US20090107335A1 - Air trap for a medical infusion device - Google Patents

Abstract

An air trap for a blood circuit and method for removing air from blood in a dialysis unit. The air trap may include a blood inlet supply line, a blood outlet supply line, and a container having an approximately spherical internal wall, an inlet at a top end of the container connected to the blood inlet supply line, and an outlet at a bottom end of the container connected to the blood outlet supply line. The inlet may be offset from a vertical axis of the approximately spherical internal wall such that blood entering the container is directed to flow in a spiral-like path. The inlet port may be arranged to introduce blood into the container in a direction that is approximately tangential to the approximately spherical inner wall of the container and/or in a direction that is approximately perpendicular to the vertical axis of the container.

Description

FIELD OF INVENTION
• The present invention generally relates to hemodialysis and similar dialysis systems, e.g., systems able to treat blood or other bodily fluids extracorporeally.
BACKGROUND
• Many factors make hemodialysis inefficient, difficult, and expensive. These factors include the complexity of hemodialysis, the safety concerns related to hemodialysis, and the very large amount of dialysate needed for hemodialysis. Moreover, hemodialysis is typically performed in a dialysis center requiring skilled technicians. Therefore any increase in the ease and efficiency of the dialysis process could have an impact on treatment cost or patient outcome.
SUMMARY OF INVENTION
• Aspects of the invention generally relate to hemodialysis and similar dialysis systems. Illustrative embodiments described herein involve, in some cases, interrelated products, alternative solutions to a particular problem, and/or a plurality of different uses of one or more systems and/or articles. Although the various systems and methods described herein are described in relation to hemodialysis, it should be understood that the various systems and method described herein are applicable to other dialysis systems and/or in any extracorporeal system able to treat blood or other bodily fluids, such as hemofiltration, hemodiafiltration, etc.
• In one aspect of the invention, an enclosure for containing a portable hemodialysis unit is provided, where the hemodialysis unit includes suitable components for performing hemodialysis including a dialyzer, one or more pumps to circulate blood through the dialyzer, a source of dialysate, and one or more pumps to circulate the dialysate through the dialyzer. The enclosure may include a housing that supports the components of the hemodialysis unit and has a front panel at which blood circuit connections and dialysate fluidic connections are located. For example, the front panel may support blood line connections for patient blood access, connections for a reagent supply, dialyzer connections for both blood flow and dialysate, etc. Thus, in one embodiment, an operator may complete all necessary fluid circuit connections for the blood circuit and reagent supply at the housing front panel. The enclosure may also include a pair of vertical, side-by-side doors hingedly mounted to the housing at opposite sides of the front panel so that the doors are movable between open and closed positions. With the doors in an open position, an operator may have access to the blood circuit connections and dialysate fluidic connections. Also, with the doors in the closed position, access to the patient access and dialysate fluidic connections may be blocked, and the doors may allow for the retention of heat in the housing suitable for disinfection during a disinfection cycle. For example, at least one of the doors may include a seal to resist air exchange between an interior and an exterior of housing when the doors are in the closed position to help retain heat and/or help resist entry of dust, dirt or other contaminants.
• In one embodiment, each of the vertical, side-by-side doors is mounted to the housing via a hinge plate that is pivotally mounted to the door at a first end, and is pivotally mounted to the housing at a second end opposite the first end. Thus, the doors may be positionable at two open positions, e.g., a first open position in which blood circuit connections and dialysate fluidic connections are exposed and the hinge plate is adjacent the housing, and a second open position in which the hinge plate is positioned away from the housing. One or more retainer members may be included to maintain the doors in an open position relative to a corresponding hinge plate. For example, the retainer member may include at least one magnet attached to the door or the hinge plate that tends to keep the door in an open position relative to the hinge plate and the housing. Also, one or more retainer members may maintain the hinge plates in a closed position relative to the housing, e.g., in a position close to the housing, and/or maintain the hinge plates in an open position away from the housing.
• In one embodiment, at least one of the doors may include a container holder that is movable between a folded position and an extended position in which the container holder is arranged to support a container, such as reagent supply container. In addition, or alternately, one or both of the doors may include a hook to support a control interface for the hemodialysis unit, such as a remote interface unit that is connected to the housing by a communication cable. These features may make use of the dialysis unit easier by supporting components in a convenient location.
• In another embodiment, the front panel may include at least one flanged portion to support blood lines of a blood circuit assembly. For example, the front panel may include several flanged sections arranged at a periphery of the front panel, such as at lower corners and at a top edge of the front panel. Blood circuit lines that connect to a patient may be relatively long (e.g., up to 3-4 feet or more), and may be wrapped around the periphery of the front panel and retained in place by the flanged portions. The flanged portions may be arranged to support the blood lines and allow the doors to be moved to the closed position without contacting the blood lines, e.g., to avoid pinching of the blood lines at door hinge points.
• In one embodiment, the blood circuit connections at the front panel include arterial and venous blood line connectors for the blood circuit, and the dialysate fluidic connections at the front panel include a connection point for a reagent supply, dialyzer dialysate connections, and a blood line connection point for connecting the arterial and venous blood lines to a directing circuit of the dialysis unit.
• The hemodialysis unit may include a control interface that is connected to the housing by a flexible cable and that is arranged to allow a user to receive information from and provide information to the hemodialysis unit. In one embodiment, the enclosure may include a control interface mounting area at a top of the enclosure where the control interface is mountable. For example, the control interface may include a foldable leg or other support that permits the control interface to be stood in a near vertical orientation on the top of the housing.
• In another embodiment, the enclosure may include an electronics section that is separated and insulated from a disinfection section that is heated to disinfect components of the hemodialysis unit. For example, the disinfection section may include all of the liquid circuit components, such as valves, pumps, conduits, etc., of the various portions of the dialysis unit. The electronics section may include motors, computers or other data processing devices, computer memory, and/or other temperature sensitive electronics or other components. By isolating the electronics section from the disinfection section (at least to some degree), components in the electronics section may be spared exposure to the heat or other environmental conditions in the disinfection section whether during a disinfection operation or otherwise.
• In another aspect of the invention, a portable hemodialysis system may be arranged so that power for the fluid circuit pumps of a dialysis unit may be provided by a modular power unit, e.g., a unit that can be selectively connected to or disconnected from the dialysis unit. As a result, failure of a power unit need not necessarily disable the entire dialysis system. Instead, the power unit may be replaced with another power unit, allowing for treatment to continue. For example, a modular assembly for a portable hemodialysis system may include a dialysis unit, e.g., including a housing that contains suitable components for performing hemodialysis, such as a dialyzer, one or more pumps to circulate blood through the dialyzer, a source of dialysate, and one or more pumps to circulate the dialysate through the dialyzer. The housing may have a front panel at which blood circuit connections and dialysate fluidic connections are located, e.g., where an operator may make patient blood access connections, connect a reagent supply, and/or connect a dialyzer. The modular assembly may also include a power unit having a housing that contains suitable components for providing operating power to the pumps of the dialysis unit. The power unit may be selectively connected to the dialysis unit and provide power to the dialysis unit for the pumps when connected to the dialysis unit, but may be incapable of providing power to the dialysis unit when disconnected from the dialysis unit. The power unit may be selectively connected to and disconnected from the dialysis unit by operation of a single handle, e.g., an operator may turn or otherwise operate a single handle to disconnect the power unit from the dialysis unit. In one embodiment, the dialysis unit and the power unit are sized and weighted to each be carried by hand by a human.
• In one embodiment, the pumps of the dialysis unit are pneumatic pumps and the power unit provides pneumatic power to the dialysis unit. For example, the power unit may provide air pressure and/or vacuum to the dialysis unit to power the pumps. The power unit may include one or more air pressure pumps and/or air vacuum pumps, and the dialysis unit may include a plurality of valves to control application of pneumatic power to the pumps. To aid with use of the hemodialysis system in the home, the power unit and dialysis unit electrical power requirements may be provided by standard residential electrical power, e.g., approximately 110 V, 15 amp electrical power. The dialysis unit may provide electrical power to the power unit, and the power unit may use the electrical power to generate operating power for the pumps.
• In another aspect of the invention, a blood circuit assembly for a dialysis unit may be arranged to allow the replacement of most or all blood circuit components in a single operation. For example, the blood circuit assembly may include an organizing tray, a pair of pneumatic pumps mounted to the organizing tray for circulating blood received from a patient through a circuit including a dialyzer unit and returned to the patient, an air trap mounted to the organizing tray arranged to remove air from blood circulating in the circuit, a pair of dialyzer connections arranged to connect to the inlet and outlet of a dialyzer unit, and a pair of blood line connectors, one inlet blood line connector for receiving blood from the patient and providing blood to the pneumatic pumps and the other outlet blood line connector for returning blood to the patient.
• In one embodiment, an anticoagulant connection is provided for engaging with an anticoagulant source and providing anticoagulant into the blood circuit. For example, the anticoagulant connection may include a pump for pumping anticoagulant from the anticoagulant source, such as heparin from a vial of heparin, to the circuit. The anticoagulant connection may include a vial holder arranged to hold two or more differently sized vials, and a spike to pierce the vial. In one embodiment, the pair of pneumatic pumps, the anticoagulant connection, and the anticoagulant pump are part of a pump cassette.
• In another embodiment, the blood circuit assembly may be selectively mounted to and removed from a dialysis unit. To aid in handling of the blood circuit assembly, the organizing tray may include a pair of handles arranged for gripping by a user. The organizing tray may also include openings adjacent each of the handles for receiving retaining tabs on a dialysis unit that engage with the blood circuit assembly and retain the blood circuit assembly on the dialysis unit.
• In one embodiment, the inlet blood line connector is connected to an inlet for the pump cassette, an outlet for the pump cassette is connected to a dialyzer inlet connector, a dialyzer outlet connector is connected to an inlet of the air trap, and an outlet of the air trap is connected to the outlet blood line connector. The inlet of the air trap may be located above the outlet of the air trap when the blood circuit assembly is mounted to a dialysis unit, e.g., to aid in trapping of air circulating in the circuit during treatment. The blood line connectors may be arranged for a threaded luer-type connection to a patient access, as well as be arranged for a press-in type connection to the dialysis unit. Such an arrangement may make it easier for an operator to connect the blood line connectors to the dialysis unit after treatment (e.g., for later disinfection and/or priming of the blood circuit) while allowing the connectors to engage with standard luer-type connectors at a patient blood access.
• In one embodiment, the organizing tray may include circuit tube engagement members having a hole or slot through which a respective circuit tube passes. The engagement members may engage with the respective circuit tube to allow the circuit tube to be pulled and stretched for engagement with an occluder of the dialysis unit. For example, the circuit tubes of the blood circuit assembly may include silicone tubing that has to be stretched (and thereby reduced in diameter) to engage with an occluder. The circuit tube engagement members may resist the pull of an operator on the tubes, allowing the tubes to be stretched and placed in engagement with the occluder.
• In another aspect of the invention, a method for replacing a blood circuit assembly of a dialysis unit includes grasping a pair of handles on an organizing tray of a blood circuit assembly that is mounted to a dialysis unit, disengaging locking tabs of the dialysis unit from the blood circuit assembly to free the blood circuit assembly from the dialysis unit, and pulling on the handles on the organizing tray of the blood circuit assembly to remove the blood circuit assembly from the dialysis unit. Disengagement of the locking tabs may be performed by flexing the locking tabs away from each other such that each locking tab is moved toward a nearest one of the handles. After removal of the blood circuit assembly, a replacement blood circuit assembly may be provided, openings in the organizing tray of the replacement blood circuit assembly may be aligned with the locking tabs so that each locking tab is received into a respective opening, and the organizing tray may be pushed relative to the dialysis unit such that the locking tabs engage with the replacement blood circuit assembly to mount the replacement blood circuit assembly to the dialysis unit. Mounting the replacement blood circuit assembly may also involve connecting control ports on the dialysis unit to mating ports on the assembly so that fluid control signals may be provided for pumps and valves of the blood circuit assembly. Other blood circuit connections may be made, such as inlet and outlet connections for the dialyzer, and the blood line connectors may be connected to receive dialysate into the blood circuit.
