72 results about "Heart-Assist Devices" patented technology

A tiny electrically powered hydrodynamic blood pump is disclosed which occupies one third of the aortic or pulmonary valve position, and pumps directly from the left ventricle to the aorta or from the right ventricle to the pulmonary artery. The device is configured to exactly match or approximate the space of one leaflet and sinus of valsalva, with part of the device supported in the outflow tract of the ventricular cavity adjacent to the valve. In the configuration used, two leaflets of the natural tri-leaflet valve remain functional and the pump resides where the third leaflet had been. When implanted, the outer surface of the device includes two faces against which the two valve leaflets seal when closed. To obtain the best valve function, the shape of these faces may be custom fabricated to match the individual patient's valve geometry based on high resolution three dimensional CT or MRI images. Another embodiment of the invention discloses a combined two leaflet tissue valve with the miniature blood pump supported in the position usually occupied by the third leaflet. Either stented or un-stented tissue valves may be used. This structure preserves two thirds of the valve annulus area for ejection of blood by the natural ventricle, with excellent washing of the aortic root and interface of the blood pump to the heart. In the aortic position, the blood pump is positioned in the non-coronary cusp. A major advantage of the transvalvular VAD is the elimination of both the inflow and outflow cannulae usually required with heart assist devices.

An apparatus for a heart assist device, comprising a processing unit for computing the blood flow rate from the arterial pressure curve and for predicting at every heartbeat the closing time of the heart valve from the curve of the blood flow rate. The processing unit is adapted to deliver a signal for controlling a heart assist device at a point in time, a period ahead in time of the closing time of the heart valve, wherein the mechanical properties of the said heart assist device are taken into account in determining the period. The apparatus adapts itself to changes in a patient's heart frequency and aortic pressure.

A heart assist device comprising a rotary pump housing having a cylindrical bore, a pumping chamber and a motor stator including an electrically conductive coil located within the housing and surrounding a portion of the cylindrical bore. A rotor has a cylindrical shaft, at least one impeller appended to one end of the shaft, and a plurality of magnets located within the shaft. The rotor shaft is positioned within the housing bore with the magnets opposite the motor stator, and the impeller is positioned within the pumping chamber. The housing bore is closely fitted to the outer surface of the shaft forming a hydrodynamic journal bearing, with the pumping chamber and journal bearing connected by a leak path of blood flow between the pumping chamber and the journal bearing. A backiron of the motor stator attracts the rotor magnets to resist longitudinal displacement of the rotor within the housing during operation. The relative orientation of positions of the inflow, outflow, and leakage flow paths may be varied within the pump, such as to accommodate different intended methods for implantation and/or use.

A ventricular assist device comprising a housing defining an interior space, at least two ports opening into said interior space, and at least one pump for pumping blood between the ports through said interior space, the ports and interior space providing a continuous blood flow path that is not interrupted by valves.

The various embodiments disclosed herein relate to transcutaneous energy transfer systems comprising an internal coil positioned within a cavity of a patient and an external coil inductively coupled to the internal coil. The systems can be coupled to any implantable medical devices, such as, for example, a heart assist device.

An apparatus and method for use in assisting a human heart are disclosed. The apparatus comprises an aortic compression means which may be fully implanatable, a fluid reservoir and a pump means adapted to pump a fluid from the reservoir to the aortic compression means so as to actuate the aortic compression means at least partly in counterpulsation with the patient's heart. In addition, the device is adapted to be wholly positioned within the right chest cavity of the patient. The aortic compression means of the device may be curved along its length so as to substantially replicate the curve of the ascending aorta.

A method of controlling the operation of a pulsatile heart assist device (14) in a patient (10). The method consisting of utilising sounds produced by the heart (12) to control the operation of the heart assist device (14).

The present invention provides methods, systems and devices that reduce dyskinesis and hypokinesis. The contoured heart assist device of the present invention includes a selectively inflatable end-systolic heart shaped bladder with one or more contoured supports configured to surround at least a portion of the heart and provide curvatures similar to the proper shape of the heart when the device is pressurized and one or more fluid connections in communication with the selectively inflatable end-systolic heart shaped bladder for pressurization and depressurization.

Heart support and assist devices for supporting and assisting the pumping action of the heart. Various embodiments include mesh support devices, devices using straps, spiral-shaped devices, catheter-based devices and related methods.

