WO1988004559A1 - Apparatus and method for collecting body fluids - Google Patents
Apparatus and method for collecting body fluids Download PDFInfo
- Publication number
- WO1988004559A1 WO1988004559A1 PCT/US1987/003334 US8703334W WO8804559A1 WO 1988004559 A1 WO1988004559 A1 WO 1988004559A1 US 8703334 W US8703334 W US 8703334W WO 8804559 A1 WO8804559 A1 WO 8804559A1
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- WO
- WIPO (PCT)
- Prior art keywords
- suctioning
- liquids
- reservoir
- housing
- gases
- Prior art date
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
- A61M1/64—Containers with integrated suction means
- A61M1/68—Containers incorporating a flexible member creating suction
- A61M1/684—Containers incorporating a flexible member creating suction bellows-type
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
- A61M1/60—Containers for suction drainage, adapted to be used with an external suction source
- A61M1/63—Containers for suction drainage, adapted to be used with an external suction source with means for emptying the suction container, e.g. by interrupting suction
Definitions
- This invention relates generally to apparatus and methods for draining body fluids. More particularly, it relates to apparatus and methods for reducing the likelihood of infection during the collection of fluids from body cavities of human and animal subjects by draining and disposing of the fluids without exposing the apparatus or the subjects to potential sources of contamination and infection.
- Contamination of drainage collection devices often arises from reusing containers designed to be filled repeatedly with drained body fluid and emptied.
- the evacuator described by McElhenny in U.S. Pat. No. 3,115,138 includes a capped fluid outlet. After the evacuator becomes filled it is emptied for reuse by removing the cap and expelling collected fluid via the outlet. During this operation the interior of the evacuator is exposed to the atmosphere and contamination of the evacuator may result.
- U.S. Pat. Nos. 3,779,243 and 3,774,611 disclose evacuators which employ a special valve over the fluid outlet. This valve operates to close the outlet at all times except for the time when fluid is actually being purged from the evacuator. Such evacuators may succeed in reducing the contamination brought on by purging. However, since these evacuators must be periodically opened for purging, they are exposed to the surrounding atmosphere and can become contaminated and therefore a source of infection.
- Goldberg and Bazell in their U.S. Patent No.
- the present invention is directed to a closed drainage apparatus for receiving fluid (liquids and gases) from body and tissue cavities including suctioning means in communication with the cavities for suctioning and receiving the drained body fluids.
- the suctioning means comprise a resilient bellows which draws body fluid from the cavities under the inherent spring back suction force produced as it returns to its normal, expanded condition.
- the apparatus also includes a reservoir into which excess body liquids from the suctioning means are automatically siphoned and into which the suctioning means may be emptied, all without exposure of the system to the atmosphere.
- the secondary reservoir consists of an impervious, flexible bag in communication with an outlet port of the suctioning means which has a one-way valve at its inlet to prevent liquid from flowing back from the reservoir.
- the secondary reservoir is vented to the atmosphere through one or more small pore hydrophobic filters to permit gases in the system to be purged without retrograde introduction of microorganisms into the reservoir.
- Yet another object of the invention is to provide a closed drainage system in which gases in the system can be purged without exposing the system to the atmosphere.
- a still further object of the present invention is to provide an economical, easy to use, closed suction drainage apparatus and method.
- FIGURE 1 is a perspective view of a closed drainage apparatus in accordance with the practice of the present invention
- FIGURE 2 is a cross-sectional elevation view of the apparatus of FIG. 1, taken generally along section line 2-2 of that figure;
- FIGURE 3 is an enlarged cross-sectional view of a one-way valve illustrated in FIG. 1, taken along section line 3-3 of FIG. 1;
- FIGURE 4 is an enlarged cross-sectional view of that portion of the apparatus of FIG. 1 containing a vent hole and filter for purging air from the apparatus, taken along section line 4-4 of FIG. 1;
- FIGURES 5 is a front elevation view of a film valve employed in the apparatus of FIG. 1;
- FIGURES 6A-6E are cross-sectional elevation views of the apparatus of FIG. 1, showing the operation of the apparatus of FIG. 1 in draining and storing body fluids. Modes for Carrying Out the Invention
- an apparatus for collecting body fluids 10 including a resilient bellows 12 mounted to a support housing 14 by way of an externally threaded neck 16 which is screwed into an internally threaded integral flange 18 of the housing.
