A pump is provided with a housing and with an upstream inlet and a downstream outlet and a fluid channel with a channel axis, said fluid channel being arranged between the inlet and outlet. A rotor which can be brought into rotation by way of a motor is arranged within the fluid channel. Furthermore, a sensor arrangement is provided which can detect an inclination of the rotation axis of the rotor.

A pumping system (200) for controlling the flow of interatrial blood comprises, housed inside a container (201), a control element (30, 30′, 30″) of the interatrial blood flow. The control element comprises: at least one worm screw (31), the rotation of which creates a two-way flow of interatrial blood; or a pair of counter-rotating propellers (31′); or a pair of membranes (31″) whose deformation creates a two-way flow of interatrial blood; or a flexible structure (31″) whose change in volume within the container (201) creates a two-way flow of interatrial blood.

The invention relates to a device for circulatory support of the heart and to a corresponding method with a holding means which is configured such that it can be implanted intracardially in the left and/or right ventricular outflow tract of the heart by means of a catheter, preferably using an endovascular method, through a femoral access and/or a percutaneous transventricular, transseptal, transapical or transvenous access, wherein the holding means comprises an anchoring means which can be fixed in the subcommissural triangle underneath the aortic valve and the pulmonary valve, respectively in the flow direction of the blood on the ventricular side of the aortic valve and the pulmonary valve, respectively, a pump which is configured such that it can be fixed in the holding means by means of a catheter, preferably using an endovascular method, through a femoral access and/or a percutaneous transventricular, transseptal, transapical or transvenous access, wherein the pump (a) can either be inserted releasably into the holding means after the holding means has been fixed by means of the anchoring means in the subcommissural triangles underneath the aortic valve and the pulmonary valve, respectively or (b) is firmly connected to the collapsible and expandable anchoring means.

Method and systems control a rotational speed of a blood pump during ventricular diastole. A method includes controlling a blood pump in accordance with a first segment operational mode. A controller monitors the blood flow rate through the blood pump. The controller determines, based on the blood flow rate, whether continued controlling of the blood pump per the first segment operational mode would result in the blood flow rate through the blood pump being less than a target minimum blood flow rate. In response to a determination that continued controlling of the blood pump per the first segment operational mode would result in the blood flow rate through the blood pump being less than the target minimum blood flow rate, the controller controls the rotational speed of the blood pump so that the blood flow rate through the blood pump is approximate to the target minimum blood flow rate.

An implantable ventricular assist device comprises an intraventricular stent used for the creation of an artificial chamber inside the ventricle, a balloon-like structure used to drive the change of the artificial chamber between a contractile configuration and a diastolic configuration, a power system used for driving the change of the balloon-like structure between the contractile configuration and the diastolic configuration. There is also a power system and a mechanical design to operate the system working, wherein in the contractile configuration, the balloon-like structure expands and occupies the space of the artificial chamber and drives the blood inside the artificial chamber flow outside the artificial chamber, wherein in the diastolic configuration, the balloon-like structure shrinks and releases the space inside the artificial chamber, and the blood outside the artificial chamber flows back into the artificial chamber. It is easy to reach the goal of cardiac function.

An implantable ventricular assist device comprises an intraventricular stent used for the creation of an artificial chamber inside the ventricle, a balloon-like structure used to drive the change of the artificial chamber between a contractile configuration and a diastolic configuration, a power system used for driving the change of the balloon-like structure between the contractile configuration and the diastolic configuration. There is also a power system and a mechanical design to operate the system working, wherein in the contractile configuration, the balloon-like structure expands and occupies the space of the artificial chamber and drives the blood inside the artificial chamber flow outside the artificial chamber, wherein in the diastolic configuration, the balloon-like structure shrinks and releases the space inside the artificial chamber, and the blood outside the artificial chamber flows back into the artificial chamber. It is easy to reach the goal of cardiac function.

The invention relates to a device (150) for monitoring the state of health of a patient (100), wherein the device (150) comprises an input interface (160) for inputting a first pressure signal (145) and a second pressure signal (155) and a processing unit (165) for processing the first pressure signal (145) and the second pressure signal (155) in order to determine a processing value (170) in order to monitor the state of health of the patient (100) based the processing value (170).

The invention relates to a device (150) for monitoring the state of health of a patient (100), wherein the device (150) comprises an input interface (160) for inputting a first pressure signal (145) and a second pressure signal (155) and a processing unit (165) for processing the first pressure signal (145) and the second pressure signal (155) in order to determine a processing value (170) in order to monitor the state of health of the patient (100) based the processing value (170).

The heart pump includes: a rotary impeller inserted in the systemic ventricle, the rotary impeller being provided with: a sealing membrane sutured onto the outer wall of the heart so as to secure the rotary impeller to the wall of the heart; a casing arranged inside the systemic ventricle such as to be able to suction and then discharge the blood; a preferably brushless motor connected to the casing and arranged inside the systemic ventricle and/or in the body of the ventricle, so as to facilitate maintenance; a managing unit installed in the epigastric region and including a preferably rechargeable power source and a unit for controlling the rotary impeller; a wired link between the managing unit and the rotary impeller; and a system for transmitting haemodynamic and rhythmic data measured by the heat pump via telemedicine.

Improved securement devices for use with intracardiac blood pump assemblies are provided. The present technology provides securement devices that may be used with a sheath assembly (e.g., an introducer sheath assembly, repositioning sheath assembly), and which are configured to restrict movement of an object (e.g., the catheter of the pump assembly) within the sheath assembly except when a mechanism (e.g., button) of the securement device is actively being actuated (e.g., pressed, held, etc.).