A method for outputting a combined power source alarm for an implantable blood pump includes determining a status for each of first and second power sources of the blood pump. A combined power source alarm based on the statuses of the first and second power sources is outputted. A method for generating an alarm based on fault detections in a mechanically assisted circulation system includes processing a series of fault detection indications to classify a fault as active or inactive. An alarm is generated if the fault is active for more than a predetermined amount of time.

A heart pump including a housing defining a cavity including at least one inlet and at least one outlet, an impeller provided within the cavity, the impeller including vanes for urging fluid from the inlet to the outlet upon rotation of the impeller, a drive that rotates the impeller within the cavity, a magnetic bearing including at least one bearing coil that controls an axial position of the impeller within the cavity, a sensor that senses an axial position of the impeller within the cavity and a controller. The controller includes an electronic processing device that, in response to a change in axial hydraulic forces on the impeller determines an axial position of the impeller within the cavity, determines a reference power in accordance with the determined axial position and controls the magnetic bearing to cause the impeller to move until a bearing power indicator indicative of the power used by the magnetic bearing reaches the reference power.

A blood pump includes a hollow body in which an impeller with blading is provided for producing an axial propulsion of blood along the impeller. An at least partly actively stabilized magnetic bearing device is provided wherein the impeller may be set into a rotation about a rotation axis of the impeller, with a motor stator. The hollow body has an inlet for the flow of blood into the hollow body in an inflow direction which is essentially parallel to the rotation axis, and an outlet for the outflow of the blood out of the hollow body in an outflow direction.

Mechanical circulatory supports configured to operate in series with the native heart are disclosed. In an embodiment, an intravascular propeller is installed into the descending aorta and anchored within via an expandable anchoring mechanism. The propeller and anchoring mechanism may be foldable so as to be percutaneously deliverable to the aorta. The propeller may have foldable blades. The blades may be magnetic and may be driven by a concentric electromagnetic stator circumferentially outside the magnetic blades. The stator may be intravascular or may be configured to be installed around the outer circumference of the blood vessel. The support may create a pressure rise between about 20-50 mmHg, and maintain a flow rate of about 5 L/min. The support may have one or more pairs of contra-rotating propellers to modulate the tangential velocity of the blood flow. The support may have static pre-swirlers and or de-swirlers. The support may be optimized to replicate naturally occurring vortex formation within the descending aorta.

Mechanical circulatory supports configured to operate in series with the native heart are disclosed. In an embodiment, an intravascular propeller is installed into the descending aorta and anchored within via an expandable anchoring mechanism. The propeller and anchoring mechanism may be foldable so as to be percutaneously deliverable to the aorta. The propeller may have foldable blades. The blades may be magnetic and may be driven by a concentric electromagnetic stator circumferentially outside the magnetic blades. The stator may be intravascular or may be configured to be installed around the outer circumference of the blood vessel. The support may create a pressure rise between about 20-50 mmHg, and maintain a flow rate of about 5 L/min. The support may have one or more pairs of contra-rotating propellers to modulate the tangential velocity of the blood flow. The support may have static pre-swirlers and or de-swirlers. The support may be optimized to replicate naturally occurring vortex formation within the descending aorta.

The present invention relates to a fluid pump that comprises a housing having an inlet opening for receiving the fluid, an outlet opening for discharging the fluid and enclosing an impeller rotating inside the housing to pump the fluid from the inlet opening to the outlet opening and a motor assembly to drive the impeller. The housing is shaped to establish a single turn volute of 360 turn angle providing a first conveying channel located peripherally around the impeller from a fluid entry point at 0 turn angle to a fluid exit point at 360 turn angle of the single turn volute being connected to the outlet opening. The first conveying channel has a first cross section area in radial direction perpendicular to the rotational plane of the impeller, where a size of the first cross section area increases as a monotonic increasing function of the turn angle between entry point and exit point.

A heart pump including: a housing forming a cavity including: at least one inlet aligned with an axis of the cavity; and, at least one outlet provided in a circumferential outer wall of the cavity; an impeller provided within the cavity, the impeller including vanes for urging fluid from the inlet to the outlet; and, a drive for rotating the impeller in the cavity and wherein a flow path through the pump has a minimal cross-sectional area of at least 50 mm.sup.2.

A heart pump including a housing forming a cavity including at least one inlet and at least one outlet, an impeller provided within the cavity, the impeller including vanes for urging fluid from the inlet to the outlet upon rotation of the impeller, a drive that rotates the impeller within the cavity, a magnetic bearing including at least one bearing coil that controls an axial position of the impeller within the cavity and a controller. The controller includes an electronic processing device that monitors changes in a bearing indicator in response to a perturbation in blood flow, the bearing indicator being at least partially indicative of operation of the magnetic bearing and controls the drive to thereby selectively change a rotational speed of the impeller at least partially in accordance with changes in the bearing indicator.

An implantable blood pump includes a control unit storing patient specific settings. The control unit is configured to store patient specific settings. The patient specific settings can be used to determine a target operating speed for the blood pump and/or a target operating mode for the blood pump. The patient specific settings can include at least one of an operating mode for the pump, a set speed for the pump, a lower speed limit for the pump, a patient hematocrit value, a patient hematocrit date, a patient blood density, and a periodic log rate for event and periodic data.

A method for outputting a combined power source alarm for an implantable blood pump includes determining a status for each of first and second power sources of the blood pump. A combined power source alarm based on the statuses of the first and second power sources is outputted. A method for generating an alarm based on fault detections in a mechanically assisted circulation system includes processing a series of fault detection indications to classify a fault as active or inactive. An alarm is generated if the fault is active for more than a predetermined amount of time.