CA1103589A - Hemodialysis ultrafiltration system with controlled liquid extraction from blood - Google Patents
Hemodialysis ultrafiltration system with controlled liquid extraction from bloodInfo
- Publication number
- CA1103589A CA1103589A CA220,363A CA220363A CA1103589A CA 1103589 A CA1103589 A CA 1103589A CA 220363 A CA220363 A CA 220363A CA 1103589 A CA1103589 A CA 1103589A
- Authority
- CA
- Canada
- Prior art keywords
- dialysate
- pressure
- pump
- dialyzer
- ultrafiltration
- 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
Links
- 238000000108 ultra-filtration Methods 0.000 title claims abstract description 63
- 238000001631 haemodialysis Methods 0.000 title claims abstract description 19
- 230000000322 hemodialysis Effects 0.000 title claims abstract description 19
- 239000007788 liquid Substances 0.000 title claims 8
- 239000008280 blood Substances 0.000 title description 16
- 210000004369 blood Anatomy 0.000 title description 16
- 238000000605 extraction Methods 0.000 title 1
- 238000005259 measurement Methods 0.000 claims abstract description 13
- 239000012528 membrane Substances 0.000 claims description 11
- 238000000502 dialysis Methods 0.000 claims description 9
- 239000012530 fluid Substances 0.000 claims description 7
- 230000017531 blood circulation Effects 0.000 claims description 2
- 239000000385 dialysis solution Substances 0.000 claims 13
- 238000005086 pumping Methods 0.000 claims 2
- 239000013641 positive control Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 claims 1
- 230000009471 action Effects 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000001419 dependent effect Effects 0.000 description 2
- 238000006073 displacement reaction Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 208000036366 Sensation of pressure Diseases 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 230000036772 blood pressure Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 210000003734 kidney Anatomy 0.000 description 1
- 230000003907 kidney function Effects 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
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
- A61M1/14—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
- A61M1/16—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
-
- 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
- A61M1/14—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
- A61M1/16—Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
- A61M1/1601—Control or regulation
-
- 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
- A61M1/34—Filtering material out of the blood by passing it through a membrane, i.e. hemofiltration or diafiltration
- A61M1/3403—Regulation parameters
- A61M1/341—Regulation parameters by measuring the filtrate rate or volume
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/14—Ultrafiltration; Microfiltration
- B01D61/145—Ultrafiltration
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/24—Dialysis ; Membrane extraction
- B01D61/243—Dialysis
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D61/00—Processes of separation using semi-permeable membranes, e.g. dialysis, osmosis or ultrafiltration; Apparatus, accessories or auxiliary operations specially adapted therefor
- B01D61/24—Dialysis ; Membrane extraction
- B01D61/28—Apparatus therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D63/00—Apparatus in general for separation processes using semi-permeable membranes
- B01D63/06—Tubular membrane modules
-
- 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
- A61M2205/00—General characteristics of the apparatus
- A61M2205/33—Controlling, regulating or measuring
- A61M2205/3331—Pressure; Flow
- A61M2205/3334—Measuring or controlling the flow rate
-
- 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
- A61M2205/00—General characteristics of the apparatus
- A61M2205/50—General characteristics of the apparatus with microprocessors or computers
Landscapes
- Health & Medical Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Engineering & Computer Science (AREA)
- Vascular Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Anesthesiology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Water Supply & Treatment (AREA)
- Emergency Medicine (AREA)
- External Artificial Organs (AREA)
Abstract
ABSTRACT
An improved hemodialysis ultrafiltration system.
Dialysate input and output pumps are linked to maintain their volume flows substantially equal. A pressure attenuator and a pressure amplifier on the dialyzer dialysate inlet and outlet, respectively, are employed to control dialyzer pressure on the dialysate side. Dialysate output in excess of dialysate input is separated through the action of the dialysate output pump for measurement. The ultrafiltration rate may be controlled through the pressure transformers and the instantaneous ultrafiltration rate and total ultrafiltration volume may be continuously monitored.
An improved hemodialysis ultrafiltration system.
Dialysate input and output pumps are linked to maintain their volume flows substantially equal. A pressure attenuator and a pressure amplifier on the dialyzer dialysate inlet and outlet, respectively, are employed to control dialyzer pressure on the dialysate side. Dialysate output in excess of dialysate input is separated through the action of the dialysate output pump for measurement. The ultrafiltration rate may be controlled through the pressure transformers and the instantaneous ultrafiltration rate and total ultrafiltration volume may be continuously monitored.
Description
~3~8~ ~
Dialysis of the blood or hemodialysis is a well known and accepted medical technique. For example t kidney malfunction or failure requires that kidney function be performed artifi~
cially, as through hemodialysis.
Successful hemodialysis involves the remo~al of was~e materials and excess water. The removal of waste materials is effectively accomplished through prior art hemodialysis systems which may also compensate, through replacement, for the removal of too much of a particular blood constituent, glucose, for example. The controlled removal of excess water, on the other hand, has proven to be a major problem in hemodialysis. Excess water is removed by ultrafiltration which is established by maintaining the dialysate pressure within the dialyzer lower than that of the blood pressure. Prior art hemodialysis systems have established this pressure condition and monitored it through the use of pressure gauges on the dialysate side. However, these prior art systems have been unable~to~even estimate the ultra-filtration rate with any accuracy~
The removal o too much water too fast will cause a 20 hemodialysis patient to go into shock. Because the ultrafiltra-tion rate cannot accurately be determined for prior art hemo-.
dialysis systems, those systems have heen operated at very lowultrafiltration rates. This has been one factor underlying the extremely long time o dialysis.
One solution to the above-mentioned difficulty in establishing ultrafiltration rate with prior art hemodialysis systems has been to place the dialysis patient on a weighing bed ~ ;
~- ~ to determine the amount of water removal by the decrease in patient weight. Obviously, this system has an extremely high cost and is available only in those situations where some control over, or a knowledge of, the ultrafiltration volume is absolutely necessary. Also, the weighing bed technique will not indicate `-; the instantaneous ultra~iltration rate.
, .
. " .. .. l , , , , :
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The present invention provides a new dialysate cir-cuit for a hemodialysis system which makes it possible to con-trol the ultrafiltration rate as well as provi~ing continuously monitoring means for the instantaneous ultrafiltration rate and total ultrafiltration volume. This is accomplished through - dialysate input and output pumps and a pressure a~tenuator and a pressure amplifier on the dialyzer dialysate inlet and outlet, respectively. The pres~ure attenuator and pressure amplifier control dialyzex pressure on the dialysate side and, thus, the ultrafiltration rate.
