U.S. patent application number 14/088543 was filed with the patent office on 2018-03-22 for respiratory secretion rentention device, system and method.
This patent application is currently assigned to Mergenet Medical, Inc.. The applicant listed for this patent is Mergenet Medical, Inc.. Invention is credited to Angelo R. Caruso, Louis Javier Collazo, Robert M. Landis, Charles A. Lewis.
Application Number | 20180078723 14/088543 |
Document ID | / |
Family ID | 43755556 |
Filed Date | 2018-03-22 |
United States Patent
Application |
20180078723 |
Kind Code |
A1 |
Caruso; Angelo R. ; et
al. |
March 22, 2018 |
RESPIRATORY SECRETION RENTENTION DEVICE, SYSTEM AND METHOD
Abstract
An apparatus, system, and method for managing respiratory
secretions and fluids in sections of artificial airways. A
secretion removal assembly configured to connect to a respiratory
secretion retention device, the respiratory secretion retention
device adapted to fluidly connect to an artificial airway, the
secretion removal assembly including a connector adapted to connect
to a port of the respiratory secretion retention device; and a bag
in fluid communication with the connector can be provided. In
another aspect of this embodiment, the bag is adapted to collect
the secretions that emit from the port of the respiratory secretion
retention device. In yet another aspect of this embodiment, the
secretion removal assembly further can include a tube having a
first end and a second end opposite the first end, the first end in
fluid communication with the connector and the second end in fluid
communication with the bag.
Inventors: |
Caruso; Angelo R.; (Boca
Raton, FL) ; Lewis; Charles A.; (Carrabelle, FL)
; Collazo; Louis Javier; (Lauderdale by the Sea, FL)
; Landis; Robert M.; (Mountainside, NJ) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Mergenet Medical, Inc. |
Coconut Creek |
FL |
US |
|
|
Assignee: |
Mergenet Medical, Inc.
Coconut Creek
FL
|
Family ID: |
43755556 |
Appl. No.: |
14/088543 |
Filed: |
November 25, 2013 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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12882162 |
Sep 14, 2010 |
8591496 |
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14088543 |
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12648033 |
Dec 28, 2009 |
8777933 |
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12882162 |
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12431069 |
Apr 28, 2009 |
8814838 |
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12648033 |
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61104597 |
Oct 10, 2008 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61M 16/0463 20130101;
A61M 16/0816 20130101; A61M 16/047 20130101; A61M 16/0808 20130101;
A61M 16/1045 20130101; A61M 16/0833 20140204; A61M 16/0488
20130101; A61M 16/0825 20140204; A61M 16/0427 20140204 |
International
Class: |
A61M 16/04 20060101
A61M016/04; A61M 16/10 20060101 A61M016/10; A61M 16/08 20060101
A61M016/08 |
Claims
1-21. (canceled)
22. A secretion removal assembly configured to connect to a
respiratory secretion retention device, the respiratory secretion
retention device adapted to fluidly connect to an artificial
airway, the secretion removal assembly comprising: a connector
adapted to connect to a port of the respiratory secretion retention
device; and, a bag in fluid communication with the connector.
23. The secretion removal assembly in claim 22, wherein the bag is
adapted to collect the secretions that emit from the port of the
respiratory secretion retention device.
24. The secretion removal assembly in claim 22, wherein the bag is
adapted to be connected to the connector by a user during use.
25. The secretion removal assembly in claim 22, wherein the bag is
adapted to be connected and disconnected to the connector during
use.
26. The secretion removal assembly in claim 22, further comprising
a tube having a first end and a second end opposite the first end,
the first end in fluid communication with the connector and the
second end in fluid communication with the bag.
27. The secretion removal assembly in claim 22, wherein the
connector sealingly engages at least a portion of the port of the
respiratory secretion retention device.
28. The secretion removal assembly in claim 22, wherein the
connector sealingly engages the port of the respiratory secretion
retention device without opening a reservoir of the respiratory
secretion retention device to atmosphere.
29. The secretion removal assembly in claim 22, further comprising
a spike coupled to the connector.
30. The secretion removal assembly in claim 29, wherein the spike
is adapted for one of breaching, engaging and repositioning a seal
of the port of the respiratory secretion retention device.
31. The secretion removal assembly in claim 22, further comprising
a control valve adapted to control contents of the bag.
32. The secretion removal assembly in claim 22, further comprising
a clamp to control the contents of the bag.
33. The secretion removal assembly in claim 22, further comprising
a bag port.
34. The secretion removal assembly in claim 22, wherein the
connector is adapted to first engage the port of the respiratory
secretion retention device in a non-sealed area of the port prior
to one of breaching, engaging and repositioning of a seal of the
port of the respiratory secretion retention device.
35. A secretion removal assembly configured to connect to a
respiratory secretion retention device, the respiratory secretion
retention device adapted to fluidly connect to an artificial
airway, the secretion removal assembly comprising: a connector
adapted to connect to a port of the respiratory secretion retention
device; wherein the secretion removal assembly is adapted to
collect the secretions that emit from the port without the use of
suction.
36. secretion removal assembly in claim 35, wherein the connector
is adapted to allow the secretions to drain into the secretions
removal assembly.
37. The secretion removal assembly in claim 35, wherein the
connector is adapted to allow the secretions into the secretions
removal assembly by use of an applied force.
38. The secretion removal assembly in claim 37, wherein the applied
force is generated by a ventilation source.
39. The secretion removal assembly in claim 37, wherein the applied
force is generated by the user.
40. The secretion removal assembly in claim 37, wherein the applied
force is generated by an instilled fluid.
41. A respiratory secretion removal system comprising: a
respiratory secretion retention assembly, the respiratory secretion
retention assembly adapted to fluidly connect to an artificial
airway; and a secretion removal assembly; wherein the secretion
removal assembly comprises a collection bag.
Description
RELATED APPLICATIONS
[0001] This application is a continuation of pending U.S.
application Ser. No. 12/882,162 filed Sep. 14, 2010 to Angelo
Caruso et al., entitled RESPIRATORY SECRETION RETENTION DEVICE,
SYSTEM AND METHOD, which application is a continuation-in-part of
pending U.S. application Ser. No. 12/648,033 filed Dec. 28, 2009 to
Robert M. Landis, et al., entitled RESPIRATORY SECRETION RETENTION
DEVICE, SYSTEM AND METHOD, which application is a
continuation-in-part of pending U.S. application Ser. No.
12/431,069 filed Apr. 28, 2009 to Robert M. Landis, et al.,
entitled RESPIRATORY SECRETION RETENTION DEVICE, SYSTEM AND METHOD,
which application claims benefit and priority from U.S. Provisional
Patent Application Ser. No. 61/104,597, filed Oct. 10, 2008, the
entire contents of all of which are incorporated herein by
reference.
BACKGROUND OF THE INVENTION
Statement of the Technical Field
[0002] The present invention relates to artificial airways and more
particularly to an airway device for controlling respiratory
secretions in artificial airways, and associated devices such as
respiratory gas delivery devices.
Discussion of the Related Art
[0003] The use of artificial airways is a common method of
maintaining an open airway for patients who require some type of
respiratory assistance. Artificial airways come in a variety of
options depending on the patient and level of respiratory
intervention required. Large numbers of artificial airways have
three common features. First, the artificial airway will be a
flexible tube that extends into the patient's trachea. Second, most
artificial airways will have an inflatable cuff near the distal end
of the tube. The inflatable cuff can be used to make an airtight
seal, e.g., for nasal tracheal, oral tracheal and tracheostomy
tubes where the entire breath of the patient is directed through
the tube. Third, the standard artificial airway has a 15 mm fitting
on the external opening of the tube to which respiratory gas
delivery devices and instruments can be attached compliant with the
ISO 5356; Anesthetic and Respiratory Equipment--Conical Connectors
standard.
[0004] One of the common issues with having the patient breathe
through these artificial airways is that respiratory secretions,
which would normally enter the pharynx and be swallowed,
expectorated or coughed out through the mouth, are forced to egress
through the lumen of the artificial airway. The presence of the
tube, being a foreign object in the airway can also stimulate
respiratory secretions.
[0005] Keeping the tube and airway clear of secretions is a
procedure performed by clinicians, which requires training and
vigilance. Depending on the condition of the patient, the frequency
of clearing the airway with a suction catheter varies greatly. When
secretions accumulate in the tube there is added resistance to
breathing and when the patient is strong enough, a forceful
exhalation sends the secretions out through the tube and into the
room or into any device attached to the tube.
[0006] Some fluid trap devices for use between an artificial airway
and respiratory gas delivery devices, such as a ventilator circuit,
have a fill volume substantially independent of orientation of the
trap within the fluid circuit. Such fluid trap devices are
disadvantageous as they impose unnecessary and excessive dead-space
(e.g., exhaled air that is re-breathed) to achieve the independent
orientation.
[0007] Typically, when a ventilator circuit or an instrument is
detached from an artificial airway, the patient coughs and
respiratory secretions and fluids are sprayed into the room. In
addition, it is common for a patient on a ventilator to have
secretions accumulate inside an artificial airway, such as
endotracheal (ET) tube, with no place to go but up the tube, down
the tube or into whatever breathing instrument is attached to the
ET tube.
[0008] In the last decade, the use of "closed suction" devices with
ventilator breathing circuits has become a standard at many medical
facilities. A closed suction device allows for access to the airway
with a suction catheter without detaching or removing the treatment
device from the artificial airway. Closed suction systems add
additional support to clinicians by greatly reducing the time and
effort necessary for clearing the airway. A closed suction device
for example, can allow a catheter to advance into the artificial
airway for suctioning and then be withdrawn into a protective
sheath where it is protected from contamination when the catheter
is not in use. The closed suction catheter may be used multiple
times without opening the device to the atmosphere, and is usually
used for one to several days. A closed suction system allows access
to the ventilator breathing circuit connected with the patient to
remain "closed" as opposed to methods that require it to be
"opened" to the atmosphere for access. Closed suction also reduces
risk of microbial contamination of the artificial airway during
suctioning thereby protecting the patient's airway from infection.
In numerous medical institutions, the infection control departments
have made the use of closed suction a standard of practice by
requiring that all intubated patients in the intensive care unit
(ICU) have a closed suction system installed.
[0009] Most clinicians find that there are a significant number of
instances when it is necessary to detach a ventilator circuit or
respiratory instrument (i.e. "open the circuit"), and having
protection from patient secretions entering the environment during
these occasions is most desirable.
[0010] There are three main problems with secretions in the tube of
an artificial airway. First, when the ventilator circuit is
disconnected, secretions can be sprayed into the room if the
patient coughs. Second, secretions in the artificial airway result
in compromised breathing. Third, when secretions are forced out
into the attached ventilator circuit, these secretions can foul the
attached instruments, such as a heat and moisture exchange (HME)
device, and the like.
SUMMARY OF THE INVENTION
[0011] Embodiments of the present invention address deficiencies of
the art in respect to artificial airways and respiratory secretions
management and provide a novel and non-obvious apparatus, system,
and method for managing respiratory secretions and fluids in a
section of an artificial airway, ventilator circuit system. In an
embodiment of the invention, a secretion removal assembly
configured to connect to a respiratory secretion retention device,
the respiratory secretion retention device adapted to fluidly
connect to an artificial airway, the secretion removal assembly
including a connector adapted to connect to a port of the
respiratory secretion retention device; and a bag in fluid
communication with the connector can be provided. In another aspect
of this embodiment, the bag is adapted to collect the secretions
that emit from the port of the respiratory secretion retention
device. In yet another aspect of this embodiment, the secretion
removal assembly further can include a tube having a first end and
a second end opposite the first end, the first end in fluid
communication with the connector and the second end in fluid
communication with the bag.
[0012] In another embodiment of the invention, a respiratory
secretion removal system can be provided. A respiratory secretion
removal system can include a respiratory secretion retention
assembly, the respiratory secretion retention assembly adapted to
fluidly connect to an artificial airway and a secretion removal
assembly, wherein the secretion removal assembly comprises a
collection bag.
[0013] In another embodiment of the invention, a secretion removal
assembly configured to connect to a respiratory secretion retention
(RSR) device can be provided. The secretion removal assembly can
include a connector configured for connecting to a sealed port of
the respiratory secretion retention device, where the connector is
configured to first engage the port in a non-sealed area of the
port prior to one of breaching, engaging and repositioning of the
seal of the port of the respiratory secretion retention device.
[0014] In yet another embodiment of the invention, a secretion
removal assembly configured to connect to a respiratory secretion
retention (RSR) device can be provided. The secretion removal
assembly can include a connector configured for connecting to a
port of the respiratory secretion retention device, where the port
has a first seal and the connector is configured to create a second
seal with the port prior to or simultaneously to one of breaching,
engaging and repositioning of the first seal of the port of the
respiratory secretion retention device.
[0015] In yet another embodiment of the invention, a secretion
removal assembly configured to connect to a respiratory secretion
retention (RSR) device can be provided. The secretion removal
assembly can include a connector configured for connecting to a
port of the respiratory secretion retention device, where the
connector is configured to first engage the port in a non-sealed
area of the port prior to one of breaching, engaging and
repositioning of the seal of the port of the respiratory secretion
retention device.
[0016] In an embodiment of the invention the RSR device may include
a port for instilling fluids, such as saline or medication.
Medication may be aerosolized for delivery of medication to the
airway.
[0017] In still another embodiment of the invention, a respiratory
secretion retention (RSR) device configured to connect to an
artificial airway can be provided. The respiratory secretion
retention (RSR) device can include a housing that defines a
passageway for the flow of respiratory gases, a chamber that is
defined by the housing, where a portion of the chamber is
configured to retain exhaled respiratory particulate and liquid,
and an expiratory port of the housing, wherein the expiratory port
is not parallel to a gas delivery port of the housing during some
phase of use of the device. In an aspect of this embodiment, the
housing is configured to provide for repositioning of the gas
delivery port with respect to the expiratory port.
[0018] The device can include a housing that defines a passageway
for the flow of respiratory gases with at least two chambers
coupled to the housing. The chambers are configured to retain
exhaled respiratory particulate and liquid. The respiratory
secretion retention further including a patient port coupled to the
housing that is in fluid communication with the artificial airway
and a repositionable barrier configured to isolate at least one of
the two chambers from the passageway.
[0019] In another embodiment, a secretion removal assembly can
connect to a respiratory secretion retention device; the secretion
removal assembly can include a connector configured for connecting
to a port of the respiratory secretion retention device and a spike
coupled to the connector. In another aspect of this embodiment, the
spike is configured for one of breaching, engaging and
repositioning of a seal of the port.
