A method of assisting a heart for the operation of a ventricular assist device comprising the steps of implanting a cannula to the heart and deploying a stent within a left ventricle, a right ventricle, a left atrium, or a right atrium of the heart. The stent may be transferable from a first compact configuration to a second open configuration to facilitate implantation. The stent may also have a flared distal end to assist with alignment, positioning, and prevent outgrowth.

Various aspects of the present disclosure are directed towards apparatuses, systems, and methods that system for delivering a blood pump. The system may include a blood pump that may include one or more impellers configured to cause blood to flow through the pump. The system may also include one or more guidewires. The guidewires may include one or more proximal sections and one or more distal sections, and the distal sections may have first dimensions and the proximal sections may have second dimensions, and the first dimensions may be greater than the second dimensions. The guidewires may also be tapered, geometrically shaped, have a curved profile, a combination thereof, or other configurations.

Various aspects of the present disclosure are directed towards apparatuses, systems, and methods that system for delivering a blood pump. The system may include a blood pump that may include one or more impellers configured to cause blood to flow through the pump. The system may also include one or more guidewires. The guidewires may include one or more proximal sections and one or more distal sections, and the distal sections may have first dimensions and the proximal sections may have second dimensions, and the first dimensions may be greater than the second dimensions. The guidewires may also be tapered, geometrically shaped, have a curved profile, a combination thereof, or other configurations.

There is provided an intravascular blood pump for insertion into a patient's heart. The blood pump comprises a slotless permanent magnet motor contained within a housing, the motor having p magnet pole pairs and n phases, where p is an integer greater than zero, and n is an integer ≥3. The motor comprises a stator extending along a longitudinal axis of the housing and having 2np coils wound to form two coils per phase per magnet pole pair. The stator comprises inner and outer windings each comprising np coils electrically connected such that the current flowing through the coils is in the same direction, the coils of the outer winding arranged on an outer surface of the coils of the inner winding.

There is provided an intravascular blood pump for insertion into a patient's heart. The blood pump comprises a slotless permanent magnet motor contained within a housing, the motor having p magnet pole pairs and n phases, where p is an integer greater than zero, and n is an integer ≥3. The motor comprises a stator extending along a longitudinal axis of the housing and having 2np coils wound to form two coils per phase per magnet pole pair. The stator comprises inner and outer windings each comprising np coils electrically connected such that the current flowing through the coils is in the same direction, the coils of the outer winding arranged on an outer surface of the coils of the inner winding.

The present document relates to a device for fixing a cardiac pump in an opening of a ventricular wall of a beating heart. The device includes: a hollow main body of overall cylindrical shape having an outer surface, this hollow main body includes a proximal end and a distal end between which said the outer surface extends, at least one portion of the outer surface of the main body intended to be placed inside ventricular cavity, except for its distal end, has a surface relief provided with protuberances and hollows, the distal end of the hollow main body forms a smooth crown having an arithmetic average roughness of less than or equal to 1 μm in order to stop the colonization of the fixing device by endothelial cells.

The present document relates to a device for fixing a cardiac pump in an opening of a ventricular wall of a beating heart. The device includes: a hollow main body of overall cylindrical shape having an outer surface, this hollow main body includes a proximal end and a distal end between which said the outer surface extends, at least one portion of the outer surface of the main body intended to be placed inside ventricular cavity, except for its distal end, has a surface relief provided with protuberances and hollows, the distal end of the hollow main body forms a smooth crown having an arithmetic average roughness of less than or equal to 1 μm in order to stop the colonization of the fixing device by endothelial cells.

The present disclosure provides catheter pump system including a catheter assembly configured to be at least partially inserted into a left ventricle (LV). The catheter assembly has a proximal end and a distal end, and includes an elongate body extending between the proximal end and the distal end. The catheter pump system further includes a pressure sensor disposed at the distal end and configured to measure a pressure within a left ventricle when the catheter assembly is inserted.

The present disclosure provides catheter pump system including a catheter assembly configured to be at least partially inserted into a left ventricle (LV). The catheter assembly has a proximal end and a distal end, and includes an elongate body extending between the proximal end and the distal end. The catheter pump system further includes a pressure sensor disposed at the distal end and configured to measure a pressure within a left ventricle when the catheter assembly is inserted.

The invention relates to an intercardiac pump device comprising a pump (11) whose distal end (13) is connected to a cannula (15) which is provided with a suction head (16) for sucking blood. Said strainer is provided with a non-sucking extension (20) for stabilizing the position of said pump device in the heart and mechanically prolonging the cannula (15) without deteriorating hydraulic conditions. Said extension is also used in the form of a spacer in order to avoid that the suction head (16) adheres to a cardiac wall.