• In another aspect of the invention, an air trap for a blood circuit in a dialysis unit includes a blood inlet supply line, a blood outlet supply line, and a container having an approximately spherical internal wall, an inlet at a top end of the container connected to the blood inlet supply line, and an outlet at a bottom end of the container connected to the blood outlet supply line. The inlet may be offset from a vertical axis of the approximately spherical internal wall such that blood entering the container through the inlet is directed to flow in around the approximately spherical wall in a spiral-like path. Such flow in the container may help to remove air bubbles from the blood as it flows from the inlet to the outlet, with any removed air remaining near the top of the container. The inlet port may be arranged to introduce blood into the container in a direction that is approximately tangential to the approximately spherical inner wall of the container and/or in a direction that is approximately perpendicular to the vertical axis of the container.
• In one embodiment, a self-sealing port may be located at a top of the container, e.g., in the form of a split septum that is arranged to permit introduction of fluid into, and withdrawal of liquid from, the container by inserting a needleless device through the split septum. The self-sealing port may be arranged to be self-cleaning when disinfection liquid is circulated through the container, e.g., the port may be suitably exposed to flowing disinfection liquid to remove debris and/or heat material on the port to achieve desired disinfection.
• In another aspect of the invention, a tube securing arrangement of a blood circuit assembly includes a organizing tray that supports components of a blood circuit assembly and includes a pair of tube engagement members each having a hole, a pair of patient inlet and outlet lines arranged to connect with patient access points for receiving liquid from and/or providing liquid to the patient, and a pair of stops on the patient inlet and outlet lines, respectively. The patient inlet and outlet lines may each pass through a hole of a respective tube engagement member so that the stop engages with the tube engagement member. With this arrangement, the tube engagement members may resist pulling and stretching of the inlet and outlet lines when engaging the lines with an occluder. The tube engagement members may be flexible to allow a user to press inwardly on the engagement member and seat the respective inlet or outlet line in the occluder, yet resist downward pulling of the line.
• In another aspect of the invention, a hemodialysis system includes a dialyzer mount arranged to support a plurality of differently sized and/or shaped dialyzer units and to accommodate different distances between dialysate connections on the dialyzer units. The dialyzer mount, which may be located on a front panel of the dialysis unit, may include a pair of flange portions that are each arranged to engage with a respective dialysate quick-connect fitting connected to a dialysate port of the dialyzer. Each flange portion may be arranged to engage with a groove on the quick connect fitting that is located between a portion of the base of the quick connect fitting and a slide element of the quick connect fitting. For example, the dialyzer mount may include a pair of keyhole features with each keyhole feature having an upper insertion area sized to receive a portion of the base of the quick-connect fitting inserted into the upper insertion area, and a lower flanged portion having a width that is smaller than an overall a width of the base of the quick-connect fitting and that engages with a groove on the quick connect fitting. The lower flanged portion may include a pair of opposite flanges that engage with the groove and allow the quick-connect fitting to slide along the flanges.
• In one embodiment, the bottom keyhole feature may include an adjustable support that is moveable in a vertical direction. For example, the adjustable support may be movable along the opposed flanges. Thus, the adjustable support may be fixable in a plurality of different positions on the flanges to support the weight of the dialyzer. In one arrangement, the adjustable support includes a “U” shaped member and at least one thumb screw that may be tightened to fix the “U” shaped member in place.
• In another aspect of the invention, a blood line connector for a blood circuit of a hemodialysis unit may have the ability to make two different types of fluid tight connections, e.g., a screw-type connection with a luer connector at a patient access and a press-in type connection with a dialysate circuit of the hemodialysis unit. For example, the blood line connector may include a tube connection end arranged to sealingly engage with a blood circuit tube, and a patient access connection end with a frustoconical member having an internally threaded portion arranged to engage with an externally threaded patient access, and a pair of locking arms extending rearwardly from the frustoconical member. The locking arms may each have a finger depression portion and a barbed portion, and may be arranged to engage with a mating connector on the dialysis unit at the barbed portions to lock the frustoconical member in sealing engagement with the mating connector when making a press-in type connection. The barbed portions may disengage from the mating connector when the finger depression portions are urged toward each other. In one embodiment, the patient access connection end may include a central tube extending from the center of the frustoconical member. The internally threaded portion of the frustoconical member and the central tube may be arranged to mate with a female luer-type patient access connector or any other suitable screw-type connection.
• In another aspect of the invention, a method for operating a dialysis unit includes connecting blood line connectors of arterial and venous blood lines for a dialysis unit to patient access connectors in communication with a patient blood system. In one embodiment, the patient access connectors may require a corresponding blood line connector to establish a threaded engagement with the patient access connector, thereby forming a luer or screw-type connection between the blood line connectors and the patient access connectors. The dialysis unit may be operated to withdraw blood from a patient access connector and into an arterial blood line, subject the withdrawn blood to a dialysis process to produce treated blood, and return the treated blood to the patient via the venous blood line and the other patient access connector. Thereafter, the blood line connectors may be disconnected from the patient access connectors by unscrewing the blood line connectors from a corresponding patient access connector, and the blood line connectors may be connected to a directing circuit of the dialysis unit. The blood line connectors may be connected to the directing circuit by a press-in connection with a corresponding connection point on the dialysis unit, e.g., by pushing the blood line connectors into the connection points to establish the press-in connection.
• In another aspect of the invention, a reagent supply arrangement for a hemodialysis system may be arranged to provide two or more reagent materials for use in preparing a dialysate and may include a connector arranged to help prevent the connection of a reagent material to the wrong port. For example, the reagent supply may include an E-prong connector having three parallel prongs with two outer prongs arranged in a common plane and a center prong arranged above the common plane, a first supply line for a first reagent connected in fluid communication with one of the outer prongs, a second supply line for a second reagent connected in fluid communication with the other of the outer prongs, a liquid line connected in fluid communication with the center prong, and a container for housing the first reagent having an inlet connected to the liquid line and an outlet connected to the first supply line for the first reagent. The E-prong connector may help prevent the improper connection of the first and second supply lines to the dialysis unit, e.g., because the central prong being located out of the plane of the two outer prongs ensure connection of the E-prong connector in only one way to the dialysis unit.
• In one embodiment, the container includes a bicarbonate material suitable for use in generating a dialysate for the hemodialysis system. The liquid line may be a water supply line that provides water to the container, allowing the water to mix with the bicarbonate (which may be in powder or other solid form) and flow to the first supply line. The second supply line may be an acid supply line that includes a connector and provides acid material to the E-prong connector. The reagent supply may also include an acid bag spike that is removably engaged with the connector of the acid supply line. The acid bag spike may include a spike member and a pair of spring clips at an end of the acid bag spike opposite the connector of the acid supply line, allowing the acid bag spike to be fluidly connected with an acid bag or other acid source.
• In another aspect of the invention, a method for operating a hemodialysis system includes providing a dialysis unit having an enclosure containing suitable components for performing hemodialysis including a dialyzer, one or more pumps to circulate blood through the dialyzer, a source of dialysate, and one or more pumps to circulate the dialysate through the dialyzer. The enclosure may include a housing that supports the components and has a front panel at which blood circuit connections and dialysate fluidic connections are made. A reagent supply may be provided including an E-prong connector, a first supply line for a first reagent connected in fluid communication with one of the outer prongs, a second supply line for a second reagent connected in fluid communication with the other of the outer prongs, a liquid line connected in fluid communication with the center prong, and a container for housing the first reagent having an inlet connected to the liquid line and an outlet connected to the first supply line for the first reagent. The E-prong connector may be engaged with a connection point at the front panel of the dialysis unit, thereby allowing the dialysis unit to provide water to the liquid line of the reagent supply, and allowing the dialysis unit to receive the first and second reagents from the first and second supply lines.
• Other advantages and novel features of the present invention will become apparent from the following detailed description of various non-limiting embodiments of the invention when considered in conjunction with the accompanying figures. In cases where the present specification and a document incorporated by reference include conflicting and/or inconsistent disclosure, the present specification shall control. If two or more documents incorporated by reference include conflicting and/or inconsistent disclosure with respect to each other, then the document having the later effective date shall control.
BRIEF DESCRIPTION OF THE DRAWINGS
• Aspects of the invention are described with reference to illustrative embodiments, which are described with reference to the drawings in which like numerals reference like elements, and wherein:
• FIG. 1 is a schematic representation of fluid handling components of a hemodialysis system in an illustrative embodiment;
• FIG. 2 shows a schematic fluid flow diagram for the dialysis system ofFIG. 1;
• FIG. 3 is a schematic fluid flow diagram for the blood flow circuit of theFIG. 2 embodiment;
• FIG. 4 is a schematic fluid flow diagram for the balancing circuit of theFIG. 2 embodiment;
• FIG. 5 is a schematic fluid flow diagram for the directing circuit of theFIG. 2 embodiment;
• FIG. 6 is a schematic fluid flow diagram for the mixing circuit of theFIG. 2 embodiment;
• FIG. 7 is a right front perspective view of a hemodialysis system in an illustrative embodiment;
• FIG. 8 is a left rear perspective view of the hemodialysis system ofFIG. 7;
• FIG. 9 is a front view of the hemodialysis system ofFIG. 7;
• FIG. 10 is a right front perspective view of the view of the hemodialysis system ofFIG. 7 with the doors in a first open position;
• FIG. 11 is a top view of the hemodialysis system ofFIG. 10;
• FIG. 12 is a front view of the hemodialysis system ofFIG. 10;
• FIG. 13 is a right side view of the hemodialysis system ofFIG. 10;
• FIG. 14 is a right front perspective view of the view of the hemodialysis system ofFIG. 7 with the doors in a second open position;
• FIG. 15 is a top view of the hemodialysis system ofFIG. 14;
• FIG. 16 is a front view of the hemodialysis system ofFIG. 14;
• FIG. 17 is a front view of the hemodialysis system ofFIG. 7 with the doors in an open position exposing a front panel of the system;
• FIG. 18 is a front view of a blood circuit assembly for use with the system ofFIG. 7;
• FIG. 19 right perspective view of a organizing tray for the blood circuit assembly ofFIG. 18;
• FIG. 20 is a left rear perspective view of the blood circuit assembly ofFIG. 18;
• FIG. 21 shows a left front perspective view of the front panel of the system ofFIG. 7;
• FIG. 22 shows a front view of the front panel of the system ofFIG. 7;
• FIG. 23 shows a front view of the front panel of the system ofFIG. 7 with a pair of mounting features for the dialyzer;
• FIG. 24 shows a side view of a dialyzer with quick-connect fittings attached to the dialysate inlet/outlet ports of the dialyzer;
• FIG. 25 shows a right perspective view of a reagent supply for use with the system ofFIG. 7;
• FIG. 26 shows a perspective view of an E-prong connector for the reagent supply ofFIG. 25 and a corresponding connection point at the front panel of the hemodialysis system;
• FIG. 27 shows a perspective view of a pair of blood line connectors for the blood circuit assembly and a corresponding connection point at the front panel of the hemodialysis system; and
• FIG. 28 shows a side view of a blood line connector and connection point ofFIG. 27.
DETAILED DESCRIPTION
• Various aspects of the invention are generally directed to new systems for hemodialysis and the like, such as hemofiltration systems, hemodiafiltration systems, plasmapheresis systems, etc. Accordingly, although the various systems and methods described herein are described in relation to hemodialysis, it should be understood that the various systems and method described herein are applicable to other dialysis systems and/or in any extracorporeal system able to treat blood or other bodily fluids, such as plasma.
• As discussed below, a hemodialysis system typically includes a blood flow path and a dialysate flow path. It should be noted that within such flow paths, the flow of fluid is not necessarily linear, and there may be any number of “branches” within the flow path that a fluid can flow from an inlet of the flow path to an outlet of the flow path. Examples of such branching are discussed in detail below. In the blood flow path, blood is drawn from a patient, and is passed through a dialyzer, before being returned to the patient. The blood is treated by the dialyzer, and waste molecules (e.g., urea, creatinine, etc.) and water are passed from the blood, through a semi-permeable membrane in the dialyzer, into a dialysate solution that passes through the dialyzer by the dialysate flow path. In various embodiments, blood may be drawn from the patient from two lines (e.g., an arterial line and a venous line, i.e., “dual needle” flow), or in some cases, blood may be drawn from the patient and returned through the same or catheter needle (e.g., the two lines or lumens may both be present within the same needle, i.e., a form of “dual lumen” flow). In still other embodiments, a “Y” site or “T” site is used, where blood is drawn from the patient and returned to the patient through one patient connection having two branches (one being the fluid path for the drawn blood, the second the fluid path for the return blood, i.e., a form of “single needle” flow). The patient may be any subject in need of hemodialysis or similar treatments, including non-human subjects, such as dogs, cats, monkeys, and the like, as well as humans.
