US3775339A - Vessel for receiving and defoaming blood - Google Patents

Vessel for receiving and defoaming blood Download PDF

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Publication number
US3775339A
US3775339A US00261127A US3775339DA US3775339A US 3775339 A US3775339 A US 3775339A US 00261127 A US00261127 A US 00261127A US 3775339D A US3775339D A US 3775339DA US 3775339 A US3775339 A US 3775339A
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blood
vessel
receptacle
disks
froth suppressor
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US00261127A
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V Kasulin
B Bobrov
Fainshtein N Super
E Balabin
A Egorov
L Makarov
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    • 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
    • A61M1/36—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3621—Extra-corporeal blood circuits
    • A61M1/3627—Degassing devices; Buffer reservoirs; Drip chambers; Blood filters
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D19/00—Degasification of liquids
    • B01D19/02—Foam dispersion or prevention
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S159/00—Concentrating evaporators
    • Y10S159/04—Foam
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S159/00—Concentrating evaporators
    • Y10S159/11—Biologicals

Definitions

  • v Said receptacle is separated from said froth suppressor device by a distribution funnel which directs the liow of coronary blood onto the ⁇ froth suppressor device.
  • the froth suppressor device comprises a hollow vertical stem for admission of donor blood and perforated disks vertically spaced on the stem, each of which is coated with a foam-breaking compound.
  • the present invention relates to medical equipment and apparatus applicable for conducting surgical operations that involve the use of artificial blood circulation, namely, to vessels for holding spare blood and reception of coronary blood.
  • the proposed vessel can be successfully used with apparatus for artificial blood circulation, as well as with arrangements for coronary blood suction.
  • One prior-art device of this nature comprises a housing made as a hollow cylinder fabricated .from organic glass. At the top of the housing there is a receiving chamber or receptacle for coronary blood, provided with ⁇ a detachable cover and an inlet pipe for the coronary blood to flow in said inlet pipe being directed tangentially with respect to the receptacle walls.
  • a froth suppressor device formed by liat metal perforated disks coated with a foam breaking compound. The disks are somewhat spaced one above another on a hollow vertical stem secured on the receptacle cover. At its bottom the vessel has an outlet pipe for the blood to discharge.
  • Spare blood is poured through the central hole of the cover and iiows down through the hollow vertical stem into the bottom portion of the vessel.
  • Coronary blood sucked from the operational wound by conventional means that need not be described herein conveys air bubbles and is passed through a tangentially arranged inlet pipe into the receptacle, wherein a rotary flow of coronary blood is formed.
  • the blood falls onto the top disk of the froth suppressor device, then flows down through the perforations therein onto the subsequent disk and so on, thus consecutively flowing down from one disk onto another to deposit onto the vessel bottom. While owing down the blood is in contact with the foam breaking compound the disks are coated with, thus liberating the same of air bubbles.
  • the blood accumulated on the vessel bottom becomes suitable for being introduced into the circulatory system of a patient.
  • the prior-art vessel for containing spare blood and reception of coronary blood fails to ensure a reasonably eiiicacious .froth suppression, this being due to the fact that part ofblood flowing down from the blood receptacle, ⁇ gets splashed over the vessel walls, thus eluding the system offroth suppressing disks.
  • a perforated distribution funnel is provided at the vessel top above the stack of perforated disks.
  • the periphery of the distribution funnel adjoin the bottom edges of the blood receptacle walls.
  • the perforated disks may be of a convexo-concave shape, have different diameters ⁇ and be arranged with their convex or cambered outward surfaces facing oppositely so that the greater diameter disks are preferably arranged with their convex cambered surface down, whereas the smaller diameter disks are arranged with their cambered outward surface up.
  • the vessel for holding spare blood and reception of coronary blood comprises a housing 1 at the top of which there is provided a receptacle 2 for coronary blood, and a cover 3 therefor.
  • the blood receptacle 2 has an inlet pipe 4 for admitting the coronary blood of a patient, said inlet pipe being arranged tangentially with respect to the receptacle inner wall.