[0020] Additional aspects of the invention will be set forth in
part in the description which follows, and in part will be obvious
from the description, or may be learned by practice of the
invention. The aspects of the invention will be realized and
attained by means of the elements and combinations particularly
pointed out in the appended claims. It is to be understood that
both the foregoing general description and the following detailed
description are exemplary and explanatory only and are not
restrictive of the invention, as claimed.
BRIEF DESCRIPTION OF THE DRAWINGS
[0021] The accompanying drawings, which are incorporated in and
constitute part of this specification, illustrate embodiments of
the invention and together with the description, serve to explain
the principles of the invention. The embodiments illustrated herein
are presently preferred, it being understood, however, that the
invention is not limited to the precise arrangements and
instrumentalities shown, herein:
[0022] FIGS. 1A and 1B are schematic illustrations of the placement
of an RSR device showing its attachment to an artificial airway in
an intubated patient, where the RSR device is also connected to a
ventilator circuit in FIG. 1A and wherein an RSR device is
connected to a closed suction catheter in FIG. 1B;
[0023] FIGS. 2A and 2B are schematic illustrations of an RSR device
according to a certain embodiment of the present invention;
[0024] FIGS. 3A and 3B are cross-sectional schematic illustrations
of yet another RSR device according to a certain embodiment of the
present invention;
[0025] FIGS. 4A, 4B and 4C shows cross-sectional schematic
illustrations of yet another RSR device according to a certain
embodiment of the present invention;
[0026] FIGS. 5A, 5B and 5C shows schematic illustrations of yet
another RSR device according to a certain embodiment of the present
invention;
[0027] FIGS. 6A, 6B and 6C shows schematic illustrations of details
of various forms of diverters which may be utilized in the RSR
device according to various embodiments of the present
invention;
[0028] FIGS. 7A and 7B shows schematic illustrations of yet another
RSR device according to a certain embodiment of the present
invention;
[0029] FIGS. 8A and 8B shows additional schematic illustrations of
the RSR device shown in FIGS. 7A and 7B according to a certain
embodiment of the present invention;
[0030] FIG. 9 shows cross-sectional schematic illustrations of
variations of the RSR device shown according to a certain
embodiment of the present invention;
[0031] FIGS. 10A and 10B shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0032] FIGS. 11A, 11B and 11C shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0033] FIGS. 12A, 12B and 12C shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0034] FIG. 13A shows lateral schematic view of a configuration of
an RSR device shown according to a certain embodiment of the
present invention;
[0035] FIG. 13B shows a frontal schematic view of the RSR device
shown in FIG. 13A;
[0036] FIG. 14 shows a cross-sectional schematic illustration of
the RSR device according to a certain embodiment of the present
invention;
[0037] FIGS. 15A, 15B and 15C shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0038] FIGS. 16A, 16B and 16C shows cross-sectional schematic
illustrations of variations of the RSR device according to a
certain embodiment of the present invention;
[0039] FIGS. 17A and 17B shows front schematic illustrations of
variations of the RSR device shown according to a certain
embodiment of the present invention;
[0040] FIGS. 18A, 18B and 18C shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0041] FIGS. 19A, 19B and 19C shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0042] FIGS. 20A and 20B shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0043] FIG. 21 shows a cross-sectional schematic illustration of
variations of the RSR device shown according to a certain
embodiment of the present invention;
[0044] FIGS. 22A and 22B shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0045] FIGS. 23A and 23B shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0046] FIGS. 24A and 24B shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0047] FIGS. 25A and 25B shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0048] FIGS. 26A, 26B and 26C shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0049] FIGS. 27A and 27B shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0050] FIG. 28 shows a cross-sectional schematic illustration of
variations of the RSR device shown according to a certain
embodiment of the present invention;
[0051] FIGS. 29A, 29B and 29C shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0052] FIGS. 30A, 30B and 30C shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0053] FIGS. 31A, 31B, 31C and 31D shows cross-sectional schematic
illustrations of variations of the RSR device shown according to a
certain embodiment of the present invention;
[0054] FIG. 32A shows perspective schematic illustrations of
variations of the RSR device shown according to a certain
embodiment of the present invention;
[0055] FIG. 32B shows a cross-sectional schematic illustration of
the RSR device shown in FIG. 32A according to a certain embodiment
of the present invention;
[0056] FIG. 33A illustrates another embodiment of an RSR device
according to a certain embodiment of the present invention;
[0057] FIG. 33B shows a cross-sectional schematic illustration of
the RSR device shown in FIG. 33A in an assembled stage according to
a certain embodiment of the present invention;
[0058] FIG. 33C is a partial longitudinal cross-sectional view of a
nonassembled RSR device taken along the plane labeled A-A shown in
FIG. 33B;
[0059] FIGS. 33D and 33E show cross-sectional views of an RSR
device in an initial sealing connection position and a final
sealing connection position;
[0060] FIGS. 34A and 34B shows schematic illustrations of
variations of the RSR device according to a certain embodiment of
the present invention;
[0061] FIG. 35A is a partial longitudinal cross-sectional view of a
nonengaged RSR device according to a certain embodiment of the
present invention;
[0062] FIGS. 35B and 35C show cross-sectional views of an RSR
device in an initial sealing connection position and a final
sealing connection position;
[0063] FIGS. 36A and 36B show cross-sectional views of an RSR
device in an initial sealing connection position and a final
sealing connection position;
[0064] FIGS. 37A and 37B show cross-sectional views of an RSR
device in a initial nonengaged position and a final engaged
position according to a certain embodiment of the present
invention;
[0065] FIG. 38A illustrates another embodiment of an RSR device
shown according to a certain embodiment of the present
invention;
[0066] FIG. 38B is a partial longitudinal cross-sectional view of a
retention assembly taken along the plane labeled A-A shown in FIG.
38A;
[0067] FIG. 38C is a partial longitudinal cross-sectional view of
an assembled RSR device taken along the plane labeled A-A shown in
FIG. 38A;
[0068] FIG. 39 illustrates a cross-sectional cutaway view of
another embodiment of an RSR device shown according to a certain
embodiment of the present invention;
[0069] FIG. 40 shows schematic illustrations of variations of the
RSR device shown according to a certain embodiment of the present
invention;
[0070] FIG. 41A shows schematic illustrations of variations of the
RSR device shown according to a certain embodiment of the present
invention;
[0071] FIG. 41B is a cross-sectional view of the RSR device shown
in FIG. 41A;
[0072] FIG. 42A shows schematic illustrations of variations of the
RSR device shown according to a certain embodiment of the present
invention;
[0073] FIG. 42B is a cross-sectional view of the RSR device shown
in FIG. 42A;
[0074] FIG. 43A shows schematic illustrations of variations of the
RSR device shown according to a certain embodiment of the present
invention;
[0075] FIGS. 43B and 43C illustrate cross-sections along lines
43-43 through the patient port from a top view of the RSR device
shown in FIG. 43A;
[0076] FIG. 43D illustrates an alternate method of secretion
clearance or removal from RSR device of FIG. 43A;
[0077] FIG. 44A shows schematic illustrations of variations of the
RSR device shown according to a certain embodiment of the present
invention;
[0078] FIG. 44B shows a cross-sectional perspective view taken
through plane B-B of RSR device of FIG. 44A in an assembled
state;
[0079] FIG. 44C is a perspective view of a plug of RSR device of
FIG. 44A that illustrates some channels; and,
[0080] FIGS. 44D, 44E, and 44F illustrate partial cross-sections of
an RSR device of FIG. 44A in non-engaged, partially engaged, and
fully engaged positions respectively.
DETAILED DESCRIPTION OF THE INVENTION
[0081] During the exhalation phase of respiration, fluid is
expelled from the lower respiratory tract. Most of the fluid is in
the form of gases, but liquid and particulate matter (respiratory
secretions) are also expelled. The RSR acts to separate the
"respiratory secretions" from the respiratory gasses. For purposes
of this disclosure, "respiratory secretions" may include sputum,
mucus, mucus plugs, and/or other all other nongaseous matter which
may be conveyed out of the lower respiratory tract and the
like.
[0082] Embodiments of the present invention address deficiencies of
the art in respect to artificial airways and respiratory secretion
management, and provide a novel and non-obvious apparatus, system,
and method for managing respiratory secretions and fluids in
artificial airways. For purposes of this disclosure "artificial
airway" may include any portion of the breathing conduit that
connects to a patient's airway. In an embodiment of the invention,
a Respiratory Secretion Retention (RSR) device for connecting to an
artificial airway can be provided. A respiratory secretion
retention device configured for connecting to an artificial airway
comprising a housing that defines a passageway for the flow of
respiratory gases, a chamber defined by the housing with a portion
of the chamber configured to retain exhaled respiratory particulate
and liquid, a patient port defined by the housing, which is in
fluid communication with an artificial airway and at least one
access port configured to provide access to the chamber and the
patient port. In another aspect of this embodiment, the at least
one access port can include a control valve, the control valve
located in a downstream position of a passage of the access port to
control access from the access port to the chamber.
[0083] In another embodiment of the invention, a respiratory
secretion retention (RSR) device can include a housing that defines
a passageway for the flow of respiratory gases, a chamber defined
by the housing with a portion of the chamber configured to retain
exhaled respiratory particulate and liquid, a patient port defined
by the housing, which is in fluid communication with an artificial
airway, a suction tube subassembly coupled to the housing, which
defines a medical instrument passage and a suction tube portion and
at least one access port configured to provide access to the
chamber and the patient port. In another aspect of this embodiment
the suction tube subassembly is coupled to a knob that provides for
translation repositioning of the suction tube subassembly with
respect to the housing.
[0084] In yet another embodiment of the invention, a respiratory
secretion retention (RSR) device configured for fluidly connecting
to an artificial airway can be provided. The respiratory secretion
retention (RSR) device can include a housing that defines a
passageway for the flow of respiratory gases, a chamber defined by
the housing with a portion of the chamber configured to retain
exhaled respiratory particulate and liquid, a patient side port
coupled with the housing, which is in fluid communication with an
artificial airway, at least one access port configured to provide
access to the chamber and the patient port and a tube coaxially
aligned and coupled to the access port and the patient port, to
define a passage between the access port and the patient port. In
another aspect of this embodiment, the tube includes a diverter in
the passage. In yet another aspect of this embodiment, the diverter
is rotatably hinged on a wall of the tube. In still yet another
aspect of this embodiment, the RSR device can include a sleeve
surrounding the tube that includes at least one first aperture and
the tube includes at least one second aperture.
[0085] In illustration, FIG. 1A is a schematic illustration of an
RSR device 200 attached to an endotracheal (ET) tube 102 in an
intubated a patient 110. The RSR device 200 also can be attached to
a ventilator circuit 104. The patient 110 is shown at an
approximately 45-degree angle from level as this position as
recommended by the Centers for Disease Control (CDC) for prevention
of ventilator associated pneumonia. This illustration shows the
relationship of the RSR device 200 used in association with a
ventilator circuit 104. The device can also be used in association
other ventilation tubes such as with a tracheostomy tubes,
pharyngeal airway, or nasotracheal tubes. RSR 200 can be used alone
with an artificial airway 102 without a ventilator 104, such as in
a spontaneously breathing patient.
[0086] FIG. 1B illustrates a closed suction device 106 that can be
connected between the RSR device 400 and the ventilator circuit
104. Certain embodiments of the present invention allow for the use
of closed suction, and allow a suction catheter 108 of the closed
suction device 106 to pass through RSR device 400 and into and
through the patient's artificial airway in accordance with an
embodiment of the present invention.
[0087] FIG. 2A is a schematic illustration of an RSR device 200
showing detail of its attachment to the endotracheal tube 102 and
to the ventilator circuit. The RSR device can be applied so that
gravity pulls secretions into a dependent area of the housing
configured to retain the respiratory secretions. In embodiments,
swivels can be added to the RSR to articulate the device in order
to adjust it into a dependent position with respect to the
collection of respiratory secretions, so that gravity pulls the
secretions into a dependent area of the housing configured to
retain the respiratory secretions.
[0088] The typically male fitting of the artificial airway 102 (as
illustrated in FIG. 2A) fits into the typically female 15 mm
fitting 202 which in preferred embodiments of this invention is
configured as a swivel fitting. The rotation of this fitting is
indicated by arrow 204. Fitting 202 can be connected to the RSR
main body 206 with tube 208. Tube 208 can be straight or tube 208
may be angled and/or rotatable. A second tube 210 can be located on
the ventilator side of the RSR device 200. Tube 210 can be straight
or tube 210 can be angled and rotatable. In embodiments, tube 208
and tube 210 can swivel to allow the reservoir area of main body
206 to be placed in a dependent orientation while allowing the
patient to be placed in a variety of positions. RSR device 200 can
be designed to be used where its reservoir area 212 is placed below
the artificial airway 102. Arrows 214 show the possible
articulation of the angled and rotatable tubes in one embodiment in
relation to the main body 206. Tube 210 is shown connected to a
female ventilator connection 216 which also can contain a swivel.
Thus, the main body 206 of the RSR 200 may move in two axes and the
reservoir area 212 can be oriented in a dependent position with
respect to gravity.
[0089] FIG. 2B further illustrates the air flow path of RSR device
200, illustrating its function. When the patient exhales, the flow
enters connector 202 through the artificial airway into the RSR
device 200 as shown by arrow 218. The momentum of the heavier
fluids (respiratory secretions) causes them to both impact the
interior surfaces of the RSR device and to fall out of the gas flow
when the flow channel widens in the RSR and gas flow slows. This
occurs in the RSR main body 206, and flow is indicated by arrows
220 and 222. Outflow of expiratory gasses is shown by arrows 224.
On inhalation the gases reverse the flow direction in this
embodiment of the invention. A fluid level of trapped respiratory
secretions 226 is shown.
[0090] FIG. 2B shows RSR device 200 according to an embodiment of
this invention which allows for control of the orientation of the
reservoir area for collection of respiratory secretions. In order
to retain the secretions, it is important that these secretions are
unlikely to exit the reservoir area of the main housing 206 and
unlikely to drain back into the patient's airway. Thus the ability
to position the reservoir in a dependent orientation is an
important feature of this invention. As the patient may be moved,
it is advantageous to have a device which allows the orientation of
the reservoir to move without disconnecting the device which would
open the airway and allow possible contamination of the airway. A
sputum trap that is insensitive to orientation has the disadvantage
of an increased dead air space, and thus creates an added burden
for CO2 removal during respiration.
[0091] FIG. 3A illustrates others embodiment of an RSR device
according to an embodiment of the present invention. In FIG. 3A,
RSR device 300 is shown as a cross-sectional schematic. Patient
airway port 302 allows for connection to artificial airway 102
typically with a 15 mm male connector via swivel connector 304.
