Abstract:
An implantable blood pump includes a tube including an inner wall, and wherein during operation of the blood pump, the impeller rotates within the tube and a distance between the inner wall of the tube and the thrust bearing decreases as a speed of the impeller increases.
Abstract:
A blood pump including a housing having an inlet element, the inlet element including a distal portion coupled to the housing and a proximal portion sized to be received within at least a portion of a heart of a patient and a rotor configured to rotate within the housing and impel blood from the heart. At least one pressure sensor is coupled to the proximal portion of the inlet element.
Abstract:
A driveline for an implantable blood pump including a percutaneous connector including an outer tube, the outer tube defining an exterior surface and having a proximal portion and a distal portion opposite the proximal portion, the proximal portion being couplable to the implantable blood pump disposed within a body of a patient and the distal portion being couplable to a controller outside of the body of the patient and at least one electronic instrument coupled to the outer tube and fluidically sealed from the exterior surface.
Abstract:
The present invention relates to kits and methods for calibrating a pump through performance of a thermal knockdown process including demagnetization of an impeller of the pump where the impeller is separate from the pump. By heat treating the impeller, a property of magnetic interaction of the pump is reduced in a repeatable manner. A kit includes a pump with impeller, a controller and an oven. The method generally involves an iterative process of testing the pump for a property related to magnetic interaction of the elements of the pump, removing the impeller from the pump, heating the impeller under controlled conditions, then placing the impeller back into the pump to repeat the test performed initially.
Abstract:
A signal processing circuit for controlling operation of an implanted ventricular assist device comprising an input module for receiving one or more signals of a patient from one or more sensors. A processor for processing the received signals is included, the processor configured to compare a total blood output on a left side of the patient's heart with a total blood output on a right side of the patient's heart; determine at least one from the group consisting of the presence of fluid imbalance between the left and right sides of the patient's heart and the absence of fluid imbalance between the left and right sides of the patient's heart based on the comparison; and when the presence of fluid imbalance is determined, control the implanted ventricular device to restore fluid balance between the left and right sides of the patient's heart.
Abstract:
The presence or absence of a suction condition in an implantable blood pump is determined at least in part based on a parameter related to flow, such as a parameter related to thrust on the rotor of the pump. A local extreme of the parameter representing the minimum flow during ventricular diastole in an earlier interval is used to establish a threshold value. A value of the parameter representing the minimum flow during ventricular diastole in a later interval is compared to this threshold. If the comparison indicates a substantial decline in the minimum flow between the earlier and later intervals is associated with a suction condition. During the absence of a suction condition, the threshold is continually updated, so that the system does not indicate presence of a suction condition if the flow decreases gradually.
Abstract:
A method of operating an implantable blood pump having a first stator, a second stator, and an impeller movably disposed there between. The method includes applying a first voltage waveform at first phase to the first stator to generate a magnetic field to rotate the impeller. A second voltage waveform is applied at a second phase shifted from the first phase to the second stator to rotate the impeller, the second voltage waveform is asymmetric to the first voltage waveform.
Abstract:
A blood pump including a housing having an inlet element, the inlet element including a distal portion coupled to the housing and a proximal portion sized to be received within at least a portion of a heart of a patient and a rotor configured to rotate within the housing and impel blood from the heart. At least one pressure sensor is coupled to the proximal portion of the inlet element.
Abstract:
A method of responding to an adverse event associated with an implantable blood pump including detecting the adverse event, reducing a pump speed of the blood pump relative to a set pump speed in response to the detected adverse event, and determining whether at least one of a group consisting of the adverse event and a second adverse event is present following the reducing of the pump speed of the blood pump. If the at least one of the group consisting of the adverse event and a second adverse event is not present, the method includes increasing the pump speed to the set pump speed and if the at least one of the group consisting of the adverse event and a second adverse event is present while increasing the pump speed to the set pump speed, the method includes reducing the pump speed to a maximum safe operating speed.
Abstract:
A method of controlling an implantable blood pump including a housing having a proximal portion including an inlet, a distal portion including an outlet, and an impeller therein, the method including detecting when a pressure in the housing exceeds a pressure threshold and executing a first vector control command to displace the impeller axially in a distal direction from a primary position to a secondary position different than the primary position in response to the pressure exceeding the pressure threshold.