CA1037881A - Protection system for mass transfer devices - Google Patents

Protection system for mass transfer devices

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Publication number
CA1037881A
CA1037881A CA203,394A CA203394A CA1037881A CA 1037881 A CA1037881 A CA 1037881A CA 203394 A CA203394 A CA 203394A CA 1037881 A CA1037881 A CA 1037881A
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CA
Canada
Prior art keywords
blood
oxygen
pressure
oxygenator
outlet
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA203,394A
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French (fr)
Other versions
CA203394S (en
Inventor
Ronald J. Leonard
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Baxter International Inc
Original Assignee
Baxter Travenol Laboratories Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Baxter Travenol Laboratories Inc filed Critical Baxter Travenol Laboratories Inc
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Publication of CA1037881A publication Critical patent/CA1037881A/en
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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3621Extra-corporeal blood circuits
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3601Extra-corporeal circuits in which the blood fluid passes more than once through the treatment unit
    • A61M1/3603Extra-corporeal circuits in which the blood fluid passes more than once through the treatment unit in the same direction
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/14Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
    • A61M1/16Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
    • A61M1/1698Blood oxygenators with or without heat-exchangers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES 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
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/36Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
    • A61M1/3621Extra-corporeal blood circuits
    • A61M1/3623Means for actively controlling temperature of blood
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S128/00Surgery
    • Y10S128/03Heart-lung

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  • Health & Medical Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Biomedical Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Cardiology (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

ABSTRACT OF THE DISCLOSURE
A safety system is provided for an oxygenator to prevent the possibility of gas embolism through the membranous barrier which separates the blood and the oxygen. The safety system includes a blood reservoir positioned at a higher horizontal level than the blood inlet, so that a gravity head is maintained. In addition, a manometer is provided which has a fluid level to permit venting of the oxygen if the oxygen pressure exceeds a predetermined gas pressure, which gas pressure is lower than the minimum pressure of the blood in the oxygenator.
The aforementioned Abstract is neither intended to define the invention of the application, which, of course, is measured by the claims, nor is it intended to be limiting as to the scope of the invention in any way.

Description

lQ37~1 BACKGROUND OF THE INVENTION

This invention relates to a safety device for a mas~
transfer system, and more particularly, to a system for prevent-ing an excessive amount of gas from transferring to a liquid on the opposite side of a membranous barrier. ~- -The system of the present invention is particularly useful as a gas embolism protection system for extracorporeal oxygenators of blood in which both oxygen and carbon dioxide are transferred across a membranous barrier separating the blood and the oxygen. An exemplary oxygenator with which the present invention can be effectively utilized is disclosed in Leonard -U.S. Patent No. 3,757,955. It is to be understood, however, ~-that the present invention may be utilized with many different ;
types of mass transfer devices, particularly those using a porous hydrophobic membranous barrier separating a liquid and a gas.
The advent of controlled pore size, nonwetting, microporous membranes has made the construction of high transfer rate membrane oxygenators possible. The membranes have open pores which permit relatively rapid transfer of oxygen, yet the nonwetting properties prevent blood loss from the system.
During operation of the oxygenator, it is important that the blood pressures exceed the oxygen pressures, because accidental reversal of oxygen and blood pressures might result in large amounts of oxygen rapidly entering the blood spaces of the oxygenator. In high flow rate oxygenators, the rapid oxygen accumulation would ov~rwhelm any reservoir or bubble trap and allow gas to enter the patient. The sizes of reservoirs or bubble traps are limited as a result of the need to limit priming volume.
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Extracorporeal oxygenators generally require a relatively high gas volumetric flow rate, and it is important for the gas spaces to be compac~ with good mixing, in order to ensure effective gas trans-fer through the microporous membrane. Since this results in some gas pressure drop in the oxygenator, gas working pressures are generally greater than atmospheric. It can be seen that if the blood pressure were reduced to zero, the gas pressure would be greater than the blood pressure. Such a reversal of gas and blood pressures could easily occur at idle condition when there is no blood flow in the 1 oxygenator.
It is extremely difficult, if not impossible, for an operator to maintain the variable pressures in an oxygenator in the proper direction. It is thus an object of the present invention to provide an automatic system of pressure control for a mass transfer system such as an oxygenator.
It is a further object of the present invention to provide a ~ -system for preventing accidental reversal of gas and liquid pressures in a mass transfer system without utilizing devices which have moving parts, springs, small orifices, or diaphragms which can become disabled or plugged up, thereby causing system failure.
Other objects and advantages of the present invention will become apparent as the description proceeds. -~

