U.S. patent number 3,814,098 [Application Number 05/279,063] was granted by the patent office on 1974-06-04 for medical suction apparatus.
This patent grant is currently assigned to Deaton Medical Company. Invention is credited to David W. Deaton.
United States Patent |
3,814,098 |
Deaton |
June 4, 1974 |
**Please see images for:
( Certificate of Correction ) ** |
MEDICAL SUCTION APPARATUS
Abstract
The specification discloses medical suction apparatus including
a generally rigid container having a lid which supports a flexible
drainage sack within the container. A pair of conduits extend from
the container for connection to a patient area to be drained and
for connection to a source of vacuum. In operation, fluid is drawn
from the area to be drained and collected within the drainage sack.
A plurality of apertures are formed through the side walls of the
sack in order that the pressure is equalized on both sides of the
sack to prevent the sack from becoming closed during suction
operation. After the sack is filled with liquid, levers are
actuated to disengage the sack from the lid and the sack is
disposed of. The sack is double lined and in the preferred
embodiment includes apertures therethrough that vary in size
according to the amount of vacuum applied to the apparatus.
Inventors: |
Deaton; David W. (Dallas,
TX) |
Assignee: |
Deaton Medical Company (Burns
Flat, OK)
|
Family
ID: |
26900971 |
Appl.
No.: |
05/279,063 |
Filed: |
August 9, 1972 |
Related U.S. Patent Documents
|
|
|
|
|
|
|
Application
Number |
Filing Date |
Patent Number |
Issue Date |
|
|
206018 |
Dec 8, 1971 |
3745999 |
|
|
|
Current U.S.
Class: |
604/320 |
Current CPC
Class: |
A61M
1/604 (20210501); A61M 1/782 (20210501); A61M
1/0001 (20130101) |
Current International
Class: |
A61M
1/00 (20060101); A61m 001/00 () |
Field of
Search: |
;128/275-278,DIG.24,294-295 |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Rosenbaum; Charles F.
Attorney, Agent or Firm: Richards, Harris & Medlock
Parent Case Text
RELATED APPLICATIONS
This application is a continuation-in-part of patent application
Ser. No. 206,018, filed Dec. 8, 1971, and entitled Medical Suction
Method and Apparatus, now U.S. Pat. No. 3,745,999.
Claims
What is claimed is:
1. A medical suction container assembly comprising:
a rigid container,
a lid for said container having a fluid inlet and a vacuum
port,
a flexible sack for being disposed within said container and having
structure in the upper portion thereof for connection to and
support by said fluid inlet, wherein said sack receives fluid from
a patient area upon application of vacuum to said vacuum port,
and
manually operable lever means for separating said sack from said
lid when it is desired to dispose of said sack and the fluid
therein.
2. The medical suction container assembly of claim 1 wherein said
lever means comprises a pair of levers pivotably connected to the
underside of said lid, inner ends of said levers operable to
separate said sack from said lid.
3. The medical suction container assembly of claim 1 wherein said
lever means comprises a manually operable lever mounted on top of
said lid for separating said sack from said lid.
4. The medical suction container assembly of claim 1 wherein said
fluid inlet includes an annular projection extending from the
underside of said lid, said sack structure frictionally receiving
said annular projection, and
said lever means manually operable to force said sack structure
from said annular projection.
5. In a medical suction container assembly including a rigid
canister having a lid supporting a flexible sack for receiving
fluid from a patient area, the combination comprising:
lever means pivotally mounted on the underside of said lid and
including a portion for being disposed between the underside of
said lid and said sack,
said lever means manually operable such that said portion is moved
downwardly to separate said sack from said lid.
6. The combination of claim 5 wherein said lever means comprises a
pair of levers mounted on opposite sides of said lid and having
outer ends operable by the fingers of an operator and inner ends
operable to separate said sack from said lid.
7. The combination of claim 5 wherein said lever means are
removably supported by pivot projections extending from the
underside of said lid.
8. In a medical suction assembly, the combination comprising:
a rigid container,
a lid for said container having a fluid inlet and a vacuum
port,
a sack for being received within said container,
a fluid inlet port device mounted in the upper portion of said sack
for being frictionally attached to said fluid inlet on the
underside of said lid,
a pair of levers pivotally mounted to the underside of said
lid,
each of said levers including an inner end for being disposed
between said port device and the underside of said lid and further
including an outer end for being manually operated,
whereby when said outer ends of said levers are manually moved
toward the underside of said lid, said inner ends are moved away
from said lid to separate said sack from said lid.
9. The combination of claim 8 and further comprising:
apertures formed in the upper portion of said sack to equalize the
pressure between the interior and exterior of said sack.
10. The combination of claim 8 and further comprising:
an annular projection extending from the underside of said lid and
communicating with said fluid inlet in said lid,
said port device comprising a resilient annular member for
frictionally receiving said annular projection and further
including an inlet conduit for extending through said fluid inlet
for connection to a tube extending to a patient area.
11. The combination of claim 8 wherein said port device includes a
diaphragm responsive to the magnitude of vacuum applied to said
assembly, wherein said port device more tightly grips said annular
projection as the magnitude of said vacuum is increased.
12. The combination of claim 8 and further comprising:
a flexible float valve attached underneath said lid and responsive
to overflow of fluid within said container to obstruct said vacuum
port in said lid.
13. In a medical suction assembly including a rigid canister and a
lid having a fluid inlet and a vacuum port, the combination
comprising:
a flexible sack for being disposed in said canister for receiving
fluid drawn through said fluid inlet upon application of vacuum to
said vacuum port,
said sack having plural walls to ensure the structural integrity
thereof, and
apertures formed through the upper portion of said plural walls to
tend to equalize pressure between the interior and exterior of said
sack to prevent collapse of said sack upon application of vacuum to
said vacuum port.
14. The combination of claim 13 wherein said apertures in said
plural walls are offset from one another to prevent splashing of
fluid therethrough as fluid is drawn into said sack through said
fluid inlet.
15. The combination of claim 13 wherein the size of said apertures
increases as the magnitude of the vacuum applied to said vacuum
port increases.
16. The combination of claim 13 and further comprising:
perforations formed in an upper corner of said sack to enable
tearing off of said corner to enable pouring out of fluid within
said sack.
17. The combination of claim 13 wherein said sack comprises an
inner sack and an outer sack, said apertures in said sacks being
positioned such that fluid may overflow from said inner sack into
said outer sack.
18. In a ported sack for being supported within a rigid medical
suction container having a lid with a fluid inlet and a vacuum
inlet, the improvement comprising:
aperture means formed through the side of said sack to prevent
collapse of said sack upon the application of vacuum to said vacuum
inlet,
said aperture means being constructed such that the size of the
aperture through the side of said sack increases as the vacuum
applied to said vacuum inlet increases.