• In the dialysate flow path, fresh dialysate is prepared and is passed through the dialyzer to treat the blood from the blood flow path. The dialysate may also be equalized for blood treatment within the dialyzer (i.e., the pressure between the dialysate and the blood are equalized), often exactly, or in some embodiments, at least within about 1% or about 2% of the pressure of the blood. In some cases, it may be desirable to maintain a greater pressure difference (either positive or negative) between the blood flow path and dialysate flow path. After passing through the dialyzer, the used dialysate, containing waste molecules (as discussed below), is discarded in some fashion. The dialysate in some cases may be re-circulated in a “multi-pass” arrangement, which may be beneficial in capturing larger molecules having low mobility across the dialyzer. In some cases, the dialysate is heated prior to treatment of the blood within the dialyzer using an appropriate heater, such as an electrical resistive heater. The dialysate may also be filtered to remove contaminants, infectious organisms, debris, and the like, for instance, using an ultrafilter. The ultrafilter may have a pore size chosen to prevent species such as these from passing therethrough. For instance, the pore size may be less than about 0.3 micrometers, less than about 0.2 micrometers, less than about 0.1 micrometers, or less than about 0.05 micrometers, etc. The dialysate is used to draw waste molecules (e.g., urea, creatinine, ions such as potassium, phosphate, etc.) and water from the blood into the dialysate through osmosis or convective transport, and dialysate solutions are well-known to those of ordinary skill in the art.
• The dialysate typically contains various ions such as sodium, chloride, bicarbonate, potassium and calcium that are similar in concentration to that of normal blood. In some cases, the bicarbonate, may be at a concentration somewhat higher than found in normal blood. Typically, the dialysate is prepared by mixing water from a water supply with one or more ingredients: an “acid” (which may contain various species such as acetic acid, dextrose, NaCl, CaCl, KCl, MgCl, etc.), sodium bicarbonate (NaHCO₃), and/or sodium chloride (NaCl). The preparation of dialysate, including using the appropriate concentrations of salts, osmolarity, pH, and the like, is well-known to those of ordinary skill in the art. As discussed in detail below, the dialysate need not be prepared at the same rate that the dialysate is used to treat the blood. For instance, the dialysate can be made concurrently or prior to dialysis, and stored within a dialysate storage vessel or the like.
• Within the dialyzer, the dialysate and the blood typically are separated by a semi-permeable membrane. Typically, the semipermeable membrane is formed from a polymer such as cellulose, polyarylethersulfone, polyamide, polyvinylpyrrolidone, polycarbonate, polyacrylonitrile, or the like, which allows the transport of ions or small molecules (e.g., urea, water, etc.), but does not allow bulk transport or convection during treatment of the blood. In some cases (such as high-flux dialyzers), even larger molecules, such as beta-2-microglobulin, may pass through the membrane. In some cases, for example, ions and molecules may pass through the dialyzer by convective flow if a hydrostatic pressure difference exists across the semi-permeable membrane.
• It should be noted that, as used herein, “fluid” means anything having fluidic properties, including but not limited to, gases such as air, and liquids such as water, aqueous solution, blood, dialysate, etc.
• FIG. 1 shows a schematic block diagram of fluid circuitry for a hemodialysis system that incorporates various aspects of the invention. In this illustrative embodiment, thedialysis system5 includes ablood flow circuit141 that draws blood from a patient, passes the blood through adialyzer14, and returns the treated blood to the patient. A balancing circuit or aninternal dialysate circuit143 receives dialysate from anultrafilter73, passes the dialysate through thedialyzer14, and receives used dialysate from thedialyzer14. A directing circuit or anexternal dialysate circuit142 provides fresh dialysate to theultrafilter73, and receives used dialysate from the internal dialysate circuit143 (which may be directed to a drain31). The directingcircuit142 can also receive water from awater supply30 and pass it to a mixingcircuit25. The mixingcircuit25 forms dialysate using water from the directingcircuit142 andreagent ingredients49, such as citric acid, salt and a bicarbonate, that may be received from a renewable source. The mixingcircuit25 may prepare dialysate, for example, on an as-needed basis, during and/or in advance of dialysis. New dialysate prepared by the mixingcircuit25 may be provided to the directingcircuit142, which may provide the dialysate to theultrafilter73, as described above. The directingcircuit142 may include a heater to heat the dialysate to a suitable temperature and/or to heat fluid in the system for disinfection. Conduits67 (shown in dotted line) may be connected between theblood flow circuit141 and the directingcircuit142, e.g., for disinfection of the hemodialysis system.
• FIG. 2 is a schematic diagram showing a more detailed circuit arrangement for thedialysis system5 shown inFIG. 1. It should be understood, of course, thatFIG. 2 is only one possible embodiment of the general hemodialysis system ofFIG. 1, and in other embodiments, other fluid circuits, modules, flow paths, layouts, etc. are possible. Examples of such systems are discussed in more detail below, and also can be found in the following, each of which is incorporated herein by reference: U.S. application Ser. No. 12/072,908, filed Feb. 27, 2008, U.S. Provisional Application 60/903,582, filed Feb. 27, 2007, U.S. Provisional Application 60/904,024, filed Feb. 27, 2007, U.S. patent application Ser. No. 11/871,680, filed Oct. 12, 2007, U.S. patent application Ser. No. 11/871,712, filed Oct. 12, 2007, U.S. patent application Ser. No. 11/871,787, filed Oct. 12, 2007, U.S. patent application Ser. No. 11/871,793, filed Oct. 12, 2007, or U.S. patent application Ser. No. 11/871,803, filed Oct. 12, 2007.
• Theblood flow circuit141 includes ananticoagulant supply11 and ablood flow pump13 which pumps blood from a patient through adialyzer14 and returns the blood to the patient. Theanticoagulant supply11, although shown in the path of blood flowing towards the dialyzer, may be instead located in another suitable location. e.g., any location upstream or downstream fromblood flow pump13. Thebalancing circuit143 includes two dialysate pumps15, which pump dialysate into thedialyzer14, and abypass pump35. The flow of blood through theblood flow circuit141 in some cases, is synchronized with the flow of dialysate in the dialysate flow path. In an embodiment, the flow of dialysate into and out of thedialyzer14 and thebalancing circuit143 is balanced volumewise using balancing chambers in thebalancing circuit143. The directingcircuit142 includes adialysate pump159, which pumps dialysate from adialysate tank169 through aheater72 and/or theultrafilter73 to thebalancing circuit143. The directingcircuit142 also receives waste fluid from balancingcircuit143 and directs it to adrain31. In some cases, theblood flow circuit141 can be connected viaconduits67 to the directingcircuit142, e.g., for disinfection, as discussed below. Dialysate in thedialysate tank169 is provided by the mixingcircuit25, which produces the dialysate using water from awater supply30 provided via the directingcircuit142 and dialysate ingredients49 (e.g., bicarbonate and acid). A series of mixingpumps180,183,184 are used to mix the various components and produce the dialysate.
• FIG. 3 shows a close-up view of theblood flow circuit141 in this illustrative embodiment. Under normal operation, blood flows from a patient througharterial line203 via blood flow pump13 to the dialyzer14 (the direction of flow during normal dialysis is indicated byarrows205; in some modes of operation, however, the flow may be in different directions, as discussed below). Optionally, an anticoagulant may be introduced into the blood viaanticoagulant pump80 from an anticoagulant supply. After passing throughdialyzer14 and undergoing dialysis, the blood returns to the patient throughvenous line204, optionally passing through an air trap and/or ablood sample port19. Thepump13 may include, for instance, pumps23 that are actuated by a control fluid.
• For example, in one embodiment, theblood flow pump13 may comprise two (or more) pod pumps23. Each pod pump, in this particular example, may include a rigid chamber with a flexible diaphragm or membrane dividing each chamber into a pumping compartment and control compartment. There may be four entry/exit valves for these compartments, two for the pumping compartment and two for the control compartment. The valves for the control compartment of the chambers may be two-way proportional valves, one connected to a first control fluid source (e.g., a high pressure air source), and the other connected to a second control fluid source (e.g., a low pressure air source) or a vacuum source. The fluid valves can be opened and closed to direct fluid flow when the pod pumps23 are operating. Non-limiting examples of pod pumps are described in U.S. Provisional Application 60/792,073, filed Apr. 14, 2006, or in U.S. patent application Ser. No. 11/787,212, filed Apr. 13, 2007, each incorporated herein by reference. If more than one pod pump is present, the pod pumps may be operated in any suitable fashion, e.g., synchronously, asynchronously, in-phase, out-of-phase, etc. For instance, in some embodiments, the two-pump pumps can be cycled out of phase to affect the pumping cycle, e.g., one pump chamber fills while the second pump chamber empties. A phase relationship anywhere between 0° (the pod pumps fill and empty in unison) and 180° (one pod pump fills as the other empties) can be selected in order to impart any desired pumping cycle. A phase relationship of 180° may yield continuous flow into and out of the set of pod pumps. This is useful, for instance, when continuous flow is desired, e.g., for use with dual needle or dual lumen catheter flow. Setting a phase relationship of 0°, however, may be useful in some cases for single needle/single lumen flow or in other cases. In a 0° relationship, the pod pumps will first fill from the needle, then deliver blood through the blood flow path and back to the patient using the same needle. In addition, running at phases between 0° and 180° can be used in some cases, to achieve a push/pull relationship (hemodiafiltration or continuous back flush) across the dialyzer.
• An anticoagulant (e.g., heparin, or any other suitable anticoagulant) may be contained within a vial11 (or other anticoagulant supply, such as a tube or a bag), andblood flow circuit141 may include a spike201 (which, in one embodiment, is a needle) that can pierce the seal of the vial. Thespike201 may be formed from plastic, stainless steel, or another suitable material, and may be a sterilizable material in some cases, e.g., the material may be able to withstand sufficiently high temperatures and/or radiation so as to sterilize the material.
• Ananticoagulant pump80, which can act as a metering chamber in some cases, can be used to control the flow of anticoagulant into the blood circuit. Theanticoagulant pump80 may be a pod pump or a membrane-based metering pump, and/or may be actuated by a control fluid, such as air. For example, theanticoagulant pump80 may include a rigid chamber with a flexible diaphragm dividing the chamber into a pumping compartment and a control compartment. One valve for the control compartment of the chamber may be connected to a first control fluid source (e.g., a high pressure air source), and the other valve connected to a second control fluid source (e.g., a low pressure air source) or a vacuum source. Valves for the pumping compartment of the chamber can be opened and closed in coordination with the control compartment, thus controlling the flow of anticoagulant into the blood. In one set of embodiments, air provided through afilter81 may also be introduced into the blood flow path by theanticoagulant pump80, e.g., to provide air into thevial11 after or before anticoagulant is withdrawn from the vial.
• Fluid Management System (“FMS”) measurements may be used to measure the volume of fluid pumped through a pump chamber during a stroke of the membrane, or to detect air in the pumping chamber. FMS methods are described in U.S. Pat. Nos. 4,808,161; 4,826,482; 4,976,162; 5,088,515; and 5,350,357, which are hereby incorporated herein by reference in their entireties. In one illustrative embodiment, the volume of liquid delivered by an anticoagulant pump, a dialysate pump, or other membrane-based fluid pump is determined using an FMS algorithm in which changes in chamber pressure are used to calculate a volume measurement at the end of a fill stroke and at the end of a delivery stroke. The difference between the computed volumes at the end of fill and delivery strokes may be used to determine the actual stroke volume. This actual stroke volume can be compared to an expected stroke volume for the particular sized chamber. If the actual and expected volumes are significantly different, the stroke has not properly completed and an error message can be generated.
• Theblood flow circuit141 may also include anair trap19 to remove air bubbles that may be present within the blood flow path. In some cases, theair trap19 is able to separate any air that may be present from the blood due to gravity, and/or may include a port for sampling blood.
• FIG. 4 shows a close-up view of thebalancing circuit143 in theFIG. 2 embodiment. In thebalancing circuit143, dialysate flows from theoptional ultrafilter73 into adialysate pump15. In this embodiment, thedialysate pump15 includes two pod pumps161,162, two balancingchambers341,342, and apump35 for bypassing the balancingchambers341,342. The balancingchambers341,342 may be constructed such that they are formed from a rigid chamber with a flexible diaphragm dividing the chamber into two separate fluid compartments, so that entry of fluid into one compartment can be used to force fluid out of the other compartment and vice versa. Non-limiting examples of pumps that can be used as pod pumps and/or balancing chambers are described in U.S. Provisional Application 60/792,073, filed Apr. 14, 2006, or in U.S. patent application Ser. No. 11/787,212, filed Apr. 13, 2007.
• In one embodiment, balancing of flow in the internal dialysate circuit works as follows. A set of pneumatically operatedvalves211,212,213,241,242 has its operation synchronized and controlled together, wherevalves211,212,213 are ganged andvalves241 and242 are ganged, and a second set of pneumatically operatedvalves221,222,223,231,232 similarly have its operation synchronized and controlled together, wherevalves221,222,223 are ganged, andvalves231 and232 are ganged. At a first point of time, the first set ofvalves211,212,213,241,242 is opened while the second set ofvalves221,222,223,231,232 is closed. Fresh dialysate flows into balancingchamber341 while used dialysate flows fromdialyzer14 intopod pump161. Fresh dialysate does not flow into balancingchamber342 sincevalve221 is closed. As fresh dialysate flows into balancingchamber341, used dialysate within balancingchamber341 is forced out and exits balancing circuit143 (the used dialysate cannot enterpod pump161 sincevalve223 is closed). Simultaneously,pod pump162 forces used dialysate present within the pod pump into balancing chamber342 (throughvalve213, which is open;valves242 and222 are closed, ensuring that the used dialysate flows into balancing chamber342). This causes fresh dialysate contained within balancingchamber342 to exit thebalancing circuit143 intodialyzer14. Also,pod pump161 draws in used dialysate fromdialyzer14 intopod pump161.
• Oncepod pump161 and balancingchamber341 have filled with dialysate, the first set ofvalves211,212,213,241,242 is closed and the second set ofvalves221,222,223,231,232 is opened. Fresh dialysate flows into balancingchamber342 instead of balancingchamber341, as valve212 is closed whilevalve221 is now open. As fresh dialysate flows into balancingchamber342, used dialysate within the chamber is forced out and exits balancing circuit, sincevalve213 is now closed. Also,pod pump162 now draws used dialysate from the dialyzer into the pod pump, while used dialysate is prevented from flowing intopod pump161 asvalve232 is now closed andvalve222 is now open.Pod pump161 forces used dialysate contained within the pod pump (from the previous step) into balancingchamber341, sincevalves232 and211 are closed andvalve223 is open. This causes fresh dialysate contained within balancingchamber341 to be directed into the dialyzer14 (sincevalve241 is now open while valve212 is now closed). At the end of this step,pod pump162 and balancingchamber342 have filled with dialysate. This puts the state of the system back into the configuration at the beginning of this description, and the cycle is thus able to repeat, ensuring a constant flow of dialysate to and from thedialyzer14. In an embodiment, the fluid (e.g. pneumatic) pressures on the control side of the balancing chamber valves are monitored to ensure they are functioning (e.g., opening and closing) properly.
