Pressure sensing in implantable medical devices

• US 7,320,676 B2
• Filed: 04/30/2004
• Issued: 01/22/2008
• Est. Priority Date: 10/02/2003
• Status: Active Grant

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Miesel, Keith A.
• Primary Examiner(s): Sirmons; Kevin C.
• Assistant Examiner(s): MacNeill; Elizabeth
• Application Number:
  US10/836,115
• Publication Number:
  US 20050075624A1
• Time in Patent Office: 1,362 Days
• Field of Search: 6048901-8921, 604/503, 604/505, 604 65- 67, 604/131
• US Class Current: 604/67
• CPC Class Codes: A61M 2205/3355 Controlling downstream pump pressure
• CPC Class Codes: A61M 2205/3523 using telemetric means
• CPC Class Codes: A61M 5/14276 specially adapted for implantation
• CPC Class Codes: A61M 5/16854 by monitoring line pressure

Abstract

An implantable medical device for delivering a therapeutic substance to a delivery site in a patient. A reservoir holds a supply of the fluid therapeutic substance. A catheter has a proximal end, a delivery region and a lumen extending from the proximal end to the delivery region. The proximal end of the catheter is operatively coupled to the reservoir. The delivery region of the catheter is adapted to be placed proximate the delivery site in the patient. The therapeutic substance is adapted to be delivered through the lumen to the patient. A sensing device is operatively coupled with the lumen of the catheter being capable of detecting a pressure of the therapeutic substance in the lumen. A controller is operatively coupled to the sensing device, the controller being capable of taking an action in response to the pressure in the lumen.

Claims

1. An implantable medical device for delivering a liquid therapeutic substance to a delivery site in a patient comprising:

a reservoir holding a supply of said fluid therapeutic substance;

a catheter having a proximal end, a delivery region and a lumen extending from said proximal end to said delivery region, said proximal end of said catheter being operatively coupled to said reservoir, said delivery region of said catheter being adapted to be placed proximate said delivery site in said patient, said therapeutic substance adapted to be delivered through said lumen to said patient;

a sensing device operatively coupled with said lumen of said catheter being capable of detecting a pressure of said therapeutic substance in said lumen;

a controller operatively coupled to said sensing device, said controller being capable of taking an action is response to said pressure in said lumen;

wherein said therapeutic substance comprises a fluid;

wherein said therapeutic substance comprises a liquid;

wherein said sensing device is further capable of detecting a reference pressure outside of said lumen and wherein said controller is capable of taking action in response to relative pressures between said pressure in said lumen and said reference pressure outside of said lumen;

wherein said location outside of said lumen is in proximity to said delivery region of said catheter; and

wherein said lumen is a first lumen and wherein said catheter has a second lumen and wherein said location outside of said first lumen is in said second lumen.

2. An implantable medical device as in claim 1 wherein said sensing device comprises:

a first pressure sensor operatively coupled with said first lumen of said catheter being capable of detecting a pressure of said therapeutic substance in said first lumen; and

a second pressure sensor being capable of detecting a pressure at a location outside of said first lumen.

3. An implantable medical device as in claim 1 wherein said action is taken when said pressure exceeds a predetermined level.

4. An implantable medical device as in claim 3 wherein said action is based upon an obstruction in said first lumen.

5. An implantable medical device as in claim 1 wherein said first lumen of said catheter has a restriction and wherein said sensing device is positioned between said reservoir and said restriction.

6. An implantable medical device as in claim 5 wherein said action is taken when said pressure drops below a predetermined level.

7. An implantable medical device as in claim 6 wherein said action is based upon a leak of said catheter.

8. An implantable medical device as in claim 5 wherein said action is taken when said pressure has a characteristic signature.

9. An implantable medical device as in claim 8 wherein said characteristic signature follows a transient in delivery rate of said therapeutic substance.

10. An implantable medical device as in claim 9 wherein said transient comprises a rise in said delivery rate of said therapeutic substance.

11. An implantable medical device as in claim 9 wherein said transient comprises a fall in said delivery rate of said therapeutic substance.

12. An implantable medical device as in claim 9 wherein said transient comprises a rise and subsequent fall in said delivery rate of said therapeutic substance.

13. An implantable medical device as in claim 12 wherein said characteristic signature is a function of a decay time of said pressure following said fall of said delivery rate of said therapeutic substance.

14. An implantable medical device as in claim 12 wherein said characteristic signature is a function of an increase in said pressure in response to an increase of said delivery rate.

15. An implantable medical device as in claim 5 further comprising a pump fluidly coupled between said reservoir and said sensing device, said pump being capable of driving said therapeutic substance through said catheter under pressure.