19. The improvement of claim 18 and further comprising:
flexible flaps being disposed in the region of said aperture
means.
20. In a medical fluid collection system wherein vacuum is applied
through a flexible collection sack, the improvement comprising:
aperture means formed in the upper part of said sack and including
slits formed through the wall of said sack to define an air outlet
aperture,
said slits also defining a resilient flap normally substantially
closing said outlet aperture upon the application of low vacuum to
said sack, said flap being responsive to the magnitude of vacuum
applied to said sack for varying the effective size of said outlet
aperture.
21. The improvement of claim 20 wherein said slits comprise a pair
of semicircular slits spaced apart at the ends thereof to form two
narrow hinges supporting said flap.
22. The improvement of claim 20 wherein said slits comprise four
semicircular slits spaced apart at the ends thereof to form four
narrow hinges supporting said flap, a pair of said hinges tending
to rupture upon the application of predetermined magnitude of
vacuum.
23. The improvement of claim 20 wherein said sack includes plural
walls, said aperture means formed through each of said walls.
24. In a medical fluid collection system, the improvement
comprising:
inner and outer disposable sacks each formed from a flexible
plastic sheet material,
said inner sack comprising a medical fluid receiving sack and said
outer sack wholly enclosing said inner sack,
medical fluid inlet means extending through said outer sack into
communication with the interior of said inner sack,
each of said sacks having aperture means formed therethrough to
equalize the pressure between the interior and exterior of said
sacks upon the application of vacuum in a region surrounding the
exterior of said outer sack,
at least one of said aperture means including one narrow slot for
defining a fluid outlet aperture and a flexible valving flap
normally substantially closing said outlet aperture upon the
application of low vacuum,
said valving flap being responsive to the magnitude of the appled
vacuum to tend to open said outlet aperture upon the application of
higher vacuum.
25. The improvement of claim 24 wherein said outlet aperture in
said inner sack is offset from said outlet aperture in said outer
sack to provide a fluid baffle.
26. The improvement of claim 24 wherein said outlet aperture in
said inner sack is positioned such that fluid overflow from said
inner sack passes through said outlet aperture and is collected in
said outer sack.
27. In a medical fluid collection system, the improvement
comprising:
inner and outer flexible disposable sacks, said inner sack
comprising a medical fluid receiving sack and said outer sack
wholly enclosing said inner sack,
medical fluid inlet means extending through both of said flexible
disposable sacks,
means for establishing a partial vacuum zone exterior to said outer
sack,
means for withdrawing air from the interior of said inner sack
through the interior of said outer sack into said vacuum zone and
thereby drawing medical fluid into the interior of said inner sack
through said medical fluid inlet means,
said air withdrawing means comprises slits formed in both of said
sacks to define relatively large diameter air outlet apertures and
resilient flaps normally substantially closing said outlet
apertures,
said flaps being responsive to the magnitude of the vacuum in said
vacuum zone to at least partially regulate the rate at which air is
withdrawn from the sacks.
28. The improvement of claim 27 wherein said slits comprise a pair
of semicircular slits spaced apart at the ends thereof to form two
narrow hinges supporting said flap.
29. The improvement of claim 27 wherein said slits comprise four
semicircular slits spaced apart at the ends thereof to form four
narrow hinges supporting said flap, a pair of hinges tending to
rupture upon the application of predetermined magnitude of
vacuum.
30. A medical suction assembly comprising:
an open topped fluid canister,
a lid for said canister including a vacuum port for being attached
to a source of vacuum,
said lid further including a fluid inlet having a downwardly
extending projection,
a flexible sack for being disposed within said canister and
including a resilient inlet member mounted in the upper portion
thereof,
said resilient inlet member dimensioned for being removably mated
with said projection wherein fluid from a patient area is drawn by
said vacuum into said sack through said resilient inlet member.
31. The medical suction assembly of claim 30 wherein said inlet
member includes a diaphragm responsive to the vacuum applied
thereto for increasing the frictional force applied by said inlet
member on said projection.
32. The medical suction assembly of claim 30 further
comprising:
lever means mounted on said lid for separating said inlet member
from said projection.
33. A medical suction apparatus comprising:
a rigid container having a lid with a fluid inlet and a vacuum
inlet,
conductive strips extending along said fluid and vacuum inlets and
connected to ground,
a conductive member extending between said fluid inlet and said
vacuum inlet and contacting said conductive strips for providing an
electrical path between said inlets.
34. The medical suction apparatus of claim 33 wherein said
conductive member comprises a flexible high carbon content rubber
strip having apertures at each end thereof for receiving said
inlets.
Description
FIELD OF THE INVENTION
This invention relates to a suction apparatus, and more
particularly relates to suction apparatus for drawing fluids from a
patient area and storing the fluid in a disposable receptacle.
THE PRIOR ART
Suction devices are commonly used in a number of medical
applications to draw various fluids from a patient area and to
store the fluids for later disposal. For example, suction devices
have heretofore been utilized to draw aspirated fluids from a
patient during a surgical operation, and during the postoperative
period. In addition, suction devices are used to drain fluids from
the gastrointestinal tract, as well as to drain pulmonary mucus in
tracheal incisions and the like.
One such suction apparatus which has long been used comprises a
rigid bottle, generally made from glass, which includes a cap
connected to a first conduit for connection to a source of reduced
pressure and a second conduit for connection to the patient area to
be drained. The reduced pressure is transmitted through the glass
bottle and draws the fluids from the patient area for storage
within the glass bottle. After filling, the cap may be removed and
the fluids poured from the bottle. The bottle must then be
sterilized for additional use. Such sterilization procedures are
not only costly and time-consuming for the hospital, but sometimes
result in cross-contamination due to inadequate sterilization.
Moreover, the use of glass bottles has often been found to be
somewhat of a hazard, due to breakage and chipping problems.
In order to reduce the problems inherent in conventional glass
suction bottles, disposable plastic containers have been developed.
Examples of such disposable fluid containers are described in U.S.
Pat. No. 3,620,408, issued Nov. 16, 1971, to Hollbrook et al. and
U.S. Pat. No. 3,646,935, issued Mar. 7, 1972, to Hollbrook et al.
However, such prior disposable plastic containers have been
relatively expensive to manufacture and ship. Moreover, prior
plastic containers have often not had sufficient strength to
withstand the high levels of vacuum required for many hospital
applications.
It has also heretofore been known to utilize a generally rigid
outer container which supports a flexible drainage bag therein for
collection of fluids. After use, the flexible drainage bag is
removed and is disposed of, leaving the outer rigid container
sterile and ready for additional use with another flexible drainage
bag. Example of such previously developed suction devices are
disclosed in U.S. Pat. No. 3,556,101, issued Jan. 19, 1971, to S.