Ventilation source port 306 is shown with a 90 degree angled arm
308, which can rotate according to one configuration of the present
invention, and is shown linked to a corrugated tubing 310 via
swivel fitting 312. Ventilation source port 306 also can have a
swivel.
[0092] Suction access ports 314 and 318 are plugged when not in
use, as shown by plug 320 which seals port 318 in FIG. 3A, and plug
322 sealing port 314 in FIG. 3B. Access port 314 allows for the
introduction of a suction catheter 316 that may suction the
artificial airway 102 as illustrated in FIG. 3A, or may be used for
the introduction of another instrument such as a bronchoalveolar
lavage tube. Access port 318 allows for introduction of a suction
catheter 316 as shown in FIG. 3B or for the introduction of another
instrument such as a needle for example for removal of collected
respiratory secretions which may collect in the reservoir area 324.
In a variation of this device (such as described in FIG. 11A) a
fitting for closed suction may be attached. Swivel connectors 304
and 312 allow for control of orientation of the RSR device 300.
[0093] FIGS. 3A and 3B also illustrate spill guards 326, which
extend from the inner wall of the RSR device 300, and help prevent
unintended emptying of the liquid contents of the reservoir back
into the artificial airway or into the gas delivery limb in the
case of movement or change in position.
[0094] FIGS. 4A, 4B and 4C show cross-sectional schematic
illustrations of another RSR device according to a certain
embodiment of this invention, and each illustration shows a
different conformational position of RSR device 400.
[0095] FIG. 4A is a cross sectional view of an RSR device 400
having a 3 sections which can rotate in reference to each other.
RSR device 400 includes a patient interface section 402, a middle
section 404 with a diverter 408, and a ventilation source section
406. FIG. 4A shows RSR sections 402, 404 and 406 in their typical
use conformational orientation. RSR device 400 changes its
conformation by changing the rotation positions of the sections
402, 404 and 406. RSR device 400 is configured so that the interior
walls form a gas flow chamber, and a reservoir area for retained
respiratory secretions.
[0096] The diverter 408 is configured to redirect the gas flow and
to separate respiratory secretions that may be expelled during
exhalation. Diverter 408 is disposed substantially perpendicular to
the inflow path of the artificial airway 102. The diverter acts as
an obstacle in the expiratory fluid pathway. As the respiratory
secretions have more mass, and thus more momentum, they do not flow
around the tortuous flow path created by the diverter as easily as
the lighter gases in the exhalation, and are more likely to impact
the surface of the diverter and the interior of the housing, to
lose velocity and thus be separated from the gas flow. The fluid
flow through the RSR devices also slows as a result of the widening
of the cross-section of the flow path within the housing where the
flow chamber is formed. This also decreases the momentum and acts
to separate the respiratory secretions from the gases in the
exhalation, and helps to retain these secretions within the
chamber. A simplified gas flow path for the RSR device 400 when in
the typical use position is illustrated by arrow 410.
[0097] The orientation of the reservoir area 418 helps retain the
heavier fluids in the body of the RSR device 400. A fluid line 420
is shown to help illustrate fluid in the reservoir area. The
dependent area 418 forms a reservoir for respiratory secretions.
Swivel 412 in artificial airway port 424 allows for orientation of
the RSR in relation to the artificial airway 102. An RSR device may
also be configured with a swivel on the ventilator source section;
however a swivel is not usually required on the ventilation source
end of the RSR device 400 where it attaches to ventilation port 424
for use with a closed suction device 106, as the closed suction
device typically contains its own swivel 110.
[0098] Also illustrated are spill guards 414 and 416, which show
that the inlets to the connection ports from the inner housing of
the RSR are configured to prevent the efflux of the retained
secretions. Spill guards 414 and 416 advantageously prevent
respiratory secretions and liquids from leaving the RSR device 400
and entering the HME, the breathing circuit and/or the artificial
airway. Accordingly, the spill guards 414 and 416 help prevent
egress of collected airway fluids into respiratory instruments when
the patient turns or moves for example, and makes the device less
susceptible to egress of retained fluids with movement of the
patient.
[0099] In FIG. 4B, middle section 404 is shown rotated 180 degrees
in relation to the typical use conformational position of sections
402 and 406. This allows diverter 408 to move out of a direct path
between the ventilation source port 422 and the artificial airway
port 424. As further illustrated in FIG. 4B, this conformational
positioning allows the suction catheter 108 of the closed suction
device 106 attached to the ventilation source port 422 to be
advanced through the body of RSR 400 and into the artificial airway
102 for suctioning. After suctioning of the artificial airway,
catheter 108 can be withdrawn into the closed suction device 106
and the RSR device 400 can be returned to it typical use
conformational alignment. Other instruments such as a bronchial
alveolar lavage device may also be passed through the RSR device in
a similar manner.
[0100] In FIG. 4C, the ventilation source section 406 of RSR device
400 is shown rotated 180 degrees with relation to the typical use
position of sections 402 and 404. This allows the suction catheter
108 of the closed suction device 106 to be advanced into the
reservoir area 418 of the body of RSR device 400 for suctioning and
evacuation of retained fluids. After clearing the retained
respiratory secretions from the reservoir area, catheter 108 can be
withdrawn into the closed suction device 106 and the RSR device 400
can be returned to it typical use position conformational
alignment.
[0101] FIG. 5A is a schematic illustration of another RSR device
according to a certain embodiment of this invention that
illustrates a diverter 506 placed in the path of the gas flow,
which allows for the passage of a suction catheter through the
diverter 506. The arrow 508 in FIG. 5A shows the flow pattern of
respiratory gasses through the chamber formed by the housing of RSR
device 500 when it is in its typical conformational position for
use for retaining respiratory secretions from exhaled respiration.
Respiratory secretions are indicated by fluid line 510 where the
housing of RSR device 500 acts as a reservoir area. The housing of
device 500 has two main chamber sections. The patient interface
section 502 is on the artificial airway side, and the ventilation
source section 504 is on the ventilation source side. These two
sections may have a circular cross section and are configured so
that they are rotatably connected to one another.
[0102] In FIG. 5A section 502 is shown with a respiratory gas
diverter 506 attached to a portion of the inner wall of device 500.
Diverter 506 features an orifice 512. Orifice 512 is shown with a
funnel shape which can act as an instrument guide for helping pass
an instrument, such as suction catheter (108) through this orifice
as shown in FIG. 5B. A valve 514, shown here as a flap valve,
closes orifice 512 and limits expiratory flow from passing through
the orifice 512, but allows the passage of an instrument as shown
in FIG. 5B. In alternative embodiments, a valve may not be required
as orifice 512 may be sized small enough such that it limits the
passing of expiratory flows and secretions
[0103] FIG. 5B illustrates RSR device 500 during the use of an
instrument intended to enter the artificial airway. Valve 514 is
shown in the open position, held open by suction catheter
instrument 108, extending from a closed suction device 106. Other
instruments such as a bronchial alveolar lavage catheter may also
be used.
[0104] FIG. 5C illustrates RSR device 500 in a second
conformational position. The two main chamber sections 502 and 504
are shown rotated 180 degrees in relationship to each other. This
conformational arrangement allows the suction catheter 108 to be
used to remove retained fluids and other respiratory secretions
from the RSR device 500 which have collected in the reservoir
area.
[0105] FIG. 5B further illustrates spill guards 518 and 520, which
can be included in RSR devices according to certain configurations
of this invention. The spill guards 518, 520 advantageously prevent
respiratory secretions and liquids from leaving the RSR device 500
and entering the HME, breathing circuit, or the patient's
artificial airway. Accordingly, the spill guards 518 and 520 help
prevent egress of collected airway fluids into respiratory
instruments or into the artificial airway, for example when the
patient turns or moves. FIG. 5C also marks a swivel 522 in the
artificial airway port connector.
[0106] FIGS. 6A, 6B and 6C show schematic illustrations of various
additional designs for diverters which allow for the passage of a
suction catheter through the diverter portion of RSR devices
according to certain configurations if this invention. FIG. 6A
shows a cross-sectional illustration of a two-stage diverter. A
first stage 602 of the diverter 600 is on the artificial airway
port side of the diverter. Multiple slits 604 are shown perforating
the first stage 602 of the diverter shown in the configuration of a
star shaped, although various forms may be used within the concept
of this invention. The first stage 602 may be thin at the center to
decrease resistance and help guide passage of an instrument such as
a suction catheter through the first stage. The first stage may use
material which is flexible and allow deformation so that wedged
shaped areas 606 formed by the perforations can bend out of the way
of an instrument being passed through this stage of the diverter.
The first stage 602 of the diverter 600 can be replaced with a
simple flap 514, as is shown in FIG. 5A.
[0107] Diverter 600 has a second stage 608. Second stage 608 may
have a larger outer diameter than the first stage 602 to enlarge
the area of respiratory gas flow diverted. The second stage 608 of
the diverter 600 is on the ventilation source side of a RSR device
Second stage 608 may have a funnel shape which can act as a guide
for directing an instrument, such as a suction catheter, through
the diverter.
[0108] FIG. 6B shows a diverter 610 with a star-shaped perforation.
Other shapes, sizes and patterns of perforations could be utilized
in different embodiments. FIG. 6C illustrates a diverter 620 with a
funnel shaped outer ring 622, and a hinged flap valve 624. This
diverter outer ring can have a sloped wall 622, which can help
guide an instrument. These illustrations are not meant to in any
way limit the type of diverter, which may be used to divert
secretions or which can be used to allow an instrument to pass
through this area of the RSR device, but rather to show some of the
possible configurations. A diverter may have one or more stages and
the stages may be of similar or different designs.
[0109] FIGS. 7A, 7B, 8A and 8B are schematic illustrations
constructed in accordance with a further embodiment of the present
invention showing an RSR device which allows conformational changes
of the device.
[0110] FIG. 7A shows a perspective view of a configuration of
another embodiment of the invention. RSR device 700 has a connector
710 which allows connection to an artificial airway port and a
connector 720 that allows connection to a ventilation source. In a
preferred configuration these connectors are standard 15 mm
respiratory connectors. In embodiments, connector 710 is a female
15 mm swivel fitting and connector 720 is a male 15 mm fitting
which can accept connection to a closed suction device or to a
ventilator circuit. RSR device 700 has a ventilation housing 705.
Housing 705 has a reservoir portion 750 for collecting secretions.
Reservoir 750 can be integral to housing 705 or a separate
component. Reservoir 750 may be suctioned through the ventilation
housing or may be suctioned through a separate port in the
reservoir itself. In embodiments, housing 705 can be flexible by
being constructed of a non-rigid material, having thin walls, or by
other means known to achieve flexibility. A flexible ventilation
housing allows for a conformational change in terms of the
alignment of the connector 720 with certain other parts of the
structure of the RSR device 700. This conformational change may be
achieved through methods such as rotation, bending, translation,
etc. A bellows area 715 in the ventilation housing 705 is shown as
a way to implement a conformational change.
[0111] FIG. 7A RSR device 700 can include a support structure 725.
Support structure 725 can interface with connector 710, connector
720 and/or ventilation housing 705. Support structure 725 can be
integral to one of these components, such as connector 710. In
embodiments, support structure 725 can contain a track 736 for
interacting with key 735 to allow the RSR device 700 to be held in
at least two different conformational positions. Key 735 may extend
from connector 720 on a support arm 740. Key 735 can move through
track 736. In another embodiment, a key feature or its mating
detail in the support structure 725 can deflect to allow for
movement and placement into different conformational positions.
Various techniques such as tracks, snaps, ratchets, detents, etc.
are known for maintaining conformational positions. Support
structure 725 also can have a cage 730. Cage 730 can protect a
reservoir portion 750 of the housing 705 from inadvertent
compression, while allowing for compression with finger pressure,
for example, when desired by the user to help evacuate the contents
of the reservoir 750.
[0112] FIG. 7A shows RSR device 700 in a straight position, which
would be used when the device is in normal use, and during
suctioning of the artificial airway with a closed suction unit, or
when introducing an instrument into the artificial airway as shown
in a cutaway view in FIG. 7B.
[0113] FIG. 8A shows device 700 in a secondary position. In the
secondary position, the control key 735 is in a secondary position
and the bellows area 715 section of ventilation housing 705 is in a
flexed position. This secondary position allows a suction catheter
to be inserted into the reservoir area 750 for evacuation of the
pooled secretions as shown in FIG. 8B. The reservoir area 750 may
be made of a flexible material and may be squeezed by the operator
during suctioning to help remove collected respiratory
secretions.
[0114] FIG. 7B shows a cutaway view of RSR device 700. The catheter
108 can be seen supported by instrument guide 760, and passing
through the second stage 608 of diverter 600, which also acts as an
instrument guide due to its funnel like shape. The catheter then
passes through the first stage 602 of the diverter 600 which acts
as a valve, diverting respiratory secretions when closed but
allowing passage of the instrument.
[0115] FIGS. 8A and 8B show the position for the RSR device in a
secondary conformational position for use during suctioning of the
reservoir.
[0116] FIG. 8B illustrates the RSR device 700 in a cross-sectional
view in a secondary conformational alignment which may be used to
remove respiratory secretions 820 from reservoir 750 using an
instrument such as closed suction catheter 108. Catheter guide 760
can help guide a flexible instrument.
[0117] FIG. 9 is a cross-sectional schematic illustration in
accordance with a certain embodiment of the present invention
configured with a connector 920 shown as a Christmas tree or male
barbed connector, for connection directly to an endotracheal tube
930. The connector 920 may also connect to the endotracheal tube
without the barbs. This configuration replaces the fitting commonly
used as the attachment to artificial airway as shown herein in
other illustrations, for example the male fitting of artificial
airway 102 and port 302 as illustrated in FIG. 3A. A connector such
as shown in FIG. 9 allows the RSR device to be integrated as a
single unit with the patient artificial airway. FIG. 9 also
illustrates that connector 920 can act as a swivel within housing
section 925 which allows the device to be rotated in relation to
the endotracheal tube. This allows for positioning of the reservoir
area of the RSR in a dependent orientation, and also decreases the
strain and traction of the artificial airway upon the patient.
[0118] In other embodiments, the RSR device 900 can be directly
attached to a tracheotomy tube, as RSR device 900 functions to
replace the adapter that is standard with ET and tracheotomy tubes.
In embodiments, RSR device 900 can be packaged and sterilized with
the artificial airways.