The amount by which the dialysate output exceeds the dialysa~e input is the ultrafiltrate volume. That is, the excess is the contribution to the total dialysate volume flow attribut-able to ultrafiltration. The excess is separated from the total dialysate output volume flow by the removal of an amount of dialysate equivalent to the dialysate input volume flow. This is accomplished through the input and output dialysate pumps which are linked to maintain their volume flow substantially equal.
That portion of the dialysate output volume flow attributable to ultrafiltration may be measured instantaneously, as by a flow meter, or the total ultrafiltration volume may be measured as in a graduated receptacle, or both. With a knowledge of the instan-taneous ultrafiltration rate and/or the total ultrafiltration volume, it is possible to make a meaningful adjustment in the ultrafiltration rate by changing the dialyzer dialysate pressure thereby providing an effective control for the ultrafiltration rate itself.
The many objects, advantages and novel features of the present invention will become apparent ~rom the following detailed description when considered in conjunction with the ;
accompanying drawings.
Dialysis of the blood or hemodialysis is a well known and accepted medical technique. For example t kidney malfunction or failure requires that kidney function be performed artifi~
cially, as through hemodialysis.
Successful hemodialysis involves the remo~al of was~e materials and excess water. The removal of waste materials is effectively accomplished through prior art hemodialysis systems which may also compensate, through replacement, for the removal of too much of a particular blood constituent, glucose, for example. The controlled removal of excess water, on the other hand, has proven to be a major problem in hemodialysis. Excess water is removed by ultrafiltration which is established by maintaining the dialysate pressure within the dialyzer lower than that of the blood pressure. Prior art hemodialysis systems have established this pressure condition and monitored it through the use of pressure gauges on the dialysate side. However, these prior art systems have been unable~to~even estimate the ultra-filtration rate with any accuracy~
The removal o too much water too fast will cause a 20 hemodialysis patient to go into shock. Because the ultrafiltra-tion rate cannot accurately be determined for prior art hemo-.
dialysis systems, those systems have heen operated at very lowultrafiltration rates. This has been one factor underlying the extremely long time o dialysis.
One solution to the above-mentioned difficulty in establishing ultrafiltration rate with prior art hemodialysis systems has been to place the dialysis patient on a weighing bed ~ ;
~- ~ to determine the amount of water removal by the decrease in patient weight. Obviously, this system has an extremely high cost and is available only in those situations where some control over, or a knowledge of, the ultrafiltration volume is absolutely necessary. Also, the weighing bed technique will not indicate `-; the instantaneous ultra~iltration rate.
, .
. " .. .. l , , , , :
~L$~
The present invention provides a new dialysate cir-cuit for a hemodialysis system which makes it possible to con-trol the ultrafiltration rate as well as provi~ing continuously monitoring means for the instantaneous ultrafiltration rate and total ultrafiltration volume. This is accomplished through - dialysate input and output pumps and a pressure a~tenuator and a pressure amplifier on the dialyzer dialysate inlet and outlet, respectively. The pres~ure attenuator and pressure amplifier control dialyzex pressure on the dialysate side and, thus, the ultrafiltration rate.
The amount by which the dialysate output exceeds the dialysa~e input is the ultrafiltrate volume. That is, the excess is the contribution to the total dialysate volume flow attribut-able to ultrafiltration. The excess is separated from the total dialysate output volume flow by the removal of an amount of dialysate equivalent to the dialysate input volume flow. This is accomplished through the input and output dialysate pumps which are linked to maintain their volume flow substantially equal.
That portion of the dialysate output volume flow attributable to ultrafiltration may be measured instantaneously, as by a flow meter, or the total ultrafiltration volume may be measured as in a graduated receptacle, or both. With a knowledge of the instan-taneous ultrafiltration rate and/or the total ultrafiltration volume, it is possible to make a meaningful adjustment in the ultrafiltration rate by changing the dialyzer dialysate pressure thereby providing an effective control for the ultrafiltration rate itself.
The many objects, advantages and novel features of the present invention will become apparent ~rom the following detailed description when considered in conjunction with the ;
accompanying drawings.
-2-:
~.~3~
Figure 1 is a diagrammatical illustration of the present invention.
Figure 2 illustrates a preferred embodiment of the flow meter in the embodiment of Figure 1.
Figure 1, which illustrates a preferred embodiment ^
of the present invention, shows a dialyzer 10 having a blood side 11 and a dialysate side 12 separated by a membrane 13. `
The dialyzer 10 may be any of those known to the prior art with regard to the configuration of membrane 13. That is, dialyzer 10 may be of the type wherein the membrane 13 is in the form of a ~ -flat sheet or, alternatively, the membrane 13 may be ~ubular or ~-any other configuration. In the tubular configuration known to the prior art, the blood flows within the tubular members formed by the membrane while the dialysate flow~ along the outer wall of the tubes. The selection of membrane material is known to the prior art and is dependent primarily upon the waste materials to be removed from the blood. With all such membranes, ultra- `
filtration may be obtained through the maintenance of proper pressure gradients across the membrane.
A dialysate source is illustrated at 15 in Figure 1 and is comprised of a dialysate reservoir 16, a dialysate degasser 17 and a dialysate heater 18. The utility of the degasser 17 and heat 18 in a hemodialysis system is well known to the prior art as are the particular conigurations of all the elements combining to form an appropriate source of dialysate.
Of course, the present system is not limited to the use of a reservoir 16, degasser 17 and heater 18 but may be employed with any dialysate makeup system known to the prior art.
Dialysate from the source 15 is passed to a pump 20 via a line 21. The exhaust of the pump 20 is connected to a pressure attenuator 24 via a line 22 and a line 23 connects -the pressure attenuator 24 to the input of the dialysate side 12 of --3~
, ~ . . ., :: :
~.~3~
Figure 1 is a diagrammatical illustration of the present invention.
Figure 2 illustrates a preferred embodiment of the flow meter in the embodiment of Figure 1.