G. Economou and U.S. Pat. No. 3,680,560, issued Aug. 1, 1972, to K.
A. Pannier et al.
Because of the use of a flexible bag, it is necessary to insure
that the bag does not collapse during the application of suction to
the interior of the bag. Therefore, the Economou patent discloses
the use of an aperture in the vacuum conduit which provides vacuum
to the area between the flexible bag and the outer rigid container
to prevent collapse of the bag. This type of suction device,
however, has been found to exert considerable stresses upon the
flexible drainage bag, and relatively heavy-weight and expensive
bags are required to be utilized in order to prevent rupture of
weak points or heat-sealed portions of the bags. In particular,
stress problems with respect to many of the flexible bags of the
prior art devices occur when the drain conduits become obstructed,
such as when a drain conduit catheter is inserted, or when mucus or
other fluids stop up the conduits. Such obstructions of the drain
conduit cause a substantial increase in the vacuum applied to the
outside of the bags, thus substantially increasing the stress on
the bag and increasing the chances of failure of the bag. Moreover,
previously developed devices utilizing flexible bags have sometimes
developed leaks around the cover of the rigid container or about
the connection of the various vacuum conduits. Due to the
construction of such prior art devices, the bags used therewith
tend to collapse upon the occurrence of a vacuum leak, and the
fluids within the bag are then sucked into the central piping
system of the hospital. Fluid overflow valves involving ball float
valves and the like have been developed to prevent such overflow
conditions, but prior overflow valves have been relatively
expensive and complex in operation.
Moreover, such prior art devices such as disclosed in the Pannier
et al patent have not only required relatively expensive
cylindrical plastic bags, but have also been difficult to attach
and remove from the container lid. With such prior art suction
devices, nurses have thus often been required to handle bags full
of contaminated fluid. In addition, the application of high vacuum
to such prior art suction devices can result in the flexible
collection sack being sucked off of the container lid, thus
resulting in contamination of the rigid outer container.
SUMMARY OF THE INVENTION
In accordance with the present invention, a medical suction
apparatus is provided which substantially eliminates or reduces the
disadvantages of prior art suction devices. The invention comprises
a medical suction assembly including a rigid container having a lid
with a fluid inlet and a vacuum port. A flexible sack is
dimensioned to be disposed within the container and includes
structure in the upper end for connection to and support by the
fluid inlet in the lid. Upon the application of vacuum to the
vacuum port, the sack receives fluid from the patient area.
Manually operable levers are provided to separate the sack from the
lid when it is desired to dispose of the sack and the fluid
contained therein.
In accordance with another aspect of the invention, the medical
suction assembly includes a rigid container and a lid having a
fluid inlet and a vacuum port. A vacuum sack is dimensioned to be
disposed in the container to receive fluid drawn through the fluid
inlet upon application of vacuum to the vacuum port. The sack has
plural walls to insure the structural integrity of the sack.
Apertures are formed through the upper portion of the plural walls
to tend to equalize pressure between the interior and exterior of
the sack to prevent collapse of the sack upon application of vacuum
to the vacuum port. In the preferred embodiment of the invention,
the apertures comprise butterfly type valves which tend to increase
the size of the apertures in dependence upon the amount of vacuum
applied to the system.
In accordance with another aspect of the invention, a fluid
container includes an annular bead extending around the upper
portion thereof. A lid is provided for the suction container which
includes a fluid inlet for communicating with the patient area and
having a vacuum port for being connected to a source of vacuum. The
lid includes an annular groove on the underside thereof for
sealingly receiving the bead to provide a vacuum tight seal from
the container. An annular side wall extends from the annular groove
and is outwardly flared to define a transient sealing portion below
the groove for abutment with the annular bead of the container. The
transient sealing portion provides a temporary vacuum seal upon the
application of vacuum to the vacuum port which is sufficient to
cause the lid to be pulled downwardly upon the container to seat
the annular bead within the annular groove.
In accordance with yet another aspect of the invention, a medical
suction assembly includes a open topped fluid canister, along with
a lid including a vacuum port for being attached to a source of
vacuum. The lid further includes a fluid inlet having a downwardly
extending projection. A flexible sack is dimensioned for being
disposed within the canister and includes a resilient inlet member
mounted in the upper portion thereof. The resilient inlet member is
dimensioned for being removably mated with the projection from the
fluid inlet, whereby fluid from a patient area is drawn by the
vacuum into the sack through the resilient inlet member.
In accordance with yet another aspect of the invention, a medical
suction canister is provided with a cylindrical upper portion and a
frustoconical lower portion separated by an inwardly directed
annular shoulder. The shoulder is operable to abut an annular
support member for support of a canister. A canister also includes
a plurality of inwardly extending projections formed on the
interior lower portion of the canister and having abutment surfaces
spaced from the bottom of the canister a sufficient distance to
abut with the bottom of the second canister to enable stacking of
the canisters.
In accordance with yet another aspect of the invention, a medical
suction device comprises a fluid canister having a lid therefor. A
vacuum inlet and a fluid inlet aperture are formed through the lid.
The fluid inlet aperture extends through an annular projection
extending from the underside of the lid. A resilient plastic port
device is provided for being frictionally attached to the annular
projection. The port device includes an inlet tube member for being
connected to a conduit extending to a patient area to receive fluid
therefrom. The port device may include a disposable fluid sack
depending therefrom for collecting fluid. Alternatively, the port
device may be connected to the upper side of the lid to provide a
disposable fluid canister.
DESCRIPTION OF THE DRAWINGS
For a more complete understanding of the present invention and for
further objects and advantages thereof, reference is now made to
the following description, taken in conjunction with the
accompanying drawings, in which:
FIG. 1 illustrates a perspective view of an embodiment of the
invention;
FIG. 2 is a sectional view taken along the upper portion of the
flexible bag shown in FIG. 1 prior to connection within the rigid
outer container;
FIG. 3 is a side view of the upper portion of the flexible bag
shown in FIG. 1;
FIG. 4 is a sectional view of the upper part of the assembled
invention taken generally along the section line 4--4 in FIG. 1
illustrating the outer rigid container and the flexible bag;
FIG. 5 is an exploded view illustrating the connection of the
drainage conduit member of FIG. 1;
FIG. 6 is a perspective illustration of the preferred embodiment of
the invention;
FIG. 7 is a perspective view of the underside of the container
assembly shown in FIG. 6;
FIG. 8 is a side view of the disposable sack constructed in
accordance with the invention;
FIG. 9 is a top view of the sack shown in FIG. 8;
FIG. 10 is a perspective view illustrating the initial attachment
of the disposable sack to the underside of the lid of the present
container;
FIG. 11 illustrates the separation of the disposable sack from the
lid of the invention;
FIG. 12 illustrates the emptying of liquids from the disposable
sack of the invention;
FIG. 13 is a sectional view through the upper portion of the
present container during attachment of the lid to the
container;
FIG. 14 is a sectional view, partially broken away, showing the
final vacuum tight connection of the lid with the container;
FIG. 15 illustrates another embodiment of the butterfly type valve
with use with the flexible sack of the invention;
FIG. 16 is a top view of the float valve of the invention;
FIG. 17 illustrates the removal of the sack separator levers of the
invention to enable application of the float valve shown in FIG.
