Abstract: Apparatus comprising and methods are described including a blood pump that includes an axial shaft, and an impeller disposed on the axial shaft. The impeller is configured to pump blood of the subject by rotating. The impeller and the axial shaft are configured to undergo axial back-and-forth motion during operation of the impeller. A distal tip element is disposed at a distal end of the blood pump. The distal tip element defines an axial-shaft-receiving tube, configured to receive at least a portion of the axial shaft during forward motion of the axial shaft. The distal tip element additionally defines an atraumatic distal tip portion disposed distally of the axial-shaft-receiving tube. Other applications are also described.

Abstract: Apparatus includes a flexible intraventricular receptacle that assumes a first volume upon passage of fluid that is not blood into the receptacle and a second, smaller volume upon passage of the fluid out of the receptacle. An expandable extracardiac receptacle expands upon transfer of the fluid into the extracardiac receptacle from the intraventricular receptacle and contracts upon passage of the fluid out of the extracardiac receptacle. A transmyocardial conduit allows passage of the fluid between the intraventricular receptacle and the extracardiac receptacle responsively to a cardiac cycle. During ventricular systole, a volume of fluid is expelled from the intraventricular receptacle, through the conduit, and into the extracardiac receptacle, producing a corresponding decrease in a total volume of the ventricle during isovolumetric contraction of the ventricle. Other embodiments are also described.

Abstract: In a method for managing a cardiac pump intended to assist the heart of a patient, the cardiac pump sends pressurized blood at a flow rate proportional to the speed of rotation Vrpm of the pump through the aortic valve of the heart. The steps, during a same ventricular systole, include: detecting mitral valve closure, rotational speed Vrpm of the pump being strictly less than a maximum value Vrpm max, increasing Vrpm of the pump such that, at time t2, after the time t corresponding to the closing of the mitral valve, the speed of rotation of the pump is equal, or substantially equal, to the maximum value Vrpm max of the speed of rotation, and keeping the speed of rotation Vrpm of the pump at this maximum value Vrpm max for at least a portion of the time period T during which the aortic valve is open.

Abstract: A method for synchronizing operation of a heart assist pump device to a patient's cardiac cycle includes obtaining a signal from a motor of a heart assist pump device and filtering the signal to remove noise. The method also includes determining a speed synchronization start point at which time the motor of the heart assist pump device will begin a change in speed of operation based on the filtered signal. The method further includes modulating a speed of the motor of the heart assist pump device to a target speed at the speed synchronization start point, thereby synchronizing the change in speed of operation with a patient's cardiac cycle.

Abstract: A method for synchronizing operation of a heart assist pump device to a patient's cardiac cycle includes obtaining a signal from a motor of a heart assist pump device and filtering the signal to remove noise. The method also includes determining a speed synchronization start point at which time the motor of the heart assist pump device will begin a change in speed of operation based on the filtered signal. The method further includes modulating a speed of the motor of the heart assist pump device to a target speed at the speed synchronization start point, thereby synchronizing the change in speed of operation with a patient's cardiac cycle.

Abstract: An extravascular pulsation blood pump possesses a bidirectionally acting pumping system (P, M) having a pump (P) which is connected via a first conduit (L1) to the left ventricle (LV) and via a second conduit (L2) to the aorta (AO). By means of a control means (St), the pump (P) is operated alternately in one and the other direction according to a given cardiac rhythm, so that alternately blood is sucked through the first conduit (L1) and simultaneously blood ejected through the second conduit (L2) to the same extent, on the one hand, and blood is sucked through the second conduit (L2) and simultaneously blood ejected through the first conduit (L1), on the other hand. The pulsation blood pump combines the functions and advantages of an extravascular copulsation pump with those of an extravascular counterpulsation blood pump.

Abstract: The invention is a new generation permanent heart assist device developed to be installed into great arteries such as trans-aortic and trans-pulmonary artery to maintain blood circulation of the patients with end-stage heart failure. This device is a sort of brushless, synchronous, servo, electric motor which uses direct driver technology. It consumes little energy and provides high blood flow. The specially designed hollow rotor without a pivot pin provides enough blood flow to the patient by pushing the blood forward with the helical winglets inside it. The risk of thromboembolic events on the foreign surface that contacts with blood is less than in the counterparts of this device. Finally, the invention; is a curved permanent heart assist device that is applied on the aortas, reinforced twice with double stators and designed in smaller size so as not to compress surrounding tissues and organs.