Figure 1, which illustrates a preferred embodiment ^
of the present invention, shows a dialyzer 10 having a blood side 11 and a dialysate side 12 separated by a membrane 13. `
The dialyzer 10 may be any of those known to the prior art with regard to the configuration of membrane 13. That is, dialyzer 10 may be of the type wherein the membrane 13 is in the form of a ~ -flat sheet or, alternatively, the membrane 13 may be ~ubular or ~-any other configuration. In the tubular configuration known to the prior art, the blood flows within the tubular members formed by the membrane while the dialysate flow~ along the outer wall of the tubes. The selection of membrane material is known to the prior art and is dependent primarily upon the waste materials to be removed from the blood. With all such membranes, ultra- `
filtration may be obtained through the maintenance of proper pressure gradients across the membrane.
A dialysate source is illustrated at 15 in Figure 1 and is comprised of a dialysate reservoir 16, a dialysate degasser 17 and a dialysate heater 18. The utility of the degasser 17 and heat 18 in a hemodialysis system is well known to the prior art as are the particular conigurations of all the elements combining to form an appropriate source of dialysate.
Of course, the present system is not limited to the use of a reservoir 16, degasser 17 and heater 18 but may be employed with any dialysate makeup system known to the prior art.
Dialysate from the source 15 is passed to a pump 20 via a line 21. The exhaust of the pump 20 is connected to a pressure attenuator 24 via a line 22 and a line 23 connects -the pressure attenuator 24 to the input of the dialysate side 12 of --3~
, ~ . . ., :: :
3`~ ~
~ :`
the dialyzer 10. The output of the dialysate side 12 of the dialyzer 10 is connected to a pressure amplifier 25 via a line 26. A line 27 connects the pressure amplifier 25 to the inlet of a pump 28 whose exhaust is connected to a drain by a line 29.
The pumps 20 and 28 are linked as at 30 to maintain their volume flow substantially equal. The link 30 may take the form o~ a mechanical linkage or any other control which will satis~y the stated condition of substantial equivalence in volume flow. Preferably, pumps 20 and 28 are positive dis-placement or constant volume pumps operated at or near æero -~-pressure drop. As is known to the prior art, this type o~ pump, when operated at the stated pressure condition, has a substan-tially constant volume flow. Also, to facilitate maintaining their volume flow substantially equal, the pumps 20 and 28 may be identical.
A flow meter 31 is connected to a receptacle 32 via `a line 33 and both are connected to the line 27 by a llne 34.
A line 35 interconnects the line 22 and the linke 34. Pressure sensors 37 are connected into the lines 23 and 26.
The dialyzer blood circuit consists essentially of a line 40 having a pump 41 connected into the blood inlet o the dialyzer 10 and a line 42 having a valve 43 connected into the blood outlet of the dialyæer 10. The lines 40 and 42 are suit-ably connected to the patient who is to undergo hemodialysis in known manner. The pressure in the blood side 11 of the dialyzer 10 is controlled through the action of the pump 41 in conjunction with the valve 43. A blood circuit may be as shown ~ r in Figure I or, alternatively, may be an~ other suitable con-figuration known to the prior art.
The pressure attenuator 24 is a pressure drop device whi-ch acts to maintain the pressure in line 23 below the pressure in line 22. The pressure amplifier 25 is a pressure rise device : -:
.
8~
which acts to maintain the pressure in line 27 above the pres-sure in line 26. Thus, the pressure attenuator 24 and pressure amplifier 25 work in conjunction to control the pressure in the dialysate side 12 of the dialy~er 10. Pressure attenuator 24 ;~
and pressure amplifier 25 may be controlled, in known manner, through suitable CQOperating controls 44 and 45 respectively.
To maintain the pressure of dialysate side 12 below that of blood side 11 and establish ultrafiltration, it is usually necessary that the pressure of the dialysate side be negative which requires that the pressure amplifier 25 be active.
That is, the conditions to establish ultrafiltration usually require that pressure amplifier 25 be a pump and preferably a variable output pump whose output may be controlled in known manner as by control 45. The pressure attenuator 24, on the ~
other hand, need only create pressure drop. Thus, pressure ` "-attenuator 24 may be either a valve or a pump, the volume flow and/or pressure drop of either being controlled in known manner as by control 44. When the pressure attenuator 24 and/or pres-~ sure amplifier 25 are pumps, it is preferred that they be positive displacement pumps with control 44 establishiny the volume flow of pressure attenuator pump 24 approximately equal to the volume flow of pump 20 and control 45 establishin~in~J the volume flow of pressure amplifier-pump 25 to be approximately ~ i equal to the volume flow of pump 20 plus the ultrafiltrate volume flow.
In operation, and assuming that pressure attenuator 24 is a valve having a volume flow rate approximately equal ` to the volume flow rate at the pump 20, the pump 20 will draw dialysate from the source 15 and pump it at a preset and rela-tively constant volume flow over the line 22 to the pressure attenuator 24. The pressure attenuator 24, in conjunction with the pressure amplifier 25, will maintain the pressure in the ~5 ~ '' .
. .. .. -- , ., .. , ,.. , . ... ,,.. . . ~ . :
dialysate side 12 of the dialyzer 10 below that of the blood side 11. Of course, on start up it may be necessary to regulate the pressure drop across pressure attenuator 24 and pressure rise across pressure amplifier 25 to obtain the initial operating ~.
conditions. With the dialysate side pressure in proper relation to the blood side pressure, ultra~iltration will occur and the volume flow of dialysate out of the dialyzer 10 will be greater than the input volume flow by an amount substantially equal to the amount of ultrafiltrateO The difference in dialysate inlet and :.
outlet volume flows is referred to herein as the ultrafiltrate volume The total volume flow out of the dialyzer dialysate side 12 will be transmitted to pressure amplifier 25 by a line 26 and, from there, into line 27. Pump 28, its volume flow being previously set ko be substantially equal to that of pump 20, will .
withdraw dialysate from the line 27 at a rate substantially equal to the rate with which dialysate is put into the system by pump 20. The amount not withdrawn from line 27 is the ultrafiltrate volume which is transmitted by a line 34 to a flow meter 31 where an instantaneous ultrafiltration rate may be estab}ished and ultimately to a receptacle 32. The receptacle 32 may be of the type having a known volume with predetermined volume markings on its side wall, as at 50, such that a total amount o water removed by ultrafiltration may be determined at any time and the ultrafiltration rate or the entire period of hemodialysis ` may be continuously monitored. It should be noted that the `
i ultrafiltrate volume is not the ultrafiltrate but, an amount of . dialysate and ultrafiltrate equal to the amount of ultrafiltrate With a precise matching of the volume flow of pressure attenuator 24 and pump 20, there will be no flow in line 35. As an alternative to precisely matching the volume flow of the pressure attenuator 24 to that o the pump 20, and particularly when the pressure attenuator 24 is a pump~ it is necessar~ -to .