16;
FIG. 18 illustrates the attachment of the present float valve to
the underside of the container lid;
FIG. 19 illustrates the connection of the sack separator lever
adjacent the float valve of the invention;
FIG. 20 is a partially sectioned view of the present container
illustrating operation of the float valve during overflow
conditions;
FIG. 21 illustrates the stacking of an embodiment of the fluid
container;
FIG. 22 is a top view of the container of FIG. 21 illustrating the
spaced apart stacking feet of the invention;
FIG. 23 illustrates a parallel connection for enabling two suction
devices according to the invention to be simultaneously filed;
FIG. 24 illustrates the use of a conductive grounding strip
according to the invention;
FIG. 25 illustrates the conversion of the present container into a
disposable container;
FIG. 26 is a sectional view of the top portion of the disposable
container shown in FIG. 25;
FIG. 27 is a perspective view of another embodiment of the presence
suction container assembly illustrating the use of a top mounted
sack separator lever;
FIG. 28 illustrates the use of the sack separator lever shown in
FIG. 27 to remove a sack from the container lid; and
FIG. 29 illustrates the removal of the disposable sack from the
underside of the container shown in FIGS. 27-28.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
FIGS. 1-5 illustrate an embodiment of the invention. Referring to
FIG. 1, a medical suction apparatus 10 comprises a generally rigid
container 12 which is preferably an open-topped transparent plastic
cylinder. Container 12 will generally include volume indicating
markings, not shown, in order to enable visual reading of the fluid
level stored in the container. A flexible drainage bag 14 is
supported within the container 12 by a conduit member or port
device 16 attached within a cover or lid 18 for the container.
Cover 18 preferably comprises a transparent plastic lid which is
snapped into place over the open top of the container 12 to tightly
seal the container for maintenance of dependable suction during
operation of the device. A flexible hose or tube 20 is connected at
one end to the conduit member 16 and extends to a patient area for
receiving fluids. A vacuum conduit member 22 extends through the
cover 18 and is connected to a flexible tube 24 which extends to a
source of reduced pressure. The source of reduced pressure may
comprise any suitable source of vacuum or suction which is commonly
found in hospitals. The conduit member 22 may comprise a plastic
port integrally formed with the cover 18, or alternatively may
comprise a metal tube which is threadedly received in an aperture
in the cover 18.
An alternate embodiment of the present device, not shown, may
comprise a second conduit member communicating with bag 14 through
the cover 18. A short tube may be connected to the second conduit
member and the tube normally clamped shut. After filling of the bag
14 with liquid, the tube may be unclamped and the liquid poured out
through the second conduit member and the short tube. The short
tube may then be clamped and the suction operation continued.
Apertures 26 are spaced along the upper portion of the flexible bag
14 in the area between the conduit members 16 and 22. Preferably,
the combined surface area of the apertures 26 is greater than the
surface area of the central opening of conduit member 22, and the
geometry and location of the apertures 26 are such that the
resistance to gas flow therethrough is slightly less than the
resistance to gas flow through conduit member 22. In this case, bag
14 will remain in a limp unstressed condition during initial
operation of the device, and will gradually become opened as it is
filled with liquid.
In some cases, it may be desirable to put a very slight initial
stress on bag 14 prior to filling with liquid. For example, if bag
14 were supported from cover 18 in a different manner than as
shown, it may be desirable to insure that the bag 14 is fully
opened prior to filling with fluid. In such instances, the
apertures 26 may be dimensioned and positioned in the bag 14 such
that the resistance to gas flow therethrough is equal to or
slightly greater than the resistance to gas flow through the
conduit member 22. By thus controlling the ratio of gas flow
resistance of apertures 26 and conduit member 22, the pressure
gradient across bag 14 may be controlled to impart a selected
amount of slight stress to bag 14. Upon the application of vacuum
to the device in this case, bag 14 will slowly become distended in
order to receive fluid. However, the apertures 26 will be
dimensioned such that bag 14 will not be stressed by an amount
sufficient to cause rupture or other damage.
In operation of the apparatus shown in FIG. 1, vacuum or suction is
applied via the tube 24 through the conduit member 22 to the space
between the flexible bag 14 and the generally rigid container 12.
The suction is communicated through the apertures 26 into the
interior of the bag 14, and is then directed through the conduit
member 16 and the tube 20 to the patient area. Fluid from the
patient area is drawn by the suction through the tube 20 and the
conduit member 16 to the bag 14 which receives and stores the
fluid. Because of the location of the apertures 26 in the upper
portion of the bag 14, no fluid escapes into the interior of the
container 12.
The application of reduced pressure to the area between the bag 14
and the container 12 insures that the bag 14 does not close up or
collapse during suction operation. However, because of the
construction of the present invention, the pressure on the exterior
and interior of the bag 14 is equalized, and thus the bag 14 is not
outwardly stressed, but instead remains in a relaxed unstressed
condition during suction operation. Elimination of outward stress
on the bag enables the use of a relatively lightweight and
inexpensive material for the construction of the bag, without
danger of rupture of the bag. After the bag is filled with liquid,
application of vacuum or suction through the tube 24 is terminated,
the cover 18 is removed and the bag 14 is then removed, emptied and
disposed of. Although not shown, a normally closed port may be
defined in the bag to enable the bag to be easily emptied when
desired. A new sterile bag 14 is then connected to the cover 18 and
inserted into the rigid container 12 for reception of additional
fluid, without the necessity of any sterilization or cleaning of
the container 12.
FIGS. 2 and 3 illustrate in greater detail the construction of the
flexible bag 14. Bag 14 preferably comprises a generally flat,
rectangular bag sealed around the peripheral edges and sealed at
the top by a heat-sealed strip 30. The conduit member 16 is mounted
through a hole in one side of the bag 14 and comprises a first
conduit member 32 having an annular base 34 which is heat-sealed or
glued to the interior of the bag 14. The first conduit member 16
also includes a hollow cylindrical extension 36 which extends from
base 34 through the hole in the bag 14. The cylindrical extension
36 includes an inwardly extending area of increased thickness to
provide a friction fit with a second conduit member 38. The second
conduit member 38 includes a central tube portion 40 having an
opening therethrough to provide a path to the interior of the bag
14. Prior to attachment of the bag 14 to the cover 18, the conduit
member 16 extends from the side of the bag in the manner shown in
FIG. 2. The bag 14 may thus be rolled into a relatively compact
shape for easy packaging and storage.