Abstract: A ventricular assist device includes a stent for placement within a cardiac artery and arranged for placement, the stent arranged to have an open configuration defining a flow path, a rotor sized to fit within the stent and arranged for percutaneous placement the flow path, the rotor including a surface disposed about a central portion and angled with respect to the flow path and having a first plurality of magnets. A collar is sized for placement about the cardiac artery and includes a stator. A power source is coupled to the stator, and the stator and the rotor are arranged to rotate the rotor about an axis. A timing control module controls a rotational speed of the rotor. Accordingly, the surface of the rotor is arranged to move blood along the flow path in response to rotation of the rotor.

Abstract: A method of estimating the blood flow rate of a heart ventricle assist device which is positioned externally of, or implanted in, a patient. The assist device comprises a blood pump having a rapidly rotating, electrically powered impeller, and comprises briefly interrupting power to the impeller to cause its rotation to slow. From this, blood viscosity can be estimated, which viscosity is used to obtain real time, estimated blood flow rates and pressure heads. Apparatus for accomplishing this is disclosed.

Abstract: A ventricular assist device includes a pump such as an axial flow pump, an outflow cannula connected to the outlet of the pump, and an anchor element. The anchor element is physically connected to the pump, as by an elongate element. The pump is implanted within the left ventricle with the outflow cannula projecting through the aortic valve but desirably terminating short of the aortic arch. The anchor element is fixed to the wall of the heart near the apex of the heart so that the anchor element holds the pump and outflow cannula in position.

Abstract: An axial-flow blood pump for pumping blood includes a substantially cylindrical outer enclosure. A tubular housing concentric with and located within the outer enclosure has at one end an inlet and at an opposite end an outlet. A motor stator is concentric with and located between the outer enclosure and the tubular housing. An impeller is concentric with and located within the tubular housing. The impeller is suspended in operation by a combination of passive magnetic forces between magnets within the impeller or magnetized regions of the impeller and the motor stator and hydrodynamic thrust forces generated as blood flows between the tubular housing and a plurality of hydrodynamic thrust bearing surfaces located on the impeller. A volute may be in fluid-tight connection with the outlet of the tubular housing for receiving blood in the axial direction and directing blood in a direction normal to the axial direction.

Abstract: A high efficiency blood pump includes a pump housing, wherein the pump housing provides an inlet and outlet. The pump includes a motor housing, wherein the motor housing contains a motor. An impeller is housed in the pump housing, wherein the impeller is radially supported by a hydrodynamic bearing providing at least one row of pattern grooves. A diaphragm provided by the pump housing separates the impeller chamber from the motor chamber. A magnetic coupling is provided between the motor and the impeller, wherein the magnetic coupling causes the impeller to rotate when the motor rotates and provides axial restraint of the impeller.

Abstract: An axial-flow blood pump for pumping blood includes a substantially cylindrical outer enclosure. A tubular housing concentric with and located within the outer enclosure has at one end an inlet and at an opposite end an outlet. A motor stator is concentric with and located between the outer enclosure and the tubular housing. An impeller is concentric with and located within the tubular housing. The impeller is suspended in operation by a combination of passive magnetic forces between magnets within the impeller or magnetized regions of the impeller and the motor stator and hydrodynamic thrust forces generated as blood flows between the tubular housing and a plurality of hydrodynamic thrust bearing surfaces located on the impeller. A volute may be in fluid-tight connection with the outlet of the tubular housing for receiving blood in the axial direction and directing blood in a direction normal to the axial direction.

Abstract: A heart pump including first and second cavities, each cavity including a respective inlet and outlet, a connecting tube extending between the first and second cavities, an impeller including: a first set of vanes mounted on a first rotor in the first cavity portion; a second set of vanes mounted on a second rotor in the second cavity portion; and, a shaft connecting the first and second rotors, the shaft extending through the connecting tube, a drive for rotating the impeller and a magnetic bearing including at least one bearing coil for controlling an axial position of the impeller, at least one of the drive and magnetic bearing being mounted outwardly of the connecting tube, at least partially between the first and second cavity portions.

