EXTRA-CARDIAC DIFFERENTIAL VENTRICULAR ACTUATION BY INERTIAL AND BARIC PARTITIONING

• US 20110196189A1
• Filed: 02/09/2010
• Published: 08/11/2011
• Est. Priority Date: 02/09/2010
• Status: Abandoned Application

• Current Assignee: Myocardiocare, Inc.
• Original Assignee: Myocardiocare, Inc.
• Inventors: Milbocker, Michael
• Application Number:
  US12/702,788
• Publication Number:
  US 20110196189A1
• Time in Patent Office: Days
• US Class Current: 600/16
• CPC Class Codes: A61M 60/191 mechanically acting upon the outside of the patient's native heart, e.g. compressive structures placed around the heart
• CPC Class Codes: A61M 60/289 Devices for mechanical circulatory actuation assisting the residual heart function by means mechanically acting upon the patient's native heart or blood vessel structure, e.g. direct cardiac compression [DCC] devices
• CPC Class Codes: A61M 60/468 the force acting on the actuation means being hydraulic or pneumatic
• CPC Class Codes: A61M 60/554 of blood pressure

Abstract

A device for extra-cardiac actuation for the support of a failing heart is provided that utilizes the inertial component of a driving fluid to provide separately adjustable quantities of supportive energy to the left and right ventricles. By partitioning the inertial and baric forms of energy delivered to a single chamber, heart encircling assist device, and by localizing the heart to minimize lateral and axial displacement a device and method for achieving balanced left-right flow is disclosed that restores the Frank-Starling mechanism to a failing heart and assists recovery by enabling the heart to achieve physiologic cardiovascular equilibrium.

Claims

1. A device for restoring cardiovascular equilibrium comprising:

a cup configured to encompass, and to seal to the atrio-ventricular groove of a heart;

said cup applying inertial and baric energy to the left ventricle and baric energy to right ventricle;

said cup localizing a heart such that motion of the heart'"'"'s center of mass is minimized.

2. The device of claim 1, wherein the ratio of inertial energy to baric energy delivered to the heart is controllable from 4 to 0.1.

3. The device of claim 1, wherein the quotient of energy delivered to the left ventricle divided by energy delivered to the right ventricle is from 4 to 1.

4. The device of claim 1, wherein the heart localization is achieved by at least one of the following:

an adjustable rim seal, hydrophilic anterior and posterior axially aligned strips positioned in the plane of the ventricular septum, or a hydrophilic circumferential apical strip encircling a portion of the heart apex.

5. The device of claim 4, further comprising:

hydrophilic strips which when exposed to body fluid become tacky and promote proteinaceous bonding between strips and epicardium.

6. The device of claim 1, wherein the actuation fluid is a gas, and the inertial component is derived by directing the flow of gas substantially perpendicular to the proximal 25% of the left ventricular free wall.

7. The device of claim 1, wherein the energy is delivered to the ventricles of a heart by delivery of an actuation fluid to a single chamber actuation volume that encircles at least 50% of the ventricular fee walls.

8. The device of claim 7, wherein the single chamber actuation volume contains two fluid flow limiting partitions running axially and located posteriorly and anteriorly and in the plane of the ventricular septum.

9. The device of claim 1, wherein the flow of blood forced out of the left and right ventricles of a heart by the device are approximately of equal volume during a cardiac cycle.

10. The device of claim 1, wherein a control means is provided that varies the ratio of inertial to baric energy supplied to the left ventricle by varying the magnitude of the first and second time derivatives of fluidic flow.

11. The device of claim 10, wherein the energy supporting actuation of the right ventricle is substantially baric energy.

12. The device of claim 11, wherein a flow liming partition delays delivery of baric energy to the right ventricle relative to delivery of baric energy to the left ventricle.

13. The device of claim 1, wherein the inertial energy delivered to the left ventricle is approximately equal to the baric energy delivered to the left ventricle and the energy delivered to the right ventricle is equal to the baric energy delivered to the left ventricle.

14. The device of claim 13, wherein the baric energy delivered to the right ventricle is delayed relative to delivery of baric energy to the left ventricle.

15. The device of claim 1, wherein the interior dimension of the cup configured to enclose the heart is approximately equal to the length of the exterior apical to base dimension of the heart and the cup has a tapered internal circular cross section approximately 25% greater in diameter than the corresponding exterior diameter of the heart.

16. The device of claim 15, wherein a rim seal located at the base of the cup configured to enclose the heart is inflatable to seal the base of the heart to the rim of the cup.

17. The device of claim 16, wherein the rim seal is an inflatable torus with outer periphery bonded hermetically to the inner surface of the cup.

18. The device of claim 17, wherein the rim seal is coated on the surface in contact with the heart with a hydrophilic and tacky coating.

19. The device of claim 18, wherein the coating is at least 1 mm thick, compliant and swells several times in thickness when exposed to body fluids.

20. The device of claim 19, wherein the action of swelling promotes bonding of proteins present in bodily fluids such that the coating bonds to the heart.

21. The device of claim 1, wherein a sheath comprised of a hydrophilic bioabsorbable material is inserted into the cup configured to enclose the heart.

22. The device of claim 21, wherein a variety of free liners can be exchangeably fitted to the interior of the cup configured to enclose the heart and improve fit between the heart and cup.