  • the housing 1 has an inlet pipe 5 for passing the venous blood of the patient in case the vessel is used as an intermediate blood container when regulating the outow of the venous blood of the patient in the artificial blood circulation system, and an outlet pipe 6 for discharging the blood from the vessel into an oxygenator (not illustrated in the drawing).
  • the frothsuppressor device which is basically a stack of perforatedA disks 7 and 8 coated with a foam-breaking compound, mounted on a vertical hollow stem 9 and being somewhat spaced one above another.
  • a perforated distribution funnel 10 Located above the top disk 7 is a perforated distribution funnel 10 likewise coated with a foam-breaking compound. The edges of the distribution funnel 10 adjoin the bottom edges of the walls of the blood receptacle 2.
  • the disks 7 and 8 are of a convexo-concave shape, the disk 7 of a greater diameter being arranged alternately with the smaller-diameter disks 8.
  • the disks 7 are mounted on the stem 9 convex-down, while the disks 8, convex-up.
  • the vessel for holding spare blood and reception of coronary blood functions as follows.
  • the donors blood is poured into the vessel through the hollow stem 9.
  • the iiow of the coronary blood of the patient is passed into the upper end of the inner space of the blood receptacle 2, wherein due to the inlet pipe 4 being arranged tangentially, a circulatory blood How is attained.
  • weight the blood decelerates its circulatory motion and flows down covering the inner surfaceof'the distribution funnel and through the perforations therein the blood gets onto subsequent disks 7 and 8 of the froth-suppressor device consecutively vowing'dovvn from the top disk onto the bottom one.
  • the distribution funnel 10 enables all of the blood toget onto the disks 7 and 8. While contacting the foam-breaking compound which coat the surface of the disks 7 and 8, the blood release the air bubbles with which the blood became enriched when sucked from the operational wound.
  • the arrangement of the disk 7 and 8, whereby the greater-diameter disks alternate the smaller-diameter ones and the disks convex surfaces are oriented in a definite manner ensures that the blood is in contact with the disks 7 and 8 throughout the surface area thereof, due to which fact the maximum froth suppressing effect is attainable.
  • the blood freed of air bubbles and accumulated at the vessel bottom, is passed through the outlet pipe 6 into the oxygenator (not shown in the drawing) and further into the patients artery.
  • a vessel for receiving and defoaming blood comprising a housing; a blood receiving receptacle located on the top portion of said housing; said receptacle having a tangential duct for admitting coronary blood thereinto; a cover on the receptacle; a froth suppressor device lo- ""tacle; said froth suppressor device comprising a hollow vertical stem for admission of donor blood passing ⁇ through said cover and receptacle and discharging into the housing, and perforated dish-like disks mounted transversely on said vertical stem in spaced positions one above another and coated with arfoam-breaking compound; the bottom of said receptacle comprising a perforated distribution funnel located directly above the uppermost of said disks; means in the bottom of said housing for lremoval of the treated blood and means in the cover to release gases.
  • a vessel as claimedin claim 1 wherein the outer periphery of said distribution funnel adjoins the bottom inner periphery of the Walls of said blood receptacle.
  • a vessel as claimed in claim 1, wherein said perforated disks are of a convexo-concave shape and of two different diameters and are arranged with their convex surfaces facing oppositely, the greater-diameter disks facing with their convex surfaces down and the smaller-diameter disks, convex up, said smaller diameter disks being interdigitated between said larger diameter disks.

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  • Health & Medical Sciences (AREA)
  • Vascular Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Anesthesiology (AREA)
  • Cardiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Dispersion Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • External Artificial Organs (AREA)

Abstract

A VESSEL FOR RECEIVING AND DEFOAMING BLOOD, WHEREIN PROVISION IS MADE FOR A FROTH SUPPRESSOR DEVICE LOCATED BENEATH THE CONONARY BLOOD RECEPTACLE. SAID RECEPTACLE IS SEPARATED FROM SAID FROTH SUPPRESSOR DEVICE BY A DISTRIBUTION FUNNEL WHICH DIRECTS THE FLOW OF CORONARY BLOOD ONTO THE FROTH SUPPRESSOR DIVICE. THE

FROTH SUPPRESSOR DEVICE COMPRISES A HOLLOW VETICAL STEM FOR ADMISSION OF DONOR BLOOD AND PERFORATED DISKS VERTICALLY SPACED ON THE STEM, EACH OF WHICH IS COATED WITH A FOAM-BREAKING COMPOUND.

