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.

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.

An electromagnetic rotary drive includes a rotor including a magnetically effective core surrounded by a stator. The stator has poles arranged around the magnetically effective core and each of the poles is delimited by an end face. The rotor is capable of being magnetically driven without contact in an operating state about an axial direction, and is capable of being magnetically levitated without contact with respect to the stator. The rotor is configured to be magnetically levitated in a radial plane and is passively magnetically stabilized in the axial direction against tilting. The magnetically effective core has a rotor height which is a maximum extension of the magnetically effective core in the axial direction, the rotor height being greater than a stator pole height defined by a maximum extension of the end faces in the axial direction.

An electromagnetic rotary drive includes a rotor and a stator. The rotor magnetically driven without contact about an axial direction, and magnetically levitated without contact with respect to the stator. The rotor actively magnetically levitated in a radial plane and passively magnetically stabilized in the axial direction against tilting. The stator has coil cores, each including a longitudinal limb extending in the axial direction and a transverse limb arranged in the radial plane. The transverse limb extends from the longitudinal limb and is bounded by an end face. A concentrated winding is arranged on each of the longitudinal limbs surrounding a respective longitudinal limb. The end faces have a first distance in the radial direction from a first portion and a second distance in the radial direction from a second portion, the second distance greater than the first distance.

The present invention relates to systems and methods for in situ inspection, interrogation, and maintenance of heart pump function in subjects with an implanted heart pump. In certain embodiments, the system comprises a catheter assembly deliverable to the inflow port and outflow port of the implanted heart pump. The system comprises additional components used to examine pump function and prevent malfunction. In certain embodiments, the invention allows for temporary, mid-term, or permanent exclusion of the implanted heart pump from cardiac function without surgically removing the pump.

The present invention relates to systems and methods for in situ inspection, interrogation, and maintenance of heart pump function in subjects with an implanted heart pump. In certain embodiments, the system comprises a catheter assembly deliverable to the inflow port and outflow port of the implanted heart pump. The system comprises additional components used to examine pump function and prevent malfunction. In certain embodiments, the invention allows for temporary, mid-term, or permanent exclusion of the implanted heart pump from cardiac function without surgically removing the pump.

A blood pump comprises a pump casing having a blood flow inlet and a blood flow outlet, and an impeller arranged in said pump casing and rotatably supported in the pump casing by a bearing so as to be rotatable about an axis of rotation. The impeller has blades for conveying blood from the blood flow inlet to the blood flow outlet. The bearing comprises at least one stationary bearing portion coupled to the pump casing and having a stationary bearing surface that faces radially outwards. The bearing further comprises a rotating bearing surface interacting with the stationary bearing surface to form the bearing, wherein the rotating bearing surface faces radially inwards and is formed on an exposed radially inner edge of the blades. The blades are designed to draw blood deposit on the stationary bearing surface in a radially outward direction.

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.

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.