A heart assist device comprising a rotary pump housing having a cylindrical bore, a pumping chamber and a motor stator including an electrically conductive coil located within the housing and surrounding a portion of the cylindrical bore. A rotor has a cylindrical shaft with an impeller and one or of magnets located within the shaft that are responsive to the motor stator to drive actuation of the rotor. The housing bore is closely fitted to the outer surface of the shaft forming a hydrodynamic journal bearing with an annular clearance defining a leakage flow path. One or more of radial or axial thrust bearings may be provided to provide rotation stability to the rotor and flow within the leakage flow path. The relative orientation of positions of the inflow, outflow, and leakage flow paths may be varied within the pump, such as to accommodate different intended methods for implantation and/or use.

The apparatus is a ventricular assist device comprising: a pump with a housing having therein radial a impeller, and a rotor for driving the impeller, both the rotor and the impeller being hydrodynamically suspended within the housing in us, the pump further including a stator for driving the rotor; an inlet cannula section arranged to extend from an internal part of the ventricle to straddle the wall of the ventricle, the stator being within the inlet cannula section to be located in the internal part of the ventricle; and an outlet for blood driven by the impeller such that the pump is a radial pump. Both the outlet and the impeller are arranged to reside outside of the heart.

In order to provide an abnormality detecting device for a heart assist device, a method for detecting an abnormality of a heart assist device and an abnormal state of a heart assist device detecting program which can early detect an abnormal state, the abnormality detecting device for a heart assist device according to the present invention includes a user information acquiring means for obtaining user information that indicates an operation state of the heart assist device implanted in a body of a user or a biological state of the user measured by the heart assist device and associating said user information with time to store in a history information storing means, and an abnormal state judging means for referring said history information storing means and judging whether or not an abnormal state is present based on a history of said user information.

The invention comprises a heart assist device. In one embodiment, the heart assist device comprises a compressible sleeve about a body part, where one or more portions of the sleeve compress to provide a force on blood generating a flow or pulse of blood in the human circulatory system. In one case, the sleeve is external to the body, such as circumferentially about a limb or about a body extremity. In another case, the sleeve is internal to the body, such as circumferentially about an artery or vein. In still another case, two or more sleeves cooperatively function in parallel and/or in series. The heart assist device is optionally configured to auto-start in an emergency system, is in on-demand or in continuous contact with an emergency response system, and/or is linked to a medical professional's system.

The invention relates to a heart assisting device, in particular to a magnetic fluid suspension type axial pump heart assisting device implanted into the human body in the field of biomedical engineering. The magnetic fluid suspension type axial pump heart assisting device is characterized in that a section of flow channel is divided into an inner flow channel and an outer flow channel by an outer ring wrapping the middle section of an impeller blade, and spiral tooth ripples are engraved on the outer wall of the ring; the top wall of the tooth ripples is in an oblique shape, so that an inflowing opening of the outer flow channel is large, and an outflowing opening is small, and an impeller is subjected to hydraulic pressure when rotating to be radially suspended; an opening is formed in the side wall of the tooth ripples; a pair of convex-concave magnetic cones are embedded in the back end of an impeller hub and a back guide blade hub, and are in the axial magnetic direction, and unlike poles attract each other; a backward pull force generated on the impeller resists the blood forward push force borne by rotating the impeller, and a stator iron core has a binding force, so that the impeller is axially suspended, and thus the impeller is fully suspended; the impeller and front and back guide blade hubs are respectively embedded with two pairs of sliding bearings, which protect the magnetic cones, blades, and the inner wall of a pump pipe, and position and help the impeller suspension.

A left-ventricular assist device (LVAD) has a generally ellipsoidal capsule fitted into a patient's ventricle, formed of a cage or frame of shape-memory wire which can be twisted open and shut to expand and collapse a thin membrane, to inflate with the incoming blood during diastole and to contract and squeeze out the blood during systole. A catheter extends from outside the patient's body through a major blood vessel and the patient's aortal valve into the left ventricle. The catheter has an external sheath, an outer tubular shaft onto which proximal ends of the shape-retaining wires are affixed, and a middle shaft extending through the hollow core of the outer shaft and which is affixed to a central shaft of the capsule. A control console has mechanical geared drives coupled to the outer and middle catheter shafts within the catheter. A sensor arrangement synchs action of the LVAD with systole and diastole of the patient's heart.