U.S. patent number 3,768,478 [Application Number 05/283,885] was granted by the patent office on 1973-10-30 for aspiration device for body fluids.
This patent grant is currently assigned to Vermitron Medical Products, Inc.. Invention is credited to Charles R. Ashley, Ira J. Fertik, Charles M. Huck.
United States Patent |
3,768,478 |
Fertik , et al. |
October 30, 1973 |
ASPIRATION DEVICE FOR BODY FLUIDS
Abstract
An aspiration device for withdrawing fluid from a patient's body
comprises a closed container and tubular members opening into the
container to define passages for suction and fluid respectively. A
control valve assembly in the container at the suction passage cuts
off suction when fluid saturates an expansible, porous pad which
then applies a nonporous, resilient sealing member to the suction
passage.
Inventors: |
Fertik; Ira J. (Queens, NY),
Huck; Charles M. (Oldwick, NJ), Ashley; Charles R.
(Somerville, NJ) |
Assignee: |
Vermitron Medical Products,
Inc. (Carlstadt, NJ)
|
Family
ID: |
23087991 |
Appl.
No.: |
05/283,885 |
Filed: |
August 25, 1972 |
Current U.S.
Class: |
604/320;
137/854 |
Current CPC
Class: |
A61M
1/784 (20210501); A61M 1/0001 (20130101); A61M
2205/7536 (20130101); Y10T 137/789 (20150401) |
Current International
Class: |
A61M
1/00 (20060101); A61m 001/00 () |
Field of
Search: |
;128/276-278,349,350
;137/409,525 ;251/63.6,334 |
References Cited
[Referenced By]
U.S. Patent Documents
Primary Examiner: Rosenbaum; Charles F.
Claims
The invention claimed is:
1. An aspiration device for withdrawing fluid from a patient's
body, comprising:
a closed container;
a first suction means defining a first passage for applying suction
to the interior of said container;
a second suction means defining a second passage for fluid to flow
into said container; and
a control valve assembly for cutting off suction from the interior
of said container after a predetermined quantity of fluid has
entered said container, said control valve comprising:
a porous expansible pad exposed to said fluid in said container for
expansion when saturated by said fluid; and
a resilient, nonporous member interposed between said pad and said
first passage and arranged to seal said first passage when said pad
expands, so that suction is cut off from said second passage to
stop withdrawal of fluid from said patient's body.
2. An aspiration device as defined in claim 1, further comprising a
cup shaped support for said pad in said container, said support
having at least one opening for exposing said pad to said fluid in
said container.
3. An aspiration device as defined in claim 2, wherein said
container comprises a generally circular cover; and a bag
pheripherally joined to said cover, whereby said bag, cover and
valve assembly can be discarded together as a unit.
4. An aspiration device as defined in claim 3, further comprising a
cylindrical base having an open top, said cover fitting removable
on said top of said base with said bag suspended inside said base,
said control valve assembly having a passage formed therein for
passing air between the inside and outside of said bag in said base
for equalizing pressure on both sides of said bag.
5. An aspiration device as defined in claim 2, wherein said first
suction means comprises a block rotatably fitted in said cup shaped
member, said first passage extending through said block, said block
having a third passage for passing suction between said first
passage and the interior of said container, said cup shaped member
having a lateral opening normally aligned with said third passage,
whereby said third passage is closed by rotation of said block in
said cup shaped member away from said lateral opening.
6. An aspiration device as defined in claim 1, wherein said
container is cylindrical in form, said first suction means
comprising a tubular member opening into one end of said
container.
7. An aspiration device as defined in claim 6, wherein said pad and
said resilient member are ring shaped and surround said tubular
member, said first passage having a cylindrical end disposed
adjacent to said resilient nonporous member for closure thereby
when said pad expands.
8. An aspiration device as defined in claim 7, further comprising
an inverted cup shaped baffle in said container disposed adjacent
to said second passage for shielding said first passage from fluid
entering said container.
