US20140291243A1 - Dialysis system with ultrafiltration control - Google Patents

Dialysis system with ultrafiltration control Download PDF

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Publication number
US20140291243A1
US20140291243A1 US14/305,952 US201414305952A US2014291243A1 US 20140291243 A1 US20140291243 A1 US 20140291243A1 US 201414305952 A US201414305952 A US 201414305952A US 2014291243 A1 US2014291243 A1 US 2014291243A1
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pump
fluid
blood
pathway
dialyzer
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US14/305,952
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James R. Curtis
Ladislaus F. Nonn
Julie Wrazel
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Outset Medical Inc
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Home Dialysis Plus Ltd
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Priority to US14/305,952 priority Critical patent/US20140291243A1/en
Assigned to HOME DIALYSIS PLUS, LTD. reassignment HOME DIALYSIS PLUS, LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: NONN, LADISLAUS F., Curtis, James R., WRAZEL, JULIE
Publication of US20140291243A1 publication Critical patent/US20140291243A1/en
Assigned to OUTSET MEDICAL, INC. reassignment OUTSET MEDICAL, INC. CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: HOME DIALYSIS PLUS, LTD.
Assigned to CRG PARTNERS III L.P., CRG PARTNERS III - PARALLEL FUND "B" (CAYMAN) L.P., CRG PARTNERS III (CAYMAN) L.P. reassignment CRG PARTNERS III L.P. SHORT-FORM PATENT SECURITY AGREEMENT Assignors: OUTSET MEDICAL, INC.
Priority to US15/225,712 priority patent/US9545469B2/en
Assigned to OUTSET MEDICAL, INC. reassignment OUTSET MEDICAL, INC. RELEASE OF PATENT SECURITY INTEREST Assignors: CRG SERVICING LLC
Abandoned legal-status Critical Current

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    • 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
    • A61M1/1621Constructional aspects thereof
    • A61M1/1647Constructional aspects thereof with flow rate measurement of the dialysis fluid, upstream and downstream of the dialyser
    • 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
    • A61M1/1601Control or regulation
    • 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
    • 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
    • A61M1/1601Control or regulation
    • A61M1/1619Sampled collection of used dialysate, i.e. obviating the need for recovery of whole dialysate quantity for post-dialysis analysis
    • 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
    • A61M1/1621Constructional aspects thereof
    • A61M1/165Constructional aspects thereof with a dialyser bypass on the dialysis fluid line
    • 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
    • A61M1/34Filtering material out of the blood by passing it through a membrane, i.e. hemofiltration or diafiltration
    • 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
    • A61M1/34Filtering material out of the blood by passing it through a membrane, i.e. hemofiltration or diafiltration
    • A61M1/3403Regulation parameters
    • 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
    • A61M1/34Filtering material out of the blood by passing it through a membrane, i.e. hemofiltration or diafiltration
    • A61M1/3413Diafiltration
    • 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
    • A61M1/34Filtering material out of the blood by passing it through a membrane, i.e. hemofiltration or diafiltration
    • A61M1/342Adding solutions to the blood, e.g. substitution solutions
    • A61M1/3424Substitution fluid path
    • A61M1/3427Substitution fluid path back through the membrane, e.g. by inverted trans-membrane pressure [TMP]
    • GPHYSICS
    • G05CONTROLLING; REGULATING
    • G05DSYSTEMS FOR CONTROLLING OR REGULATING NON-ELECTRIC VARIABLES
    • G05D7/00Control of flow
    • G05D7/06Control of flow characterised by the use of electric means
    • G05D7/0617Control of flow characterised by the use of electric means specially adapted for fluid materials
    • G05D7/0629Control of flow characterised by the use of electric means specially adapted for fluid materials characterised by the type of regulator means
    • G05D7/0676Control of flow characterised by the use of electric means specially adapted for fluid materials characterised by the type of regulator means by action on flow sources
    • 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
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/33Controlling, regulating or measuring
    • A61M2205/3331Pressure; Flow
    • 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
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/33Controlling, regulating or measuring
    • A61M2205/3331Pressure; Flow
    • A61M2205/3334Measuring or controlling the flow rate
    • 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
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/70General characteristics of the apparatus with testing or calibration facilities
    • 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
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/70General characteristics of the apparatus with testing or calibration facilities
    • A61M2205/702General characteristics of the apparatus with testing or calibration facilities automatically during use

Definitions

  • a dialyzer is a device for cleansing blood through hemodialysis by a process of diffusion and/or convection of waste products, dissolved solutes and fluid from the blood across a semi permeable membrane into a dialysis solution known as dialysate.
  • a dialysis system is an assembly that includes the dialyzer and associated equipment to support the dialyzer, such a plumbing and pumps.
  • Diffusion is the principal mechanism in which dialysis removes waste products such as urea, creatinine, phosphate and uric acid, among others, from the blood.
  • a differential between the chemical composition of the dialysate and the chemical composition of the blood causes the waste products to be drawn through the semi-permeable membrane from the blood into the dialysate.
  • Ultrafiltration is a process in dialysis where fluid is caused to move across the membrane from the blood into the dialysate for the purpose of removing excess fluid from the patient's blood stream. Along with water, some solutes are also drawn across via convection rather than diffusion.
  • Ultrafiltration is a result of a pressure differential between the blood compartment of the dialyzer and the dialysate compartment of the dialyzer where fluid will move from a higher pressure to a lower pressure.
  • fluid in the dialysate compartment is higher than the blood compartment, causing fluid to move from the dialysate compartment into the blood compartment. This is commonly referred to as reverse ultrafiltration.
  • the system includes a first pump for pumping dialysate into a dialyzer and a second pump for pumping dialysate out of the dialyzer.
  • the system also includes a third pump that provides improved control of a level of ultrafiltration, hemodiafiltration, or both, as described in detail below.
  • a method of performing dialysis comprising: operating a first pump to pump dialysate at a first flow rate through a fluid inlet pathway into a dialyzer; operating a second pump to pump the dialysate through a fluid outlet pathway out of the dialyzer; operating a third pump to pump the dialysate through the fluid outlet pathway in cooperation with the second pump, wherein the second and third pumps cooperate to collectively achieve a second flow rate through the fluid outlet pathway from the dialyzer; and pumping blood through the dialyzer in communication with the dialysate such that the dialyzer dialyzes the blood.
  • a method of performing dialysis comprising: providing a dialysis system having an inlet conduit through which fluid flows in an inward direction toward a dialyzer and an outlet conduit through which fluid flows in an outward direction from the dialyzer; pumping fluid through the inlet conduit using a first pump; pumping fluid through the outlet conduit using a second pump; and using a third pump to supplement the pumping of the second pump through the outlet conduit.
  • a dialysis system comprising: a dialyzer having a blood flow pathway through which blood flows; a fluid inlet pathway configured to provide incoming fluid to the dialyzer; a fluid outlet pathway configured to receive outgoing fluid from the dialyzer; a first pump coupled to the fluid inlet pathway and configured to pump the fluid through the fluid inlet pathway toward the dialyzer; a second pump coupled to the fluid outlet pathway and configured to pump the fluid through the fluid outlet pathway away from the dialyzer; and a third pump coupled to the fluid outlet pathway, the third pump configured to work in cooperation with the second pump to achieve a desired flow rate of fluid to or from the blood flowing through the dialyzer.
  • FIG. 1A shows a schematic view of a dialysis system adapted to perform dialysis of a patient's blood.
  • FIG. 1B shows a schematic view of another embodiment of a dialysis system.
  • FIG. 2 is a schematic view of a dialyzer of the dialysis system.
  • FIG. 3 shows a schematic representation of the system running in a calibration mode.
  • FIG. 4 shows a schematic representation of the system running in a dialysis mode.
  • FIG. 5 is a cross-sectional view of a compliance control device.
  • FIG. 6 is a cross-sectional view of another embodiment of a compliance control device.
  • FIG. 1A shows a schematic view of a dialysis system adapted to perform hemodialysis of a patient's blood.
  • the system includes an arrangement of three or more pumps that provide improved control over the type of hemodialysis being performed. By varying the relative pump speeds of the three pumps, an operator can vary the level of blood filtration and can also selectively achieve ultrafiltration and hemodiafiltration of the blood.
  • Ultrafiltration is a process in dialysis where fluid is caused to move across a dialyzer membrane via diffusion from the blood into the dialysate for the purpose of removing excess fluid from the patient's blood stream. Along with water, some solutes are also drawn across the membrane via convection rather than diffusion. Ultrafiltration is a result of a pressure differential between the blood compartment and the dialysate compartment where fluid will move from a higher pressure to a lower pressure.
  • fluid in the dialysate compartment is higher than the blood compartment causing fluid to move from the dialysate compartment into the blood compartment. This is commonly referred to as reverse ultrafiltration.
  • the dialysis system includes a dialyzer 105 that is fluidly connected to a source 110 of fluid (such as dialysate) and also to a source 115 of blood to be dialyzed.
  • the source 115 of blood may be a patient.
  • the source 110 of fluid may be a dialysate preparation system that prepares dialysate for use in the dialysis system.
  • the dialysate preparation system may include a water purification system that purifies water pursuant to systems and methods described in co-pending U.S. patent application Ser. No. 12/795,382 entitled “Fluid Purification System”, which is filed concurrently herewith and which is incorporated by reference in its entirety.
  • dialyzer 105 may be at least partially configured with microfluidic pathways as described in co-pending U.S. patent application Ser. No. 12/795,371 entitled “Microfluidic Devices”, filed concurrently herewith, which claims priority to U.S. Provisional Application Ser. No. 61/220,117, filed on Jun. 24, 2009, which applications are incorporated by reference in their entirety.
  • U.S. patent application Ser. No. 12/795,444 entitled “Dialysis System”, filed concurrently herewith, is also incorporated by reference in its entirety. Dialysate flows into the dialyzer 105 through a fluid inlet 120 and out of the dialyzer 105 through a fluid outlet 125 .
  • the dialyzer 105 is described in more detail below.
  • the dialysis system includes plumbing that forms a plurality of fluid flow pathways, which may be any type of conduit through which a fluid such as dialysate may flow.
  • the fluid flow pathways include an inlet pathway 132 through which a fluid such as unused dialysate flows from the source 110 toward and into the dialyzer 105 .
  • At least a first pump 135 is positioned along or in communication with the inlet pathway 132 for pumping the fluid toward the dialyzer 105 at a desired flow rate.
  • One or more sensors S may be coupled to the fluid flow pathway for sensing one or more characteristics of the incoming fluid, such as pressure, flow rate, temperature, conductivity, etc.
  • one or more sample ports P may be coupled to the fluid flow pathways that provide access to fluid flowing through the piping.
  • FIG. 1 shows the sensors S and sample ports P coupled to the fluid flow pathways at specific locations, although the quantity and locations of the sensors S and sample ports P may vary.
  • the fluid flow pathways further include an outlet pathway 137 through which used dialysate flows out of the dialyzer 105 toward one or more drains 140 .
  • the dialysate exiting the dialyzer may be used to pre-heat other incoming fluids in the system, such as the water stream entering the heat exchange and purification system, before reaching the drain 140 .
  • the outlet pathway 137 bifurcates into two or more outlet pathways including a main outlet pathway 137 a and a secondary outlet pathway 1137 b.
  • At least a second pump 155 is positioned along or in communication with the main outlet pathway 137 a for pumping the dialysate out of and away from the dialyzer 105 through the main outlet pathway 137 a.
  • a third pump 160 is positioned along or in communication with the secondary outlet pathway 137 b.
  • the third pump 160 can be used to augment fluid flow through the fluid flow pathways such as to selectively achieve differentials in flow rates between the inflow pathway 132 and the outflow pathway 132 pursuant to achieving various types of dialysis, including hemodialysis, ultrafiltration, and hemodiafiltration, as described more fully below.
  • the third pump pumps dialysate through the fluid flow pathways when the system is in dialysis mode.
  • the third pump may also pump another fluid, such as water or disinfectant, when the system is in a different mode, such as in a calibration mode or in a cleaning mode.
  • the third pump 160 can also be used to calibrate flow rates between the first pump 135 and the second pump 155 , as described more fully below.
  • the third pump 160 is positioned along the inflow pathway 132 upstream of the inlet 120 of the dialyzer 105 .
  • the secondary outlet pathway 137 branches off the inlet pathway 132 at a location downstream of the first pump 135 and upstream of the first valve 170 .
  • the third pump 160 pumps fluid toward the drain 140 .
  • the embodiment of FIG. 1A may be more efficient than the embodiment of FIG. 1B because the third pump 160 in FIG. 1B pumps fresh, unused dialysate into the drain 140 while the third pump in FIG. 1A pumps used dialysate into the drain 140 .
  • the third pump 160 and the second pump 155 are both positioned along a single, non-bifurcating outflow pathway.
  • first, second and third pumps may be used for the first, second and third pumps.
  • the pumps are nutating pumps.
  • the pumps could be rotary lobe pumps, progressing cavity pumps, rotary gear pumps, piston pumps, diaphragm pumps, screw pumps, gear pumps, hydraulic pumps, vane pumps, regenerative (peripheral) pumps, or peristaltic pumps, or any combination thereof.
  • Other types of pumps can also be used.
  • the first pump 135 and the second pump 155 may be driven by a common shaft to ensure synchrony of the pump strokes and the volume of fluid pumped. It is understood that first pump 135 and the second pump 155 may also be fully independent from each other.
  • any of a variety of fluid conduits may be used to form the fluid flow pathways.
  • at least a portion of the fluid flow pathway is formed of piping having an inside diameter from 1 ⁇ 8 inch to 1 ⁇ 2 inch.
  • the flow rate in the piping could range between about 50 ml/min to about 1,000 ml/min. In an embodiment, the flow rate is in the range of between about 100 ml/min and about 300 ml/min.
  • the fluid flow pathways further include a bypass pathway 165 that fluidly directly connects the inlet pathway 132 and the outlet pathway 137 .
  • An exemplary purpose of the bypass pathway 165 is to provide a fluid flow pathway where fluid can flow into and out of the dialysis system and bypass the dialyzer 105 , such as for flushing, cleaning or calibrating the system.
  • the junction between the inlet pathway 132 and bypass pathway 165 is located upstream of the fluid inlet 120 of the dialyzer 105
  • the junction between the bypass pathway 165 and the outlet pathway is located downstream of the fluid outlet 125 of the dialyzer 105 .
  • other configurations of the bypass pathway 165 can be used to achieve bypassing of the dialyzer 105 .
  • a first valve 170 is positioned at the junction between the inlet pathway 132 and the bypass pathway 165 .
  • a second valve 175 is positioned at the junction between the bypass pathway 165 and the outlet pathway 137 .
  • the first valve 170 and second valve 175 are three-way valves, such as solenoid valves, that can be used to selectively regulate fluid flow through the fluid flow pathways. That is, the first valve 170 can be set to either of two or more settings including (1) a dialysis setting wherein the first valve directs all incoming fluid along the inlet pathway 132 toward the dialyzer 105 (as represented by arrow A in FIG.
  • the second valve 175 can also be set to either of two settings including (1) a bypass setting wherein the second valve 175 directs incoming fluid from the bypass pathway 165 into the outlet pathway 137 (as represented by arrow C in FIG. 1 ); or (2) a dialysis setting wherein the second valve 175 closes flow from the bypass valve 165 such that outgoing fluid from the dialyzer outlet 125 continues to flow outward along the outlet pathway 137 (as represented by arrow D in FIG. 1 .)
  • the first valve 175 and the second valve 160 are generally both set in tandem to either the bypass setting or the dialysis setting.
  • the system may include a control and safety system that ensures that the first and second valves are not set to incompatible settings.
  • FIGS. 1A and 1B The arrangement of the various components of the dialysis system shown in FIGS. 1A and 1B are exemplary and other arrangements are possible.
  • the flow pathways and the pumps may be placed in different locations along the flow pathways from what is shown in FIG. 1 .
  • the third pump 160 is positioned in the flow pathway at a location upstream of the dialyzer 105 and downstream of the first valve 170 or the third pump can be positioned downstream of the dialyzer 105 and upstream of the second valve 175 .
  • the system can employ more than three pumps.
  • FIG. 2 is a schematic, cross-sectional view of the dialyzer 105 , which defines a blood compartment having a blood flow pathway 205 and a dialysate compartment having a dialysate flow pathway 210 separated by a semi-permeable membrane 215 .
  • the blood enters the blood flow pathway 205 via the blood inlet 130 , flows through the blood flow pathway 205 , and exits via the blood outlet 133 .
  • the dialysate enters the dialysate flow pathway 210 via the fluid inlet 120 , flows through the dialysate flow pathway 210 , and exits via the fluid outlet 125 .
  • the semi-permeable membrane 215 is configured to allow the transfer of one or more substances from the blood in the blood flow pathway 205 to the dialysate in the dialysate flow pathway 210 , or visa-versa.
  • materials that may be used as the semipermeable membrane 215 include polymers, copolymers, metals, ceramics, composites, and/or liquid membranes.
  • a composite membrane is polysulfone-nanocrystalline cellulose composite membrane such as AN69 flat sheet membranes available from Gambro Medical.
  • Gas-liquid contactor membranes may also be employed for transferring a substance between a liquid and gas such as for oxygenation of blood, whereby the membrane allows transfer of carbon dioxide and oxygen, such that oxygen transfers to blood from oxygen or oxygen-enriched air, and carbon dioxide transfers from the blood to the gas.
  • Fluid membranes may also be employed. Fluid membranes comprise a lamina having through cut microchannels containing fluid and a first and second membrane support positioned to contain fluid in the microchannels.
  • the blood and the dialysate may flow in a counter-flow configuration wherein blood flows through the blood flow pathway 205 in one direction and the dialysate flows through the dialysate flow pathway 210 in the opposite direction.
  • the dialyzer 105 is described in the context of having a counter-flow configuration although a cross-flow configuration may also be used.
  • hemodialysis occurs. That is, waste solutes move across the semipermeable membrane 215 from the blood into the dialysate via diffusion as a result of the differential of solute concentration between the blood and the dialysate.
  • the flow of the blood and dialysate which may be counter-, cross- or concurrent-flow, maintains the concentration gradient of solutes between the blood and dialysate, which helps to remove more urea and creatinine from the blood.
  • concentrations of solutes for example potassium, phosphorus, and urea
  • the concentrations of solutes may be undesirably high in the blood, but low or absent in the dialysate and constant replacement of the dialysate ensures that the concentration of undesired solutes is kept low on the dialysate side of the membrane.
  • the dialysate has levels of minerals like potassium and calcium that are similar to their natural concentration in healthy blood.
  • the dialysate level is set at a slightly higher level than in normal blood, to encourage diffusion of bicarbonate into the blood, to maintain a patient's CO2 level, and act as a pH buffer to neutralize the metabolic acidosis that is often present in these patients.
  • the dialyzer 105 is also configured to perform ultrafiltration wherein a pressure differential across the membrane 215 results in fluid and dissolved solutes passing across the membrane 215 from the blood to the dialysate.
  • the dialyzer 105 is also configured to perform hemodiafiltration wherein solute movement across the semipermeable membrane 215 is governed by convection rather than by diffusion.
  • a positive hydrostatic pressure differential between the blood flow pathway 205 and the dialysate flow pathway 210 drives water and solutes across the semipermeable membrane 215 from the blood flow pathway to the fluid flow pathway. Solutes of both small and large molecules get dragged through the semipermeable membrane 215 along with the fluid.
  • the direction of water and solute movement is oscillated between moving water and solutes from the blood into the dialysate and moving water and solutes from the dialysate into the blood.
  • the dialysis system achieves hemodialysis without ultrafiltration when the flow rate through the inlet pathway 132 is equal to or substantially equal to the flow rate through the outlet pathway 137 .
  • hemodialysis without ultrafiltration is achieved where the amount of dialysate flowing into dialyzer 105 via the inlet pathway 137 is substantially equal to the amount of dialysate flowing out of the dialyzer via the outlet pathway 137 over a period time.
  • the system performs a hemodialysis procedure utilizing all three pumps in an active state substantially continuously throughout the hemodialysis procedure.
  • the system adjusts the pump rate of the third pump 160 to achieve a desired balance of equal flow rates between the inlet pathway 132 and the outlet pathway 137 .
  • the first pump 135 , second pump 155 , and third pump 160 are all active throughout the hemodialysis procedure with the first and second pumps operating at different pump rates and the third pump operating at a pump rate that achieves a balanced flow rate between the inlet pathway 132 and the outlet pathway 136 .
  • the third pump is typically operated at a pump rate that is equal to the differential between the pump rate of the first pump and the pump rate of the second pump. In this manner, the second and third pumps collectively achieve a flow rate through the outlet pathway 137 that is equal to the flow rate through the inlet pathway 132 .
  • the first pump 135 is set to provide a flow rate of 100 ml/min through the inlet pathway 132 and the second pump 155 is deliberately set out of balance with the first pump 135 , to provide, for example, a flow rate of only 80 ml/min. This would provide a flow rate differential of 20 ml/min between the first pump and the second pump.
  • the pump rate of third pump 160 is set to provide a flow rate of 20 ml/min, which is equal to the differential between the flow rates of the first and second pumps.
  • the second pump 155 and the third pump 160 collectively achieve a flow rate of 100 ml/min through the outlet pathway 137 which is equal to the flow rate of through the inlet pathway 132 such that the flow rates are balanced across the dialyzer. Under such conditions, waste solutes move across the dialyzer's semipermeable membrane from the blood stream into the dialysate via diffusion to perform hemodialysis.
  • the flow rates through the inlet pathway 132 and the outlet pathway 137 may be measured using one or more of the sensors S.
  • the sensors are flow rate sensors that directly measure flow rates through the inlet pathway 132 and outlet pathway 137 .
  • the sensors are pressure sensors that provide indications as to the fluid pressure within the inlet pathway 132 and the fluid pressure within the outlet pathway 137 . Fluid pressure is a function of the flow rate through the flow pathways and therefore provides an indirect measurement of flow rate. Where the fluid pressure in the inlet pathway 132 is equal to the fluid pressure in the outlet pathway 137 , this is an indication that the flow rates are balanced between the inlet pathway and outlet pathway.
  • the system of fluid pathways may include one or more damping mechanisms for dampening any extreme fluctuations in pressure within the fluid pathways.
  • the pump rate of the third pump 160 may be adjusted in response to a pressure differential between the inlet and outlet pathways such as in a calibration procedure, to achieve a balanced flow rate between the inlet pathway 132 and outlet pathway 137 .
  • the calibration procedure may optionally be performed with the system in a calibration mode such that the first and second valves are set to cause fluid to flow through the bypass pathway 165 and bypass the dialyzer 105 , as represented in FIG. 3 and described in more detail below.
  • the flow of the third pump 160 may be appropriately adjusted ‘on the fly’ to increase or decrease the third pump's speed to achieve the desired flow rate in the outlet pathway 137 without having to turn the pump on or off.
  • the pressure sensors S and the three pumps, as well as the valves 175 may be connected in a closed loop control system to achieve automatic balancing of the flow rates.
  • a balanced flow rate between the inlet pathway 132 and the outlet pathway 137 is achieved in theory at least by the first pump 135 and the second pump 155 operating at the same pump rate to achieve equal flow rates through the inlet pathway 132 and outlet pathway 137 .
  • various factors may result in the actual fluid flow rate in the inlet pathway 132 differing from the actual fluid flow rate in the outlet pathway 137 .
  • the factors may include trapped air, hardware wear, and fluid leakage, which can cause the flow rates of the first and second pumps to diverge over time from a preset or desired value. Typical technologies in dialysis systems are unable to correct the flow balance for these types of factors.
  • the third pump 160 can be used to correct the differing flow rates by being activated to pump fluid through the secondary outlet pathway 1137 b at a rate that is equal to the delta between the fluid flow rate through the inlet pathway 132 and the fluid flow rate through the outlet pathway 137 .
  • the system is preferably configured such that the first pump 135 is prevented from pumping less fluid than the second pump 155 such that the first pump 135 always pumps at a higher rate than the second pump 155 .
  • the system preferably includes a control system that detects a condition where the first pump 135 inadvertently pumps at a slower rate than the second pump 155 and sets off an alarm or moves the system out of dialysis mode if such a situation occurs.
  • the sensors S ( FIG. 1 ) are used to measure the flow rates through the inlet pathway 132 and the outlet pathway 137 .
  • a comparison is performed between the flow rate through the inlet pathway 132 and the flow rate through the outlet pathway 137 .
  • the third pump 160 is activated from a de-activated state to cause fluid to flow into the secondary outlet pathway 137 b at a rate selected to cause the overall flow rate in the outlet pathway 137 to be equal to the flow rate in the inlet pathway 132 .
  • a mechanism such as a servo mechanism may be used to adjust the stroke volume of the first pump 135 and/or the second pump 155 until balance of the flow rates is restored (as may be evidenced, for example, by the presence of the same fluid pressure in both the inlet pathway 132 and the outlet pathway 137 ).
  • the sensors S may be communicatively coupled to a control system and to the three pumps in a closed loop system.
  • the control system includes hardware and/or software that automatically activates and/or deactivates the third pump 160 or adjusts the pump rate of the third pump 160 as needed in response to differences in detected flow rates from predetermined values or from each other, to equalize the flow rates between the inlet pathway 132 and outlet pathway 137 .
  • other measurements such as fluid pressure in the inlet and outlet pathways, may be used to indirectly calculate the flow rates rather than directly measuring the flow rates.
  • the fluid pressures within the inlet pathway and the outlet pathway may be measured for any detectable change in pressure from a predetermined value or from each other.
  • the flow pathways may be adapted to be essentially non-compliant so that a small difference in the flow rates of the first pump 135 and the second pump 155 will cause a rapid pressure change either negative or positive in magnitude.
  • the system may initially and/or periodically run in a calibration mode (sometimes also referred to as a UF checking mode) wherein a fluid (which may or may not be dialysate) is flowed through the flow pathways with the first valve 170 and second valve 137 set to the “bypass setting” such that fluid flowing through the system bypasses the dialyzer 105 via the bypass pathway 165 .
  • FIG. 3 shows a schematic representation of the system running in such a calibration mode where the dialyzer 105 is bypassed.
  • the first and second pumps are initially deliberately set to achieve unbalanced flow rates.
  • the sensors S in the flow pathway are then used to measure the fluid flow rate or pressure through the inlet pathway and the fluid flow rate or pressure through the outlet pathway.
  • the third pump 160 is then set at a pump speed that achieves a substantially balanced flow rate between the inlet pathway 132 and outlet pathway 137 .
  • the first pump 135 and second pump 155 are initially set to achieve equal flow rates without necessarily requiring the assistance of the third pump 160 , which is initially inactive.
  • the sensors S in the flow pathway are then used to measure the fluid flow rate through the inlet pathway and the fluid flow rate through the outlet pathway.
  • the third pump 160 remains inactive.
  • the third pump 160 is run at a rate that compensates for the discrepancy in flow rates between the inlet pathway 132 and outlet pathway 137 .
  • the third pump 160 may operate in a closed-loop relationship with the flow rate sensors and/or the pressure sensors.
  • FIG. 3 shows the third pump 160 in phantom lines to represent the third pump may or may not be activated depending on whether there is a flow rate differential between the inlet pathway 132 and outlet pathway 137 .
  • the calibration procedure that does not require activating and de-activating the third pump is preferred as the system may run more efficiently when all three pumps are continuously operating.
  • the valves 170 and 175 may be set to the “dialysis setting” such that fluid flows from the source 110 , through the inlet pathway 132 , into the dialyzer 105 , out of the dialyzer, and into the outlet pathway 137 from the dialyzer 105 .
  • the system can be used for dialysis by flowing dialysate into and out of the dialyzer 105 via the inlet and outlet pathways, and by also by flowing blood into and out of the dialyzer via the blood flow pathway 124 .
  • the previously described calibration procedure may be periodically repeated, such as at predetermined intervals, to ensure that the flow rates of the inlet and outlet pathways remain within desired ranges.
  • calibration is run only at the beginning of a dialysis session. In a more preferred embodiment, calibration is run periodically during the dialysis session, to ensure that the desired flow balance is maintained throughout the session.
  • the control system can cycle the valves 170 and 175 controlling incoming flow stream between the dialysis setting and the bypass setting and run the calibration steps without additional interruptions to the dialysis session.
  • the dialysate fluid bypasses the dialyzer 105 , dialysis of the blood that passes through the dialyzer during that period of time is unhampered due to no fresh dialysate being provided to the dialyzer 105 , though the blood may cool slightly.
  • the calibration step can be conducted over a relatively short period of time relative to the time between calibrations, the calibration has no material effect on the quality of dialysis being provided to the patient.
  • the dialysis system can be cycled between calibration for one minute followed by 60 minutes of dialysate being delivered through the dialyzer.
  • the dialysis system can be cycled between calibration for 30 seconds followed by 120 minutes of dialysate being delivered through the dialyzer.
  • Various different cycle times between calibration and dialysis may be chosen based on how frequently the system's calibration is to be verified and/or adjusted. If no adjustment to any of the pumps is necessary during calibration, the calibration step may be concluded in a much shorter period of time than 30-seconds, for example 5-10 seconds.
  • FIG. 4 schematically shows the system running in a dialysis mode.
  • the third pump 160 and the flow arrow 405 through the secondary outlet pathway 137 b are shown in phantom lines to indicate that the third pump 160 may or may not be active while the system is in dialysis mode.
  • the third pump 160 may be active in the situation where the third pump 160 is needed to equalize the flow rates between the inlet pathway and outlet pathways. Or, the flow rates of the inlet and outlet pathways may be equal without the assistance of the third pump 160 , in which case the third pump 160 remains inactive.
  • the dialysis system achieves ultrafiltration in the situation where the flow rate through the inlet pathway 132 differs from the flow rate through the outlet pathway 137 such that there is an unbalanced flow rate across the dialyzer.
  • the dialyzer 105 pulls fluid from the blood across the semipermeable membrane by a convective process in order to compensate for the unbalanced flow rate.
  • the system utilizes all three pumps substantially continuously throughout the procedure and the pump rate of the third pump 160 is adjusted to achieve a desired flow rate differential between the inlet pathway 132 and the outlet pathway 137 to perform ultrafiltration.
  • first pump 135 , second pump 155 , and third pump 160 are all active with the first and second pumps operating at different pump rates.
  • the third pump is then operated at a pump rate that intentionally achieves a desired imbalance of flow rates between the inlet pathway 132 and the outlet pathway 136 sufficient to cause ultrafiltration.
  • the first pump 135 is set to provide a flow rate of 100 ml/min through the inlet pathway 132 and the second pump 155 is deliberately set out of balance with the first pump 135 , to provide, for example, a flow rate of only 80 ml/min.
  • the third pump 160 is then set to provide a flow rate of 30 ml/min such that the second and third pumps collectively provide a flow rate of 110 ml/min through the outlet pathway 137 .
  • the dialyzer 105 compensates for the 10 ml/min flow rate differential by transferring 10 ml/min of fluid from the blood stream into the dialysate.
  • the first pump 135 is set to provide a flow rate of 100 ml/min through the inlet pathway 132 and the second pump 155 is again deliberately set out of balance with the first pump 135 , to provide, for example, a flow rate of only 80 ml/min.
  • the third pump 160 is then set to provide a flow rate of only 10 ml/min such that the second and third pumps collectively provide a flow rate of 90 ml/min through the outlet pathway 137 .
  • the speed of the third pump 160 can be varied to selectively vary an amount of ultrafiltration. For example, if it is determined that the ultrafiltration is greater than desired when pulling fluid out of the blood, for example, the pump speed of the third pump 160 can be slowed down, reducing the amount of extra fluid that the third pump 160 draws out of the dialyzer. Where the ultrafiltration is not great enough when compared against a desired predetermined value, the pump speed of the third pump 160 may be increased in the case where fluid is being pulled out of the blood into the dialysate, for example, to draw an even greater amount of fluid out of the dialyzer and, hence, the blood.
  • the third pump 160 may be coupled to a source of fluid such that the third pump 160 outputs extra fluid into the flow pathway via the secondary outlet pathway 137 b, such as in the embodiment of FIG. 1B .
  • the extra fluid introduced into the flow pathway is transferred across the semi-permeable membrane 215 into the blood.
  • the dialysis system is configured to achieve hemodiafiltration by oscillating the speed of the third pump between (1) a first speed such that the second and third pump collectively achieve a flow rate through the outlet pathway that is greater than the flow rate through the inlet pathway; and (2) a second speed such that the second and third pump collectively achieve a flow rate through the outlet pathway that is less than the flow rate through the inlet pathway.
  • the third pump 160 can be used to intermittently alternate the flow rate differential between a state where the dialyzer 105 pulls fluid from the blood stream into the dialysate and a state where the dialyzer 105 pushes fluid from the dialysate into the blood stream.
  • the dialyzer 105 Over a predetermined span of time, there should be a zero net loss (or substantially a zero net loss) of fluid from the blood and a zero net gain (or substantially a zero net gain) of fluid into the blood for the process of hemodiafiltration. However, during that span of time, the dialyzer 105 periodically transfers fluid into the blood from the dialysate and periodically transfers fluid out of the blood into the dialysate. If ultrafiltration is desired to be performed at the same time as the hemodiafiltration, then the pumps can be operated in such a way so that in addition to the cycling of fluid into and out of the blood over time, there also occurs a net gain or loss of fluid to or from the blood over a predetermined span of time.
  • the first pump 135 is set to provide a flow rate of 100 ml/min through the inlet pathway 132 and the second pump 155 is again deliberately set out of balance with the first pump 135 , to provide, for example, a flow rate of only 80 ml/min.
  • the speed of pump 160 can be cycled between a rate of 10 ml/min for a period of 30 seconds and 30 ml/min for a period of 30 seconds.
  • the total flow rate through the outlet pathway 137 is 90 ml/min with the flow rate through the inlet pathway 132 at 100 ml/min, resulting in an unbalanced flow rate that causes the dialyzer 105 to transfer 10 ml/min of fluid into the blood stream.
  • the total flow rate through the outlet pathway 137 is 110 ml/min with the flow rate through the inlet pathway 132 at 100 ml/min, resulting in an unbalanced flow rate that causes the dialyzer 105 to transfer 10 ml/min of fluid from the blood stream into dialysate.
  • the third pump is located on the inlet flow side of the dialyzer instead of on the outlet flow path, such that the first and third pumps collectively achieve the desired inlet flow rate and the second pump achieves the desired outlet flow rate to perform one or more of hemodialysis, ultrafiltration and hemodiafiltration.
  • the flow pathways may be rinsed and/or disinfected.
  • a rinse fluid such as, but not limited to disinfectant solution and water, is routed through the flow pathways while the valves are in the bypass setting.
  • the third pump 160 may or may not be operated with the first pump 135 and second pump 155 to achieve fluid flow through the system.
  • the inherently high sensitivity of the methods described above might provide a challenge for controlling the flow rate as the small diameter and largely non-compliant flow pathways coupled with the pulsatile nature of the flow may make it difficult to measure pressures and pressure change rates sufficient to control the flow during dialysis.
  • the pulsatile pressure signals present in a pulsatile flow configuration may be filtered out using appropriate signal conditioning. But the small volume and rigid flow pathways might cause too rapid of a pressure shift, quickly driving the pressure magnitude beyond the range of the pressure sensors. This may be particularly true for large, temporary mismatches associated with air being present in the flow pathways.
  • FIG. 5 is a cross-sectional view of a compliance control device 500 that may be positioned in fluid communication with the flow pathways of the system.
  • the device 500 is adapted to smooth out the pulsatile nature of the flow.
  • the compliance control device 500 comprises a chamber 505 divided by a compliant diaphragm 510 defining a first chamber 515 and a second chamber 520 .
  • the first chamber 505 comprises a first chamber inlet 525 and a first chamber outlet 530 adapted for fluid communication with the flow pathways of the system.
  • the second chamber 520 is in fluid communication with a control valve 535 and air plenum 540 , wherein a non-compliant fluid 545 , such as, but not limited to an inert liquid or gel, is disposed in the second chamber 520 and a compliant gas 550 is disposed in the air plenum 540 .
  • a non-compliant fluid 545 such as, but not limited to an inert liquid or gel
  • control valve 535 may be closed restricting the flow of the non-compliant fluid 545 to the second chamber 520 creating a substantially non-compliant flow circuit as the compliant diaphragm 510 is restricted from complying (elastically deforming) against the now relatively rigid non-compliant fluid 545 .
  • control valve 535 may be opened, allowing the non-compliant fluid 545 to react with the gas 550 in the air plenum in reaction to pressure transients of the fluid in the pathway acting against the diaphragm 510 .
  • the diaphragm 510 moves in response to the pressure change and the gas 550 in the air plenum tends to moderate and smooth the pressure changes, allowing for a more precise pressure detection during calibration for flow compensation by the third pump 160 .
  • FIG. 6 is a cross-sectional view of another compliance control device 600 adapted for fluid communication with the flow pathways of the system and adapted to smooth out the pulsatile nature of the flow such as during calibration.
  • the compliance control device 600 comprises a chamber 605 divided by a compliant diaphragm 510 defining a first chamber 610 and a second chamber 615 .
  • the first chamber 610 comprises a first chamber inlet 620 and a first chamber outlet 625 adapted for fluid communication with the flow pathways of the system.
  • the second chamber 615 comprises a second chamber inlet 630 and a second chamber outlet 635 adapted for fluid communication with a source of non-pulsatile flow of substantially non-compliant fluid 640 .
  • the fluid flow into the second chamber inlet 630 is controlled by a control valve 535 and the second chamber outlet 635 is in fluid communication with a drain.
  • control valve 535 is opened, allowing the flow of non-compliant fluid 640 to flow into the second chamber 615 and against the diaphragm 510 which restricts the movement of the diaphragm 510 and therefore creates a substantially non-compliant flow circuit.
  • control valve 535 is closed, restricting the flow of the non-compliant fluid 640 into the second chamber 615 with the non-compliant fluid 640 left in the second chamber 615 free to flow to the drain.
  • the fluid can react against the diaphragm 510 unconstrained by the non-compliant fluid 640 .
  • the diaphragm 510 elastically moves in response to any pressure change in the flow circuit moderating and smoothing the pressure change, allowing for a more precise pressure detection in the flow pathways for flow compensation by the third pump 160 .
  • the compliance control devices 500 and 600 can be placed in fluid communication at any location in the flow pathways of the system such as upstream of the first valve 170 and downstream of the second valve 175 , suitable for a particular purpose.