35~
:
provide some means o~ compensation for any differences in volume flow. This compensation is accomplished throuyh the line 35.
When operating with a pump as pressure attenuator 24, ~he pump 20 will again withdraw a preset amount of dialysate from the dialysate source 15. The pressure attenuator 24 and pressure amplifier 25 (both pumps in this embodiment) will operate as described above to maintain a pressure in the dialysate side below that of the blood side of the dialyzer 10. Again, the pump 28 will withdraw from the line 27 an amount of dialysate equiva-lent to that put into the system by the pump 20. If there is a difference in volume flow between the pump 20 and pump 24, there will be a dialysate flow established in the line 35. That is, if the pump 20 has a vo]ume flow greater than that of the pump 24, a dialysate flow in the line 35 will be established to the flow meter 31. On the other hand, if the pump 24 has a greater ~olume flow than that of the pump 20 a dialysate flow through the line 35 to the pump 24 will be established. In either case, the volume flow of the pressure attenuator-pump 24 will establish the actual dialysate input into the dialyæer 10. .
Since the amount of the dialysate withdrawn from line 27 by the pump 28 is matched to that of the input to line 22 of the pump 20, the amount withdrawn from the line 27 may not pre- ~
cisely correspond to the actual dialysate input via the pressure ;
attenuator-pump 24. However, any dialysate flow in the line 35 will be summed with the dialysate flow in the line 34 to give a precise measurement of ultrafiltration rate. For example, if the pressure attenuator-pump 24 has a volume flow less than that of pump 2~ (and thus pump 28) the amount withdrawn by the pump 28 will exceed the actual dialysate input. The amount by which the amount withdrawn by pump 28 exceeds actual dialysate input will correspond to the amount flowing in the line 35. Thus, when the amount of dialysate flowing in the line 35 is summed with the ~3~
volume flow in line 34 and metered at 31, the ultrafiltration rate measurement will be accura-te. Conversely, if the volume flow of pressure attenuator-pump 24 exceeds that of pump 20 .
the amount of dialysate input into the dialyzer will be in ~ :
excess of that withdrawn by a pump 28. However, this excess will be withdrawn from the line 34 over the line 35 and thus will not be measured in the flow meter 31. It should be noted that the preferable, but not critical, condition is to have the line 35 carrying a flow from the pump 20 to the flow meter 31 in either the valve or pump mode of pressure attenuator 24. This eliminates the need for precisely matchiny ~he volume flow of pump 20 and ;~
pressure attenuator 24 while assuring that once circulated dialysate is not recirculated.
From the above, it is apparent that the present inven-tion provides a novel ultrailtration system having the capability to measure the ultrafiltration rate during hemodialysis. Since an accurate measurement of ultrafiltration rate is possible, it is also possible to precisely control the ultrafiltration rate.
For example, if the ultrafiltration is too low the dialysate side pressure may be raduced by operating on either or both of the . pressure attenuator 24 and pressure amplifier 25 through their respective controls 44 and 45. Conversely, if the ultrafiltra-tion rate is too high for patient safety the dialysate side .pressure may be increased - while maintaining it below a blood side pressure - by operating upon the pressure attenuator 24 ~: and/or pressure amplifier 25 through their respective controls ~ 44 and 45. While both modes discussed herein (valve and pump : as pressure attenuator 24) provide ultrafiltration rate measure-ment and control not heretofore available in any prior ar~ system it has been found advantageous to operate in the pump mode.
This results from the fact that a pump operating as attenuator 24 ~: will automatically adjust to changes in output pressure to : -8-35~3~
, , maintain the transmembrance pressure and, thus, the ultrafiltra-tion rate relatively constant. Such pressure changes and their causes are known to the prior art. Also, with a dual pump operation it is possible to reverse the transmembrane pressure gradient to accomplish "reverse" ultrafiltration (i.e., from dialysate to blood).
The pressure sensors 37 are tapped into either or both ~ -of the lines 23 and 26 to give an indication of the dialysate side pressure. The controls 44 and 45 are adjusted to control dialysate side pressure in accordance with the measurement of ~ . .
ultrafiltration rate and the dialysate side pressure may be read with appropriate pressure sensors 37. Also~ if the dialysate side pressure gets too negative, there is the danger that the membrane 13 will rupture. The pressure sensors 37 may be employed to sound an alarm or otherwise give an indication of unsafe pressure on the dialysate side 12 or shut down the system. , Referring now to Figure 2 there is shown a flow meter 31 suitable for use within the embodiment of Figure l. The flow ;
meter 31 is of the type commonly referred to as a ball type flow meter having a transparent vextical tubular member 51 with flow rate markings 52 marked on the side wall. A ball 53 having a , mass selected for the particular fluid to be measured is positioned within the member 51 and a flow oE fluid whose flow rate is to be determined is introduced into the member 51 in the direction indicated by the arrow 54. Gravity will act upon the ball 53 tending to bring it to the bottom of the tube while the force exerted on the ball 53 by the flow through the member 51 will tend to raise the ball 53. Assuming a constant flow rate, these two forces acting on the ball will cause the ball to establish a vertical equilibrium position within the member 51 corresponding to the flow rate. At lower flow rates, the ball - will-assume a lower position while higher flow rates will cause ;
_ g _ 3~
the ball to rise within the member 51. Ball type flow meters of the type illustrated are well known in the art and their calibration is within the knowledge of those of ordinary skill in the art.
Hemodialysis is often performed with a dialysate input volume flow rate of 500 cc/minute. The ultrafiltration rate normally falls within the range of 0-20 cc/minute. The ultra-filtration system of the present invention is capable, with a proper selection of components, of operating at the nominal rates of the prior art devices and any other desired dialysate flow rateO Also, there is no limit to the ultrafiltration rate attain-able by the ultrafiltration system of the present invention except as limited by the rupture strength of the membrane 13. Thus, the system of the present invention provides ultrafiltration rate measurement and control not heretofore available in prior art systems. With a proper selection of components, it is possible to maintain the control of the ultra~iltration rate with any desired limits although, it is anticipated that an accuracy in the ranye of 1 cc/minute will be more than adequate.