FIG. 4 illustrates in greater detail the support of the bag 14
within the container 12. The first conduit member 32 extends
through an aperture in the cover 18 and frictionally receives the
second conduit member 38 in order to secure the bag to the cover
18. The drainage tube 20 is then secured to the central tube
portion 40 and is extended to the patient area to receive fluid.
The cover 18 includes an annular extension 44 which is dimensioned
to be securely received by the interior side walls of container 12.
An O-ring 46 is carried by the extension 44 to ensure a vacuum
tight seal. The conduit 22 extends through the cover 18 and is
rigidly connected thereto in order to receive the vacuum tube 24 in
the manner previously described.
FIG. 5 illustrates an exploded view illustrating the manner of
connection of the first conduit member 32 and the second member 38
to the cover 18. Bag 14 is omitted from FIG. 5 for ease of
illustration. The first conduit member 32 is extended through a
hole 48 formed in the cover 18. An annular lip 50 on the
cylindrical extension 36 abuts with the lower edge of the hole 48
to properly position the first conduit member 32. The second
conduit member 38 is then disposed through the hole 48 from the top
of cover 18 and manually snapped into frictional fit inside the
cylindrical extension 36. An annular lip 52 formed on the conduit
member 38 properly positions the conduit member 38 relative to the
cover 18. The drainage tube 20 is then connected to the tube
portion 40, wherein fluids from the patient area may be directed
into the interior of the bag 14. The above-described conduit member
construction enables ease of attachment of the bag 14 to the cover
18, while maintaining a vacuum tight connection. However, due to
the provision of apertures 26 in bag 14, vacuum leaks in the
conduit members or in the cover do not cause the bag 14 to
collapse, as is the case with some prior art devices.
FIG. 6 illustrates a medical suction apparatus 60 which includes a
number of improvements over the device shown in FIGS. 1-5 and which
is the preferred embodiment of the present invention. Suction
apparatus 60 comprises an open top container or canister 62 and a
lid 64. Lid 64 includes a vacuum inlet 66 to which may be attached
a flexible tube 68 which leads to a source of reduced pressure. Lid
64 also includes a fluid inlet port 70 through which extends a
fluid inlet conduit 72. A rubber hose 74 may be attached to the
conduit 72 and extended to a patient area in order to draw fluid
from the patient. A double walled bag or sack 76 is connected to
the fluid inlet conduit in a manner to be subsequently described
and is disposed within the container 62 in order to receive the
fluid drained from the patient area. Sack 76 preferably includes
indicia 78 printed thereon in order to enable measurement of the
amount of fluid contained within the sack.
FIG. 7 illustrates the underside of the container 62 and lid 64. As
will be described later in greater detail, the underside of lid 64
includes a downwardly extending annular projection 80 through which
the fluid inlet port 70 extends. The upper portion of the sack 76
includes a resilient fluid inlet conduit member or port device 82.
Preferably, the port device 82 is constructed of plastic and is
shaped to be frictionally fit over the annular projection 80 in
order to support the sack 76 within the container 62 in the manner
illustrated. The port device 82 is bonded to the top of the sack 76
by means of an annular heat seal 84. The port device 82 includes a
fluid inlet conduit 86 which communicated with conduit 72 in order
to admit fluid received from the hose 74 into the interior of the
sack 76.
A vacuum inlet port 88 extends through the lid 64 for communication
with the vacuum inlet 66 and the hose 68 in order to admit a
partial vacuum to the space between the exterior of the sack 76 and
the container 62. Apertures 90 and 92, to be later described in
detail, are formed through the sidewalls of the sack 76 in order to
tend to equalize the pressure between the interior and the exterior
of the sack 76 to prevent collapse thereof upon application of
vacuum.
An important aspect of the present invention is the provision of a
pair of sack separator levers 94 and 96. Levers 94 and 96 are
pivoted to the underside of the lid 64 and include end portions
which are disposed between the underside of the lid 64 and the port
device 82 of the sack 76. As will be subsequently described, when
the sack 76 is full of fluid, the levers 94 and 96 may be manually
pivoted in order to separate the sack 76 from the lid 64 to enable
disposal of the sack 76. A float valve 97 is mounted to the
underside of the lid 64 above the sack separator 96. In a manner to
be subsequently described, the float valve 97 prevents passage of
liquid through the vacuum inlet 88 upon overflow of fluid within
the container 62.
FIG. 8 is a side view of the rectangular sack 76. Preferably, the
sack 76 is constructed from a suitable transparent flexible plastic
such as polyethylene modified with ethyl vinyl acetate. Sack 76
includes an inner flat sack 98 constructed by an upper heat seal
100 and a lower heat seal 102 made on a section of plastic flat bag
stock. The inner sack is disposed within an outer sack 104 which is
constructed of the same transparent plastic material. The outer
sack 104 is also constructed from conventional flat bag stock and
includes an upper heat seal 106 and a lower heat seal 108. The port
device 82 comprises a two piece member constructed in a similar
manner as the conduit member 16 shown in FIG. 2. The port device 82
is heat sealed by a circular heat seal 110 through the tops of the
bags 98 and 104.
In the preferred embodiment, a line of perforations 112 is defined
in one upper end portion of the sack 76. After the sack is filled
with fluid, the nurse or other operator may grasp the corner of the
sack and tear the corner of the sack along the perforations 112.
The fluid within the sack may then be quickly dispensed from the
sack.
The aperture 90 is formed through the side wall of the outer sack
104, while the aperture 92 is formed through the side wall of the
inner sack 98. In the preferred embodiment, a pair of apertures 90
are formed through the front and back of sack 104 by a punch
operation, while a similar pair of apertures 92 are formed through
the front and back of sack 98. The apertures 90 and 92 are spaced
apart in this manner to provide a splash guard function for the
system. When fluid is introduced into the sack 76, fluid tends to
splash and form an aerosol type medium which tends to exit through
a conventional open aperture. By the spacing of the apertures 90
and 92 in the manner illustrated, the apertures act as a baffle to
aerosol to prevent leakage within the container 62. The provision
of the double sack shown in FIG. 8 ensures the integrity of the bag
and substantially reduces the possibility of a fluid leak. In
addition, in case of overflow of the inner bag 98, the outer bag
104 would serve as an auxiliary collection receptacle.
