A ventricular assist device is provided, including a blood pump, a driveline and a feedthrough. The blood pump includes a pump housing, an axi-symmetric oval-shaped blood sac and stem assembly received in the pump housing, and a pressure sensing system embedded in the pump housing. The driveline includes a pneumatic lumen, at least one electric wire and a tether included in a wall of the driveline, wherein the electric wires and the tether are disposed on the pneumatic lumen. The feedthrough connects the driveline to the pump housing.

An intravascular blood pump for percutaneous insertion into a patient’s vasculature comprises a pumping device and a supply catheter. The pumping device comprises a pump section with a blood flow inlet, blood flow outlet, and impeller for conveying blood from the inlet to the outlet and further comprises a drive section connected to the pump section and adapted to drive the impeller. The supply line supplies the drive section with electric energy for driving the impeller. The supply catheter supplies electric energy for driving the impeller. The pump section is axially arranged between the drive section and the supply line. The pump section includes a flexibly bendable cannula, and electric lines are arranged across the cannula in a manner to prevent their rupture in the event that the cannula is subject to bending.

A circulatory support device includes a flexible cannula having a fluid outlet at a proximal end; and a pump assembly disposed at a distal end of the flexible cannula. The pump assembly includes a pump housing having a fluid inlet defined therein; a motor disposed within a distal end of the housing; and an impeller, driven to rotate by the motor, and configured to push blood toward the fluid outlet.

Apparatus is provided for treating heart failure, the apparatus including one or more propeller blades and a controller, which is configured to rotate the one or more propeller blades to produce continuous non-pulsatile blood flow not synchronized with a cardiac cycle of a subject. An intra-atrial anchor includes a stent surrounding the one or more propeller blades. The intra-atrial anchor is coupled to the one or more propeller blades and configured to be anchored in a left atrium of the subject so as to position the one or more propeller blades in the left atrium oriented such that the one or more propeller blades, when rotated by the controller, draw blood from the left atrium and expel the blood in the left atrium toward a mitral valve, thereby increasing atrial pressure above the mitral valve. Other embodiments are also described.

Apparatus is provided for treating heart failure, the apparatus including one or more propeller blades and a controller, which is configured to rotate the one or more propeller blades to produce continuous non-pulsatile blood flow not synchronized with a cardiac cycle of a subject. An intra-atrial anchor includes a stent surrounding the one or more propeller blades. The intra-atrial anchor is coupled to the one or more propeller blades and configured to be anchored in a left atrium of the subject so as to position the one or more propeller blades in the left atrium oriented such that the one or more propeller blades, when rotated by the controller, draw blood from the left atrium and expel the blood in the left atrium toward a mitral valve, thereby increasing atrial pressure above the mitral valve. Other embodiments are also described.

The invention relates to a fluid pump having a housing delimiting a fluid chamber and having a conveying element for the fluid disposed in the fluid chamber, the housing, with respect to the shape and/or size thereof, being able to be changed between at least a first, expanded state and a second, compressed state. The object, to stabilise adequately a corresponding housing, is achieved according to the invention by the housing having at least one stabilisation chamber which can be supplied with a fluid pressure and is different from the fluid chamber, the first state of the housing being assigned to a first fluid pressure in the stabilisation chamber and the second state of the housing being assigned to a second fluid pressure.

The invention relates to a fluid pump having a housing delimiting a fluid chamber and having a conveying element for the fluid disposed in the fluid chamber, the housing, with respect to the shape and/or size thereof, being able to be changed between at least a first, expanded state and a second, compressed state. The object, to stabilise adequately a corresponding housing, is achieved according to the invention by the housing having at least one stabilisation chamber which can be supplied with a fluid pressure and is different from the fluid chamber, the first state of the housing being assigned to a first fluid pressure in the stabilisation chamber and the second state of the housing being assigned to a second fluid pressure.

An implantable right ventricular assist device configured to be implanted within the right ventricle of a heart, including a percutaneously deliverable centrifugal pump configured to carry the blood from the right ventricle to the pulmonary artery; an exit cylinder configured to secure directly or indirectly the centrifugal pump within a portion of the pulmonary artery; and a power source. Also, a method to percutaneously and transluminally implant the right ventricular assist device within the right ventricle of a patient's heart. Further, the use of the right ventricular assist device to long-term assist of the right ventricle of a patient's heart.

A circulatory assist apparatus comprising: an inflatable pumping balloon having a proximal end joined to an elongated balloon catheter, the balloon catheter having a distal end joined to the pumping balloon and a proximal end, separated from the distal end by a length sufficient to extend from within a circulatory lumen to the outside of a patient's body, for receiving positive and negative pressure pulses from a pump to inflate and deflate the pumping balloon; and a radially expandable frame, mounted on one of a segment extending distally from the pumping balloon, the balloon catheter, and a sleeve tube surrounding the balloon catheter. The expandable frame is manipulate to expand within the circulatory lumen, and functions to space apart the inflatable balloon from the circulatory lumen, having a first diameter in a collapsed configuration for intraluminal delivery and a second, larger diameter in an expanded configuration achieved by said manipulation.

A minimally invasive circulatory support platform that utilizes an aortic stent pump or pumps. The platform uses a low profile catheter-based techniques and provides temporary and chronic circulatory support depending on the needs of the patient. Also described is a catheter-based temporary assist pump to treat patients with acute decompensated heart failure and provide circulatory support to subjects undergoing high risk percutaneous coronary intervention (“PCI”). Further described is a wirelessly powered circulatory assist pump for providing chronic circulatory support for heart failure patients. The platform and system are relatively easy to place, have higher flow rates than existing systems, and provide improvements in the patient's renal function.