- the bellows which comprises the suctioning means of the invention, is preferably constructed of polyethylene, although it may be made of other impervious resilient materials such as polypropylene.
- the suctioning may be accomplished using any sort of reservoir capable of producing sufficient negative pressure, when evacuated, to draw blood, serum, pus, gases and other fluids from a wound site.
- resilient bellows 12 has a liquid capacity in its normal extended state of about 150cc.
- a conventional drain 20 of the type placed in body or tissue cavities of patients undergoing urinary, wound, biliary, gastro-intestinal drainage, peritoneal dialysis, and hyperalimentation treatment is connected to a suction port 22 of the apparatus by way of an appropriate length of flexible tubing 24 affixed at one end to the drain and at the other to the proximal end of the suction port.
- Suction port 22 passes through housing 14 and into the area circumscribed by flange 18.
- a one-way gross reflux valve 24 (FIG. 3) is affixed to the distal end of the suction port, positioned as near as practical to the top of bellows 12.
- a duckbill valve be used as the gross reflux valve
- other conventional one-way valves such as ball, check and diaphragm valves.
- the primary consideration in the choice of the valve is that it prevent fluid reflux and that it not interfere with the bellows when the bellows is compressed during " operation of the apparatus.
- a drainage port 26 passes through housing 14 and into the area circumscribed by flange 18 to communicate with the interior of bellows 12.
- the distal end of the drainage port is connected to a tube 28 located within the housing which is routed into the top of a secondary reservoir 30.
- secondary reservoir 30 is a clear, flexible polyethylene bag although other impervious containers (flexible or rigid) could be used.
- the size of the reservoir is a matter of choice, although in typical applications where a polyethylene bag is used, the reservoir will be large enough to the contain 500, 1000, or 2000cc of liquid.
- reservoir 30 has a 500cc capacity and is marked to indicate its level of fill.
- Reservoir 30 is attached and heat sealed to a flange 32 protruding downwardly from housing 14.
- a rigid tube 29 protrudes from the flange into the top of reservoir 30 where it terminates in a second anti-reflux valve 50.
- Anti-reflux valve 50 must be chosen for maximum contact sealing area to prevent blood clots and other solids from causing leakage across the valve. While a conventional Heimlich valve could be used, a film valve 50 particularly useful in this application is illustrated in FIGURE 5. In addition to its excellent sealing properties (even in the presence of solids in the sealing area), the film valve is particularly well adapted to the present application since it does not create dead space in secondary reservoir 30.
- the film valve is made up of two pieces of virtually any type of plastic film, such as polyethylene, mylar, nylon or PVC, as well as laminates of these materials.
- plastic films such as polyethylene, mylar, nylon or PVC, as well as laminates of these materials.
- the only requirement in choosing the plastic films is that the combination of plastics do not adhere.
- Housing 14 includes a vent 34 (FIG. 4) in communication with reservoir 30.
- Vent 34 permits air from the secondary reservoir to escape as it is filled with liquid during the drainage procedure.
- the vent also permits gases which may be drawn into the system from the drain site by way of drain 20 to escape. Absent vent 34, reservoir 30 would not be able to be filled to capacity with liquid due to space taken up by gases in the system. Also, by eliminating gases from the system through vent 34, the reservoir may be maintained in a lower and easier to handle profile.
- a small pore hydrophobic filter 36 is heat sealed into vent cup 34 which is friction fit onto a flange 40 encircling port 34.
- Filter 36 prevents the migration of bacteria into the system. It also makes it possible to vent gases without impairing the "closed" nature of the system.
- the vent cap is positioned at the top of the housing in order to prevent the filter from getting wet, which could cause clogging.
- Hydrophobic filter 36 must have a pore size less than or equal to 0.45 microns in order to prevent bacterial migration.
- One useful filter material is an expanded PTFE membrane available from W.L. Gore & Associates, Inc. of Elkton, Maryland under the name "GORE-TEX EXPANDED PTFE".
- Alternative materials include woven fabric filters such as those available from PALL Bio-Medical Products Corporation of Glencove, New York under the trademark "PALLFLEX”.
- FIGURES 6A-E The operation of the apparatus of the present invention is illustrated in FIGURES 6A-E. It is to be understood in this discussion of the operation of the apparatus of the invention that the apparatus is affixed to the patient's bed or clothing by way of hook 42 (FIG. 1) or other fastening devices at a position below the wound site.