23. The device of claim 22, wherein the liner is comprised of closed cell pores and has a modulus less than 25 Shore A.

24. The device of claim 22, wherein liner is comprised of open pores designed to draw body fluid into the liner and conduct vacuum across the surface of the heart such that the Poisson ratio increases to 0.5 over the period of approximately 1 hour.

25. The device of claim 1, wherein cup is localized on the heart by supplying suction at the apex of the cup.

26. The device of claim 25, wherein energy is applied to the ventricles of a heart by fluidically and cyclically filling and evacuating a chamber situated between the ventricular free walls of a heart and a semi-rigid cup structure surrounding it.

27. The device of claim 25, wherein positive pressure is supplied by a pressurized reservoir and negative pressure is supplied by an evacuated reservoir and a switching means is provided for cyclically connecting the cup to said reservoirs.

28. The device of claim 27, wherein the inertial energy component is controlled by adjusting the target pressure of the pressurized reservoir.

29. The device of claim 1, wherein the heart is supported in its pumping in both systolic and diastolic phases of the cardiac cycle.

30. A method for restoring cardiovascular equilibrium comprising:

(a) providing a cup configured to encompass, and to seal to the atrio-ventricular groove of a heart;

(b) applying, using the cup, inertial and baric energy to the left ventricle and baric energy to right ventricle; and

(c) localizing a heart such that motion of the heart'"'"'s center of mass is minimized such that a state of cardiovascular equilibrium is reached.

31. The method of claim 30, wherein variation of the ratio of inertial to baric components of energy applied to the heart places the patient in a state of cardiovascular equilibrium that responds to changes in ventricular after load and preload in a manner substantially equivalent to the Frank-Starling mechanism.

32. The method of claim 30, wherein the ratio of inertial to baric energy applied to the heart is controlled by selecting a target pressure for a pressure supply reservoir.

33. The method of claim 30, wherein the ratio of inertial to baric energy applied to the heart is controlled by regulating the first time derivative of fluid flow supplied to the cup.

34. The method of claim 30, wherein the ratio of inertial to baric energy applied to the heart is controlled by regulating the first and second time derivatives of fluid flow supplied to the cup.

35. The method of claim 30, wherein the majority of energy supplied to the right ventricle is baric and the majority of energy supplied to the left ventricle is inertial.

36. The method of claim 30, wherein at least half the energy supplied to the heart is stored proximal to the heart during the systolic phase of the cardiac cycle.

37. The method of claim 30, wherein greater than 50% of the energy supplied to the heart is supplied to the right side of the heart to support a heart in predominately right ventricular failures.

38. The method of claim 30, wherein greater than 50% of the energy supplied to the heart is supplied to the left side of the heart to support a heart in predominately left ventricular failure.

39. The method of claim 30, further comprising:

(d) weaning a heart off support supplied by an extra-cardiac assist device by

(d1) actuating the heart in synchrony with native ventricular contraction,

(d2) actuating the heart on every other cardiac cycle,

(d3) assessing the health of the heart during the non-assist cycles by measuring change in cup volume while the driveline is freely open to the atmosphere,

(d4) measuring the change in cup volume during the assist cycles,

(d5) determining a measure of heart health by comparing the changes in cup volume during assist cycles and during non-assist cycles, and

(d6) gradually reducing the amount of support energy until the heart is beating substantially on its own.

40. The method of claim 39, wherein gradually reducing the amount of support energy until the heart is beating substantially on its own commences, when the measure of heart health is less than a predetermined value.

41. The method of claim 39, wherein weaning a heart off support supplied by an extra-cardiac assist device further comprises (d7) releasing the seal around the base of the heart, (d8) making the suction line pressure slightly positive, and (d9) gradually increasing the support level until the heart decouples from the device.

42. The method of claim 41, wherein when the heart decouples from the device the liner is retained on the heart.

43. The method of claim 30, further comprising:

(d) weaning a heart off support supplied by an extra-cardiac assist device by

(d1) actuating the heart in synchrony with native ventricular contraction,

(d2) gradually reducing the amount of support energy and plotting the aortic flow as a function of aortic or ventricular pressure,

(d3) drawing a line through the end systolic points,

(d4) comparing the slope of this line to the slope of a normal heart under increasing after load conditions and

(d5) by this comparison deciding whether the heart possesses a viable Frank-Starling mechanism sufficient for terminating support.

44. The method of claim 30, wherein support level during recuperation of a heart is adjusted based on the robustness of the Frank-Starling mechanism.

45. The method of claim 30, wherein the need for continued mechanical respiratory support is alleviated by increasing the inertial component of energy supplied to a supported heart.

46. The method of claim 30, wherein a patient with abnormally high venous pressure has their venous pressure reduced by increasing the inertial component of energy supplied to a supported heart.

47. The method of claim 30, wherein poor end organ perfusion is improved by increasing the inertial component of energy supplied to a supported heart.

48. The method of claim 30, wherein donor organs are preserved longer by increasing the inertial component of energy supplied to a supported heart.

49. The method of claim 30, wherein a patient with coronary stenosis has their coronary artery perfusion improved by reducing the proportional duration of systole and maximizing the potential energy stored proximal to the heart.

50. The method of claim 30, wherein a sheath is used for patients who have recently received bypass graft surgery.

51. The method of claim 30, wherein a liner is used with an inflexible patch embedded in the otherwise flexible construction of the liner to prevent force being directly applied to a friable region of a supported heart.

52. The method of claim 30, wherein a patient is initially supported in an asynchronous mode and later supported in a synchronous mode.