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BRIEF DESCRIPTION OF THE INVENTION
In accordance with the present invention, a safety system is provided for a mass transfer system of the type wherein a mem-branous barrier separates a liquid and a gas, and including a liquid inlet, a liquid outlet, and a gas inlet and outlet. The improvement comprises means for maintaining at all times a liquid pressure which i6 higher than the gas pressure. A gas pressure sensing device is coupled to the gas inlet with the gas pressure sensing device com-prising means for venting the gas to prevent the pressure of the gas from exceeding the pressure of the liquid.
In the illustrative embodiments of the invention, the liquid pressure maintaining means comprises a liquid reservoir positioned at a higher horizontal level than the liquid inlet, whereby gravity liquid pressure is maintained. A first pump is located downstream of the reservoir for drawing liquid therefrom, with the reservoir -being collapsible to prevent a negative pressure on the mass transfer device if the pumping action is excessive.
In the illustrative embodiments of the invention, the gas pres-sure sensing device comprises a manometer having a fluid level that prevents gas from venting unless the gas pressure exceeds a pre-determined maximum gas pressure. The fluid level of the manometer is such that it permits gas to vent if the gas pressure exceeds the maximum gas pressure,l with the maximum gas pressure being a pres-sure that is lower than the minimum pressure of the liquid in the oxygenator.
In one embodiment of the invention, another manometer is provided,and iæ operable in response to a pressure of the liquid for variably adjusting the first-mentioned manometer.
, , , ........ . . - . . .. - -, . . . .

10378~31 In one particular aspect the present invention provides in an extracorporeal oxygenator system wherein oxygen and car-bon dioxide are transferred across a porous, hydrophobic mem--branous barrier separating the blood and the oxygen, said oxygenator having a blood inlet, a blood outlet, and an oxygen inlet and outlet; the improvement comprising, in combination: a blood reservoir coupled to said blood outlet downstream therefrom, ~.
said blood reservoir bein~ positioned at a higher level than said blood outlet to provide to blood adjacent the membranous barrier a predetermined minimum pressure; and manometer means which comprises an open liquid container being at least partially filled . .
with a liquid; an oxygen supply line coupled to said oxygen inlet, ~-venting conduit means coupled with said oxygen line and communica-ting with said liquid within said container and having an outlet therein, said liquid having a level that is selected to provide . --a pressure at said venting conduit means outlet but to permit venting of the oxygen in order to prevent the pressure of the oxygen from exceeding said minimum pressure of said blood. .
In another aspect the present invention provides in an 20 oxygen and blood delivery system for use in conjunction with a -membrane-type blood oxygenator having a blood inlet and outlet .
and an oxygen inlet and outlet for diffusion therebetween across a porous, hydrophobic membrane, the improvement comprising~
blood and oxygen conduit means for operatively communicating with .
said respective blood and oxygen inlets and outlets of said - ~ .
oxygenator, and for conveying such materials to and from said ~ .
oxygenator; means forIcarrying a blood reservoir in a position .
elevated above the position of said oxygenator, receptacle means, I
open to the atmosphere, for containing a liquid; an oxygen line having one end thereof diposed within said receptacle means, for immersion in liquid disposed in said receptacle means to create .
a predetermined pressure head at said one end, said oxygen line .~ .

;
~ -4a- .. -" 1037B~31 communicating with said oxygen conduit means, whereby the oxygen pressure in said conduit means is limited in a manner dependent upon said predetermined pressure head.
In a further aspect the present invention provides in an extracorporeal oxygenation system in which oxygen and carbon :-dioxide are transferred across a porous hydrophobic membranous barrier separating the blood and the oxygen, said oxygenator having a blood inlet, a blood outlet, and an oxygen inlet and outlet; the improvement comprising, in combination: a blood ~ .
10 reservoir coupled to said blood outlet downstream therefrom, said ~ -blood reservoir being positioned at a higher level than said blood - outlet to provide to blood adjacent the membranous barrier a pre-determined minimum pressure; and manometer means which comprises a liquid container, open to the atmosphere, being at least par-tially filled with a liquid; an oxygen supply line coupled to said oxygen inlet, venting conduit means coupled with said oxygen line ~1 and communicating with said liquid within said container and :- :
having an outlet therein, said liquid having a level that is selected to provide a pressure at said venting conduit means outlet but-to permit the venting of the oxygen in order to prevent the pressure of the oxygen from exceeding said minimum pressure of said blood, and further including second manometer means .~ ..
coupled to $he blood inlet line, said second manometer means .
being also operatively connected to sald liquid in the container, - - .
and responsive to the pressure of the blood in said blood inlet line to automatically adjust the level of said liquid in said .
- container. I :

