Implantable ventricular assist device

• US 6,264,601 B1
• Filed: 04/02/1999
• Issued: 07/24/2001
• Est. Priority Date: 04/02/1999
• Status: Expired due to Term

• Current Assignee: World Heart Corporation (Medtronic Plc)
• Original Assignee: World Heart Corporation (Medtronic Plc)
• Inventors: Miller, Phillip J., LaForge, David H., Jassawalla, Jal S.
• Primary Examiner(s): EVANISKO, GEORGE ROBERT
• Application Number:
  US09/285,933
• Time in Patent Office: 844 Days
• Field of Search: 600/16, 600/17, 623/3.1, 623/3.11, 623/3.16, 623/3.17, 623/3.18, 623/3-9-
• US Class Current: 600/16
• CPC Class Codes: A61M 60/148 in line with a blood vessel using resection or like techniques, e.g. permanent endovascular heart assist devices
• CPC Class Codes: A61M 60/178 drawing blood from a ventricle and returning the blood to the arterial system via a cannula external to the ventricle, e.g. left or right ventricular assist devices
• CPC Class Codes: A61M 60/462 Electromagnetic force
• CPC Class Codes: A61M 60/531 using blood pressure data, e.g. from blood pressure sensors
• CPC Class Codes: A61M 60/896 having flexible or resilient parts, e.g. flap valves
• CPC Class Codes: F04B 2205/01 Pressure before the pump inlet
• CPC Class Codes: F04B 43/04 Pumps having electric drive
• CPC Class Codes: H02K 33/16 with polarised armatures moving in alternate directions by reversal or energisation of a single coil system

Abstract

An implantable ventricular assist device (VAD) has a small size to provide full-implantable capabilities. The VAD has two variable-volume chambers and an actuator for expelling blood from the chambers in sequence and to a common outlet, thus operating as a positive-displacement pump. The variable-volume chambers may be flexible sacs and the pump is operable at a substantially continuous flow, such as during the systolic phase of the assisted ventricle. A method of operation includes operating the pump at a first frequency during systole and a second lower frequency during diastole. The VAD pump includes a pair of coils housed within a frame and disposed in a spaced relationship to generate a coil flux through a pair of poles. A plate including an armature and a magnet is disposed within the frame such that the armature is between the poles and the magnet is between the coils. Gaps are defined between the armature and each of the poles and the coil flux displaces the armature across the gap. The coil flux follows a donut-shaped path including the frame, one of the poles, one of the gaps, the armature, the other the gap, and the other the pole, and no coil flux passes through the magnet. The magnet is not subject to depolarization and may be made substantially smaller than those of conventional devices. The magnet generates a bias flux that offsets a portion of the coil flux around the frame. A spring may be provided to counteract the unstable action of the bias magnet. The volume of the chambers is a fraction of the ventricular volume, and may be about 20 ml. To pump a typical 80-ml volume of a left ventricle, the controller may activate the coils four times during systole, or once every 40 msec.

Claims

1. A device for assisting the pumping capacity of one ventricle, comprising:

an implantable housing;

a pair of variable-volume chambers mounted in the housing, each of the chambers having an inlet port and an outlet port;

at least one ventricular outflow conduit adapted to be connected between the ventricle and the inlet ports said ventricular outflow conduit comprising a device inlet conduit branching to the two inlet ports;

and an actuator disposed to alternately contract one of the variable-volume chambers while expanding the other, and vice versa, to provide a positive displacement pump.

2. The device of claim 1, further including at least one one way valve provided in said ventricular outflow conduit to prevent upstream regurgitation from each of said variable volume chambers.

3. The device of claim 2, further including at least one device outlet conduit adapted to be connected between the outlet ports and at least one arterial vessel, and at least one one way valve provided in said outlet conduit to prevent downstream regurgitation into each of said variable volume chambers.

4. The device of claim 3, wherein the device outlet conduit comprises a single conduit branching to the two outlet ports.

5. The device of claim 1, wherein the variable-volume chambers are flexible sacs, and the actuator comprises a movable plate therebetween.

6. The device of claim 5, wherein the movable plate is free of mechanical connections to the housing and is sandwiched between opposing faces of the flexible sacs.

