Patent classifications
A61M60/50
Systems and methods for determining cardiac performance
The systems and methods described herein determine metrics of cardiac performance via a mechanical circulatory support device and use the cardiac performance to calibrate, control and deliver mechanical circulatory support for the heart. The systems include a controller configured to operate the device, receive inputs indicative of device operating conditions and hemodynamic parameters, and determine vascular performance, including vascular resistance and compliance, and native cardiac output. The systems and methods operate by using the mechanical circulatory support device (e.g., a heart pump) to introduce controlled perturbations of the vascular system and, in response, determine heart parameters such as stroke volume, vascular resistance and compliance, left ventricular end diastolic pressure, and ultimately determine native cardiac output.
Transcutaneous energy transfer systems
The present disclosure relates to an improved transcutaneous energy transfer (TET) system that generates and wirelessly transmits a sufficient amount of energy to power one or more implanted devices, including a heart pump, while maintaining the system's efficiency, safety, and overall convenience of use. The disclosure further relates one or more methods of operation for the improved system.
Blood pump
The invention concerns a control device for controlling a blood flow of an intravascular blood pump for percutaneous insertion into a patient's blood vessel, the blood pump comprising a pump unit with a drive unit for driving the pump unit and configured to convey blood from a blood flow inlet towards a blood flow outlet, wherein the control device is configured to operate the blood pump in a selectable zero-flow control mode, wherein a blood flow command signal is selected, and the control device comprises a first controller and a second controller, wherein the first controller is configured to control the blood flow by adjusting a speed command signal for the drive unit, and the second controller is configured to control a drive speed of the drive unit.
Blood pump
The invention concerns a control device for controlling a blood flow of an intravascular blood pump for percutaneous insertion into a patient's blood vessel, the blood pump comprising a pump unit with a drive unit for driving the pump unit and configured to convey blood from a blood flow inlet towards a blood flow outlet, wherein the control device is configured to operate the blood pump in a selectable zero-flow control mode, wherein a blood flow command signal is selected, and the control device comprises a first controller and a second controller, wherein the first controller is configured to control the blood flow by adjusting a speed command signal for the drive unit, and the second controller is configured to control a drive speed of the drive unit.
Devices for pumping blood, related systems, and related methods
An intravascular device for pumping blood includes a catheter comprising a membrane chamber located between a proximal end and a distal end of the catheter. An inflatable membrane is disposed within the membrane chamber. The intravascular device includes a first one-way valve and optionally a second one-way valve configured to permit blood flow in a first direction. The first one-way valve may be positioned proximal to the membrane chamber, and the second one-way valve may be positioned distal to the membrane chamber. Methods related to intravascular devices and their respective use are provided.
Devices for pumping blood, related systems, and related methods
An intravascular device for pumping blood includes a catheter comprising a membrane chamber located between a proximal end and a distal end of the catheter. An inflatable membrane is disposed within the membrane chamber. The intravascular device includes a first one-way valve and optionally a second one-way valve configured to permit blood flow in a first direction. The first one-way valve may be positioned proximal to the membrane chamber, and the second one-way valve may be positioned distal to the membrane chamber. Methods related to intravascular devices and their respective use are provided.
BLOOD PUMP
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.
CARDIOVASCULAR ASSIST SYSTEM THAT QUANTIFIES HEART FUNCTION AND FACILITATES HEART RECOVERY
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.
Systems and Methods for Inertial Sensing for VAD Diagnostics and Closed Loop Control
A blood circulation assist system includes a ventricular assist device (VAD) and a controller. The VAD is attachable to a heart of a patient to pump blood from a ventricle of the heart into a blood vessel of the patient. The VAD includes an impeller, a motor stator operable to rotate the impeller, and an accelerometer generating an accelerometer output indicative of accelerations of the VAD. The controller controls operation of the motor stator to control rotational speed of the impeller based on the accelerometer output.
A VASCULAR COUPLING DEVICE
A vascular coupling device (10), comprising a first and a second coupling element (21, 22) wherein each one of said first and second coupling elements (21, 22) has an external surface (23′, 23″) facing an external side, a coupling surface (25′, 25″) facing a coupling side, a central opening (27′, 27″), and a first and a second tubular connecting element (31, 32). Each one of said first and second tubular connecting elements (31, 32) is arranged in a corresponding central opening (27′, 27″) of the first and second coupling elements (21, 22) respectively, and with second open ends (37, 38) protruding through said central openings (27′, 27″) on said external side of each of said first and second coupling elements (21, 22). The first and second coupling elements (21, 22) being removably connected to each other into a locked configuration, or disconnected from each other into an unlocked configuration by means of a first and second locking structure (41, 42) being arranged on a centerline A and opposite to each other on an outer perimeter of said vascular coupling device (10). The vascular device further comprises a fail-safe arrangement comprising first and second cut-in portions (91, 92) arranged on said first coupling element (21) configured to receive first and second projecting elements (93, 94) arranged on said second coupling element (22), thereby preventing erroneous connection of said first and second coupling elements (21, 22) to each other.