- FIG. 6A the apparatus is shown in an empty condition, with bellows 12 extended.
- FIG. 6B the bellows are manually compressed, forcing the air in the bellows through tube 28, past valve 50 and out of the system through hydrophobic filter 34.
- the resilient bellows are permitted to expand. Since the system is sealed (film valve 50 is closed due to the suction created by the bellows), liquid and gases are drawn from the wound site through the suction port 22 past gross reflux valve 24 and into the bellows.
- the bellows continue filling with liquid (FIG. 6D) until the liquid reaches the bellows top. At that point, due to the siphon effect produced by the positioning of the apparatus below the wound site, surplus liquid automatically enters tube 28 and flows into reservoir 30, as shown in FIG. 6E. The fluid entering the bag displaces any gases therein which exit the system through vent 34 and filter 36.
Abstract
A closed drainage apparatus for suctioning and storing fluid from body and tissue cavities including draining means for suctioning and receiving fluid, reservoir means for siphoning and storing excess fluids, and a small pore hydrophobic filter for venting air without retrograde introduction of microorganisms.
Description
TITLE OF INVENTION: APPARATUS AND METHOD FOR COLLECTING BODY FLUIDS Technical Field
This invention relates generally to apparatus and methods for draining body fluids. More particularly, it relates to apparatus and methods for reducing the likelihood of infection during the collection of fluids from body cavities of human and animal subjects by draining and disposing of the fluids without exposing the apparatus or the subjects to potential sources of contamination and infection. Background Art
In modern medical practice it is often necessary or desirable to catheterize patients for drainage of bladder, closed wound or other body cavities. In such situations, it is essential to prevent undesirable micro-organisms from gaining access to the catheterized cavity.
Unfortunately, conventional drainage devices are a prime source of infection in catheterized patients. For example, in the area of bladder drainage, a large proportion of catheterized patients suffer from urinary tract infections attributable to contaminated drainage devices. In many cases, the drainage collection device itself becomes contaminated in use and infection then ascends in a retrograde manner from the drainage collection device to the patient via the drainage catheter. Such retrograde infection from a contaminated drainage or infusion device has been observed, for example, in patients undergoing urinary, wound, biliary, or gastro-intestinal drainage, peritoneal
dialysis, and hyperalimentation treatment. See, e.g. E.M. Goldberg, et al., "Peritoneal Dialysis", Dialysis and Transplantation, June/July 1975, Vol. 4 #4; J.H. Isaccs, et al., "Foley Catheter Drainage Systems and Bladder Damage", Surgery, Gynecology & Obstetrics, May 1971, p.889; R.E. Desautels, "The Causes of Catheter-Induced Urinary Infections and Their" Prevention", J. Urology, 1969, 101:757; R.E. Desautels, et al. "Technical Advances in the Prevention of Urinary Tract Infection", J. Urology, 1962, 87:487; R.E. Desautels, "Aseptic Management of Catheter Drainage", New Eng. J. Med., I960, 263:189; E.H. Kass, et al., "Prevention of Infection of Urinary Tract in Presence of Indwelling Catheters", J.A.M.A. 1959, 169:1181; and E.H. Kass, et al. "Entry of Bacteria into the Urinary Tracts of Patients with Inlying Catheters" New Eng. J. Med., 1957, 256: 556.
Contamination of drainage collection devices often arises from reusing containers designed to be filled repeatedly with drained body fluid and emptied. For example, the evacuator described by McElhenny in U.S. Pat. No. 3,115,138 includes a capped fluid outlet. After the evacuator becomes filled it is emptied for reuse by removing the cap and expelling collected fluid via the outlet. During this operation the interior of the evacuator is exposed to the atmosphere and contamination of the evacuator may result.