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A more detailed explanation of the invention is provided in the following description and claims, and is illustrated in the accompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS
Figure 1 is a schematic flow diagram of a safety fluid nOw system for mass transfer devices in accordance with the principles of the present invention. - --Figure 2 i8 a schematic flow diagram of a modified safety fluid flow system for mass transfer devices according to a second embodiment of the present invention.
''',,, DETAILED DESCRIPTION OF THE
_ILLUSTRATIVE ~3MBODIMENTS ~ -Referring to Figure 1, a mass transfer system is shown ~ -therein in the form of an extracorporeal oxygenator system, including a main console 10 to which a venous reservoir 12 and an arterial reser-voir 14 are attached. Console 10 has an oxygen outlet 15 to which a conduit 16 is connected to feed a regulated nOw of oxygen to the inlet 18 of an oxygenator 20. After passing through oxygenator 20, the spent gas exits via outlet 19. Main console 10 contains a gas nOw rotometer, an oxygenator shim pressure control, a temperature readout meter, and the necessary selector buttons and switches, all as is well-known in the art. Console 10 is located to be within the operator's easy reach, but out of the way of possible fluid contamination.

. .

'``` 10;~78~1 Oxygenator 20 is a typical oxygenator wherein oxygen and carbon dioxide are transferred in opposite directions ~cross a membranous barrier separating the blood and the oxygen.
Such oxygenators are disclosed in the United States patent application in aforementioned Leonard U.S. Patent No. 3,757,955.
It is to be understood that the system of the present invention is particularly suitable for use with any oxygenator using a microporous hydrophobic membrane. A typical suitable membrane material is polytetrafluoroethylene sheeting having a pore size of less than 0.5 micron and being about 0.005 inch -thick. Another exemplary membrane is formed of polypropylene sheeting approximately 0.001 inch thick and having a pore size of about 0.1 micron. The membranes can be laminated to screen~
ing for strengthening support.
A blood conduit 22 is connected from an outlet 24 of venous reservoir 12 to blood inlet 26 of oxygenator 20. The blood and oxygen flow through oxygenator 20 on opposite sides of the membrane contained therewithin and the blood exits via conduit 28 to a heat exchanger 30, which regulates the blood temperature. A typical heat exchanger which could be utilized with the system of the present invention is disclosed in -Leonard et al U.S. Patent No. 3,640,340, issued February 8, 1~72. The blood is then returned via conduit 32 to an inlet 34 .. .. . . .
of arterial reservoir 14.
An arterial pump 36 is utilized to pump oxygenated blood from arterial reservoir 14 via conduit 38 for flow to the , patient's artery. A venous pump 40 is utilized to pump the blood from venous reservoir 12 to blood inlet 26. Line 43 provides blood from the patient's venous supply to venous re-8ervoir 12. The two pumps (venous pump 40 and arterial pump 36) aid to protectthe oxygenator and heat exchanger from over-pres-8urization. Venous pump 40 draws blood from venous reservoir 12 rc~ 6 -: - . .