Abstract

Systems and methods are disclosed for performing hemodialysis that include fluid handling systems that provide accurate control over the type and level of hemodialysis being performed. The system includes a first pump for pumping dialysate into a dialyzer and a second pump for pumping dialysate out of the dialyzer. The system also includes a third pump that provides improved control of a level of ultrafiltration, hemodiafiltration, or both.

Description

    REFERENCE TO PRIORITY DOCUMENT
  • This application is a continuation of U.S. patent application Ser. No. 12/795,498, titled “Dialysis System With Ultrafiltration Control,” filed Jun. 7, 2010, that in turn claims priority to U.S. Provisional Patent Application Ser. No. 61/267,043, filed Dec. 5, 2009. Priority of the filing date of Dec. 5, 2009, is hereby claimed, and the disclosures of the aforementioned patent applications are hereby incorporated by reference, each in its entirety.
  • BACKGROUND
  • Chronic dialysis has been performed on patients with kidney failure since the early 1960's. A dialyzer is a device for cleansing blood through hemodialysis by a process of diffusion and/or convection of waste products, dissolved solutes and fluid from the blood across a semi permeable membrane into a dialysis solution known as dialysate. A dialysis system is an assembly that includes the dialyzer and associated equipment to support the dialyzer, such a plumbing and pumps.
  • Diffusion is the principal mechanism in which dialysis removes waste products such as urea, creatinine, phosphate and uric acid, among others, from the blood. A differential between the chemical composition of the dialysate and the chemical composition of the blood causes the waste products to be drawn through the semi-permeable membrane from the blood into the dialysate. Ultrafiltration is a process in dialysis where fluid is caused to move across the membrane from the blood into the dialysate for the purpose of removing excess fluid from the patient's blood stream. Along with water, some solutes are also drawn across via convection rather than diffusion. Ultrafiltration is a result of a pressure differential between the blood compartment of the dialyzer and the dialysate compartment of the dialyzer where fluid will move from a higher pressure to a lower pressure. In some circumstances, by design or unintentionally, fluid in the dialysate compartment is higher than the blood compartment, causing fluid to move from the dialysate compartment into the blood compartment. This is commonly referred to as reverse ultrafiltration.
  • It would be convenient for a patient to be able to perform dialysis in his or her home. Unfortunately, current dialysis systems are large in size, making them generally unsuitable for use in a patient's home. Current dialysis systems are also energy-inefficient in that they use large amounts of energy and require enormous amounts of water for proper use. Although some home dialysis systems are available, they generally use complex flow-balancing technology that is relatively expensive to manufacture and most systems are designed with a system of solenoid valves that create high noise levels. As a result, most dialysis treatments are performed at dialysis centers.
  • SUMMARY
  • In view of the foregoing, there is a need for improved dialysis systems that are smaller, more portable, consume less water and that provide precise control over a level of ultrafiltration. Disclosed are systems and methods for performing hemodialysis that include fluid handling systems and provide accurate control over the type and level of hemodialysis being performed. The system includes a first pump for pumping dialysate into a dialyzer and a second pump for pumping dialysate out of the dialyzer. The system also includes a third pump that provides improved control of a level of ultrafiltration, hemodiafiltration, or both, as described in detail below.
  • In one aspect, there is disclosed a method of performing dialysis, comprising: operating a first pump to pump dialysate at a first flow rate through a fluid inlet pathway into a dialyzer; operating a second pump to pump the dialysate through a fluid outlet pathway out of the dialyzer; operating a third pump to pump the dialysate through the fluid outlet pathway in cooperation with the second pump, wherein the second and third pumps cooperate to collectively achieve a second flow rate through the fluid outlet pathway from the dialyzer; and pumping blood through the dialyzer in communication with the dialysate such that the dialyzer dialyzes the blood.
  • In another aspect, there is disclosed a method of performing dialysis, comprising: providing a dialysis system having an inlet conduit through which fluid flows in an inward direction toward a dialyzer and an outlet conduit through which fluid flows in an outward direction from the dialyzer; pumping fluid through the inlet conduit using a first pump; pumping fluid through the outlet conduit using a second pump; and using a third pump to supplement the pumping of the second pump through the outlet conduit.
  • In another aspect, there is disclosed a dialysis system, comprising: a dialyzer having a blood flow pathway through which blood flows; a fluid inlet pathway configured to provide incoming fluid to the dialyzer; a fluid outlet pathway configured to receive outgoing fluid from the dialyzer; a first pump coupled to the fluid inlet pathway and configured to pump the fluid through the fluid inlet pathway toward the dialyzer; a second pump coupled to the fluid outlet pathway and configured to pump the fluid through the fluid outlet pathway away from the dialyzer; and a third pump coupled to the fluid outlet pathway, the third pump configured to work in cooperation with the second pump to achieve a desired flow rate of fluid to or from the blood flowing through the dialyzer.
  • Other features and advantages should be apparent from the following description of various embodiments, which illustrate, by way of example, the principles of the disclosed devices and methods.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1A shows a schematic view of a dialysis system adapted to perform dialysis of a patient's blood.
  • FIG. 1B shows a schematic view of another embodiment of a dialysis system.
  • FIG. 2 is a schematic view of a dialyzer of the dialysis system.
  • FIG. 3 shows a schematic representation of the system running in a calibration mode.
  • FIG. 4 shows a schematic representation of the system running in a dialysis mode.
  • FIG. 5 is a cross-sectional view of a compliance control device.
  • FIG. 6 is a cross-sectional view of another embodiment of a compliance control device.
  • DETAILED DESCRIPTION
  • In order to promote an understanding of the principals of the disclosure, reference is made to the drawings and the embodiments illustrated therein. Nevertheless, it will be understood that the drawings are illustrative and no limitation of the scope of the disclosure is thereby intended. Any such alterations and further modifications in the illustrated embodiments, and any such further applications of the principles of the disclosure as illustrated herein are contemplated as would normally occur to one of ordinary skill in the art.
  • FIG. 1A shows a schematic view of a dialysis system adapted to perform hemodialysis of a patient's blood. The system includes an arrangement of three or more pumps that provide improved control over the type of hemodialysis being performed. By varying the relative pump speeds of the three pumps, an operator can vary the level of blood filtration and can also selectively achieve ultrafiltration and hemodiafiltration of the blood.
  • Ultrafiltration is a process in dialysis where fluid is caused to move across a dialyzer membrane via diffusion from the blood into the dialysate for the purpose of removing excess fluid from the patient's blood stream. Along with water, some solutes are also drawn across the membrane via convection rather than diffusion. Ultrafiltration is a result of a pressure differential between the blood compartment and the dialysate compartment where fluid will move from a higher pressure to a lower pressure.
  • In some circumstances, by design or unintentional, fluid in the dialysate compartment is higher than the blood compartment causing fluid to move from the dialysate compartment into the blood compartment. This is commonly referred to as reverse ultrafiltration.
  • In hemodiafiltration a high level of ultrafiltration is created, greater than the amount required to remove fluid from the patient's blood, for the purpose of increasing convective solute transport across the membrane. The amount of fluid in excess of what is required to be removed from the patient's blood must therefore be returned to the blood stream in order to avoid an adverse blood reaction. This is accomplished by intentionally increasing the pressure in the dialysate compartment of the dialyzer to cause the appropriate amount of reverse ultrafiltration. This process of ultrafiltration alternating with reverse ultrafiltration is often referred to as “push-pull hemodiafiltration”. This is a significant improvement over more common methods of hemodiafiltration where sterile fluid is administered to the patient in a location outside of the dialyzer.
  • The dialysis system includes a dialyzer 105 that is fluidly connected to a source 110 of fluid (such as dialysate) and also to a source 115 of blood to be dialyzed. The source 115 of blood may be a patient. The source 110 of fluid may be a dialysate preparation system that prepares dialysate for use in the dialysis system. The dialysate preparation system may include a water purification system that purifies water pursuant to systems and methods described in co-pending U.S. patent application Ser. No. 12/795,382 entitled “Fluid Purification System”, which is filed concurrently herewith and which is incorporated by reference in its entirety. In addition, the dialyzer 105 may be at least partially configured with microfluidic pathways as described in co-pending U.S. patent application Ser. No. 12/795,371 entitled “Microfluidic Devices”, filed concurrently herewith, which claims priority to U.S. Provisional Application Ser. No. 61/220,117, filed on Jun. 24, 2009, which applications are incorporated by reference in their entirety. U.S. patent application Ser. No. 12/795,444 entitled “Dialysis System”, filed concurrently herewith, is also incorporated by reference in its entirety. Dialysate flows into the dialyzer 105 through a fluid inlet 120 and out of the dialyzer 105 through a fluid outlet 125. Blood flows through the dialyzer 105 via a blood flow pathway 124 that includes a blood inlet 130 into the dialyzer 105 and a blood outlet 133 out of the dialyzer. From the dialyzer 105, the blood flows back to the patient. The dialyzer 105 is described in more detail below.
  • The dialysis system includes plumbing that forms a plurality of fluid flow pathways, which may be any type of conduit through which a fluid such as dialysate may flow. The fluid flow pathways include an inlet pathway 132 through which a fluid such as unused dialysate flows from the source 110 toward and into the dialyzer 105. At least a first pump 135 is positioned along or in communication with the inlet pathway 132 for pumping the fluid toward the dialyzer 105 at a desired flow rate. One or more sensors S may be coupled to the fluid flow pathway for sensing one or more characteristics of the incoming fluid, such as pressure, flow rate, temperature, conductivity, etc. In addition, one or more sample ports P may be coupled to the fluid flow pathways that provide access to fluid flowing through the piping. FIG. 1 shows the sensors S and sample ports P coupled to the fluid flow pathways at specific locations, although the quantity and locations of the sensors S and sample ports P may vary.
  • The fluid flow pathways further include an outlet pathway 137 through which used dialysate flows out of the dialyzer 105 toward one or more drains 140. In some embodiments, the dialysate exiting the dialyzer may be used to pre-heat other incoming fluids in the system, such as the water stream entering the heat exchange and purification system, before reaching the drain 140. The outlet pathway 137 bifurcates into two or more outlet pathways including a main outlet pathway 137 a and a secondary outlet pathway 1137 b. At least a second pump 155 is positioned along or in communication with the main outlet pathway 137 a for pumping the dialysate out of and away from the dialyzer 105 through the main outlet pathway 137 a.
  • A third pump 160 is positioned along or in communication with the secondary outlet pathway 137 b. The third pump 160 can be used to augment fluid flow through the fluid flow pathways such as to selectively achieve differentials in flow rates between the inflow pathway 132 and the outflow pathway 132 pursuant to achieving various types of dialysis, including hemodialysis, ultrafiltration, and hemodiafiltration, as described more fully below. The third pump pumps dialysate through the fluid flow pathways when the system is in dialysis mode. The third pump may also pump another fluid, such as water or disinfectant, when the system is in a different mode, such as in a calibration mode or in a cleaning mode. The third pump 160 can also be used to calibrate flow rates between the first pump 135 and the second pump 155, as described more fully below.
  • In another embodiment, shown in FIG. 1B, the third pump 160 is positioned along the inflow pathway 132 upstream of the inlet 120 of the dialyzer 105. In this embodiment, the secondary outlet pathway 137 branches off the inlet pathway 132 at a location downstream of the first pump 135 and upstream of the first valve 170. The third pump 160 pumps fluid toward the drain 140. The embodiment of FIG. 1A may be more efficient than the embodiment of FIG. 1B because the third pump 160 in FIG. 1B pumps fresh, unused dialysate into the drain 140 while the third pump in FIG. 1A pumps used dialysate into the drain 140. In another embodiment, the third pump 160 and the second pump 155 are both positioned along a single, non-bifurcating outflow pathway.
  • Various types of pumps may be used for the first, second and third pumps. In an embodiment, the pumps are nutating pumps. On other embodiments, the pumps could be rotary lobe pumps, progressing cavity pumps, rotary gear pumps, piston pumps, diaphragm pumps, screw pumps, gear pumps, hydraulic pumps, vane pumps, regenerative (peripheral) pumps, or peristaltic pumps, or any combination thereof. Other types of pumps can also be used. The first pump 135 and the second pump 155 may be driven by a common shaft to ensure synchrony of the pump strokes and the volume of fluid pumped. It is understood that first pump 135 and the second pump 155 may also be fully independent from each other.
  • As mentioned, any of a variety of fluid conduits may be used to form the fluid flow pathways. In an embodiment, at least a portion of the fluid flow pathway is formed of piping having an inside diameter from ⅛ inch to ½ inch. The flow rate in the piping could range between about 50 ml/min to about 1,000 ml/min. In an embodiment, the flow rate is in the range of between about 100 ml/min and about 300 ml/min.
  • With reference again to FIGS. 1A, the fluid flow pathways further include a bypass pathway 165 that fluidly directly connects the inlet pathway 132 and the outlet pathway 137. An exemplary purpose of the bypass pathway 165 is to provide a fluid flow pathway where fluid can flow into and out of the dialysis system and bypass the dialyzer 105, such as for flushing, cleaning or calibrating the system. In an embodiment, the junction between the inlet pathway 132 and bypass pathway 165 is located upstream of the fluid inlet 120 of the dialyzer 105, and the junction between the bypass pathway 165 and the outlet pathway is located downstream of the fluid outlet 125 of the dialyzer 105. However, other configurations of the bypass pathway 165 can be used to achieve bypassing of the dialyzer 105.
  • A first valve 170 is positioned at the junction between the inlet pathway 132 and the bypass pathway 165. A second valve 175 is positioned at the junction between the bypass pathway 165 and the outlet pathway 137. The first valve 170 and second valve 175 are three-way valves, such as solenoid valves, that can be used to selectively regulate fluid flow through the fluid flow pathways. That is, the first valve 170 can be set to either of two or more settings including (1) a dialysis setting wherein the first valve directs all incoming fluid along the inlet pathway 132 toward the dialyzer 105 (as represented by arrow A in FIG. 1) and prevents incoming fluid from flowing into the bypass pathway 165; or (2) a bypass setting wherein the first valve 170 diverts all the incoming fluid into the bypass pathway 165 (as represented by arrow B in FIG. 1) and the prevents incoming fluid from flowing past the first valve toward the dialyzer 105.
  • The second valve 175 can also be set to either of two settings including (1) a bypass setting wherein the second valve 175 directs incoming fluid from the bypass pathway 165 into the outlet pathway 137 (as represented by arrow C in FIG. 1); or (2) a dialysis setting wherein the second valve 175 closes flow from the bypass valve 165 such that outgoing fluid from the dialyzer outlet 125 continues to flow outward along the outlet pathway 137 (as represented by arrow D in FIG. 1.) The first valve 175 and the second valve 160 are generally both set in tandem to either the bypass setting or the dialysis setting. The system may include a control and safety system that ensures that the first and second valves are not set to incompatible settings.
  • The arrangement of the various components of the dialysis system shown in FIGS. 1A and 1B are exemplary and other arrangements are possible. For example, the flow pathways and the pumps may be placed in different locations along the flow pathways from what is shown in FIG. 1. In an embodiment, the third pump 160 is positioned in the flow pathway at a location upstream of the dialyzer 105 and downstream of the first valve 170 or the third pump can be positioned downstream of the dialyzer 105 and upstream of the second valve 175. Moreover, the system can employ more than three pumps.
  • Dialyzer and Various Forms of Dialysis
  • FIG. 2 is a schematic, cross-sectional view of the dialyzer 105, which defines a blood compartment having a blood flow pathway 205 and a dialysate compartment having a dialysate flow pathway 210 separated by a semi-permeable membrane 215. The blood (from a patient) enters the blood flow pathway 205 via the blood inlet 130, flows through the blood flow pathway 205, and exits via the blood outlet 133. The dialysate enters the dialysate flow pathway 210 via the fluid inlet 120, flows through the dialysate flow pathway 210, and exits via the fluid outlet 125. The semi-permeable membrane 215 is configured to allow the transfer of one or more substances from the blood in the blood flow pathway 205 to the dialysate in the dialysate flow pathway 210, or visa-versa. Some examples of materials that may be used as the semipermeable membrane 215 include polymers, copolymers, metals, ceramics, composites, and/or liquid membranes. One example of a composite membrane is polysulfone-nanocrystalline cellulose composite membrane such as AN69 flat sheet membranes available from Gambro Medical. Gas-liquid contactor membranes may also be employed for transferring a substance between a liquid and gas such as for oxygenation of blood, whereby the membrane allows transfer of carbon dioxide and oxygen, such that oxygen transfers to blood from oxygen or oxygen-enriched air, and carbon dioxide transfers from the blood to the gas. Fluid membranes may also be employed. Fluid membranes comprise a lamina having through cut microchannels containing fluid and a first and second membrane support positioned to contain fluid in the microchannels.
  • When flowing through the dialyzer 105, the blood and the dialysate may flow in a counter-flow configuration wherein blood flows through the blood flow pathway 205 in one direction and the dialysate flows through the dialysate flow pathway 210 in the opposite direction. The dialyzer 105 is described in the context of having a counter-flow configuration although a cross-flow configuration may also be used. As the blood and water flow along the membrane 215, hemodialysis occurs. That is, waste solutes move across the semipermeable membrane 215 from the blood into the dialysate via diffusion as a result of the differential of solute concentration between the blood and the dialysate. The flow of the blood and dialysate, which may be counter-, cross- or concurrent-flow, maintains the concentration gradient of solutes between the blood and dialysate, which helps to remove more urea and creatinine from the blood. The concentrations of solutes (for example potassium, phosphorus, and urea) may be undesirably high in the blood, but low or absent in the dialysate and constant replacement of the dialysate ensures that the concentration of undesired solutes is kept low on the dialysate side of the membrane. The dialysate has levels of minerals like potassium and calcium that are similar to their natural concentration in healthy blood. For another solute, bicarbonate, the dialysate level is set at a slightly higher level than in normal blood, to encourage diffusion of bicarbonate into the blood, to maintain a patient's CO2 level, and act as a pH buffer to neutralize the metabolic acidosis that is often present in these patients.
  • The dialyzer 105 is also configured to perform ultrafiltration wherein a pressure differential across the membrane 215 results in fluid and dissolved solutes passing across the membrane 215 from the blood to the dialysate.
  • The dialyzer 105 is also configured to perform hemodiafiltration wherein solute movement across the semipermeable membrane 215 is governed by convection rather than by diffusion. A positive hydrostatic pressure differential between the blood flow pathway 205 and the dialysate flow pathway 210 drives water and solutes across the semipermeable membrane 215 from the blood flow pathway to the fluid flow pathway. Solutes of both small and large molecules get dragged through the semipermeable membrane 215 along with the fluid. In a typical hemodiafiltration procedure, the direction of water and solute movement is oscillated between moving water and solutes from the blood into the dialysate and moving water and solutes from the dialysate into the blood. Over a predetermined span of time, there is a net zero loss and zero net gain of fluid from the blood into the dialysate. However, during discrete time periods within that span of time, there can be a net loss of fluid from the blood into the dialysate and a net gain of fluid into the blood from the dialysate.
  • Operation of Pumps to Achieve Hemodialysis without Ultrafiltration
  • With reference again to FIG. 1A, the dialysis system achieves hemodialysis without ultrafiltration when the flow rate through the inlet pathway 132 is equal to or substantially equal to the flow rate through the outlet pathway 137. In other words, hemodialysis without ultrafiltration is achieved where the amount of dialysate flowing into dialyzer 105 via the inlet pathway 137 is substantially equal to the amount of dialysate flowing out of the dialyzer via the outlet pathway 137 over a period time. This can be achieved by operating the first pump 135 at a first pump rate to provide a first flow rate through the inlet pathway 132 and operating the second pump 155 and the third pump 160 at respective pump rates that collectively achieve a flow rate through the outlet pathway 137 that is equal to the flow rate through the inlet pathway 132.
  • In an embodiment, the system performs a hemodialysis procedure utilizing all three pumps in an active state substantially continuously throughout the hemodialysis procedure. The system adjusts the pump rate of the third pump 160 to achieve a desired balance of equal flow rates between the inlet pathway 132 and the outlet pathway 137. In this embodiment, the first pump 135, second pump 155, and third pump 160 are all active throughout the hemodialysis procedure with the first and second pumps operating at different pump rates and the third pump operating at a pump rate that achieves a balanced flow rate between the inlet pathway 132 and the outlet pathway 136. The third pump is typically operated at a pump rate that is equal to the differential between the pump rate of the first pump and the pump rate of the second pump. In this manner, the second and third pumps collectively achieve a flow rate through the outlet pathway 137 that is equal to the flow rate through the inlet pathway 132.
  • For example, to achieve a desired flow rate of, for example, 100 ml/min through the dialyzer, the first pump 135 is set to provide a flow rate of 100 ml/min through the inlet pathway 132 and the second pump 155 is deliberately set out of balance with the first pump 135, to provide, for example, a flow rate of only 80 ml/min. This would provide a flow rate differential of 20 ml/min between the first pump and the second pump. The pump rate of third pump 160 is set to provide a flow rate of 20 ml/min, which is equal to the differential between the flow rates of the first and second pumps. In this manner, the second pump 155 and the third pump 160 collectively achieve a flow rate of 100 ml/min through the outlet pathway 137 which is equal to the flow rate of through the inlet pathway 132 such that the flow rates are balanced across the dialyzer. Under such conditions, waste solutes move across the dialyzer's semipermeable membrane from the blood stream into the dialysate via diffusion to perform hemodialysis.
  • The flow rates through the inlet pathway 132 and the outlet pathway 137 may be measured using one or more of the sensors S. In an embodiment, the sensors are flow rate sensors that directly measure flow rates through the inlet pathway 132 and outlet pathway 137. In another embodiment, the sensors are pressure sensors that provide indications as to the fluid pressure within the inlet pathway 132 and the fluid pressure within the outlet pathway 137. Fluid pressure is a function of the flow rate through the flow pathways and therefore provides an indirect measurement of flow rate. Where the fluid pressure in the inlet pathway 132 is equal to the fluid pressure in the outlet pathway 137, this is an indication that the flow rates are balanced between the inlet pathway and outlet pathway. Where the fluid pressure in the inlet pathway 132 is less than the fluid pressure through the outlet pathway 137, this is an indication that the flow rate through the inlet pathway 132 is less than the flow rate through the outlet pathway 137. Where the fluid pressure in the inlet pathway 132 is greater than the fluid pressure through the outlet pathway 137, this is an indication that the flow rate through the inlet pathway 132 is greater than the flow rate through the outlet pathway 137. The system of fluid pathways may include one or more damping mechanisms for dampening any extreme fluctuations in pressure within the fluid pathways.
  • In the latter two situations, the pump rate of the third pump 160 may be adjusted in response to a pressure differential between the inlet and outlet pathways such as in a calibration procedure, to achieve a balanced flow rate between the inlet pathway 132 and outlet pathway 137. The calibration procedure may optionally be performed with the system in a calibration mode such that the first and second valves are set to cause fluid to flow through the bypass pathway 165 and bypass the dialyzer 105, as represented in FIG. 3 and described in more detail below. When the calibration procedure is performed by bypassing the dialyzer 105 and a pressure differential is detected between the inlet and outlet pathways, the flow of the third pump 160 may be appropriately adjusted ‘on the fly’ to increase or decrease the third pump's speed to achieve the desired flow rate in the outlet pathway 137 without having to turn the pump on or off. In this regard, the pressure sensors S and the three pumps, as well as the valves 175, may be connected in a closed loop control system to achieve automatic balancing of the flow rates.
  • In another embodiment, a balanced flow rate between the inlet pathway 132 and the outlet pathway 137 is achieved in theory at least by the first pump 135 and the second pump 155 operating at the same pump rate to achieve equal flow rates through the inlet pathway 132 and outlet pathway 137. Although it is theoretically possible to match the flow rates of the first pump 135 and the second pump 137, various factors may result in the actual fluid flow rate in the inlet pathway 132 differing from the actual fluid flow rate in the outlet pathway 137. The factors may include trapped air, hardware wear, and fluid leakage, which can cause the flow rates of the first and second pumps to diverge over time from a preset or desired value. Typical technologies in dialysis systems are unable to correct the flow balance for these types of factors.
  • Thus, there may come a time when a balanced flow rate cannot easily be achieved through use of the first and second pumps alone, and thus when there exists a need for correction to equalize the flow rates between the inlet pathway 132 and outlet pathway 137. Where the fluid flow rates are different, the third pump 160 can be used to correct the differing flow rates by being activated to pump fluid through the secondary outlet pathway 1137 b at a rate that is equal to the delta between the fluid flow rate through the inlet pathway 132 and the fluid flow rate through the outlet pathway 137. The system is preferably configured such that the first pump 135 is prevented from pumping less fluid than the second pump 155 such that the first pump 135 always pumps at a higher rate than the second pump 155. The system preferably includes a control system that detects a condition where the first pump 135 inadvertently pumps at a slower rate than the second pump 155 and sets off an alarm or moves the system out of dialysis mode if such a situation occurs.
  • According to a flow rate correction process, the sensors S (FIG. 1) are used to measure the flow rates through the inlet pathway 132 and the outlet pathway 137. A comparison is performed between the flow rate through the inlet pathway 132 and the flow rate through the outlet pathway 137. Where the flow rates are different, the third pump 160 is activated from a de-activated state to cause fluid to flow into the secondary outlet pathway 137 b at a rate selected to cause the overall flow rate in the outlet pathway 137 to be equal to the flow rate in the inlet pathway 132. A mechanism such as a servo mechanism may be used to adjust the stroke volume of the first pump 135 and/or the second pump 155 until balance of the flow rates is restored (as may be evidenced, for example, by the presence of the same fluid pressure in both the inlet pathway 132 and the outlet pathway 137).
  • As mentioned, the sensors S may be communicatively coupled to a control system and to the three pumps in a closed loop system. The control system includes hardware and/or software that automatically activates and/or deactivates the third pump 160 or adjusts the pump rate of the third pump 160 as needed in response to differences in detected flow rates from predetermined values or from each other, to equalize the flow rates between the inlet pathway 132 and outlet pathway 137. It should be appreciated that other measurements, such as fluid pressure in the inlet and outlet pathways, may be used to indirectly calculate the flow rates rather than directly measuring the flow rates. In this regard, the fluid pressures within the inlet pathway and the outlet pathway may be measured for any detectable change in pressure from a predetermined value or from each other. The flow pathways may be adapted to be essentially non-compliant so that a small difference in the flow rates of the first pump 135 and the second pump 155 will cause a rapid pressure change either negative or positive in magnitude.
  • The system may initially and/or periodically run in a calibration mode (sometimes also referred to as a UF checking mode) wherein a fluid (which may or may not be dialysate) is flowed through the flow pathways with the first valve 170 and second valve 137 set to the “bypass setting” such that fluid flowing through the system bypasses the dialyzer 105 via the bypass pathway 165. FIG. 3 shows a schematic representation of the system running in such a calibration mode where the dialyzer 105 is bypassed. In the embodiment where the system utilizes all three pumps in an active state substantially continuously throughout the hemodialysis procedure, the first and second pumps are initially deliberately set to achieve unbalanced flow rates. The sensors S in the flow pathway are then used to measure the fluid flow rate or pressure through the inlet pathway and the fluid flow rate or pressure through the outlet pathway. The third pump 160 is then set at a pump speed that achieves a substantially balanced flow rate between the inlet pathway 132 and outlet pathway 137.
  • In the other embodiment, the first pump 135 and second pump 155 are initially set to achieve equal flow rates without necessarily requiring the assistance of the third pump 160, which is initially inactive. The sensors S in the flow pathway are then used to measure the fluid flow rate through the inlet pathway and the fluid flow rate through the outlet pathway. Where the fluid flow rates are equal, the third pump 160 remains inactive. However, where the fluid flow rates are not equal, the third pump 160 is run at a rate that compensates for the discrepancy in flow rates between the inlet pathway 132 and outlet pathway 137. As mentioned, the third pump 160 may operate in a closed-loop relationship with the flow rate sensors and/or the pressure sensors. FIG. 3 shows the third pump 160 in phantom lines to represent the third pump may or may not be activated depending on whether there is a flow rate differential between the inlet pathway 132 and outlet pathway 137. The calibration procedure that does not require activating and de-activating the third pump is preferred as the system may run more efficiently when all three pumps are continuously operating.
  • After the calibration procedure is completed, the valves 170 and 175 may be set to the “dialysis setting” such that fluid flows from the source 110, through the inlet pathway 132, into the dialyzer 105, out of the dialyzer, and into the outlet pathway 137 from the dialyzer 105. When configured as such, the system can be used for dialysis by flowing dialysate into and out of the dialyzer 105 via the inlet and outlet pathways, and by also by flowing blood into and out of the dialyzer via the blood flow pathway 124. During dialysis, the previously described calibration procedure may be periodically repeated, such as at predetermined intervals, to ensure that the flow rates of the inlet and outlet pathways remain within desired ranges.
  • In an embodiment, calibration is run only at the beginning of a dialysis session. In a more preferred embodiment, calibration is run periodically during the dialysis session, to ensure that the desired flow balance is maintained throughout the session. The control system can cycle the valves 170 and 175 controlling incoming flow stream between the dialysis setting and the bypass setting and run the calibration steps without additional interruptions to the dialysis session. During the calibration process, when the dialysate fluid bypasses the dialyzer 105, dialysis of the blood that passes through the dialyzer during that period of time is unhampered due to no fresh dialysate being provided to the dialyzer 105, though the blood may cool slightly. As long as the calibration step can be conducted over a relatively short period of time relative to the time between calibrations, the calibration has no material effect on the quality of dialysis being provided to the patient. In an embodiment, the dialysis system can be cycled between calibration for one minute followed by 60 minutes of dialysate being delivered through the dialyzer. In another embodiment, the dialysis system can be cycled between calibration for 30 seconds followed by 120 minutes of dialysate being delivered through the dialyzer. Various different cycle times between calibration and dialysis may be chosen based on how frequently the system's calibration is to be verified and/or adjusted. If no adjustment to any of the pumps is necessary during calibration, the calibration step may be concluded in a much shorter period of time than 30-seconds, for example 5-10 seconds.
  • FIG. 4 schematically shows the system running in a dialysis mode. The third pump 160 and the flow arrow 405 through the secondary outlet pathway 137 b are shown in phantom lines to indicate that the third pump 160 may or may not be active while the system is in dialysis mode. The third pump 160 may be active in the situation where the third pump 160 is needed to equalize the flow rates between the inlet pathway and outlet pathways. Or, the flow rates of the inlet and outlet pathways may be equal without the assistance of the third pump 160, in which case the third pump 160 remains inactive.
  • Operation of Pumps to Achieve Ultrafiltration
  • The dialysis system achieves ultrafiltration in the situation where the flow rate through the inlet pathway 132 differs from the flow rate through the outlet pathway 137 such that there is an unbalanced flow rate across the dialyzer. Where the flow rate through the outlet pathway 137 is greater than the flow rate through the inlet pathway 132, the dialyzer 105 pulls fluid from the blood across the semipermeable membrane by a convective process in order to compensate for the unbalanced flow rate. In an embodiment, the system utilizes all three pumps substantially continuously throughout the procedure and the pump rate of the third pump 160 is adjusted to achieve a desired flow rate differential between the inlet pathway 132 and the outlet pathway 137 to perform ultrafiltration. That is, the first pump 135, second pump 155, and third pump 160 are all active with the first and second pumps operating at different pump rates. The third pump is then operated at a pump rate that intentionally achieves a desired imbalance of flow rates between the inlet pathway 132 and the outlet pathway 136 sufficient to cause ultrafiltration.
  • For example, to achieve the removal of fluid at a rate 10 ml/min from the blood stream, the first pump 135 is set to provide a flow rate of 100 ml/min through the inlet pathway 132 and the second pump 155 is deliberately set out of balance with the first pump 135, to provide, for example, a flow rate of only 80 ml/min. The third pump 160 is then set to provide a flow rate of 30 ml/min such that the second and third pumps collectively provide a flow rate of 110 ml/min through the outlet pathway 137. With a flow rate of 100 ml/min through the inlet pathway 132 and a flow rate of 110 ml/min through the outlet pathway, the dialyzer 105 compensates for the 10 ml/min flow rate differential by transferring 10 ml/min of fluid from the blood stream into the dialysate.
  • In another example, to achieve the addition of fluid at a flow rate of 10 ml/min into the blood stream, the first pump 135 is set to provide a flow rate of 100 ml/min through the inlet pathway 132 and the second pump 155 is again deliberately set out of balance with the first pump 135, to provide, for example, a flow rate of only 80 ml/min. The third pump 160 is then set to provide a flow rate of only 10 ml/min such that the second and third pumps collectively provide a flow rate of 90 ml/min through the outlet pathway 137. With a flow rate of 100 ml/min through the inlet pathway 132 and a flow rate of 90 ml/min through the outlet pathway, there is a transfer of 10 ml/min from the dialysate into the blood stream in order to compensate for the flow rate differential. It should be appreciated that the flow rate values in the preceding examples and following examples are only for purpose of example and that the actual flow rates as well as the relative flow rates can vary to achieve a desired level of ultrafiltration or reverse ultrafiltration.
  • The speed of the third pump 160 can be varied to selectively vary an amount of ultrafiltration. For example, if it is determined that the ultrafiltration is greater than desired when pulling fluid out of the blood, for example, the pump speed of the third pump 160 can be slowed down, reducing the amount of extra fluid that the third pump 160 draws out of the dialyzer. Where the ultrafiltration is not great enough when compared against a desired predetermined value, the pump speed of the third pump 160 may be increased in the case where fluid is being pulled out of the blood into the dialysate, for example, to draw an even greater amount of fluid out of the dialyzer and, hence, the blood.
  • In another embodiment, the third pump 160 may be coupled to a source of fluid such that the third pump 160 outputs extra fluid into the flow pathway via the secondary outlet pathway 137 b, such as in the embodiment of FIG. 1B. The extra fluid introduced into the flow pathway is transferred across the semi-permeable membrane 215 into the blood.
  • Operation of Pumps to Achieve Hemodiafiltration
  • The dialysis system is configured to achieve hemodiafiltration by oscillating the speed of the third pump between (1) a first speed such that the second and third pump collectively achieve a flow rate through the outlet pathway that is greater than the flow rate through the inlet pathway; and (2) a second speed such that the second and third pump collectively achieve a flow rate through the outlet pathway that is less than the flow rate through the inlet pathway. In this manner, the third pump 160 can be used to intermittently alternate the flow rate differential between a state where the dialyzer 105 pulls fluid from the blood stream into the dialysate and a state where the dialyzer 105 pushes fluid from the dialysate into the blood stream. Over a predetermined span of time, there should be a zero net loss (or substantially a zero net loss) of fluid from the blood and a zero net gain (or substantially a zero net gain) of fluid into the blood for the process of hemodiafiltration. However, during that span of time, the dialyzer 105 periodically transfers fluid into the blood from the dialysate and periodically transfers fluid out of the blood into the dialysate. If ultrafiltration is desired to be performed at the same time as the hemodiafiltration, then the pumps can be operated in such a way so that in addition to the cycling of fluid into and out of the blood over time, there also occurs a net gain or loss of fluid to or from the blood over a predetermined span of time.
  • For example over an exemplary time span of ten minutes, the first pump 135 is set to provide a flow rate of 100 ml/min through the inlet pathway 132 and the second pump 155 is again deliberately set out of balance with the first pump 135, to provide, for example, a flow rate of only 80 ml/min. The speed of pump 160 can be cycled between a rate of 10 ml/min for a period of 30 seconds and 30 ml/min for a period of 30 seconds. During the periods when the speed of the third pump 160 is at a rate of 10 ml/min, the total flow rate through the outlet pathway 137 is 90 ml/min with the flow rate through the inlet pathway 132 at 100 ml/min, resulting in an unbalanced flow rate that causes the dialyzer 105 to transfer 10 ml/min of fluid into the blood stream. During the periods when the speed of the third pump 160 is at a rate of 30 ml/min, the total flow rate through the outlet pathway 137 is 110 ml/min with the flow rate through the inlet pathway 132 at 100 ml/min, resulting in an unbalanced flow rate that causes the dialyzer 105 to transfer 10 ml/min of fluid from the blood stream into dialysate. Over the span of ten minutes with alternating periods of 30 seconds as described above, there is a net balanced flow rate of 100 ml/min across the dialyzer without any net addition or subtraction of fluid from the blood. This serves the purpose of passing fluid to the blood across the membrane and then fluid from the blood to the dialysate across the membrane to achieve hemodiafiltration of the blood and increases the removal of large-molecular waste products that would not otherwise be effectively dialyzed. In this way, operation of the three or more-pump system can achieve all of hemodialysis, ultrafiltration and hemodiafiltration through how the speeds of the first, second, and third pumps are controlled. This type of operation has heretofore not been possible in other dialysis systems.
  • In another embodiment, shown in FIG. 1B, the third pump is located on the inlet flow side of the dialyzer instead of on the outlet flow path, such that the first and third pumps collectively achieve the desired inlet flow rate and the second pump achieves the desired outlet flow rate to perform one or more of hemodialysis, ultrafiltration and hemodiafiltration.
  • Between dialysis treatments, the flow pathways may be rinsed and/or disinfected. A rinse fluid, such as, but not limited to disinfectant solution and water, is routed through the flow pathways while the valves are in the bypass setting. During rinse mode, the third pump 160 may or may not be operated with the first pump 135 and second pump 155 to achieve fluid flow through the system.
  • Control of Flow Rates Using Pulsatile Pumps
  • In embodiments wherein the flow through flow pathways has a pulsatile nature, such as might be produced by certain types of pumps, the inherently high sensitivity of the methods described above might provide a challenge for controlling the flow rate as the small diameter and largely non-compliant flow pathways coupled with the pulsatile nature of the flow may make it difficult to measure pressures and pressure change rates sufficient to control the flow during dialysis.
  • In an embodiment, the pulsatile pressure signals present in a pulsatile flow configuration may be filtered out using appropriate signal conditioning. But the small volume and rigid flow pathways might cause too rapid of a pressure shift, quickly driving the pressure magnitude beyond the range of the pressure sensors. This may be particularly true for large, temporary mismatches associated with air being present in the flow pathways.
  • FIG. 5 is a cross-sectional view of a compliance control device 500 that may be positioned in fluid communication with the flow pathways of the system. The device 500 is adapted to smooth out the pulsatile nature of the flow. The compliance control device 500 comprises a chamber 505 divided by a compliant diaphragm 510 defining a first chamber 515 and a second chamber 520. The first chamber 505 comprises a first chamber inlet 525 and a first chamber outlet 530 adapted for fluid communication with the flow pathways of the system. The second chamber 520 is in fluid communication with a control valve 535 and air plenum 540, wherein a non-compliant fluid 545, such as, but not limited to an inert liquid or gel, is disposed in the second chamber 520 and a compliant gas 550 is disposed in the air plenum 540.
  • When the dialysis system is performing hemodialysis, the control valve 535 may be closed restricting the flow of the non-compliant fluid 545 to the second chamber 520 creating a substantially non-compliant flow circuit as the compliant diaphragm 510 is restricted from complying (elastically deforming) against the now relatively rigid non-compliant fluid 545.
  • During calibration of the dialysis system, the control valve 535 may be opened, allowing the non-compliant fluid 545 to react with the gas 550 in the air plenum in reaction to pressure transients of the fluid in the pathway acting against the diaphragm 510. The diaphragm 510 moves in response to the pressure change and the gas 550 in the air plenum tends to moderate and smooth the pressure changes, allowing for a more precise pressure detection during calibration for flow compensation by the third pump 160.
  • FIG. 6 is a cross-sectional view of another compliance control device 600 adapted for fluid communication with the flow pathways of the system and adapted to smooth out the pulsatile nature of the flow such as during calibration. The compliance control device 600 comprises a chamber 605 divided by a compliant diaphragm 510 defining a first chamber 610 and a second chamber 615. The first chamber 610 comprises a first chamber inlet 620 and a first chamber outlet 625 adapted for fluid communication with the flow pathways of the system. The second chamber 615 comprises a second chamber inlet 630 and a second chamber outlet 635 adapted for fluid communication with a source of non-pulsatile flow of substantially non-compliant fluid 640. The fluid flow into the second chamber inlet 630 is controlled by a control valve 535 and the second chamber outlet 635 is in fluid communication with a drain.
  • During hemodialysis operation of the system, the control valve 535 is opened, allowing the flow of non-compliant fluid 640 to flow into the second chamber 615 and against the diaphragm 510 which restricts the movement of the diaphragm 510 and therefore creates a substantially non-compliant flow circuit. During calibration of the system, the control valve 535 is closed, restricting the flow of the non-compliant fluid 640 into the second chamber 615 with the non-compliant fluid 640 left in the second chamber 615 free to flow to the drain. Without the flow of non-compliant fluid 640 reacting against the diaphragm 510 and the remaining fluid 640 in the second chamber 615 free to drain, the fluid can react against the diaphragm 510 unconstrained by the non-compliant fluid 640. The diaphragm 510 elastically moves in response to any pressure change in the flow circuit moderating and smoothing the pressure change, allowing for a more precise pressure detection in the flow pathways for flow compensation by the third pump 160.
  • It is appreciated that the compliance control devices 500 and 600, such as provided in FIGS. 5 and 6, can be placed in fluid communication at any location in the flow pathways of the system such as upstream of the first valve 170 and downstream of the second valve 175, suitable for a particular purpose.
  • While this specification contains many specifics, these should not be construed as limitations on the scope of an invention that is claimed or of what may be claimed, but rather as descriptions of features specific to particular embodiments. Certain features that are described in this specification in the context of separate embodiments can also be implemented in combination in a single embodiment. Conversely, various features that are described in the context of a single embodiment can also be implemented in multiple embodiments separately or in any suitable sub-combination. Moreover, although features may be described above as acting in certain combinations and even initially claimed as such, one or more features from a claimed combination can in some cases be excised from the combination, and the claimed combination may be directed to a sub-combination or a variation of a sub-combination. Similarly, while operations are depicted in the drawings in a particular order, this should not be understood as requiring that such operations be performed in the particular order shown or in sequential order, or that all illustrated operations be performed, to achieve desirable results.
  • Although embodiments of various methods and devices are described herein in detail with reference to certain versions, it should be appreciated that other versions, embodiments, methods of use, and combinations thereof are also possible. Therefore the spirit and scope of the appended claims should not be limited to the description of the embodiments contained herein.

