High-efficiency external counterpulsation apparatus and method for performing the same

• US 20060004245A1
• Filed: 06/30/2004
• Published: 01/05/2006
• Est. Priority Date: 06/30/2004
• Status: Active Grant

• Current Assignee: David Anthony Pickett, James Russell Lusk
• Original Assignee: David Anthony Pickett, James Russell Lusk
• Inventors: Lusk, James Russell, Pickett, David Anthony
• Granted Patent: US 7,074,177 B2
• Time in Patent Office: Days
• US Class Current: 600/16
• CPC Class Codes: A61H 1/006 Apparatus for applying pressure or blows for compressive stressing of a part of the skeletal structure, e.g. for preventing or alleviating osteoporosis
• CPC Class Codes: A61H 2201/0103 inflatable
• CPC Class Codes: A61H 2201/1238 with hydraulic or pneumatic drive
• CPC Class Codes: A61H 2201/165 Wearable interfaces
• CPC Class Codes: A61H 2201/5007 computer controlled
• CPC Class Codes: A61H 2201/5056 pneumatically controlled
• CPC Class Codes: A61H 2203/0456 Supine
• CPC Class Codes: A61H 2230/04 Heartbeat characteristics, e.g. E.G.C., blood pressure modulation
• CPC Class Codes: A61H 31/005 with feedback for the user
• CPC Class Codes: A61H 31/006 Power driven
• CPC Class Codes: A61H 31/008 Supine patient supports or bases, e.g. improving air-way access to the lungs
• CPC Class Codes: A61H 9/0078 with intermittent or alternately inflated bladders or cuffs mattresses for preventing bed-sores with alternated pressurized chambers A61G7/05776

Abstract

The embodiments of the invention generally provide an external counterpulsation apparatus having an efficient cuff and bladder system. The embodiments generally allow effective treatment at lower pressures and a reduced total body surface area being compressed. An accurate and reliable combination of automatic and preset timing for inflation and deflation of the bladder system is used to simplify use of the apparatus.

Claims

1. An external counterpulsation system which compresses a limited area of the lower limbs and buttocks;

does not require high inflation pressures;

reduces skin irritation; and

reduces or eliminates the need for bladder deflation during a premature ventricular contraction, comprising;

six air pressurizable bladders, wherein each said air bladder has a compression surface area of about forty square inches;

a right and left lower thigh cuff, each said lower thigh cuff adapted for holding one said air bladder against the lower thigh of a patient and transmitting force generated by pressurization of said bladder to said patient through said compression surface area;

a right and left upper thigh cuff, each said upper thigh cuff adapted for holding one said air bladder against the upper thigh of said patient and transmitting force generated by pressurization of said bladder to said patient through said compression surface area;

a buttock cuff adapted for holding two said air bladders against the buttocks of said patient and transmitting force generated by pressurization of said bladders to said patient through said compression surface areas;

wherein said cuffs are no more than six inches in width;

an air compressor for pressurizing said bladders;

a pressure regulator for limiting the pressurization of said bladders to no greater than 240 mm Hg;

a plurality of valves for controlling the timing of said pressurization of said bladders;

an ECG signal from an external ECG monitor connected to said patient;

an ECG signal input connector that is capable of accepting ECG signals from different external ECG monitors;

a programmable logic controller programmed to receive said ECG signal and generating valve timing signals from peaks in said ECG signal;

wherein said programmable logic controller is programmed not to terminate the valve timing signals upon detection of a premature ventricular contraction.

2. A method for performing external counterpulsation which compresses a limited area of the lower limbs and buttocks;

does not require high inflation pressures;

reduces skin irritation; and

reduces or eliminates the need for bladder deflation during a premature ventricular contraction, comprising;

providing an external counterpulsation apparatus having a plurality of cuffs and bladders, a pressure source for pressurizing said bladders, a physiological sensor and a pressure controller,

wherein said bladders each have a compression surface area of less than about 40 square inches and the total compression surface area of said bladders is less than about 240 square inches;

attaching said bladders to a patient;

sensing heart activity in said patient;

limiting the pressure of said bladders to no greater than 240 mm Hg; and

compressing said patient with said bladders in coordination with said heart activity;

wherein said compressing step comprises compression of the lower thighs, the upper thighs and the buttocks of said patient; and

said compressing step does not require compression of other areas on the lower limbs or pelvic region.

3. An external counterpulsation system, comprising:

a plurality of pressurizable bladders, said bladders each having a compression surface area for transmitting pressure;

wherein said compression surface area of each said bladder is generally less than about 80 square inches and the total compression surface area of said bladders is less than about 600 square inches;

a plurality of cuffs adapted for holding said bladders against the body of said patient;

a pressure source for pressurizing said bladders;

an ECG signal source for providing an ECG signal;

a valve controller for receiving said ECG signal and generating at least one control signal;

a plurality of valves for receiving said control signals and controlling pressurization of said bladders; and

said valves having a first position that allows depressurization of said bladders and a second position that allows pressurization of said bladders by said pressure source.

4. The system of claim 3, wherein said cuffs are generally about six inches or less in width.

5. The system of claim 3, wherein the total compression surface area of said bladders is less than about 216 square inches.

