A blood pump comprises a pump casing having a blood flow inlet and a blood flow outlet connected by a passage, and an impeller rotatable about an axis of rotation. A surface of the impeller faces a surface of the pump casing spaced from said surface of the impeller by a clearance, the clearance being in fluid connection with the passage at a clearance transition point. At least one wash out channel extends through the impeller and is in fluid connection with the passage via a first opening and with the clearance via a second opening. The first opening of the wash out channel is arranged in an area of the impeller that is under a higher pressure than the clearance transition point so as to cause a blood flow from the first opening through the wash out channel and the clearance to the clearance transition point.

Systems and methods are provided herein for treating a patient in cardiogenic shock. An intravascular heart pump system is inserted into vasculature of the patient. The heart pump system has a cannula, pump outlet, pump inlet, and rotor. The heart pump system is positioned within the patient such that the cannula extends across the patient's aortic valve, the pump inlet is located within the patient's left ventricle, and the pump outlet is located within the patient's aorta. Data related to time-varying parameters of the heart pump system is acquired from the heart pump system. A plurality of features are extracted from the data. A probability of survival of the patient is determined based on the plurality of features and using a prediction model. The heart pump system is operated to treat the patient.

Systems and methods are provided herein for treating a patient in cardiogenic shock. An intravascular heart pump system is inserted into vasculature of the patient. The heart pump system has a cannula, pump outlet, pump inlet, and rotor. The heart pump system is positioned within the patient such that the cannula extends across the patient's aortic valve, the pump inlet is located within the patient's left ventricle, and the pump outlet is located within the patient's aorta. Data related to time-varying parameters of the heart pump system is acquired from the heart pump system. A plurality of features are extracted from the data. A probability of survival of the patient is determined based on the plurality of features and using a prediction model. The heart pump system is operated to treat the patient.

A method includes detecting a startup of an apheresis machine; in response to detecting start up, transmitting data to a server; determining, based on the data, whether software of the apheresis machine is current; receiving, in response to the data, a response from the server; and preventing usage of apheresis machine if the response indicates the software is not current. The data transmitted to the server may include one or more of a data log, a firmware version identifier, and an error log. The response may include a lockout signal. The response may include a software update. The software update may include a firmware update. The method may include automatically initiating installation of the software update. The method may include ceasing prevention of usage of the apheresis machine following installation of the software update.

A method includes detecting a startup of an apheresis machine; in response to detecting start up, transmitting data to a server; determining, based on the data, whether software of the apheresis machine is current; receiving, in response to the data, a response from the server; and preventing usage of apheresis machine if the response indicates the software is not current. The data transmitted to the server may include one or more of a data log, a firmware version identifier, and an error log. The response may include a lockout signal. The response may include a software update. The software update may include a firmware update. The method may include automatically initiating installation of the software update. The method may include ceasing prevention of usage of the apheresis machine following installation of the software update.

The invention relates to a transmitter unit (12) comprising a housing (20), a transmitter coil (18) arranged in the housing (20) for inductively transferring electrical energy to a receiver unit (14) which is provided with a receiver coil (16) and is arranged in the tissue (2) of the body (1) of a patient when the housing (20) having a contact surface (22) is placed on the body (1), and comprising a control device (30) for controlling the operation of the transmitter coil (18). According to the invention, a temperature sensor (26) is provided in the transmitter unit for determining a heating of the tissue (2) of the body (1) caused by the inductive transfer of electrical energy to the receiver unit (14). The invention also relates to methods for determining the temperature (T.sub.Korr) of the tissue (2) of a body (1) on a surface (38), by which electrical energy is inductively transmitted for supplying an electrical consumer arranged in the tissue (2) of the body (1), and to a method for inductively transferring electrical energy.

The invention relates to a transmitter unit (12) comprising a housing (20), a transmitter coil (18) arranged in the housing (20) for inductively transferring electrical energy to a receiver unit (14) which is provided with a receiver coil (16) and is arranged in the tissue (2) of the body (1) of a patient when the housing (20) having a contact surface (22) is placed on the body (1), and comprising a control device (30) for controlling the operation of the transmitter coil (18). According to the invention, a temperature sensor (26) is provided in the transmitter unit for determining a heating of the tissue (2) of the body (1) caused by the inductive transfer of electrical energy to the receiver unit (14). The invention also relates to methods for determining the temperature (T.sub.Korr) of the tissue (2) of a body (1) on a surface (38), by which electrical energy is inductively transmitted for supplying an electrical consumer arranged in the tissue (2) of the body (1), and to a method for inductively transferring electrical energy.

An impeller (1) for an implantable vascular support system (2) is provided. The impeller includes an impeller body (3) having a first longitudinal portion (4) and a second longitudinal portion (5) forming a first inner rotor (12) having at least one magnet encapsulated in the second longitudinal portion (5). At least one blade (6) formed in the first longitudinal portion (4) is configured to axially convey a fluid upon rotation. A second outer rotor (13) extends axially and includes at least one magnet. The first rotor (12) and the second rotor (13) form a magnetic coupling (14). The magnets of the first and second rotor being arranged to partially axially overlap with an axial offset and are entirely radially offset.

Apparatus and methods are described including a blood pump that includes a catheter, a first impeller disposed on the catheter, and a second impeller disposed on the catheter, proximally to the first impeller. A control unit drives the first and second impellers to pump blood of a subject, by driving the first and second impellers to rotate. The blood pumps is configured such that (a) the first and second impellers are shaped differently from each other when the first and second impellers are in non-radially-constrained configurations, (b) the first and second impellers are sized differently from each other when the first and second impellers are in non-radially-constrained configurations, and/or (c) the first and second impellers are driven by the control unit to rotate under respective rotation conditions that are different from each other. Other applications are also described.

Apparatus and methods are described including a blood pump that includes a catheter, a first impeller disposed on the catheter, and a second impeller disposed on the catheter, proximally to the first impeller. A control unit drives the first and second impellers to pump blood of a subject, by driving the first and second impellers to rotate. The blood pumps is configured such that (a) the first and second impellers are shaped differently from each other when the first and second impellers are in non-radially-constrained configurations, (b) the first and second impellers are sized differently from each other when the first and second impellers are in non-radially-constrained configurations, and/or (c) the first and second impellers are driven by the control unit to rotate under respective rotation conditions that are different from each other. Other applications are also described.