IP Library Granted Patent US 8,585,571
Granted Patent B2
US 8,585,571 · App. 13/041,220 · Granted Nov 19, 2013

Portable controller with integral power source for mechanical circulation support systems

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Quick Facts
Patent No.
US 8,585,571
App. No.
13/041,220
Granted
Nov 19, 2013
Kind
B2
Abstract

A portable external device for a mechanical circulation support system includes first and second power sources, e.g. batteries and control electronics for redundant uninterrupted operation of an implantable blood pump. The control and power source module may be configured to accommodate a variety of wearable configurations for patient convenience and comfort.

Claims (66)

1. A portable external device for a mechanical circulation support (MCS) system comprising:

a housing;

a first battery removably connected to the housing, wherein the first battery, when connected to the housing, forms an integral portion of the housing and wherein the first battery comprises an energy dense battery;

a second battery arranged within the housing, wherein the second battery comprises a power dense battery; and

control electronics arranged within the housing, powered by at least one of the first or the second batteries, and configured to control an implantable pump.

2. The device of claim 1 , wherein the first battery comprises a first rechargeable battery configured to operate without recharge for a period of time in a range from approximately 4 hours to approximately 12 hours.

3. The device of claim 2 , wherein the first rechargeable battery is configured to operate without recharge for a period of time approximately equal to 8 hours.

4. The device of claim 1 , wherein the second battery comprises a second rechargeable battery configured to operate without recharge for a period of time in a range from approximately 15 minutes to approximately 2 hours.

5. The device of claim 4 , wherein the second rechargeable battery is configured to operate without recharge for a period of time approximately equal to 1 hour.

6. The device of claim 1 , wherein the housing comprises a width in a range from approximately 60 millimeters to approximately 90 millimeters, a length in a range from approximately 100 millimeters to approximately 140 millimeters, and a depth in a range from approximately 20 millimeters to approximately 40 millimeters.

7. The device of claim 1 , wherein the housing comprises a volume in a range from approximately 120 centimeters cubed to approximately 504 centimeters cubed.

8. The device of claim 1 , wherein the portable external device comprises a weight in a range from approximately 0.25 kilograms to approximately 1.0 kilograms.

9. The device of claim 1 further comprising a latch configured to release the first battery for removal from the housing, wherein the latch is configured to be actuated to release the first battery for removal from the housing by at least two independent motions.

10. The device of claim 9 , wherein the latch comprises two push buttons, each of which is biased into a locked position that inhibits removal of the first battery from the housing, and both of which are configured to be pushed into an unlocked position simultaneously to release the first battery for removal from the housing.

11. The device of claim 10 , wherein the two push buttons are arranged on opposing sides of the housing such that the two buttons are configured to be pushed in approximately opposite directions to one another.

12. The device of claim 9 , wherein the latch comprises a channel and a post biased into a locked position toward a first end of the channel that inhibits removal of the first battery from the housing, and wherein the post is configured to be pushed in at least two directions toward a second end of the channel into an unlocked position to release the first battery for removal from the housing.

13. The device of claim 1 , wherein each of the first and second batteries is configured to power the implantable pump.

14. The device of claim 1 , wherein a ratio of power consumed by the control electronics to power consumed by the implantable pump is in a range from approximately 1/100 to approximately 4/20.

15. The device of claim 14 , wherein the ratio of power consumed by the control electronics to power consumed by the implantable pump is approximately equal to 4/20.

16. The device of claim 14 , wherein the ratio of power consumed by the control electronics to power consumed by the implantable pump is approximately equal to 1/100.

17. The device of claim 1 , wherein the energy dense first battery comprises a lithium-ion (Li-ion), nickel-metal hydride (NiMH), or nickel-cadmium (NiCd) rechargeable battery.

18. The device of claim 1 , wherein the power dense second battery comprises lithium polymer (Lipoly) rechargeable battery.

19. The device of claim 1 , wherein the energy dense first battery comprises an energy density in a range from approximately 455 watt-hours per liter to approximately 600 watt-hours per liter.

