Device to assist the performance of a heart

Abstract

A method and device to assist the performance of a heart with at least one pump that is formed as a rotary pump and driven via magneto coupling. The pump includes a magnetically driven rotor rotatable within a surrounding rotor housing to act upon blood flowing from an inflow tube toward the magnetically driven rotor, and a second magnetic device axially aligned with the inflow tube and positioned to magnetically drive rotation of the magnetically driven rotor via the magneto coupling.

Claims

1. A system for assisting the blood circulation of a heart, comprising: a heart assist pump device deliverable to the heart and comprising: an inflow tube defining a blood inflow path; a magnetically driven rotor axially aligned with the inflow tube and being rotatable within a surrounding rotor housing to act upon blood flowing from the inflow tube toward the magnetically driven rotor, the magnetically driven rotor being rotatable about a central axis and being rigidly coupled to a first magnetic device that is located within the surrounding rotor housing, wherein both the magnetically driven rotor and first magnetic device are entirely spaced apart from the surrounding rotor housing by a gap during rotation of the magnetically driven rotor; a magnetic drive system comprising a second magnetic device axially aligned with the central axis of the magnetically driven rotor and spaced apart from the magnetically driven rotor such that a wall of the surrounding rotor housing is positioned between the magnetically driven rotor and the second magnetic device, the second magnetic device positioned axially closer to the first magnetic device than to the magnetically driven rotor so as to provide a magneto coupling with the first magnetic device to drive rotation of the magnetically driven rotor; a blood outflow port positioned radially adjacent the magnetically driven rotor such that blood driven by the magnetically driven rotor is configured to exit the surrounding rotor housing in a direction substantially perpendicular from the blood inflow path and the central axis of the magnetically driven rotor, wherein the magneto coupling orients the magnetically driven rotor so that, in response to rotation of the magnetically driven rotor, the magnetically driven rotor is spaced apart from the surrounding rotor housing by the blood flowing in the gap and to the blood outflow port; and an external control unit configured to regulate operation of the second magnetic device, the external control unit connectable to the heart assist pump device for controlling the second magnetic device to thereby magnetically drive the rotation of the magnetically driven rotor via the magneto coupling with the first magnetic device.

2. The system of claim 1, wherein the magnetically driven rotor comprises guide surfaces to produce centrifugal flow components.

3. The system of claim 2, wherein the first magnetic device rotates together with the magnetically driven rotor relative to the surrounding rotor housing.

4. The system of claim 3, wherein the magnetically driven rotor has a maximum width greater than a maximum width of the first magnetic device.

5. The system of claim 1, wherein the magnetically driven rotor is sealed from both the second magnetic device and a drive source that regulates the operation of the second magnetic device.

6. The system of claim 5, wherein the drive source comprises a hydraulically or pneumatically operated drive wheel.

7. The system of claim 1, wherein the heart assist pump device is formed as an intravasal rotary pump.

8. The system of claim 1, wherein the first magnetic device comprises a bar magnet.

9. The system of claim 1, wherein the second magnetic device comprises a bar magnet.

10. The system of claim 1, wherein the magnetically driven rotor is positioned axially side-by-side with the first magnetic device and rotates together with the first magnetic device within the surrounding rotor housing.

11. The system of claim 10, further comprising one or more sensors that deliver feedback signals to the external control unit.

12. The system of claim 10, wherein the external control unit is connectable to the heart assist pump device to deliver energy to the second magnetic device.

13. The system of claim 12, wherein the external control unit delivers energy to the second magnetic device via delivery of a driving fluid.

14. The system of claim 1, wherein the external control unit is configured to regulate operation of the second magnetic device based on a fixed control value.

15. The system of claim 14, wherein the fixed control value comprises a defined cardiac output for control of the heart assist pump device.

16. The system of claim 1, wherein the second magnetic device is positioned closer to the blood outflow port than to a suction end of the inflow tube that is insertable into a heart ventricle.

17. The system of claim 1, wherein heart assist pump device is a catheter device.

18. The system of claim 17, further comprising a drive wheel configured to urge rotation of the second magnetic device.

19. The system of claim 1, wherein the magnetically driven rotor is positioned at a distal end of a catheter.

20. The system of claim 1, wherein the second magnetic device is configured to rotate during rotation of the magnetically driven rotor.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) The invention is explained in further detail below by use of an exemplary embodiment which is illustrated diagrammatically in the drawings, in which

(2) FIG. 1 shows a diagrammatic illustration of the arrangement of the pump and of the drive,

(3) FIG. 2 shows a diagrammatic illustration of the distal end of a catheter which is used according to the invention, and

(4) FIG. 3 shows an enlarged illustration of the part of the catheter bearing the balloon, in section.

