment is completed.
[0063] An embodiment of a third version of the present invention is
illustrated in FIG. 9. In this embodiment, the present invention
includes an appliance 310 that is generally comprised of a
treatment device 320, a vacuum system 330, a drainage system 350,
and a forced entry treatment system 360. In this embodiment, the
treatment device 320 is further comprised of a chamber 321 having
an opening 323, sealing means (a flexible sleeve 324 in FIG. 7) to
seal the opening 323 so that reduced pressure may be maintained in
the volume within the chamber 321, and a liner 380. In the
illustrated embodiment, the liner 380 is positioned over the
portion of the body 312 to be treated, which extends through the
opening 323 so that the portion 312 may be treated with reduced
pressure by the appliance 310. The vacuum system 330 is generally
comprised of a reduced pressure supply source, illustrated
schematically and generally designated 331, and reduced pressure
supply means 332 that operably connect the reduced pressure supply
source 331 to the chamber 321 so that reduced pressure is supplied
to the volume within the chamber 321 at the portion of the body 312
to be treated. In the various embodiments of this third version of
the present invention, the vacuum system 330 may have substantially
the same structure, features, characteristics and operation as the
embodiments of the vacuum system 30 described above and illustrated
in connection with FIG. 1. The forced entry treatment system 360 is
generally comprised of a forced entry supply source, illustrated
schematically and generally designated 361, and forced entry supply
means 362 that operably connect the forced entry supply source 361
to the chamber 321 so that various treatments may be supplied to
the volume within the chamber 321 at the portion of the body 312 to
be treated. In the various embodiments of this third version of the
present invention, the forced entry treatment system 360 may have
substantially the same structure, features, characteristics and
operation as the embodiments of the forced entry treatment system
60 described above and illustrated in connection with FIG. 1. It is
to be noted that in some embodiments there may be more than one
forced entry treatment system 360 and in other embodiments there
may not be any forced entry treatment system 360. The drainage
system 350 may be generally comprised of combinations of an overlay
351, wound packing means 352, draining means 353, valves 354, and
collection system 356. In the various embodiments of this third
version of the present invention, the drainage system 350 may have
substantially the same structure, features, characteristics and
operation as the embodiments of the drainage system 50 described
above and illustrated in connection with FIG. 1. It is to be noted
that in some embodiments there may be more than one drainage system
350 and in other embodiments there may not be any drainage system
350. In yet other embodiments, the drainage system 350 may contain
all of the components of the illustrated drainage system 350, while
in still other embodiments the drainage system 350 may contain only
some of the components.
[0064] In some embodiments of this third version of the present
invention, the chamber 321 may have substantially the same
structure, features, characteristics and operation as the
embodiments of the flexible chamber 21 and its supporting
collapsible frame 22 described above and illustrated in connection
with FIG. 1. In other embodiments, the chamber 321 may have a
different structure, shape or size. For example, the chamber 321
may be comprised of a rigid or semi-rigid material and may have a
rectangular cross-sectional shape. In addition, the sealing means
324 utilized in the various embodiments of this third version of
the present invention may generally be comprised of any of the
sealing means 24 described above and illustrated in connection with
FIG. 1. The liner 380 is generally adapted to be of a size and
shape to cover the portion 312 of the body to be treated, as well
as an additional portion 313 of the body that extents to at least
the sealing portion 324a of the flexible sleeve 324. Thus, in this
version of the invention, the sealing means (the flexible sleeve
324) may be sealed against the liner 380 rather than the portion
313 of the body adjacent to the sealing portion 324a of the
flexible sleeve 324. This seal may provide for permanent
attachment, or for removable attachment, and seal of the liner 380
to the flexible sleeve 324. The portion 313 of the body that is
approximately adjacent to the sealing portion of the liner 380a is
also sealed in a manner so that reduced pressure may be maintained
in the volume within the chamber 321. Such sealing means may be
comprised of any suitable means, such as adhesives, adhesive tapes,
the reduced pressure within the chamber 321, or other means or
combinations of such means. The liner 380 is generally comprised of
a material that is impermeable or semi-permeable with respect to
fluids (liquids and gases). Where semi-permeable materials are
used, the reduced pressure within the chamber 321 is also applied
to the portion of the body 312 enclosed by the liner 380, but any
exudate aspirated from such portion 312 of the body is generally
not able to pass through the liner 380 to the interior volume of
the chamber 321. For example, the liner 380 may be constructed of
polyurethane or other semi-permeable polymers (such as that sold by
the 3M Corporation under the trademark IOBAN), or combinations of
such materials. This enables the application of reduced pressure to
the portion 312 of the body to be treated, without contamination of
the chamber 321 by any exudate aspirated from the portion 312 of
the body to be treated. It is to be noted that the liner 380 may be
used in other embodiments of this third version of the present
invention with or without an overlay 351, draining means 353, or
wound packing means 352. The method of using the embodiments of
this third version of the invention is substantially similar to the
method used to operate the embodiments of the first version of the
present invention described above and illustrated in connection
with FIG. 1, except that this version includes the steps of placing
the portion 312 of the body to be treated into the liner 380,
sealing the liner 380 to the portion 313 of the body adjacent to
the sealing portion 380a of the liner 380, and where necessary,
sealing the flexible sleeve 324 to the liner 380.
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