. s Obviously, many modifications and alterations of the present invention will be apparent to those skilled in the art from the above description. For example, either the flow meter 31 or the receptacle 32 may be eliminated dependent upon the ;~
circumstances surrounding the hemodlalysis. Also, depending on ;
the transmembrane pressure gradient, the present attenuator 24 and pressure amplifier 25 may be either a pump or a valve. The ultrafiltration system of the present invention may be utilized within a common dialyzer-dialysate circuit, as illustrated, or, -alternatively, may be employed within a separate ultrafiltration ; 30 circuit. It is therefore to be understood that the invention may be practiced otherwise than is specifically described within the scope of the appended claims.
~ :`
the dialyzer 10. The output of the dialysate side 12 of the dialyzer 10 is connected to a pressure amplifier 25 via a line 26. A line 27 connects the pressure amplifier 25 to the inlet of a pump 28 whose exhaust is connected to a drain by a line 29.
The pumps 20 and 28 are linked as at 30 to maintain their volume flow substantially equal. The link 30 may take the form o~ a mechanical linkage or any other control which will satis~y the stated condition of substantial equivalence in volume flow. Preferably, pumps 20 and 28 are positive dis-placement or constant volume pumps operated at or near æero -~-pressure drop. As is known to the prior art, this type o~ pump, when operated at the stated pressure condition, has a substan-tially constant volume flow. Also, to facilitate maintaining their volume flow substantially equal, the pumps 20 and 28 may be identical.
A flow meter 31 is connected to a receptacle 32 via `a line 33 and both are connected to the line 27 by a llne 34.
A line 35 interconnects the line 22 and the linke 34. Pressure sensors 37 are connected into the lines 23 and 26.
The dialyzer blood circuit consists essentially of a line 40 having a pump 41 connected into the blood inlet o the dialyzer 10 and a line 42 having a valve 43 connected into the blood outlet of the dialyæer 10. The lines 40 and 42 are suit-ably connected to the patient who is to undergo hemodialysis in known manner. The pressure in the blood side 11 of the dialyzer 10 is controlled through the action of the pump 41 in conjunction with the valve 43. A blood circuit may be as shown ~ r in Figure I or, alternatively, may be an~ other suitable con-figuration known to the prior art.
The pressure attenuator 24 is a pressure drop device whi-ch acts to maintain the pressure in line 23 below the pressure in line 22. The pressure amplifier 25 is a pressure rise device : -:
.
8~
which acts to maintain the pressure in line 27 above the pres-sure in line 26. Thus, the pressure attenuator 24 and pressure amplifier 25 work in conjunction to control the pressure in the dialysate side 12 of the dialy~er 10. Pressure attenuator 24 ;~
and pressure amplifier 25 may be controlled, in known manner, through suitable CQOperating controls 44 and 45 respectively.
To maintain the pressure of dialysate side 12 below that of blood side 11 and establish ultrafiltration, it is usually necessary that the pressure of the dialysate side be negative which requires that the pressure amplifier 25 be active.
That is, the conditions to establish ultrafiltration usually require that pressure amplifier 25 be a pump and preferably a variable output pump whose output may be controlled in known manner as by control 45. The pressure attenuator 24, on the ~
other hand, need only create pressure drop. Thus, pressure ` "-attenuator 24 may be either a valve or a pump, the volume flow and/or pressure drop of either being controlled in known manner as by control 44. When the pressure attenuator 24 and/or pres-~ sure amplifier 25 are pumps, it is preferred that they be positive displacement pumps with control 44 establishiny the volume flow of pressure attenuator pump 24 approximately equal to the volume flow of pump 20 and control 45 establishin~in~J the volume flow of pressure amplifier-pump 25 to be approximately ~ i equal to the volume flow of pump 20 plus the ultrafiltrate volume flow.
In operation, and assuming that pressure attenuator 24 is a valve having a volume flow rate approximately equal ` to the volume flow rate at the pump 20, the pump 20 will draw dialysate from the source 15 and pump it at a preset and rela-tively constant volume flow over the line 22 to the pressure attenuator 24. The pressure attenuator 24, in conjunction with the pressure amplifier 25, will maintain the pressure in the ~5 ~ '' .
. .. .. -- , ., .. , ,.. , . ... ,,.. . . ~ . :
dialysate side 12 of the dialyzer 10 below that of the blood side 11. Of course, on start up it may be necessary to regulate the pressure drop across pressure attenuator 24 and pressure rise across pressure amplifier 25 to obtain the initial operating ~.
conditions. With the dialysate side pressure in proper relation to the blood side pressure, ultra~iltration will occur and the volume flow of dialysate out of the dialyzer 10 will be greater than the input volume flow by an amount substantially equal to the amount of ultrafiltrateO The difference in dialysate inlet and :.
outlet volume flows is referred to herein as the ultrafiltrate volume The total volume flow out of the dialyzer dialysate side 12 will be transmitted to pressure amplifier 25 by a line 26 and, from there, into line 27. Pump 28, its volume flow being previously set ko be substantially equal to that of pump 20, will .
withdraw dialysate from the line 27 at a rate substantially equal to the rate with which dialysate is put into the system by pump 20. The amount not withdrawn from line 27 is the ultrafiltrate volume which is transmitted by a line 34 to a flow meter 31 where an instantaneous ultrafiltration rate may be estab}ished and ultimately to a receptacle 32. The receptacle 32 may be of the type having a known volume with predetermined volume markings on its side wall, as at 50, such that a total amount o water removed by ultrafiltration may be determined at any time and the ultrafiltration rate or the entire period of hemodialysis ` may be continuously monitored. It should be noted that the `
i ultrafiltrate volume is not the ultrafiltrate but, an amount of . dialysate and ultrafiltrate equal to the amount of ultrafiltrate With a precise matching of the volume flow of pressure attenuator 24 and pump 20, there will be no flow in line 35. As an alternative to precisely matching the volume flow of the pressure attenuator 24 to that o the pump 20, and particularly when the pressure attenuator 24 is a pump~ it is necessar~ -to .
35~
:
provide some means o~ compensation for any differences in volume flow. This compensation is accomplished throuyh the line 35.
When operating with a pump as pressure attenuator 24, ~he pump 20 will again withdraw a preset amount of dialysate from the dialysate source 15. The pressure attenuator 24 and pressure amplifier 25 (both pumps in this embodiment) will operate as described above to maintain a pressure in the dialysate side below that of the blood side of the dialyzer 10. Again, the pump 28 will withdraw from the line 27 an amount of dialysate equiva-lent to that put into the system by the pump 20. If there is a difference in volume flow between the pump 20 and pump 24, there will be a dialysate flow established in the line 35. That is, if the pump 20 has a vo]ume flow greater than that of the pump 24, a dialysate flow in the line 35 will be established to the flow meter 31. On the other hand, if the pump 24 has a greater ~olume flow than that of the pump 20 a dialysate flow through the line 35 to the pump 24 will be established. In either case, the volume flow of the pressure attenuator-pump 24 will establish the actual dialysate input into the dialyæer 10. .