20. The device of claim 1 , wherein the power dense second battery comprises a power density in a range from approximately 700 watts per liter to approximately 6 kilowatts per liter.

21. The device of claim 1 , wherein the control electronics comprises two processors, each of which is configured to control at least one of the first battery, the second battery, the implantable pump, or one or more components of the control electronics.

22. The device of claim 1 , further comprising at least one piezoelectric speaker controlled by the control electronics to emit one or more audible sounds.

23. The device of claim 1 , further comprising a first telemetry module configured to communicate information between the portable external device and one or more other devices according to a first wireless communication technique.

24. The device of claim 23 , further comprising a second telemetry module configured to communicate information between the portable external device and one or more other devices according to a second wireless communication technique.

25. The device of claim 24 , wherein the first wireless communication technique is different than the second wireless communication technique.

26. The device of claim 1 , further comprising a user interface comprising a capacitive sensor configured to receive user input.

27. The device of claim 26 , further comprising a depression in which the capacitive sensor is arranged.

28. The device of claim 1 , wherein power consumed by the control electronics is in a range from approximately 0.25 to approximately 1.25 watts.

29. A mechanical circulation support system comprising:

an implantable pump; and

a portable external device comprising:

a housing;

a first battery removably connected to the housing, wherein the first battery, when connected to the housing, forms an integral portion of the housing and wherein the first battery comprises an energy dense battery;

a second battery arranged within the housing, wherein the second battery comprises a power dense battery; and

control electronics arranged within the housing, powered by at least one of the first or the second power batteries, and configured to control an implantable pump.

30. The system of claim 29 , wherein the first battery comprises a first rechargeable battery configured to operate without recharge for a period of time in a range from approximately 4 hours to approximately 12 hours.

31. The system of claim 30 , wherein the first rechargeable battery is configured to operate without recharge for a period of time approximately equal to 8 hours.

32. The system of claim 29 , wherein the second battery comprises a second rechargeable battery configured to operate without recharge for a period of time in a range from approximately 15 minutes to approximately 2 hours.

33. The system of claim 32 , wherein the second rechargeable battery is configured to operate without recharge for a period of time approximately equal to 1 hour.

34. The system of claim 29 , wherein the housing comprises a width in a range from approximately 60 millimeters to approximately 90 millimeters, a length in a range from approximately 100 millimeters to approximately 140 millimeters, and a depth in a range from approximately 20 millimeters to approximately 40 millimeters.

35. The system of claim 29 , wherein the housing comprises a volume in a range from approximately 120 centimeters cubed to approximately 504 centimeters cubed.

36. The system of claim 29 , wherein the portable external device comprises a weight in a range from approximately 0.25 kilograms to approximately 1.0 kilograms.

37. The system of claim 29 , further comprising a latch configured to release the first battery for removal from the housing, wherein the latch is configured to be actuated to release the first battery for removal from the housing by at least two independent motions.

38. The system of claim 37 , wherein the latch comprises two push buttons, each of which is biased into a locked position that inhibits removal of the first battery from the housing, and both of which are configured to be pushed into an unlocked position simultaneously to release the first battery for removal from the housing.

39. The system of claim 38 , wherein the two push buttons are arranged on opposing sides of the housing such that the two buttons are configured to be pushed in approximately opposite directions to one another.

40. The system of claim 37 , wherein the latch comprises a channel and a post biased into a locked position toward a first end of the channel that inhibits removal of the first battery from the housing, and wherein the post is configured to be pushed in at least two directions toward a second end of the channel into an unlocked position to release the first battery for removal from the housing.

41. The system of claim 29 , wherein each of the first and second batteries is configured to power the implantable pump.

42. The system of claim 29 , wherein a ratio of power consumed by the control electronics to power consumed by the implantable pump is in a range from approximately 1/100 to approximately 4/20.

43. The system of claim 42 , wherein the ratio of power consumed by the control electronics to power consumed by the implantable pump is approximately equal to 4/20.