Claims (18)

1. A method of performing dialysis, comprising:
operating a first pump to pump dialysate at a first flow rate through a fluid inlet pathway into a dialyzer;
operating a second pump to pump the dialysate through a fluid outlet pathway out of the dialyzer;
operating a third pump to pump the dialysate through the fluid outlet pathway in cooperation with the second pump, wherein the second and third pumps cooperate to collectively achieve a second flow rate through the fluid outlet pathway from the dialyzer;
pumping blood through the dialyzer in communication with the dialysate such that the dialyzer dialyzes the blood; and
varying the pumping speed of at least one of the first pump, second pump and third pump to allow the dialyzer to individually perform hemodialysis, ultrafiltration and hemodiafiltration based on relative pumping speeds between the first pump, second pump and third pump.
2. The method of claim 1, wherein the first, second and third pumps operate to maintain balance between the fluid flow rates in the inlet pathway and outlet pathway such that substantially no fluid is added to or removed from the blood during operation.
3. The method of claim 1, wherein the first, second and third pumps operate to maintain balance between the fluid flow rates in the inlet pathway and outlet pathway such that a desired rate of fluid addition to the blood during operation is achieved.
4. The method of claim 1, wherein the first, second and third pumps operate to maintain balance between the fluid flow rates in the inlet pathway and outlet pathway such that a desired amount of fluid is removed from the blood during operation.
5. The method of claim 1, wherein the first, second and third pumps operate to maintain balance between the fluid flow rates in the inlet pathway and outlet pathway such that a desired amount of fluid is added to the blood during a time span of operation.
6. The method of claim 1, wherein the first, second and third pumps operate to maintain balance between the fluid flow rates in the inlet pathway and outlet pathway such that amount of fluid is removed to the blood during a time span of operation.
7. The method of claim 1, wherein the first, second and third pumps operate to achieve a desired level of hemodiafiltration by cycling the third pump between a lower speed and a higher speed substantially without a net addition of fluid to the blood.
8. The method of claim 1, wherein the first, second and third pumps operate to achieve a desired level of hemodiafiltration and a desired rate of fluid addition to the blood by cycling the third pump between a lower speed and a higher speed.
9. The method of claim 1, wherein the first, second and third pumps operate to achieve a desired level of hemodiafiltration and a desired rate of fluid removal from the blood by cycling the third pump between a lower speed and a higher speed.
10. A method of performing dialysis, comprising:
providing a dialysis system having an inlet conduit through which fluid flows in an inward direction toward a dialyzer and an outlet conduit through which fluid flows in an outward direction from the dialyzer;
pumping fluid through the inlet conduit using a first pump;
pumping fluid through the outlet conduit using a second pump;
using a third pump to supplement the pumping of the second pump through the outlet conduit; and
varying the pumping speed of at least one of the first pump, second pump and third pump to allow the dialyzer to individually perform hemodialysis, ultrafiltration and hemodiafiltration based on relative pumping speeds between the first pump, second pump and third pump.
11. A method as in claim 10, further comprising measuring a first fluid pressure in the inlet conduit and a second fluid pressure in the outlet conduit and adjusting a pump speed of the third pump based on the first and second fluid pressures.
12. A method as in claim 10, wherein adjusting a pump speed of the third pump based on the first and second fluid pressures comprises adjusting the pump speed of the third pump based on a pressure differential between the first fluid pressure and the second fluid pressure.
13. A method as in claim 10, wherein the fluid is dialysate and further comprising pumping blood through the dialyzer to achieve dialysis of the blood, and further comprising operating the third pump in a manner such that no fluid is added or removed from the blood during dialysis.
14. A method as in claim 10, wherein the fluid is dialysate and further comprising pumping blood through the dialyzer to achieve dialysis of the blood, and further comprising operating the third pump in a manner such that fluid is added to the blood from the dialysate during dialysis.
15. A method as in claim 10, wherein the fluid is dialysate and further comprising pumping blood through the dialyzer to achieve dialysis of the blood, and further comprising operating the third pump in a manner such that fluid is removed from dialysate into the blood during dialysis.
16. A method as in claim 10, wherein the fluid is dialysate and further comprising pumping blood through the dialyzer to achieve dialysis of the blood, and further comprising operating the third pump in a manner such that fluid is removed from the blood into the dialysate, and then operating the third pump in a manner such that fluid is added into the blood from the dialysate.
17. A method as in claim 16, wherein there is substantially no net gain of fluid into the blood and no loss of fluid from the blood over a predetermined span of time.
18. A method as in claim 10, wherein a first valve and a second valve control the flow of fluid through the bypass conduit.
US14/305,952 2009-12-05 2014-06-16 Dialysis system with ultrafiltration control Abandoned US20140291243A1 (en)

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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9402945B2 (en) 2014-04-29 2016-08-02 Outset Medical, Inc. Dialysis system and methods
US9545469B2 (en) 2009-12-05 2017-01-17 Outset Medical, Inc. Dialysis system with ultrafiltration control
US9849226B2 (en) 2014-12-19 2017-12-26 Fenwal, Inc. Systems and methods for real time calibration of pump stroke volumes during a blood separation procedure
US10179896B2 (en) 2015-05-12 2019-01-15 Baker Group, LLP Method and system for a bioartificial organ
US20200405941A1 (en) * 2018-03-26 2020-12-31 Nikkiso Company Limited Blood Purification Apparatus and Method of Trapping Bubbles Therein
US11298446B2 (en) 2014-12-19 2022-04-12 Fenwal, Inc. Systems and methods for calibrating pump stroke volumes during a blood separation procedure
US11534537B2 (en) 2016-08-19 2022-12-27 Outset Medical, Inc. Peritoneal dialysis system and methods
US11724013B2 (en) 2010-06-07 2023-08-15 Outset Medical, Inc. Fluid purification system
US11951241B2 (en) 2022-11-28 2024-04-09 Outset Medical, Inc. Peritoneal dialysis system and methods

Families Citing this family (66)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7744553B2 (en) 2003-12-16 2010-06-29 Baxter International Inc. Medical fluid therapy flow control systems and methods
US9308307B2 (en) 2007-09-13 2016-04-12 Fresenius Medical Care Holdings, Inc. Manifold diaphragms
US8040493B2 (en) 2007-10-11 2011-10-18 Fresenius Medical Care Holdings, Inc. Thermal flow meter
US8597505B2 (en) 2007-09-13 2013-12-03 Fresenius Medical Care Holdings, Inc. Portable dialysis machine
US8240636B2 (en) 2009-01-12 2012-08-14 Fresenius Medical Care Holdings, Inc. Valve system
US8105487B2 (en) 2007-09-25 2012-01-31 Fresenius Medical Care Holdings, Inc. Manifolds for use in conducting dialysis
US9199022B2 (en) 2008-09-12 2015-12-01 Fresenius Medical Care Holdings, Inc. Modular reservoir assembly for a hemodialysis and hemofiltration system
US9358331B2 (en) 2007-09-13 2016-06-07 Fresenius Medical Care Holdings, Inc. Portable dialysis machine with improved reservoir heating system
US8535522B2 (en) 2009-02-12 2013-09-17 Fresenius Medical Care Holdings, Inc. System and method for detection of disconnection in an extracorporeal blood circuit
CA3057807C (en) 2007-11-29 2021-04-20 Thomas P. Robinson System and method for conducting hemodialysis and hemofiltration
CN105148344B (en) 2008-10-07 2019-06-11 弗雷塞尼斯医疗保健控股公司 System and method are charged for dialysis system
WO2010062698A2 (en) 2008-10-30 2010-06-03 Xcorporeal, Inc. Modular, portable dialysis system
US8685251B2 (en) * 2009-12-05 2014-04-01 Home Dialysis Plus, Ltd. Ultra-pasteurization for dialysis machines
US9861733B2 (en) 2012-03-23 2018-01-09 Nxstage Medical Inc. Peritoneal dialysis systems, devices, and methods
WO2012129501A2 (en) 2011-03-23 2012-09-27 Nxstage Medical, Inc. Peritoneal dialysis systems, devices, and methods
DE102011078695A1 (en) * 2011-07-05 2013-01-10 Charité - Universitätsmedizin Berlin Dialysis procedure for removing protein-bound toxins from the blood of patients using high-frequency electromagnetic fields
EP3165245B1 (en) 2011-08-02 2019-02-20 Medtronic, Inc. Hemodialysis system having a flow path with a controlled compliant volume
EP2744537B1 (en) 2011-08-16 2018-01-24 Medtronic, Inc. Modular hemodialysis system
WO2013052680A2 (en) 2011-10-07 2013-04-11 Home Dialysis Plus, Ltd. Heat exchange fluid purification for dialysis system
DE102012009043A1 (en) * 2012-05-04 2013-11-07 Fresenius Medical Care Deutschland Gmbh Balancing device, dialysis machine, extracorporeal circuit and method for balancing liquids with a flow cell
ES2534477T5 (en) * 2012-05-09 2018-07-20 D_Med Consulting Ag Procedure for priming a hemodialysis device
US9201036B2 (en) 2012-12-21 2015-12-01 Fresenius Medical Care Holdings, Inc. Method and system of monitoring electrolyte levels and composition using capacitance or induction
US9157786B2 (en) 2012-12-24 2015-10-13 Fresenius Medical Care Holdings, Inc. Load suspension and weighing system for a dialysis machine reservoir
US10010663B2 (en) 2013-02-01 2018-07-03 Medtronic, Inc. Fluid circuit for delivery of renal replacement therapies
US10850016B2 (en) 2013-02-01 2020-12-01 Medtronic, Inc. Modular fluid therapy system having jumpered flow paths and systems and methods for cleaning and disinfection
US9623164B2 (en) 2013-02-01 2017-04-18 Medtronic, Inc. Systems and methods for multifunctional volumetric fluid control
US10543052B2 (en) 2013-02-01 2020-01-28 Medtronic, Inc. Portable dialysis cabinet
GB201305755D0 (en) 2013-03-28 2013-05-15 Quanta Fluid Solutions Ltd Re-Use of a Hemodialysis Cartridge
ES2723348T3 (en) * 2013-07-15 2019-08-26 Gambro Lundia Ab Individual pump calibration for ultrafiltration control in a dialysis machine
ES2728778T3 (en) 2013-07-15 2019-10-28 Gambro Lundia Ab Relative pump calibration to control ultrafiltration in a dialysis unit
GB201314512D0 (en) 2013-08-14 2013-09-25 Quanta Fluid Solutions Ltd Dual Haemodialysis and Haemodiafiltration blood treatment device
US9354640B2 (en) 2013-11-11 2016-05-31 Fresenius Medical Care Holdings, Inc. Smart actuator for valve
DE102013019356A1 (en) * 2013-11-19 2015-06-03 Fresenius Medical Care Deutschland Gmbh Apparatus and method for balancing fluids for an extracorporeal blood treatment device
DE102013021012A1 (en) * 2013-12-13 2015-06-18 Fresenius Medical Care Deutschland Gmbh Device for extracorporeal blood treatment
JP6540705B2 (en) * 2013-12-19 2019-07-10 ジーイー・ヘルスケア・バイオサイエンス・アクチボラグ Teleoperated valve for biological fluid handling system
US10451591B1 (en) * 2013-12-19 2019-10-22 Ge Healthcare Bio-Sciences Ab Remotely actuated valve for a biological liquid treatment system
JP2017510396A (en) * 2014-02-27 2017-04-13 イージーダイアル インク Portable hemodialysis machine and disposable cartridge
GB201409796D0 (en) 2014-06-02 2014-07-16 Quanta Fluid Solutions Ltd Method of heat sanitization of a haemodialysis water circuit using a calculated dose
US10980929B2 (en) 2014-09-12 2021-04-20 Diality Inc. Hemodialysis system with ultrafiltration controller
US10016550B2 (en) 2014-09-12 2018-07-10 Easydial, Inc. Portable hemodialysis assembly with ammonia sensor
US10525182B2 (en) 2014-10-10 2020-01-07 Nxstage Medical, Inc. Flow balancing devices, methods, and systems
US10098993B2 (en) * 2014-12-10 2018-10-16 Medtronic, Inc. Sensing and storage system for fluid balance
US9713665B2 (en) 2014-12-10 2017-07-25 Medtronic, Inc. Degassing system for dialysis
US10874787B2 (en) 2014-12-10 2020-12-29 Medtronic, Inc. Degassing system for dialysis
US9895479B2 (en) 2014-12-10 2018-02-20 Medtronic, Inc. Water management system for use in dialysis
US9763325B2 (en) * 2015-04-07 2017-09-12 Oregon State University Microreactor-assisted printing of conductive traces with in-situ reactive inks
US11040172B2 (en) 2015-07-20 2021-06-22 Strataca Systems Limited Ureteral and bladder catheters and methods of inducing negative pressure to increase renal perfusion
AU2016296866B2 (en) * 2015-07-20 2018-07-19 Roivios Limited Ureteral and bladder catheters and methods for inducing negative pressure to increase renal perfusion
US10926062B2 (en) 2015-07-20 2021-02-23 Strataca Systems Limited Ureteral and bladder catheters and methods of inducing negative pressure to increase renal perfusion
US10918827B2 (en) 2015-07-20 2021-02-16 Strataca Systems Limited Catheter device and method for inducing negative pressure in a patient's bladder
GB2543801A (en) * 2015-10-28 2017-05-03 Quanta Fluid Solutions Ltd Dialysis machine and ultrafiltration
DE102015015636A1 (en) * 2015-12-02 2017-06-08 Fresenius Medical Deutschland Gmbh Method for testing the rigidity of a disposable
GB201523104D0 (en) 2015-12-30 2016-02-10 Quanta Fluid Solutions Ltd Dialysis machine
CN105999447B (en) * 2016-07-15 2018-01-12 重庆弘善医疗设备有限公司 Haemodialysis and the control method of ultrafiltration
GB2570050B (en) 2016-07-18 2020-01-01 Nxstage Medical Inc Apparatus for controlling fluid flow in a circuit
DE102016008755A1 (en) * 2016-07-18 2018-01-18 Fresenius Medical Care Deutschland Gmbh Dialysis machine with a control unit for carrying out a conditioning of the dialysis membrane
GB201622119D0 (en) 2016-12-23 2017-02-08 Quanta Dialysis Tech Ltd Improved valve leak detection system
GB201703048D0 (en) 2017-02-24 2017-04-12 Quanta Dialysis Tech Ltd Testing rotor engagement of a rotary peristaltic pump
GB201710547D0 (en) * 2017-06-30 2017-08-16 Quanta Dialysis Tech Ltd A dialysis system
USD907211S1 (en) 2017-09-28 2021-01-05 Quanta Dialysis Technologies Ltd. Dialysis machine
US11278654B2 (en) 2017-12-07 2022-03-22 Medtronic, Inc. Pneumatic manifold for a dialysis system
US10881347B2 (en) 2017-12-29 2021-01-05 Fresenius Medical Care Holdings, Inc. Closed loop dialysis treatment using adaptive ultrafiltration rates
US11033667B2 (en) 2018-02-02 2021-06-15 Medtronic, Inc. Sorbent manifold for a dialysis system
US11110215B2 (en) 2018-02-23 2021-09-07 Medtronic, Inc. Degasser and vent manifolds for dialysis
AU2019228526B2 (en) 2018-02-28 2021-11-25 Nxstage Medical, Inc. Fluid preparation and treatment devices, methods, and systems
JP7227459B2 (en) * 2018-11-22 2023-02-22 澁谷工業株式会社 Flow calibration device for replacement fluid pump in hemodialysis machine