• As a specific example, a vacuum (e.g., 4 p.s.i. of vacuum) can be applied to the port for the first set of valves, causing those valves to open, while positive pressure (e.g., 20 p.s.i. of air pressure) is applied to the second set of valves, causing those valves to close (or vice versa). The pod pumps each urge dialysate into one of the volumes in one of the balancingchambers341,342. By forcing dialysate into a volume of a balancing chamber, an equal amount of dialysate is squeezed by the diaphragm out of the other volume in the balancing chamber. In each balancing chamber, one volume is occupied by fresh dialysate heading towards the dialyzer and the other volume is occupied by used dialysate heading from the dialyzer. Thus, the volumes of dialysate entering and leaving the dialyzer are kept substantially equal.
• Thebypass pump35 can direct the flow of dialysate from thedialyzer14 through balancingcircuit143 without passing through either of pod pumps161 or162. In this embodiment, thebypass pump35 is a pod pump, similar to those described above, with a rigid chamber and a flexible diaphragm dividing each chamber into a fluid compartment and a control compartment. This pump may be the same or different from the other pod pumps and/or metering pumps described above. When control fluid is used to actuate thebypass pump35, the additional drop in pressure on the exiting (spent) dialysate side of the dialyzer causes additional ultrafiltration of fluid from the blood in the dialyzer. This may cause a net efflux of fluid from the patient's blood, through the dialyzer, and ultimately to drain. Such a bypass may be useful, for example, in reducing the amount of fluid a patient has, which is often increased due to the patient's inability to excrete excess fluid (primarily water) through the kidneys. As shown inFIG. 4, thebypass pump35 may be controlled by a control fluid (e.g., air), irrespective of the operation of pod pumps161 and162. This configuration may allow for easier control of net fluid removal from a patient, without having to operate the inside dialysate pumps either out of balance or out of phase with the blood pumps in order to achieve such fluid withdrawal from the patient.
• To achieve balanced flow across the dialyzer, the blood flow pump, the pumps of the balancing circuit, and the pumps of the directing circuit (discussed below) may be operated to work together to ensure that flow into the dialyzer is generally equal to flow out of the dialyzer. If ultrafiltration is required, the ultrafiltration pump (if one is present) may be run independently of some or all of the other blood and/or dialysate pumps to achieve the desired ultrafiltration rate.
• To prevent outgassing of the dialysate, the pumps of the balancing circuit may be kept at pressures above atmospheric pressure. In contrast, however, the blood flow pump and the directing circuit pumps use pressures below atmosphere to pull the diaphragm towards the chamber wall to complete a fill stroke. Because of the potential of fluid transfer across the semi-permeable membrane of the dialyzer and because the pumps of the balancing circuit run at positive pressures, the balancing circuit pumps may be able to use information from the blood flow pump(s) in order to synchronize the delivery strokes of the balancing circuit chambers to the dialyzer with the delivery strokes of the blood pumps.
• In one set of embodiments, when running in such a balanced mode, if there is no delivery pressure from the blood flow pump, the balancing circuit pump diaphragm will push fluid across the dialyzer into the blood and the alternate pod of the balancing circuit will not completely fill. For this reason, the blood flow pump reports when it is actively delivering a stroke. When the blood flow pump is delivering a stroke the inside dialysate pump operates. When the blood flow pump is not delivering blood, the valves that control the flow from the dialyzer to the inside dialysate pumps (and other balancing valves ganged together with these valves, as previously discussed) may be closed to prevent any fluid transfer from occurring from the dialysate side to the blood side. During the time the blood flow pump is not delivering, the inside dialysate pumps are effectively frozen, and the inside dialysate pump delivery stroke resumes once the blood flow pump starts delivering again. The inside dialysate pump fill pressure can be set to a minimal positive value to ensure that the pump operates above atmosphere at minimal impedance. Also, the inside dialysate pump delivery pressure can be set to the blood flow pump pressure to generally match pressures on either side of the dialyzer, minimizing flow across the dialyzer during delivery strokes of the inside dialysate pump.
• In another embodiment, the inside dialysate pump delivers dialysate to the dialyzer at a pressure slightly above the pressure at which blood is delivered to the dialyzer. This ensures that a full balance chamber of clean dialysate gets delivered to the dialyzer. On the return side, the inside dialysate pump can fill with spent dialysate from the dialyzer at a slightly lower pressure than the outlet pressure on the blood side of the dialyzer, ensuring that the receiving dialysate pump chamber can fill. This in turn ensures that there is enough dialysate available to complete a full stroke in the balancing chamber. Flows across the semi-permeable membrane caused by these differential pressures will tend to cancel each other; and the pumping algorithm otherwise attempts to match the average pressures on the dialysate and blood sides of the dialyzer.
• It is generally beneficial to keep the blood flow as continuous as possible during therapy, as stagnant blood flow can result in blood clots. In addition, when the delivery flow rate on the blood flow pump is discontinuous, the balancing pump may pause its stroke more frequently, which can result in discontinuous and/or low dialysate flow rates. However, the flow through the blood flow pump can be discontinuous for various reasons. For instance, pressure may be limited within the blood flow pump, e.g., to +600 mmHg and/or −350 mmHg to provide safe pumping pressures for the patient. For instance, during dual needle flow, the two pod pumps of the blood flow pump can be programmed to run 180° out of phase with one another. If there were no limits on pressure, this phasing could always be achieved. However to provide safe blood flow for the patient these pressures are limited. If the impedance is high on the fill stroke (due to a small needle, very viscous blood, poor patient access, etc.), the negative pressure limit may be reached and the fill flow rate will be slower then the desired fill flow rate. Thus the delivery stroke must wait for the previous fill stroke to finish, resulting in a pause in the delivery flow rate of the blood flow pump. Similarly, during single needle flow, the blood flow pump may be run at 0° phase, where the two blood flow pump pod pumps are simultaneously emptied and filled. When both pod pumps are filled, the volumes of the two pod pumps are delivered. In an embodiment, the sequence of activation causes a first pod pump and then a second pod pump to fill, followed by the first pod pump emptying and then the second pod pump emptying. Thus the flow in single needle or single lumen arrangement may be discontinuous.
• One method to control the pressure saturation limits would be to limit the desired flow rate to the slowest of the fill and deliver strokes. Although this would result in slower blood delivery flow rates, the flow rate would still be known and would be more continuous, which would allow for more accurate and continuous dialysate flow rates. Another method to make the blood flow rate more continuous in single needle operation would be to use maximum pressures to fill the pods so the fill time would be minimized. The desired deliver time could then be set to be the total desired stroke time minus the time that the fill stroke took. However, the less continuous the blood flow, the more the dialysate flow rate may have to be adjusted upward during blood delivery to the dialyzer to make up for the time that the dialysate pump is stopped when the blood flow pump is filling. If this is done with the correct timing, an average dialysate flow rate taken over several strokes can still match the desired dialysate flow rate.
• FIG. 5 shows a close up of the directingcircuit142 in theFIG. 2 embodiment. In this embodiment, the directingcircuit142 can provide dialysate from adialysate tank169 via adialysate pump159 to aheater72 and theultrafilter73. Theheater72 may be used to warm the dialysate to body temperature, and/or a temperature such that the blood in the blood flow circuit is heated by the dialysate, and the blood returning to the patient is at body temperature or higher. In some cases, theheater72 may be connected to a control system such that dialysate that is incorrectly heated (i.e., the dialysate is too hot or too cold) may be recycled (e.g., back to the dialysate tank169) or sent to drain instead of being passed to the dialyzer. Theheater72 may also be used, in some embodiments, for disinfection or sterilization purposes. For instance, water may be passed through the hemodialysis system and heated using the heater such that the water is heated to a temperature able to cause disinfection or sterilization to occur, e.g., temperatures of at least about 70° C., at least about 80° C., at least about 90° C., at least about 100° C., at least about 110° C., etc.
• The flow of dialysate through the directingcircuit142 may be controlled (at least in part) by operation of thedialysate pump159. In addition, thedialysate pump159 may control flow through thebalancing circuit143. For instance, as discussed above, fresh dialysate from the directingcircuit142 flows into balancingchambers341 and342 of balancingcircuit143. Thedialysate pump159 may be used as a driving force to cause the fresh dialysate to flow into these balancing chambers. In one set of embodiments,dialysate pump159 includes a pod pump, e.g., similar to those described above.
• The dialysate may also be filtered to remove contaminants, infectious organisms, pathogens, pyrogens, debris, and the like, for instance, using anultrafilter73. Theultrafilter73 may be positioned in any suitable location in the dialysate flow path, for instance, between the directing circuit and the balancing circuit, e.g., as shown, and/or theultrafilter73 may be incorporated into the directing circuit or the balancing circuit. If an ultrafilter is used, its pore size may be chosen to prevent species such as these from passing through the filter.
• In some cases, theultrafilter73 may be operated such that waste from the filter (e.g., the retentate stream) is passed to a waste stream, such aswaste line39 inFIG. 5. In some cases, the amount of dialysate flowing into the retentate stream may be controlled. For instance, if the retentate is too cold (i.e.,heater72 is not working, orheater72 is not heating the dialysate to a sufficient temperature, the entire dialysate stream (or at least a portion of the dialysate) may be diverted to wasteline39, and optionally, recycled todialysate tank169 usingline48. Flow from thefilter73 may also be monitored for several reasons, e.g., using temperature sensors (e.g.,sensors251 and252), conductivity sensors (for confirming dialysate concentration, e.g., sensor253), or the like. An example of such sensors is discussed below; further non-limiting examples can be seen in a U.S. patent application Ser. No. 12/038,474, filed Feb. 27, 2008.
• The ultrafilter and the dialyzer may provide redundant screening methods for the removal of contaminants, infectious organisms, pathogens, pyrogens, debris, and the like. Accordingly, any contaminant would have to pass through both the ultrafilter and the dialyzer before reaching a patient's blood. Even in the event that either the ultrafilter or dialyzer integrity fails, the other may still be able to maintain dialysate sterility and prevent contaminants from reaching the patient's blood.
• The directingcircuit142 may also be able to route used dialysate coming from a balancing circuit to a drain, e.g., throughwaste line39 to drain31. The drain may be, for example, a municipal drain or a separate container for containing the waste (e.g., used dialysate) to be properly disposed of. In some cases, one or more check or “one-way” valves (e.g.,check valves215 and216) may be used to control flow of waste from the directingcircuit142 and from thesystem5. Also, in certain instances, a blood leak sensor (e.g., sensor258) may be used to determine if blood is leaking through thedialyzer14 into the dialysate flow path. In addition, a liquid sensor can be positioned in a collection pan at the bottom of the hemodialysis unit to indicate leakage of either blood or dialysate, or both, from any of the fluid circuits.
• The directingcircuit142 may receive water from awater supply30, e.g., from a container of water such as a bag, and/or from a device able to produce water, e.g., a reverse osmosis device. In some cases, the water entering the system is set at a certain purity, e.g., having ion concentrations below certain values. The water entering into the directingcircuit142 may be passed on to various locations, e.g., to a mixingcircuit25 for producing fresh dialysate and/or to wasteline39. In some cases, valves to thedrain31 and various recycle lines are opened, andconduits67 may be connected between directingcircuit142 andblood flow circuit141, such that water is able to flow continuously around the system. Ifheater72 is also activated, the water passing through the system will be continuously heated, e.g., to a temperature sufficient to disinfect the system.
• FIG. 6 shows a close-up view of the mixingcircuit25 in the illustrative embodiment ofFIG. 2. Water from the directingcircuit142 flows into the mixingcircuit25 due to action of apump180. In this embodiment, thepump180 includes one or more pod pumps, similar to those described above. In some cases, a portion of the water is directed toreagent ingredients49, e.g., for use in transporting the ingredients, such as thebicarbonate28, through the mixingcircuit25. In some cases, sodium chloride and/or thesodium bicarbonate28 may be provided in a powdered or granular form, which is mixed with water provided by thepump180. Bicarbonate frombicarbonate source28 is delivered viabicarbonate pump183 to a mixing line186, which also receives water from the directingcircuit142. Acid from an acid source29 (which may be in a liquid form) is also pumped via anacid pump184 to the mixing line186. The ingredients49 (water, bicarbonate, acid, NaCl, etc.) are mixed in mixingchamber189 to produce dialysate, which then flows out of mixingcircuit25 to the directingcircuit142.Conductivity sensors178 and179 are positioned along mixing line186 to ensure that as each ingredient is added to the mixing line, it is added at proper concentrations. The volumes delivered by thewater pump180 and/or the other pumps may be directly related to the conductivity measurements, so the volumetric measurements may be used as a cross-check on the composition of the dialysate that is produced. This may ensure that the dialysate composition remains safe even if a conductivity measurement becomes inaccurate during a therapy.