9. An aspiration device as defined in claim 7, further comprising a
cup shaped support for said pad in said container, said support
having at least one opening for exposing said pad to said fluid in
said container.
10. An aspiration device as defined in claim 9, wherein said cup
shaped support is inverted to define a baffle adjacent to said
second passage for shielding said first passage from fluid entering
said container.
Description
This invention relates to the art of aspiration devices for body
fluids and more particularly concerns an aspiration device having
novel valve control means for cutting off suction when the level of
fluid in a container rises to a predetermined level.
Aspiration devices heretofore have either lacked means for cutting
off suction automatically, or have employed complex valve control
means for controlling suction.
The present invention is directed to an improved and simplified
valve control means for cutting off suction in as aspiration
device. According to the invention, the valve control means
includes an expansible porous pad which expands upon absorbing
moisture. When the pad is fully saturated it expands to cut off a
passage through which suction is applied to a patient for
withdrawing body fluids. The valve control can be installed in a
cover of a fluid container, or it can be installed in an overflow
unit interposed between a suction pump and a fluid container.
It is therefore a primary object of the present invention to
provide a novel, improved and simplified valve control means for
cutting off suction in an aspiration device for body fluids.
Another object of the present invention is to provide a valve
control means as described in which an expansible pad is disposed
to cut off suction when the pad becomes fully saturated and
expanded by absorbed liquid.
A further object of the present invention is to provide an
aspiration device for collecting body fluids, comprising a
throw-away fluid container and cover therefor, with valve control
means as described above installed in the cover.
These and other objects and many of the attendant advantages of
this invention will be readily appreciated as the same become
better understood by reference to the following detailed
description when considered in connection with the accompanying
drawings in which:
FIG. 1 is a perspective view of an aspiration device embodying the
invention, part being broken away to show internal
construction;
FIG. 2 is a top plan view of the device;
FIG. 3 is an enlarged vertical sectional view taken along line 3--3
of FIG. 2, parts being broken away;
FIG. 4 is an exploded perspective view of parts of a valve control
assembly employed in the aspiration device of FIGS. 1-3;
FIG. 5 is a side elevational view of another aspiration device
according to the invention which includes a fluid collection
container and overflow unit;
FIG. 6 is an enlarged vertical sectional view of the overflow unit,
taken along line 6--6 of FIG. 5;
FIG. 7 is a horizontal sectional view taken along line 7--7 of FIG.
6;
FIG. 8 is a vertical sectional view similar to FIG. 6 of another
overflow unit embodying a modification of the invention;
FIG. 9 is a side elevational view partially in section of a further
aspiration device including another fluid collection container and
another overflow unit; and
FIG. 10 is an enlarged vertical sectional view taken along line
10--10 of FIG. 9.
Referring now to the drawings wherein like reference characters
designate like or corresponding parts throughout, there is
illustrated in FIGS. 1-3, an aspiration device generally designated
by reference numeral 20 comprising a hollow cylindrical container
22 open at the top and having a closed circular bottom 24. On the
annular top of a cylindrical wall 25 is a reilient ring gasket 26
(FIG. 3). The annular top of the wall 25 fits frictionally into a
circumferential groove 28 formed in a channel shaped rim 29 of a
circular cover 30 which may be lifted off the base 22 by means of a
handle 32 integrally formed with a flange 34 extending tangentially
of the cover 30 and integral with the rim 29 as clearly shown in
FIG. 2. The handle 32 folds up at creases or notches 36 formed at
ends of the flange 34.
The cover 30 has a central inwardly dished body 38 and extending
upwardly therefrom is a first integral nipple 40 to which may be
connected a tube which will convey fluids under suction from the
body of a patient. The fluids are collected in a cylindrical bag 42
whose upper open end is fused by heat sealing to a short, vertical
cylindrical wall 43 disposed between the dished body 38 and a flat,
annular, circumferential ledge 44 which is integrally joined to the
inner side of the channel shaped rim 29 of the cover 30. The wall
43 is integral with the periphery of the body 38 and the inner edge
of ledge 44. The cover 30 and bag 42 form a unit for collecting
fluid. This unit can be lifted clear of the base and discarded.