Efforts have been made to reduce the contamination of drainage devices during periodic emptying. For example, U.S. Pat. Nos. 3,779,243 and 3,774,611 disclose evacuators which employ a special valve over the fluid outlet. This valve operates to close the outlet at all times except for the time when fluid is actually being purged
from the evacuator. Such evacuators may succeed in reducing the contamination brought on by purging. However, since these evacuators must be periodically opened for purging, they are exposed to the surrounding atmosphere and can become contaminated and therefore a source of infection. Goldberg and Bazell, in their U.S. Patent No. 4,435,171 for Apparatus to Be Worn And Method For Removing Fluid From A Living Subject, describe a closed, gravity drainage system designed to minimize retrograde introduction of microorganisms into a patient. This system, however, has no provision for suction drainage. Disclosure of Invention
The present invention is directed to a closed drainage apparatus for receiving fluid (liquids and gases) from body and tissue cavities including suctioning means in communication with the cavities for suctioning and receiving the drained body fluids. In an important embodiment, the suctioning means comprise a resilient bellows which draws body fluid from the cavities under the inherent spring back suction force produced as it returns to its normal, expanded condition.
The apparatus also includes a reservoir into which excess body liquids from the suctioning means are automatically siphoned and into which the suctioning means may be emptied, all without exposure of the system to the atmosphere. In an important embodiment of the invention, the secondary reservoir consists of an impervious, flexible bag in communication with an outlet port of the suctioning means which has a one-way valve at its inlet to prevent liquid from flowing back from the reservoir.
In yet another important embodiment of the invention, the secondary reservoir is vented to the atmosphere through one or more small pore hydrophobic filters to permit gases in the system to be purged without retrograde introduction of microorganisms into the reservoir.
It is therefore an object of the present invention to provide an improved apparatus and method for draining body fluids from a body cavity under suction in which potential retrograde infection due to contamination of drainage devices on exposure to the atmosphere is eliminated.
It is a further object of the present invention to provide an improved apparatus and method for collecting body fluids including liquids and gases from a body cavity under suction in which collected liquids are siphoned into disposable containers for disposal and collected gases are vented to the atmosphere without exposing the system to the atmosphere and without exposure of hospital personnel to the container contents.
Yet another object of the invention is to provide a closed drainage system in which gases in the system can be purged without exposing the system to the atmosphere.
A still further object of the present invention is to provide an economical, easy to use, closed suction drainage apparatus and method. These and other objects of the present invention will become apparent to those skilled in the art upon consideration of the accompanying specification, claims and drawings.
Brief Description of the Drawings
The features of this invention which are believed to be novel are set forth with particularity in the appended claims. The invention, together with its objects and advantages, may be best understood by reference to the following description, taken in conjunction with the following drawings, in which like reference numerals identify like elements in the several figures and in which:
FIGURE 1 is a perspective view of a closed drainage apparatus in accordance with the practice of the present invention; FIGURE 2 is a cross-sectional elevation view of the apparatus of FIG. 1, taken generally along section line 2-2 of that figure;
FIGURE 3 is an enlarged cross-sectional view of a one-way valve illustrated in FIG. 1, taken along section line 3-3 of FIG. 1;
FIGURE 4 is an enlarged cross-sectional view of that portion of the apparatus of FIG. 1 containing a vent hole and filter for purging air from the apparatus, taken along section line 4-4 of FIG. 1;
FIGURES 5 is a front elevation view of a film valve employed in the apparatus of FIG. 1; and
FIGURES 6A-6E are cross-sectional elevation views of the apparatus of FIG. 1, showing the operation of the apparatus of FIG. 1 in draining and storing body fluids. Modes for Carrying Out the Invention
Turning now to FIGURES 1 and 2, an apparatus for collecting body fluids 10 is illustrated including a resilient bellows 12 mounted to a support housing 14 by way of an externally threaded neck 16 which is screwed into an internally threaded integral flange 18 of the housing.
The bellows, which comprises the suctioning means of the invention, is preferably constructed of polyethylene, although it may be made of other impervious resilient materials such as polypropylene. In fact, the suctioning may be accomplished using any sort of reservoir capable of producing sufficient negative pressure, when evacuated, to draw blood, serum, pus, gases and other fluids from a wound site. In the illustrated embodiment, resilient bellows 12 has a liquid capacity in its normal extended state of about 150cc.
A conventional drain 20 of the type placed in body or tissue cavities of patients undergoing urinary, wound, biliary, gastro-intestinal drainage, peritoneal dialysis, and hyperalimentation treatment is connected to a suction port 22 of the apparatus by way of an appropriate length of flexible tubing 24 affixed at one end to the drain and at the other to the proximal end of the suction port. Suction port 22 passes through housing 14 and into the area circumscribed by flange 18. A one-way gross reflux valve 24 (FIG. 3) is affixed to the distal end of the suction port, positioned as near as practical to the top of bellows 12. Although it is preferred that a duckbill valve be used as the gross reflux valve, other conventional one-way valves may be used, such as ball, check and diaphragm valves. The primary consideration in the choice of the valve is that it prevent fluid reflux and that it not interfere with the bellows when the bellows is compressed during "operation of the apparatus.