~0;~7~Bl and propels it through oxygenator 20 and heat exchanger 30, and into arterial reservoir 14. Arterial pump 36 draws blood from arterial reservoir 14 and propels it back to an artery of the perfused subject.
Since the exact matching of the pumping rate of the two pumps is difficult, if not impossible, the venous pump 40 is set to run at a slightly greater speed than the arterial pump 14. A recirculation line 42 between the arterial reservoir 14 and venous reservoir 12 allows the extra flow generated by venous pump 40 to return to the venous reservoir. This assures that the arterial reservoir 14 has blood in it at all times while protecting the oxygenator 20 from over-pressure due to blood accumulation.
Venous reservoir 12 and arterial reservoir 14 are preferably formed of a medical grade polyvinylchloride plastic, or silicone rubber, and are collapsible. Thus in the event the output of either venous pump 40 or arterial pump 36 exceeds the input into a reservoir, the respec-tive reservoir collapses to restrict outflow, thereby preventing a reduced pressure from forming upstream of the reservoir. This is particularly important with respect to arterial reservoir 14 because it is necessary to maintain a minimum blood pressure on the oxygenator so long as there is blood in the system by maintaining a blood pressure head in conduits 22, 32, and 28.
It is important that reservoir 14, and preferably also reservoir 12, is supported so that its lower edges are above the upper port of the oxygenator generally by at least about 3 inches. In this manner, -~
a gravity-induced liquid pressure head is always exerted on the oxy-genator by the blood in the reservoir. The gravity head of the blood is 1037~bl arranged as described below to be always greater than the gas pres-sure in the oxygenator, to guard against the possibility of gas bubbles passing through the microporous membrane.
A safe, positive, direct method of pressure control is provided by coupling to oxygen inlet 18 a gas pressure sensing means 60. Gas pressure sensing means 60 comprises a manometer including an open container 62 having liquid 64, such as water, filled to a predetermined level. A venting conduit 66 is coupled from oxygen inlet 18, to the inside of container 62, passing downwardly through the top of container 62, to form the manometer construction. Fluid 64 is filled to that level which requires enough back pressure in venting conduit 66 to thereby prcvent the gas from venting unless the gas pressure exceeds the predetermined maximum gas pressure, and to permit the gas to vent if the gas pressure exceeds such maximum gas pressure. The maximum gas pressure is selected to be a pressure that is lower than a pressure of the blood in the oxygenator created by the pressure head in line 34, that is, lower than the pressure of the blood in the oxygenator at the vertically highest point of the blood flow path therein. Thus, the vertical distance between outlet 34 of reservoir 14 and oxygen inlet 18 of oxygenator 20 must be greater than the vertical distance between lower end 68 of conduit 66 and surface 70 of fluid 64. In that manner, the gas pressure must always be lower than the blood head, which typically is about 18-19 inches minimum at inlet 26. Thus gas cannot bubble through the membrane to enter the blood spaces. Typically, a 14 inch pressure head of water exists in manometer 60 when the gas pressure is sufficient to cause flow through line 66. When gas is not flowing, the pressure head is slightly less, since then water resides within line 66, lowering the liquid level in container 62.

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The system is fail-safe because if the fluid 64 were to evaporate, thc gas would be vented at a lower pressure than before evaporation. Thus, evaporation of fluid 64 only permits the gas to vent at a lower pressure, and the oxygenator remains safe from the possibility of a gas embolism passing through the membrane.
A line 43 connected to the patient's venous blood supply feeds blood to venous reservoir 12.
The system also may include a cardiotomy reservoir 44, such as is shown in U. S. Patent No. 3, 507, 395, the inlet of which is coupled to the incision site of the patient via suction line 46. Blood spilled in the incision site of the patient is sucked by means of a suc-tion pump 48 to which line 46 is connected. Conduit 50 couples the outlet of cardiotomy reservoir 44 to venous reservoir 12 through an optional auxiliary filter 52 which filters out any remaining clots and other gross particles in the blood, and then passes the blood to the venous reservoir. The cardiotomy reservoir is usually also located above the venous and arterial reservoirs to assist in providing a gravity head of blood.
Where coronary perfusion or other localized perfusion of an organ is desired, a perfusion conduit 54 is coupled to an outlet of arterial reservoir 14, and the fluid is pumped through line 54 by means of a perfusion pump 56.
A modified gas pressure sensing means is illustrated in Figure 2. As the remainder of the system may be identical to the Figure 1 system, like reference numerals have been used for like structure. The gas pressure sensing means 60' of Figure 2 com-prises a manometer formed by container 62' and having an open top _ g _ . .