Another clean, sterilized bag and cover can then be replaced on the
base. A pour spout 48 having a removable plug 49 is provided on the
cover for pouring fluid from the closed bag 42.
Suction is applied to the interior of the bag via a nipple 47
forming part of a valve control assembly generally designated by
reference 50 installed in the cover 30. The valve control assembly
50 comprises a cylindrical block 52 as best shown in FIG. 4.
Integral with the top of the block 52 and extending radially of the
nipple 47 are radial flanges 54 which serve as finger grips for
turning the block for purposes to be hereinafter described. A
circumferential bead or ridge 56 is formed on the side of the block
52 and engages slidably in a circumferential groove 58 formed in a
cylindrical cup 60 integral with the body 38 of the cover 30. The
cup 60 has circumferentially spaced slots or apertures 61 formed in
its sides 62 and bottom 64. Seated inside the cup is a porous,
expansible cylindrical pad 66 which may be made of spongy or felt
material. Disposed on the porous pad 66 is a circular, resilient,
nonporous disk 68 made of rubber or the like. The top of disk 68 is
disposed below a vertical central passage 70 passing axially
through the block 52 and the nipple 47. A right angle passage 72 is
also formed in block 52 and communicates between the bottom of the
block and its side where passage 72 registers with an opening 74
formed in the side of the cup 60 (FIG. 3). The passage 72 is used
to equalize the air pressure on the outside of the bag 42.
When liquid collects in the bag 42 and its level rises to reach pad
66, this pad will expand and raise disk 68 to close both of the
passages 70 and 72. Closing of the passage 70 will cut off suction
applied to the interior of the bag via the nipple 47 and will cut
off application of suction to the exterior of the bag via the
passage 72 and the opening 74 in the side of the cup 60. By
manually turning the block 52 with the finger grips 54 mentioned
above, passage 72 is located out of alignment with the opening 74
so that fluid cannot leak through this opening when the collection
unit is tipped over to empty it via the pour spout 48.
Suction is applied via nipple 40 from the interior of the bag and
cover unit to the patient. When suction is cut off at the valve
control assembly 50, suction is of course cut off at the patient's
body from which fluid is being withdrawn. The tube connected
between the patient's body and the nipple 40 can then be removed.
Another tube 80 or the same tube indicated by dotted lines in FIG.
3 can then be fitted at opposite ends on both of the nipples 40 and
47 to serve as closures therefor. The entire bag and cover unit can
be removed from the base 22 by lifting the handle 32. It is perhaps
preferable that a part of the liquid in the bag 42 be removed via
the spout 48 by tipping the entire unit while the bag 42 is still
in the base 22. This will limit the strain on the handle 32 and on
the bag 42 itself after the partially filled bag and cover unit is
removed from the base 22.
It will be noted that the valve control assembly 50 is discarded
along with the bag 42 and the cover 30. Only the base 22 is
retained. This can be sterilized before a fresh bag and cover are
replaced in the base. All parts of the cover and bag are preferably
made of lightweight, tough plastic material such as polyethylene or
polystyrene. The pad 66 can be made of any suitable spongy material
such as compressed sponge, or it can be made of rayon fibers. The
disk 68 can be made of an elastomer such as natural or artificial
rubber. The base 22 can be made of rigid plastic material.
Alternatively it can be made of metal such as stainless steel.
However it is preferable that both the base, bag and cover be made
of transparent or translucent material so that the flow of fluid
into the bag can be observed.
FIGS. 5, 6 and 7 illustrate another aspiration device generally
designated as reference numeral 20A. A cylindrical container 90 has
an annular top 91 into which extends one end of a tube 92 which can
be connected to the patient from which fluid is being drawn. The
container 90 is closed by a removable cover or cap 93. Another tube
97 for applying suction to the interior of the container 90 is
connected at one end to a top 91 of the container 90 and at the
other end to a nipple 94 at the top of an overflow unit generally
designated by reference numeral 100.