In construction of the sack 76, two different sizes of flat bag
stock are utilized. Suitable lengths are cut from the two different
sizes of bag stock and indicia 78 is printed upon the smallest size
bag stock. Additional indicia may be printed upon the larger bag
stock, if desired. The upper ends of each of the bag portions are
then heat sealed to form sacks 98 and 104. A circular hole is then
punched into the top of each of the sacks and the inner sack 98 is
then inserted through the bottom of the outer sack 104. The port
device 82 is inserted through the circular hole and the circular
heat seal 110 is made to firmly connect the port device 82 to both
of the sacks 98 and 104. The lower open end of the sack 104 is then
peeled back and the heat seal 102 is made along the bottom of the
inner sack 98. The heat seal 108 is then made on the bottom of the
sack 104 in order to form the complete sack 76.
FIG. 9 is a top view of a folded sack 76. In this folded
configuration, the sack 76 may be easily packaged in a small
plastic bag to maintain the sack 76 in a sanitary condition during
transportation and storage. FIG. 9 also illustrates in greater
detail the annular heat seal 110 which bonds the port device 82 to
the top of the sacks 98 and 104.
FIG. 10 illustrates connection of the sack 76 to the underside of
the lid 64. The lid 64 is placed in an upsidedown position and the
port device 82 is placed on the top of the annular projection 80.
The thumbs of the operator are then used to push the port device 82
down over the projection 80. The port device 82 is preferably
constructed from a resilient plastic material such as polyethylene
or the like and is dimensioned to tightly receive the projection
80. As shown in FIG. 10, the sack separator levers 94 and 96 are
pivotally connected to the underside of a lid 64 by means of pivots
116 and 118. As the port device 82 is pushed over the projection
80, the levers 94 and 96 are pivoted such that the semicircular end
portions 120 and 122 of the levers are disposed between the
underside of the lid 64, the sack is disposed within the container
62 and the lid 64 is placed on the top of container 62. Suction is
applied to hose 68 and causes the lid 64 to be snapped into place
on the top of the container 62. Fluid may then be drawn from a
patient area through the hose 74 into the sack 76.
FIG. 11 illustrates the disengagement of the sack 76 from the lid
64 after the sack 76 is filled with fluid. Generally, the nurse or
other operator of the suction system will remove the lid 64 from
the container 62 and carry the fluid-filled sack to a sink or other
disposal location. The nurse will then place her thumbs on the top
of the lid 64 and place the ends of her fingers on pads 124 and 126
which are integral end portions of the levers 94 and 96,
respectively. The nurse then pulls the pads 124 and 126 toward the
underside of the lid 64 and the curved end portions 120 and 122
push the port device 82 off the annular projection 80. The
fluid-filled sack 76 is separated from the lid 64 and a new sack
may be attached to the lid 64 and additional fluid collected.
FIG. 12 illustrates the tearing of the corner of the sack 76 along
the line of perforations 112. This opens the upper corner of both
the outer sack 104 and the inner sack 98 and enables the fluid
contained within the sack 76 to be quickly poured into a sink or
other suitable receptacle. The sack 76 may then be disposed of in
the trash or the like. In the preferred embodiment, it has been
found desirable to pour out the contents of fluid of the sack 76
prior to disposal of the sack in order to prevent subsequent
contamination of personnel which are required to handle the sack
during incineration or other disposal.
FIG. 13 illustrates a partially sectioned view of the present
assembly during the attachment of the sack-bearing lid 64 to the
container 62. In FIG. 13, sack 76 has been attached to the
underside of lid 64 by forcing the port device 82 over the annular
projection 80 in the manner previously described. As shown in FIG.
13, the port device 82 comprises two interlocking plastic pieces
130 and 132. An important aspect of the invention is that piece 134
includes an annular diaphragm which supports in the center thereof
the fluid inlet conduit 72. The diaphragm 134 is constructed to be
responsive to the magnitude of vacuum applied to the interior of
the container 62. The greater the vacuum applied, the more the
diaphragm 134 is flexed to cause the side-walls of piece 130 to
more tightly grip the outer walls of the annular projection 80.
This prevents the port device 82 from being sucked off from the
annular projection 80 upon the application of high vacuum.
As shown in FIG. 13, the lid 64 includes a downwardly directed
concavo-convex top portion 140 having in the center thereof the
fluid inlet port 70 which extends through the projection 80. The
particular downwardly directed concavo-convex construction of the
top 140 provides great strength to the top and enables the top to
be integrally constructed from injection molded plastic such as
nylon or the like. The vacuum inlet 66 is integrally formed from
the lid and extends upwardly to enable connection of a hose 58
thereto.
An annular groove 142 is formed about the underside periphery of
the lid 64, with the groove being shaped with a bead 144 which
extends about the upper lid of the container 62. A downwardly
extending outwardly flared side 146 integrally extends below the
groove 142. The side 146 includes an annularly outwardly directed
flange 148 to enable ease of handling of the lid.
An important aspect of the present lid is that a transient seal
portion 150 is provided on the interior of the side 146. As shown
in FIG. 13, when the lid 64 is initially set upon the top of the
container 62, the bead 144 abuts the transient sealing portion 150
of the side 146. Vacuum is applied through the hose 68 and through
the vacuum port 88 into the container 62. If the hose 74 is then
temporarily obstructed by the nurse or operator, sufficient suction
is applied to the lid 64 in order to move the lid 64 downwardly
such that the bead 144 snaps into place into the groove 142. The
mating of the bead 144 within the groove 142 is illustrated in FIG.
14. As the lid 64 is pulled downwardly into seating engagement with
the container 62, the sidewall 146 is slightly cammed outwardly
until the bead 144 snaps into place into the groove 142. A vacuum
fit is then provided at the juncture of the bead 144 and the groove
142. No O-ring is required for the lid 64. The lid 64 is preferably
constructed from a flexible plastic such as nylon or the like to
enable the outward bending of the side 146 during attachment of the
lid 64 to the container 62. Similarly, the edge 146 may be
outwardly bent by the hands of a nurse in order to enable easy
removal of the lid 64.
FIG. 13 also illustrates in detail the pivotal connection of the
levers 94 and 96 to the underside of the lid 64. Pivots 116 and 118
are integrally formed on the underside of the lid 64 and include
openings therein for receiving cylindrical pivot members 160 and
162. Pivot member 160 is carried by a flange 164 integrally formed
with lever 94, while pivot member 162 is carried by a flange 166
integrally formed to the lever 96. The pads 124 and 126 of the
levers are provided with corrugations in order to improve the
strength of the levers. As previously noted, upon manual depression
of the pads 124 and 126, the levers 94 and 96 may be pivoted in
order to remove the port device 82 from the annular projection
80.