7. The device of claim 6, wherein the movable plate is attached to each of the flexible sacs.

8. The device of claim 5, wherein the movable plate comprises a bias magnet, and a portion of the housing is magnetically permeable so that the plate is unstable in a central position between the two flexible sacs, and is biased toward one or the other sac upon a slight displacement in that direction.

9. The device of claim 8, wherein the flexible sacs and movable plate are generally circular and axially aligned.

10. The device of claim 8, further including a spring positioned in the housing to apply a centering force to the plate.

11. The device of claim 8, wherein the actuator comprises an armature with a magnetically permeable portion, the device including electromagnetic coils situated so as to generate a coil flux path through the housing and magnetically permeable portion of the armature, and wherein the coil flux generated by the coils displaces the armatures toward one of the two flexible sacs depending on the current direction through the electromagnetic coils.

12. The device of claim 1, wherein the actuator comprises an armature with a magnetically permeable portion, the device including electromagnetic coils situated so as to generate a coil flux path through the housing and magnetically permeable portion of the armature, and wherein the coil flux generated by the coils displaces the armature toward one of the two variable-volume chambers depending on the current direction through the electromagnetic coils.

13. The device of claim 12, wherein the armature includes a bias magnet portion generating a magnetic flux, and a portion of the housing is magnetically permeable and situated so as to provide a magnetic flux path for the bias magnet, and wherein the armature is unstable in a central position between the two variable-volume chambers, and is biased toward one or the other variable-volume chamber upon a slight displacement in that direction by the magnetic flux.

14. The device of claim 13, further including a spring positioned in the housing to apply a centering force to the armature.

15. The device of claim 13, wherein the bias magnet portion is out of the coil flux path.

16. The device of claim 13, wherein the variable-volume chambers are circular flexible sacs and the actuator comprises a circular movable plate therebetween and axially aligned therewith, and wherein the movable plate is free of mechanical connections to the housing and is sandwiched between opposing faces of the flexible sacs.

17. The device of claim 16, wherein there are two of the coils, annularly shaped and disposed in axial alignment with and on opposite sides of the sandwiched plate and sacs, and wherein bias magnet portion of the armature is annular and positioned in axial alignment with and generally between the annular coils.

18. The device of claim 12, further including a controller connected to supply current to the electromagnetic coils, and an input sensor positioned in the ventricular outflow conduit and connected to provide physiological data to the controller, the controller supplying current to the coils based on the physiological data so provided.

19. A ventricular assist device, comprising:

a frame;

a pair of coils including a first coil and a second coil disposed in a spaced relationship within the frame, the coils generating coil flux and defining a pair of poles including a first pole and a second pole when electrically activated;

a plate including an armature and a bias magent, the plate being disposed within the frame such that the armature is between the poles, and a gap being defined between the armature and each of the poles; and

a pair of compressible chambers including a first chamber and a second chamber respectively disposed between the plate and each of the coils;

the device being configured so that the coil flux follows a path including one of the poles, one of the gaps, the armature, the other gap, and the other pole, and such that the bias magnet is substantially free of the coil flux.

20. A ventricular assist device as claimed in claim 19, wherein the bias magnet has an energy density that produces a substantially constant bias flux.

21. A ventricular assist device as claimed in claim 19, further comprising a power supply connected to the coils, and a controller connected to the power supply for selectively supplying power to the coils.

22. A ventricular assist device as claimed in claim 19, wherein the compressible chambers are flexible sacs.

23. A ventricular assist device as claimed in claim 19, further comprising:

a power supply connected to and for electrically activating the coils; and

a controller connected to the power supply for controlling when the power supply activates the coils.

24. A ventricular assist device as claimed in claim 23, wherein the controller causes the coils to move the plate at a stroke time of less than about 100 msec.

25. A ventricular assist device as claimed in claim 19, wherein the frame and the plate are substantially cylindrical, and the coils are annular, all being axially aligned.

26. A ventricular assist device as claimed in claim 25, wherein the armature is centrally located in the plate, the magnet annularly surrounding the armature and being between the coils.