Since the amount of the dialysate withdrawn from line 27 by the pump 28 is matched to that of the input to line 22 of the pump 20, the amount withdrawn from the line 27 may not pre- ~
cisely correspond to the actual dialysate input via the pressure ;
attenuator-pump 24. However, any dialysate flow in the line 35 will be summed with the dialysate flow in the line 34 to give a precise measurement of ultrafiltration rate. For example, if the pressure attenuator-pump 24 has a volume flow less than that of pump 2~ (and thus pump 28) the amount withdrawn by the pump 28 will exceed the actual dialysate input. The amount by which the amount withdrawn by pump 28 exceeds actual dialysate input will correspond to the amount flowing in the line 35. Thus, when the amount of dialysate flowing in the line 35 is summed with the ~3~
volume flow in line 34 and metered at 31, the ultrafiltration rate measurement will be accura-te. Conversely, if the volume flow of pressure attenuator-pump 24 exceeds that of pump 20 .
the amount of dialysate input into the dialyzer will be in ~ :
excess of that withdrawn by a pump 28. However, this excess will be withdrawn from the line 34 over the line 35 and thus will not be measured in the flow meter 31. It should be noted that the preferable, but not critical, condition is to have the line 35 carrying a flow from the pump 20 to the flow meter 31 in either the valve or pump mode of pressure attenuator 24. This eliminates the need for precisely matchiny ~he volume flow of pump 20 and ;~
pressure attenuator 24 while assuring that once circulated dialysate is not recirculated.
From the above, it is apparent that the present inven-tion provides a novel ultrailtration system having the capability to measure the ultrafiltration rate during hemodialysis. Since an accurate measurement of ultrafiltration rate is possible, it is also possible to precisely control the ultrafiltration rate.
For example, if the ultrafiltration is too low the dialysate side pressure may be raduced by operating on either or both of the . pressure attenuator 24 and pressure amplifier 25 through their respective controls 44 and 45. Conversely, if the ultrafiltra-tion rate is too high for patient safety the dialysate side .pressure may be increased - while maintaining it below a blood side pressure - by operating upon the pressure attenuator 24 ~: and/or pressure amplifier 25 through their respective controls ~ 44 and 45. While both modes discussed herein (valve and pump : as pressure attenuator 24) provide ultrafiltration rate measure-ment and control not heretofore available in any prior ar~ system it has been found advantageous to operate in the pump mode.
This results from the fact that a pump operating as attenuator 24 ~: will automatically adjust to changes in output pressure to : -8-35~3~
, , maintain the transmembrance pressure and, thus, the ultrafiltra-tion rate relatively constant. Such pressure changes and their causes are known to the prior art. Also, with a dual pump operation it is possible to reverse the transmembrane pressure gradient to accomplish "reverse" ultrafiltration (i.e., from dialysate to blood).
The pressure sensors 37 are tapped into either or both ~ -of the lines 23 and 26 to give an indication of the dialysate side pressure. The controls 44 and 45 are adjusted to control dialysate side pressure in accordance with the measurement of ~ . .
ultrafiltration rate and the dialysate side pressure may be read with appropriate pressure sensors 37. Also~ if the dialysate side pressure gets too negative, there is the danger that the membrane 13 will rupture. The pressure sensors 37 may be employed to sound an alarm or otherwise give an indication of unsafe pressure on the dialysate side 12 or shut down the system. , Referring now to Figure 2 there is shown a flow meter 31 suitable for use within the embodiment of Figure l. The flow ;
meter 31 is of the type commonly referred to as a ball type flow meter having a transparent vextical tubular member 51 with flow rate markings 52 marked on the side wall. A ball 53 having a , mass selected for the particular fluid to be measured is positioned within the member 51 and a flow oE fluid whose flow rate is to be determined is introduced into the member 51 in the direction indicated by the arrow 54. Gravity will act upon the ball 53 tending to bring it to the bottom of the tube while the force exerted on the ball 53 by the flow through the member 51 will tend to raise the ball 53. Assuming a constant flow rate, these two forces acting on the ball will cause the ball to establish a vertical equilibrium position within the member 51 corresponding to the flow rate. At lower flow rates, the ball - will-assume a lower position while higher flow rates will cause ;
_ g _ 3~
the ball to rise within the member 51. Ball type flow meters of the type illustrated are well known in the art and their calibration is within the knowledge of those of ordinary skill in the art.
Hemodialysis is often performed with a dialysate input volume flow rate of 500 cc/minute. The ultrafiltration rate normally falls within the range of 0-20 cc/minute. The ultra-filtration system of the present invention is capable, with a proper selection of components, of operating at the nominal rates of the prior art devices and any other desired dialysate flow rateO Also, there is no limit to the ultrafiltration rate attain-able by the ultrafiltration system of the present invention except as limited by the rupture strength of the membrane 13. Thus, the system of the present invention provides ultrafiltration rate measurement and control not heretofore available in prior art systems. With a proper selection of components, it is possible to maintain the control of the ultra~iltration rate with any desired limits although, it is anticipated that an accuracy in the ranye of 1 cc/minute will be more than adequate.
. s Obviously, many modifications and alterations of the present invention will be apparent to those skilled in the art from the above description. For example, either the flow meter 31 or the receptacle 32 may be eliminated dependent upon the ;~
circumstances surrounding the hemodlalysis. Also, depending on ;
the transmembrane pressure gradient, the present attenuator 24 and pressure amplifier 25 may be either a pump or a valve. The ultrafiltration system of the present invention may be utilized within a common dialyzer-dialysate circuit, as illustrated, or, -alternatively, may be employed within a separate ultrafiltration ; 30 circuit. It is therefore to be understood that the invention may be practiced otherwise than is specifically described within the scope of the appended claims.
Claims (19)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. In a hemodialysis system, an improved ultrafiltration circuit which comprises:
(a) input pump means;
(b) pressure attenuator means interconnecting said input pump means and the dialyzer dialysate input;
(c) output pump means;
(d) pressure amplifier means interconnecting said output pump means and the dialyzer dialysate output, said pressure attentuator means and said pressure amplifier means cooperating to control dialyzer pressure on the dialysate side;
(e) means for maintaining the volume flow of said input and output pump means substantially equal; and (f) means for accepting any dialysate from the dialyzer output which exceeds the volume flow of said output pump means.