6. The system of claim 3, wherein at least one said cuff is adapted for placement at about an upper posterior knee area of said patient.

7. The system of claim 3, wherein at least one said cuff is adapted for placement at about an inguinal area of said patient.

8. The system of claim 7, wherein said bladders of said cuffs adapted for placement at about the inguinal areas have an average compression surface area of less than about 40 square inches.

9. The system of claim 3, wherein at least one said cuff adapted for placement at about the buttocks of said patient.

10. The system of claim 9, wherein said bladder of said cuff adapted for placement at about the buttocks comprises a single bladder connector and has a compression surface area of less than about 90 square inches.

11. The system of claim 3, wherein said pressure source comprises a first air compressor connected to said valves.

12. The system of claim 3, wherein said pressure source comprises an external compressed air source.

13. The system of claim 3, wherein said ECG signal source comprises an external ECG signal from an external ECG monitor connected to said patient.

14. The system of claim 3, wherein said ECG signal source originates from an ECG monitor integrated within said system.

15. The system of claim 3, wherein at least one said cuff forms a portion of at least one said bladder.

16. The system of claim 3, wherein said cuffs each comprise at least one buckle for holding said bladders against said body.

17. The system of claim 16, wherein said cuffs further comprise a buckle roller for reducing the effort of tightening the cuff.

18. The system of claim 16, wherein said cuffs further comprise a buckle shield to reduce pinching of the skin of said body.

19. The system of claim 3, further comprising a pressure regulator attached to said pressure source.

20. The system of claim 19, wherein said pressure regulator is configured to provide a maximum bladder pressure of about 160 mm Hg to about 240 mm Hg.

21. The system of claim 3, wherein said valve controller is configured to generate a first control signal following a first delay interval after the detection of a QRS complex;

wherein said first delay interval is calculated upon the heart rate; and

wherein said first control signal terminates following a fixed interval after detection of said QRS complex.

22. The system of claim 21, wherein said valve controller is further configured to generate at least one secondary control signal following a fixed delay interval from said first control signal and terminating following a fixed interval after detection of said QRS complex.

23. The system of claim 22, wherein said fixed delay intervals of said control signals are not user-selectable.

24. The system of claim 3, wherein said valves are configured to be in said first position in the absence of a control signal and in said second position while receiving said control signal.

25. The system of claim 3, wherein said valves are configured to be in said first position in the while receiving said control signal and in said second position in the absence of said control signal.

26. The system of claim 21, wherein said valve controller is configured to have a refractory period for detecting said QRS complexes during generation of said control signals.

27. The system of claim 21, wherein said first delay interval for said first control signal pre-set to about 280 milliseconds.

28. The system of claim 21, wherein said first delay interval for said first control signal is equal to about 25% of the average duration of the last eight peak-to-peak ECG intervals of a detected ECG signal.

29. The system of claim 21, wherein said first delay interval for said first control signal is equal to about 25% of the longest duration of the last eight peak-to-peak intervals in said ECG signal.

30. The system of claim 21, wherein said valve controller is configured to generate a first control signal based upon detection of signal peaks after processing said ECG signal.

31. The system of claim 21, wherein said valve controller is configured to generate a first control signal based upon detection of R wave peaks of said ECG signal.

32. An external counterpulsation system, comprising:

a plurality of pressurizable bladders, said bladders each having a compression surface area for transmitting pressure of about 40 square inches or less;

a bladder selector capable of inactivating at least one of said bladders to limit the total compression surface area of bladders used during a treatment to less than about 240 square inches;

a plurality of cuffs adapted for holding said bladders against the body of said patient;

a pressure source for pressurizing said bladders;

an ECG signal source for providing an ECG signal;

a valve controller for receiving said ECG signal and generating at least one control signal;

a plurality of valves for receiving said control signals and controlling pressurization of said bladders; and

said valves having a first position that allows depressurization of said bladders and a second position that allows pressurization of said bladders by said pressure source.

33. The method of claim 32, wherein said bladder inactivator comprises programming of said valve controller to not send control signals to inactive bladders.

34. The method of claim 32, wherein said bladder inactivator comprises a plurality of switches capable of blocking control signals from said valve controller.

35. The method of claim 32, wherein said bladder inactivator comprises a plurality of shut-off valves connected to said bladders for preventing inflation of said bladders.

36. An external counterpulsation system, comprising:

a plurality of compression members, each said compression member having a compression surface area for transmitting pressures;

wherein said compression surface areas of each said compression member is has a compression surface area generally less than about 40 square inches and the total compression surface area of said compression members is less than about 240 square inches;

wherein said compression members have a first position that is capable of applying compression against said body and a second position that relieves compression of said body.

a plurality of cuffs for holding said compression members against the body of said patient;

wherein said cuffs are generally about 6 inches or less in width;

a energy source for activating said compression members;

an ECG signal source for providing an ECG signal;

a main controller for receiving said ECG signal and generating at least one control signal; and

a plurality of compression member controllers for receiving said control signals and controlling said position of said compression members.