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4209391A (en) * 1978-11-06 1980-06-24 Cordis Dow Corp. Apparatus and method for automatically controlling hemodialysis at a pre-selected ultrafiltration rate
US6716356B2 (en) * 2000-01-11 2004-04-06 Nephros, Inc. Thermally enhanced dialysis/diafiltration system
US20140021111A1 (en) * 2006-06-05 2014-01-23 Baxter Healthcare S.A. Dynamic weight balancing of flow in kidney failure treatment systems

Family Cites Families (624)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3356360A (en) 1964-08-25 1967-12-05 Task Corp Apparatus for supporting stacked and bonded laminations for electrical apparatus
DE1926907C3 (en) 1968-12-05 1975-07-10 Veb Filmfabrik Wolfen, X 4440 Wolfen Multi-chamber cell for electrodialysis
US3695445A (en) 1969-04-24 1972-10-03 Becton Dickinson Co Pleated membrane transfer device
DK123074B (en) 1970-07-13 1972-05-15 Inst Produktudvikling Support plate for the membranes of a dialyzer, in particular for hemodialysis.
US3809309A (en) 1970-08-14 1974-05-07 Trw Inc Diffusion bonding apparatus
US3710237A (en) 1970-09-08 1973-01-09 Nalco Chemical Co Probe for a conductivity testing device
US3762032A (en) 1971-08-19 1973-10-02 Gen Motors Corp Bonding
US3965008A (en) 1974-03-15 1976-06-22 Dawson Gerald C Portable water sterilization device
US4172033A (en) 1974-12-23 1979-10-23 DWS, Inc. Artificial kidney proportioning system
SE396887B (en) 1976-02-16 1977-10-10 Gambro Ab DEVICE FOR DIFFUSION OF THE SUBJECT BETWEEN TWO FLUIDA VIA SEMIPERMEABLE MEMBRANE
DE2636290A1 (en) 1976-08-12 1978-02-16 Fresenius Chem Pharm Ind DEVICE FOR CONTROLLING AND MONITORING BLOOD FLOW DURING BLOOD DIALYSIS, PERFUSION AND DIAFILTRATION USING ONLY ONE CONNECTION POINT TO THE PATIENT'S BLOOD CIRCUIT (SINGLE NEEDLE TECHNOLOGY)
SE401894B (en) 1976-10-14 1978-06-05 Gambro Ab DIALYSIS SYSTEM
US4110220A (en) 1976-10-18 1978-08-29 Lavender Ardis R Mass transfer device
US4115273A (en) 1976-11-15 1978-09-19 Extracorporeal Medical Specialties, Inc. Wave patterned support for dialyzer membrane
NL7614605A (en) 1976-12-30 1978-07-04 Stork Amsterdam METHOD AND DEVICE FOR THE REGULAR HEATING OF A LIQUID PRODUCT.
US4100068A (en) 1977-01-13 1978-07-11 The United States Of America As Represented By The Secretary Of The Interior System for the dielectrophoretic separation of particulate and granular material
US4089456A (en) 1977-06-28 1978-05-16 United Technologies Corporation Controlled-pressure diffusion bonding and fixture therefor
GB2003053B (en) 1977-08-19 1982-07-14 Kuraray Co Plate type fluid treatment apparatus
DE2739335B2 (en) 1977-09-01 1980-01-10 Blutspendedienst Der Landesverbaende Des Deutschen Roten Kreuzes Niedersachsen, Oldenburg Und Bremen Gemeinnuetzige Gmbh, 3257 Springe Process for obtaining germ-free and particle-free water for medical injections and for technical purposes
US4155157A (en) 1978-03-06 1979-05-22 United Aircraft Products, Inc. Braze fixture
US4229299A (en) * 1978-03-22 1980-10-21 Hoechst Aktiengesellschaft Peristaltic dialysate solution pump
GB2023427B (en) * 1978-06-15 1982-11-24 Honda Motor Co Ltd Artificial kindey
US4204628A (en) 1978-07-24 1980-05-27 General Electric Company Method for thermo-compression diffusion bonding
DE2838414C2 (en) 1978-09-02 1984-10-31 Fresenius AG, 6380 Bad Homburg Device for hemodialysis and for withdrawing ultrafiltrate
DE3005408A1 (en) 1979-02-15 1980-08-21 Daicel Chem SEMIPERMEABLES MEMBRANE ELEMENT
WO1982000775A1 (en) 1980-09-03 1982-03-18 Lefebvre M Fluid treatment apparatus
FR2493707A1 (en) 1980-11-13 1982-05-14 Hospal Sodip APPARATUS, USEFUL AS AN ARTIFICIAL REINFORCEMENT, HAVING DISCOVERED CHANNEL PLATES
US4486303A (en) 1981-10-06 1984-12-04 Brous Donald W Ultrafiltration in hemodialysis
DE3223051C2 (en) 1982-06-21 1984-09-13 Fresenius AG, 6380 Bad Homburg Dialysis device with regulated dialysis solution
JPS5958002U (en) 1982-10-08 1984-04-16 株式会社日本メデイカル・サプライ Stacked dialyzer
US4476022A (en) 1983-03-11 1984-10-09 Doll David W Spirally wrapped reverse osmosis membrane cell
SE451801B (en) 1983-11-29 1987-11-02 Gambro Lundia Ab DEVICE FOR BREATHING A FLUID THROUGH A PIPE
JPS60143803U (en) 1984-03-06 1985-09-24 丸井産業株式会社 Large floor retainer for buildings
US4647748A (en) 1984-05-17 1987-03-03 Smith International, Inc. Graphite electrode construction and method of making
CS248305B1 (en) 1984-06-18 1987-02-12 Miroslav Skala Blood cleaning instrument
US4661246A (en) 1984-10-01 1987-04-28 Ash Medical Systems, Inc. Dialysis instrument with dialysate side pump for moving body fluids
US4770787A (en) 1985-06-25 1988-09-13 Cobe Laboratories, Inc. Method of operating a fluid flow transfer device
US4689108A (en) 1985-11-04 1987-08-25 Gte Government Systems Corporation Apparatus for assembling electrochemical batteries and similar articles
US4769134A (en) 1985-11-20 1988-09-06 C D Medical Open patient fluid management method and system
FR2597753B1 (en) 1986-04-25 1990-09-28 Hospal Ind ARTIFICIAL KIDNEY WITH DEVICE FOR CONTROLLING THE QUANTITIES OF LIQUID FLOWING IN THE DIALYSIS LIQUID CIRCUIT
US4756835A (en) 1986-08-29 1988-07-12 Advanced Polymer Technology, Inc. Permeable membranes having high flux-density and low fouling-propensity
DE3636995A1 (en) 1986-10-30 1988-05-11 Fresenius Ag METHOD AND DEVICE FOR EXTRACTING HEAT FROM BLOOD IN THE EXTRACORPORAL CIRCUIT
US5868930A (en) 1986-11-26 1999-02-09 Kopf; Henry B. Filtration cassette article and filter comprising same
DE8702995U1 (en) 1987-02-24 1987-05-07 Mehnert, Kurt
US4773991A (en) 1987-03-13 1988-09-27 Baxter Travenol Laboratories, Inc. Water purification system fluid path
US4827430A (en) 1987-05-11 1989-05-02 Baxter International Inc. Flow measurement system
FR2615289B1 (en) 1987-05-15 1989-07-21 Hospal Ind METHOD FOR DETERMINING THE NATREMIA OF A PATIENT AND ARTIFICIAL KIDNEY USING THE SAME
EP0392010B1 (en) 1987-05-29 1993-12-01 Terumo Kabushiki Kaisha Body fluid filter having flat film permeative membranes having protrusions
SE457605B (en) 1988-01-18 1989-01-16 Gambro Ab DEVICE FOR DIFFUSION OF THE SUBSTANCES BETWEEN TWO FLUIDS
SE465404B (en) 1988-03-03 1991-09-09 Gambro Ab DIALYSIS SYSTEM
US5015379A (en) 1988-03-16 1991-05-14 Mordeki Drori Coiled filter strip with upstream and downstream butt ends
US4869421A (en) 1988-06-20 1989-09-26 Rohr Industries, Inc. Method of jointing titanium aluminide structures
US4875619A (en) 1988-09-01 1989-10-24 Anderson Jeffrey J Brazing of ink jet print head components using thin layers of braze material
JPH0630764B2 (en) 1989-03-06 1994-04-27 森田化学工業株式会社 Ultrapure water line sterilization method
DE3909967A1 (en) 1989-03-25 1990-09-27 Fresenius Ag HAEMODIALYSIS DEVICE WITH AUTOMATIC ADJUSTMENT OF THE DIALYSIS FLUID FLOW
US5087930A (en) 1989-11-01 1992-02-11 Tektronix, Inc. Drop-on-demand ink jet print head
US5227049A (en) 1990-08-20 1993-07-13 Hospal Industrie Single-needle circuit for circulating blood outside the body in blood treatment apparatus
AU658845B2 (en) 1990-08-20 1995-05-04 Abbott Laboratories Medical drug formulation and delivery system
US5344392A (en) 1990-09-28 1994-09-06 Baxter International Inc. Method and apparatus for preparation of solutions from concentrates
US5308320A (en) * 1990-12-28 1994-05-03 University Of Pittsburgh Of The Commonwealth System Of Higher Education Portable and modular cardiopulmonary bypass apparatus and associated aortic balloon catheter and associated method
US5232145A (en) 1991-03-29 1993-08-03 Watkins-Johnson Company Method of soldering in a controlled-convection surface-mount reflow furnace
US5247434A (en) 1991-04-19 1993-09-21 Althin Medical, Inc. Method and apparatus for kidney dialysis
US5326476A (en) 1991-04-19 1994-07-05 Althin Medical, Inc. Method and apparatus for kidney dialysis using machine with programmable memory
FR2678177B1 (en) 1991-06-25 1994-09-09 Lescoche Philippe INORGANIC MEMBRANE FOR FILTRATION AND, FILTER UNIT OBTAINED.
IT1255260B (en) 1991-07-16 1995-10-20 Hospal Dasco Spa METHOD OF SURVEILLANCE OF A THERAPY IN A DIALYTIC TREATMENT.
SE502103C2 (en) 1991-08-01 1995-08-14 Gambro Dialysatoren Filter unit for transfer of pulp and / or heat containing cavity fibers
US5365516A (en) 1991-08-16 1994-11-15 Pinpoint Communications, Inc. Communication system and method for determining the location of a transponder unit
US5336165A (en) 1991-08-21 1994-08-09 Twardowski Zbylut J Artificial kidney for frequent (daily) Hemodialysis
FR2680976B1 (en) * 1991-09-10 1998-12-31 Hospal Ind ARTIFICIAL KIDNEY PROVIDED WITH BLOOD CHARACTERISTIC MEANS OF DETERMINATION AND CORRESPONDING DETERMINATION METHOD.
US6139754A (en) 1991-11-15 2000-10-31 Baxter International Inc. Hemodialysis conductivity servo-proportioning system and method
IT1250558B (en) 1991-12-30 1995-04-20 Hospal Dasco Spa DIALYSIS MACHINE WITH SAFETY CONTROL AND RELATED SAFETY CONTROL METHOD.
US5236476A (en) 1992-02-21 1993-08-17 Klick Ronald C Air purification system for enclosed arenas
DE4208274C1 (en) 1992-03-13 1993-10-21 Medical Support Gmbh Method and arrangement for rinsing and filling the extracorporeal blood circuit of dialysis machines
US5313023A (en) 1992-04-03 1994-05-17 Weigh-Tronix, Inc. Load cell
US5312550B1 (en) 1992-04-27 1996-04-23 Robert L Hester Method for detecting undesired dialysis recirculation
CA2094102A1 (en) 1992-04-30 1993-10-31 David S. Utterberg Blood air trap chamber
US5385623A (en) 1992-05-29 1995-01-31 Hexcel Corporation Method for making a material with artificial dielectric constant
EP0620429A4 (en) 1992-10-07 1995-02-08 Daikin Ind Ltd Optically measuring device.
DE4239937C2 (en) 1992-11-27 1995-08-24 Fresenius Ag Method for determining the functionality of a partial device of a hemodialysis machine and device for carrying out this method
SE470377B (en) 1993-02-11 1994-02-07 Gambro Dialysatoren Drip and / or expansion chamber with built-in filter and method for making one
US5749226A (en) 1993-02-12 1998-05-12 Ohio University Microminiature stirling cycle cryocoolers and engines
US5540808A (en) 1993-02-24 1996-07-30 Deka Products Limited Partnership Energy director for ultrasonic welding and joint produced thereby
US5534328A (en) 1993-12-02 1996-07-09 E. I. Du Pont De Nemours And Company Integrated chemical processing apparatus and processes for the preparation thereof
US5610645A (en) 1993-04-30 1997-03-11 Tektronix, Inc. Ink jet head with channel filter
US5346472A (en) 1993-06-02 1994-09-13 Baxter International Inc. Apparatus and method for preventing hypotension in a dialysis patient
US5409612A (en) 1993-07-16 1995-04-25 Cobe Laboratories, Inc. Method and apparatus for cleaning a dialysate circuit downstream of a dialyzer
JPH0777192A (en) 1993-09-10 1995-03-20 Nikkiso Co Ltd Performance estimating method for centrifugal pump having thrust balance mechanism
US5394732A (en) 1993-09-10 1995-03-07 Cobe Laboratories, Inc. Method and apparatus for ultrasonic detection of air bubbles
US5342326A (en) 1993-09-22 1994-08-30 B. Braun Medical, Inc. Capless medical valve
US5395351A (en) 1993-09-29 1995-03-07 Baxter International Inc. Self-valving connector and interface system and a method of using same
IT1260992B (en) 1993-10-15 1996-04-29 Hospal Dasco Spa MACHINE FOR EXTRA-BODY DIALYSIS.
US5498253A (en) 1993-11-23 1996-03-12 Baxter International Inc. Port adaptor and protector and container having same
US5360395A (en) 1993-12-20 1994-11-01 Utterberg David S Pump conduit segment having connected, parallel branch line
ES2133472T3 (en) 1993-12-29 1999-09-16 Braun Melsungen Ag INFUSION SYSTEM WITH REGULATORY DEVICE.
US5536258A (en) 1994-02-14 1996-07-16 Fresenius Usa, Inc. Antibacterial medical tubing connector
SE513524C2 (en) 1994-02-18 2000-09-25 Gambro Med Tech Ab Systems and method for calculating and / or monitoring a fluid flow in a dialysis apparatus
US5439451A (en) 1994-03-22 1995-08-08 B. Braun Medical, Inc. Capless medical backcheck valve
US5580523A (en) 1994-04-01 1996-12-03 Bard; Allen J. Integrated chemical synthesizers
US5421208A (en) 1994-05-19 1995-06-06 Baxter International Inc. Instantaneous volume measurement system and method for non-invasively measuring liquid parameters
US5595712A (en) 1994-07-25 1997-01-21 E. I. Du Pont De Nemours And Company Chemical mixing and reaction apparatus
FR2723002B1 (en) 1994-07-26 1996-09-06 Hospal Ind DEVICE AND METHOD FOR PREPARING A FILTRATION PROCESSING LIQUID
US6129973A (en) 1994-07-29 2000-10-10 Battelle Memorial Institute Microchannel laminated mass exchanger and method of making
US6126723A (en) 1994-07-29 2000-10-03 Battelle Memorial Institute Microcomponent assembly for efficient contacting of fluid
US5811062A (en) 1994-07-29 1998-09-22 Battelle Memorial Institute Microcomponent chemical process sheet architecture
US5611214A (en) 1994-07-29 1997-03-18 Battelle Memorial Institute Microcomponent sheet architecture
SE9402720D0 (en) 1994-08-15 1994-08-15 Gambro Ab Insert for pressure transducer
SE504166C2 (en) 1994-08-15 1996-11-25 Gambro Ab Drip chamber head
SE510512C2 (en) 1994-08-23 1999-05-31 Gambro Lundia Ab Method and connection unit for sterile transfer of a solution
US5993174A (en) 1994-08-23 1999-11-30 Nikkiso Co., Ltd. Pulsation free pump
US5533996A (en) 1994-08-24 1996-07-09 Baxter International, Inc. Transfer set connector with permanent, integral cam opening closure and a method of using the same
WO1996011033A1 (en) 1994-10-11 1996-04-18 Baxter International Inc. Easy-to-clamp tubing and a method for clamping the tubing
US6635226B1 (en) 1994-10-19 2003-10-21 Agilent Technologies, Inc. Microanalytical device and use thereof for conducting chemical processes
DE4440556A1 (en) 1994-11-12 1996-05-15 Polaschegg Hans Dietrich Dr Device and method for determining the amount of uremia toxins removed during hemodialysis treatment
DE4442352C1 (en) 1994-11-29 1995-12-21 Braun Melsungen Ag Valve arrangement provided in connector for use e.g. with cannula
US5698916A (en) 1994-11-30 1997-12-16 Nikkiso Co., Ltd. Slender motor for canned motor pump
US5591016A (en) 1994-11-30 1997-01-07 Nikkiso Co., Ltd. Multistage canned motor pump having a thrust balancing disk
US6234773B1 (en) 1994-12-06 2001-05-22 B-Braun Medical, Inc. Linear peristaltic pump with reshaping fingers interdigitated with pumping elements
SE510513C2 (en) 1994-12-07 1999-05-31 Gambro Lundia Ab Method and apparatus for measuring the ultrafiltration volume of a dialysis machine and method for calibrating the apparatus
DE4443714C2 (en) 1994-12-09 1996-10-17 Fresenius Ag Device for controlling a fluid flow
US5643190A (en) 1995-01-17 1997-07-01 Medisystems Technology Corporation Flow-through treatment device
US5932103A (en) 1995-02-13 1999-08-03 Aksys, Ltd. Withdrawal of priming fluid from extracorporeal circuit of hemodialysis machines or the like
US5788851A (en) 1995-02-13 1998-08-04 Aksys, Ltd. User interface and method for control of medical instruments, such as dialysis machines
US5788099A (en) * 1995-02-13 1998-08-04 Akysys, Ltd. Vessel for containing batch quantities of dialysate or other physiologic solution chemicals
US5591344A (en) 1995-02-13 1997-01-07 Aksys, Ltd. Hot water disinfection of dialysis machines, including the extracorporeal circuit thereof
US6153102A (en) 1995-02-13 2000-11-28 Aksys, Ltd. Disinfection of dead-ended lines in medical instruments
US5630804A (en) 1995-02-24 1997-05-20 Baxter International Inc. Metallic silver-plated silicon ring element for exit site disinfection and a method for preventing contamination at an exit site
DE69635566T2 (en) 1995-03-16 2006-06-14 Murata Manufacturing Co Monolithic ceramic component and its manufacture
US6329139B1 (en) 1995-04-25 2001-12-11 Discovery Partners International Automated sorting system for matrices with memory
US5618268A (en) 1995-06-06 1997-04-08 B. Braun Medical Inc. Medical infusion devices and medicine delivery systems employing the same
US5618441A (en) 1995-06-07 1997-04-08 Rosa; Jim Single microcontroller execution of control and safety system functions in a dialysis machine
US5650071A (en) 1995-06-07 1997-07-22 Cobe Laboratories, Inc. Technique for priming and recirculating fluid through a dialysis machine to prepare the machine for use
US5685835A (en) 1995-06-07 1997-11-11 Cobe Laboratories, Inc. Technique for using a dialysis machine to disinfect a blood tubing set
US6790195B2 (en) 1995-06-07 2004-09-14 Gambro Inc Extracorporeal blood processing methods and apparatus
US5623969A (en) 1995-06-07 1997-04-29 B. Braun Medical Inc. Normally closed aspiration valve
US5624572A (en) 1995-06-07 1997-04-29 Cobe Laboratories, Inc. Power management system and method for maximizing heat delivered to dialysate in a dialysis machine
US5629871A (en) 1995-06-07 1997-05-13 Cobe Laboratories, Inc. Wear trend analysis technique for components of a dialysis machine
US5647984A (en) 1995-06-07 1997-07-15 Cobe Laboratories, Inc. Extracorporeal fluid treatment systems selectively operable in a treatment mode or a disinfecting mode
US5620608A (en) 1995-06-07 1997-04-15 Cobe Laboratories, Inc. Information entry validation system and method for a dialysis machine
US5693008A (en) 1995-06-07 1997-12-02 Cobe Laboratories, Inc. Dialysis blood tubing set
US5609770A (en) 1995-06-07 1997-03-11 Cobe Laboratories, Inc. Graphical operator machine interface and method for information entry and selection in a dialysis machine
IT1276468B1 (en) 1995-07-04 1997-10-31 Hospal Dasco Spa AUTOMATIC DIALYSIS METHOD AND EQUIPMENT
US5772624A (en) 1995-07-20 1998-06-30 Medisystems Technology Corporation Reusable blood lines
US5648684A (en) 1995-07-26 1997-07-15 International Business Machines Corporation Endcap chip with conductive, monolithic L-connect for multichip stack
US5582600A (en) 1995-08-03 1996-12-10 Baxter International Inc. Transfer set connector with a locking lid and a method of using the same
US5779833A (en) 1995-08-04 1998-07-14 Case Western Reserve University Method for constructing three dimensional bodies from laminations
US5938634A (en) 1995-09-08 1999-08-17 Baxter International Inc. Peritoneal dialysis system with variable pressure drive
US5928177A (en) 1995-09-15 1999-07-27 Cobe Laboratories, Inc. Technique for loading a pump header within a peristaltic pump of a dialysis machine
US5711883A (en) 1995-09-27 1998-01-27 Fresenius Usa, Inc. Method for testing dialyzer integrity prior to use
US6003556A (en) 1995-10-06 1999-12-21 Cobe Laboratories, Inc. Hinged cap fluid connector
EP0856352B1 (en) 1995-10-09 2003-07-09 Asahi Kasei Kabushiki Kaisha Polysulfone membrane for purifying blood
DE19540292C1 (en) 1995-10-28 1997-01-30 Karlsruhe Forschzent Static micromixer
US6058934A (en) 1995-11-02 2000-05-09 Chiron Diagnostics Corporation Planar hematocrit sensor incorporating a seven-electrode conductivity measurement cell
WO1997022535A1 (en) 1995-12-15 1997-06-26 Medisystems Technology Corporation Medical connector with integral closure
FR2742665B1 (en) 1995-12-21 1998-02-27 Braun Celsa Sa BI-DIRECTIONAL AXIAL SLOT VALVE CATHETER
US5858238A (en) 1996-03-08 1999-01-12 Baxter Research Medical, Inc. Salvage of autologous blood via selective membrane/sorption technologies
IT1285623B1 (en) 1996-03-18 1998-06-18 Bellco Spa EQUIPMENT FOR DIALYSIS TREATMENTS
US5689966A (en) 1996-03-22 1997-11-25 Battelle Memorial Institute Method and apparatus for desuperheating refrigerant
US5743892A (en) 1996-03-27 1998-04-28 Baxter International Inc. Dual foam connection system for peritoneal dialysis and dual foam disinfectant system
US5928213A (en) 1996-05-13 1999-07-27 B. Braun Medical, Inc. Flexible multiple compartment medical container with preferentially rupturable seals
US5910138A (en) 1996-05-13 1999-06-08 B. Braun Medical, Inc. Flexible medical container with selectively enlargeable compartments and method for making same