(a) input pump means;
(b) pressure attenuator means interconnecting said input pump means and the dialyzer dialysate input;
(c) output pump means;
(d) pressure amplifier means interconnecting said output pump means and the dialyzer dialysate output, said pressure attentuator means and said pressure amplifier means cooperating to control dialyzer pressure on the dialysate side;
(e) means for maintaining the volume flow of said input and output pump means substantially equal; and (f) means for accepting any dialysate from the dialyzer output which exceeds the volume flow of said output pump means.
2. The ultrafiltration circuit of claim 1 wherein said dialysate accepting means comprises means for providing a measurement of instantaneous ultrafiltration rate.
3. The ultrafiltration circuit of claim 1 wherein said dialysate accepting means comprises means for providing a measurement of total ultrafiltration volume.
4. The ultrafiltration circuit of claim 1 wherein said dialysate accepting means comprises first means for providing an instantaneous ultrafiltration rate and second means for providing a measurement of total ultrafiltration volume.
- Page 1 of Claims -
- Page 1 of Claims -
5. The ultrafiltration circuit of claim 1 wherein said pressure attenuator means and said pressure amplifier means comprise pump means.
6. The ultrafiltration circuit of claim 1 wherein at least one of said pressure attenuator means and said pressure amplifier means comprises pump means.
7. The ultrafiltration circuit of claim 6 wherein said dialysate accepting means comprises means for measuring the ultrafiltration rate.
8. An ultrafiltration control and measurement system for a hemodialysis system which includes a dialyzer having blood flow ports and dialysate input and output ports, comprising:
a first pressure control means connected to the dialysate input port of said dialyzer;
a second pressure control means connected to the dialysate output port of said dialyzer, said first and second pressure control means co-operating to establish and control the dialysate pressure in said dialyzer so as to establish ultrafiltration therein;
conduit means connected from the output of said second pressure control means to the input of said first pressure control means, said conduit means providing a fluid path in which dialysate recirculation may take place;
a receptacle connected to said conduit means in fluid communication therewith;
dialysate input pump means for pumping dialysate with the output of said pump connected to the portion of said conduit between said receptacle and said first pressure control means for supplying dialysate thereto; and - Page 2 of Claims -dialysate exhaust pump means connected to the portion of said conduit between said second pressure control means and said receptacle for withdrawing fluid from the conduit at a flow rate substantially equal to the dialysate supply flow rate provided by said dialysate input pump means, whereby a volume of fluid flow equal to the ultrafiltration rate is diverted to said receptacle.
a first pressure control means connected to the dialysate input port of said dialyzer;
a second pressure control means connected to the dialysate output port of said dialyzer, said first and second pressure control means co-operating to establish and control the dialysate pressure in said dialyzer so as to establish ultrafiltration therein;
conduit means connected from the output of said second pressure control means to the input of said first pressure control means, said conduit means providing a fluid path in which dialysate recirculation may take place;
a receptacle connected to said conduit means in fluid communication therewith;
dialysate input pump means for pumping dialysate with the output of said pump connected to the portion of said conduit between said receptacle and said first pressure control means for supplying dialysate thereto; and - Page 2 of Claims -dialysate exhaust pump means connected to the portion of said conduit between said second pressure control means and said receptacle for withdrawing fluid from the conduit at a flow rate substantially equal to the dialysate supply flow rate provided by said dialysate input pump means, whereby a volume of fluid flow equal to the ultrafiltration rate is diverted to said receptacle.
9. Apparatus according to claim 8 wherein said first pressure control means comprises a pressure attenuator, and said second pressure control means comprises a pressure amplifier.
10. Apparatus according to claim 8 wherein said first pressure control means comprises a valve and said second pressure control means comprises a pump.
11. Apparatus according to claim 10 further including control devices connected to said valve and to said pump which comprises said second pressure control means, said control devices operable for controlling the pressure in the dialysate side of said dialyzer.
12. Apparatus according to claim 8 wherein said first and second pressure control means each comprises a pump.
13. Apparatus according to claim 12 further including control devices connected to said pumps which comprise the first and second pressure control means, said control device operable for adjusting the pressure on the dialysate side of said dialyzer.
14. Apparatus according to claim 8 further including flow meter means connected in fluid communication with said conduit means and said receptacle for providing an instantan-- Page 3 of Claims -eous ultrafiltration rate measurement.
15. Apparatus according to claim 8 wherein said receptacle includes means for providing a measurement of the total ultrafiltration volume.
16. Apparatus according to claim 8 further including pump control means connected to said dialysate input pump means and said dialysate exhaust pump means, for controlling the pumping rate thereof.
17. In a hemodialysis system, an improved ultrafiltration circuit which comprises:
input pump means;
first pressure control means interconnecting said input pump means and the dialyzer dialysate input;
output pump means;
second pressure control means interconnecting said output pump means and the dialyzer dialysate output, said first and second pressure control means cooperating to control dialyzer pressure on the dialysate side;
means for maintaining the volume flow of said input and output pump means substantially equal; and means for accepting any dialysate from the dialyzer output which exceeds the volume flow of said output pump means.
input pump means;
first pressure control means interconnecting said input pump means and the dialyzer dialysate input;
output pump means;
second pressure control means interconnecting said output pump means and the dialyzer dialysate output, said first and second pressure control means cooperating to control dialyzer pressure on the dialysate side;
means for maintaining the volume flow of said input and output pump means substantially equal; and means for accepting any dialysate from the dialyzer output which exceeds the volume flow of said output pump means.