• FIG. 7 shows a perspective view of ahemodialysis system5 that incorporates various aspects of the invention. In accordance with one aspect of the invention, thesystem5 includes adialysis unit51 and apower unit module52 that are shown joined together. In this embodiment, thedialysis unit51 has a housing that contains suitable components for performing hemodialysis, such as a dialyzer, one or more pumps to circulate blood through the dialyzer, a source of dialysate, and one or more pumps to circulate the dialysate through the dialyzer. For example, thedialysis unit51 may include the mixingcircuit25,blood flow circuit141, thebalancing circuit143 and the directingcircuit142 as described above. Thedialysis unit51 may also include all blood circuit connections and dialysate fluidic connections needed for operation of thesystem5. Patient access and other connections may be revealed by opening side-by-sidevertical doors53 via ahandle54 at a front side of thedialysis unit51 housing. In this embodiment, thedialysis unit51 includes a control interface55 (attached to the housing by a flexible cable in this embodiment) that a user may use to control operation of thedialysis unit51. Thecontrol interface55 may include a display screen with a touch sensitive overlay to allow touch control and interaction with a graphical user interface presented on the screen. Thecontrol interface55 may also include other features, such as push buttons, a speaker, a microphone for receiving voice commands, a digital camera, and so on. The back side of thecontrol interface55 may include a retractable “kick-stand” (not shown) that allows thecontrol interface55 to be positioned on top of thedialysis unit51 housing. Deploying the retractable “kick-stand” permits thecontrol interface55 to be placed in a near-vertical position to allow proper viewing of the display screen.
• Thepower unit52 housing may contain suitable components for providing operating power to thedialysis unit51, e.g., pneumatic pressure/vacuum to power the pumps, valves and other components of thedialysis unit51. “Pneumatic,” as used herein, means using air or other gas to move a flexible diaphragm or other member. (It should be noted that air is used by way of example only, and in other embodiments, other control fluids, such as nitrogen (N₂), CO₂, water, an oil, etc., may be used). As discussed above, the pumps and valves of thedialysis unit51 may operate on pneumatic power, and thus thepower unit52 may provide one or more pneumatic sources for use by thedialysis unit51. In this way, thedialysis unit51 need not necessarily be arranged to generate and/or store the necessary pneumatic power needed, but instead may rely on thepower unit module52. Thepower unit52 may include one or more pneumatic pumps to generate desired air pressure and/or vacuum, one or more accumulators or other devices to store pneumatic power, valves, conduits and/or other devices to control flow of pneumatic power in thepower unit52, as well as a controller having suitable components, such as a programmed general purpose data processor, memory, sensors (e.g., to detect pressure, temperature, etc.), relays, actuators, and so on.
• In one embodiment, the pneumatic power (e.g., air under suitable pressure/vacuum) may be supplied by thepower unit52 to thedialysis unit51 via one or more supply tanks or other pressure sources. For instance, if two tanks are used in thepower unit52, one supply tank may be a positive pressure reservoir, and in one embodiment, has a set point of 750 mmHg (gauge pressure) (1 mmHg is about 133.3 pascals). The other supply tank can be a vacuum or negative pressure reservoir, and in one embodiment, has a set point of −450 mmHg (gauge pressure). This pressure difference may be used, for instance, between the supply tanks and the required pod pump pressure to allow for accurate control of the variable valves to the pod pumps. The supply pressure limits can be set based on maximum pressures that can be set for the patient blood flow pump plus some margin to provide enough of a pressure difference for control of the variable valves. Thus, in some cases, the two tanks may be used to supply pressures and control fluids for all of thedialysis unit51 functions.
• In one embodiment, thepower unit52 may include two independent compressors to service the supply tanks. Pressure in the tanks can be controlled using any suitable technique, for instance, with a simple “bang-bang” controller (a controller that exists in two states, i.e., in an on or open state, and an off or closed state), or with more sophisticated control mechanisms, depending on the embodiment. As an example of a bang-bang controller, for the positive tank, if the actual pressure is less than a set point, the compressor servicing the positive tank is turned on. If the actual pressure is greater than a set point, the compressor servicing the positive tank is turned off. The same logic may be applied to the vacuum tank and control of the vacuum compressor with the exception that the sign of the set point term is reversed. If the pressure tanks are not being regulated, the compressor is turned off and the valves are closed.
• Tighter control of the pressure tanks can be achieved by reducing the size of the hysteresis band, however this may result in higher cycling frequencies of the compressor. If very tight control of these reservoirs is required, the bang-bang controller could be replaced with a proportional-integral-derivative (“PID”) controller and using pulse width modulation (“PWM”) signals on the compressors. Other methods of control are also possible.
• Other pressure sources may be used in other embodiments, and in some cases, more than one positive pressure source and/or more than one negative pressure source may be used. For instance, more than one positive pressure source may be used that provides different positive pressures (e.g., 1000 mmHg and 700 mmHg), which may be used to minimize leakage. For example, high positive pressure can be used to control valves, whereas lower positive pressures can be used to control pumps. This limits the amount of pressure that can potentially be sent to the dialyzer or to the patient, and helps to keep actuation of the pumps from overcoming the pressures applied to adjacent valves. A non-limiting example of a negative pressure is −400 mmHg. In some cases, the negative pressure source may be a vacuum pump, while the positive pressure pump may be an air compressor.
• Moreover, thepower unit52 may be selectively connectable to thedialysis unit51, e.g., to allowdifferent power units52 to be interchanged. For example, thedialysis unit51 may be arranged to work with different types ofpower units52, such aspower units52 that use electrical power to generate the pneumatic power supply, as well aspower units52 that use stored pneumatic power (e.g., pressurized air stored in one or more high pressure tanks). Thus, apower unit52 may be interchanged for anotherunit52, in case of failure or other requirements. For example, it may be desired to use thesystem5 in an area where noise generation is unacceptable, such as when nearby people are sleeping. In this case, it may be desirable to use apower unit52 that uses stored pneumatic power, rather than aunit52 that generates pneumatic power by running pumps or other noise generating equipment. As shown inFIG. 8, thepower unit52 may be disconnected from thedialysis unit51 by manipulating ahandle521. For example, turning thehandle521 may unlock thepower unit52 from thedialysis unit51, disengaging not only mechanical connections between the housings, but also power and/or communications connections between the two. An interface (not shown) between thedialysis unit51 and thepower unit52 may permit the units to exchange pneumatic power (from thepower unit52 to the dialysis unit51) as well as electrical power, control communications, and other. Thedialysis unit51 may have connection points for electrical power (e.g., standard 115V, 15 amp power found in most home power outlets), external communication (such as Ethernet, or any other suitable connection suitable for communication), a water supply, and so on. Thedialysis unit51 may provide electrical power or other connections to thepower unit52, if desired.
• Thedialysis unit51 may include a controller to control flow of control fluid for various components of thesystem5, as well as perform other desired functions. In some cases, the control fluid may be held at different pressures within the various tubes or conduits. For instance, some of the control fluid may be held at positive pressure (i.e., greater than atmospheric pressure), while some of the control fluid may be held at negative pressures (less than atmospheric pressure). In addition, in certain embodiments, the controller may have components that are kept separate from the various liquid circuits. This configuration has a number of advantages. For example, in one embodiment, the liquid circuits in thedialysis unit51 may be heated to disinfection temperatures and/or exposed to relatively high temperatures or other harsh conditions (e.g., radiation) to effect disinfection, while electronic components of the controller may not be exposed to such harsh conditions, and may even be kept separate by an insulating wall (e.g., a “firewall”) or the like. That is, the dialysis unit housing may have two or more compartments, e.g., one compartment with electronic and other components that may be sensitive to heat or other conditions, and another compartment with liquid circuit components that are heated or otherwise treated for disinfection.
• Thus, in some embodiments, thesystem5 may include a “cold” section (which is not heated), and a “hot” section, portions of which may be heated, e.g., for disinfection purposes. The cold section may be insulated from the hot section through insulation. In one embodiment, the insulation may be molded foam insulation, but in other embodiments can be any type of insulation, including but not limited to a spray insulation, an air space, insulation cut from sheets, etc. In one embodiment, the cold section includes a circulation system, e.g., a fan and/or a grid to allow air to flow in and out of the cold box. In some cases, the insulation may be extended to cover access points to the “hot” section, e.g., doors, ports, gaskets, and the like. For instance, when the “hot” section is sealed, the insulation may completely surround the “hot” section in some cases.
• Non-limiting examples of components that may be present within the “cold” section include power supplies, electronics, power cables, pneumatic controls, or the like. In some cases, at least some of the fluids going to and from the “hot” section may pass through the “cold” section; however, in other cases, the fluids may pass to the “hot” section without passing through the “cold” section.
• Non-limiting examples of components that may be present within the “hot” section include cassettes (if present), fluid lines, temperature and conductivity sensors, blood leak sensors, heaters, other sensors, switches, emergency lights, or the like. In some cases, some electrical components may also be included in the “hot” section. These include, but are not limited to, a heater. In one embodiment, the heater can be used to heat the hot box itself, in addition to fluid. In some embodiments, theheater72 heats the entire “hot” section to reach a desired temperature.
• In accordance with an aspect of the invention, thedialysis unit51 housing may include vertical side-by-side doors that can be opened to expose all mechanical interface points for blood flow circuitry and connections for dialysate circuitry, i.e., all connection points for patient blood connections and acid/bicarbonate connections, that must be made by a user to use thedialysis unit51.FIG. 9 shows a front view of thedialysis unit51 with the vertical side-by-side doors53 in a closed state. In this arrangement, thedoors53 may block access to connection points for patient blood connections and acid/bicarbonate connections as well as seal the interior of the unit housing so as to allow heat retention suitable for disinfection. The seal provided by thedoors53 may be hermetic, preventing or substantially resisting any air exchange between the housing interior and an exterior environment, or may be of a somewhat lesser quality yet still allow for disinfection.
• In this embodiment, thedoors53 are connected to thedialysis unit51 housing by a dual hinge arrangement such that thedoors53 can be opened to two different states of opening.FIGS. 10-13 show thedoors53 in a first state of opening. In this state, thedoors53 expose all user-made connections for the blood circuit connections and for the dialyzer circuitry, including thedialyzer14 itself and for reagent materials, such as consumable acid/bicarbonate materials. This position also exposes several other features, such asholders531 for an acid/bicarbonate container (not shown) and hooks532 that may be used to hold any suitable item, such as thecontrol interface55, which may be hung by its handle on one of thehooks532. (See alsoFIG. 7 which shows ahook532 on the front of theleft door53 which may be folded out to receive thecontrol interface55 or other item.) Theholders531 in this embodiment may be folded down from their position shown in the figures (i.e., folded up and into recesses in the doors53) so as to extend horizontally from thedoors53. Theholders531 have a “C” shaped receiving section to receive and hold an acid/bicarbonate container, but of course could be shaped or otherwise arranged in any suitable way.
• FIGS. 14-16 show thedoors53 in a second state of opening in which ahinge plate533 for eachdoor53 is pivoted outward and away from thedialysis unit housing51. Thehinge plates533, which in this embodiment extend vertically along almost the entire height of thedialysis unit housing51, are pivotally attached to thedoors53 at a first, outer end, and are pivotally attached at a second inner end to thedialysis unit housing51. (Of course, it should be understood that thehinge plates533 could be arranged and/or positioned differently, e.g., at the top and bottom of thedoors53 as is found in many refrigerator door arrangements, eachplates533 may include two or more portions that are vertically separated from each other, etc.)Magnets534 attached to thehinge plates533 may interact with corresponding magnets (or other suitable components, such as a steel elements) attached to thedialysis unit housing51 so as to attract thehinge plates533 toward thedialysis unit housing51, thus tending to keep thehinge plates533 in the position shown inFIGS. 10-13. (Of course, themagnets534 could be positioned on the unit housing, and thehinge plates533 could have suitable elements (such as pieces of steel) that are attracted to themagnets534.) Thedoors53 in this embodiment also include magnets attached near thehinge plates533 so that when thedoors53 are opened to the first state as shown inFIGS. 10-13, the magnets interact with corresponding magnets in thehinge plates533 to help keep thedoors53 in an open position relative to thehinge plate533. These magnets will also help maintain the relative position of thedoors53 and thehinge plates533 when thehinge plates533 are opened to the second state shown inFIGS. 13-16.
• Although magnets are used in this illustrative embodiment as part of a retainer member to help thedoors53 and/or hingeplates533 stay in a particular state of opening or closing, other arrangements for a retainer member are possible. For example, the hinge connection between thedoors53 and thehinge plates533 and/or the connection between thehinge plates533 and thehousing51 may include a detent arrangement that serves to resiliently hold thedoor53 orhinge plate533 in a particular position relative to the other part (the hinge plate or housing, respectively). In another embodiment, one or more springs may be used to help maintain thedoors53 in an open position relative to thehinge plates533. In yet another embodiment, thehinge plates533 may have a friction or interference fit with a portion of thehousing51 that tends to maintain thehinge plates533 in the closed position (adjacent the housing). Accordingly, a retainer member that functions to help maintain adoor53 in a particular position relative to itshinge plate533, and/or that functions to help maintain ahinge plate533 in a particular position relative to thehousing51, may take any one of a number of possible arrangements.