US5944709A (en) 1996-05-13 1999-08-31 B. Braun Medical, Inc. Flexible, multiple-compartment drug container and method of making and using same
SE510126C2 (en) 1996-06-13 1999-04-19 Althin Medical Ab Dialysis machine with movable control panel
US5932940A (en) 1996-07-16 1999-08-03 Massachusetts Institute Of Technology Microturbomachinery
US5885456A (en) 1996-08-09 1999-03-23 Millipore Corporation Polysulfone copolymer membranes and process
US6387069B1 (en) 1996-09-23 2002-05-14 Dsu Medical Corporation Blood set priming method and apparatus
US7166084B2 (en) 1996-09-23 2007-01-23 Dsu Medical Corporation Blood set priming method and apparatus
US5895368A (en) 1996-09-23 1999-04-20 Medisystems Technology Corporation Blood set priming method and apparatus
US6258276B1 (en) 1996-10-18 2001-07-10 Mcmaster University Microporous membranes and uses thereof
JP3168927B2 (en) 1996-11-19 2001-05-21 住友金属工業株式会社 Method for manufacturing duplex stainless steel joint
ES2208806T3 (en) 1996-11-21 2004-06-16 Fresenius Medical Care Deutschland Gmbh HIBLE FIBER MEMBRANE SEPARATOR DEVICE.
SE9604370D0 (en) 1996-11-28 1996-11-28 Gambro Ab Method and system for preventing intradialytic symptomatology
US6109994A (en) 1996-12-12 2000-08-29 Candescent Technologies Corporation Gap jumping to seal structure, typically using combination of vacuum and non-vacuum environments
AU5895898A (en) 1996-12-20 1998-07-17 Gamera Bioscience Corporation An affinity binding-based system for detecting particulates in a fluid
JP3992159B2 (en) 1997-01-24 2007-10-17 フレセニウス メディカル ケア ドイチランド ゲーエムベーハー Method for measuring hemodialysis parameters and apparatus for carrying out such a method
US6036680A (en) 1997-01-27 2000-03-14 Baxter International Inc. Self-priming solution lines and a method and system for using same
WO1998033585A1 (en) 1997-02-05 1998-08-06 California Institute Of Technology Microfluidic sub-millisecond mixers
US5903211A (en) 1997-02-07 1999-05-11 Althin Medical, Inc. Medical treatment device with a user interface adapted for home or limited care environments
US20010016699A1 (en) 1997-02-14 2001-08-23 Jeffrey H. Burbank Hemofiltration system
US6579253B1 (en) 1997-02-14 2003-06-17 Nxstage Medical, Inc. Fluid processing systems and methods using extracorporeal fluid flow panels oriented within a cartridge
US5858239A (en) 1997-02-14 1999-01-12 Aksys, Ltd. Methods and apparatus for adjustment of blood drip chamber of dialysis machines using touchscreen interface
US6979309B2 (en) 1997-02-14 2005-12-27 Nxstage Medical Inc. Systems and methods for performing blood processing and/or fluid exchange procedures
US6554789B1 (en) 1997-02-14 2003-04-29 Nxstage Medical, Inc. Layered fluid circuit assemblies and methods for making them
US5813235A (en) 1997-02-24 1998-09-29 The State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Resonantly coupled α-stirling cooler
US5983947A (en) 1997-03-03 1999-11-16 Medisystems Technology Corporation Docking ports for medical fluid sets
US5928180A (en) 1997-03-25 1999-07-27 Krivitski; Nikolai M. Method and apparatus for real time monitoring of blood volume in a filter
US6432309B1 (en) 1997-05-19 2002-08-13 Asahi Medical Co, Ltd Polysulfone-base hollow-fiber hemocathartic membrane and processes for the production thereof
US5957898A (en) 1997-05-20 1999-09-28 Baxter International Inc. Needleless connector
US6261282B1 (en) 1997-05-20 2001-07-17 Baxter International Inc. Needleless connector
SE509602C2 (en) 1997-06-05 1999-02-15 Gambro Med Tech Ab Two-way valve
US5974867A (en) 1997-06-13 1999-11-02 University Of Washington Method for determining concentration of a laminar sample stream
US6514412B1 (en) 1998-06-18 2003-02-04 3M Innovative Properties Company Microstructured separation device
US6010623A (en) 1997-08-01 2000-01-04 Medisystems Technology Corporation Bubble trap with flat side
US6375871B1 (en) 1998-06-18 2002-04-23 3M Innovative Properties Company Methods of manufacturing microfluidic articles
DE19734002C1 (en) 1997-08-06 1998-09-17 Fresenius Medical Care De Gmbh Blood dialysis process with process monitoring system on dialysis machine
DE59814205D1 (en) 1997-08-13 2008-05-21 Fresenius Medical Care De Gmbh A blood treatment device comprising a device for determining parameters of hemodialysis and methods for its determination
FR2767477B1 (en) * 1997-08-21 1999-10-08 Hospal Ind DIALYSIS APPARATUS FOR INDEPENDENTLY CONTROLLING THE CONCENTRATION OF AT LEAST TWO IONIC SUBSTANCES IN THE INTERIOR OF A PATIENT
US6280406B1 (en) 1997-09-12 2001-08-28 Gambro, Inc Extracorporeal blood processing system
DE19742637C5 (en) 1997-09-26 2005-06-02 Fresenius Medical Care Deutschland Gmbh Device and method for operating medical devices
US5976115A (en) 1997-10-09 1999-11-02 B. Braun Medical, Inc. Blunt cannula spike adapter assembly
US5951870A (en) 1997-10-21 1999-09-14 Dsu Medical Corporation Automatic priming of blood sets
US6187198B1 (en) 1997-10-21 2001-02-13 Dsu Medical Corporation Automatic priming of connected blood sets
DE19746377C1 (en) 1997-10-21 1999-07-01 Fresenius Medical Care De Gmbh Blood treatment device with a device for continuous monitoring of the patient's blood pressure
DE69840028D1 (en) 1997-10-23 2008-10-30 Morinaga Milk Industry Co Ltd METHOD AND DEVICE FOR CONTINUOUS HEATING TEMPERATURE OF LIQUIDS
US6100463A (en) 1997-11-18 2000-08-08 The Boeing Company Method for making advanced thermoelectric devices
US6030472A (en) 1997-12-04 2000-02-29 Philip Morris Incorporated Method of manufacturing aluminide sheet by thermomechanical processing of aluminide powders
SE9900077D0 (en) 1999-01-14 1999-01-14 Gambro Ab Procedure and Device for Uber Testing of Sensors
US6365041B1 (en) 1997-12-23 2002-04-02 Jonathan Hoadley Filtration process utilizing heat exchanger apparatus
DE19757523C1 (en) 1997-12-23 1999-04-22 Fresenius Medical Care De Gmbh Method of monitoring functioning of blood distributing machine for dialysis
DE29800107U1 (en) 1998-01-07 1998-03-05 Braun Melsungen Ag Hose coupling for a medical transfer system
DE19800529A1 (en) 1998-01-09 1999-07-15 Bayer Ag Process for phosgenation of amines in the gas phase using microstructure mixers
DE19801768C2 (en) 1998-01-19 2001-04-19 Fresenius Medical Care De Gmbh Method and device for providing operational dialysis fluid
US6167910B1 (en) 1998-01-20 2001-01-02 Caliper Technologies Corp. Multi-layer microfluidic devices
US6048432A (en) 1998-02-09 2000-04-11 Applied Metallurgy Corporation Method for producing complex-shaped objects from laminae
US7004924B1 (en) 1998-02-11 2006-02-28 Nxstage Medical, Inc. Methods, systems, and kits for the extracorporeal processing of blood
US6212333B1 (en) 1998-02-13 2001-04-03 M. Joseph Olk Medical unit water line sterilization system
EP1058006B1 (en) 1998-02-17 2012-09-12 Nikkiso Company, Ltd. Diaphragm pump
US6582385B2 (en) 1998-02-19 2003-06-24 Nstage Medical, Inc. Hemofiltration system including ultrafiltrate purification and re-infusion system
DE19814687C1 (en) 1998-04-01 1999-02-18 Fresenius Medical Care De Gmbh Blood dialysis assembly
JP3537349B2 (en) 1998-04-20 2004-06-14 日機装株式会社 Thrust balance device
US6123798A (en) 1998-05-06 2000-09-26 Caliper Technologies Corp. Methods of fabricating polymeric structures incorporating microscale fluidic elements
US6071269A (en) 1998-05-13 2000-06-06 Medisystems Technology Corporation Blood set and chamber
DE19821534C1 (en) 1998-05-14 1999-08-19 Braun Melsungen Ag Blood cleaning machine
DE19823811C1 (en) 1998-05-28 1999-11-25 Fresenius Medical Care De Gmbh Safety device for a blood treatment device and method for increasing the safety of a blood treatment device
DE19823836C2 (en) 1998-05-28 2000-05-04 Fresenius Medical Care De Gmbh Device and method for non-contact measurement of the conductivity of a liquid in a flow channel
DE19824015C1 (en) 1998-05-29 1999-08-26 Fresenius Ag Method of cleaning haemodialysis circuit
SE525639C2 (en) 1998-06-04 2005-03-22 Thore Falkvall Determination of slag products in dialysis fluid by means of optical sensor
US6142008A (en) 1998-06-12 2000-11-07 Abbott Laboratories Air bubble sensor
DE19827473C1 (en) 1998-06-19 1999-08-26 Sartorius Gmbh Cross flow filter cartridge suiting diverse range of medical, industrial and laboratory applications
SE513838C2 (en) * 1998-06-25 2000-11-13 Gambro Lundia Ab Method and apparatus for calibrating sensing means in a system with a flowing fluid
DE19828651C2 (en) 1998-06-26 2000-07-13 Fresenius Medical Care De Gmbh Connector element with closure part for medical technology
US6323662B2 (en) 1998-06-26 2001-11-27 B. Braun Melsungen Ag Device for the precise measurement of magnitudes and method of verification of correct functioning of the device
DE29811529U1 (en) 1998-06-27 1999-11-25 Braun Melsungen Ag Filters for medical liquids
US6041801A (en) 1998-07-01 2000-03-28 Deka Products Limited Partnership System and method for measuring when fluid has stopped flowing within a line
US6343614B1 (en) 1998-07-01 2002-02-05 Deka Products Limited Partnership System for measuring change in fluid flow rate within a line
US6616909B1 (en) 1998-07-27 2003-09-09 Battelle Memorial Institute Method and apparatus for obtaining enhanced production rate of thermal chemical reactions
FR2781380B1 (en) 1998-07-27 2000-09-15 Braun Celsa Sa RING FOR CONNECTING A DEFORMABLE FLEXIBLE TUBE AND A CRUSH-RESISTANT ROD, AND MEDICAL ASSEMBLY PROVIDED WITH SUCH A RING
DE69800630T2 (en) 1998-07-29 2001-08-23 Agilent Technologies Inc Chip for electrophoretic separation of molecules and method for using the same
US6331252B1 (en) 1998-07-31 2001-12-18 Baxter International Inc. Methods for priming a blood compartment of a hemodialyzer
US6357332B1 (en) 1998-08-06 2002-03-19 Thew Regents Of The University Of California Process for making metallic/intermetallic composite laminate materian and materials so produced especially for use in lightweight armor
US6793831B1 (en) * 1998-08-06 2004-09-21 State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Microlamination method for making devices
US6044691A (en) 1998-08-26 2000-04-04 Aksys, Ltd. Blood tubing set integrity tests for extracorporeal circuits
US6121539A (en) 1998-08-27 2000-09-19 International Business Machines Corporation Thermoelectric devices and methods for making the same
SE513522C2 (en) 1998-09-10 2000-09-25 Gambro Ab Device for monitoring a fluid tube
WO2000016873A1 (en) 1998-09-18 2000-03-30 Rockwell Medical Technologies, Inc. Method and apparatus for preparing liquid dialysate
US6050278A (en) 1998-09-24 2000-04-18 Minntech Corporation Dialyzer precleaning system
US6575927B1 (en) 1998-09-25 2003-06-10 The Regents Of The University Of Michigan System and method for determining blood flow rate in a vessel
US6117115A (en) 1998-10-12 2000-09-12 B. Braun Medical, Inc. Medical tubing slide clamp device for determining proper tubing size and functional characteristics
US6064797A (en) 1998-10-12 2000-05-16 B. Braun Medical, Inc. Volumetric flow equalizing drive control wheel
CA2346814A1 (en) 1998-10-16 2000-04-27 Mission Medical, Inc. Blood processing system
US6148635A (en) 1998-10-19 2000-11-21 The Board Of Trustees Of The University Of Illinois Active compressor vapor compression cycle integrated heat transfer device
US7670491B2 (en) 1998-10-20 2010-03-02 Advanced Renal Technologies Buffered compositions for dialysis
DE19848235C1 (en) 1998-10-20 2000-03-16 Fresenius Medical Care De Gmbh Method for monitoring supply to vessel and extra-corporeal blood treatment device for monitoring supply to vessel; inputs blood circulation pressure to computer to calculate values to identify errors in supply during dialysis
US6726647B1 (en) 1998-10-23 2004-04-27 Gambro Ab Method and device for measuring access flow
DE19849787C1 (en) 1998-10-28 2000-02-24 Fresenius Medical Care De Gmbh Dialysis machine includes distributed operational and auxiliary computers with bus interconnections, sensors and actuators in high-integrity redundant architecture safeguarding life-critical systems
AU1334600A (en) 1998-11-02 2000-05-22 Lifestream International, Inc. Cardioplegia heat exchanger
DE19852557C2 (en) 1998-11-13 2002-11-07 Fresenius Medical Care De Gmbh closure element
US6223130B1 (en) 1998-11-16 2001-04-24 Deka Products Limited Partnership Apparatus and method for detection of a leak in a membrane of a fluid flow control system
DE19852982C1 (en) 1998-11-17 2000-03-16 Braun Melsungen Ag Cartridge holder for dialysis machine has lower cheek with outlet connection and upper cheek with inflow connection, with cartridge being insertable between cheeks
US6383158B1 (en) 1998-12-01 2002-05-07 Dsu Medical Corporation Dialysis pressure monitoring with clot suppression
DE60043476D1 (en) 1999-01-12 2010-01-21 Gambro Ind Sas Device for dialysis with heating of the blood
US7316780B1 (en) 1999-01-29 2008-01-08 Pall Corporation Range separation devices and processes
DE29903286U1 (en) 1999-02-24 2000-08-10 Braun Melsungen Ag Catheter coupling
US6334301B1 (en) 1999-02-25 2002-01-01 Vacco Industries, Inc. Assembly of etched sheets forming a fluidic module
US6254567B1 (en) 1999-02-26 2001-07-03 Nxstage Medical, Inc. Flow-through peritoneal dialysis systems and methods with on-line dialysis solution regeneration
US6488842B2 (en) 1999-02-26 2002-12-03 Tadayoshi Nagaoka Filtering device
US6749814B1 (en) 1999-03-03 2004-06-15 Symyx Technologies, Inc. Chemical processing microsystems comprising parallel flow microreactors and methods for using same
US6202312B1 (en) 1999-03-08 2001-03-20 Levelite Technology, Inc. Laser tool for generating perpendicular lines of light on floor
US6192596B1 (en) 1999-03-08 2001-02-27 Battelle Memorial Institute Active microchannel fluid processing unit and method of making
KR20020010132A (en) 1999-03-30 2002-02-02 아스케토르프 괴단 Method and apparatus for sterilising a heat sensitive fluid
SE9903331D0 (en) 1999-09-16 1999-09-16 Gambro Lundia Ab Method and apparatus for sterilizing a heat sensitive fluid
DE19917197C1 (en) 1999-04-16 2000-07-27 Fresenius Medical Care De Gmbh Method to determine blood flow in vessel entrance of haemodialysis unit; involves measuring arterial and venous pressures when vessel entrance is open to allow blood flow and closed to prevent blood flow
DE19925297C1 (en) 1999-06-02 2000-07-13 Braun Melsungen Ag Dialysis machine filter cartridge holder uses radial tensioner elements to seal onto cartridge connections when positioned using keyhole holder connections taking cartridge connection grooves.
JP2003501639A (en) 1999-06-03 2003-01-14 ユニバーシティ オブ ワシントン Microfluidic devices for transverse and isoelectric focusing
ATE306312T1 (en) 1999-06-08 2005-10-15 Nitto Denko Corp MEMBRANE MODULE FOR SEPARATING LIQUIDS AND METHOD FOR PRODUCING IT
US6616877B2 (en) 1999-06-10 2003-09-09 Nicholas H. Danna Resilient article and method of manufacturing same using recycled material
US6530252B1 (en) * 1999-06-21 2003-03-11 Aida Engineering Co., Ltd. Hydroforming method and hydroforming device
US6322551B1 (en) 1999-07-09 2001-11-27 Gambro Inc. Break-apart tubing connectors for use in dialysis blood tubing sets
US6905479B1 (en) 1999-07-20 2005-06-14 Deka Products Limited Partnership Pumping cartridge having an integrated filter and method for filtering a fluid with the cartridge
US6416293B1 (en) 1999-07-20 2002-07-09 Deka Products Limited Partnership Pumping cartridge including a bypass valve and method for directing flow in a pumping cartridge
US6382923B1 (en) 1999-07-20 2002-05-07 Deka Products Ltd. Partnership Pump chamber having at least one spacer for inhibiting the pumping of a gas
US6877713B1 (en) 1999-07-20 2005-04-12 Deka Products Limited Partnership Tube occluder and method for occluding collapsible tubes
US6302653B1 (en) 1999-07-20 2001-10-16 Deka Products Limited Partnership Methods and systems for detecting the presence of a gas in a pump and preventing a gas from being pumped from a pump
US6604908B1 (en) 1999-07-20 2003-08-12 Deka Products Limited Partnership Methods and systems for pulsed delivery of fluids from a pump
KR100677860B1 (en) 1999-07-23 2007-02-05 보드 오브 트러스티스 오브 유니버스티 오브 일리노이즈 Microfabricated Devices and Method of Manufacturing The Same
ITTO990148U1 (en) 1999-07-30 2001-01-30 Hospal Dasco Spa FILTRATION UNIT FOR A DIALYSIS MACHINE.
IT1310659B1 (en) * 1999-07-30 2002-02-19 Hospal Dasco Spa METHOD OF CONTROL OF A DIALYSIS MACHINE WITH A SEMI-PERMANENT FILTER.
US6526357B1 (en) 1999-08-09 2003-02-25 Gambro, Inc. Associated parameter measuring and/or monitoring such as in the evaluation of pressure differences
DE19940624C5 (en) 1999-08-27 2006-11-16 Fresenius Medical Care Deutschland Gmbh A safety device for a blood treatment device and method for increasing the safety of a blood treatment device
US6309673B1 (en) 1999-09-10 2001-10-30 Baxter International Inc. Bicarbonate-based solution in two parts for peritoneal dialysis or substitution in continuous renal replacement therapy
US20040215129A1 (en) 1999-09-16 2004-10-28 Gambro Ab Method and cycler for the administration of a peritoneal dialysis fluid
DE19945604A1 (en) 1999-09-23 2003-08-07 Aclara Biosciences Inc Method of joining workpieces made of plastic and its use in microstructure and nanostructure technology
US6355161B1 (en) 1999-10-12 2002-03-12 Aksys, Ltd. Bottles for dialysis machines and method for automatically identifying such bottles
CN100371595C (en) 1999-11-12 2008-02-27 日机装株式会社 Diaphragm type reciprocative pump
US6251279B1 (en) 1999-12-09 2001-06-26 Dialysis Systems, Inc. Heat disinfection of a water supply
DE19960226C1 (en) 1999-12-14 2001-05-10 Fresenius Ag Connection system, for two or more sterile systems, comprises male and female connectors with threshold breakage points inside the fluid supply system.
DE19961257C2 (en) 1999-12-18 2002-12-19 Inst Mikrotechnik Mainz Gmbh micromixer
US6346084B1 (en) 2000-01-10 2002-02-12 Dsu Medical Corporation Measuring vascular access pressure
EP1259887A4 (en) 2000-01-25 2003-08-13 Vistaprint Usa Inc Managing print jobs
EP1120150B1 (en) 2000-01-26 2006-02-08 ENVIRO-CHEMIE GmbH Membrane separation apparatus
US6537506B1 (en) 2000-02-03 2003-03-25 Cellular Process Chemistry, Inc. Miniaturized reaction apparatus
US6415860B1 (en) 2000-02-09 2002-07-09 Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College Crossflow micro heat exchanger
WO2001064262A2 (en) 2000-02-28 2001-09-07 Valemont Participation Corp. Method and system for hemodialysis for use in a non-clinical environment
DE60108482T2 (en) 2000-03-07 2006-02-16 Symyx Technologies, Inc., Santa Clara PROCESS OPTIMIZING REACTOR WITH PARALLEL FLOW
DE10011724C1 (en) 2000-03-10 2001-04-26 Fresenius Medical Care De Gmbh Connector for sterile packed fluid systems, such as kidney dialysis fluid flow system, comprises connections at both ends, each having inner slides with limit stops
DE10013665C2 (en) 2000-03-20 2003-11-06 Fresenius Medical Care De Gmbh Medical device with double communication bus
DE20005691U1 (en) 2000-03-28 2000-06-29 Braun Melsungen Ag Reusable tap
IT1320024B1 (en) * 2000-04-07 2003-11-12 Gambro Dasco Spa METHOD FOR ADJUSTING THE INFUSION IN A DIALYSIS MACHINE AND DIALYSIS MACHINE FOR THE APPLICATION OF THE MENTIONED METHOD.
US7776021B2 (en) 2000-04-28 2010-08-17 The Charles Stark Draper Laboratory Micromachined bilayer unit for filtration of small molecules
US6544229B1 (en) 2000-05-01 2003-04-08 Baxter International Inc Linearly motile infusion pump
US7168334B1 (en) 2000-05-30 2007-01-30 Gambro Lundia Ab Arrangement for measuring a property of a fluid present in a tube
AU2002213592A1 (en) 2000-06-05 2001-12-17 The State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of The University Of Oregon Mutiscale transport apparatus and methods
US7125540B1 (en) 2000-06-06 2006-10-24 Battelle Memorial Institute Microsystem process networks
US6666909B1 (en) 2000-06-06 2003-12-23 Battelle Memorial Institute Microsystem capillary separations