In addition to suction port 22, a drainage port 26 passes through housing 14 and into the area circumscribed by flange 18 to communicate with the interior of bellows 12. The distal end of the drainage port
is connected to a tube 28 located within the housing which is routed into the top of a secondary reservoir 30. In the illustrated embodiment, secondary reservoir 30 is a clear, flexible polyethylene bag although other impervious containers (flexible or rigid) could be used. The size of the reservoir is a matter of choice, although in typical applications where a polyethylene bag is used, the reservoir will be large enough to the contain 500, 1000, or 2000cc of liquid. As illustrated in the figures, reservoir 30 has a 500cc capacity and is marked to indicate its level of fill. Reservoir 30 is attached and heat sealed to a flange 32 protruding downwardly from housing 14. A rigid tube 29 protrudes from the flange into the top of reservoir 30 where it terminates in a second anti-reflux valve 50.
Anti-reflux valve 50 must be chosen for maximum contact sealing area to prevent blood clots and other solids from causing leakage across the valve. While a conventional Heimlich valve could be used, a film valve 50 particularly useful in this application is illustrated in FIGURE 5. In addition to its excellent sealing properties (even in the presence of solids in the sealing area), the film valve is particularly well adapted to the present application since it does not create dead space in secondary reservoir 30.
The film valve is made up of two pieces of virtually any type of plastic film, such as polyethylene, mylar, nylon or PVC, as well as laminates of these materials. The only requirement in choosing the plastic films is that the combination of plastics do not adhere.
Also, it has been found to be preferable to use films with a combined
thickness in the- range of about 3-5 mils. The edges of the two film members of the valve are heat sealed to each other with a tortuous profile 51 at the closed edges of the valve in order to prevent fluid leakage. Housing 14 includes a vent 34 (FIG. 4) in communication with reservoir 30. Vent 34 permits air from the secondary reservoir to escape as it is filled with liquid during the drainage procedure. The vent also permits gases which may be drawn into the system from the drain site by way of drain 20 to escape. Absent vent 34, reservoir 30 would not be able to be filled to capacity with liquid due to space taken up by gases in the system. Also, by eliminating gases from the system through vent 34, the reservoir may be maintained in a lower and easier to handle profile.
A small pore hydrophobic filter 36 is heat sealed into vent cup 34 which is friction fit onto a flange 40 encircling port 34. Filter 36 prevents the migration of bacteria into the system. It also makes it possible to vent gases without impairing the "closed" nature of the system. The vent cap is positioned at the top of the housing in order to prevent the filter from getting wet, which could cause clogging. Although only a single vent cup and filter are illustrated in order to simplify the figures, two or more cups and filters could be used.
Hydrophobic filter 36 must have a pore size less than or equal to 0.45 microns in order to prevent bacterial migration. One useful filter material is an expanded PTFE membrane available from W.L. Gore & Associates, Inc. of Elkton, Maryland under the name "GORE-TEX EXPANDED PTFE". Alternative materials include woven fabric filters such as those available from PALL Bio-Medical Products Corporation of Glencove, New York under the trademark "PALLFLEX".
The operation of the apparatus of the present invention is illustrated in FIGURES 6A-E. It is to be understood in this discussion of the operation of the apparatus of the invention that the apparatus is affixed to the patient's bed or clothing by way of hook 42 (FIG. 1) or other fastening devices at a position below the wound site.
Looking first to FIG. 6A, the apparatus is shown in an empty condition, with bellows 12 extended. In FIG. 6B the bellows are manually compressed, forcing the air in the bellows through tube 28, past valve 50 and out of the system through hydrophobic filter 34.
In FIG. 6C, the resilient bellows are permitted to expand. Since the system is sealed (film valve 50 is closed due to the suction created by the bellows), liquid and gases are drawn from the wound site through the suction port 22 past gross reflux valve 24 and into the bellows.