16. An implantable medical device as in claim 15 wherein said pump comprises a peristaltic pump.

17. An implantable medical device as in claim 16 wherein said peristaltic pump comprises a tubular structure and a plurality of rollers driving said therapeutic substance through said tubular structure, said peristaltic pump creating a pressure dip each time one of said plurality of rollers lifts off of said tubular structure and wherein said characteristic signature comprises said pressure dropping below a predetermined threshold in combination with a lack of said pressure dip.

18. An implantable medical device as in claim 17 wherein said action comprises modifying operation of said pump.

19. An implantable medical device as in claim 1 wherein said action comprises ceasing delivery of said therapeutic substance to said patient.

20. An implantable medical device as in claim 19 further comprising a pump fluidly coupled between said reservoir and said catheter, said pump being capable of driving said therapeutic substance through said catheter under pressure.

21. An implantable medical device as in claim 20 wherein said action comprises modifying operation of said pump.

22. A drug delivery system for delivering a liquid therapeutic substance to a delivery site in a patient comprising:

an implantable medical device, comprising;

a reservoir holding a supply of said fluid therapeutic substance; and

a pump fluidly coupled to said reservoir, said pump being capable of fluidly driving said therapeutic substance to said delivery site under pressure;

a catheter having a proximal end, a delivery region and a lumen extending from said proximal end to said delivery region, said proximal end of said catheter being operatively coupled to said reservoir, said delivery region of said catheter being adapted to be placed proximate said delivery site in said patient, said therapeutic substance adapted to be delivered through said lumen to said patient;

a sensing device operatively coupled with said lumen of said catheter being capable of detecting a pressure of said therapeutic substance in said lumen;

a controller operatively coupled to said sensing device, said controller being capable of taking an action in response to said pressure in said lumen;

wherein said sensing device is further capable of detecting a reference pressure outside of said lumen and wherein said controller is capable of taking action in response to relative pressures between said pressure in said lumen and said reference pressure outside of said lumen;

wherein said location outside of said lumen is in proximity to said delivery region of said catheter; and

wherein said lumen is a first lumen and wherein said catheter has a second lumen and wherein said location outside of said first lumen is in said second lumen.

23. A drug delivery system as in claim 22 wherein said sensing device comprises:

a first pressure sensor operatively coupled with said first lumen of said catheter being capable of detecting a pressure of said therapeutic substance in said first lumen; and

a second pressure sensor being capable of detecting a pressure at a location outside of said first lumen and inside of said second lumen.

24. A drug delivery system as in claim 22 wherein said action is taken when said pressure exceeds a predetermined level.

25. A drug delivery system as in claim 24 wherein said action is based upon an obstruction in said first lumen.

26. A drug delivery system as in claim 22 wherein said first lumen of said catheter has a restriction and wherein said sensing device is positioned between said reservoir and said restriction.

27. A drug delivery system as in claim 26 wherein said restriction is located near said distal end of the said catheter.

28. A drug delivery system as in claim 26 wherein said action is taken when said pressure drops below a predetermined level.

29. A drug delivery system as in claim 28 wherein said action is based upon a leak of said catheter.

30. A drug delivery system as in claim 29 wherein said action is taken when said pressure has a characteristic signature.

31. A drug delivery system as in claim 30 wherein said characteristic signature follows a transient in delivery rate of said therapeutic substance.

32. A drug delivery system as in claim 31 wherein said transient comprises a rise in said delivery rate of said therapeutic substance.

33. A drug delivery system as in claim 31 wherein said transient comprises a fall in said delivery rate of said therapeutic substance.

34. A drug delivery system as in claim 31 wherein said transient comprises a rise and subsequent fall in said delivery rate of said therapeutic substance.

35. A drug delivery system as in claim 34 wherein said characteristic signature is a function of a decay time of said pressure following said fall of said delivery rate of said therapeutic substance.

36. A drug delivery system as in claim 34 wherein said characteristic signature is a function of an increase in said pressure in response to an increase of said delivery rate.

37. A drug delivery system as in claim 22 wherein said pump comprises a peristaltic pump.

38. A drug delivery system as in claim 37 wherein said peristaltic pump comprises a tubular structure and a plurality of rollers driving said therapeutic substance through said tubular structure, said peristaltic pump creating a pressure dip each time one of said plurality of rollers lifts off of said tubular structure and wherein said characteristic signature comprises said pressure dropping below a predetermined threshold in combination with a lack of said pressure dip.

39. A drug delivery system as in claim 38 wherein said action comprises stopping operation of said pump.

40. A drug delivery system as in claim 22 wherein said action comprises ceasing delivery of said therapeutic substance to said patient.

41. A drug delivery system as in claim 40 wherein said action comprises stopping operation of said pump.