~037t~1 and bottom. Container 62' contains lluid, such as water 64', and has oxygen line 66 inserted therein in a manner similar to the previous embodiment. The manometer formed by container 62', fluid 64', and line 66 operates similarly to gas sensing means 60 of the Figure 1 embodiment. However, the gas sensing means 60' of the Figure 2 embodiment permits the maximum gas pressure to be raised if the blood pressure is raised, due to a change in blood nOw rate or the like. However, it is still mandatory that the gas pressure be limited and remain less than the blood pressure. To this end, a closed blood manometer 70 is provided. Manometer 70 contains an amount of blood 72, which is dependent on the pressure in line 22, to which it is connected. This provides a variable gas pressure in the space 74 above blood 72 which also depends on the pressure in line 22. Hence, the height of fluid 64' is thereby dependent upon the pressure in space 74, tube 76, and line 22. The outlet of tube 76 communicates with sealed container 78, into which container 62' is positioned. A micro-porous plug 77 prevents blood from entering the control manometer 60' and provides a sterile barrier through which only the gas in space 74 and container 78 can pass. Plug 77 can be made of the same porous, hydrophobic membrane material as can be used in oxygenator 20.
It can be seen that a shift in the level of blood 72 will cause a pressure shift in space 74 and tube 76, thereby creating a fluid shift with respect to fluid 64~. Assuming that the blood pressure in line 22 is increased by an increased flow rate or other reason, the level of blood 72 will rise, thereby increasing the pressure in closed container 78.
This will cause fluid 64 to rise in container 62', thereby permitting a higher oxygen pressure before venting from line 66 will occur. On the other hand, if the blood pressure in line 22 is decreased, the level of . . , - .: - .

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blood 72 in manometer 70 will be lowered, thereby decreasing the pressure upon fluid 64 and causing a drop in the height of fluid 64' within container 62'. Thus the gas will vent at a lower pressure as is required.
The above system provides additional efficiency coupled with safety, in that higher gas pressures may be used when higher blood pressures exist, but upon a sudden drop in blood pressure, the limiting maximum gas pressure will also drop to safe levels.
It is seen that an automatic system of pressure control has been provided for a mass transfer system, such as an oxygenator.
The system is operative to prevent accidental reversal of gas and liquid pressures in a mass transfer system, without utilizing devices having moving parts, springs, small orifices, or diaphragms. The invention not only provides a safety system, but also permits effective operation of an oxygenation system at high altitudes, since manometers 60, 60' permit the safe use of gas pressures in an oxygenator which may exceed the ambient atmospheric pressure.
Furthermore, the use of manometers 60, 60' permit the con-tinued lifesaving oxygenation of a patient even in the event of a gas delivery pressure valve failure or the like causing excess pressure, since the excess gas pressure is simply bled off by manometers 60, 60', while the oxygenator remains exposed to whatever predetermined maximum gas pressure has been selected.
Although two illustrative embodiments of the invention have been illustrated and described, it is to be underætood that various modifications and substitutions may be made by those skilled in the art without departing from the novel spirit and scope of the present invention.

