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Publication numberUS3834386 A
Publication typeGrant
Publication dateSep 10, 1974
Filing dateSep 7, 1972
Priority dateSep 7, 1972
Publication numberUS 3834386 A, US 3834386A, US-A-3834386, US3834386 A, US3834386A
InventorsSisley J
Original AssigneeSweden Freezer
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Blood drip chamber
US 3834386 A
Abstract
A blood drip chamber is provided with a cap having a large penetration area which includes a self-sealing rubber supported by a layer of stiffer material. The inner surface of the stiffening material is at the same general level as the remainder of the inner surface of the cap so that blood is not held by capillary action in the penetration area. The blood drip chamber includes a reservoir having a sidewall, a lower discharge port and an upper end. A blood inlet port is positioned centrally in the cap so that the inflow of blood is maintained away from the sidewalls of the reservoir.
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Description  (OCR text may contain errors)

United States Patent [191 Sisley [52] US. Cl. 128/214 C, 215/37 R [51] Int. Cl A61m 5/16 [58] Field of Search 128/214 R, 214 C, 214 D,

l28/2l4.2; 215/37 R, 38 R [56] References Cited UNITED STATES PATENTS 2,129,983 9/1938 Bacon 128/214 C 2,438,149 3/1948 Cutter et al 128/214 R X 2,838,046 6/1958 Butler 128/214 D 3,092,278 6/1963 Jarnhall 215/37 R 3,216,418 11/1965 Scislowicz 128/214 C [11] 3,834,386 Sept. 10, 1974 11/1965 Scislowlcz 128/214 C 7/1967 Brody 128/214 R [5 7] ABSTRACT A blood drip chamber is provided with a cap having a large penetration area which includes a self-sealing rubber supported by a layer of stiffer material. The inner surface of the stiffening material is at the same general level as the remainder of the inner surface of the cap so that blood is not held by capillary action in the penetration area. The blood drip chamber includes a reservoir having a sidewall, a lower discharge port and an upper end. A blood inlet port is positioned centrally in the cap so that the inflow of blood is maintained away from the sidewalls of the reservoir.

4 Claims, 2 Drawing Figures BLOOD DRIP CHAMBER BACKGROUND OF THE INVENTION 1. Field of the Invention This invention pertains to blood drip chambers for hemodialysis or the like.

2. Description of the Prior Art I-lemodialysis requires removal of the bloodifrom the circulatory system of the patient and then after dialysis the blood is returned into the circulatory system. Blood drip chambers are added to the arterial and or venous vessels to reduce the possibility of air leakage. into the circulatory system. A blood. drip chamber generally in. cludes an elongated tubular reservoir having a bottom discharge port and an upper end covered by acap. The cap is provided with a blood inlet port' and a penetration region and generally with some form of optional monitoring port. The blood inlet port directs the blood into the reservoir where the level is maintained at approximately one-half the height. of the. reservoir so-that air bubbles in the blood are freeto rise and be released into the air in the top portion of the reservoir. The penetration region is provided for the insertion. of a syringe into the reservoir either to remove blood for sampling or for maintaining a proper levelv in the reservoir or for the introduction of medication into the blood during fibrin formation (clotting) occurswithin hemodialysis sets in use, the patients-well-being is jeopardized.

In prior art drip chambers fibrin formation frequently occurs since the blood inlet port generally is near the sidewall of the chamber with the blood being directed against the sidewall before it reaches the pool of blood at the lower end of the reservoir. As the blood touches the sidewall it begins to coagulate frequently leaving a residue on the sidewall. Secondly, non-flowing blood in a small vertical tube will be held in the tube against gravity due to the capillary action of the tube. In prior art drip chambers the penetration region for introducing syringes into the chamber consists of a small tube projecting up from the cap of the chamber. Consequently, blood splashing into the tube is held causing a fibrin build up situation.

An additional shortcoming of prior art blood drip chambers is that the penetration region is a cap secured to a short small diameter tube in the cap of the chamber and is difficult to hit with a syringe needle. The diameter is so small that a non-axially inserted needle will frequently penetrate the side of the tube. Furthermore, because of the small diameter and thus small surface area the selfsealing rubber in the penetration area can only tolerate a relatively few number of needle penetrations before losing its self-sealing capability.

SUMMARY OF THE INVENTION It is an object of this invention to provide a blood drip chamber in which the blood inlet port is centrally positioned in the cap of the chamber.

It is an object of this invention to provide a blood drip chamber which has a large penetration areafor theinsertion of hypodermic syringes.

' losing its capability to seal.

blood drip chamber having a central blood. inlet port partially encircled, by a large penetration area.

It is an object of this invention to provide a cap for a blood drip chamber in which blood deposits are minimized.