Abstract: An axial-flow blood pump for pumping blood includes a substantially cylindrical outer enclosure. A tubular housing concentric with and located within the outer enclosure has at one end an inlet and at an opposite end an outlet. A motor stator is concentric with and located between the outer enclosure and the tubular housing. An impeller is concentric with and located within the tubular housing. The impeller is suspended in operation by a combination of passive magnetic forces between magnets within the impeller or magnetized regions of the impeller and the motor stator and hydrodynamic thrust forces generated as blood flows between the tubular housing and a plurality of hydrodynamic thrust bearing surfaces located on the impeller. A volute may be in fluid-tight connection with the outlet of the tubular housing for receiving blood in the axial direction and directing blood in a direction normal to the axial direction.

Abstract: A high efficiency cardiac support system is suitable for chronic use in treating heart failure, wherein the system includes an implantable rotary blood pump, an implantable power module, a wireless power transfer subsystem, a patient monitor, and a programmer. In a cardiac support system, the cumulative efficiencies of the components of the system are capable of providing therapeutically effective blood flow for a typical day of awake hours using the energy from a single wireless recharge of an implanted rechargeable energy source. Moreover, the implantable rechargeable energy source may be recharged during a normal sleep period of 8 hours or less. The system may provide full or partial cardiac support without the need for external wearable batteries, controllers, or cables.

Abstract: A method of estimating the blood flow rate of a heart ventricle assist device which is positioned externally of, or implanted in, a patient. The assist device comprises a blood pump having a rapidly rotating, electrically powered impeller, and comprises briefly interrupting power to the impeller to cause its rotation to slow. From this, blood viscosity can be estimated, which viscosity is used to obtain real time, estimated blood flow rates and pressure heads. Apparatus for accomplishing this is disclosed.

Abstract: An impeller for a blood pump such as a magnetically driven, rotary ventricular assist device for pumping blood of a patient, the impeller being substantially entirely made of an alloy which consists essentially of about 70-80 weight percent of platinum and 20-30 weight percent of cobalt.

Abstract: A blood pump consisting of an inflow cannula, a stator fixed to the pump housing, a flow straightener, an impeller, and a diffuser. The pump may include a flow straightener assembly consisting of the flow straightener body and front shaft. The pump may include an impeller assembly with a bearing on the front hub section. The pump may have a body contour which is shaped such that the rear section of the flow straightener body blends into the inserted shaft and there is no axial gap between the end of the flow straightener other than the ends of the blades and the front hub of the impeller.

Abstract: A high efficiency cardiac support system is suitable for chronic use in treating heart failure, wherein the system includes an implantable rotary blood pump, an implantable power module, a wireless power transfer subsystem, a patient monitor, and a programmer In a cardiac support system, the cumulative efficiencies of the components of the system are capable of providing therapeutically effective blood flow for a typical day of awake hours using the energy from a single wireless recharge of an implanted rechargeable energy source. Moreover, the implantable rechargeable energy source may be recharged during a normal sleep period of 8 hours or less. The system may provide full or partial cardiac support without the need for external wearable batteries, controllers, or cables.

Abstract: By inserting a protruding portion (8b), which is installed to a center position of a rear end surface (8x) of a fixed body (8), into a hole (4a), which is provided to a center position of an end surface (4x) on a side of a fixed body (8) of a fixed shaft (4) that is connected to a fixed body (3), the fixed bodies (3) and (8) and the fixed shaft (4) are connected. As a result, a sleeve (5) can be removed only by dismantling the fixed body (3).

Abstract: An artificial heart pump system is provided independently with a controlling processor for controlling an operation status of a blood pump so as to perform in a preset condition and with an observing processor for controlling a display unit displaying an operation status and an operation condition of the blood pump. In addition, a memory device is mounted in an outside-the-body type battery pack included in the artificial heart pump system; data such as pump data, event log or the like is stored therein; and data are collected and managed automatically by a battery charger when charging the battery charger for a daily performance. Further, an interface unit of an artificial heart pump is proposed where a user can confirm displayed contents of the controller without exposing the controller externally.