WO2001095955A1 (en) 2000-06-15 2001-12-20 Jms Co., Ltd. Automatic dialyzer and dialyzing method
US6503062B1 (en) 2000-07-10 2003-01-07 Deka Products Limited Partnership Method for regulating fluid pump pressure
IT1320784B1 (en) 2000-07-21 2003-12-10 Gambro Dasco Spa METHOD OF SETTING A DIALYTIC TREATMENT IN A PERDIALYSIS MACHINE.
IT1320247B1 (en) 2000-07-21 2003-11-26 Gambro Dasco Spa METHOD AND DEVICE FOR SETTING A DIALYTIC TREATMENT IN A DIALYSIS MACHINE.
AU2001281076A1 (en) 2000-08-07 2002-02-18 Nanostream, Inc. Fluidic mixer in microfluidic system
US6913877B1 (en) 2000-09-11 2005-07-05 State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Methods for detecting bioactive compounds
DE10046651A1 (en) 2000-09-20 2002-04-04 Fresenius Medical Care De Gmbh Valve
IT1320264B1 (en) 2000-09-29 2003-11-26 Gambro Dasco Spa DIALYSIS EQUIPMENT AND METHOD OF VERIFICATION OF THE FUNCTIONALITY OF A DIALYSIS EQUIPMENT.
EP1322949A2 (en) 2000-10-05 2003-07-02 E.I. Du Pont De Nemours And Company Polymeric microfabricated fluidic device suitable for ultraviolet detection
DE10049393A1 (en) 2000-10-05 2002-04-25 Braun Melsungen Ag Extracorporeal blood treatment system
US6623860B2 (en) 2000-10-10 2003-09-23 Aclara Biosciences, Inc. Multilevel flow structures
DE10051943B4 (en) 2000-10-19 2015-01-15 Fresenius Medical Care Deutschland Gmbh Method and device for pulse wave transit time determination and extracorporeal blood treatment device with such a device
JP2002127492A (en) 2000-10-27 2002-05-08 Ricoh Co Ltd Optical write unit and apparatus for inspecting optical write unit
US6607644B1 (en) 2000-10-31 2003-08-19 Agilent Technolgoies, Inc. Microanalytical device containing a membrane for molecular identification
US6585675B1 (en) 2000-11-02 2003-07-01 Chf Solutions, Inc. Method and apparatus for blood withdrawal and infusion using a pressure controller
AU2002225716A1 (en) 2000-11-10 2002-05-21 Gentex Corporation Visibly transparent dyes for through-transmission laser welding
US20020108859A1 (en) 2000-11-13 2002-08-15 Genoptix Methods for modifying interaction between dielectric particles and surfaces
US6744038B2 (en) 2000-11-13 2004-06-01 Genoptix, Inc. Methods of separating particles using an optical gradient
JP2002143298A (en) 2000-11-16 2002-05-21 Toray Ind Inc Blood treatment apparatus
US7378280B2 (en) 2000-11-16 2008-05-27 California Institute Of Technology Apparatus and methods for conducting assays and high throughput screening
US7033498B2 (en) 2000-11-28 2006-04-25 Renal Solutions, Inc. Cartridges useful in cleaning dialysis solutions
US6672502B1 (en) * 2000-11-28 2004-01-06 The State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Method for making devices having intermetallic structures and intermetallic devices made thereby
KR100382523B1 (en) 2000-12-01 2003-05-09 엘지전자 주식회사 a tube structure of a micro-multi channel heat exchanger
FR2817754B1 (en) 2000-12-08 2003-09-12 Hospal Internat Marketing Man DEVICE FOR PRESSURE MEASUREMENT COMPRISING A MEMBRANE MOLDED IN A CASSETTE
FR2817756B1 (en) 2000-12-08 2008-10-31 Hospal Internat Marketing Man DEVICE FOR PRESSURE MEASUREMENT COMPRISING A MOTORIZED EFFORT SENSOR
FR2817755B1 (en) 2000-12-08 2003-01-24 Hospal Internat Marketing Man DEVICE FOR MEASURING NEGATIVE PRESSURES IN AN EXTRACORPOREAL BLOOD CIRCUIT
US6936031B2 (en) 2000-12-12 2005-08-30 Gambro Dasco S.P.A. Site for access to the inside of a channel, and corresponding cannula
WO2002053209A1 (en) 2000-12-27 2002-07-11 Philips Japan, Ltd. Biological information and blood treating device information control system, biological information and blood treating device information control device, and biological information and blood treating device information control method
US6592558B2 (en) 2000-12-28 2003-07-15 Baxter International Inc. Clamp device, method and system for exchanging a solution
DE10103048A1 (en) 2001-01-24 2002-07-25 Braun Melsungen Ag Therapy apparatus for extracorporeal blood cleaning has blood pressure measuring device, and replaces blood pressure measurements with hypothetical values at some time points
US20020108869A1 (en) 2001-02-09 2002-08-15 Alex Savtchenko Device and technique for multiple channel patch clamp recordings
US6432695B1 (en) 2001-02-16 2002-08-13 Institute Of Microelectronics Miniaturized thermal cycler
EP1236479B1 (en) 2001-02-19 2005-05-04 Nipro Corporation Dialyzing system
NL1017570C2 (en) 2001-03-12 2002-09-13 Stichting Hogeschool Van Utrec Blood treatment device.
EP1383575A4 (en) 2001-03-28 2010-01-20 Televital Inc System and method for real-time monitoring, assessment, analysis, retrieval, and storage of physiological data over a wide area network
US6572641B2 (en) 2001-04-09 2003-06-03 Nxstage Medical, Inc. Devices for warming fluid and methods of use
US6773412B2 (en) 2001-04-13 2004-08-10 Chf Solutions, Inc. User interface for blood treatment device
DE10123093A1 (en) 2001-05-07 2002-11-21 Inst Mikrotechnik Mainz Gmbh Method and static micromixer for mixing at least two fluids
US6863867B2 (en) 2001-05-07 2005-03-08 Uop Llc Apparatus for mixing and reacting at least two fluids
WO2002094440A2 (en) 2001-05-22 2002-11-28 Northeastern University Microchip integrated multichannel electroosmotic pumping system
US7771379B2 (en) 2001-05-24 2010-08-10 Nxstage Medical, Inc. Functional isolation of upgradeable components to reduce risk in medical treatment devices
JP3942945B2 (en) 2001-05-31 2007-07-11 株式会社神戸製鋼所 Injection compression molding apparatus, injection compression molding method and injection compression molded product by the method
ITBO20010355A1 (en) 2001-06-05 2002-12-05 Gambro Dasco Spa METHOD AND DEVICE TO DETECT BLOOD PRESSURE IN A CIRCUIT OF A DIALYSIS MACHINE IN A NON-INTRUSIVE WAY
ITBO20010354A1 (en) 2001-06-05 2002-12-05 Gambro Dasco Spa METHOD OF FILLING AND WASHING OF A FILTER OF A DIALYSIS MACHINE
JP2005516171A (en) 2001-06-06 2005-06-02 バッテル・メモリアル・インスティチュート Fluid processing apparatus and method
US6981522B2 (en) 2001-06-07 2006-01-03 Nanostream, Inc. Microfluidic devices with distributing inputs
US6685664B2 (en) 2001-06-08 2004-02-03 Chf Solutions, Inc. Method and apparatus for ultrafiltration utilizing a long peripheral access venous cannula for blood withdrawal
US7014705B2 (en) 2001-06-08 2006-03-21 Takeda San Diego, Inc. Microfluidic device with diffusion between adjacent lumens
US6797056B2 (en) 2001-06-08 2004-09-28 Syrrx, Inc. Microfluidic method employing delivery of plural different fluids to same lumen
US7211442B2 (en) 2001-06-20 2007-05-01 Cytonome, Inc. Microfluidic system including a virtual wall fluid interface port for interfacing fluids with the microfluidic system
US7147615B2 (en) 2001-06-22 2006-12-12 Baxter International Inc. Needle dislodgement detection
US6477058B1 (en) 2001-06-28 2002-11-05 Hewlett-Packard Company Integrated circuit device package including multiple stacked components
ITMI20011395A1 (en) 2001-06-29 2002-12-29 Gambro Dasco Spa METHOD AND DEVICE FOR DETECTION OF VENOUS NEEDLE FROM A PATIENT DURING AN EXTRACORPOREAL BLOOD TREATMENT IN A MACHINE
US6572576B2 (en) 2001-07-07 2003-06-03 Nxstage Medical, Inc. Method and apparatus for leak detection in a fluid line
US6649063B2 (en) 2001-07-12 2003-11-18 Nxstage Medical, Inc. Method for performing renal replacement therapy including producing sterile replacement fluid in a renal replacement therapy unit
US20030010718A1 (en) 2001-07-12 2003-01-16 Nxstage Medical, Inc. Hemodilution cap and methods of use in blood-processing procedures
US20030010717A1 (en) 2001-07-13 2003-01-16 Nx Stage Medical, Inc. Systems and methods for handling air and/or flushing fluids in a fluid circuit
US6743193B2 (en) 2001-07-17 2004-06-01 Nx Stage Medical, Inc. Hermetic flow selector valve
US6775577B2 (en) 2001-07-18 2004-08-10 Fresenius Usa, Inc. Method and system for controlling a medical device
JP4225198B2 (en) 2001-08-01 2009-02-18 株式会社ジェイ・エム・エス Blood purification device that can improve purification efficiency
WO2003016075A1 (en) 2001-08-15 2003-02-27 Florida State University Method of manufacturing and design of microreactors, including microanalytical and separation devices
DE10143137C1 (en) 2001-09-03 2003-04-17 Fresenius Medical Care De Gmbh Measuring device and method for determining parameters of medical liquids and method for calibrating such a device
US20030047288A1 (en) 2001-09-12 2003-03-13 Thaddeus Soberay Low profile vacuum press
WO2003023366A2 (en) 2001-09-12 2003-03-20 The State Of Oregon, Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Method and system for classifying a scenario
EP1427515B1 (en) 2001-09-20 2007-08-08 Millipore Corporation Process for making a fluid processing module
US6868309B1 (en) 2001-09-24 2005-03-15 Aksys, Ltd. Dialysis machine with symmetric multi-processing (SMP) control system and method of operation
DE10147903C1 (en) 2001-09-28 2003-04-17 Fresenius Medical Care De Gmbh Membrane device for dialysis and / or filtration and housing jacket of such a membrane device
SE523610C2 (en) 2001-10-02 2004-05-04 Gambro Lundia Ab Method of controlling dialysis device
US20030156991A1 (en) 2001-10-23 2003-08-21 William Marsh Rice University Optomechanically-responsive materials for use as light-activated actuators and valves
US6878283B2 (en) 2001-11-28 2005-04-12 Renal Solutions, Inc. Filter cartridge assemblies and methods for filtering fluids
DE10158924B4 (en) 2001-11-30 2006-04-20 Bruker Daltonik Gmbh Pulser for time-of-flight mass spectrometers with orthogonal ion injection
ITTO20011222A1 (en) 2001-12-27 2003-06-27 Gambro Lundia Ab BLOOD FLOW CONTROL EQUIPMENT IN A BLOOD CIRCUIT-EXTRA-BODY.
US20030128125A1 (en) 2002-01-04 2003-07-10 Burbank Jeffrey H. Method and apparatus for machine error detection by combining multiple sensor inputs
US7040142B2 (en) 2002-01-04 2006-05-09 Nxstage Medical, Inc. Method and apparatus for leak detection in blood circuits combining external fluid detection and air infiltration detection
DE10201109C1 (en) 2002-01-15 2003-01-23 Fresenius Medical Care De Gmbh Detecting leak in liquid system of blood treatment system involves deriving leakage rate from change in pressure in defined intervals, driving leakage volume from leakage rate
US6695807B2 (en) 2002-01-18 2004-02-24 Dsu Medical, Inc. Blood flow reversing system
US7918993B2 (en) 2002-01-24 2011-04-05 James Harraway Portable dialysis machine
US7708714B2 (en) 2002-02-11 2010-05-04 Baxter International Inc. Dialysis connector with retention and feedback features
US6814859B2 (en) 2002-02-13 2004-11-09 Nanostream, Inc. Frit material and bonding method for microfluidic separation devices
US6852231B2 (en) 2002-02-15 2005-02-08 Denco, Inc. Spin-hemodialysis assembly and method
ITMI20020359A1 (en) 2002-02-22 2003-08-22 Gambro Lundia Ab METHOD OF CONTROL OF THE OPERATION OF A FLOW INTERDICTION BODY AND A FLOW STOP DEVICE FOR AN EXTRA-BODY CIRCUIT
KR100450818B1 (en) 2002-03-09 2004-10-01 삼성전자주식회사 Multi chamber PCR chip
ES2402057T3 (en) 2002-03-11 2013-04-26 Fresenius Medical Care Deutschland Gmbh Connector, container with such connector and fluid preparation device with a coupling connector for such container
DE10212247C1 (en) 2002-03-19 2003-12-18 Fresenius Medical Care De Gmbh Method for determining a treatment parameter on a hemofiltration device and hemofiltration device for using the method
US7312085B2 (en) 2002-04-01 2007-12-25 Fluidigm Corporation Microfluidic particle-analysis systems
US7052480B2 (en) 2002-04-10 2006-05-30 Baxter International Inc. Access disconnection systems and methods
US7022098B2 (en) 2002-04-10 2006-04-04 Baxter International Inc. Access disconnection systems and methods
ITMI20020819A1 (en) 2002-04-18 2003-10-20 Gambro Lundia Ab CONNECTION ELEMENT AND CONNECTION DEVICE FOR MEDICAL USE PIPES
DE20206474U1 (en) 2002-04-24 2003-09-04 Braun Melsungen Ag Pressure sensor for infusion hose pumps
US7021148B2 (en) 2002-04-30 2006-04-04 Baxter International Inc. Apparatus and method for sealing pressure sensor membranes
US7455771B2 (en) 2002-05-14 2008-11-25 Hepa Wash Gmbh Means for removing protein-bound substances
US6731216B2 (en) 2002-05-20 2004-05-04 B. Braun Medical, Inc. Proper tubing installation testing method and apparatus for a peristaltic pump
US7033539B2 (en) 2002-05-24 2006-04-25 Baxter International Inc. Graphical user interface for automated dialysis system
US7153286B2 (en) 2002-05-24 2006-12-26 Baxter International Inc. Automated dialysis system
US6869538B2 (en) 2002-05-24 2005-03-22 Baxter International, Inc. Method and apparatus for controlling a medical fluid heater
US7115228B2 (en) 2002-05-24 2006-10-03 Baxter International Inc. One-piece tip protector and organizer
US6929751B2 (en) 2002-05-24 2005-08-16 Baxter International Inc. Vented medical fluid tip protector methods
US6892781B2 (en) 2002-05-28 2005-05-17 International Business Machines Corporation Method and apparatus for application of pressure to a workpiece by thermal expansion
WO2003103533A2 (en) 2002-06-06 2003-12-18 Nxstage Medical, Inc. Last-chance quality check and/or air/pyrogen filter for infusion systems
US7063512B2 (en) 2002-06-21 2006-06-20 Nikkiso Company, Ltd. Pump stabilizer and method
DE20209663U1 (en) 2002-06-21 2003-10-23 Braun Melsungen Ag infusion pump
ATE426420T1 (en) 2002-06-24 2009-04-15 Gambro Lundia Ab GAS SEPARATION DEVICE
TWI220046B (en) 2002-07-04 2004-08-01 Au Optronics Corp Driving circuit of display
DE20210502U1 (en) 2002-07-06 2003-11-20 Braun Melsungen Ag Peristaltic peristaltic pump
DE10230413B4 (en) 2002-07-06 2004-07-22 Fresenius Medical Care Deutschland Gmbh Device for determining the blood volume during extracorporeal blood treatment
JP3730601B2 (en) 2002-07-11 2006-01-05 日機装株式会社 Self-priming vortex pump
US7122149B2 (en) 2002-07-12 2006-10-17 Applied Research Associates, Inc. Apparatus and method for continuous depyrogenation and production of sterile water for injection
JP4129866B2 (en) 2002-07-18 2008-08-06 日機装株式会社 Blood processing equipment
JP4129867B2 (en) 2002-07-18 2008-08-06 日機装株式会社 Hematocrit sensor
US7238164B2 (en) 2002-07-19 2007-07-03 Baxter International Inc. Systems, methods and apparatuses for pumping cassette-based therapies
US20040016700A1 (en) 2002-07-23 2004-01-29 Benjamin Kellam System and a method for determining integrity of a dialyzer
US6796172B2 (en) 2002-07-31 2004-09-28 Hewlett-Packard Development Company, L.P. Flow sensor
US6746514B2 (en) 2002-08-08 2004-06-08 Baxter International Inc. Gas venting device and a system and method for venting a gas from a liquid delivery system
US7163531B2 (en) 2002-08-19 2007-01-16 Baxter International, Inc. User-friendly catheter connection adapters for optimized connection to multiple lumen catheters
US20040035462A1 (en) 2002-08-20 2004-02-26 Mccarty Michael W. Integral control valve and actuator
US20040035452A1 (en) 2002-08-22 2004-02-26 Joen-Shen Ma Umbrella having worm-gear based driving system
ATE298595T1 (en) 2002-09-05 2005-07-15 Gambro Lundia Ab CONTROL FOR A BLOOD TREATMENT DEVICE
ITMI20021895A1 (en) 2002-09-06 2004-03-07 Gambro Lundia Ab FLOW INTERCEPTION BODY.
US7094345B2 (en) 2002-09-09 2006-08-22 Cytonome, Inc. Implementation of microfluidic components, including molecular fractionation devices, in a microfluidic system
US6878271B2 (en) 2002-09-09 2005-04-12 Cytonome, Inc. Implementation of microfluidic components in a microfluidic system
JP4384044B2 (en) 2002-09-11 2009-12-16 フレゼニウス メディカル ケアー ドイチュラント ゲゼルシャフト ミット ベシュレンクテル ハフツング Blood treatment equipment
US7279134B2 (en) 2002-09-17 2007-10-09 Intel Corporation Microfluidic devices with porous membranes for molecular sieving, metering, and separations
US7112273B2 (en) 2002-09-27 2006-09-26 Nxstage Medical, Inc. Volumetric fluid balance control for extracorporeal blood treatment
US8182440B2 (en) 2002-09-27 2012-05-22 Baxter International Inc. Dialysis machine having combination display and handle
US20040157096A1 (en) 2002-10-07 2004-08-12 Peterson Richard B. Plug-compatible modular thermal management packages
US7115206B2 (en) 2002-10-15 2006-10-03 Gambro Lundia Ab Method for in-line preparation of liquid for an extracorporeal blood treatment apparatus
US7118920B2 (en) 2002-10-22 2006-10-10 Battelle Memorial Institute Multiphasic microchannel reactions
US6886929B2 (en) 2002-10-25 2005-05-03 Hewlett-Packard Development Company, L.P. Techniques for improving pressure sensor shock robustness in fluid containment devices
US6652627B1 (en) 2002-10-30 2003-11-25 Velocys, Inc. Process for separating a fluid component from a fluid mixture using microchannel process technology
WO2004039436A1 (en) 2002-10-30 2004-05-13 Gambro Lundia Ab A method and an apparatus for determining the efficiency of dialysis
US7932098B2 (en) 2002-10-31 2011-04-26 Hewlett-Packard Development Company, L.P. Microfluidic system utilizing thin-film layers to route fluid
US7264723B2 (en) 2002-11-01 2007-09-04 Sandia Corporation Dialysis on microchips using thin porous polymer membranes
US6654660B1 (en) 2002-11-04 2003-11-25 Advanced Micro Devices, Inc. Controlling thermal expansion of mask substrates by scatterometry
US20040084371A1 (en) 2002-11-06 2004-05-06 Kellam Benjamin A. Dialysis system and method for automatically priming a dialyzer
US6989134B2 (en) 2002-11-27 2006-01-24 Velocys Inc. Microchannel apparatus, methods of making microchannel apparatus, and processes of conducting unit operations
ATE434454T1 (en) 2003-01-07 2009-07-15 Nxstage Medical Inc BATCH FILTRATION SYSTEM FOR PRODUCING A STERILE REPLACEMENT LIQUID FOR KIDNEY TREATMENTS
WO2004066121A2 (en) 2003-01-15 2004-08-05 Nxstage Medical Inc. Waste balancing for extracorporeal blood treatment systems
US8235931B2 (en) 2003-01-15 2012-08-07 Nxstage Medical, Inc. Waste balancing for extracorporeal blood treatment systems
DE10302691B3 (en) 2003-01-24 2004-04-29 Fresenius Medical Care Deutschland Gmbh Supplying dialysis device with dialyzing liquid involves adjusting dialyzing liquid rate so that defined residual quantity of concentrate or none remains in accommodation unit at end of treatment
EP2095835B1 (en) 2003-01-28 2013-04-03 Gambro Lundia AB Apparatus for monitoring a vascular access
US7223338B2 (en) 2003-02-07 2007-05-29 Gambro Lundia Ab Support element for an integrated module for blood treatment, an integrated module for blood treatment, and a manufacturing process for an integrated module for blood treatment
US7247146B2 (en) 2003-02-07 2007-07-24 Gambro Lundia Ab Support element for an integrated blood treatment module, integrated blood treatment module and extracorporeal blood treatment apparatus equipped with said integrated module
US7232418B2 (en) 2003-02-07 2007-06-19 Gambro Lundia Ab Support element, an integrated module for extracorporeal blood treatment comprising the support element, an apparatus for extracorporeal blood treatment equipped with the integrated module, and an assembly process for an integrated module for extracorporeal blood treatment
US7223336B2 (en) 2003-02-07 2007-05-29 Gambro Lundia Ab Integrated blood treatment module and extracorporeal blood treatment apparatus
WO2004076056A2 (en) 2003-02-26 2004-09-10 Lake Shore Cryotronics Inc. Microfluidic chemical reactor for the manufacture of chemically-produced nanoparticles
DE102004011264B4 (en) 2003-03-11 2014-03-27 B. Braun Medizintechnologie Gmbh dialysis Center
ATE510605T1 (en) 2003-03-14 2011-06-15 Univ Columbia SYSTEMS AND METHODS FOR BLOOD BASED THERAPY USING A MEMBRANELESS MICROFLUID EXCHANGE DEVICE
US7470265B2 (en) 2003-03-20 2008-12-30 Nxstage Medical, Inc. Dual access spike for infusate bags
US7175697B2 (en) 2003-03-21 2007-02-13 Gambro Lundia Ab Device for protecting medical apparatus
US6871838B2 (en) 2003-04-03 2005-03-29 B. Braun Medical Inc. Injection port valve
DE10317024A1 (en) 2003-04-11 2004-11-11 Fresenius Medical Care Deutschland Gmbh Blood treatment device