Basically the invention comprises a reservoir having a lower discharge port and an. open upper end. A cap is provided over the upper end. The cap has a centrallylocated blood inlet port and a large targetarea covering approximately a third or'more of the remainder of the cap. The inner surface of the penetration area. is generally aligned with the remainder of the inner surface of the cap. Self-sealing material is provided on the penetration area.

DESCRIPTION OF THE DRAWINGS FIG. 1 is an isometric of the preferred form of blood drip chamber with parts removed for clarity.

FIG. 2 is a fragmentary section taken along the line 2.-2 of FIG. 1.

DESCRIPTION OF THE PREFERRED EMBODIMENTS The blood drip chamber 10 includes a reservoir 12 havinga smooth sidewall 14 and alower discharge; port 16. The-upper end of the reservoir is provided with an open end, 18' which is covered by acap 20. The cap and reservoir are all formed from medical-grade, waterclear, non-pyrogenic, non-toxic polyvinyl chloride. Preferably the polyvinyl chloride material is soft enough to milk or squeeze blood from the chamber but stiff enough to withstand negative pressures that are typical in a dialysis. system.

The cap 20 is uniquely provided with a centrally positioned blood inlet port 24 which is coupled to a tube 26 in a conventional manner. Blood flowing through the tube 26 is discharged into the reservoir forming a pool of blood B with an air space above it. Since the blood is fed centrally into the reservoir there is less opportunity for blood to strike the sidewall above the level of the pool B where it can coagulate.

A second unique feature ofthe invention is the provision of a large self-sealing penetration (injection) area or region28. As best shown in FIG. 1 the penetration area is substantially kidney-shaped extending all the way from the diameter on one side of the inlet port to the diameter on the other side of the inlet port. The penetration region has an upright wall 30 which houses a self-sealing material 32 of a type conventional in this art. A thin layer of polyvinyl chloride 34 is left in the molding process at the inside of the penetration area. The purpose of the thin layer of polyvinyl chloride is to provide stiffening support for the self-sealing material throughout the large surface of the penetration area. During both insertion of a syringe needle through the penetration area and the removal of the needle the selfsealing material clings to the needle. The support 34 holds the self-sealing material from thus pulling out or being-pushed in by the. needle. Since the polyvinyl chloride is relatively thin it provides little obstruction to the penetration of the needle. The large surface allows-the needle to be inserted at variable angles and provides for numerous insertions without the selfsealing material As is best shown in FIG. Zt-he, thin polyvinyl chloride layer 34 forming the bottom of the penetration area terminates generally flush (relative to prior art tubes) with the remainder of the inner surface of the cap indicated by the reference character 38. The width of the penetration area above the surface 38 is substantially large so that no capillary action is present to capture and hold blood in the penetration area.

If desired, an optional monitoring inlet 40 (not shown) may be provided as is conventional.

While the preferred form of the invention has been illustrated and described it should be understood that variations and alternatives will be apparent to one skilled in the art without departing from the principals thereof. Accordingly, the invention is not to be limited to the specific embodiment described but rather only by a literal interpretation of the claims appended hereto.

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:

l. A blood drip chamber for hemodialysis or the like comprising a reservoir for holding a quantity of blood and having a lower end with a discharge port, an upper end, and sidewalls extending between said ends; and a cap covering said upper end, said cap having a generally centrally located inlet port means for directing blood into said reservoir inwardly away from the sidewalls of the reservoir and for forming a pool of blood at the bottom of the reservoir, and penetration means in said cap for introducing a syringe needle into said reservoir and including a self-sealing medium for closing the penetration means when the needle is withdrawn, said penetration means extending approximately at least a third of the way around said inlet port means for providing a large penetration area for a syringe needle, said penetration means including a layer of stiffening material bonded to the underside of the self-sealing material for avoiding contaminable air gaps between the self-sealing material and for supporting the self-sealing material when a syringe needle is inserted or withdrawn by strengthening the self-sealing material for withstanding the stress resulting from multiple insertions of the syringe needle, said stiffening material being bonded to said self-sealing medium over substantially the entire area of contact between said selfsealing medium and said stiffening material.

2. The blood drip chamber of claim 1, said penetration means including an inner surface at generally the same level as the inner surface of the remainder of said cap.

3.'A blood drip chamber for hemodialysis or the like comprising a reservoir for holding a quantity of blood and having a lower end with a discharge port, an upper end, and sidewalls extending between said ends; and a cap covering said upper end, said cap having an inlet port means for directing blood into said reservoir away from the sidewalls of the reservoir and for forming a pool of blood at the bottom of the reservoir, and a penetration area covering a substantial region of said cap for the insertion of a syringe needle through said cap,

said penetration area including a soft self-sealing material, and a layer of supporting material below said selfsealing material and bonded thereto over substantially the area of contact between said self sealing medium and said supporting material to prevent contamination of the surfaces between the self-sealing material and the supporting material and to support the latter from stress of a syring needle when inserted or withdrawn.