Abstract: Provided are a magnetic coupling as an axial bearing including a driven magnet (11B3) that is a permanent magnet provided to a rotating body (11) inside a casing (12) and a drive magnet (23A) that is a permanent magnet placed face to face with the driven magnet in a radial direction of the rotating body outside the casing to be magnetically coupled with the driven magnet, a driving motor (22) that rotatably drives the drive magnet about an axis (P) of the rotating body, a radial bearing that is a dynamic bearing having annular bearing surfaces (12B1, 11B1) centering on the axis on an inner wall of the casing and the rotating body, each of the annular bearing surfaces being arranged with a gap between the drive magnet and the driven magnet in the radial direction of the rotating body, and a closed impeller (11A) including a front shroud (11A1) arranged on a front side in the axis direction in the rotating body, a rear shroud (11A2) arranged on a rear side in the axis direction of the front shroud, and a vane (

Abstract: An axial-flow blood pump for pumping blood includes a substantially cylindrical outer enclosure. A tubular housing concentric with and located within the outer enclosure has at one end an inlet and at an opposite end an outlet. A motor stator is concentric with and located between the outer enclosure and the tubular housing. An impeller is concentric with and located within the tubular housing. The impeller is suspended in operation by a combination of passive magnetic forces between magnets within the impeller or magnetized regions of the impeller and the motor stator and hydrodynamic thrust forces generated as blood flows between the tubular housing and a plurality of hydrodynamic thrust bearing surfaces located on the impeller. A volute may be in fluid-tight connection with the outlet of the tubular housing for receiving blood in the axial direction and directing blood in a direction normal to the axial direction.

Abstract: A demand responsive physiological control system for use with a rotary blood pump; said system including a pump controller which is capable of controlling pump speed of said pump; said system further including a physiological controller, and wherein said physiological controller is adapted to analyse input data relating to physiological condition of a user of said pump; and wherein said physiological controller determines appropriate pumping speed and sends a speed control signal to said pump controller to adjust pump speed; said system further including a physiological state detector which provides said input data indicative of at least one physiological state of said user, in use, to said physiological controller.

Abstract: A method of estimating the blood flow rate of a heart ventricle assist device which is positioned externally of, or implanted in, a patient. The assist device comprises a blood pump having a rapidly rotating, electrically powered impeller, and comprises briefly interrupting power to the impeller to cause its rotation to slow. From this, blood viscosity can be estimated, which viscosity is used to obtain real time, estimated blood flow rates and pressure heads. Apparatus for accomplishing this is disclosed.

Abstract: Systems and methods to control the movement of one or more pistons in a pumping chamber. The systems and methods may include a sensor to sense an external variable provide an output signal. The systems and methods may also include a microprocessor configured to receive the output signal from the sensor and to change an operating parameter of the pump in response to the output signal.

Abstract: Systems and methods for providing a variable pumping stroke from a pump comprising a pumping chamber, a pump inlet, a pump outlet, a valving mechanism, and a drive piston.

Abstract: A blood pump comprises a pump housing; a rotor positioned in the housing and comprising an impeller having a hydrodynamic surface for pumping blood; and a motor including a plurality of magnets carried by the impeller, plus a rotor stator, including an electrically conductive coil located adjacent to or within the housing. The impeller comprises radially outwardly extending, bladelike projections that define generally longitudinally extending spaces between the projections. The shape of the projections and the spaces therebetween tend to drive blood in the spaces in an axial direction as the impeller is rotated. The spaces collectively have a total width along most of their lengths at the radial periphery of the rotor, that is substantially equal to or less than the collective width of the projections along most of their lengths at the radial periphery. Thus, the bladelike projections are thicker, achieving significant advantages.

Abstract: In order to optimize the clearances between both end surfaces of a sleeve 5 and each of the end surfaces of the fixed bodies 3 and 5, respectively, magnetic forces of repulsion being caused by each of the permanent magnets 3a, 5b, 5c and 8a is adjusted. At this time, by adjusting each of the distances between the permanent magnets 3a, 5b, 5c, 8a, respectively, by adjusting the quantity of the adjustment rings 9, the magnetic force of repulsion being caused by each of the permanent magnets 3a, 5b, 5c and 8a is adjusted.