Description

Nov. 27, 1973 v, s. KASULIN ETAL 3,7759339 VESSEL FOR RECEIVING AND DEFOAMING BLOGD Filed June v8, 1972 United States Patent l3,775,339 VESSEL FOR RECEIVING AND DEFOAMINGV BLOOD U.S. Cl. 252--361 Claims ABSTRACT OF THE DISCLOSURE A vessel for receiving and defoaming blood, wherein provision is made-for a froth suppressor device located beneath the coronary blood receptacle.
v Said receptacle is separated from said froth suppressor device by a distribution funnel which directs the liow of coronary blood onto the` froth suppressor device. The froth suppressor device comprises a hollow vertical stem for admission of donor blood and perforated disks vertically spaced on the stem, each of which is coated with a foam-breaking compound.
This is a continuation of application Ser. No. 72,726, filed Sept. 15, 1970, now abandoned.
The present invention relates to medical equipment and apparatus applicable for conducting surgical operations that involve the use of artificial blood circulation, namely, to vessels for holding spare blood and reception of coronary blood. x
The proposed vessel can be successfully used with apparatus for artificial blood circulation, as well as with arrangements for coronary blood suction.
One prior-art device of this nature comprises a housing made as a hollow cylinder fabricated .from organic glass. At the top of the housing there is a receiving chamber or receptacle for coronary blood, provided with `a detachable cover and an inlet pipe for the coronary blood to flow in said inlet pipe being directed tangentially with respect to the receptacle walls. Located beneath the blood receptacle is a froth suppressor device formed by liat metal perforated disks coated with a foam breaking compound. The disks are somewhat spaced one above another on a hollow vertical stem secured on the receptacle cover. At its bottom the vessel has an outlet pipe for the blood to discharge.
Spare blood is poured through the central hole of the cover and iiows down through the hollow vertical stem into the bottom portion of the vessel.
Coronary blood sucked from the operational wound by conventional means that need not be described herein conveys air bubbles and is passed through a tangentially arranged inlet pipe into the receptacle, wherein a rotary flow of coronary blood is formed.
Further, the blood falls onto the top disk of the froth suppressor device, then flows down through the perforations therein onto the subsequent disk and so on, thus consecutively flowing down from one disk onto another to deposit onto the vessel bottom. While owing down the blood is in contact with the foam breaking compound the disks are coated with, thus liberating the same of air bubbles.
As a result the blood accumulated on the vessel bottom becomes suitable for being introduced into the circulatory system of a patient.
However, the prior-art vessel for containing spare blood and reception of coronary blood fails to ensure a reasonably eiiicacious .froth suppression, this being due to the fact that part ofblood flowing down from the blood receptacle, `gets splashed over the vessel walls, thus eluding the system offroth suppressing disks.
It is an object of the present invention to provide such a vessel for holding spare blood and reception of coronary blood that would enable an eiiicacious froth suppression in all of the coronary blood passing into the vessel.
The above-stated object is 'accomplished due to the fact that in a vessel for holding spare blood and reception of coronary blood, wherein provision is made for a froth suppressor device located beneath the coronary blood receptacle and comprising a stack of perforated disks coated with a foam-breaking compound `and somewhat spaced one above another on a vertical stem, according to the invention a perforated distribution funnel is provided at the vessel top above the stack of perforated disks.
It is desirable that the periphery of the distribution funnel adjoin the bottom edges of the blood receptacle walls.
The perforated disks may be of a convexo-concave shape, have different diameters `and be arranged with their convex or cambered outward surfaces facing oppositely so that the greater diameter disks are preferably arranged with their convex cambered surface down, whereas the smaller diameter disks are arranged with their cambered outward surface up.
In what follows the present invention is exemplified by the description of an embodiment thereof to be had in conjunction with the accompanying drawing, wherein a longitudinal section view of a vessel for holding spare blood and reception of coronary blood, according to the invention, is represented.