44. The system of claim 42 , wherein the ratio of power consumed by the control electronics to power consumed by the implantable pump is approximately equal to 1/100.

45. The system of claim 29 , wherein the energy dense first battery comprises a lithium-ion (Li-ion), nickel-metal hydride (NiMH), or nickel-cadmium (NiCd) rechargeable battery.

46. The system of claim 29 , wherein the power dense second battery comprises lithium polymer (Lipoly) rechargeable battery.

47. The system of claim 29 , wherein the energy dense first battery comprises an energy density in a range from approximately 455 watt-hours per liter to approximately 600 watt-hours per liter.

48. The system of claim 29 , wherein the power dense second battery comprises a power density in a range from approximately 700 watts per liter to approximately 6 kilowatts per liter.

49. The system of claim 29 , wherein the control electronics comprises two processors, each of which is configured to control at least one of the first battery, the second battery, the implantable pump, or one or more components of the control electronics.

50. The system of claim 29 , further comprising at least one piezoelectric speaker controlled by the control electronics to emit one or more audible sounds.

51. The system of claim 29 , further comprising a first telemetry module configured to communicate information between the portable external device and one or more other devices according to a first wireless communication technique.

52. The system of claim 51 , further comprising a second telemetry module configured to communicate information between the portable external device and one or more other devices according to a second wireless communication technique.

53. The system of claim 52 , wherein the first wireless communication technique is different than the second wireless communication technique.

54. The system of claim 29 , further comprising a user interface comprising a capacitive sensor configured to receive user input.

55. The system of claim 54 , further comprising a depression in which the capacitive sensor is arranged.

56. The system of claim 29 , wherein power consumed by the control electronics is in a range from approximately 0.25 to approximately 1.25 watts.

Assignments (8)
RELEASE OF PATENT SECURITY AGREEMENT - REEL/FRAME 054795/0607, SUPPLEMENTAL PATENT SECURITY AGREEMENT - REAL/FRAME 056240/0147 AND ASSIGNMENT ID: 885388 Recorded Oct 1, 2025
From: TEXAS CAPITAL BANK, AS AGENT
To: MINNETRONIX MEDICAL, INC.
Reel/Frame 073434/0838 →
SECURITY INTEREST Recorded Sep 30, 2025
From: INTRICON CORPORATION; MINNETRONIX, INC.
To: CAPITAL ONE, NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 072428/0878 →
ASSIGNMENT OF SECURITY INTEREST IN PATENT COLLATERAL RECORDED ON REEL 054795 FRAME 0607 AND SUPPLEMENTAL PATENT SECURITY AGREEMENT RECORDED ON REEL 056240 FRAME 0147 Recorded Mar 13, 2025
From: FIRST HORIZON BANK
To: TEXAS CAPITAL BANK, AS SUCCESSOR AGENT
Reel/Frame 073460/0969 →
SECURITY INTEREST Recorded Jan 4, 2021
From: MINNETRONIX MEDICAL, INC.; MINNETRONIX NEURO, INC.
To: FIRST HORIZON BANK, AS ADMINISTRATIVE AGENT
Reel/Frame 054795/0607 →
RELEASE OF SECURITY INTEREST Recorded Dec 31, 2020
From: MINNESOTA BANK & TRUST
To: MINNETRONIX MEDICAL, INC.; MINNETRONIX NEURO, INC.
Reel/Frame 054788/0122 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 7, 2016
From: BROEN, KENNETH E.
To: MINNETRONIX, INC.
Reel/Frame 037428/0247 →
SECURITY INTEREST Recorded Dec 16, 2014
From: MINNETRONIX, INC.
To: MINNESOTA BANK & TRUST
Reel/Frame 034518/0602 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2011
From: BACHMAN, TIMOTHY A.; BOLYARD, NATHAN J.; BROWN, COREY D.; EVANS, DON E.W.; KNIPFER, MICHAEL A.; NAZARIAN, RICHARD A.
To: MINNETRONIX INC.
Reel/Frame 025906/0047 →