18. In a dialysis system which includes dialysis solution conduit means for passing dialysis solution through a membrane dialyzer, the improvement comprising:
means for supplying precisely controlled volumes of fresh dialysis solution to, and means for withdrawing - Page 4 of Claims -precisely controlled volumes of used dialysis solution from, a portion of said dialysis solution conduit means and a dialyzer connected to said conduit means, to positively control the input and output of the dialysis solution to and from said conduit portion and connected dialyzer;
an outlet conduit, communicating with said withdrawing means for removing said used, withdrawn dialysis solution from said dialysis system;
container means capable of holding a variable liquid volume and connected to said portion of the dialysis solution conduit means which is under precise, positive control of the input and output of dialysis solution; and means for measuring the liquid volume of dialysis solution in said precisely, positively controlled conduit portion and connected dialyzer, said liquid volume being less than the entire liquid volume of dialysis solution in said dialysis system, whereby changes in said liquid volume not attributable to said dialysis solution input and output indicate the amount of ultrafiltration during dialysis.
means for supplying precisely controlled volumes of fresh dialysis solution to, and means for withdrawing - Page 4 of Claims -precisely controlled volumes of used dialysis solution from, a portion of said dialysis solution conduit means and a dialyzer connected to said conduit means, to positively control the input and output of the dialysis solution to and from said conduit portion and connected dialyzer;
an outlet conduit, communicating with said withdrawing means for removing said used, withdrawn dialysis solution from said dialysis system;
container means capable of holding a variable liquid volume and connected to said portion of the dialysis solution conduit means which is under precise, positive control of the input and output of dialysis solution; and means for measuring the liquid volume of dialysis solution in said precisely, positively controlled conduit portion and connected dialyzer, said liquid volume being less than the entire liquid volume of dialysis solution in said dialysis system, whereby changes in said liquid volume not attributable to said dialysis solution input and output indicate the amount of ultrafiltration during dialysis.
19. The dialysis device of claim 18 in which said means for supplying and withdrawing controlled volumes of solution is adapted to supply and withdraw identical liquid volumes, whereby the liquid volume attributable to dialysis solution in said conduit portion and connected dialyzer remains constant.
- Page 5 of Claims -
- Page 5 of Claims -
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US44370074A | 1974-02-19 | 1974-02-19 | |
US443,700 | 1974-02-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1103589A true CA1103589A (en) | 1981-06-23 |
Family
ID=23761857
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA220,363A Expired CA1103589A (en) | 1974-02-19 | 1975-02-18 | Hemodialysis ultrafiltration system with controlled liquid extraction from blood |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS5512262B2 (en) |
CA (1) | CA1103589A (en) |
DE (1) | DE2506039C2 (en) |
FR (1) | FR2261018B1 (en) |
GB (1) | GB1502859A (en) |
NL (1) | NL176638C (en) |
SE (1) | SE418801B (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2544258C2 (en) * | 1975-10-03 | 1984-04-19 | Fresenius AG, 6380 Bad Homburg | Hemodialysis machine |
JPS5272379A (en) * | 1975-12-15 | 1977-06-16 | Toray Ind Inc | Separation of fluid |
JPS5281995A (en) * | 1975-12-27 | 1977-07-08 | Musashi Eng Kk | Artificial liver |
GB1560660A (en) * | 1975-12-30 | 1980-02-06 | Rhone Poulenc Ind | Dialyser system and control unit therefor |
FR2368963A1 (en) * | 1976-10-27 | 1978-05-26 | Abg Semca | Blood dialysis unit with an ultrafiltration membrane - including carefully rated pumps and pressure control systems |
JPS5444396A (en) * | 1977-09-13 | 1979-04-07 | Koujinkai | Method of measuring quantity of ultraafiltration of artificial kidney dialyzer and its device |
JPS5563653A (en) * | 1978-11-06 | 1980-05-13 | Kawasumi Lab Inc | Ultrafiltration capacity measuring method of artificial kidney |
US4209391A (en) * | 1978-11-06 | 1980-06-24 | Cordis Dow Corp. | Apparatus and method for automatically controlling hemodialysis at a pre-selected ultrafiltration rate |
FI61739C (en) * | 1980-07-01 | 1982-09-10 | Valmet Oy | TORKNINGSFOERFARANDE OCH ANORDNING |
DE3439661A1 (en) * | 1984-10-30 | 1986-05-07 | Fresenius AG, 6380 Bad Homburg | Haemodialysis unit |
FR2574664B1 (en) * | 1984-12-14 | 1987-03-06 | Issautier Gerald | HEMODIALYSIS DEVICE FOR AUTOMATICALLY CONTROLLING WEIGHT LOSS |
GB8524972D0 (en) * | 1985-10-10 | 1985-11-13 | Atomic Energy Authority Uk | Liquid treatment |
DE3819704C1 (en) * | 1988-06-09 | 1989-09-28 | Kraft Europe R & D, Inc. Zweigniederlassung Muenchen, 8000 Muenchen, De | |
DE102011016870B4 (en) * | 2011-04-13 | 2013-06-20 | Fresenius Medical Care Deutschland Gmbh | Device for conveying a fluid to a filter unit of a medical treatment device and method for measuring the pressure in the fluid flow system of such a device |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3563381A (en) * | 1968-12-18 | 1971-02-16 | Andrew Charles Edelson | Dialysis apparatus |
FR2041436A5 (en) * | 1969-04-24 | 1971-01-29 | Thomson Medical Telco | Artificial kidney metering device |
US3669880A (en) * | 1969-06-30 | 1972-06-13 | Cci Aerospace Corp | Recirculation dialysate system for use with an artificial kidney machine |
DE2101168B1 (en) * | 1971-01-12 | 1972-05-25 | B. Braun Melsungen AG, 3508 MeIsungen | Dosing system for peritoneal dialysis |
JPS4861196A (en) * | 1971-12-01 | 1973-08-27 |
-
1975
- 1975-02-07 SE SE7501357A patent/SE418801B/en not_active IP Right Cessation
- 1975-02-13 DE DE2506039A patent/DE2506039C2/en not_active Expired
- 1975-02-14 NL NLAANVRAGE7501755,A patent/NL176638C/en not_active IP Right Cessation
- 1975-02-18 CA CA220,363A patent/CA1103589A/en not_active Expired
- 1975-02-18 FR FR7504956A patent/FR2261018B1/fr not_active Expired
- 1975-02-19 GB GB6975/75A patent/GB1502859A/en not_active Expired
- 1975-02-19 JP JP2079475A patent/JPS5512262B2/ja not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB1502859A (en) | 1978-03-08 |
NL176638B (en) | 1984-12-17 |
SE7501357L (en) | 1975-08-20 |
FR2261018B1 (en) | 1980-06-27 |
DE2506039C2 (en) | 1982-05-13 |
JPS50118597A (en) | 1975-09-17 |
DE2506039A1 (en) | 1975-08-21 |
JPS5512262B2 (en) | 1980-03-31 |
FR2261018A1 (en) | 1975-09-12 |
SE418801B (en) | 1981-06-29 |
NL7501755A (en) | 1975-08-21 |
NL176638C (en) | 1985-05-17 |
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Legal Events
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