[0119] FIGS. 10A and 10B are yet other schematic illustrations of
RSR device embodiments according to the present disclosure where
the respiratory inflow tract enters at the patient end of the RSR
device, and the exhaled gasses pass through the RSR device. This
has the added advantage of greatly reducing the volume of dead air
space while still providing a larger reservoir. This inspiratory
bypass that allows a larger reservoir area, and can be used alone
or in combination with valves to prevent efflux of respiratory
secretions back into the airway. FIG. 10A illustrates an RSR device
1000 similar to device 200 shown in FIG. 2A. FIG. 10B illustrates
an RSR device 1060 similar to RSR device 500. In FIG. 10A, the gas
supply enters through delivery port 1020 close to the artificial
airway. In device 200, the gas flow is bi-directional and reverses
direction during the respiratory cycle. In contrast, in device 1000
flow though the RSR body passes in one direction; away from the
patient. Arrow 1015 illustrated the direction of delivery of
respiratory gas to the subject from the delivery arm of the
ventilator circuit. During expiration breath passes through the RSR
device 1000 as shown by arrow 1025 and into the exhalation arm of
the ventilator circuit.
[0120] In FIG. 10B, the gas supply enters the RSR device through
delivery port 1020 and flows to the subject near to the artificial
airway 102 as shown by arrow 1055. In similar device 500, the gas
flow is bi-directional and reverses direction during the
respiratory cycle. In contrast, in RSR device 1050, flow thought
the RSR body passes in one direction; away from the patient, as
shown by arrow 1065, and flows towards expiratory port 1010.
[0121] Another advantage to having a gas inflow tract on the
patient side is that if the reservoir side is opened for
suctioning, negative pressure is unlikely to occur, and there is
less likelihood of patient contamination from the environment.
Alternative to having a patient end inflow port configured integral
into the RSR, a Tee can be added on the patient end which is placed
between the artificial airway and the RSR device. A disadvantage of
this that the suction catheter must be extended further to suction
the artificial airway.
[0122] FIGS. 11A and 12A illustrate additional embodiments of the
current invention, wherein closed suction allows clearance of
respiratory secretions from the artificial airway and from the RSR
device. FIG. 11A shows a RSR device 1100 with an integrated closed
suction catheter. In RSR device 1100, a suction catheter 1116 can
be connected by a fitting 1114. Fitting 1114 allows the suction
catheter 1116 to be advanced and withdrawn into and through the
body 1122 of RSR device 1100. Fitting 1114 also can pivot to allow
the catheter 1116 to enter into the artificial airway for
suctioning as shown in FIG. 11B or to enter the reservoir area 1118
for evacuation of accumulated respiratory secretions from the RSR
device as illustrated in FIG. 11C. Catheter 1116 is sealed within a
protective sheath 1124, which is only partially visible in FIGS.
11A, 11B and 11C. Sheath 1124 is flexible and allows the catheter
to be advanced into and retracted from the housing of the RSR
device, and prevents contamination of the catheter from the
external environment.
[0123] FIG. 12A illustrates yet another embodiment of the invention
showing an RSR device with an integrated fitting for a closed
suction connection. Device 1200 is configured to attach to
artificial airway 102 with connector port 1202. A swivel connector,
such as 1204 allows a connection, which places less stress on the
artificial airway. Stress on the artificial airway may be injurious
to the patient, may cause damage to the trachea, and may induce
leaking of seal of the balloon of the endotracheal balloon. This
may allow upper airway secretions to enter the lung, which is
considered to be a risk factor for ventilator associated
pneumonia.
[0124] FIGS. 12A and 12B show a gas flow path diverter 1206.
Diverter 1206 contains a valve 1208 and bevels 1210 which act an
instrument guide. A suction catheter 108 is illustrated in FIG. 12B
through the diverter. The diverter 1206 is shown as being supported
by support arms 1212. In other configurations, the diverter could
be attached to an interior wall, a swivel connector, or to the
ventilation source side of the RSR device.
[0125] FIGS. 12B and 12C show device 1200 illustrated with a
fitting 1214 to allow for connection to a closed suction device
106. The fitting 1214 is designed to allow flow of gas. Fitting
1214 can pivot to allow the catheter 108 to enter into the
artificial airway for suctioning as shown in FIG. 12B or to enter
the reservoir area 1216 for evacuation of accumulated respiratory
secretions from the RSR device 1200 as illustrated in FIG. 12C. The
catheter 108 would be withdrawn into the closed suctioning device
during its typical use.
[0126] FIG. 13 illustrates yet another embodiment of an RSR device
according to the present invention. RSR device 1300 is configured
to fit to a tracheostomy tube 1350. A connector 1302, e.g., a
swivel connector, is shown in FIG. 13A which allows orientation of
the reservoir area 1320 in a dependent position for collection of
respiratory secretions. In contrast to having a single gas flow
vent (e.g., exhalation port) configured to couple with another
device, device 1300 is an example of a configuration of an RSR
device with multiple perforations or vents 1304 for direct flow to
and from the device to the atmosphere. Vents are illustrated on the
anterior surface, but can be on other surfaces. The anterior and
upper portion is shown containing heat and moisture exchange (HME)
material 1306 which acts as a filter helping to protect the
patient's airway from airborne pathogens. The HME material also
acts to capture heat and humidity from the patient's exhaled
breath, and release it back to the patient upon inhalation, thus
avoiding drying of the airways and avoiding energy loss from the
patient. A large total vent area is advantageous in that it
provides low flow resistance and efficient heat and moisture
exchange. FIG. 13B illustrates that within device 1300, an airflow
diverter wall 1308 helps capture respiratory secretions and guide
them towards the reservoir area 1310 and towards the lower internal
surface of the housing. Diverter wall 1308 helps to separate
respiratory secretions from the gas flow. RSR device 1300 also has
spill guards 1312 which help retain secretions in the reservoir
area and help prevent spillage of retained respiratory secretions
in the event that the patient's position is moved.
[0127] The exhaled breath flows first towards the deflector and
then flows through the HME material 1306 where heat and moisture is
captured and the remaining exhaled gas can pass to the atmosphere
through vents 1304. On inspiration, atmospheric gas enters through
vents 1304 is filtered, heated and humidified before flowing into
the patient airway.
[0128] The device in FIG. 13B shows an orifice 1318 with a cap 1314
on the front surface of device 1300 which may be opened if
suctioning is desired. Deflector wall 1308 is illustrated in FIG.
13B with a valve 1316 that allows a suction catheter or other
instrument to be introduced into the artificial airway 1350 with
access being given by opening cap 1314. In certain embodiments, RSR
device 1300 may be configured so that a suction catheter or other
instrument may be directed to enter reservoir area 1310. This
allows for removal of respiratory secretions from the device. In
other configurations, the RSR device 1300 can be configured without
these features.
[0129] Not shown in the illustration, the cap may cover a second
valve at the surface of the RSR device 1300. Such a valve would
help prevent sputum from entering the room during suctioning, and
limit inhalation of unfiltered air. Valve 1316 can have, for
example a conformation similar to valve 610 shown in FIG. 6B. In
another embodiment, the device can be made with a valve without a
cap. In a configuration of the invention, one or more valves can be
configured as an anti-asphyxiation valve which would open in the
case that the resistance to flow through HME material and surface
vents became higher than desirable.
[0130] Device 1300 may be preferentially constructed with a housing
made of a flexible material, such as silicone, to make wearing the
device more comfortable for the patient. The device may also be
configured so that it may be cleansed and the HME material or HME
section may be replaced.
[0131] FIG. 14 illustrates another embodiment of an RSR device 1400
according to the present invention. Housing 1405 has a patient port
1420 for connection to an artificial airway and a ventilation port
1430 for connection to a closed suction device and/or ventilation
source (not shown). The ports can have swivel connectors to
facilitate orientation of the RSR device. Housing 1405 also has a
reservoir 1450 for collection of respiratory secretions. Opening
1490 allows secretions to enter the reservoir as they pass through
the housing. The opening may be sized large enough to maximize the
entry of the secretions. Features such as a diverter, which were
described in other embodiments of this invention, can also be
located in RSR device 1400 to further separate secretions from the
gas flow and direct them into the reservoir. The RSR device 1400
may be disposed of with the contained secretions, or the secretions
may be removed by a variation of methods such as removing the
reservoir, draining the reservoir, or suctioning the reservoir
and/or housing, etc. In embodiments, the reservoir may be flexible.
A flexible reservoir may be collapsed, for example by squeezing, or
translated into the housing in order to move the secretions into
main section of the housing. Once the secretions are moved there,
the secretions may be removed, for example by a suction catheter
1410.
[0132] FIG. 15A illustrates a RSR device 1500 similar to RSR device
1400. Housing 1505 can include a diverter 1520 as shown. Housing
1505 further can include a flexible portion 1570 with a guide 1580.
The flexible portion 1570 can provide the guide to translate with
respect to the interior of the housing. In FIG. 15B, a suction
catheter 1510 is shown passing through the housing in order to
suction an artificial airway of a patient. In FIG. 15C, the guide
is shown translated further into the housing and therefore
directing the suction catheter into a reservoir 1550 in order to
remove secretions.
[0133] FIG. 16A illustrates a RSR device 1600 similar to RSR device
1400. Housing 1605 has a diverter 1620 as shown. Housing 1605 has a
guide 1680 that can direct an instrument, such as a suction
catheter, towards the diverter or towards a reservoir 1650. Guide
1680 can be integral to housing 1605 or it could be a separate
piece. If a separate piece, guide 1680 may pivot within housing
1605 allowing for increased directional control of a suction
catheter. A pivoting guide may extend through the housing in a
sealed manner to allow a user to externally control the angle of
the guide. An external knob or similar detail could be attached to
the extended part of the guide to allow the user to pivot the
guide. In FIG. 16B, a suction catheter 1610 is shown passing above
the guide in the housing in order to suction an artificial airway
of a patient. In FIG. 16C, a suction catheter 1610 is shown passing
below the guide directing the suction catheter into a reservoir
1650 in order to remove secretions.
[0134] FIGS. 17A and 17B illustrate another embodiment of and RSR
device 1700 according to the present invention. Housing 1705 has a
patient port 1720 for connection to an artificial airway and a
ventilation port 1730 for connection to a closed suction device
and/or ventilation source (not shown). The ports may have swivels
to facilitate orientation of the RSR device. Housing 1705 also has
a reservoir 1750 for collection of respiratory secretions. The
reservoir 1750 may be flexible or have a flexible extension, which
allows the size of the reservoir to be controlled. Features such as
a diverter, which were described in other embodiments of this
invention, may also be located in the RSR device 1700 to further
separate secretions from the gas flow and direct them into the
reservoir 1750. A drain or vacuum port 1760 may be included which
allows for emptying the contents of the reservoir. In one
embodiment, a RSR device 1700 can include a drain port 1760 and a
fluid instillation port 1765. Instillation port 1765 can be used to
instill saline or other fluid to help clear the respiratory
secretions which have collected in the reservoir, especially if
these secretions are thick or tenacious.
[0135] A clip 1770 can be applied to the reservoir 1750 to divide
the volume of the reservoir to an upper area 1752 above the clip
1770 and a lower area 1754 below the clip 1770. A smaller reservoir
volume is advantageous to limit dead space volume, especially for
example in smaller patients and in patients with certain
respiratory diseases. A larger reservoir volume is advantageous to
allow for less frequent clearing of the secretions in the RSR
device 1700. The position of the clip 1770 may be adjustable on the
reservoir and therefore limiting the volume in the upper area 1752
as desired by the user.
[0136] As shown in FIG. 17B, clip 1770 could be removed and then
attached above the fluid instillation port 1765, allowing the
reservoir to be cleared while maintaining a minimum deadspace in
the upper area 1752, maintaining a closed air circuit, and
preventing the patient from experiencing the effects of the
clearing, such as with a vacuum. When the reservoir 1750 begins to
fill with respiratory secretions during use, the clip position may
be adjusted to enlarge the upper area 1752. The clip 1770 also can
be removed to allow the secretions to pool in the lower area 1754
of the reservoir, and then the clip may be reattached to again
limit the reservoir volume. The clip 1770 could then also be used
as a tool to force the secretions lower into the lower area 1754 of
the reservoir. The secretions now in the lower area 1754 of the
reservoir may be drained through a port 1760 or may be maintained
there until the device or reservoir is disposed.
[0137] Several other possible configurations of this invention can
easily come to mind by those skilled in the art, which are within
the scope of this invention. For example, the route for passage of
a suction catheter in most configurations may as well be used for
passage of a stylette for use in facilitating intubation, for
passage of a bronchoscope or the like. The connection port for the
artificial airway for RSR devices can have a 15 mm inner diameter
(ID); however, it could be any ID necessary to connect with various
artificial airway tubes or the like. The connection port of the
ventilation source can have 15 mm outer diameter; however, it could
be any ID necessary to connect with a ventilator circuit, closed
suction device, or similar device, or may be used open to the
atmosphere.
[0138] All RSR device embodiments of this invention could be
integrated into other components found in breathing circuits, such
as artificial airways, medical instruments (for example suction
catheters), HMEs, medication delivery devices, tubing, fittings,
etc. Tubing could also be connected between any ports described in
all RSR device embodiments of this invention and other components
found in breathing circuits. For example, tubing, such as flexible
tubing, can be connected between the RSR device and the artificial
airway and/or a HME. It is also understood that many of the RSR
device embodiments of the inventions are bi-directional and will
function to trap liquid coming from either side of the RSR device.
In fact, with slight modification, all of the disclosed embodiments
could function bi-directionally as would be apparent to one skilled
in the art.
[0139] Many of the respiratory secretion retention (RSR) devices
discussed above include an instrument port for receiving a medical
instrument, e.g., a catheter of a closed suction device, a catheter
of an open suction device, a bronchoscope, a drug delivery device,
and the like. In embodiments, the instrument port can be configured
on a RSR device so that the artificial airway is still closed to
the atmosphere even when the medical instrument is not present. For
example, plugs 320 and 322 shown in FIGS. 3A and 3B respectively
can accomplish this. Alternatively, a valve could be used to
maintain a closed system. For example, when a medical instrument is
not present, a valve can be configured so it remains in a closed
state. When a medical instrument is inserted, the valve can open to
allow the medical instrument to enter into and/or through the RSR
device. Various valve types configured to allow passage in one
direction can be utilized, e.g., a flapper valve, a check valve, a
biased valve, a pucker valve, a duckbill valve and the like. Also,
valves that open when a certain pressure is reached (i.e. "cracking
pressure") can be utilized, such as a valve that activates when
medication is introduced via a syringe that is connected to an RSR
device.
[0140] In illustration, FIG. 18A is a cross-sectional view of
another embodiment of an RSR device 1800 according to the present
invention. Housing 1802 can include an instrument port 1840 for
receiving a medical instrument, a patient port 1820 for connection
to an artificial airway and a ventilation port 1830 for connection
to a closed suction device and/or ventilation source (not shown).
