Rotary lobe pump, comprising a pump housing (2, 9, 10) with a substantially cylindrical pump chamber (8) and a rotary lobe as rotor (1) with at least two blades (3) arranged opposite each other or evenly distributed in the circumferential direction and at least one sealing valve (4), characterized in that at least two sealing valves (4a, 4b) arranged opposite one another or uniformly distributed in the circumferential direction are provided, the at least two sealing valves (4a, 4b) being rotatable or pivotable, and an inlet duct (11) to at least two inlet openings (6) into the pump chamber (8) and an outlet duct (12) from at least two outlet openings (7) out of the pump chamber (8) being provided axially in a rotor axial tube (18), extending from the opposite axial ends and separated from one another.

The invention concerns a control device for controlling a blood flow of an intravascular blood pump for percutaneous insertion into a patient's blood vessel, the blood pump comprising a pump unit with a drive unit for driving the pump unit and configured to convey blood from a blood flow inlet towards a blood flow outlet, wherein the control device is configured to operate the blood pump in a selectable zero-flow control mode, wherein a blood flow command signal is selected, and the control device comprises a first controller and a second controller, wherein the first controller is configured to control the blood flow by adjusting a speed command signal for the drive unit, and the second controller is configured to control a drive speed of the drive unit.

A blood circulation assist system includes a ventricular assist device (VAD) and a controller. The VAD is attachable to a heart of a patient to pump blood from a ventricle of the heart into a blood vessel of the patient. The VAD includes an impeller, a motor stator operable to rotate the impeller, and an accelerometer generating an accelerometer output indicative of accelerations of the VAD. The controller controls operation of the motor stator to control rotational speed of the impeller based on the accelerometer output.

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.

Method and systems control a rotational speed of a blood pump during ventricular diastole. A method includes controlling a blood pump in accordance with a first segment operational mode. A controller monitors the blood flow rate through the blood pump. The controller determines, based on the blood flow rate, whether continued controlling of the blood pump per the first segment operational mode would result in the blood flow rate through the blood pump being less than a target minimum blood flow rate. In response to a determination that continued controlling of the blood pump per the first segment operational mode would result in the blood flow rate through the blood pump being less than the target minimum blood flow rate, the controller controls the rotational speed of the blood pump so that the blood flow rate through the blood pump is approximate to the target minimum blood flow rate.

A blood pump system including a blood pump, an intravascular flow cannula, and a pressure sensor. The intravascular flow cannula is in flow communication with the blood pump and has a distal end portion distally from the blood pump and a proximal end portion closer to the blood pump. The intravascular flow cannula has at least one blood flow through opening at its distal end portion for blood to enter or exit the flow cannula. The blood flow through opening has a borderline surrounding the through opening. The pressure sensor is configured radially within the flow cannula and borders a proximal portion of the borderline.

A blood pump system including a blood pump, an intravascular flow cannula, and a pressure sensor. The intravascular flow cannula is in flow communication with the blood pump and has a distal end portion distally from the blood pump and a proximal end portion closer to the blood pump. The intravascular flow cannula has at least one blood flow through opening at its distal end portion for blood to enter or exit the flow cannula. The blood flow through opening has a borderline surrounding the through opening. The pressure sensor is configured radially within the flow cannula and borders a proximal portion of the borderline.

A dialysis cassette includes a cassette housing having a plurality of channels fluidly coupled to a plurality of connectors and a plurality of valves disposed within the plurality of channels. The dialysis cassette also includes a pump assembly disposed within the cassette housing. The pump assembly includes a pump housing and a flexible rotor having a plurality of flexible vanes, where the flexible rotor is rotatable in either a clockwise direction or a counterclockwise direction to move a fluid through the plurality of channels.

A dialysis cassette includes a cassette housing having a plurality of channels fluidly coupled to a plurality of connectors and a plurality of valves disposed within the plurality of channels. The dialysis cassette also includes a pump assembly disposed within the cassette housing. The pump assembly includes a pump housing and a flexible rotor having a plurality of flexible vanes, where the flexible rotor is rotatable in either a clockwise direction or a counterclockwise direction to move a fluid through the plurality of channels.

The invention relates to a method for determining at least one flow parameter of a fluid (31) flowing through an implanted vascular support system (10), comprising the following steps: a) estimating the flow velocity of the fluid (31), b) carrying out a pulsed Doppler measurement using an ultrasound sensor (18) of the support system (10) in an observation window (201) inside the support system (10), wherein the observation window (201) is displaced at an observation window velocity which is determined using the flow velocity estimated in Step a), c) determining the at least one flow parameter of the fluid using at least one measurement result of the pulsed Doppler measurement or a measurement result of the pulsed Doppler measurement and the observation window velocity.