A cardiac assist device is provided. The cardiac assist device may comprise a structure surrounding at least a portion of a heart. The cardiac assist device may comprise an inner cup enclosing at least a portion of the structure. The cardiac assist device may comprise an outer cup enclosing at least a portion of the inner cup. The outer cup may comprise an opening. Gas may be conducted into a space between the outer cup and the inner cup, using a pump, to cause a first motion of the structure, associated with a first rotation of a first portion of the heart in a first direction. The gas may be conducted from the space to outside of the outer cup, using the pump, to cause a second motion of the structure, associated with a second rotation of the first portion of the heart in a second direction.

The disclosure relates to a heart support system with at least one system unit that includes a pump arrangement, a first connection apparatus connected to the pump arrangement and a second connection apparatus connected to the pump arrangement, wherein the pump arrangement has a first pump that is fluidically connected in a first flow path between the first and the second connection apparatus. The pump arrangement further has an intermediate reservoir and a second pump, which are connected in series together with the first pump in the first flow path, wherein the intermediate reservoir is fluidically arranged between the first pump and the second pump. The disclosure further relates to a cannula arrangement for a heart support system of this kind and a corresponding use of the heart support system.

The present disclosure provides intravascular ventricular assist devices for insertion into the vasculature of an individual to improve the overall blood flow of the individual. In many embodiments, the intravascular ventricular assist devices described herein provide an individual with an intravascular ventricular assist device that is sized and configured for insertion into an aortic root or pulmonary root such that its reduced size and placement provide the individual with an improved quality of life.

A cardiac assist device is provided. The cardiac assist device may comprise a structure surrounding at least a portion of a heart. The cardiac assist device may comprise an inner cup enclosing at least a portion of the structure. The cardiac assist device may comprise an outer cup enclosing at least a portion of the inner cup. The outer cup may comprise an opening. Gas may be conducted into a space between the outer cup and the inner cup, using a pump, to cause a first motion of the structure, associated with a first rotation of a first portion of the heart in a first direction. The gas may be conducted from the space to outside of the outer cup, using the pump, to cause a second motion of the structure, associated with a second rotation of the first portion of the heart in a second direction.

A heart pump including: a housing forming a cavity including: at least one inlet aligned with an axis of the cavity; and, at least one outlet provided in a circumferential outer wall of the cavity; an impeller provided within the cavity, the impeller including vanes for urging fluid from the inlet to the outlet; and, a drive for rotating the impeller in the cavity and wherein a flow path through the pump has a minimal cross-sectional area of at least 50 mm.sup.2.

A heart pump device may be provided with an implantable heart pump, which has at least one sensor, wherein at least one of the sensors is a sensor for a rotor of the heart pump, and with a control device, which is connected to the heart pump by means of a transcutaneous line, characterised by a signal processing device, which on the one hand is connected by means of the transcutaneous line to the control device, and which on the other hand is connected to at least one sensor of the heart pump and transmits signals of at least one sensor via the transcutaneous line to the control unit. The signal processing device may be for a pre-processing of the sensor data for more efficient transmission via the transcutaneous line.

A heart pump including: a housing forming a cavity including: at least one inlet aligned with an axis of the cavity; and, at least one outlet provided in a circumferential outer wall of the cavity; an impeller provided within the cavity, the impeller including vanes for urging fluid from the inlet to the outlet; and, a drive for rotating the impeller in the cavity and wherein a flow path through the pump has a minimal cross-sectional area of at least 50 mm.sup.2.

A system for generating a blood circulation in at least part of an organ of a vertebrate, including a first artificial cavity and a second artificial cavity. The cavities each include a flexible membrane capable of beating under the action of a gas. Each of the membranes separate in a sealed manner a blood circulation chamber and a chamber containing the gas. The system also includes: a first low pressure gas buffer reservoir; a second high-pressure gas buffer reservoir; a gas distribution; and a pneumatic pump.

A heart pump device may be provided with an implantable heart pump, which has at least one sensor, wherein at least one of the sensors is a sensor for a rotor of the heart pump, and with a control device, which is connected to the heart pump by means of a transcutaneous line, characterized by a signal processing device, which on the one hand is connected by means of the transcutaneous line to the control device, and which on the other hand is connected to at least one sensor of the heart pump and transmits signals of at least one sensor via the transcutaneous line to the control unit. The signal processing device may be for a pre-processing of the sensor data for more efficient transmission via the transcutaneous line.

A blood pump control system includes a local processing terminal and a remote processing terminal. The local processing terminal is configured to transmit to the remote processing terminal, collected current state parameters of the blood pump and heart activity indexes, and to drive and control the blood pump according to blood pump adjusting parameters received from the remote processing terminal. The remote processing terminal is configured to obtain current blood pump adjusting parameters according to the current state parameters, and the heart activity indexes received from the local processing terminal, and set adjusting conditions; and to transmit the blood pump adjusting parameters back to the local processing terminal.