Referring now to the drawing by numerals of reference, the vessel for holding spare blood and reception of coronary blood comprises a housing 1 at the top of which there is provided a receptacle 2 for coronary blood, and a cover 3 therefor. The blood receptacle 2 has an inlet pipe 4 for admitting the coronary blood of a patient, said inlet pipe being arranged tangentially with respect to the receptacle inner wall. The housing 1 has an inlet pipe 5 for passing the venous blood of the patient in case the vessel is used as an intermediate blood container when regulating the outow of the venous blood of the patient in the artificial blood circulation system, and an outlet pipe 6 for discharging the blood from the vessel into an oxygenator (not illustrated in the drawing).
Located beneath the blood receptacle 2 is the frothsuppressor device which is esentially a stack of perforatedA disks 7 and 8 coated with a foam-breaking compound, mounted on a vertical hollow stem 9 and being somewhat spaced one above another. Located above the top disk 7 is a perforated distribution funnel 10 likewise coated with a foam-breaking compound. The edges of the distribution funnel 10 adjoin the bottom edges of the walls of the blood receptacle 2.
The disks 7 and 8 are of a convexo-concave shape, the disk 7 of a greater diameter being arranged alternately with the smaller-diameter disks 8. The disks 7 are mounted on the stem 9 convex-down, while the disks 8, convex-up.
The vessel for holding spare blood and reception of coronary blood functions as follows.
The donors blood is poured into the vessel through the hollow stem 9. The iiow of the coronary blood of the patient is passed into the upper end of the inner space of the blood receptacle 2, wherein due to the inlet pipe 4 being arranged tangentially, a circulatory blood How is attained. Under the effect of centrifugal forces and its own s l 3 t; weight the blood decelerates its circulatory motion and flows down covering the inner surfaceof'the distribution funnel and through the perforations therein the blood gets onto subsequent disks 7 and 8 of the froth-suppressor device consecutively vowing'dovvn from the top disk onto the bottom one. The distribution funnel 10 enables all of the blood toget onto the disks 7 and 8. While contacting the foam-breaking compound which coat the surface of the disks 7 and 8, the blood release the air bubbles with which the blood became enriched when sucked from the operational wound.
The arrangement of the disk 7 and 8, whereby the greater-diameter disks alternate the smaller-diameter ones and the disks convex surfaces are oriented in a definite manner ensures that the blood is in contact with the disks 7 and 8 throughout the surface area thereof, due to which fact the maximum froth suppressing effect is attainable.
In case of necessity to reactivate the foam-breaking compound one can readily remove the cover 3 complete with the stem 9 secured thereto and carrying the disks 7 and 8 and to recoat the disks 7 and 8 with the fresh foam-breaking compound.
The blood freed of air bubbles and accumulated at the vessel bottom, is passed through the outlet pipe 6 into the oxygenator (not shown in the drawing) and further into the patients artery.
The provision of the distribution funnel and the froth suppressor device of the construction disclosed above, makes it possible to add much to the effectiveness of the froth suppressing process in the herein-proposed vessel for holding spare blood and reception of coronary blood as compared to the prior-art vessels for the same purpose.
What is claimed is:
1. A vessel for receiving and defoaming blood comprising a housing; a blood receiving receptacle located on the top portion of said housing; said receptacle having a tangential duct for admitting coronary blood thereinto; a cover on the receptacle; a froth suppressor device lo- ""tacle; said froth suppressor device comprising a hollow vertical stem for admission of donor blood passing `through said cover and receptacle and discharging into the housing, and perforated dish-like disks mounted transversely on said vertical stem in spaced positions one above another and coated with arfoam-breaking compound; the bottom of said receptacle comprising a perforated distribution funnel located directly above the uppermost of said disks; means in the bottom of said housing for lremoval of the treated blood and means in the cover to release gases.
2. A vessel as claimedin claim 1, wherein the outer periphery of said distribution funnel adjoins the bottom inner periphery of the Walls of said blood receptacle.
3. A vessel as claimed in claim 1, wherein said perforated disks are of a convexo-concave shape and of two different diameters and are arranged with their convex surfaces facing oppositely, the greater-diameter disks facing with their convex surfaces down and the smaller-diameter disks, convex up, said smaller diameter disks being interdigitated between said larger diameter disks.
References Cited UNITED STATES PATENTS 37,258 12/1862 Miller 159-13 R 651,000 6/1900 Webster 159-15 1,257,854 2/1918 Harris 159-15 FOREIGN PATENTS 147,777 1/1902 Germany 159-15 234,618 10/1969 Russia 128-214 NORMAN YUDKOFF, Primary Examiner I. SOFER, Assistant Examiner U.S. Cl. X.R.
159-15, Dig. 4; 55-178
US00261127A 1972-06-08 1972-06-08 Vessel for receiving and defoaming blood Expired - Lifetime US3775339A (en)