FIG. 13 also illustrates the attachment of the float valve 97
between the lever 96 and the underside of the lid 64. In the normal
position, the float valve 96 hangs downwardly out of contact with
the vacuum inlet 88. During an overflow condition, as will be
subsequently described, the float valve 97 floats on the surface of
the fluid in order to obstruct the opening of the vacuum inlet 88
to prevent fluid from being drawn therethrough.
FIG. 13 also illustrates in greater detail the construction of the
apertures 90 and 92 formed through the sack 76. Each of the
apertures are formed by a pair of semicircular slits 166 and 168.
Under low vacuum conditions, air is drawn through the slits 166 and
168 in order to equalize the pressure between the interior and
exterior of the sack 76. The slits 166 and 168 define small spaced
apart hinge portions 170 and 172 of plastic material which support
a valve flap 174 of flexible plastic. In low vacuum conditions, the
flap 164 substantially obstructs the apertures 90 and 92 except for
the small openings provided by the slits 166 and 168.
However, upon the application of greater vacuum, the edges of the
flaps 174 tend to be bent to provide a larger effective opening for
the apertures 90 and 92. The flaps 174 thus tend to act as a
butterfly type valve in order to provide sufficient resistance to
flow through the apertures so that the sack 76 will fully expand
under low vacuum. However, upon the application of high vacuum and
resulting high air flow through the apertures, the flaps 174 are
bent to provide an enlarged flow opening to eliminate the
possibility of rupture of the sack at a weak point. Additionally,
as previously noted, aperture 90 is formed in an outer sack 104,
while the aperture 92 is formed in an inner sack 98 to provide a
splash baffle to prevent leakage of medical fluid into the interior
of the container 62.
FIG. 15 illustrates another embodiment of the aperture valving
invention. In this embodiment, the apertures are formed by four
semicircular slits 180-186 to provide four small plastic hinges
which support a flexible valve flap 188. Due to the molecular
orientation of sheets of plastic, two of the four hinges defined by
the slits 180-186 will be weaker than the remaining two hinges.
Upon application of low vacuum to the system, the slits 180-186
provide a relatively small opening to ensure that the sack 76 is
fully expanded for suction of medical fluid. However, under higher
fluid flow, two of the small hinges formed by the slits 180-186
will rupture to provide a larger effective opening for increased
flow rates through the aperture. Provision of the four slots
180-186 provides improved resistance control to the flap 188 during
very low vacuum pressure application.
FIGS. 16-20 illustrate in detail the construction and operation of
the float valve of the invention. FIG. 16 is a top view of the
float valve 97 which comprises an elongated strip of flexible
plastic material having low fluid absorption characteristics. The
float valve includes a free end portion 190 which hangs below the
vacuum inlet port during normal operating conditions and which
obstructs the vacuum during overflow conditions. A generally curved
cutout portion 192 is provided in the other end of the strip for
abutting with the exterior of the projection 80 of the lid 64. A
generally U-shaped cutout portion 194 defines a rectangular tab 196
which includes a slot 198 for receiving a pivot member depending
from the underside of the lid 62. Rubber material which has been
found to work well for the present float valve is a closed cell
Neoprene rubber, manufactured and sold by B. F. Goodrich Company.
Preferably, the material for constructing the float valve 97
comprises a cellular rubber or plastic material which has
flexibility and low fluid absorption characteristics, but yet which
has sufficient strength to obstruct the vacuum inlet during
overflow conditions.
FIG. 17 illustrates how the sack separator lever 96 may be removed
from the underside of the lid 64 by manually pulling the
cylindrical projection 162 away from the pivot projection 118 which
extends from the underside of the lid 64.
After removal of the lever 96, the float valve 97 is inserted over
the pivot projection 118 as shown in FIG. 18. FIG. 18 illustrates
how the slot 198 of the float valve 97 receives the pivot
projection 118. FIG. 19 also illustrates how the curved end portion
192 abuts against the annular projection 80 to provide additional
support to the inwardly directed end of the float valve 97. The
U-shaped cutout portion 194 provides for greater flexibility of the
float valve 97 while enabling the pivot projection 118 to be
utilized both as a support for the float valve and as a pivot
support for the lever 96. As shown in FIG. 19, after the float
valve 97 is firmly attached to the pivot projection 118, the lever
96 is again snapped into pivotal connection with the projection
118. The float valve 97 is then firmly attached to the underside of
lid 64.
FIG. 20 illustrates the operation of the float valve 97 during
overflow conditions. Under some operating conditions, excessive
fluid may be introduced into the sack 76. When this occurs, the
fluid first overflows from the inner sack 98 into the outer sack
104. If additional fluid is then directed into the sack 76, the
fluid overflows into the aperture 90 into the interior of the
container 62. When the lever of fluid between the container 62 and
the exterior of the sack 76 reaches the level of the float valve
97, the float valve 97 floats on the surface of the fluid and the
free end 190 is carrid upwardly by the fluid until the vacuum inlet
orifice 88 is obstructed by the free end portion 190 as shown in
FIG. 20. With the use of the proper types of flexible cellular
material, the end portion 190 will be deformed upwardly into the
vacuum inlet 88 and the air cells within the cellular material are
compressed in order to provide a fluid tight obstruction to prevent
fluid from being sucked into the vacuum system of the hospital.
After an overflow condition occurs, the present float valve 97 may
be snapped out of place and a fresh float valve installed as shown
in FIGS. 17-19. The present float valve is extremely simple and
economical to construct and manufacture and provides
maintenance-free operation.
FIG. 21 illustrates another configuration of a container for use
with the present invention which provides stacking for shipping and
storage of the rigid container. As shown in FIG. 21, a first
open-topped container 200a includes an upper cylindrical portion
202a which is joined with a lower frustoconical portion 204a by
means of an annular shoulder 206a. Shoulder 206a may be utilized to
support the container in an annular wall bracket. A second annular
shoulder 208a is provided in the lower portion of the container for
abutment with a lower container in a manner to be described. As
shown in FIGS. 21 and 22, on the lower interior of the container
200a are three feet or projections 210a. The bottom of container
200a has an upwardly directed conical configuration.
A second container 200b is illustrated in a stacking configuration
within container 200a. Container 200b is identical to container
200a and includes a cylindrical upper portion 202b, a shoulder 206b
and a conical lower portion 204b. As shown in FIG. 21, the lower
annular shoulder 208b of container 200b abuts with the top of the
feet 210a to prevent the container 200b from being too tightly
inserted within the container 200a. The length of the feet 210a is
such that the shoulder 208b abuts with the top of the feet 210a
prior to abutment of shoulder 206b with the top of container 200a.