27. A ventricular assist device as claimed in claim 26, wherein the armature has a hollow central portion.

28. A ventricular assist device as claimed in claim 26, further comprising a magnetically permeable shoe disposed between the bias magnet and an inner surface of the frame, wherein the shoe has a narrow neck which becomes magnetically saturated as the bias magnet nears the inner surface of the frame.

29. A ventricular assist device as claimed in claim 19;

wherein the bias flux shifts according to movement of the plate which results in a negative spring force generated by a magnetic field induced thereby, and wherein the compressible chambers possess an elasticity that acts in opposition to the negative spring.

30. A ventricular assist device as claimed in claim 19, wherein each of the chambers has an elasticity, further comprising springs disposed between the frame and the plate and augmenting the elasticity of the chambers.

31. A device for assisting the cardiovascular system of a patient, the cardiovascular system including an arterial vessel and a heart having a ventricle with an ejection volume, the device comprising:

a pump including;

a frame;

a pair of coils including a first coil and a second coil disposed in a spaced relationship within the frame, the coils generating coil flux and defining a pair of poles including a first pole and a second pole when electrically activated;

a plate including an armature and a magnet, the plate being disposed within the frame such that the armature is between the poles; and

a pair of compressible chambers including a first chamber and a second chamber respectively disposed between the plate and each of the coils, each of the chambers having a volume less than about one-half of the ejection volume of the ventricle; and

cannulation for connecting the pump to the cardiovascular system of the patient.

32. A device as claimed in claim 31, wherein each of the chambers has a volume of about one-quarter the ejection volume of the ventricle.

33. A device as claimed in claim 31, wherein the cannulation comprises:

an inlet conduit connected to the pump to be in communication with the chambers for receiving blood from the ventricle; and

an outlet conduit connected to the pump to be in communication with the chambers for delivering blood to an artery of the patient.

34. A device as claimed in claim 33, wherein each of the chambers is connected to the inlet conduit and the outlet conduit such that each of the chambers receives blood when the other the chamber ejects blood.

35. A device as claimed in claim 33, wherein one of the chambers is connected to the inlet conduit and the other chamber is connected to the outlet conduit;

the pump further including a transfer conduit connected between the chambers.

36. A device as claimed in claim 31, wherein the pump is substantially cylindrical with an external diameter of less than about 100 millimeters.

37. A device as claimed in claim 31, further comprising a controller connected to supply current to the electromagnetic coils, and an input sensor positioned in the inlet conduit and connected to provide physiological data to the controller, the controller supplying current to the coils based on the physiological data so provided.

38. A device as claimed in claim 37, wherein the input sensor senses pressure in the inlet conduit and the controller causing the coils to continuously move the plate when the pressure sensed is above a threshold value.

39. A method of ventricular assist, comprising:

providing a ventricular assist pump including two pumping chambers, valved inlet and outlet conduits for each chamber, and an actuator;

directing an inflow of blood from a single ventricle to both of the chambers; and

actuating the pumping chambers with the actuator during a systolic phase of the assisted ventricle to alternately expel blood from one of the chambers while drawing blood into the other of the chambers.

40. The method of claim 39, further including resting the pumping chambers during the diastolic phase.

41. The method of claim 40, further including sensing the pressure of the ventricle and controlling actuation of the pumping chambers based on the pressure sensed.

42. The method of claim 39, wherein the actuator is an armature and the pump includes coils for generating a coil flux to displace the armature, and wherein the actuator further includes a bias magnet generating a bias flux, the pump being configured so that a portion of the path of the coil flux interacts with a portion of the path of the bias flux.

43. A method of ventricular assist, comprising:

providing a positive displacement pulsatile pump having two variable-volume chambers each with a volume less than about one-half of the ejection volume of the ventricle;

implanting the pump in a patient so as to be in fluid communication with the blood circulatory system;

actuating the pump during systole to provide substantially continuous flow output and propel the ventricular ejection volume into an arterial vessel; and

resting the pump during a diastolic phase of the assisted ventricle.

44. The method of claim 43, further including sensing the pressure of the ventricle and controlling actuation of the pump based on the pressure sensed.