Once started, the bellows continue filling with liquid (FIG. 6D) until the liquid reaches the bellows top. At that point, due to the siphon effect produced by the positioning of the apparatus below the wound site, surplus liquid automatically enters tube 28 and flows into reservoir 30, as shown in FIG. 6E. The fluid entering the bag displaces any gases therein which exit the system through vent 34 and filter 36.
While particular embodiments of the invention have been shown and described, it will be obvious to those skilled in the art that various changes and modifications may be made therein without departing from the spirit and scope of the invention and, therefore, it is intended in the appended claims to cover all such changes and modifications which fall within the true spirit and scope of the invention.
Claims
1. A closed drainage apparatus for suctioning liquids and gases and for storing liquids suctioned from body and tissue cavities comprising: a housing; suctioning means, attached to said housing, in communication with the body and tissue cavities, for suctioning and receiving liquids and gases from the cavities; and reservoir means, attached to said housing, for receiving and storing excess liquids from said suctioning means, said reservoir means being in sealed communication with said suctioning means through a conduit, said conduit being supported in said housing to permit fluid communication between said suctioning means and said reservoir means at all times.
2. The closed drainage apparatus of claim 1 wherein said suctioning means comprises a resilient container which is compressible to create a suctioning force as it returns to its normal expanded condition.
3. The closed drainage apparatus of claim 1 wherein said suctioning means comprises a resilient bellows which produces a suctioning force as it returns to its normal expanded condition.
4. The closed drainage apparatus of claim 1 wherein said reservoir means comprises an impervious, flexible bag.
5. The closed drainage apparatus of claim 1 including a one-way valve at the inlet of said conduit to prevent liquids and gases from flowing back from said reservoir and into said suctioning means.
6. The closed drainage apparatus of claim 1 wherein said apparatus is provided with means for venting gases.
7. The closed drainage apparatus of claim 6 wherein said venting means is provided with a small pore hydrophobic filter for preventing retrograde introduction of microorganisms into said reservoir.
8. The closed drainage apparatus of claim 1 wherein said draining means includes a suction port for receiving the liquids and gases from the body and tissue cavities, said suction port being fitted with reflux valve means for preventing reflux of liquids and gases from said suctioning means to the body and tissue cavities.
9. The closed drainage apparatus of claim 9 wherein said reflux valve means comprises a duckbill valve.
10. A closed drainage apparatus for suctioning liquids and gases and for storing liquids suctioned from body and tissue cavities comprising: a housing; suctioning means, attached to said housing, in communication with the body and tissue cavities, for suctioning and receiving liquids and gases from the cavities; reservoir means, attached to said housing, for receiving and storing excess liquids from said suctioning means, said reservoir means being in sealed communication with said suctioning means through a conduit, said conduit being supported in said housing to maintain fluid communication between said suctioning means and said reservoir means at all times; and means for venting gases from said reservoir, said venting means including a small pore hydrophobic filter for preventing retrograde introduction of microorganisms into said reservoir.
11. A method for collecting fluids from body and tissue cavities comprising the steps of: locating means within the body and tissue cavities for draining the body fluids; attaching to said draining means and maintaining at a position below the body and tissue cavities, a closed drainage apparatus comprising a housing supporting a resilient container and reservoir means in sealed continuous one-way communication through a conduit supported in said housing to maintain said suctioning means and said reservoir means in fluid communication at all times, and means for venting gases from said reservoir means without the retrograde of microorganisms; compressing said resilient container to expel air therefrom through said venting means; permitting said resilient container to expand, drawing fluid from the body or tissue cavity into said resilient container; and siphoning surplus liquids into said reservoir means. -13-
12. A closed drainage apparatus for suctioning liquids and gases and for storing liquids from body and tissue cavities comprising: a housing; suctioning means attached to said housing, in communication 5 with the body and tissue cavities, for suctioning and receiving liquids and gases from the cavities; reservoir means attached to said housing, in sealed continuous one-way communication with said suctioning means, for siphoning and storing excess liquids without permitting the excess 10 liquids to return to said suctioning means; and means for affixing said housing in a location relative to the body and tissue cavities such that said suctioning means and said reservoir means are positioned below the body and tissue cavities.