Container 200b also includes three feet or pedestals 210b to enable
stacking of a third container in the manner illustrated.
FIG. 23 illustrates the interconnection of two of the present
suction systems to enable parallel simultaneous filling of the two
containers from a single patient area. A first container 220
includes a lid 222 which supports a flexible sack within the
container in the manner previously described. A second suction
container 224 includes a lid 226 which supports a second flexible
sack within the container 224. A vacuum source is connected through
a hose 228 to a Y-connection 230 for connection to a hose 232 which
extends to a suction inlet lid 226. The Y-connection 230 is also
connected to a second hose 234 which is connected to the suction
inlet of lid 222. A hose 236 is connected to the fluid inlet port
of the lid 222 and is connected to one end of a Y-connection 238. A
second tube 240 is connected to the fluid inlet port of lid 226 and
is connected to the other end of the Y-connection 238. A hose 242
extends from the Y-connection 238 to the patient area. Upon
application of vacuum to hose 228, fluid is drawn from a patient
area through tube 242 and tubes 236 and 240 into the flexible sacks
within containers 220 and 224. The parallel connected system
enables the system to be utilized for large operations and other
instances when large fluid collection capacity is required.
FIG. 23 also includes the use of roll about supports for the fluid
container of the invention. The support includes a lower generally
X-shaped support 250 from which extend four upright members 252.
The containers 220 and 224 are received between the upper members
252. Wheels 254 enable the supports to be freely rolled about an
operating table or floor when desired.
FIG. 24 illustrates a conductive grounding strip for use with the
invention. A container 260 includes a lid 262 constructed in
accordance with the present invention. A tube 264 extends to a
patient area and is connected to the fluid inlet port of the lid
262. A vacuum regulator 266 is connected to the vacuum inlet of the
lid 262 and is connected through a tube 268 to a source of vacuum.
The tubes 268 and 264 include conductive paths in order to prevent
electric shock of the patient. However, if the tube 264 terminates
in a plastic insulated lid, a path to ground will not be provided
from the patient. Therefore, a black high carbon content rubber
strip 270 is provided which includes an aperture 272 for receiving
the end of the hose 264. The strip 270 includes an aperture at the
other end thereof for receiving an end of the regulator 266. As the
rubber strip 270 is conductive, tubing 264 is shorted to tubing 268
which is normally grounded. In this manner, a path to ground is
provided from the patient to prevent sparks and the like from
igniting the explosive oxygen atmosphere often present in operating
rooms and the like.
FIG. 25 illustrates how the present container and lid may be
modified to provide a disposable rigid medical fluid collecting
system. The container 280 is constructed from transparent plastic
in the same manner as the previously described container. A fluid
level indicia 280 is printed upon the exterior of the container. A
lid 284 is provided to cover the open top of the container 280. Lid
284 is constructed in the identical configuration as that
previously described. A vacuum inlet port 286 is integrally formed
in the lid 284 for connection to a source of reduced pressure.
In this embodiment, a plastic nipple 288 is rigidly fitted within
the fluid inlet port of the lid 284. As shown in FIG. 26, the lid
284 is provided with a downwardly directed concavo-convex shape in
the manner previously described. The plastic nipple is shaped in
the same manner as the part 130 shown in FIG. 13 and includes an
upper extending conduit 290 for connection to tubing which leads to
a patient area. In this embodiment, the flexible sack of the
invention is not required. Suction is merely applied to the vacuum
inlet port 286 and fluid is drawn from the patient area through the
conduit 290 into the container 280. Caps may be placed over the
port 286 and the conduit 290 and the resulting closed system may
then be completely disposed of if desired. In some cases, the
container 280 may be cleaned and reutilized.
FIGS. 27-29 illustrate another embodiment of the present invention
utilizing a different embodiment of a sack separating lever. FIG.
27 illustrates a rigid container 300 which threadedly receives a
rigid plastic domed top 302. A vacuum inlet nipple 304 is attached
to the top 302 and may be connected to a flexible hose 306 for
connection to a source of reduced pressure. A fluid inlet conduit
308 is mounted in the top for connection to a hose 310 leading to a
patient area to receive fluid. A post 312 is rigidly affixed to the
top 302 and pivotally supports a rigid plate 314 having a
cylindrical projection 316.
In use of the system shown in FIG. 27, a sack constructed in the
previously described manner is connected beneath the lid 302.
Vacuum is then applied through the hose 306 and fluid from the
patient area is drawn through the tube 310 for collection within
the collection sack within the container 300. When it is desired to
separate the fluid filled sack from the container 300, the lid 302
is removed and the plate 314 is moved to the position shown in FIG.
28. The projection 316 is placed directly over the plastic port
device 318 connected to the sack, and downward pressure is applied
by the nurse or the operator. As shown in FIG. 29, the downward
pressure causes the plastic port device 318 to the sack 320 to be
disengaged from the annular downward projection 322 of the lid 302.
In this manner, the sack 320 may be emptied and disposed of in the
previously described manner. A new sack may then be inserted over
the annular member projection 322 and the lid reattached to the
container 300 for additional use of the system.
It may thus be seen that the present suction device may be very
economically manufactured and utilized. Due to the flexible nature
of the bags utilized, the suction apparatus may be conveniently
stored in a relatively small package, thereby resulting in
considerable space-saving in hospital environments. Because of the
particular operation of the device, the flexible bags utilized are
not subject to excessive stress during suction operation, and
therefore may comprise relatively lightweight and economical
plastic bags. The present device is extremely simple in design and
construction, and thus is not generally subject to maintenance
problems and may be operated with a minimum of instruction.
Moreover, the bags of the present device do not tend to collapse in
case of a vacuum leak in the cover or in the conduit members. The
flexible bags of the invention are also completely disposable so
that cross-contamination from patient to patient is reduced.
In addition, the present invention provides an improved medical
suction device having a lid which is automatically attached to a
container by application of vacuum thereto. The double lined
flexible sack of the invention provides improved fluid integrity.
The novel aperture valving structure of the invention enables the
system to work with various degrees of suction. The float valve of
the invention prevents fluid overflow from the system into the
vacuum supply of a hospital. The sack separating levers of the
invention enable a fluid filled sack to be easily disengaged from
an upper lid without requiring a nurse to touch the fluid filled
sack. Construction of the fluid inlet port device of the invention
prevents the sack from being sucked off the lid during heavy
application of pressure. The provision of the stacking feet in the
lower interior of the container enables a plurality of the
containers to be stacked together for ease in shipping and
storage.
Whereas the present invention has been described with respect to
specific embodiments thereof, it will be understood that various
changes and modifications will be suggested to one skilled in the
art, and it is intended to encompass such changes and modifications
as fall within the scope of the appended claims.
* * * * *