A61M1/341

BLOOD RINSEBACK SYSTEM AND METHOD
20190167884 · 2019-06-06 ·

A hemodialysis system is provided and includes a dialyzer, a dialysis fluid circuit in fluid communication with the dialyzer, a blood circuit, a blood detector and a blood rinseback scheme, wherein the blood rinseback scheme includes transferring blood to the patient using a physiologically acceptable fluid, wherein the physiologically acceptable fluid is introduced from its source into an arterial line between an arterial line patient end and a blood pump of the blood circuit, and flowed through the dialyzer, through a venous drip chamber and to the blood detector along a venous line of the blood circuit, where the physiologically acceptable fluid is sensed by the blood detector to indicate an end of the blood rinseback.

Dialysis method and system including wireless patient data

A dialysis method includes: receiving at least one of blood pressure data from a blood pressure monitor or patient weight data from a weight scale at a dialysis machine at least one of (i) before or (ii) after each treatment performed by the dialysis machine; generating ultrafiltration (UF) removed data over a treatment performed by the dialysis machine; sending the UF removed data and at least one of the blood pressure data or the patient weight data to a server; determining at least one of a UF trend, a blood pressure trend or a patient weight trend from the UF removed data, the blood pressure data or the patient weight data, respectively; and displaying at least one of the UF trend, the blood pressure trend or the patient weight trend so that a therapy adjustment can be made if necessary.

Device and method for regulating a treatment device

A method and a device are disclosed for regulating an ultrafiltration in a dialysis treatment, in which the blood to be ultrafiltered in an extracorporeal blood circulation (109) flows through a blood chamber (110) of a dialyzer (113), which is subdivided by a semipermeable membrane (111) into a blood chamber (110) and a dialysis fluid chamber (108), and dialysis fluid in a dialysis fluid circulation (109) flows through the dialysis fluid chamber (108) of the dialyzer (113). The device has a blood pump (115) for controlling a blood flow in the extracorporeal blood circulation (112), a dialysis fluid pump (107) for controlling a dialysis fluid flow in the dialysis fluid circulation (109) upstream or downstream from the dialyzer (113), for controlling the dialysis fluid flow upstream of downstream from the dialyzer, a balancing device (104) for setting up a fluid balance in the dialysis fluid circulation between an inflow (106) and an outflow (105) of the dialysis fluid chamber (113) as a measure of the ultrafiltration, as well as a regulating unit (101) for regulating the blood pump (115), the throttle (117) and/or the dialysis fluid pump (107). The pumps or the throttles (117) are regulated so that a predetermined ultrafiltration is achieved.

DIALYSIS SYSTEM HAVING ADAPTIVE PRESCRIPTION MANAGEMENT
20240207498 · 2024-06-27 ·

An example peritoneal dialysis system is disclosed. The example peritoneal dialysis system includes at least one pump and a memory device configured to store therapy prescriptions including a first ultrafiltration (UF) therapy prescription for removing ultrafiltrate from a patient, and a second UF therapy prescription for removing less ultrafiltrate from the patient compared to the first UF therapy prescription. The system further includes a logic implementer configured to receive UF removed data, use the UF removed data to form or update a moving average UF removed trend, and compare the moving average UF removed trend to an expected UF removal trend or an expected UF removal minimum value. When the moving average UF removed trend is below the expected UF removal trend or the expected UF removal minimum value, the logic implementer provides a recommendation that the first UF therapy prescription should be selected for a next peritoneal dialysis treatment.

Method for recovering residual blood from an extracorporeal circulation circuit and equipment for collecting and recovering residual blood in the extracorporeal circulation circuit

The processes and equipment for collecting and recovering residual blood from cardiopulmonary bypass provide increased efficiency in hemoconcentrators and hemodialysers. Residual blood collection and recovery equipment for extracorporeal circulation circuits include a flow-limiting valve disposed at an exit of a hemofilter, which automatically regulates a resistance in a line as a function of an inlet pressure. The valves of the residual blood collection and recovery equipment also include an opening that is proportional to a flow and a hematocrit. The systems and methods for blood recovery can be used after surgery or for hemodialysis, in addition to other applications.

Multiple Mode Treatment Devices Methods and Systems
20240181145 · 2024-06-06 · ·

A blood treatment system employing at least two pumps for performing a low blood flow treatment is operable for high blood flow treatments such as extracorporeal membrane oxygenation (ECMO) by providing a fluid circuit with parallel blood flow paths and recruiting multiple ones of the pumps for parallel blood flow.

Extracorporeal blood filtering machine and methods

An extracorporeal blood filtering machine can include a blood circuit, an effluent circuit, and a source fluid circuit and can be controlled by a controller. The extracorporeal blood filtering machine can also include access ports for connecting the source fluid circuit to the blood circuit, as well as blood sensors to detect possible issues with the extracorporeal blood filtering machine. The extracorporeal blood filtering machine can include density sensors and flow sensors that enable it to be more accurate and to operate while being transported. The extracorporeal blood filtering machine can further include a user interface and can display fluid inflow/outflow information. A medical fluid container can automatically empty after being filled. An apparatus for supporting a medical fluid container can include a hanger and an attachment member with the apparatus able to adjust to ensure the medical fluid container remains properly oriented directly under a medical fluid container scale.

Dialysis system including cassette with pumping tubes

A hemodialysis system includes a blood treatment machine, a blood pump housed by the blood treatment machine, a first dialysate pump housed by the blood treatment machine, a second dialysate pump housed by the blood treatment machine; and a fluid cassette including an upper portion and a lower portion. The fluid cassette further includes a blood pumping tube extending from the upper portion to the lower portion of the fluid cassette, a first dialysate pumping tube extending from the upper portion to the lower portion of the fluid cassette, and a second dialysate pumping tube extending from the upper portion to the lower portion of the fluid cassette.

METHOD FOR TESTING THE RIGIDITY OF A DISPOSABLE

The present invention concerns a method for testing the rigidity of a particular disposable for volumetric balancing, for a blood treatment device, comprised of the following steps: filling the disposable or portion thereof with a liquid, enclosing the filled liquid, so that a certain volume of liquid is present in the disposable unit or the portion thereof, supplying and/or discharging a certain volume of liquid, and measuring the change in pressure caused by the supply and/or discharge of the volume of liquid. The present invention further concerns a blood treatment device.

Renal therapy system including a blood pressure monitor

An example renal therapy system includes a blood pressure monitor configured to output blood pressure data concerning a patient and a renal therapy machine communicatively coupled to the blood pressure monitor. The renal therapy machine is configured to generate ultrafiltration (UF) removed data from a prescribed renal therapy treatment performed by the renal therapy machine on the patient, and transmit the UF removed data and the blood pressure data via a network. At least one of a UF trend or a blood pressure trend from the UF removed data or the blood pressure data is determined, enabling a further determination as to at least one of (a) whether a prescribed renal therapy treatment adjustment or a new prescribed renal therapy treatment needs to be made, (b) whether the patient is complying with the prescribed renal therapy treatment, or (c) whether a condition related to an alarm or an alert exists.