Abstract: A method of estimating the blood flow rate of a heart ventricle assist device which is positioned externally of, or implanted in, a patient. The assist device comprises a blood pump having a rapidly rotating, electrically powered impeller, and comprises briefly interrupting power to the impeller to cause its rotation to slow. From this, blood viscosity can be estimated, which viscosity is used to obtain real time, estimated blood flow rates and pressure heads.

Abstract: A pump for pumping sensitive fluids, such as blood, having no mechanical contact between the impeller and any other structure. The pump comprises a pump housing, an impeller disposed within the pump housing, a magnetic bearing system for supporting and stabilizing the impeller in five degrees of freedom, and a conformally shaped magnetically linked motor for rotating the impeller. The magnetic bearing system and motor advantageously comprise electromagnets and permanent magnets for stability and control of the impeller, and to reduce size, weight, and pump power consumption. Permanent and electromagnets are disposed on the pump housing and permanent magnets are disposed on the impeller such that by controlling electric current through the electromagnets on the housing, the magnetically suspended impeller functions as the rotor, and the housing as the stator of a D.C. motor.

Abstract: A control system for a continuous flow rotary blood pump is provided. A normal operating range of the blood pump is established. The normal operating range may comprise a normal pump flow range and a normal pressure head range. A target rotational speed of the pump is set in accordance with the normal operating range. A current operating condition of the blood pump is determined. The current operating condition may comprise a current pump flow, a current pressure head, and a current rotational speed of the pump. The current operating condition is compared with the normal operating range. An appropriate control algorithm is selected from a plurality of available control algorithms based on the comparison. The target rotational speed of the pump is adjusted using the selected control algorithm to maintain or recover the normal operating range.

Abstract: A blood pump has an impeller rotatably disposed and magnetically suspended within a cavity of a stator by a plurality of magnetic bearings (passive permanent and active electromagnetic) having impeller magnets on the impeller and stator magnets or coils/poles on the stator. A motor includes impeller magnets on the impeller and coils/poles associated with the stator. A single, annular blood flow path extends axially through the cavity between the impeller and the stator, and between the impeller magnets on the impeller and the stator magnets or the coils/poles on the stator.

Abstract: A blood pump has an impeller rotatably disposed and magnetically suspended within a cavity of a stator by a plurality of magnetic bearings including an axial bearing to support the impeller axially in the cavity. The axial bearing includes adjacent impeller magnets and adjacent stator magnets with axially aligned polarities and reverse polarities with respect to adjacent magnets. A motor includes impeller magnets on the impeller and coils and poles associated with the stator. Radial permanent magnet and electromagnetic bearings are also included. The magnetic bearings and the motor have stator magnets or coils and poles disposed radially across the fluid passage from corresponding impeller magnets to define an annular gap positioned radially between the impeller and the stator, and positioned radially between all of the plurality of magnetic bearings, creating a straight through blood path without secondary flow paths.

Abstract: A rotary mechanism includes a stator body defining a chamber and an elongated rotor operationally disposed within the chamber. The elongated rotor has opposed ends with a central axis defining an axis of rotation, with magnetic driven elements disposed on the rotor and positioned outwardly of the rotor axis between the opposed ends. Passive magnetic bearing pairs are positioned along opposed ends of the rotor body with each bearing pair being similarly polarized so as to be in mutually attracting or mutually repelling relationship.

Abstract: An artificial heart pump includes a casing (4, 15) having a blood inflow port (5) in its upper part, a blood outflow port (6) in its side surface part and a plurality of electromagnets (22) on its inner peripheral surface; a fixed shaft (17) projecting from the bottom surface of the casing and having thrust receptacles (18, 16) at its upper and lower end parts (12, 10), respectively; an impeller section (2) having a blood inflow section (3) in its center part and a blood outflow section (9) in its side surface part; an impeller support member (7) supporting the impeller section from below and having on its outer peripheral surface a plurality of permanent magnets (2) and in its center a hole part fitted on the fixed shaft to rotatably support the impeller section within the casing; a radial hydrodynamic bearing part formed between the inner peripheral surface of the hole part of the impeller support member and the outer peripheral surface of the fixed shaft; and thrust hydrodynamic bearings formed between the

Abstract: An implantable magnetic suspension blood pump having a rotor magnetically suspended and having blood flow gaps at the axial ends of the rotor so that blood in the gaps is washed out by flow in a conduit along the axis of the rotor connecting the fluid gaps. The blood pump impeller includes main and secondary blades, an exit diffuser uses a plurality of low divergence blades wrapped circumferentially around the pump axis, and concentric cones are used at the pump outlet, all to eliminate flow separation. The trailing edges of all blades are limited to an included angle of fifteen degrees, also to eliminate flow separation.