EP1466657B1 (en) 2003-04-11 2012-10-03 Gambro Lundia AB Filter device having more than one filtration compartment
US6986428B2 (en) 2003-05-14 2006-01-17 3M Innovative Properties Company Fluid separation membrane module
US6952963B2 (en) 2003-05-23 2005-10-11 Gambro Dasco S.P.A. Method for detecting a liquid level in a container in a circuit and a dialysis machine for actuating the method
WO2004105589A2 (en) 2003-05-28 2004-12-09 Hemocleanse Technologies, Llc Sorbent reactor for extracorporeal blood treatment systems, peritoneal dialysis systems, and other body fluid treatment systems
US7291123B2 (en) 2003-06-04 2007-11-06 Gambro Lundia Joint for fluid transport lines for medical use
JP4352775B2 (en) 2003-06-19 2009-10-28 株式会社ジェイ・エム・エス Hemodiafiltration machine
DE10328435B3 (en) 2003-06-25 2005-03-24 Fresenius Medical Care Deutschland Gmbh Device for extracorporeal blood treatment with a device for checking a sterile filter and method for checking a sterile filter of an extracorporeal blood treatment device
US7327443B2 (en) 2004-07-01 2008-02-05 Gambro Bct, Inc Stroboscopic LED light source for blood processing apparatus
US7191790B1 (en) 2003-07-04 2007-03-20 Scott Technologies, Inc. Quick connect pressure reducer/cylinder valve for self-contained breathing apparatus
US7289335B2 (en) 2003-07-08 2007-10-30 Hewlett-Packard Development Company, L.P. Force distributing spring element
ATE422938T1 (en) 2003-08-15 2009-03-15 Gambro Lundia Ab CONNECTING DEVICE AND METHOD FOR CONNECTING MEDICAL SUBSYSTEMS
US7559911B2 (en) 2003-09-05 2009-07-14 Gambro Lundia Ab Blood chamber for extracorporeal blood circuits and a process for manufacturing the blood chamber
US7354426B2 (en) 2003-09-12 2008-04-08 B. Braun Medical Inc. Flexible container with a flexible port and method for making the same
ITMO20030259A1 (en) 2003-09-25 2005-03-26 Gambro Lundia Ab USER INTERFACE FOR A TREATMENT MACHINE
US7029456B2 (en) 2003-10-15 2006-04-18 Baxter International Inc. Medical fluid therapy flow balancing and synchronization system
US20070029365A1 (en) * 2003-10-24 2007-02-08 Paul Brian K High volume microlamination production of devices
EP2368589B1 (en) 2003-10-28 2016-08-03 Baxter International Inc. Apparatuses for medical fluid systems
US7671974B2 (en) 2003-10-29 2010-03-02 Chf Solutions Inc. Cuvette apparatus and system for measuring optical properties of a liquid such as blood
US8038639B2 (en) 2004-11-04 2011-10-18 Baxter International Inc. Medical fluid system with flexible sheeting disposable unit
US8029454B2 (en) 2003-11-05 2011-10-04 Baxter International Inc. High convection home hemodialysis/hemofiltration and sorbent system
EP1691882B1 (en) 2003-11-07 2010-09-08 NxStage Medical, Inc. Apparatus for leak detection in blood processing systems
WO2005049113A1 (en) 2003-11-20 2005-06-02 Gambro Lundia Ab Method, apparatus and software program for measurement of a parameter relating to a heart-lung system of a mammal.
US7434411B2 (en) 2003-12-15 2008-10-14 Drost Kevin M Droplet desorption process and system
US7744553B2 (en) 2003-12-16 2010-06-29 Baxter International Inc. Medical fluid therapy flow control systems and methods
ES2427513T3 (en) 2003-12-18 2013-10-30 Gambro Lundia Ab Apparatus for determining a patient parameter or treatment or device during an extracorporeal blood treatment
US7152469B2 (en) 2004-01-13 2006-12-26 Baxter International Inc. Fluid flow sensor, method and system
SE0400330D0 (en) 2004-02-12 2004-02-12 Gambro Lundia Ab Pressure sensing
WO2005080901A1 (en) 2004-02-24 2005-09-01 Spec Co., Ltd Micro heat exchanger for fuel cell and manufacturing method thereof
US7507380B2 (en) 2004-03-19 2009-03-24 State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Microchemical nanofactories
ITMO20040086A1 (en) 2004-04-20 2004-07-20 Gambro Lundia Ab METHOD TO CHECK AN INFUSION DEVICE.
ITMO20040085A1 (en) 2004-04-20 2004-07-20 Gambro Lundia Ab INFUSION DEVICE FOR MEDICAL FLUIDS.
DE102004026561B4 (en) 2004-05-27 2007-02-22 Fresenius Medical Care Deutschland Gmbh Hemodialysis machine with emergency activator
US7520919B2 (en) 2004-06-22 2009-04-21 Gambro Lundia Ab Transducer-protector device for medical apparatus
US7968250B2 (en) 2004-06-25 2011-06-28 Ultracell Corporation Fuel cartridge connectivity
US7648792B2 (en) 2004-06-25 2010-01-19 Ultracell Corporation Disposable component on a fuel cartridge and for use with a portable fuel cell system
US7971449B2 (en) 2004-08-14 2011-07-05 State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Heat-activated heat-pump systems including integrated expander/compressor and regenerator
US7204277B2 (en) 2004-09-16 2007-04-17 B. Braun Medical Inc. By-pass line connector for compounding system
ITMO20040235A1 (en) 2004-09-17 2004-12-17 Gambro Lundia Ab SNAGUE ROOM FOR AN EXTRAXORPOREO CIRCUIT.
US20080193961A1 (en) 2004-09-29 2008-08-14 Easley Christopher J Localized Control of Thermal Properties on Microdevices and Applications Thereof
JP4094600B2 (en) 2004-10-06 2008-06-04 日機装株式会社 Blood purification equipment
US7955504B1 (en) 2004-10-06 2011-06-07 State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Microfluidic devices, particularly filtration devices comprising polymeric membranes, and method for their manufacture and use
CA2583360C (en) 2004-10-06 2016-01-26 State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Microtechnology-based dialyzer
US20060079698A1 (en) 2004-10-07 2006-04-13 Glenmark Pharmaceuticals Limited Process for the preparation of intermediates of trandolapril and use thereof for the preparation of trandolapril
JP4260092B2 (en) 2004-10-15 2009-04-30 日機装株式会社 Hemodialysis machine
WO2006049822A1 (en) 2004-10-28 2006-05-11 Nxstage Medical, Inc Blood treatment dialyzer/filter design to trap entrained air in a fluid circuit
EP1658869A1 (en) 2004-11-17 2006-05-24 Fresenius Medical Care Deutschland GmbH Membrane unit, housing of a pressure measuring unit and pressure measuring unit
US7615028B2 (en) 2004-12-03 2009-11-10 Chf Solutions Inc. Extracorporeal blood treatment and system having reversible blood pumps
JP2006187685A (en) 2004-12-28 2006-07-20 Fuji Xerox Co Ltd Microstructure, microreactor, heat exchanger and manufacturing method of microstructure
US7510545B2 (en) 2005-02-09 2009-03-31 B. Braun Medical Inc. Needleless access port valves
SE532147C2 (en) 2005-02-16 2009-11-03 Triomed Ab Portable dialysis system
DE102005008271A1 (en) 2005-02-22 2006-08-24 Behr Gmbh & Co. Kg Micro heat transfer device for cooling electronic components has channels open at top and bottom, and closed towards side surfaces
US7114701B2 (en) 2005-03-02 2006-10-03 B. Braun Medical, Inc. Needleless access port valves
ATE411061T1 (en) 2005-03-04 2008-10-15 Braun B Avitum Ag DIALYSIS MACHINE WITH MAINTENANCE INDICATOR
DE102005013418A1 (en) 2005-03-23 2006-09-28 B. Braun Medizintechnologie Gmbh Blood treatment device with alarm device
US7615035B2 (en) 2005-03-24 2009-11-10 B. Braun Medical Inc. Needleless access port valves
US7314061B2 (en) 2005-03-25 2008-01-01 B. Braun Medical Inc. Needleless access port valves
WO2006123197A1 (en) 2005-05-18 2006-11-23 Gambro Lundia Ab An apparatus for controlling blood flow in an extracorporeal circuit.
US20060266692A1 (en) 2005-05-25 2006-11-30 Innovative Micro Technology Microfabricated cross flow filter and method of manufacture
EP1902397B1 (en) 2005-06-09 2010-04-14 Gambro Lundia AB Medical apparatus and method for setting up a medical apparatus
JP5158830B2 (en) 2005-06-22 2013-03-06 日機装株式会社 Dialysis treatment device
US7337674B2 (en) 2005-06-29 2008-03-04 Nx Stage Medical, Inc. Pressure detector for fluid circuits
US7503908B2 (en) 2005-07-22 2009-03-17 B. Braun Medical Inc. Needleless access port valves
US7846489B2 (en) 2005-07-22 2010-12-07 State of Oregon acting by and though the State Board of Higher Education on behalf of Oregon State University Method and apparatus for chemical deposition
ES2397731T3 (en) 2005-08-25 2013-03-11 Gambro Lundia Ab Medical device
US7551043B2 (en) 2005-08-29 2009-06-23 The Regents Of The University Of Michigan Micromechanical structures having a capacitive transducer gap filled with a dielectric and method of making same
US20070125489A1 (en) 2005-09-08 2007-06-07 Oregon State University Microfluidic welded devices or components thereof and method for their manufacture
WO2007051118A2 (en) 2005-10-25 2007-05-03 Nxstage Medical, Inc Safety features for medical devices requiring assistance and supervision
US8092414B2 (en) 2005-11-09 2012-01-10 Nxstage Medical, Inc. Diaphragm pressure pod for medical fluids
US20070128707A1 (en) 2005-11-10 2007-06-07 Oregon State University Method for making metal oxides
US8679587B2 (en) 2005-11-29 2014-03-25 State of Oregon acting by and through the State Board of Higher Education action on Behalf of Oregon State University Solution deposition of inorganic materials and electronic devices made comprising the inorganic materials
US7794593B2 (en) 2005-11-30 2010-09-14 3M Innovative Properties Company Cross-flow membrane module
US7766075B2 (en) 2005-12-09 2010-08-03 The Boeing Company Microchannel heat exchanger
CN101395611A (en) 2006-01-06 2009-03-25 雷纳尔解决方法公司 Dialysis machine with transport mode
CN101394875B (en) 2006-01-06 2011-04-20 雷纳尔解决方法公司 Dual purpose acute and home treatment dialysis machine
US7713226B2 (en) 2006-01-06 2010-05-11 Renal Solutions, Inc. On demand and post-treatment delivery of saline to a dialysis patient
US8187250B2 (en) 2006-01-30 2012-05-29 The Regents Of The University Of California Peritoneal dialysis methods and apparatus
US7591449B2 (en) 2006-02-14 2009-09-22 B. Braun Medical Inc. Needleless access port valves
US8047405B2 (en) 2006-03-20 2011-11-01 Hewlett-Packard Development Company, L. P. Volumetric is fluid dispensing devices, systems, and methods
JP2007268490A (en) 2006-03-31 2007-10-18 Fujifilm Corp Micro device and catalytic reaction method using the same
DE102006016846B4 (en) 2006-04-07 2010-02-11 Nikkiso Medical Systems Gmbh Connecting element for releasably sealed connection of a fluid conduit system with a pressure transducer and pressure transducer for this purpose
US20080058697A1 (en) 2006-04-14 2008-03-06 Deka Products Limited Partnership Heat exchange systems, devices and methods
US20090306573A1 (en) 2006-04-27 2009-12-10 Johan Gagner Remote Controlled Medical Apparatus
EP2021438A4 (en) 2006-06-01 2010-09-29 Oregon State Microreactor process for making biodiesel
US20070295651A1 (en) 2006-06-26 2007-12-27 Martinez F Jesus Dialysis bag system
JP4984685B2 (en) 2006-06-30 2012-07-25 澁谷工業株式会社 Dialysis machine cleaning method
JP2008032395A (en) 2006-07-26 2008-02-14 Yokogawa Electric Corp Blood diagnosing method of artificial dialysis patient, and dialyzer
CN200951223Y (en) 2006-08-22 2007-09-26 重庆山外山科技有限公司 Flat-plate heating apparatus used blood purification
US8926550B2 (en) 2006-08-31 2015-01-06 Fresenius Medical Care Holdings, Inc. Data communication system for peritoneal dialysis machine
US20080108122A1 (en) * 2006-09-01 2008-05-08 State of Oregon acting by and through the State Board of Higher Education on behalf of Oregon Microchemical nanofactories
EP2407191B1 (en) 2006-10-30 2012-12-12 Gambro Lundia AB Air separator extracorporeal fluid treatment sets
WO2008057478A2 (en) 2006-11-03 2008-05-15 The Regents Of The University Of Michigan Method and system for determining volume flow in a blood conduit
US7656527B2 (en) 2006-11-07 2010-02-02 Deka Products Limited Partnership Method and apparatus for determining concentration using polarized light
WO2008065470A1 (en) 2006-12-01 2008-06-05 Gambro Lundia Ab Blood treatment apparatus
US7758082B2 (en) 2006-12-05 2010-07-20 Nxstage Medical, Inc. Fluid line connector safety device
US20080149563A1 (en) 2006-12-22 2008-06-26 Renal Solutions, Inc. Method of controlling dialysis using blood circulation times
US7661294B2 (en) 2007-09-21 2010-02-16 Cosense, Inc. Non-invasive multi-function sensor system
US8152751B2 (en) 2007-02-09 2012-04-10 Baxter International Inc. Acoustic access disconnection systems and methods
US8409441B2 (en) 2007-02-27 2013-04-02 Deka Products Limited Partnership Blood treatment systems and methods
US8562834B2 (en) 2007-02-27 2013-10-22 Deka Products Limited Partnership Modular assembly for a portable hemodialysis system
US8357298B2 (en) 2007-02-27 2013-01-22 Deka Products Limited Partnership Hemodialysis systems and methods
EP4309691A2 (en) 2007-02-27 2024-01-24 DEKA Products Limited Partnership Hemodialysis systems
US8210049B2 (en) 2007-03-15 2012-07-03 Nxstage Medical, Inc. Pressure measurement device
CA2682544C (en) 2007-03-30 2012-09-25 Jms Co., Ltd. Blood circuit, blood purification control apparatus, and priming method
US7775986B2 (en) 2007-04-10 2010-08-17 B. Braun Medizintechnologie Gmbh Therapy device with a time-variable blood regulation
DE102007024463A1 (en) 2007-05-25 2008-11-27 Fresenius Medical Care Deutschland Gmbh Method and device for checking the correct coupling of an adding device to a therapy device
CN101778646B (en) 2007-05-29 2013-01-30 弗雷塞尼斯医疗保健控股公司 Solutions, dialysates, and related methods
US8287724B2 (en) 2007-07-05 2012-10-16 Baxter International Inc. Dialysis fluid measurement systems using conductive contacts
US8512553B2 (en) 2007-07-05 2013-08-20 Baxter International Inc. Extracorporeal dialysis ready peritoneal dialysis machine
TW200907306A (en) 2007-08-07 2009-02-16 Promos Technologies Inc Liquid level sensing apparatus with self-diagnosis function and method for self-diagnosing thereof
US8622606B2 (en) 2007-09-25 2014-01-07 State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Micro-channels, micro-mixers, and micro-reactors
US7934912B2 (en) 2007-09-27 2011-05-03 Curlin Medical Inc Peristaltic pump assembly with cassette and mounting pin arrangement
US7892331B2 (en) 2007-10-01 2011-02-22 Baxter International Inc. Dialysis systems having air separation chambers with internal structures to enhance air removal
WO2009049235A2 (en) 2007-10-12 2009-04-16 Deka Products Limited Partnership Systems, devices and methods for cardiopulmonary treatment and procedures
US8123947B2 (en) 2007-10-22 2012-02-28 Baxter International Inc. Priming and air removal systems and methods for dialysis
US8114276B2 (en) 2007-10-24 2012-02-14 Baxter International Inc. Personal hemodialysis system
US9415150B2 (en) 2007-11-09 2016-08-16 Baxter Healthcare S.A. Balanced flow dialysis machine
ES2536403T3 (en) 2007-12-21 2015-05-25 Gambro Lundia Ab Disposable extracorporeal blood circuit and apparatus for extracorporeal blood treatment
CA2712945C (en) 2008-01-23 2017-06-06 Deka Products Limited Partnership Pump cassette and methods for use in medical treatment system using a plurality of fluid lines
US7892423B2 (en) 2008-02-14 2011-02-22 Baxter International Inc. Dialysis system including multi-heater power coordination
US20090211977A1 (en) 2008-02-27 2009-08-27 Oregon State University Through-plate microchannel transfer devices
US8414182B2 (en) 2008-03-28 2013-04-09 State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Micromixers for nanomaterial production
AU2008357106B2 (en) 2008-05-26 2013-02-07 Gambro Lundia Ab A hemodialysis or hemo(dia)filtration apparatus and a method for controlling a hemodialysis or hemo(dia)filtration apparatus
US8323503B2 (en) 2008-06-11 2012-12-04 Fresenius Medical Care Holdings, Inc. User interface processing device
CN102076368B (en) 2008-06-26 2014-09-03 甘布罗伦迪亚股份公司 Method and device for processing a time-dependent measurement signal
US8062513B2 (en) 2008-07-09 2011-11-22 Baxter International Inc. Dialysis system and machine having therapy prescription recall
US10265454B2 (en) 2008-07-25 2019-04-23 Baxter International Inc. Dialysis system with flow regulation device
US8192388B2 (en) 2008-07-25 2012-06-05 Baxter International Inc. System and method for detecting access disconnection
US20100051552A1 (en) 2008-08-28 2010-03-04 Baxter International Inc. In-line sensors for dialysis applications
FR2936713B1 (en) 2008-10-06 2012-01-27 Rd Nephrologie EXTRACORPOREAL BLOOD TREATMENT APPARATUS AND METHOD FOR MANAGING SUCH APPARATUS.
US8293113B2 (en) 2008-10-10 2012-10-23 Gambro Lundia Ab Heat exchanger and method for heat exchanging
WO2010062698A2 (en) 2008-10-30 2010-06-03 Xcorporeal, Inc. Modular, portable dialysis system
JP5294985B2 (en) 2008-12-16 2013-09-18 日機装株式会社 Blood purification apparatus and priming method thereof
WO2010085764A2 (en) 2009-01-23 2010-07-29 State Of Oregon Acting By Andthrough The State Board Of Higher Education On Behalf Of Oregon State University Method, apparatus, and compositions making anti-reflective coatings for substrates
US8506536B2 (en) 2009-02-20 2013-08-13 Nxstage Medical, Inc. Medical devices and methods for assisting in sub-scab access
CN102361657B (en) 2009-03-24 2015-12-16 甘布罗伦迪亚股份公司 dialysis machine
US8236599B2 (en) 2009-04-09 2012-08-07 State of Oregon acting by and through the State Board of Higher Education Solution-based process for making inorganic materials
US8587516B2 (en) 2009-04-24 2013-11-19 Baxter International Inc. User interface powered via an inductive coupling
US8190651B2 (en) 2009-06-15 2012-05-29 Nxstage Medical, Inc. System and method for identifying and pairing devices
WO2010147873A1 (en) 2009-06-17 2010-12-23 Ysi Incorporated Wipeable conductivity probe and method of making same
JP2012531256A (en) * 2009-06-24 2012-12-10 ステイト オブ オレゴン アクティング バイ アンド スルー ザ ステイト ボード オブ ハイヤー エデュケーション オン ビハーフ オブ オレゴン ステイト ユニバーシティー Microfluidic device for dialysis
US8801922B2 (en) * 2009-06-24 2014-08-12 State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Dialysis system
US8685251B2 (en) 2009-12-05 2014-04-01 Home Dialysis Plus, Ltd. Ultra-pasteurization for dialysis machines
US8460228B2 (en) 2009-10-27 2013-06-11 Nxstage Medical Inc. Methods, devices, and systems for parallel control of infusion device
WO2011056582A1 (en) 2009-10-27 2011-05-12 Nxstage Medical Inc. Fluid line safety device
US8632485B2 (en) 2009-11-05 2014-01-21 Fresenius Medical Care Holdings, Inc. Patient treatment and monitoring systems and methods
US8753515B2 (en) 2009-12-05 2014-06-17 Home Dialysis Plus, Ltd. Dialysis system with ultrafiltration control
WO2011069110A1 (en) 2009-12-05 2011-06-09 Home Dialysis Plus, Ltd. Modular dialysis system
AU2010338448B2 (en) 2009-12-17 2014-01-23 Gambro Lundia Ab System and method for monitoring the presence of blood
DE102009060330A1 (en) 2009-12-23 2011-06-30 Fresenius Medical Care Deutschland GmbH, 61352 Dialysis machine, in particular peritoneal dialysis machine
US8529491B2 (en) 2009-12-31 2013-09-10 Fresenius Medical Care Holdings, Inc. Detecting blood flow degradation
US9220832B2 (en) 2010-01-07 2015-12-29 Fresenius Medical Care Holdings, Inc. Dialysis systems and methods
US20110295175A1 (en) 2010-03-16 2011-12-01 Marv Enterprises Llc Sequential Extracoporeal Treatment of Bodily Fluids
US8506513B2 (en) 2010-04-20 2013-08-13 Sorin Group Italia S.R.L. Blood reservoir with ultrasonic volume sensor
US8501009B2 (en) 2010-06-07 2013-08-06 State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University Fluid purification system
US20120138533A1 (en) 2010-12-01 2012-06-07 Curtis James R Dialysis system control system with user interface
MX344664B (en) 2011-05-24 2017-01-04 Deka Products Lp Blood treatment systems and methods.
US20130056419A1 (en) 2011-08-30 2013-03-07 James R. Curtis Dialysate mixing and dialyzer control for dialysis system
WO2013052680A2 (en) 2011-10-07 2013-04-11 Home Dialysis Plus, Ltd. Heat exchange fluid purification for dialysis system
WO2015168280A1 (en) 2014-04-29 2015-11-05 Outset Medical, Inc. Dialysis system and methods
EP3193963B1 (en) 2014-09-18 2019-07-31 Outset Medical, Inc. Dialysis machine having a conductivity sensor for determining fluid properties