Housing 1802 also can have a reservoir 1804 for collection of
respiratory secretions. In embodiments, housing 1802 can be similar
to housing 705 of RSR device 700 to allow for conformational change
in terms of the alignment of the instrument port 1840 with certain
other parts of the structure of the RSR device 1800. RSR device
1800 further can include a valve 1842 located in the instrument
port 1840. In FIG. 18A, the valve 1842 is shown in a closed
position or state. FIG. 18B illustrates a medical instrument 1812,
e.g., a closed suction device connected to the instrument port
1840. FIG. 18C illustrates catheter 1810 of the closed suction
device 1812 inserted through valve 1842. Valve 1842 is shown in an
open position or state. Referring again to FIG. 18B, RSR device
1800 also can have a fluid instillation port 1862. Fluid may be
instilled through port 1862 to lavage or clean a portion of the
medical instrument 1812, such as a portion of catheter 1810 of a
closed suction device 1812. Closed valve 1842 prevents the fluid
from entering portions of the RSR device that are closed to the
atmosphere during this cleaning process. Referring again to FIG.
18A, ventilation port 1830 could be at an angle, for example 45 or
90 degrees, or could be parallel to the patient port 1820. Any of
the ports 1820, 1830, or 1840 could have swivels as discussed in
previous RSR device embodiments. Features such as a diverter, which
were described in other embodiments of this invention, may also be
located in the RSR device 1800 to further separate secretions from
the gas flow. Features and methods for clearing an RSR device of
respiratory secretions described in other embodiments of this
invention, drain ports, and/or or suction ports may also be located
in the RSR device 1800. Also, other RSR device embodiments
discussed in the present invention could have a valve, a fluid
instillation port, and/or ventilation port.
[0141] FIG. 19A illustrates another embodiment of an RSR device.
RSR device 1900 can include a housing 1902, which can include a
patient port 1920, a ventilation port 1930, an instrument port 1940
and a rotatable housing section 1904. All three ports 1920, 1930
and 1940 can have swivel connectors. The instrument port 1940 can
include a control valve 1942, as described in other embodiments,
which controls access to reservoir 1950 and maintains a closed
system to atmosphere. The patient port 1920 and the ventilation
port 1930 are configured to extend sufficiently far into reservoir
1950 of RSR device 1900 to prevent the unintended emptying or
displacement of liquid contents from the reservoir 1950 into an
artificial airway of a patient or into the ventilation delivery
branch or limb. In FIG. 19A, the ventilation port 1930 and the
instrument port 1940 are shown parallel to each other. The
instrument port 1940 and the patient port 1920 can be aligned so a
medical instrument 1910 can enter into the reservoir 1950 of RSR
device 1900 and travel through to the patient port 1920. Instrument
port 1940 can be repositioned as shown in FIG. 19B, to enable a
medical instrument 1910 to enter the reservoir 1950 at a different
angle. The different angle can facilitate the removal of the fluid
contents 1956 by use of medical instrument 1910, such as a suction
catheter. FIG. 19C further illustrates a cross-sectional
perspective view of RSR device 1900. The rotatable housing section
1904 can include a first connecting section 1906 and a second
connecting section 1908. In operation, as rotatable housing section
1904 is rotated downward from a first position to a second
position, the two connecting sections 1906 and 1908 maintain a
sealed connection with the inner wall of housing 1902. The sealed
connection will insure that no fluid contents 1956 escape from
reservoir 1950.
[0142] FIG. 20A illustrates another embodiment of an RSR device.
RSR device 2000 can include a housing 2002, which can include a
patient port 2020, a ventilation port 2030 and an instrument port
2040. All three ports 2020, 2030 and 2040 can have swivel
connectors. The instrument port 2040 can include a control valve
2042 as described in other embodiments. The patient port 2020 and
the ventilation port 2030 are configured to extend sufficiently far
into reservoir 2050 of the RSR device 2000 to prevent the
unintended emptying or displacement of liquid contents from the
reservoir 2050 into an artificial airway of a patient or into the
ventilation delivery branch. Patient port 2020 and ventilation port
2030 may be on the same plane as shown in FIG. 20A or may be on
different planes similar to the patient and ventilation ports of
RSR device 1900. In this embodiment, it is preferred that the
ventilation port 2030 and the instrument port 2040 be angled
relative to each other to allow adequate clearance between a
medical instrument 2012 and a ventilator circuit (not shown). This
angle may facilitate the setup of the ventilator circuit. For
example, as illustrated in FIG. 20A, the ventilation port 2030 and
the patient port 2020 are at a substantially 90 degree angle of
orientation to each other. The instrument port 2040 and the patient
port 2020 can be aligned so the medical instrument 2010 could enter
into RSR device 2000 and move through the patient port 2020. FIG.
20B illustrates RSR device 2000 in a tilted position, which can
allow the fluid contents 2056 to shift towards the instrument port
2040. A catheter 2010 of suction device 2012 is illustrated
removing the fluid contents 2056 from the reservoir 2050. If
additional secretions enter the reservoir 2050 through the patient
port 2020 and splash the top surface of the fluid contents, the
angled relationship between the ventilation port 2030 and the
patient port 2020 makes it less likely that any liquid contents
will splash into the ventilation port 2030. In embodiments, a drain
or an additional port can be included in another portion of the RSR
device 2000 to allow for further removal of the liquid contents of
reservoir 2050. In embodiments, a flexible tube (not shown) may be
connected between the patient port 2020 and the artificial airway.
In embodiments, a flexible tube (not shown) may be connected
between ventilation port 2030 and the ventilation circuit (not
shown). Flexible tubes connected to a RSR device can facilitate the
setup of the ventilator circuit, as well as facilitate
repositioning a RSR device.
[0143] Each of the RSR device embodiments described in this
specification can have a housing portion with a fitting portion.
FIG. 21 illustrates a RSR device 2100 that is similar to RSR device
1800. RSR device 2100 includes a housing portion 2102 and a fitting
portion 2104. Housing 2102 can include a patient port 2120 and a
connection port 2110. The housing 2102 is designed to retain
secretions as described in previous embodiments. In embodiments,
the patient port 2120 and the connection port 2110 can have swivel
connectors. Connected to the connection port 2110 is a fitting
portion 2104 of RSR device 2100. The fitting portion 2104 can
include an instrument port 2140 for receiving a medical instrument.
The fitting portion 2104 also can include a ventilation port 2130.
Ventilation port 2130 can be affixed to the fitting portion 2104 at
an angle, for example 30 or 90 degrees, or can be parallel to any
other port. One or more of ports 2110, 2130, 2140 on the fitting
portion 2104 can have swivel connectors as discussed in previous
RSR device embodiments. Similar to RSR device 1800, RSR device 2100
may include a valve 2142 located within the instrument port and can
include a fluid instillation port 2162. In embodiments, fitting
portion 2104 could be a separate part. In embodiments, a tube may
be positioned between or instead of the fitting portion 2104 of RSR
device 2100. Additional features such as a diverter (not shown),
which are described in other embodiments of this invention, also
can be located in the RSR device 2100 to further separate
secretions from the gas flow. FIG. 21 also illustrates a suction
tube assembly 2154 that serves as a drain port for RSR device 2100.
Suction tube assembly 2154 can be connected to a suction device to
clear the RSR device of any contained respiratory secretions.
Suction tube assembly 2154 may be capped or plugged externally (not
shown) when suction is not required. Suction tube assembly 2154,
which is mounted to housing 2102, may be repositioned by
translation, rotation, or both to facilitate removal of secretions
from reservoir 2150. Suction tube assembly 2154 may have an angled
tip portion to allow it to access different areas of RSR device
2100 when suction tube assembly 2154 is repositioned. Any
embodiment of this invention can have a drain port similar to the
suction tube assembly 2154.
[0144] FIG. 22A illustrates another embodiment of an RSR device.
RSR device 2200 can include a housing 2202, which can include a
patient port 2220, a ventilation port 2230 and an instrument port
2240. Any of the ports 2220, 2230, or 2240 could have swivel
connectors as discussed in previous RSR device embodiments. In
embodiments, housing 2202 can include a side cavity 2252 configured
to assist in the removal of liquid contents of reservoir 2250. In
FIG. 22A, the instrument port 2240 is shown in a coaxial alignment
with the patient port 2220; however, the two ports can be in a
non-coaxial alignment as well. In this embodiment, the patient port
2220 and the ventilation port 2230 are provided with pivoting
features, for example ball and socket joints, which allow for the
rotation of the housing 2202 without exerting undue stress on any
attached artificial airway tubing or ventilation tubing connected
to patient port 2220 and ventilation port 2230, respectively. For
example, as the housing 2202 is rotated downward, the side cavity
2252 translates to a substantially downward orientation, as
illustrated in FIG. 22B, and the fluid contents 2256 of reservoir
2250 collect in side cavity 2252. A medical instrument 2210, e.g.,
a suction catheter, can be inserted through the instrument port
2240 and introduced to into side cavity 2252 to allow the removal
of the liquid contents, e.g., secretions from the reservoir 2250.
In FIG. 22B, repositioning of the RSR device 2200 is actuated by
use of ball and socket joints at the patient and ventilation ports
2220, 2230. In other embodiments, repositioning can be actuated by
use of translating fittings, swivels (single axis or multiple axes)
and/or other rotational and translational mechanisms located at the
patient and ventilation ports 2220, 2230. Even though the housing
2202 is shown repositioned in FIG. 22B, the patient port 2220 and
the ventilation port 2230 are still oriented as in FIG. 22A and are
still oriented at the same angle with respect to one another. This
allows the housing 2202 to be repositioned without affecting the
artificial airway or the ventilation circuit. In embodiments,
patient port 2220, ventilation port 2230, and/or housing 2202 may
have features to maintain a desired position with respect to one
another, such as locking features, and/or features to limit range
of repositioning.
[0145] FIG. 23A illustrates another embodiment of an RSR device.
RSR device 2300 can include a housing 2302, which can include a
patient port 2320 and an access port 2330 that can function as both
a ventilation port and an instrument port. Any of the ports 2320 or
2330 could have swivel connectors as discussed in previous RSR
device embodiments. In embodiments, housing 2302 can include a
suction tube assembly 2354, which is mounted to the housing 2302
and connected to an actuation mechanism 2370, such as a knob, a
dial, a button or the like, that provides for repositioning of the
suction tube assembly 2354 within the housing 2302 by rotation,
translation or other means of motion. Referring again to FIG. 23A,
a medical instrument 2310, e.g., a catheter, passes through a
passage 2372 of the suction tube assembly 2354 and through the
patient port 2320 into an artificial airway. In a second position,
the catheter 2310 can couple with a suction tube portion 2374 of
the suction tube assembly 2354 such that suction is directed to the
bottom of the reservoir 2350 to drain the fluid contents 2356. In
embodiments, suction tube portion 2374 could have a funnel shaped
entrance to facilitate entry of the catheter. In embodiments,
suction tube portion 2374 could have a valve or membrane that seals
around the catheter when it is inserted into the suction tube
portion. FIG. 23B illustrates the suction tube assembly 2354
positioned to suction the reservoir 2350. Suction tube assembly
2354 and/or actuation mechanism 2370 may be locked into a certain
position(s) if desired.
[0146] FIG. 24 illustrates another embodiment of an RSR device. RSR
device 2400 can include a housing 2402, which can include a patient
port 2420 and an access port 2430 that can function as both a
ventilation port and an instrument port. Any of the ports 2420 or
2430 could have swivel connectors as discussed in previous RSR
device embodiments. In embodiments, housing 2402 can include a
suction tube assembly 2454, which is mounted within the housing
2402. Referring to FIG. 24A, a medical instrument 2410, e.g., a
catheter, passes through a passage 2456 (FIG. 24B) and a valve 2442
of the suction tube assembly 2454 and through the patient port 2420
into an artificial airway. In a second position, as illustrated by
FIG. 24B, the catheter 2410 can couple with a suction tube fluid
removal portion 2458 of the suction tube assembly 2454 such that
suction is directed to the bottom of the reservoir 2450 to drain
the fluid contents 2456. In this embodiment, the medical instrument
2410 is not extended through the valve 2442, which remains closed,
but is seated near the top of the suction tube fluid removal
portion 2458 to suction the fluid contents 2456 of reservoir 2450.
Suction tube assembly 2454 could have at least one additional valve
or membrane 2444 that seals around the catheter when it is inserted
into the suction tube assembly. In embodiments, suction tube
assembly 2454 could have a funnel shaped entrance to facilitate
entry of the catheter. An additional port may be included in the
RSR device to remove secretions.
[0147] FIG. 25A illustrates another embodiment of an RSR device.
RSR device 2500 can include a housing 2502, which can include a
patient port 2520 and an access port 2530 that can function as both
a ventilation port and an instrument port, and a tube 2560
coaxially aligned and positioned between the patient port 2520 and
the access port 2530. Any of the ports 2520 or 2530 could have
swivel connectors as discussed in previous RSR device embodiments.
Tube 2560 can include a diverter 2514 that is attached to an inner
bottom wall at a hinge point 2516 to the tube 2560. In embodiments,
diverter 2514 can attach along any portion of the inner wall of
tube 2560 at any hinge point or points. The tube 2560 further can
include a first opening or aperture 2562 and second opening or
aperture 2564 in the top and bottom walls, respectively, of tube
2560. First aperture 2562 and second aperture 2564 can be located
near the midpoint of tube 2560 on opposing walls. In embodiments,
the apertures could be located at any point and on any wall of tube
2560 as long as the apertures are on different sides of the
diverter. As illustrated in FIG. 25A, the flow diverter 2514 is in
a first position, where the fluid expirations from the patient port
2520 can strike flow diverter 2514 and exit tube 2560 via second
aperture 2564 into reservoir 2550 where the liquids are retained
while the gases flow around the outside of tube 2560 and reenter
tube 2560 via first aperture 2562, and then flow on to access port
2530. FIG. 25B illustrates when a medical instrument 2510, e.g., a
catheter, is inserted into access port 2530, to pass through tube
2560, the catheter can force the flow diverter 2514 into an open
position allowing the medical instrument to access patient port
2520 and any artificial airway connected to patient port 2520. In
embodiments, patient port 2520 and access port 2530 are coaxially
aligned. In embodiments, flow diverter 2514 can be pushed into an
open position via a manual operation. Manual operation could be
accomplished by a button, switch, knob, or other means of
mechanical operation. By pushing the flow diverter into an open
position or going through the flow diverter, a medical instrument
2510, e.g., a suction catheter can be passed from the access port
2530 into the artificial airway. In embodiments, the flow diverter
2514 can also be configured in such a way so as to allow the
medical instrument 2510 to pass through it as discussed in previous
embodiments. For example, diverter 2514 could be a valve. In
embodiments, the diverter 2514 may redirect the medical instrument
into the reservoir 2550, for example to suction the reservoir of
retained secretions. Other features and methods for clearing an RSR
device of respiratory secretions described in other embodiments of
this invention, including drain ports and/or or suction ports may
also be located in the RSR device 2500.
