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.

A diaphragm pump, includes a case, a diaphragm dividing a space in the case into a first space and a second space, a liquid feed flow path including an inflow path to introduce a liquid to be fed into the first space and an outflow path to discharge the liquid to be fed from the first space, a drive unit including a compression/decompression device that repeatedly causes displacement of the diaphragm by repeating compression and decompression of a driving fluid filling the second space, and a valve mechanism to open and close the inflow path and the outflow path. The drive unit includes a pressure release mechanism to release pressure of the driving fluid after the driving fluid is compressed or decompressed by the compression/decompression device.

A diaphragm pump, includes a case, a diaphragm dividing a space in the case into a first space and a second space, a liquid feed flow path including an inflow path to introduce a liquid to be fed into the first space and an outflow path to discharge the liquid to be fed from the first space, a drive unit including a compression/decompression device that repeatedly causes displacement of the diaphragm by repeating compression and decompression of a driving fluid filling the second space, and a valve mechanism to open and close the inflow path and the outflow path. The drive unit includes a pressure release mechanism to release pressure of the driving fluid after the driving fluid is compressed or decompressed by the compression/decompression device.

A system for treating a patient with a heart condition includes an atrial assist device (AAD) configured to be positioned in the patients heart to pump blood from an atrium of the patients heart into a ventricle associated with the atrium. The system also includes a controller operatively connected to the AAD and being configured to control the AAD to pump blood from the atrium of the patients heart into the ventricle associated with the atrium.

A blood pump housing device designed to enclose and protect a total artificial heart when implanted in a subject is disclosed. The blood pump housing device comprises a first and second artificial heart pump receiving part (3a, 3b) configured to receive and partly enclose a first and a second artificial heart pump (20a, 20b) of a total artificial heart (TAH); and a first and second pump actuation enclosing part (4a, 4b) configured to partly enclose a first and second pump actuation means (60a, 60b), said artificial heart pump receiving parts (3a, 3b) and pump actuation means enclosing parts (4a, 4b) are arranged to connect to each other in a leak-free manner.

Described are systems and methods for administration of nitric oxide (NO) with use of left ventricular assists devices (LVADs), as well as systems and methods for monitoring the NO delivery devices and/or the LVAD.

A heart pump assembly includes an elongate catheter with a proximal portion and a distal portion, a rotor at the distal portion of the elongate catheter, a driveshaft, and a bearing. The rotor can include an impeller blade shaped to induce fluid flow in a first axial direction. The drive shaft may be coupled to or integrally formed with a proximal end of the rotor and can include a pump element formed in a surface of the drive shaft. The bearing can include a bore into which the drive shaft extends. The pump element is shaped so as to induce fluid flow through the bore in a second axial direction which can be the same or opposite to the first axial direction.

An apparatus for starting operation of a motor of an implantable blood pump including a memory storing one or more default parameters for at least one of controlling and monitoring the startup operation. A processor operatively coupled to the motor is included, the processor is configured to: commence the startup operation based on the one or more default parameters; detect an error during the startup operation; adjust at least one of the one or more default parameters in response to the detected error; store the at least one adjusted parameter in the memory; and commence subsequent startup operations based at least in part on the at least one adjusted parameter.

The systems, devices, and methods presented herein use a heart pump to obtain measurements of cardiovascular function. The heart pumps described herein can operate in parallel with and unload the heart. The system can quantify the functioning of the native heart by measuring certain parameters/signals such as pressure or motor current, then calculate and display one or more metrics of cardiovascular function. These metrics, such as left ventricular end diastolic pressure (LVEDP), left ventricular pressure, and contractility, provide valuable information to a user regarding a patient's state of heart function and recovery.

Blood pump for percutaneous insertion into a heart's ventricle comprising an electrical motor for driving the blood pump, the electrical motor comprising at least tree motor winding units, wherein each motor winding unit is individually connectable to a power supply via two separate phase supply lines connected to the respective motor winding unit terminals. Motor controller for driving and controlling the electrical motor of the blood pump, wherein the motor controller comprises corresponding phase supply line driving units for each motor winding units of the electrical motor of the blood pump which phase supply line driving units are connected via the corresponding two phase supply lines with the corresponding motor winding unit. Blood pump system comprising the blood pump and the motor controller. Control method for controlling the power supply to the motor winding units of the blood pump, wherein the method comprises: detecting a fault of one of the motor winding units, and in case of a detected faulty motor winding unit, switching off the corresponding phase supply line driving unit of the faulty motor winding unit and further operating the electrical motor by the remaining motor winding units, or, alternatively, adjusting driving parameters of the faulty motor winding unit and further operating the electrical motor by all motor winding units. Use of at least three independent motor winding units in an electrical motor for driving of a blood pump for percutaneous insertion, which motor winding units are individually connected to corresponding power supply via corresponding two separate phase supply lines connected to respective motor winding unit terminals of one of the at least three motor winding units.