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4209391A (en) * 1978-11-06 1980-06-24 Cordis Dow Corp. Apparatus and method for automatically controlling hemodialysis at a pre-selected ultrafiltration rate
US6716356B2 (en) * 2000-01-11 2004-04-06 Nephros, Inc. Thermally enhanced dialysis/diafiltration system
US20140021111A1 (en) * 2006-06-05 2014-01-23 Baxter Healthcare S.A. Dynamic weight balancing of flow in kidney failure treatment systems

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9545469B2 (en) 2009-12-05 2017-01-17 Outset Medical, Inc. Dialysis system with ultrafiltration control
US11724013B2 (en) 2010-06-07 2023-08-15 Outset Medical, Inc. Fluid purification system
US9402945B2 (en) 2014-04-29 2016-08-02 Outset Medical, Inc. Dialysis system and methods
US9504777B2 (en) 2014-04-29 2016-11-29 Outset Medical, Inc. Dialysis system and methods
US9579440B2 (en) 2014-04-29 2017-02-28 Outset Medical, Inc. Dialysis system and methods
US11305040B2 (en) 2014-04-29 2022-04-19 Outset Medical, Inc. Dialysis system and methods
US9849226B2 (en) 2014-12-19 2017-12-26 Fenwal, Inc. Systems and methods for real time calibration of pump stroke volumes during a blood separation procedure
US11298446B2 (en) 2014-12-19 2022-04-12 Fenwal, Inc. Systems and methods for calibrating pump stroke volumes during a blood separation procedure
US10179896B2 (en) 2015-05-12 2019-01-15 Baker Group, LLP Method and system for a bioartificial organ
US11534537B2 (en) 2016-08-19 2022-12-27 Outset Medical, Inc. Peritoneal dialysis system and methods
US20200405941A1 (en) * 2018-03-26 2020-12-31 Nikkiso Company Limited Blood Purification Apparatus and Method of Trapping Bubbles Therein
US11951241B2 (en) 2022-11-28 2024-04-09 Outset Medical, Inc. Peritoneal dialysis system and methods

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US20160339162A1 (en) 2016-11-24

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