DETAILED DESCRIPTION

(5) In FIG. 1, a heart is designated by 1, into which a heart ventricle catheter 2 is introduced. The catheter is introduced here for example via the femoral artery and the aortic arch 3 into the heart chamber and carries a series of sensors 4 via which the volume can be determined. The measurement signals are passed to a control arrangement 5. The heart ventricle catheter is formed with several lumina, as additionally illustrated below in further figures of the drawings, with fluid being supplied via such lumina to drive a rotor, arranged at the distal end, which forms the pump to assist the blood circulation and is designated by 6 in FIG. 1. The positioning of this rotor is indicated in FIG. 1 by the arrow 8. The driving medium for the rotor or the pump is guided in a circular flow by means of a fluid pump 7 which can be regulated in a synchronised manner as a function of the control signals generated in the control arrangement 5. The distal region in which the pump is arranged is designated diagrammatically by 8, the catheter 2 having at its distal end a tube 9 leading to the suction end 10. A reservoir for driving fluid is designated by 11, which provides additional driving medium for filling the balloon 12 serving for an occlusion of the artery, and which receives again the volume of driving medium occurring on deflation of the balloon.

(6) The volumetric measurement in the cardiac chamber allows differences to be reliably detected between the diastolic and systolic volume and allows corresponding correction signals to be made available for the output of the synchronised fluid pump 7. Furthermore, in the control circuit 5, corresponding fixed values can be provided, such as for example a defined cardiac output, which is referred to on deviation of the measured cardiac output to control the pump.

(7) A retroperfusion can take place via a conventional balloon catheter which is occluded in a correspondingly synchronized manner, so that the directed return is in fact guaranteed during the diastole. Hereby the corresponding measurement values for the heart rate or for the correct moment of the diastole can be obtained from ECG data.

(8) In FIG. 2, the distal end of a modified catheter 2 is now illustrated. The end side 13 of this catheter has two pocketshaped chambers 14 and 15, in which bar magnets are respectively arranged. The bar magnet 16 is connected here at the distal end outwards via a shaft 17 with a rotor 18, whereas the bar magnet 19 lying on the inside is connected via a shaft 20 with a drive wheel 21. The drive wheel 21 is formed here as a paddle wheel and is acted upon with fluid via a lumen 22, this fluid flowing off again via the lumen 23 of the catheter. The rotation of the paddle wheel 21 is regulated here accordingly by corresponding control of the fluid pressure in the lumen 22 serving for the supply of fluid, in which the magnet 19, which is connected so as to be locked against relative rotation with the paddle wheel 21, is set into corresponding rotation. At the outer side, which is completely sealed with respect to the lumina 22 and 23, the magnet 16 is subsequently entrained accordingly and drives the rotor 18 via the shaft 17, whereby a flow is formed in the region of the tube 9, as is indicated by the arrows 24, and which assists the natural blood flow in the vessel 26, illustrated by the arrow 25.

(9) In FIG. 3, the partial region of the balloon 12, which is connected in a sealing manner to the catheter 2, is illustrated on an enlarged scale. The two lumina leading away from the fluid pump 7 and back to the fluid pump 7 are designated in turn by 22 and 23. In the region of the balloon 12, the wall of these lumina is provided with valves which can be actuated magnetically for example. The valves are indicated diagrammatically by 27 and 28. An opening of the valve 27 leads to the fluid, coming from the fluid pump 7, which is under pressure, which is indicated by the “+” sign, being pumped into the balloon 12, with which the overall quantity of the circulating driving fluid would of course be reduced, in so far as the reservoir 11, indicated diagrammatically in FIG. 1, is not provided. By closing the valve 27, the occlusion is closed off, the collapsing of the balloon 12 being able to be brought about by opening the valve 28 and the fluid now being drawn off via the lumen 23, leading back to the pump, which lumen 23 is at a slightly lower pressure which is indicated by the “−” sign. As the overall volume of the fluid in the circulating system is now to be reduced, a portion of this volume must be pumped back again into the reservoir 11 according to FIG. 1.