[0148] FIG. 26A illustrates a cross-sectional perspective view of
another embodiment of an RSR device. RSR device 2600 can include a
housing 2602, which can include a patient port 2620, a ventilation
port 2630, and an instrument port 2640. Any of the ports 2620,
2630, or 2640 could have swivel connectors as discussed in previous
RSR device embodiments. In embodiments, housing 2602 can include a
suction tube assembly 2654, which is mounted to the housing 2602
and connected to an actuation mechanism 2670, such as a knob, a
dial, a button or the like, that provides for repositioning of the
suction tube assembly 2654 within the housing 2602 by rotation.
FIGS. 26B and 26C illustrate cross-sections through the patient
port 2620. Referring to FIG. 26B, a medical instrument 2610, e.g.,
a catheter passes through a passage 2672 of the suction tube
assembly 2654 and through the patient port 2620 into an artificial
airway. In a second position as illustrated in FIG. 26C, the
catheter 2610 can couple with a suction tube portion 2674 of the
suction tube assembly 2654 such that suction is directed to the
bottom of the reservoir 2650 to drain the fluid contents 2656. FIG.
26C illustrates the suction tube assembly 2654 rotated relative to
its position in FIG. 26B in order to suction the reservoir 2650.
Suction tube assembly 2654 and/or actuation mechanism 2670 may be
locked into a certain position(s) if desired.
[0149] In the position illustrated in FIG. 26B, the suction tube
assembly 2654 itself also can function as a diverter to further
separate secretions from the gas flow. In all embodiments of this
invention that have a feature to divert secretions from the gas
flow, an actuation mechanism such as actuation mechanism 2670 could
be provided to the RSR device to allow for repositioning of the
diverter feature. For example, RSR device 1600 has a diverter 1620
that is shown in the gas flow path. An actuation mechanism may be
connected to diverter 1620 that allows the diverter to be
repositioned to a new position where it is not in the gas flow
path. This new position could facilitate the insertion of a medical
instrument through the RSR device by allowing the medical
instrument to go around diverter 1620 instead of through diverter
1620.
[0150] As previously discussed, all of the RSR device embodiments
in this invention may be located at any point in the breathing
circuit in order to protect either the downstream (towards the
patient) or upstream (towards the ventilation source) circuit
components from patient secretions or any other liquid in the
circuit. For example, a RSR device can be placed between a closed
suction system and an HME or ventilator circuit, as illustrated in
FIG. 27A. RSR device 2700 is connected between closed suction
system 2706 and HME 2708. It is understood that the RSR device can
be connected to other components found in breathing circuits, such
as tubing, fittings (e.g., wyes, tees, connectors, elbows, adapters
and spacers), medication delivery device, etc. Also shown are an
artificial airway 2702 and a ventilator circuit 2704. In this
embodiment, RSR device 2700 may have a port 2760 located on the
housing for the removal of fluids which have been trapped by the
device. FIG. 27B, a cross-sectional view of RSR device 2700,
illustrates that the RSR device may include a patient side port
2720, a ventilator side port 2730, and a reservoir 2750. The RSR
device may also include a diverter 2714, similar to diverters
described in other embodiments of this invention. RSR device 2700
may have spill guards 2726 which prevent patient secretions from
reentering the circuit once they are trapped. Both ports 2720 and
2730 may include swivel connectors as discussed in previous RSR
device embodiments.
[0151] As previously discussed, all of the RSR device embodiment of
this invention may include drain ports to facilitate removal of
respiratory secretions. Drain ports may include a valve for the
application of suction. The actuation of the valve could be via
insertion of a medical instrument, manual user operation as with a
push button valve, by automated electrical operation as with a
computer controlled solenoid valve, or any other suitable means of
actuation.
[0152] FIG. 28 illustrates another embodiment of an RSR device. RSR
device 2800 can include a housing 2802, a patient port 2820, a
ventilation port 2830, a tube 2832, which can defined patient port
2820 and ventilation port 2830 and one or more drain ports 2860.
Any of the ports 2820 or 2830 could have swivel connectors as
discussed in previous RSR device embodiments. Housing 2802 can have
a reservoir 2850 for collection of fluids. Housing 2802 can contain
a tube 2832 that has a plurality of holes 2846. The holes 2846 can
take any shape or configuration such that fluid may pass through
the holes 2846 and into reservoir 2850. As secretions move through
tube 2832, air pressure and/or gravity can force the secretions out
through holes 2846 and into reservoir 2850. Housing 2802 can be
configured in a conical shape, which can aid in the retention and
clearance of secretions from the reservoir 2850. Gravity can aid in
the movement of secretions through the reservoir towards a drain
port 2860. Secretions can be drained or suctioned through the at
least one drain port. In this embodiment, a plurality of drain
ports increases the number of positions that RSR device 2800 may be
cleared of secretions. As discussed previously, any or all of the
drain ports could include a control valve (not shown). In
embodiments, holes 2846 are positioned in such a way as to create
an area above and below the holes for secretions to accumulate in
reservoir 2850 for when RSR device 2900 is positioned with the axis
of tube 2832 in a vertical orientation. This prevents unintended
emptying of secretions from reservoir 2850 back into tube 2832.
[0153] FIG. 29A illustrates a cross-sectional perspective view of
an embodiment of an RSR device. RSR device 2900 includes a tube
2932 (best shown in FIG. 29B), which defines a patient port 2920
and a ventilation port 2930. Any of ports 2920 or 2930 can have
swivel connectors as discussed in previous RSR device embodiments.
RSR device 2900 also includes housing 2902 attached to tube 2932,
which defines drain port 2960 and fluid instillation port 2965.
Housing 2902 can be comprised of a flexible material such as thin
plastic. Sleeve 2942 surrounds tube 2932 and has sleeve slots 2944.
Referring to the cross-section illustrated in FIG. 29B, tube 2932
is also shown to have slots, tube slots 2934. Slots 2934 and 2944
can take any shape or configuration such that fluid could pass
through the slots and could be considered as holes or the like. RSR
device 2900 is configured such that the sleeve 2942 may be rotated
angularly with respect to the tube 2932. This rotation can allow
sleeve slots 2944 to reposition relative to tube slots 2934 into
two distinct configurations. FIG. 29B shows a configuration where
sleeve slots 2944 and tube slots 2934 are aligned. FIG. 29C shows a
configuration where sleeve slots 2944 and tube slots 2934 are not
aligned. Referring to FIG. 29B, in this configuration is the RSR
device 2900 can trap liquids such as patient secretions. As
secretions travel through tube 2932, air pressure and/or gravity
can force the secretions out through both tube slots 2934 and
sleeve slots and into reservoir 2950. Referring to FIG. 29C, this
configuration is configured to facilitate clearing retained
secretions from the reservoir 2950. Sleeve 2942 blocks tube slots
2934 and therefore shields the interior of tube 2932 from the
contents of the reservoir 2950. Secretions can be drained or
suctioned through the drain port 2960. The instillation of fluid,
such as saline, through the fluid instillation port 2965 can
facilitate clearing of secretions. When tube slots 2934 are
blocked, instilled fluids, liquids, secretions, atmosphere, etc.,
cannot enter the tube 2932. Housing 2902 may also be repositioned
or manipulated, such as by squeezing, to aid in moving secretions
through the reservoir and towards drain port 2960. In embodiments,
a flexible housing 2902 may aid in clearing secretions when suction
is applied as the reservoir 2950 may decrease in size and push the
secretions towards drain port 2960. In embodiments, slots 2934 and
2944 are configured in such a way as to limit their length, thereby
creating an area above and below the slots 2934 and 2944 for
secretions to accumulate for when RSR device 2900 is positioned
with the axis of tube 2932 in a vertical orientation. This further
prevents unintended emptying of secretions from reservoir 2950 back
into tube 2932. In embodiments, sleeve 2942 may be repositioned
with respect to tube 2932 by any means such as translation,
rotation, etc. In embodiments, sleeve 2942, tube 2932, and/or
housing 2902 may have features that maintain a desired position
with respect to one another, such as locking features, and/or
features to limit the range of repositioning.
[0154] FIGS. 30A and 30B illustrate another embodiment of an RSR
device. RSR device 3000 can include a housing 3002, which can
include a patient port 3020, a ventilation port 3030, a reservoir
3050 defined by housing 3002, and a drain port 3060. RSR device
3000 can include tube portions 3070, which can be flexible to
increase the utility of the device, e.g. by reducing the stresses
in the circuit. Ports 3020 and 3030 can have swivel connectors as
discussed in previous RSR device embodiments. In this embodiment,
swivel connectors are particularly desirable, because the swivel
connectors allow the positioning of the drain port 3060 in a
downwards orientation thereby facilitating draining of trapped
secretions or other fluids. In addition, if flexible tube portions
3070 are present, these flexible tube portions can also assist in
positioning the device for draining. Tube portions 3070 may be
integral to the housing 3002 or may be attached to housing 3002. If
the tube portions 3070 are attached to the housing 3002, it is
preferred for the attachment points to have swivel connectors. As
discussed previously, drain port 3060 may include an integral valve
to facilitate applying suction to the reservoir. As illustrated in
the cross-sectional view FIG. 30B, the reservoir 3050 has a
dog-bone shape to facilitate the entrapment of secretions. RSR
device 3000 also may contain a diverter 3008 as described in
previous embodiments. FIG. 30C illustrates another configuration
similar to RSR device 3000. RSR device 3001 has a patient port
3021, a ventilation port 3031, a reservoir 3051 defined by housing
3003, and a drain port 3061. RSR device 3001 can include a single
tube portion 3071. Ports 3021 and 3031 can have swivel connectors
as discussed in previous RSR device embodiments. For example, port
3021 is shown having a swivel connector 3023. Having a single tube
portion further reduces the deadspace of the RSR device. RSR device
3001 may have a diverter 3009 as described in previous embodiments.
A baffle type of diverter system with more than one diverter, which
can be angled, is shown as one example.
[0155] FIG. 31A illustrates another embodiment of an RSR device.
RSR device 3100 has a housing 3102. Housing 3102 may be rigid to
maintain a "horseshoe" shape whereby secretions can be trapped in
several locations. Housing 3102 may also be flexible to allow for
some repositioning or adjustability of shape. RSR device 3100 may
include a patient port 3120, a ventilation port 3130, and one or
more drain ports 3160. Ports 3120 and 3130 can have swivel
connectors as discussed in previous RSR device embodiments. In this
embodiment, swivel connectors are desirable as they allow
positioning of the device to maximize secretion collection. FIG.
31B illustrates secretions 3156 trapped in RSR device 3100 in one
orientation. FIG. 31C illustrates secretions trapped in RSR device
3100 in a second orientation. FIG. 31D illustrates secretions 3156
trapped in RSR device 3100 in a third orientation. As shown in FIG.
31D, RSR device 3100 can have a curved housing to further increase
the retention of respiratory secretions within the RSR device.
[0156] FIG. 32A illustrates another embodiment of an RSR device.
RSR device 3200 can include a housing 3202 which defines a tube
portion and a plurality of grooves 3206. The RSR device also
includes a patient port 3220 and a ventilation port 3230, and one
or more drain ports (not shown). Ports 3220 and 3230 can have
swivel connectors as discussed in previous RSR device embodiments.
As patient secretions advance within housing 3202, the secretions
become trapped in the grooves 3206. Grooves 3206 can have a depth
of 1 mm or greater to become effective fluid traps. It is also
preferred to have at least two grooves if the grooves are
individual features, such as circumferential grooves. In
embodiments, the grooves may be formed by one helical feature. The
configuration of the grooves also limits the resistance to flow in
the main tube portion of housing 3202. RSR device 3200 may be
flexible and/or may be comprised of a flexible material, such as
polyethylene, silicone and the like. The flexibility of the RSR
device can add to the utility of the device by relieving stresses
in the circuit. In addition, the RSR device 3200 may also be
comprised of rigid material such as polycarbonate or polypropylene.
In embodiments, RSR device 3200 may have a curved housing to
further increase the retention of respiratory secretions within the
RSR device. FIG. 32B illustrates a cross-sectional view of RSR
device 3200. The passive collection of secretions may function in
any orientation and may be aided by flexibility in the RSR device
3200. In embodiments, RSR device 3200 can have no drain port and
simply can be disposed of after becoming saturated with
secretions.
[0157] In addition, although not required for function of this
invention, the use of clear materials is desirable as it aids in
determining the amount of fluid sequestered in the RSR device. In
addition, the RSR device can be made of or coated with
antimicrobial substances or materials to prevent the growth of
bacteria, and other microbes, for example antimicrobial substances
that prevent the formation of biofilms on or within the RSR device.
Further coatings containing silver or a silver alloy may be used to
prevent or decrease the formation of biofilms and/or inhibit the
growth of bacteria on or within the RSR device. Further coatings or
materials with hydrophilic properties may be used to improve the
retention of secretions in a reservoir area. Further coatings or
materials with hydrophobic properties may be used to decrease
adhesion of secretions to the diverter or other surfaces in the RSR
device. A hydrophobic diverter is more likely to shed tenacious
secretions off the diverter and into the reservoir during high flow
ventilation.
[0158] FIG. 33A illustrates another embodiment of an RSR device.
RSR device 3300 includes a retention assembly 3302 and suction
assembly 3304. Retention assembly 3302 can include a ventilator
port 3330, a patient port 3320, connection port 3306 and an
optional tube 3332 disposed between the patient port 3320 and
ventilator port 3330 and in fluid communication with a reservoir
3350. Tube 3332 may be collapsible and provides additional strain
relief between the RSR device 3300 and a ventilator circuit (not
shown). Ports 3320, 3330, and 3306 can have swivel connectors as
discussed in previous RSR device embodiments. Suction assembly 3304
can include a connector 3308 having a fluid instillation port 3365
and a suction port 3360 in fluid communication with the suction
assembly 3304 via optional tubing 3313. Suction assembly 3304
further can include an actuation mechanism 3370, e.g., a thumb
valve and the like, disposed between tubing 3313 and suction port
3360. The actuation mechanism 3370 provides for controlling a
hospital suction line (not shown) that connects to suction port
3360. In embodiments, the actuation mechanism 3370 could be engaged
or integrated directly into connector 3308. As illustrated in FIG.