• In accordance with another aspect of the invention, opening of the doors to the dialysis unit housing may reveal all of the user-made connections for blood circuit connections and dialysate fluidic connections needed for operation of thesystem5. For example, as shown inFIG. 17, with thedoors53 in an open position (either the first or second state of opening) afront panel511 of thedialysis unit51 may be exposed. In this embodiment, thefront panel511 carries several items or connection points that must be accessed by a user. For example, thedialyzer14, which must be periodically replaced, is mounted to thefront panel511. Thedialyzer14 must be connected not only to theblood flow circuit141, but also thebalancing circuit143. Also, aconnection point512 for an acid/bicarbonate source49 is located at a lower end of thefront panel511. It is at thisconnection point512 that a user may connect a source ofconsumable reagent ingredients49 used by thedialysis unit51 in making dialysate. Anoccluder513 is also mounted on thefront panel511. Theoccluder513 receives tubes of the blood flow circuit and controls the open/closed state of the tubes based on system operation. The function of theoccluder513 is discussed in more detail in U.S. application Ser. No. 12/198,947, filed Aug. 27, 2008 (under Attorney Docket Number D0570.70020US00 (G28)) and below. In short, theoccluder513 allows flow through the arterial and venous lines of the blood flow circuit unless there is a system problem, such as a leak, pump failure, overpressure situation, etc. In such case, theoccluder513 automatically closes the blood lines to prevent all flow to or from the patient. Also exposed on thefront panel511 are blood line connection points514 for connecting the arterial andvenous blood lines203,204 of theblood flow circuit141 with the directing circuit142 (as explained above with reference toFIGS. 2 and 3, theblood flow circuit141 may be connected to the directing circuit142). This connection is normally made at the end of treatment to allow the system to clean and disinfect theblood flow circuit141. Thefront panel511 also has a set ofcontrol ports515 that mate with corresponding control ports on the blood pump portion of theblood flow circuit141. Thecontrol ports515 provide controlled levels of air pressure and/or vacuum to control the open/closed state of valves and to power the pumps of theblood flow circuit141.
• Also exposed on thefront panel511 is auser control panel510. Theuser control panel510 includes one or more buttons permitting the user to bypass the graphical user interface oncontrol interface55, providing an alternate method to control certain functions (e.g., critical functions) during hemodialysis. This may be important, for example, if thecontrol interface55 should ever fail during a dialysis treatment session. Non-limiting examples of critical functions can include a “stop dialysis” or “pause dialysis” command and an “infuse dialysate solution” command.
• FIG. 17 does not show the arterial andvenous lines203,204 for theblood flow circuit141 because in this embodiment and in accordance with another aspect of the invention, theblood flow circuit141 is formed as a blood circuit assembly that is removable from thefront panel511 of thedialysis unit51, and the blood circuit assembly is not mounted on thefront panel511 inFIG. 17.FIG. 18 shows a front view of theblood circuit assembly17 in this embodiment along with thedialyzer14. Theblood circuit assembly17 includes various components discussed above, for example with reference toFIG. 3, that are mounted to a bloodcircuit organizing tray171. The arterial andvenous lines203 and204 (e.g., including lengths of flexible silicone tubing) are terminated with blood line connectors that, in one aspect of the invention, are arranged to provide a plug-in or press-in connection with the blood line connection points514 as well as provide a screw-type connection used with standard patient access points (e.g., luer type patient access connectors). Thearterial line203 leads to an inlet at the top of theblood pump13, which includes two pod pumps23, valves and other components for controlling blood flow. Associated with theblood pump13 are anair filter81, an anticoagulant pump80 (not shown), and an anticoagulant supply11 (such as a vial of heparin). (Details regarding theblood pump13 in this illustrative embodiment may be found in U.S. patent application Ser. No. 11/871,680, filed Oct. 12, 2007, entitled “Pumping Cassette”; U.S. patent application Ser. No. 11/871,712, filed Oct. 12, 2007, entitled “Pumping Cassette”; U.S. patent application Ser. No. 11/871,787, filed Oct. 12, 2007, entitled “Pumping Cassette”; U.S. patent application Ser. No. 11/871,793, filed Oct. 12, 2007, entitled “Pumping Cassette”; and U.S. patent application Ser. No. 11/871,803, filed Oct. 12, 2007, entitled “Cassette System Integrated Apparatus.”) Blood output from the blood pump13 (the outlet is located at a bottom of the pump13) flows to an inlet of the dialyzer14 (at the top of the dialyzer14), and out of the dialyzer (the dialyzer blood outlet is located at the bottom of the dialyzer14) to the inlet of theair trap19. The outlet of theair trap19 is connected to thevenous blood line204. Connections to the inlet and outlet blood ports of thedialyzer14 are made with typical screw-type connections.
• In accordance with another aspect of the invention, theair trap19 is placed in the blood flow path after the blood exits the dialyzer and before it is returned to the patient. In an embodiment,air trap19 can have a spherical or spheroid-shape container (i.e., a container having an approximately spherical inner wall), and have its inlet port located near the top and offset from the vertical axis of the container, and an outlet at a bottom of the container. (The vertical axis of the container is arranged in a vertical direction passing through the top and bottom “poles” of the approximately spherical container.) With the inlet port offset from the vertical axis (in this case set back toward the tray171), blood is introduced into the container in a direction that is approximately perpendicular to the vertical axis of the container and that is approximately tangential to the spherical inner wall of the container. The curved shape of the inside wall of the trap can thus direct the blood to circulate along the inside wall as the blood gravitates to the bottom of the container (e.g., in a spiral like fashion), facilitating the removal of air bubbles from the blood. Air present in the blood exiting the outlet of thedialyzer14 will enter at the top of theair trap19 and remain at the top of the container as blood flows out the outlet at the bottom and to thevenous blood line204. By locating the inlet port near the top oftrap19, it is also possible to circulate blood through the trap with minimal or no air present within the container (as a “run-full” air trap. The ability to avoid an air-blood interface for routine circulation of blood in the trap can be advantageous. Placing the inlet port at or near the top of the container also allows most or all of the air present in the trap to be removed from the trap by reversing the flow of fluid through the blood tubing (i.e. from the bottom to the top of thetrap19, exiting through the inlet port of the trap19).
• In an embodiment, a self-sealing port, such as a self-sealing stopper with a split septum or membrane, or another arrangement, is located at the top of the trap, allowing the withdrawal of air from the container (e.g., by syringe). The blood-side surface of the self-sealing membrane can be situated nearly flush with the top of the interior of the trap, in order to facilitate cleaning of the self-sealing port during disinfection, e.g., by reversing flow through the air trap using a dialysate or other cleaning fluid. Also, the inlet, outlet and internal wall of the container and the self-sealing port may be arranged to substantially eliminate stagnation regions, i.e., allow for few or no regions where blood can stagnate or clot. The self-sealing port can also serve as a blood sampling site, and/or to allow the introduction of liquids, drugs or other compounds into the blood circuit. A sealed rubber-type stopper can be used if access with a needle is contemplated. Using a self-sealing stopper with split septum permits sampling and fluid delivery using a needleless system.
• FIG. 19 shows the organizingtray171 for theblood circuit assembly17 without the variousblood circuit assembly17 components mounted. In accordance with one aspect of the invention, the organizingtray171 includes handles172 (in this embodiment, finger pulls) that a user can grip when mounting/dismounting theblood circuit assembly17 to thefront panel511. Inward of thehandles172 areopenings173 that allow spring tabs on thefront panel511 to pass through and engage with the organizingtray171 and/or theblood pump13 cassette to hold theblood circuit assembly17 in place on thefront panel511. In accordance with another aspect of the invention, the organizingtray171 includes bloodline engagement members174 that each have a C-shaped recess or other hole through which a correspondingblood line203,204 passes. (In this context, a “hole” includes a recess like that shown inFIG. 19, a throughbore that has a continuous wall, e.g., as may be made by a drill, or other suitable opening.) As described in more detail below, the bloodline engagement members174 are used when mounting theblood lines203,204 in theoccluder513. In short, when mounting theblood lines203,204 in theoccluder513, theblood lines203,204 must be pulled and stretched downwardly (so as to reduce the outside diameter of the line) while being pushed horizontally into slots for theoccluder513. The bloodline engagement members174 function to both resist downward pulling on theblood lines203,204 (e.g., eachline203,204 may include a stop ring above therespective engagement member174 that cannot be pulled through the recess in the engagement member174) as well as permit the user to press inwardly on theengagement member174 to seat thelines203,204 in the occluder slots. Theengagement members174 are formed integrally with the organizingtray171 so that a “living hinge” or relatively flexible portion of the organizing tray is positioned between theengagement member174 and the main body of the organizingtray171. This arrangement allows theengagement members174 to be pushed inwardly relative to the organizingtray171 as the connection portion between theengagement members174 and the organizing tray main body flexes.
• FIG. 20 shows a rear view of theblood circuit assembly17 with the organizingtray171 removed. This view shows the rear side of theblood pump13 section with control ports exposed. These control ports mate with correspondingports515 on the front panel511 (seeFIG. 17) so that pneumatic control (e.g., suitable air pressure or vacuum) can be applied to the pumps and valves to control their operation and flow through theblood circuit assembly17.FIG. 20 also shows the offset of the inlet port of theair trap19, i.e., the inlet port at the top of theair trap19 is arranged to the rear of the vertical axis of the generally spherical container portion of theair trap19.
• FIG. 21 shows a perspective view of thefront panel511 of thedialysis unit51 with theblood circuit assembly17 mounted to thefront panel511 without the organizingtray171. (Normally, theblood circuit assembly17 would include the organizingtray171, but thetray171 is not shown in the example so as to more clearly show components at thefront panel511.) On opposite sides of theblood pump13 cassette, thefront panel511 hasspring tabs516 that extend forwardly and resiliently engage with the blood pump cassette and/or the organizingtray171 to retain theblood circuit assembly17 in place. Thetabs516 may include a barb or other feature to help retain theblood circuit assembly17 in place. Thespring tabs516 may be flexed outwardly to release their hold on theblood circuit assembly17, allowing its removal. However, in the absence of an outwardly directed force on thespring tabs516, thetabs516 will remain engaged with theblood circuit assembly17.FIG. 22 shows a front view of thefront panel511 with the organizingtray171 of theblood circuit assembly17 included. To remove theblood circuit assembly17 from thefront panel511, a user may place index fingers behind thehandles172 while simultaneously placing thumbs on the inner side of the spring tabs516 (the sides nearest the blood pumps23) and flexing thespring tabs516 outwardly and away from thepumps23. This causes thespring tabs516 to release theblood circuit assembly17, e.g., disengagement of barbs on thetabs516 from theblood pump13 and/or the organizingtray171. Of course, to remove theblood circuit assembly17, other connections must be removed, including connections to thedialyzer14 and the blood line connection points514, as well as removal of thelines203,204 from theoccluder513. When mounting theblood circuit assembly17 to thefront panel511, the organizingtray171 may be grasped at thehandles172 and properly aligned, e.g., so that thespring tabs516 are aligned to pass through theopenings173 and the control ports of theblood pump13 cassette are aligned with the correspondingports515 on thefront panel511. Theblood circuit assembly17 may then be simply pushed into place, so that thespring tabs516 engage with the organizingtray171 and/or the blood pump cassette. Other connections can then be made, such as connections to thedialyzer14, mounting of theblood lines203,204 with theoccluder513, etc.
• FIG. 21 also shows theslots517 that hold theblood lines203,204 for leading into theoccluder513. Theslots517 define a channel that is slightly smaller than the outside diameter of theblood lines203,204 so that thelines203,204 tend to remain in theslots517 after placement in the slots. This helps to ensure proper association of the lines with theoccluder513. Once theblood circuit assembly17 is mounted on thespring tabs516, the user may then engage theblood lines203,204 with theslots517 by stretching thelines203,204 downward (with theengagement members174 on the organizingtray171 engaging the stop ring or other feature on therespective line203,204 and resisting the downward pull) and pushing thelines203,204 into a corresponding slot. Thelines203,204 can be pushed into place by pressing inwardly on theengagement members174, which as described above, are flexible and bend inwardly relative to the organizingtray171. Thelines203,204 can then be routed through theoccluder513.
• In accordance with another aspect of the invention, thefront panel511 includes a blood line wrap feature around the periphery of thefront panel511. In this illustrative embodiment, thefront panel511 includesflanged portions518 along the top edge and at lower corners of thefront panel511. This allows a user to wrap theblood lines203,204 around the periphery of thefront panel511 by placing thelines203,204 in a channel defined by theflanged portions518. Thelines203,204 may be wrapped in a clockwise direction, starting from a point near the bottom of thedialyzer14, and ending at a point near the lower right corner of thefront panel511. The blood lines203,204 may then be connected at the blood line connection points514, e.g., to allow disinfecting fluid to be circulated through theblood lines203,204. As a result, theblood lines203,204 can be neatly retained on thefront panel511, allowing easy access to other components on thefront panel511 and allowing the user to close thedoors53 with minimal concern for pinching theblood lines203,204 between thedoors53 and thedialyzer unit housing51. Alternatively, theblood lines203,204 may be first connected at the blood line connection points514, and then wrapped in a clockwise direction, starting from a point near the bottom of thedialyzer14, and ending at a point near the lower right corner of thefront panel511. This ensures that the blood lines are properly distributed along theflanged portions518 to reach the connection points514.Vertical fences519 may also be provided along the left and right sides of thefront panel511 to help keep theblood lines203,204 in a desired position and away from thehinge plates533 and other possible pinch points.
