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.

A catheter blood pump includes a cannula with an expandable central portion having a proximal end, a distal end and a blood flow conduit therebetween. A flexible inlet portion at the distal end is provided with a plurality of spaced apart inlet struts configured to prevent an obstruction from entering, and a flexible outlet portion is provided with a plurality of spaced apart outlet struts operative to reduce a swirl velocity of blood, wherein the plurality of spaced apart inlet struts and the plurality of spaced apart outlet struts are fabricated from a collapsible shape memory material.

A catheter blood pump includes a cannula with an expandable central portion having a proximal end, a distal end and a blood flow conduit therebetween. A flexible inlet portion at the distal end is provided with a plurality of spaced apart inlet struts configured to prevent an obstruction from entering, and a flexible outlet portion is provided with a plurality of spaced apart outlet struts operative to reduce a swirl velocity of blood, wherein the plurality of spaced apart inlet struts and the plurality of spaced apart outlet struts are fabricated from a collapsible shape memory material.

A device to assist the performance of a heart with at least one pump that is formed as a rotary pump and driven via a magneto coupling.

A device to assist the performance of a heart with at least one pump that is formed as a rotary pump and driven via a magneto coupling.

An apparatus for a heart of a patient having a cardiac assist device adapted to be implanted into the patient to assist the heart with pumping blood. The apparatus has a sensor adapted to be implanted into the patient. The sensor in communication with the cardiac assist device and the heart which measures native volume of the heart. Alternatively, the sensor monitors the heart based on admittance while the cardiac assist device. Alternatively, the sensor monitors the heart based on impedance.

An apparatus for a heart of a patient having a cardiac assist device adapted to be implanted into the patient to assist the heart with pumping blood. The apparatus has a sensor adapted to be implanted into the patient. The sensor in communication with the cardiac assist device and the heart which measures native volume of the heart. Alternatively, the sensor monitors the heart based on admittance while the cardiac assist device. Alternatively, the sensor monitors the heart based on impedance.

Systems and methods for detecting suction events in blood pumps by monitoring pump motor current. A pump suction event is detected based on a comparison of a pulsatility index that is calculated based on a filtered pump motor current signal with a first predetermined threshold or based on a comparison of a calculated index associated with a normalized band-pass filtered pump motor current signal with a second predetermined threshold. A suction event is also detected based on comparisons of both the calculated pulsatility index and the calculated index associated with the normalized band-pass filtered pump motor current signal with respective first and second predetermined thresholds.

A transcatheter valve implant assembly has a ventricular assist device, a prosthetic valve, a stent frame structure, and a docking station, and is implanted at an aortic or a pulmonary valve. During implantation, the native valve leaflets of the respective valve at the implantation site are engaged with the prosthetic valve and/or the stent frame structure while the stent frame structure is connected to the docking station with the prosthetic valve adjacent to the proximal end of the stent frame structure. The ventricular assist device is inserted into the interior the stent frame structure with an inlet of ventricular assist device positioned in the respective ventricle associated with the implantation site and the outlet of the ventricular assist device positioned to discharge into the respective blood vessel associated with the implantation site. The ventricular assist device is releasably connected with the stent frame structure and the docking station.

A catheter pump system includes a catheter assembly having a proximal end, a distal end, and an elongate body extending therebetween. The catheter pump system also includes a motor assembly including a shaft assembly extending at least partially within the elongate body of the catheter assembly. The shaft assembly is configured to rotate about an axis. The catheter pump system further includes a flow diverter housing defining a chamber and a fluid pathway through which a proximally-conveyed fluid flows. The shaft assembly extends outward from the chamber into an inner lumen of the elongate body. The catheter pump system also includes a seal configured to extend around and engage the shaft assembly to inhibit fluid within the elongate body of the catheter assembly from entering the chamber at least about an outer periphery of the shaft assembly.