4. The blood drip chamber of claim 3 said supporting material lying generally in the plane of the inner surface of the remainder of said cap.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2129983 *Apr 6, 1936Sep 13, 1938Harvey Bacon JaySurgical appliance
US2438149 *Dec 18, 1945Mar 23, 1948Cutter LabStopper
US2838046 *Apr 6, 1955Jun 10, 1958Cutter LabContainer for blood and the like
US3092278 *Sep 19, 1958Jun 4, 1963Astra Apotekarnes Kem FabCap for a container for an injection liquid
US3216418 *Jun 1, 1962Nov 9, 1965Abbott LabApparatus for administering parenteral solutions
US3216419 *Oct 17, 1963Nov 9, 1965Abbott LabApparatus for administering a parenteral solution provided with a diaphragm float valve
US3332418 *May 28, 1964Jul 25, 1967Baxter Don IncInjection site for venoclysis apparatus
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US4465479 *Sep 8, 1982Aug 14, 1984C. R. Bard, Inc.Air vent splash guard for drip chamber
US4586925 *Sep 7, 1983May 6, 1986Gambro Lundia AbHose set for extracorporeal treatment of blood and similar liquids
US4976685 *Jun 15, 1988Dec 11, 1990Block Jr Frank EMethod of blood-gas interface control in surgical gas traps
US5163902 *Sep 13, 1990Nov 17, 1992James R. LongacrePatient fluid manifold
US5503801 *Nov 29, 1993Apr 2, 1996Cobe Laboratories, Inc.Extracorporeal treatment of blood
US5591251 *Dec 22, 1994Jan 7, 1997Cobe Laboratories, Inc.Side flow bubble trap apparatus and method
US5674199 *Sep 21, 1995Oct 7, 1997Cobe Laboratories, Inc.Top flow bubble trap method
US5830185 *Oct 12, 1995Nov 3, 1998Instrumentarium Corp.Position-independent fluid trap
US7871462Oct 1, 2007Jan 18, 2011Baxter International Inc.Dialysis systems having air separation chambers with internal structures to enhance air removal
US7892331Oct 1, 2007Feb 22, 2011Baxter International Inc.Dialysis systems having air separation chambers with internal structures to enhance air removal
US7892332Oct 1, 2007Feb 22, 2011Baxter International Inc.Dialysis systems having air traps with internal structures to enhance air removal
US7988768Dec 28, 2010Aug 2, 2011Baxter International Inc.Dialysis systems having spiraling fluid air separation chambers
US8025714Feb 15, 2011Sep 27, 2011Baxter International Inc.Dialysis systems and methods having vibration-aided air removal
US8025716Feb 18, 2011Sep 27, 2011Baxter International Inc.Fluid delivery systems and methods having floating baffle aided air removal
US8080091Feb 18, 2011Dec 20, 2011Baxter International Inc.Dialysis systems and methods including cassette with fluid heating and air removal
US8114276Oct 23, 2008Feb 14, 2012Baxter International Inc.Personal hemodialysis system
US8123947Oct 22, 2007Feb 28, 2012Baxter International Inc.Priming and air removal systems and methods for dialysis
US8221529Nov 21, 2011Jul 17, 2012Baxter InternationalDialysis systems and methods including cassette with air removal
US8323492Aug 19, 2011Dec 4, 2012Baxter International Inc.Hemodialysis system having clamping mechanism for peristaltic pumping
US8329030Aug 19, 2011Dec 11, 2012Baxter International Inc.Hemodialysis system with cassette and pinch clamp
US8382711Dec 29, 2010Feb 26, 2013Baxter International Inc.Intravenous pumping air management systems and methods
US8444587Sep 24, 2008May 21, 2013Baxter International Inc.Fluid and air handling in blood and dialysis circuits
US8632624Oct 13, 2011Jan 21, 2014General Electric CompanyFluid trap and method of separating fluids
US20120091048 *Jun 16, 2010Apr 19, 2012Reiner SpickermannChamber for a blood treatment system, blood tubing system, and blood treatment system
DE102009030283A1Jun 24, 2009Jan 5, 2011Fresenius Medical Care Deutschland GmbhKammer für ein Blutbehandlungssystem, Blutschlauchsystem sowie Blutbehandlungssystem
EP0106026A1Jul 4, 1983Apr 25, 1984Gambro Lundia ABA tube set intended for extracorporeal treatment of blood and similar perishable liquids
WO2010133343A1 *May 18, 2010Nov 25, 2010Fresenius Kabi Deutschland GmbhDrip chamber for an infusion device and infusion device having a drip chamber
Classifications
U.S. Classification604/251, 604/415, 215/309, 604/86, D24/117
International ClassificationA61M1/36, A61M5/14
Cooperative ClassificationA61M1/3627, A61M5/1411
European ClassificationA61M1/36C4, A61M5/14F