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NL (1) NL144156B (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4033486A (en) * 1975-11-13 1977-07-05 Seaquist Valve Company Anti-foaming assembly and method
US4230467A (en) * 1978-09-18 1980-10-28 Tii Corporation Apparatus for removing foam
US4534939A (en) * 1982-10-15 1985-08-13 Hemotec, Inc. Gas flow cartridge with improved coagulation detection and expanded analytical test capability
US4642089A (en) * 1985-01-29 1987-02-10 Shiley, Inc. Unitary venous return reservoir with cardiotomy filter
FR2592815A1 (en) * 1984-07-23 1987-07-17 Vish Khim T DEVICE FOR PURIFYING STEAM CONDENSATE CONTAINING, AS IMPURITIES, OILS AND SALTS
US4737139A (en) * 1985-01-29 1988-04-12 Shiley Inc. Unitary venous return reservoir with cardiotomy filter
US7699966B2 (en) 2004-05-17 2010-04-20 Medtronic, Inc. Point of care heparin determination system
WO2019099157A1 (en) * 2017-11-14 2019-05-23 Fresenius Medical Care Holdings, Inc. Removal of microbubbles through drip chamber nucleation sites

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4033486A (en) * 1975-11-13 1977-07-05 Seaquist Valve Company Anti-foaming assembly and method
US4230467A (en) * 1978-09-18 1980-10-28 Tii Corporation Apparatus for removing foam
US4534939A (en) * 1982-10-15 1985-08-13 Hemotec, Inc. Gas flow cartridge with improved coagulation detection and expanded analytical test capability
FR2592815A1 (en) * 1984-07-23 1987-07-17 Vish Khim T DEVICE FOR PURIFYING STEAM CONDENSATE CONTAINING, AS IMPURITIES, OILS AND SALTS
US4642089A (en) * 1985-01-29 1987-02-10 Shiley, Inc. Unitary venous return reservoir with cardiotomy filter
US4737139A (en) * 1985-01-29 1988-04-12 Shiley Inc. Unitary venous return reservoir with cardiotomy filter
US7699966B2 (en) 2004-05-17 2010-04-20 Medtronic, Inc. Point of care heparin determination system
US20100181210A1 (en) * 2004-05-17 2010-07-22 Wei Qin Point of Care Heparin Determination System
US8801918B2 (en) 2004-05-17 2014-08-12 Medtronic, Inc. Point of care heparin determination system
WO2019099157A1 (en) * 2017-11-14 2019-05-23 Fresenius Medical Care Holdings, Inc. Removal of microbubbles through drip chamber nucleation sites
CN111356488A (en) * 2017-11-14 2020-06-30 费森尤斯医疗保健控股公司 Microbubble removal by drip chamber nucleation sites
US11160913B2 (en) 2017-11-14 2021-11-02 Fresenius Medical Care Holdings, Inc. Removal of microbubbles through drip chamber nucleation sites
AU2018369039B2 (en) * 2017-11-14 2024-02-01 Fresenius Medical Care Holdings, Inc. Removal of microbubbles through drip chamber nucleation sites
US11998674B2 (en) 2017-11-14 2024-06-04 Fresenius Medical Care Holdings, Inc. Removal of microbubbles through drip chamber nucleation sites

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NL7014005A (en) 1972-03-24
NL144156B (en) 1974-12-16
BE756128A (en) 1971-03-15
FR2105602A5 (en) 1972-04-28
CH512249A (en) 1971-09-15

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