33A, retention assembly 3302 and suction assembly 3304 are in a
nonassembled stage. At the discretion of the user (e.g. when
reservoir 3350 has collected secretions), the user attaches the
suction assembly 3304 to the retention assembly 3302 of the RSR
device 3300 via the connection port 3306 and the connector 3308 so
that suction can be performed on the reservoir 3350 of the RSR
device 3300.
[0159] FIG. 33B is a perspective view of RSR device 3300 in an
assembled stage. FIG. 33B illustrates a cross-section plane labeled
A-A. In operation, a clinician can activate the actuation mechanism
3370 to apply suction to the reservoir 3350. Saline or another
fluid that passes through fluid instillation port 3365 can be used
by the clinician to assist in keeping the suction line from
becoming clogged or blocked with secretions.
[0160] FIG. 33C is a partial longitudinal cross-sectional view of a
nonassembled RSR device 3300 taken along the plane labeled A-A
shown in FIG. 33B. The connection port 3306 can include an outer
wall 3340, which can have an annular shape and be configured to
engage an outer wall 3348 of the connector 3308. Connection port
3306 can include a plug 3344 and a cap 3342. In an embodiment, cap
3342 is attached to the plug 3344 by a cap tether 3346. The plug
3344 can have an inner wall 3343. Connector 3308 can have a spike
3309, which can be a hollow tube that includes an outer wall and an
inner wall that defines a conduit or passageway for the passage of
secretions and other fluids. In embodiments, the tip of spike 3309
can have a smaller diameter than the base of spike 3309. The
diameter of the hollow tube can increase from a tip portion of
spike 3309 to the base portion of spike 3309, for example in a
sloping manner. As the connector 3308 is advanced towards the
connection port 3306, as shown by arrow 3351 of FIG. 33D, the outer
wall of spike 3309 will contact an inner wall 3343 of plug 3344 to
create an initial sealing connection 3347 (FIG. 33D). Sealing
connection 3347 advantageously prevents exposure of the reservoir
3350 and/or its contents to atmosphere once cap 3342 is pushed away
from the plug 3344. As illustrated by FIG. 33E, the clinician may
now further advance connector 3308 such that spike 3309 forces cap
3342 to be opened and thereby provide for the capability to drain
or suction the reservoir 3350.
[0161] Similar to FIG. 33C, FIG. 34A is a partial longitudinal
cross-sectional view of a nonengaged RSR device 3400. FIG. 34A
illustrates an alternate structure and mode for achieving a seal
while engaging a suction assembly 3404. The connection port 3406 of
retention assembly 3402 can include an outer wall 3440, which can
have an annular shape and be configured to engage an outer wall
3448 of the connector 3408 of suction assembly 3404. Connection
port 3406 can have a valve 3442 (e.g., a duckbill valve, a dome
valve, spring-loaded valve, and the like) which provides a seal for
reservoir 3450. FIG. 34B is a partial longitudinal cross-sectional
view of a fully engaged RSR device 3400. As the connector 3408 is
advanced towards the connection port 3406, as shown by arrow 3451
of FIG. 34A, the outer surface of spike 3409 will contact the valve
3442 to create a sealing connection 3447 (FIG. 34B). Sealing
connection 3447 advantageously prevents exposure of the reservoir
3450 and/or its contents to atmosphere. Valve 3442 may reseal the
reservoir 3450 when suction assembly 3404 is removed.
[0162] Similar to FIG. 33C, FIG. 35A is a partial longitudinal
cross-sectional view of a nonengaged RSR device 3500. FIG. 35A
illustrates an alternate structure and mode for achieving a seal
while engaging a suction assembly 3504. The connection port 3506 of
retention assembly 3502 can include an outer wall 3540, which can
have an annular shape and be configured to engage an outer wall
3548 of the connector 3508 of suction assembly 3504, and can
include a cap 3542 that provides a seal for reservoir 3550. Suction
assembly 3504 can have a sealing ring 3544 (e.g., an O-ring,
gasket, and the like). FIG. 35B is a partial longitudinal
cross-sectional view of a partially engaged RSR device 3500. As the
connector 3508 is advanced towards the connection port 3506, as
shown by arrow 3551 of FIG. 35B, the sealing ring 3544 will contact
the inner surface of the outer wall of the connection port 3506 to
create an sealing connection 3547 (FIG. 35B). Sealing connection
3547 advantageously prevents exposure of the reservoir 3550 and/or
its contents to atmosphere once cap 3542 is pushed open. As
illustrated in FIG. 35C, the clinician may now further advance
connector 3508 such that spike 3509 forces cap 3542 to be opened
and thereby provide for the capability to drain or suction the
reservoir 3550.
[0163] Similar to FIG. 33C, FIG. 36A is a partial longitudinal
cross-sectional view of a nonengaged RSR device 3600. FIG. 36A
illustrates an alternate structure and mode for achieving a seal
while engaging a suction assembly 3604. The connection port 3606 of
retention assembly 3602 can include an outer wall 3640, which can
have an annular shape and be configured to engage an outer wall
3648 of the connector 3608, and can include a membrane 3642 (e.g.,
a thin film and the like), which provides a seal for reservoir
3650. FIG. 36B is a partial longitudinal cross-sectional view of a
fully engaged RSR device 3600. As the connector 3608 is advanced
towards the connection port 3606, as shown by arrow 3651 of FIG.
36A, the outer surface of spike 3609 will contact the membrane 3642
to create an sealing connection 3647 (FIG. 36B). Sealing connection
3647 advantageously prevents exposure of the reservoir 3650 and/or
its contents to atmosphere. In embodiments, RSR device 3600 can
include a sealing ring (not shown) similar to sealing ring 3544 of
FIG. 35A. In embodiments, spike 3609 may only open or puncture
membrane 3642 without engaging it in a sealing connection.
[0164] Similar to FIG. 33C, FIG. 37A is a partial longitudinal
cross-sectional view of a nonengaged RSR device 3700. FIG. 37A
illustrates an alternate structure and mode for achieving a seal
while engaging a suction assembly 3704. The connection port 3706 of
retention assembly 3702 can include a valve 3742, which provides a
seal for reservoir 3750, and a retention spring 3743 used to bias
the valve in a closed position. FIG. 37B is a partial longitudinal
cross-sectional view of a fully engaged RSR device 3700. As shown
by arrow 3751 of FIG. 37B, a suction assembly 3704 (FIG. 37B) can
be inserted into access port 3709 to move the valve 3742 the
direction shown by arrow 3751 and thereby open valve 3742 to allow
the reservoir 3750 to be drained or suctioned. Suction assembly
3704 may form a sealing connection 3747 with port 3709 prior to
engaging valve 3742. Sealing connection 3747 advantageously
prevents exposure of the reservoir 3750 and/or its contents to
atmosphere. Suction assembly 3704 may take the form of a syringe
and needle (as shown), a catheter, a spike, a lumen, or the like.
Valve 3742 can reseal the reservoir 3750 when suction assembly 3704
is removed. In embodiments, connection port 3706 of retention
assembly 3702 can be configured to engage a connector (not shown)
of suction assembly 3704, where the connector can be similar to
connector 3448 of FIG. 34A. This connector could have a spike (not
shown) similar to spike 3409 shown in FIG. 35A that could engage
with access port 3709.
[0165] FIG. 38A illustrates another embodiment of an RSR device.
RSR device 3800 includes a retention assembly 3802. Retention
assembly 3802 can include a ventilator port 3830, a patient port
3820, a connection port 3806 (FIG. 38B) and an optional tube 3832
disposed between the patient port 3820 and ventilator port 3830 and
in fluid communication with the reservoir 3850. Tube 3832 may be
collapsible and provides additional strain relief between the RSR
device 3800 and a ventilator circuit (not shown). Ports 3820, 3830,
and 3806 can have swivel connectors as discussed in previous RSR
device embodiments. Retention assembly 3802 can include an
actuation mechanism 3870 (e.g., a knob, a dial, a button or the
like) that provides for repositioning, such as by rotation,
translation or other means of motion, of a valve 3842 (FIG. 38B)
that is positioned within the retention assembly 3802.
[0166] FIG. 38B is a partial longitudinal cross-sectional view of a
retention assembly 3802 taken along the plane labeled A-A shown in
FIG. 38A. Referring to FIG. 38B, the connection port 3806 of
retention assembly 3802 can be configured to engage a cap 3862, and
can include a valve 3842 that provides a seal for reservoir 3850.
With the valve 3842 positioned in a closed position as demonstrated
in FIG. 38B, cap 3862 can be removed prior to engaging a suction
assembly without exposing the reservoir 3850 and/or its contents to
atmosphere.
[0167] At the discretion of the user (e.g. when reservoir 3850 has
collected secretions), the user attaches the suction assembly 3804
to the retention assembly 3802 of the RSR device 3800. FIG. 38C is
a partial longitudinal cross-sectional view of an assembled RSR
device 3800 taken along the plane labeled A-A shown in FIG. 38A.
The connection port 3806 can include an outer wall 3840, which can
have an annular shape and be configured to engage an outer wall
3848 of the suction assembly connector 3808. As the suction
assembly connector 3808 is advanced towards the connection port
3806, as shown by arrow 3851 of FIG. 38C, the inner surface of
outer wall 3848 of suction assembly connector 3808 will contact the
outer wall 3840 of connection port 3806 to create an initial
sealing connection 3847 (FIG. 38C). Sealing connection 3847
advantageously prevents exposure of the reservoir 3850 and/or its
contents to atmosphere. As illustrated by FIG. 38C, the clinician
may now open the valve 3842 by activating the actuation mechanism
3870 and thereby provide for the capability to drain or suction the
reservoir 3850 through a drain port 3860. In operation, a clinician
advantageously now has the capability to directly control suction
(i.e. no suction, less suction, more suction) via the actuation
mechanism 3870 and the valve 3842. The valve 3842 can be closed to
reseal the reservoir 3850 and then suction assembly 3804 can be
removed without exposing the reservoir 3850 and/or its contents to
atmosphere.
[0168] FIG. 39 illustrates a cross-sectional cutaway view of
another embodiment of an RSR device. RSR device 3900 can include a
housing 3902, which defines a tube portion 3932, and can include an
absorbent media 3910 that is designed to trap respiratory
secretions. The RSR device also includes a patient port 3920 and a
ventilation port 3930. Ports 3920 and 3930 can have swivel
connectors as discussed in previous RSR device embodiments. As
patient secretions advance within the tube portion 3932 of housing
3902, the secretions become trapped in the absorbent media 3910. In
operation, the absorbent media 3910 provides the clinician
additional time between circuit changes. For example the clinician
can rotate RSR device 3900 to expose fresh absorbent media once one
side becomes saturated with secretions. RSR device 3900 may be
flexible and/or may be comprised of a flexible material, such as
polyethylene, silicone and the like. The flexibility of the RSR
device can add to the utility of the device by relieving stresses
in the circuit. In addition, the RSR device 3900 may also be
comprised of rigid material such as polycarbonate or polypropylene.
RSR device 3900 simply can be disposed of after becoming saturated
with secretions. In embodiments, RSR device 3900 can have a drain
port (not shown) to remove secretions. In embodiments, RSR device
can have a plurality of grooves 3906. The absorbent media 3910 can
fill the grooves 3906, providing for additional volume for holding
trapped secretions. Secretions can wick from the portion of the
media 3910 nearest the axis of tube 3932 towards the portion of the
media 3910 in the grooves. In embodiments, the media may not fill
the grooves 3906 but may just lay over the grooves 3906. In this
embodiment, the media 3910 is constructed to first initially
capture the secretions, second to wick the secretions into the
grooves 3906, and third to not allow the secretions to exit from
the grooves (e.g. by trapping due to material properties or
nano-sized details in the media 3910).
[0169] FIG. 40 illustrates another embodiment of a RSR device 4000,
which is similar to RSR device 1700. RSR device 4000 includes a
housing 4002, a patient side port 4020, and a ventilation side port
4030, and may include a tube 4032. Any of the ports 4020 or 4030
could have swivel connectors as discussed in previous RSR device
embodiments. Housing 4002 can have a reservoir 4050 for collection
of fluids. Similar to RSR device 1700, reservoir 4050 can be made
of a flexible material, which allows the reservoir 4050 to deform
and allows the size of the reservoir to be controlled. A drain port
4060 may be included which allows for emptying the contents of the
reservoir, such as by suctioning. In one embodiment, a RSR device
4000 can include a fluid instillation port 4065. Instillation port
4065 can be used to instill saline or other fluid to help clear the
respiratory secretions which have collected in the reservoir,
especially if these secretions are thick or heavily viscous.
[0170] A clip 4070 can be applied to the reservoir 4050 to divide
the volume of the reservoir to an upper area 4052 above the clip
4070 and a lower area 4054 below the clip 4070. Clip 4070 can
compress reservoir 4050 locally, preventing any of the contents in
the upper area 4052 from draining into the lower area 4054. Clip
4070 is configured so a user can actuate it by pushing or squeezing
in order to temporarily allow it to not compress reservoir 4050.
During this non-compressed state, contents in the upper area 4052
could move into the lower area 4054. In one embodiment, clip 4070
could have a button 4072 to facilitate this actuation. Any method
or feature known to one skilled in the art that would allow the
clip 4070 to actuate in a manner that it would not compress
reservoir 4050 would be suitable.
[0171] Actuation of clip 4070 may also allow the user to move the
clip 4070 to a different location on the reservoir 4050. This would
allow a user to adjust the volume of the upper area 4052 of the
reservoir 4050 as desired. A smaller reservoir volume is
advantageous to limit dead space volume, especially for example in
smaller patients and in patients with certain respiratory diseases.
A larger reservoir volume is advantageous to allow for less
frequent clearing of the secretions in the RSR device 4000. The
position of the clip 4070 may be adjustable on the reservoir,
similar to RSR device 1700, and therefore adjusting the volume in
the upper area 4052 as desired by the user. Reservoir 4050 may also
have markings 4056 to indicate different reservoir volumes and
deadspace. In other embodiments features such as a diverter (not
shown), which were described in other embodiments of this
invention, may also be located in the RSR device 4000 to further
separate secretions from the gas flow and direct them into the
reservoir 4050.
[0172] FIG. 41A illustrates another embodiment of a RSR device
4100, which functions similarly to RSR device 2900. RSR device 4100
includes a tube 4132, which defines a patient end port 4120 and a
ventilation port 4130. Any of ports 4120 or 4130 can have swivel
connectors as discussed in previous RSR device embodiments. RSR
device 4100 also includes housing 4102 that encloses a first
portion 4134 (best shown in FIG. 41B) of tube 4132. Housing 4102
can be comprised of a flexible material such as thin plastic.