• In accordance with another aspect of the invention, thefront panel511 of the dialysis unit51 (or other suitable component) may be arranged to accommodate a variety of differently sized and/or shapeddialyzer units14. Different patients, and in some cases even the same patient over time, may be prescribed different dialyzers so as to provide different treatment conditions. Thus, thedialysis unit51 is preferably arranged to operate with multiple different types ofdialyzers14. In many cases,different dialyzers14 have different dimensions, such as the overall diameter and/or length of the dialyzer unit. In this illustrative embodiment as shown inFIG. 23, thefront panel511 includes a dialyzer mount with a pair of “keyhole” features520 that are arranged to engage with a respective dialysate quick-connect fitting on thedialyzer14. Each keyhole feature520 includes anupper insertion area520asized to receive a portion of the quick-connect fitting and a lowerflanged portion520bthat has a width that is smaller than an overall diameter of the quick-connect fitting and that engages with a grooved area of the quick-connect fitting. So as to aid in understanding of these features,FIG. 24 shows adialyzer14 withquick connect fittings14aattached at dialysate inlet and outlet ports of thedialyzer14. (Blood inlet and outlet ports are located at the extreme top and bottom of thedialyzer14 shown inFIG. 24.) Thequick connect fittings14ashown are of a standard type, and most, if not all, dialyzers14 have dialysate inlet/outlet ports that are arranged to engage with the standardquick connect fittings14a. Thequick connect fittings14aeach include aslide element14bthat is moved to the right (as shown inFIG. 24) relative to a base14cto allow the fitting14ato be engaged with a dialysate port on thedialyzer14. When theslide element14bis moved to allow the fitting14ato be attached to thedialyzer14, agroove14dis closed. However, once the fitting14ais properly seated on the inlet/outlet port of thedialyzer14, theslide element14bmay be released, allowing a spring (not shown) to move the slide to the left as shown inFIG. 24, reestablishing thegroove14dto the condition shown inFIG. 24. Thus, when the quick connect fitting14ais properly engaged with thedialyzer14, thegroove14dwill be present as shown inFIG. 24.
• To mount thedialyzer14 to the keyhole features520, thequick connect fittings14amay be partially inserted into theupper insertion area520aof the top and bottom keyhole features, respectively, so that thegroove14dof each fitting14ais aligned with a flange of the lowerflanged portion520bof the keyhole features520. (Note that theupper insertion area520 of the bottom keyhole feature520 may be made longer than that shown inFIG. 23 to allow the accommodation of a wider range of dialyzer lengths.) With thegrooves14daligned with the flanges, thedialyzer14 may be lowered so that thequick connect fittings14aare fully received into the lowerflanged portions520bof the keyhole features520.
• In accordance with another aspect of the invention, one or both of the keyhole features520 may be adjustable so that the weight of thedialyzer14 is shared by both lowerflanged portions520bof the keyhole features520. For example, in this illustrative embodiment, the bottom keyhole feature520 has part of the lowerflanged portion520badjustable in vertical position relative to thetop keyhole feature520. In this way, the portion of the lowerflanged portion520bmay be adjusted in vertical position so that, with the top quick connect fitting14asupported by theflanged portion520bof thetop keyhole feature520, the movable portion of theflanged portion520bof the bottom keyhole feature can be moved, e.g., upwardly, so that the bottom quick connect fitting14ais also supported by theflanged portion520b. Thus, the weight of thedialyzer14 can be shared by both keyhole features520. Theflanged portion520bmay be made adjustable in any suitable way. In this embodiment, theflanged portion520bhas a “U” shapedmember520cthat is vertically slidable along the vertical flanges and can be fixed in place by tightening a set of thumb screws. The “U” shapedmember520cmay engage the quick connect fitting14aso that the “U” shapedmember520csupports the weight (at least in part) of thedialyzer14.
• Although in the embodiment above, thedialyzer14 is supported by keyhole features in thefront panel511, a support arrangement for the dialyzer may be configured in other ways. For example, theupper insertion area520ais not necessarily required. Instead, only flange portions (e.g., in the shape of a “U” shaped flange having opposed flange portions) may be provided to engage the dialyzer quick connect fittings. The flange portions may be offset from the front surface of thefront panel511 to provide clearance for the fitting and allow the flange portions to engage with the grooves of the quick connect fittings. Also, the flange portions need not be provided in a vertical orientation as shown, but instead may be oriented at an angle to the vertical, e.g., in a horizontal arrangement. The flange portions may have a detent, catch, or other feature to help maintain the dialyzer in place as well.
• In accordance with another aspect of the invention, a bicarbonate, acid and/or other reagent supply device may be selectively associated with the dialysis unit. As described above, thedialysis unit51 requires a supply of certain chemicals to generate dialysate and/or other materials needed for system operation.FIG. 25 shows areagent supply49 used to provide acid, bicarbonate and/or other materials to thedialysis unit52. (FIG. 21 shows thereagent supply49 attached to the acid/bicarbonate connection point512 on thefront panel511.) Thereagent supply49 in this illustrative embodiment includes anE-prong connector491 that is arranged to mate with the acid/bicarbonate connection point512. As with other connections made by the user at thefront panel511, e.g., including the blood line connections at theconnection point514, the mating connectors may be color coded or otherwise marked to help ensure proper connections are made. For example, theE-prong connector491 and the acid/bicarbonate connection point512 may be colored orange, while thearterial line203 and its mating connection at theconnection point514 may be colored red, and thevenous line204 and its mating connection at theconnection point514 are colored blue. Leading from theE-prong connector491 are abicarbonate supply line492, awater supply line493 and anacid supply line494. (SeeFIG. 6 and the accompanying description regarding the function of these lines.) Thewater supply line493 provides water to a bicarbonate supply28 (which in this embodiment is a 750 g Altracart Bicarbonate cartridge (#500750A) sold by Baxter International Inc. that includes a powdered bicarbonate material, but may be any suitable supply), which provides bicarbonate to thedialysis unit51 via thebicarbonate supply line492. In this embodiment, theacid supply line494 leads to anacid bag spike495, which may be used to pierce and draw a suitable acid from a IV-type bag or other container. In this embodiment, theacid bag spike495 includes aspike member495aand a pair of spring clips495b. The spring clips495bare joined together at center portions by a connecting bar such that the spring clips495band the connecting bar form an “H” shape and allow the spring clips495bto be pivoted relative to each other when proximal ends of the spring clips495bare squeezed toward each other. The spring clips495bmay be arranged to engage with a connector element on an acid bag (or other acid supply, not shown) so that thespike member495aremains engaged with the bag until a user disengages theclips495b. For example, distal ends of theclips495bmay include barbs that engage with the acid supply, and the clips may be disengaged from the acid supply by squeezing proximal ends of theclips495btogether to disengage the barb elements at the distal ends of theclips495bfrom the acid supply. Theacid bag spike495 may also include avalve495c(in this case, a pinch clamp) to open/close the line of theacid bag spike495. In accordance with one aspect of the invention, theacid bag spike495 may be replaced (disconnected from theacid supply line494 at a cap connector496) with another component, such as an acid jug straw (not shown) or other arrangement. When used with a jug straw, thecap connector496 may be engaged with an acid jug opening such that thecap connector496 covers the opening, like a cap. Alternatively, the jug straw can terminate in a spike, which then has the ability to penetrate a self-sealing (e.g. rubber) membrane covering the opening of the acid jug. Thus, different types of components may be attached to theacid supply line494 depending on the acid supply arrangement (such as a jug, bottle, bag, or other).
• FIG. 26 shows a close up view of theE-prong connector491 and thecorresponding connection point512 at thefront panel511. TheE-prong connector491 has three parallel prongs (corresponding to the bicarbonate andacid supply lines492 and494 and the water supply line493) that that engage with corresponding receiving holes in theconnection point512. TheE-prong connector491 and receiving holes in theconnection point512 are arranged so that a center lumen (the water supply line493) is arranged above, or otherwise out of, a common plane of the two outer lumens (the bicarbonate andacid supply lines492 and494). In this way, it is ensured that the bicarbonate andacid supply lines492 and494 are properly connected since theE-prong connector491 cannot be engaged with theconnection point512 unless appropriately oriented. TheE-prong connector491 includes a pair ofspring tabs491athat can be engaged withcorresponding slots512ain theconnection point512, e.g., when the prongs are properly seated in receiving holes of theconnection point512. With thetabs491aengaged in theslots512a, theE-prong connector491 cannot be easily removed from theconnection point512, helping reduce the likelihood of an accidental disconnection. TheE-prong connector491 may be disconnected by pressing thetabs491atoward each other so that barbs at the distal ends of thetabs491adisengage from theslots512a. Theconnection point512 hassimilar spring tabs512bwhich allow theconnection point512 to be connected to and disconnected from thefront panel511.
• In accordance with another aspect of the invention, a disinfect connector (not shown) engages withconnection point512 for use during a disinfection procedure. The disinfect connector has three parallel prongs having a similar orientation as theE-prong connector491, so that the prongs may engage with the receiving holes inconnection point512. The channels in the prongs of the disinfect connector terminate within a common chamber within the disinfect connector. Thus, during a disinfect procedure, the bicarbonate flow line, acid flow line and water flow line are all interconnected, permitting disinfection of each of these flow lines during the disinfect procedure. (This is shown as a dashed inverted “T” line at49 inFIG. 6).
• In accordance with another aspect of the invention, theblood lines203,204 are equipped with a connector that enables two types of connections to be made. One type of connection is a plug-in or press-in connection by which the connector can be pushed into a receiving lumen and a leakfree connection made without requiring rotation of the connector or the receiving lumen. A second type of connection is a screw-type connection by which a leakfree connection can be made by a threaded engagement of the connector with a complementary element. For example,FIGS. 27 and 28 show a perspective view and a side view of ablood line connector202 that is used with theblood lines203,204 and that can engage with the bloodline connection point514 on thefront panel511. Theconnector202 includes a tube connection end202athat connects to the correspondingblood line203,204, and a patientaccess connection end202bthat is arranged to connect to both a patient access as well as theconnection point514 to establish a leakfree connection. At the patientaccess connection end202b, theconnector202 includes afrustoconical member202cthat has an internally threaded portion arranged to engage with an externally threaded patient access. For example, thefrustoconical member202cmay be part of a male-type luer connector that includes thecentral tube202eextending from the center of thefrustoconical member202c. When making the luer connection, thetube202emay extend into a female luer connector at the patient access and the threaded portion on the interior of thefrustoconical member202cmay engage with a thread on the female luer connector of the patient access (whether arterial or venous). Such luer connections are standard when connecting blood lines to a patient access. However, theconnector202 may also be engaged with theconnection point514 by simply pushing the patientaccess connection end202binto a receiving hole of theconnection point514. When making this connection, the exterior of thefrustoconical member202cmay engage with a suitable seat, or other surface or element in the connection point514 (such as a valve seat, O-ring, or other) so that a seal is formed between thefrustoconical member202cand theconnection point514. Thecentral tube202emay also, or instead, be used to engage with theconnection point514 to establish a suitable seal. Lockingarms202dthat extend rearwardly from thefrustoconical member202cmay engage withholes514ain the connection point514 (e.g., barbed portions on thearms202dmay engage with theholes514a) to help maintain theconnector202 in the receiving hole of theconnection point514. Theconnector202 may be released by pressing thearms202dtoward each other (e.g., by pressing on finger depression portions at the distal ends of thearms202d), thereby disengaging the barbs from theholes514a, and withdrawing theconnector202. Note that theconnection point514 may includespring tabs514bto allow theconnection point514 to be selectively engaged/disengaged at thefront panel511. Theconnectors202 may be made in any suitable way, such as by molding of plastic as a single unitary part.
• The following are each incorporated herein by reference in their entireties: U.S. Provisional Patent Application Ser. No. 60/903,582, filed Feb. 27, 2007, entitled “Hemodialysis System and Methods”; U.S. Provisional Patent Application Ser. No. 60/904,024, filed Feb. 27, 2007, entitled “Hemodialysis System and Methods”; U.S. patent application Ser. No. 11/787,213, filed Apr. 13, 2007, entitled “Heat Exchange Systems, Devices and Methods”; U.S. patent application Ser. No. 11/787,212, filed Apr. 13, 2007, entitled “Fluid Pumping Systems, Devices and Methods”; U.S. patent application Ser. No. 11/787,112, filed Apr. 13, 2007, entitled “Thermal and Conductivity Sensing Systems, Devices and Methods”; U.S. patent application Ser. No. 11/871,680, filed Oct. 12, 2007, entitled “Pumping Cassette”; U.S. patent application Ser. No. 11/871,712, filed Oct. 12, 2007, entitled “Pumping Cassette”; U.S. patent application Ser. No. 11/871,787, filed Oct. 12, 2007, entitled “Pumping Cassette”; U.S. patent application Ser. No. 11/871,793, filed Oct. 12, 2007, entitled “Pumping Cassette”; and U.S. patent application Ser. No. 11/871,803, filed Oct. 12, 2007, entitled “Cassette System Integrated Apparatus.” In addition, the following are incorporated by reference in their entireties: U.S. Pat. No. 4,808,161, issued Feb. 28, 1989, entitled “Pressure-Measurement Flow Control System”; U.S. Pat. No. 4,826,482, issued May 2, 1989, entitled “Enhanced Pressure Measurement Flow Control System”; U.S. Pat. No. 4,976,162, issued Dec. 11, 1990, entitled “Enhanced Pressure Measurement Flow Control System”; U.S. Pat. No. 5,088,515, issued Feb. 18, 1992, entitled “Valve System with Removable Fluid Interface”; and U.S. Pat. No. 5,350,357, issued Sep. 27, 1994, entitled “Peritoneal Dialysis Systems Employing a Liquid Distribution and Pumping Cassette that Emulates Gravity Flow.” Also incorporated herein by reference are a U.S. patent application entitled “Sensor Apparatus Systems, Devices and Methods,” filed on even date herewith (Docket No. F63, now Ser. No. 12/038,474), and a U.S. patent application entitled “Cassette System Integrated Apparatus,” filed on even date herewith (Docket No. F62).
• While several embodiments of the present invention have been described and illustrated herein, those of ordinary skill in the art will readily envision a variety of other means and/or structures for performing the functions and/or obtaining the results and/or one or more of the advantages described herein, and each of such variations and/or modifications is deemed to be within the scope of the present invention. More generally, those skilled in the art will readily appreciate that all parameters, dimensions, materials, and configurations described herein are meant to be exemplary and that the actual parameters, dimensions, materials, and/or configurations will depend upon the specific application or applications for which the teachings of the present invention is/are used. Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. It is, therefore, to be understood that the foregoing embodiments are presented by way of example only and that, within the scope of the appended claims and equivalents thereto, the invention may be practiced otherwise than as specifically described and claimed.
• The indefinite articles “a” and “an,” as used herein in the specification and in the claims, unless clearly indicated to the contrary, should be understood to mean “at least one.”