37. The system of claim 36, wherein said compression members comprise electrically actuated pistons.

38. The system of claim 36, wherein said compression members comprise pneumatically actuated pistons.

39. The system of claim 36, wherein said energy source comprises an air compressor.

40. The system of claim 36, wherein said compression members comprise inflatable bladders.

41. The system of claim 36, wherein said energy source comprises an air compressor.

42. An external counterpulsation system, including:

pressurizable bladders for compressing the superior-posterior knee regions, the inguinal regions and buttocks but not the remaining portions of the legs and pelvic regions of the patient; and

retention members adapted to hold said bladders against the body of said patient.

43. The system of claim 42, wherein said retention members comprise cuffs.

44. The system of claim 43, wherein said cuffs comprise pockets for holding said bladders.

45. The system of claim 42, wherein said retention members comprise friction or slip-resistant pads.

46. The system of claim 42, wherein said retention members comprise protective padding.

47. A compression system for an external counterpulsation system, including:

compression members for compressing the body of a patient; and

retention members adapted to hold said bladders against the superior-posterior knee regions, the inguinal regions and buttocks but not the remaining portions of the legs and pelvic regions of the patient.

48. The system of claim 47, wherein said compression members comprise inflatable bladders.

49. The system of claim 47, wherein said compression members comprise electromechanical actuators.

50. The system of claim 47, wherein said retention members comprise cuffs.

51. The system of claim 47, wherein at least one said compression member and one said retention member are integrally formed.

52. A method for performing external counterpulsation, comprising the steps of:

providing an external counterpulsation apparatus, the apparatus comprising a pressurized fluid source;

a plurality of valves, a valve controller, a physiological sensor and a plurality of active bladders having a total compression surface area of less than about 480 square inches;

applying said compression surface areas of said active bladders to a patient;

attaching at least one physiological sensor to said patient;

detecting the systolic and diastolic phases of heart contraction from said physiological sensor;

pressurizing said active bladders during said diastolic phase to no greater than about 220 mm Hg;

compressing said patient with said compression surface areas of said active bladders during said diastolic phase; and

deflating said bladders.

53. The method of claim 52, wherein said apparatus of said providing step further comprises inactive bladders that are not pressurized during said pressuring step.

54. The method of claim 52, wherein the step of applying said bladders to said patient comprises applying said bladders to the inguinal region of said patient.

55. The method of claim 52, wherein the step of applying said bladders to said patient comprises applying said bladder to the upper posterior knee region of said patient.

56. The method of claim 52, wherein the step of applying said bladders to said patient comprises applying said bladder to the buttock region of said patient.

57. The method of claim 52, wherein the step of applying said bladders to said patient further comprises applying said bladders to at least one femoral vein near the inguinal line of said patient.

58. The method of claim 57, wherein said compressing step comprises occlusion of said femoral vein.

59. The method of claim 57, wherein said compressing step comprises occlusion of said femoral artery.

60. The method of claim 52, wherein the step of applying said bladders to said patient comprises applying all said bladders to sites superior to the knees of said patient.

61. The method of claim 52, wherein the step of applying said bladders to said patient comprises applying said bladders to the lower thighs, upper thighs and buttocks.

62. The method of claim 52, wherein said compressing step comprises compressing less than 10% of the total body surface area of said patient.

63. The method of claim 52, wherein the step of applying said bladders comprises using cuffs to apply said bladders.

64. A method for performing external counterpulsation, comprising the steps of:

providing an external counterpulsation apparatus, the apparatus comprising a pressurized fluid source;

a plurality of valves, a valve controller, a physiological sensor and a plurality of bladders each having a compression surface area;

applying said bladders to a patient;

selecting a subset of said plurality of bladders for pressurization, said subset having a total compression surface area of about 240 square inches or less;

detecting the systolic and diastolic phases of heart contraction from said physiological sensor;

pressurizing said subset of bladders during said diastolic phase;

compressing said patient with said compression surface areas of said active bladders during said diastolic phase; and

deflating said subset of bladders.

65. A method for performing external counterpulsation, comprising the steps of:

providing an external counterpulsation apparatus, the apparatus comprising a pressurized fluid source;

a plurality of valves, a valve controller, a physiological sensor and a plurality of bladders each having a compression surface area;

applying said bladders to a patient;

detecting heart activity from said physiological sensor;

pressurizing said bladders during said diastolic phase;

compressing about 240 square inches or less of said patient'"'"'s body with said pressurized bladders during said diastolic phase; and

deflating said bladders.

66. A method for performing external counterpulsation, comprising:

providing an external counterpulsation apparatus having a plurality of activateable compression members, an energy source for activating said compression members, a physiological sensor and a compression member controller;

attaching said compression members to a patient;

sensing heart activity in said patient;

compressing said patient with said activateable compression members in synchrony with said heart activity;

wherein said compressing step comprises less than about 10 percent of the total body surface area of said patient.

67. The method of claim 66, wherein said compression members each have a compression surface area of less than about 40 square inches and the total compression surface area of said compression members is less than about 240 square inches.

68. The method of claim 66, wherein said compressing step comprises temporarily occluding the femoral veins of said patient at about the inguinal ligament.