The overflow unit 100 is a closed cylindrical container formed by
fusing two cup shaped members 102 and 104 together at their rims to
form a hermetically sealed joint 103. The nipple 94 is integrally
formed with a top 106 of the inverted cup shaped member 102.
Located inside of the member 102 and supported by a plurality of
radial ribs 108 is an inverted cup shaped baffle 110 which serves
as a guide for fluid entering the unit via the nipple 94. Supported
inside of the baffle 110 by a plurality of ribs 112 is another cup
shaped member 114 which surrounds a cylindrical skirt 116 formed at
the top of a suction tube 118. The tube 118 is secured and sealed
at a joint 119 to the center of the bottom 117 of the member 104.
The tube 118 extends axially, vertically upward and terminates
short of the member 114 to define a vertical passage 120 which
communicates with a cylindrical passage 122 between the member 114
and the skirt 116. Surrounding the tube 118 and slidable thereon is
a resilient, non-porous rubber ring 124, and below the ring 124 is
an expansible, porous ring-like pad 125 which, like the pad 66
hereinbefore described above, expands when it becomes saturated
with a liquid. The pad 125 rests on the bottom 117 of the cup
shaped member 104 and expands to lift the ring 124 which then
closed the cylindrical passage 122 to cut off suction from the tube
97 and from the container 90.
Another overflow unit, generally designated as reference numeral
100a is illustrated in FIG.8, which is similar to the unit 100 and
corresponding parts are identically numbered. In the unit 100a, a
baffle 110a extends down to and rests on the bottom 117 of the cup
shaped member 104. A plurality of axially extending
circumferentially spaced slots or openings 126 are formed in the
bottom portion of a cylindrical wall 128 of the baffle 110a. Liquid
collecting in the member 104, reaches the pad 125 which is disposed
inside the baffle 110a and surrounds the tube 118. The pad 125
expands when saturated to lift the resilient ring 124, which closes
the passage 122 and cuts off suction from the nipple 94 and the
tube 97.
FIGS. 9 and 10 show another aspirator device, generally designated
as reference numeral 20B, which includes another container 90a and
another overflow unit generally designated as reference numeral
100B. In container 90a is a stopper 130. A tube 92a is connected at
one end to the patient's body and terminates at its other end
inside the container 90a, after passage through an opening 132 in
the stopper 130. A suction tube 134 is connected between the
container 90a and a nipple 136 at the bottom of the overflow unit
100B. The tube 134 passes through a passage 135 in the stopper 130.
When fluid is collected in the container 90a, foam tends to be
generated at the upper surface of the fluid. The unit 100B is
arranged as a container to prevent passage of foam to a suction
pump (not shown) connected to a suction tube 140. The tube 140 is
connected to the upper end of a tube 141 which is secured at a
joint 143 in the top of a cup shaped member 102a and extends
axially vertically downward inside cup shaped support and strainer
member 142 which is secured by sealing at a circumferential joint
145, to the inside of the member 102a. The member 102a and a member
104a are secured together by a hermetically sealed joint 103a. A
plurality of circumferentially spaced slots or openings 144 are
formed in the sides and the bottom of the strainer member 142. A
porous expansible pad 146 is seated in the member 142 and on this
pad 146 is a resilient, nonporous disc 148 which closes the open
bottom of a suction tube 141. It will be apparent that the overflow
unit 100B effectively blocks passage of foam or liquid from the
container 90a so that it cannot pass to the suction generating pump
(not shown) connected to the suction tube 140.
In all forms of the invention described, the valve control
assemblies employ a porous, expansible spongy or felt pad in
conjunction with a nonporous resilient sealing or closure member to
close a suction passage. As described the valve control assembly
can form part of the fluid container, or it can be installed in a
separate overflow container.
It should be understood that the foregoing relates to only
preferred embodiments of the invention, and that it is intended to
cover all changes and modifications of the examples of the
invention herein chosen for the purpose of the disclosure which do
not constitute departures from the spirit and scope of the
invention.
* * * * *