Claims (17)

1. An air trap for a blood circuit in a dialysis unit, comprising:

a blood inlet supply line;

a blood outlet supply line; and

a container having an approximately spherical internal wall, an inlet at a top end of the container connected to the blood inlet supply line, and an outlet at a bottom end of the container connected to the blood outlet supply line, the inlet being offset from a vertical axis of the approximately spherical internal wall such that blood entering the container through the inlet is directed to flow in around the approximately spherical wall in a spiral-like path;

wherein when blood is supplied to the container via the blood inlet supply line and blood in the container is removed from the container via the blood outlet supply line, air in the blood entering the container remains in the container.

2. The air trap ofclaim 1, wherein the container is formed by an approximately spherical shell.

3. The air trap ofclaim 1, wherein the blood circuit includes a dialyzer and the air trap receives blood via the blood inlet supply line from the dialyzer.

4. The air trap ofclaim 1, further comprising:

a self-sealing port located at a top of the container.

5. The air trap ofclaim 4, wherein the self-sealing port is formed by a split septum.

6. The air trap ofclaim 4, wherein the split septum is arranged to permit introduction of fluid into, and withdrawal of liquid from, the container by inserting a needleless device through the split septum.

7. The air trap ofclaim 4, wherein the self-sealing port is arranged to be self-cleaning when disinfection liquid is circulated through the container.

8. The air trap ofclaim 7, wherein an inner surface of the self-sealing port is approximately flush with the internal wall of the container at a top of the container.

9. The air trap ofclaim 8, wherein the self-sealing port is cleaned by introducing liquid into the container via the blood outlet supply line and removing liquid from the container via the blood inlet supply line.

10. The air trap ofclaim 1, wherein the inlet port is arranged to receive air in the container when liquid is introduced into the container via the outlet port during a priming operation.

11. The air trap ofclaim 1, wherein the inlet port is arranged to introduce blood into the container in a direction that is approximately tangential to the approximately spherical inner wall of the container.

12. The air trap ofclaim 1, wherein the inlet port is arranged to introduce blood into the container in a direction that is approximately perpendicular to the vertical axis of the container.

13. A method for removing air from a flow of blood in a dialysis unit, comprising:

introducing blood into an upper portion of an approximately spherical container;

causing the blood to flow in a spiral-like path in the container; and

removing the blood from a lower portion of the approximately spherical container.

14. The method ofclaim 13, wherein the step of introducing comprises:

introducing blood into the container in a direction that is approximately tangential to an approximately spherical inner wall of the container.

15. The method ofclaim 13, wherein the step of introducing comprises:

introducing blood into the container in a direction that is approximately perpendicular to the vertical axis of the container.

16. An air trap for a blood circuit in a dialysis unit, comprising:

a blood inlet supply line;

a blood outlet supply line;

a container having an approximately spherical internal wall, an inlet at a top end of the container connected to the blood inlet supply line, and an outlet at a bottom end of the container connected to the blood outlet supply line, the inlet being offset from a vertical axis of the approximately spherical internal wall such that blood entering the container through the inlet is directed to flow in around the approximately spherical wall in a spiral-like path; and

a self-sealing port located at a top of the container, the self-sealing port having an inner surface that is approximately flush with the internal wall of the container at the top of the container,

wherein when blood is supplied to the container via the blood inlet supply line and blood in the container is removed from the container via the blood outlet supply line, air in the blood entering the container remains in the container, and wherein any air in the container is substantially completely removed by introducing liquid into the container via the blood outlet supply line and removing liquid from the container via the blood inlet supply line.

17. The air trap ofclaim 16, wherein the inlet, outlet and internal wall of the container and the self-sealing port are arranged to substantially eliminate stagnation regions.

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