Claims (7)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN EXCLUSIVE
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. In an extracorporeal oxygenator system wherein oxy-gen and carbon dioxide are transferred across a porous, hydro-phobic membranous barrier separating the blood and the oxygen, said oxygenator having a blood inlet, a blood outlet, and an oxygen inlet and outlet; the improvement comprising, in combina-tion: a blood reservoir coupled to said blood outlet downstream therefrom, said blood reservoir being positioned at a higher level than said blood outlet to provide to blood adjacent the membranous barrier a predetermined minimum pressure; and mano-meter means which comprises an open liquid container being at least partially filled with a liquid; an oxygen supply line cou-pled to said oxygen inlet, venting conduit means coupled with said oxygen line and communicating with said liquid within said con-tainer and having an outlet therein, said liquid having a level that is selected to provide a pressure at said venting conduit means outlet but to permit venting of the oxygen in order to prevent the pressure of the oxygen from exceeding said minimum pressure of said blood.
2. An extracorporeal oxygenator system as described in claim 1, wherein the further improvement comprises said blood reservoir having an inlet and outlet for blood, and further in-cluding a first pump located downstream of and operatively con-nected to said outlet of said blood reservoir for drawing blood from said reservoir, said blood reservoir being collapsible to prevent a negative pressure upon the blood side of the oxygenator membranous barrier if the pumping action is excessive; and a second pump located upstream of and operatively connected to said blood inlet of said oxygenator for propelling blood to said blood inlet of said oxygenator said second pump being operated to pump at a greater flow rate than said first pump, and means for re-circulating the extra flow of blood from upstream of said first pump to upstream of said second pump.
3. In an oxygen and blood delivery system for use in conjunction with a membrane-type blood oxygenator having a blood inlet and outlet and an oxygen inlet and outlet for diffusion therebetween across a porous, hydrophobic membrane, the improve-ment comprising:
blood and oxygen conduit means for operatively communica-ting with said respective blood and oxygen inlets and outlets of said oxygenator, and for conveying such materials to and from said oxygenator;
means for carrying a blood reservoir in a position ele-vated above the position of said oxygenator, receptacle means, open to the atmosphere, for containing a liquid;
an oxygen line having one end thereof disposed within said receptacle means, for immersion in liquid disposed in said receptacle means to create a predetermined pressure head at said one end, said oxygen line communicating with said oxygen conduit means, whereby the oxygen pressure in said conduit means is limited in a manner dependent upon said predetermined pressure head.
4. The system of claim 3 in which means are provided for assuring a continuous minimum blood pressure comprising the further improvement in said oxygenator.
5. The system of claim 4 comprising the further improve-ment in which said oxygen line communicates with said gas conduit means upstream from said oxygenator.
6. The system of claim 3, 4 or 5 wherein said blood reservoir is flexible.
7. In an extracorporeal oxygenation system in which oxygen and carbon dioxide are transferred across a porous hydrophobic membranous barrier separating the blood and the oxygen, said oxygenator having a blood inlet, a blood outlet, and an oxygen inlet and outlet; the improvement comprising, in combination: a blood reservoir coupled to said blood outlet downstream therefrom, said blood reservoir being positioned at a higher level than said blood outlet to provide to blood adjacent the membranous barrier a predetermined minimum pressure; and manometer means which comprises a liquid container, open to the atmosphere, being at least partially filled with a liquid; an oxygen supply line coupled to said oxygen inlet, venting conduit means coupled with said oxygen line and communicating with said liquid within said container and having an outlet therein, said liquid having a level that is selected to provide a pressure at said venting conduit means outlet but to permit the venting of the oxygen in order to prevent the pressure of the oxygen from exceeding said minimum pressure of said blood, and further in-cluding second manometer means coupled to the blood inlet line, said second manometer means being also operatively connected to said liquid in the container, and responsive to the pressure of the blood in said blood inlet line to automatically adjust the level of said liquid in said container.
CA203,394A 1973-08-22 1974-06-25 Protection system for mass transfer devices Expired CA1037881A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US390567A US3927980A (en) 1973-08-22 1973-08-22 Oxygen overpressure protection system for membrane-type blood oxygenators

Publications (1)

Publication Number Publication Date
CA1037881A true CA1037881A (en) 1978-09-05

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US (1) US3927980A (en)
JP (1) JPS5430237B2 (en)
AR (1) AR201146A1 (en)
BE (1) BE814984A (en)
BR (1) BR7405230A (en)
CA (1) CA1037881A (en)
DE (1) DE2434571C2 (en)
DK (1) DK447774A (en)
FR (1) FR2241336B1 (en)
GB (1) GB1471308A (en)
IL (1) IL45020A (en)
IT (1) IT1017486B (en)
NL (1) NL165935C (en)
NO (1) NO743005L (en)
ZA (1) ZA742754B (en)

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IL45020A0 (en) 1974-09-10
BE814984A (en) 1974-09-02
JPS5430237B2 (en) 1979-09-28
NL165935C (en) 1981-06-15
AR201146A1 (en) 1975-02-14
IT1017486B (en) 1977-07-20
NL165935B (en) 1981-01-15
GB1471308A (en) 1977-04-21
JPS5045498A (en) 1975-04-23
DE2434571A1 (en) 1975-03-06
BR7405230A (en) 1976-02-24
ZA742754B (en) 1975-05-28
NL7408795A (en) 1975-02-25
DE2434571C2 (en) 1984-10-04
FR2241336A1 (en) 1975-03-21
AU6983874A (en) 1975-12-11
FR2241336B1 (en) 1983-04-01
DK447774A (en) 1975-04-28
IL45020A (en) 1977-05-31
US3927980A (en) 1975-12-23
NO743005L (en) 1975-03-24

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