A blood purification apparatus in which the error in the amount of discharge from a blood pump that is caused by the change in the suction pressure of the blood pump is reduced. A blood purification apparatus includes a blood circuit through which blood of a patient is extracorporeally circulated; a dialyzer connected to proximal ends of an arterial blood circuit and a venous blood circuit and that purifies the blood extracorporeally circulating through the blood circuit; a squeezable tube connected to the arterial blood circuit; a blood pump allowing liquid in the squeezable tube to flow by squeezing the squeezable tube in a lengthwise direction while compressing the squeezable tube in a radial direction; and a pressure-detecting device attached to a predetermined position of the arterial blood circuit that is nearer to a distal end than a position where the blood pump is provided, the pressure-detecting device being capable of detecting a suction pressure of the blood pump.

The invention relates to an infusate holder for use in dialysis. The infusate holder can include one or more interior compartments for holding infusate containers or infusates. The interior compartments are aligned to cooperate with fluid connectors of a dialysis system, ensuring that the proper infusates are added to the dialysis system at a proper location.

The present invention relates to a method and to an apparatus for preparing a dialysis solution, wherein the apparatus has a first circuit and a second circuit, wherein the first circuit has a container for receiving the consumed dialysis solution or fresh water or another fluid, the primary side of a filter connected downstream of the container, and a return line from the primary side of the filter into the container, wherein the filter is configured to prepare purified water from the consumed dialysis solution or from fresh water or from another fluid, and wherein the second circuit has the secondary side of the filter, the dialyzate side of a dialyzer, a reservoir, a line that leads from the reservoir to the secondary side of the filter, by means of which dialyzate or a dialyzate concentrate can be supplied to the secondary side of the filter, and a filtrate line that leads away from the secondary side of the filter.

The present specification provides a dialysate management system for generating, weighing, and heating a dialysate fluid during a dialysis treatment. The dialysate management system includes a container and base enclosure. A bottom surface of the container rests within the base enclosure, which is configured to weigh the fluid in the container and measure its conductivity. The fluid may be heated using a heater integrated into the base enclosure or positioned in-line with a fluid pathway. The base of the container is preferably sloped and positioned within the internal volume of the container is a disposable prescription bag having a predefined quantity of prescription compositions that dissolve when water is poured into the container.

The invention relates to a system for treating blood, which includes a single cassette capable of carrying out the various CRRT treatments.

A pulmonary artery (PA) via trans-septal to left atrial (LA) percutaneous dual lumen cannulation system which reduce the pressure of the right ventricle provides drainage of pulmonary artery blood with bypassing the lung while return the blood to the Left Atrium (LA) without the need for thoracotomy for a wearable pump less extra corporeal lung assist (pECLA) to remove CO.sub.2, pump less extra corporeal membrane oxygenation (ECMO), para-corporeal pump driven CO.sub.2 removal, extra corporeal CO.sub.2 removal (ECCO.sub.2R) pump driven, para-corporeal pump driven membrane oxygenation, or extra corporeal membrane oxygenation (ECMO) with extra-corporeal pump. By establishing percutaneously a shunt with a dual lumen cannula between PA and LA using the PA-LA pressure gradient as the driving force for the blood flow through the drainage lumen, CO.sub.2 removal device, or oxygenator and return cannula lumen in the vascular system.

Systems and methods are provided for separating a red blood cell-containing fluid into separated red blood cells and another fluid constituent. A suitable system includes a disposable fluid flow circuit and a durable, reusable separation system, with the circuit being mounted onto or otherwise associated with the separation system. The circuit includes a membrane separator for separating the fluid into its constituent parts, as well as a leukoreduction filter. The leukoreduction filter may be used before or after the red blood cell-containing fluid has been passed into the membrane separator. The red blood cell-containing fluid (if the leukoreduction filter is positioned upstream of the membrane separator) or the separated red blood cells (if the leukoreduction filter is positioned downstream of the membrane separator) may also be passed through a microaggregate filter prior to passing through the leukoreduction filter.

The invention relates to a method and a system for synthesizing a medical preparation, a peristaltic pump being used for pumping liquid from a plurality of source containers. According to the invention, micro-amounts are extracted only in the linear region of the peristaltic pump.

An apparatus for treating blood with veno-venous access comprising: a blood circuit (C1, C2) provided with an inlet branch (C3) and an outlet branch (C4), an oxygenator (OX), a blood pump (P) adapted for drawing blood from the patient and returning it to the patient at a first blood flow value. The blood pump (P) is a volumetric peristaltic pump; the blood circuit (C1, C2) comprises a high-speed portion (C1) and a recirculation circuit (C2); the apparatus (100) comprises at least one pressure measuring means (PA; PR; PP), as well as automatic flow regulation means (FD) acting on the recirculation circuit to determine a second blood flow value in the same recirculation circuit (C2) so that in the high speed portion (C1) the flow value is the sum of said first and second flow values.

The present invention relates to a sorbent manifold and related systems and methods having a plurality of passageways fluidly connectable to one or more valves and one or more sensors and components for use in a sorbent dialysis system. The sorbent manifold can control the one or more valves to direct fluid to either pass through a sorbent cartridge or bypass the sorbent cartridge based on measurements obtained from sensors.