[0173] Referring to cross-sectional view FIG. 41B of RSR device
4100, a first portion 4134 of tube 4132 is preferably made of a
material and design that allows it to compress axially, such as by
collapsing into itself like a bendable or compressible drinking
straw. First portion 4134 can have apertures 4138. When the first
portion 4134 is in its extended position, apertures 4138 are open.
When the first portion 4134 is compressed axially, apertures 4138
are sealed against the opposing outer wall of the tubing 4132.
Apertures 4138 can take any shape or configuration such that a
fluid could pass through the apertures and could be considered as
holes or the like. In the position shown in FIG. 41B, RSR device
4100 can trap liquids such as patient secretions. As secretions
travel through tube 4132, air pressure and/or gravity can force the
secretions out through apertures 4138 into a reservoir 4150 of
housing 4102.
[0174] In the configuration when the first portion 4134 is
compressed axially to force apertures 4138 to seal, the RSR device
4100 is configured to facilitate clearing retained secretions from
the reservoir 4150. Since the apertures 4138 are sealed, the
interior of tube 4132 is shielded from the contents of the
reservoir 4150. Secretions can be drained or suctioned through the
drain port 4160. Suctioning the reservoir 4150 while the apertures
4138 are sealed, prevents the suctioning procedure from affecting
the pressure or flows within the tubing 4132. The instillation of
fluid, such as saline, through a fluid instillation port 4165 can
facilitate clearing of secretions. When apertures 4138 are sealed,
instilled fluids, liquids, secretions, atmosphere, etc., cannot
enter the tube 4132. Housing 4102 may also be repositioned or
manipulated, such as by squeezing, to aid in moving secretions
through the reservoir and towards drain port 4160. In embodiments,
a flexible housing 4102 may aid in clearing secretions when suction
is applied as the reservoir 4150 may decrease in size and push the
secretions towards drain port 4160. In embodiments, tube 4132,
and/or housing 4102 may have features that maintain a desired
position with respect to one another, such as locking features,
and/or features to limit the range of repositioning. Tubing 4132
may have a second portion 4136 that is external to housing 4102. In
embodiments, first portion 4134 and second portion 4136 could be
two different tubes. In the extended configuration shown in FIG.
41B, if the housing 4102 is flexible, this may allow the user to
determine the pressure inside the housing 4102 by observing the
amount the inflation of the flexible housing. In embodiments, the
housing 4102 may also have markings (not shown) to indicate
different inflation levels that may correlate to different
pressures.
[0175] FIGS. 42A and 42B illustrate another embodiment of a RSR
device 4200. RSR device 4200 includes a housing 4202, a patient
side port 4220, and a ventilation side port 4230. Any of the ports
4220 or 4230 could have swivel connectors and/or tubing extensions
as discussed in previous RSR device embodiments. Housing 4202 can
have a reservoir 4250 for collection of fluids. A drain port 4260
can be included which allows for emptying of respiratory secretions
that may collect in the reservoir. Housing 4202 can have a valve
4242 that prevents unintended emptying of the reservoir contents.
Valves have been discussed previously in other RSR device
embodiments. In embodiments, any feature apparent to one skilled in
the art that prevents unintended emptying of the contents could be
used, such as a thin plastic film.
[0176] Methods for emptying the collected respiratory secretions in
an RSR device have been discussed in other embodiments. Some of
these methods included draining, squeezing, and suctioning, such as
by a suction device or by a syringe. Once secretions have collected
inside RSR device 4200, a secretion removal assembly 4204 that
includes a bag 4290 may be utilized to collect secretions that emit
from the drain port 4260. Bag 4290 can be connected to the RSR
device 4200 at any time, for example at the discretion of the user.
In one embodiment, bag 4290 may have a fitting 4292 and an optional
tube 4213. Fitting 4292 can connect to drain port 4260, preferably
in a sealing manner. When connected, fitting 4292 can open valve
4242. The contact area between the fitting 4292 and valve 4242 may
also create a secondary seal. In other embodiments when a film is
used instead of a valve, the fitting 4292 would pierce the film.
Once the bag 4290 is assembled to the RSR device 4200, the
secretions could be transferred from the reservoir 4250 to the bag
4290. When bag 4290 is full, it may be removed and discarded
without requiring the RSR device 4200 to be removed from the
ventilation circuit. A new bag may be connected when needed. In
other embodiments, bag 4290 may be permanently attached or attached
in a non-removable manner. When a valve 4242 is utilized, the valve
4242 will close when bag 4290 is removed and therefore any
additional secretions will be maintained in the reservoir 4250 and
the inside of the circuit will not be exposed to atmosphere or the
pressures inside of the circuit will not be affected. Bag 4290 can
be made of a rigid or flexible material and can be inflatable. In
embodiments, bag 4290, tube 4213, or fitting 4292 can also have a
control valve (not shown), such as biased valve, anti-reflux valve,
or any other feature previously discussed or commonly known that
prevents unintended emptying of the bag contents. In embodiments,
tube 4213 could be simply clamped (such as by a clamp or clip),
pinched, or tied off to prevent unintended emptying of the bag
contents.
[0177] The collection bag approach presents a method of removing
secretions from a RSR device without affecting the pressures inside
of the system. Transfer of the secretions from the RSR device 4200
to the bag 4290 may occur passively due to gravity or the pressure
inside the system. In embodiments reservoir 4250 may be flexible
and allow the user the option to squeeze the reservoir 4250 to
assist in transferring the secretions into the bag 4290. In other
embodiments, the bag 4290 may have a bag port (not shown) that
allows the bag 4290 to be drained or suctioned. This would allow
the bag 4290 to be emptied of secretions without requiring it to be
removed from the rest of the RSR device 4200. Also, suction applied
to bag 4290 may facilitate the transfer of the sections from the
reservoir 4250 to the bag 4290. In yet other embodiments, RSR
device 4200 can include a fluid instillation port (not shown). A
fluid instillation port can be used to instill saline or other
fluid to help clear or transfer the respiratory secretions which
have collected in the reservoir or bag, especially if these
secretions are thick or heavily viscous.
[0178] FIG. 43A illustrates another embodiment of a RSR device
4300. RSR device 4300 can include a housing 4302 with a patient
port 4320 and a ventilation port 4330. Any of the ports 4320 or
4330 could have swivel connectors and/or tubing extensions as
discussed in previous RSR device embodiments. Housing 4302 can have
at least two reservoirs, first reservoir 4351 and second reservoir
4352, for collection of fluids. By having more than one reservoir,
RSR device 4300 can retain more secretions. Housing 4302 can
include an actuation mechanism 4370 (e.g., a knob, a dial, a button
or the like) that provides for repositioning, such as by rotation,
translation or other means of motion, of a wall 4304 (FIGS. 43B and
43C) that is positioned within the housing 4302. FIGS. 43B and 43C
illustrate cross-sections along lines 43-43 through the patient
port 4320 from a top view. Referring to FIG. 43B, wall 4304 is
positioned to isolate first reservoir 4351 from the flow path
inside of housing 4302. In this configuration, secretions that pass
through housing 4302 would be retained in the second reservoir
4352. The deadspace of RSR device 4300 in this configuration
includes the internal volumes of the housing 4302 and second
reservoir 4352. Because first reservoir 4351 is sealed off by wall
4304, it is not included as part of the deadspace. In embodiments,
various features known to one skilled in the art that would allow
the flow path to be redirected towards only one reservoir or that
isolates one reservoir from the flow path could serve the purpose
of wall 4304. Examples of these features include switches, valves,
overlapping walls, diverters and the like.
[0179] When the second reservoir 4352 is full of secretions, the
user may reposition actuation mechanism 4370 in order to move wall
4304. FIG. 43C illustrates one example of this process. Wall 4304
has been moved so as to isolate the second reservoir 4352 from the
flow path inside of housing 4302 and to expose first reservoir 4351
to the flow path. In this configuration, secretions that pass
through housing 4302 would now be retained in first reservoir 4351.
The deadspace of RSR device 4300 includes the internal volumes of
the housing 4302 and first reservoir 4351. Since second reservoir
4352 is sealed off by wall 4304, it is not included as part of the
deadspace in this configuration. This method of repositioning wall
4304 allows for a RSR device that has increased capacity for
secretion retention without increased deadspace. Alternatively, the
user may move wall 4304 to a position where it does not seal either
first reservoir 4351 or second reservoir 4352. In this
configuration, both first reservoir 4351 and second reservoir 4352
can retain secretions and can be in the fluid flow path through the
RSR device 4300. Actuation mechanism 4370 and/or wall 4304 may be
locked into a certain position(s) if desired.
[0180] Referring to FIG. 43A, drain ports 4360 may be included in
reservoirs 4351 and 4352 to provide for content removal from the
reservoirs 4351 and 4352 by various methods, such as by suctioning
and the like. The removal of secretions from a reservoir that it is
isolated from the gas path by wall 4304 (shown in FIGS. 43B and
43C) is advantageous because it allows the secretions to be removed
without affecting the pressure or fluid flows within the RSR device
4300. Another advantage is that the inside of the circuit will not
be exposed to atmosphere during the removal process. In one
embodiment, RSR device 4300 can include a fluid instillation port
(not shown), which can be used to instill saline or other fluid to
help clear the respiratory secretions that have collected in
reservoirs 4531, 4532, especially if these secretions are thick or
heavily viscous
[0181] FIG. 43D illustrates an alternate method of secretion
clearance or removal from RSR device 4300. If the user positions
actuation mechanism 4370 as shown in FIG. 43B, first reservoir 4351
is isolated from the flow path. The user may now remove first
reservoir 4351 from housing 4302 without affecting the pressure
within the RSR device 4300 and without exposing to the inside of
the circuit to atmosphere. The user may now clear first reservoir
4351 of secretions or simply dispose first reservoir 4351, and then
sealingly engage a reservoir back into the vacant reservoir opening
in housing 4302. This method of replacing or clearing reservoirs
that are not currently in the flow path allows the user to
endlessly clear out secretions without removing the RSR device 4300
from the ventilation circuit.
[0182] FIG. 44A illustrates another embodiment of an RSR device.
RSR device 4400 includes a retention assembly 4402 and suction
assembly 4404. Retention assembly 4402 can include a ventilator
port 4430, a patient port 4420, a connection port 4406 and an
optional tube 4432 disposed between the patient port 4420 and
ventilator port 4430 and in fluid communication with the reservoir
4450. Tube 4432 may be collapsible and provides additional strain
relief between the RSR device 4400 and a ventilator circuit (not
shown). Ports 4420, 4430, and 4406 can have swivel connectors as
discussed in previous RSR device embodiments. Suction assembly 4404
can include a connector 4408 in fluid communication with a fluid
instillation port 4465 and a suction port 4460. Suction assembly
4404 further can include a tubing 4413 and an actuation mechanism
(not shown), e.g., a thumb valve and the like, similar to actuation
mechanism 3370 of RSR 3300. In embodiments, the actuation mechanism
could be coupled or integrated directly into connector 4408. The
actuation mechanism provides for controlling a hospital suction
line (not shown) that fluidly connects to suction port 4460. As
illustrated in FIG. 44A, retention assembly 4402 and suction
assembly 4404 are in an assembled stage. At the discretion of the
user (e.g. when reservoir 3350 has collected secretions), the user
attaches the suction assembly 4404 to the retention assembly 4402
of the RSR device 4400 via the connection port 4406 and the
connector 4408 so that suction can be performed on the reservoir
4450 of the RSR device 4400.
[0183] FIG. 44A includes two section planes A-A and B-B that
subsequent figures reference. FIG. 44B shows a cross-sectional
perspective view taken through plane B-B of RSR device 4400 in an
assembled state. This view illustrates that connection port 4406
includes a plug 4444 that has channels 4445, which in this
configuration allow fluid communication from reservoir 4450 to
suction assembly 4404. FIG. 44C is a perspective view of plug 4444
of RSR device 4400 and illustrates the channels 4445.
[0184] FIGS. 44D, 44E, and 44F illustrate partial cross-sections of
RSR device 4400 in non-engaged, partially engaged, and fully
engaged positions respectively. FIG. 44D is a partial longitudinal
cross-sectional view of a nonassembled RSR device 4400 taken along
the plane labeled A-A shown in FIG. 44A. The connection port 4406
can include an outer wall 4440, which can have an annular shape and
be configured to engage an outer wall 4448 of the connector 4408 of
suction assembly 4404, and can include a plug 4444. The plug 4444
can include an inner wall 4443. Connector 4408 can include a spike
4409.
[0185] FIG. 44E is a partial longitudinal cross-sectional view of a
partially engaged RSR device 4400 taken along the plane labeled A-A
shown in FIG. 44A. As the connector 4408 is advanced by the user
towards the connection port 4406, as shown by arrow 4451 of FIG.
44E, the outer surface of spike 4409 will contact the inner wall
4443 of plug 4444 to create an initial sealing connection 4447
(FIG. 44E). Sealing connection 4447 advantageously prevents
exposure of the reservoir 4450 and/or its contents to atmosphere
once plug 4444 is pushed upward further into reservoir 4450.
[0186] FIG. 44F is a partial longitudinal cross-sectional view of a
fully engaged (i.e. assembled) RSR device 4400 taken along the
plane labeled A-A shown in FIG. 44A. As the connector 4408 is
further advanced towards the connection port 4406, as shown by
arrow 4451 of FIG. 44F, the spike 4409 forces plug 4444 to
reposition further into reservoir 4450 and thereby places channels
4445 in fluid communication with the reservoir 4450 (as shown in
FIG. 44B). In the assembled position, the suction assembly 4404 can
provide for the capability to drain or suction the reservoir 4450.
Outer wall 4440 of connection port 4406 and outer wall 4448 of
connector 4408 can snap together as shown. In embodiments, any
method or feature for coupling two parts known to one skilled in
the art such as threads, clips, bands, press fit, etc. could be
utilized. Coupling methods or features such as these could apply to
any of the suction assembly and retention assembly embodiments
previously described, such as devices 3400, 3500, 3600, etc. For
example, walls 4440 and 4448 of RSR device 4400 could have threads
(not shown). Depending on the coupling method or feature, the
advancement direction of the connector assembly may vary. For
example, a press fit connection of connector 4408 onto connection
port 4406 would have an advancement direction as shown by arrow
4451 of FIG. 44E. However, in an embodiment where a threaded
connection (not shown) exists between connector 4408 and connection
port 4406, advancement direction could be best described by a
helical arrow (not shown).
[0187] While the invention has been described in terms of what is
presently considered to be the most practical and preferred
embodiments, it is to be understood that the invention needs not be
limited to the disclosed embodiment. On the contrary, it is
intended to cover various modifications and similar arrangements
included within the spirit and scope of the appended claims, which
are to be accorded with the broadest interpretation so as to
encompass all such modifications and similar structures.
* * * * *