Abstract: An artificial heart device for minimizing the damage to blood cells having electromagnetically driven pistons which move the blood around and through a toroidal chamber. In first and second preferred embodiments no motor is used to drive the pistons and the pistons are suspended within the toroid by cycling of electromagnets. In a third preferred embodiment the pistons are moved with the use of motor-driven magnets. In each embodiment blood is sucked into the toroidal chamber through one or more intake openings and blood exits the toroidal chamber through one or more outflow openings.

Abstract: This invention is a non-contact axial flow turbo blood pump for propelling blood, which is composed of a pump housing (24) that defines a pump axis, with inlet, outlet openings at opposite axial ends of the pump housing, a rotor unit (17) that defines a rotor axis, and opposing rotor axial ends. The pump magnetically suspends the rotor within the pump housing at the rotor axial ends so as to avoid causing physical contact between the housing to define fluid gaps between the rotor axial ends, and the magnetic suspension elements (13)(13′).

Abstract: A blood pump intended to be carried by a freely moving patient uses perpendicular magnetic and electrical fields to propel blood. A rod mounted coaxially inside a tube has electrodes in blood contact for establishing a radial electric field, and an inductor having windings parallel to the axis of the tube is used to establish a circumferential magnetic field. To avoid the evolution of gas at the electrode surfaces the magnetic and electric fields are periodically reversed, and the electrodes are made to have very high surface areas. The blood pump is powered by batteries or fuel cells (or a combination of both) to provide long service between recharging and to reduce the weight carried by the patient.

Abstract: A blood pump for assisting a heart is provided having a stator and a rotor. The rotor is magnetically radially supported creating a suspension gap between the stator and the rotor. The rotor can be supported axially by a Lorentz force bearing and can be magnetically rotated. The stator can have a single or double volute pump chamber and the rotor can have an impeller portion for pumping blood. The rotor can have a center bore as a primary blood flowpath. The suspension gap can be a secondary blood flowpath. The blood pump can also have an axial position controller and a flow rate controller. The axial position controller can cause the axial bearing to adjust the position of the rotor. The flow rate controller can have a member for measuring a dimension of a heart ventricle to control the flow rate to avoid overly distending or contracting the ventricle. A method of operating the flow rate controller to create a pulsatile flow rate is also provided.

Abstract: A blood pump for assisting a heart is provided having a stator and a rotor. The rotor is magnetically radially supported creating a suspension gap between the stator and the rotor. The rotor can be supported axially by a Lorentz force bearing and can be magnetically rotated. The stator can have a single or double volute pump chamber and the rotor can have an impeller portion for pumping blood. The rotor can have a center bore as a primary blood flowpath. The suspension gap can be a secondary blood flowpath. The blood pump can also have an axial position controller and a flow rate controller. The axial position controller can cause the axial bearing to adjust the position of the rotor. The flow rate controller can have a member for measuring a dimension of a heart ventricle to control the flow rate to avoid overly distending or contracting the ventricle. A method of operating the flow rate controller to create a pulsatile flow rate is also provided.

Abstract: A blood pump for assisting a heart is provided by a stator and a rotor. The rotor is magnetically supported creating a suspension gap between the stator and the rotor. The rotor can be supported axially by a Lorentz force bearing and can be magnetically rotated. The stator can have a volute pump chamber and the rotor can have an impeller portion for pumping blood. The rotor can have a center bore as a primary blood flowpath. The suspension gap can be a first retrograde blood flowpath. An axial gap between the impeller and the volute housing can be a second retrograde blood flowpath. The blood pump can also have an axial position controller. The axial position controller can cause the axial bearing to adjust the position of the rotor. The axial position of the rotor. The axial position of the magnetic suspension components can be adjusted to compensate for changes in the magnetic fields of the magnetic suspension components. The blood pump can also have a flow rate controller.