13. The apparatus of claim 1 wherein said affixing means comprises a hook which is integral with said housing.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US94176986A | 1986-12-15 | 1986-12-15 | |
US941,769 | 1986-12-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1988004559A1 true WO1988004559A1 (en) | 1988-06-30 |
Family
ID=25477033
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1987/003334 WO1988004559A1 (en) | 1986-12-15 | 1987-12-15 | Apparatus and method for collecting body fluids |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0293456A1 (en) |
JP (1) | JPH01501528A (en) |
CA (1) | CA1304645C (en) |
WO (1) | WO1988004559A1 (en) |
Cited By (6)
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EP0378296A2 (en) * | 1989-01-12 | 1990-07-18 | Smiths Industries Public Limited Company | Suction pump assemblies |
GB2234902A (en) * | 1989-08-18 | 1991-02-20 | Peter Griggs | Mucus removing device |
EP0592730A1 (en) * | 1992-10-15 | 1994-04-20 | Inmed Limitada | Portable disposable device for post-surgical suction |
CN103598901A (en) * | 2013-10-24 | 2014-02-26 | 苏雪莲 | Fat transplantation device |
US8679079B2 (en) | 2006-10-13 | 2014-03-25 | Kci Licensing, Inc. | Reduced pressure delivery system having a manually-activated pump for providing treatment to low-severity wounds |
US10238787B2 (en) | 2013-09-25 | 2019-03-26 | Transell Co., Ltd. | Blood component separation device |
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JP2011055916A (en) * | 2009-09-07 | 2011-03-24 | Terumo Corp | Blood container for examination and blood sampling instrument |
JP6019272B2 (en) * | 2012-02-29 | 2016-11-02 | アルケア株式会社 | Body fluid suction pump and body fluid suction and collection device using the body fluid suction pump |
JP5938568B2 (en) * | 2012-02-29 | 2016-06-22 | アルケア株式会社 | Body fluid suction pump and body fluid suction and collection device using the body fluid suction pump |
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JPS61289996A (en) * | 1985-06-14 | 1986-12-19 | Nikko Sogyo Kk | Treatment device for dehydrating and drying sludge or the like |
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1987
- 1987-12-15 CA CA000554305A patent/CA1304645C/en not_active Expired - Lifetime
- 1987-12-15 JP JP63500729A patent/JPH01501528A/en active Pending
- 1987-12-15 EP EP88900438A patent/EP0293456A1/en not_active Withdrawn
- 1987-12-15 WO PCT/US1987/003334 patent/WO1988004559A1/en not_active Application Discontinuation
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DE2103187A1 (en) * | 1970-02-02 | 1971-08-19 | Astra Meditec AB, Göteborg (Schwe den) | Liquid suction device |
US3875941A (en) * | 1974-04-03 | 1975-04-08 | Medical Dynamics Inc | System for evacuating fluids from the body |
FR2279425A1 (en) * | 1974-07-25 | 1976-02-20 | Crilly Robert | Vacuum-assisted sterile drainage system for catheter - has elastic elongated valve oscillating in chamber (BR300376) |
EP0175830A1 (en) * | 1984-09-26 | 1986-04-02 | Bay, Otto, Dipl.-Ing. | Aspirator bottle for use in the draining of wounds |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0378296A2 (en) * | 1989-01-12 | 1990-07-18 | Smiths Industries Public Limited Company | Suction pump assemblies |
EP0378296A3 (en) * | 1989-01-12 | 1991-02-20 | Smiths Industries Public Limited Company | Suction pump assemblies |
GB2234902A (en) * | 1989-08-18 | 1991-02-20 | Peter Griggs | Mucus removing device |
EP0592730A1 (en) * | 1992-10-15 | 1994-04-20 | Inmed Limitada | Portable disposable device for post-surgical suction |
US8679079B2 (en) | 2006-10-13 | 2014-03-25 | Kci Licensing, Inc. | Reduced pressure delivery system having a manually-activated pump for providing treatment to low-severity wounds |
US9561312B2 (en) | 2006-10-13 | 2017-02-07 | Kci Licensing, Inc. | Reduced pressure delivery system having a manually-activated pump for providing treatment to low-severity wounds |
US10238787B2 (en) | 2013-09-25 | 2019-03-26 | Transell Co., Ltd. | Blood component separation device |
CN103598901A (en) * | 2013-10-24 | 2014-02-26 | 苏雪莲 | Fat transplantation device |
Also Published As
Publication number | Publication date |
---|---|
CA1304645C (en) | 1992-07-07 |
EP0293456A1 (en) | 1988-12-07 |
JPH01501528A (en) | 1989-06-01 |
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