Catheter with temporary stimulation electrode

• US 20050256541A1
• Filed: 04/29/2005
• Published: 11/17/2005
• Est. Priority Date: 04/30/2004
• Status: Abandoned Application

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Stypulkowski, Paul H.
• Application Number:
  US11/119,390
• Publication Number:
  US 20050256541A1
• Time in Patent Office: Days
• US Class Current: 607/3
• CPC Class Codes: A61N 1/05 for implantation or insertion into the body, e.g. heart electrode A61N1/06 takes precedence

Abstract

A catheter has at least one removable, temporary stimulation electrode for positioning of the catheter prior to delivery of a therapeutic substance, such as pharmaceutical or biological therapy, to the nervous system of a patient. A stylet having at least one temporary stimulation electrode disposed at its distal end is removably positioned within a lumen of the catheter. A test stimulation is delivered via the temporary stimulation electrode to produce a patient response. If the patient response is not consistent with proper positioning of the distal end of the catheter with respect to the target tissue, the distal end of the catheter is repositioned and another test stimulation is delivered. This process is repeated until the patient response is consistent with proper positioning of the distal end of the catheter. The stylet and its associated temporary stimulation electrode are then removed from the lumen, leaving the catheter in position with respect to the target tissue. A therapeutic substance may then be delivered to the target tissue via the lumen.

Claims

1. A device comprising:

a catheter having a proximal end and a distal end and a lumen extending between the proximal end and the distal end of the catheter to deliver a therapeutic substance to target tissue;

a stylet removably positioned within the lumen and having a proximal end and a distal end, wherein the distal end of the stylet extends beyond the distal end of the catheter; and

at least one stimulation electrode disposed at the distal end of the stylet to verify proper positioning of the distal end of the catheter with respect to the target tissue.

2. The device of claim 1, further including an electrical stimulation generator coupled to the stimulation electrode to deliver a test stimulation to the target tissue via the stimulation electrode to produce a patient response.

3. The device of claim 1, further including a therapy delivery device coupled to the catheter to deliver a therapeutic agent to the target tissue after removal of the stylet from the lumen.

4. The device of claim 1, wherein the therapeutic substance includes at least one of a pharmaceutical therapy, a biological therapy or a neuropharmaceutical agent.

5. The device of claim 4, wherein the pharmaceutical therapy includes at least one of an anesthetic or a narcotic.

6. The device of claim 4, wherein the biological therapy includes at least one of a gene therapy agent or a growth factor.

7. The device of claim 1, wherein the catheter has a size selected for introduction into a brain or a spinal column of a patient.

8. The device of claim 1, wherein the catheter comprises a flexible material.

9. The device of claim 8, wherein the catheter comprises a medical grade silicon elastomer, a polyurethane, or polytetrafluoroethylene (PTFE).

10. The device of claim 1, wherein the stylet comprises at least one of a tungsten or a titanium material.

11. The device of claim 1, wherein the stimulation electrode includes one of a monopolar electrode, a bipolar electrode, or a multi-polar electrode.

12. The device of claim 1, wherein the distal end of the stylet extends from between 1 millimeters and 5 millimeters beyond the distal end of the catheter.

13. The device of claim 1, wherein the stimulation electrode comprises a conductive layer disposed at the distal end of the stylet.

14. The device of claim 13, wherein the conductive layer comprises a biocompatible material.

15. The device of claim 13, wherein the conductive layer comprises one of platinum, platinum-iridium or stainless steel.

16. The device of claim 1, wherein the stimulation electrode comprises a bipolar electrode including a conductive layer disposed at the distal end of the stylet and a circumferential ring electrode.

17. The device of claim 1, further including an electrical stimulation generator external to the body of the patient.

18. The device of claim 1, further comprising a fluid delivery device to deliver the therapeutic substance to the target tissue via the lumen following removal of the stylet.

19. A method comprising:

introducing a catheter having a temporary stimulation electrode removably positioned therein to target tissue within a body of a patient such that a distal end of the temporary stimulation electrode extends beyond a distal end of the catheter;

delivering a test stimulation via the temporary stimulation electrode to produce a patient response;

determining, based on the patient response, whether the catheter is properly positioned with respect to the target tissue; and

removing the temporary stimulation electrode from the catheter when the catheter is properly positioned.

20. The method of claim 19, further comprising delivering a therapeutic substance to the target tissue via the catheter after removing the temporary stimulation electrode.

21. The method of claim 20, wherein delivering a therapeutic substance includes delivering at least one of a pharmaceutical or a biological therapy.

22. The method of claim 21, wherein delivering a pharmaceutical therapy includes delivering at least one of an anesthetic or narcotic.

23. The method of claim 21, wherein delivering a biological therapy includes delivering a gene therapy agent.

24. The method of claim 19, further comprising:

repositioning the catheter when the patient response is not consistent with proper positioning of the catheter; and

delivering an additional test stimulation via the stimulation electrode.

25. The method of claim 19, wherein the patient response includes one of symptom reduction, evoked potentials, subjective sensations, or paraesthesia.

26. A device comprising:

a catheter having a proximal end and a distal end and a lumen extending between the proximal end and the distal end of the catheter to deliver a therapeutic substance to target tissue;

a stiffening stylet removably positioned within the lumen and having a proximal end and a distal end, wherein the distal end of the stylet extends beyond the distal end of the catheter; and

at least one stimulation electrode disposed at the distal end of the stylet to verify proper positioning of the distal end of the catheter with respect to the target tissue.

27. The device of claim 26, wherein the stylet comprises at least one of a tungsten or a titanium material.

28. The device of claim 26, wherein the stimulation electrode includes one of a monopolar electrode, a bipolar electrode, or a multi-polar electrode.

29. The device of claim 26, wherein the distal end of the stylet is substantially flush with the distal end of the catheter.

30. The device of claim 26, wherein the distal end of the stylet extends beyond the distal end of the catheter.

31. The device of claim 30, wherein the distal end of the stylet extends from between 1 millimeters and 5 millimeters beyond the distal end of the catheter.

32. The device of claim 26, wherein the stimulation electrode comprises a conductive layer disposed at the distal end of the stylet.

33. The device of claim 32, wherein the conductive layer comprises a biocompatible material.

34. The device of claim 32, wherein the conductive layer comprises one of platinum, platinum-iridium or stainless steel.

35. The device of claim 26, wherein the stimulation electrode comprises a bipolar electrode including a conductive layer disposed at the distal end of the stylet and a circumferential ring electrode.

36. A method comprising:

introducing a catheter having a stiffening stylet removably positioned therein to target tissue within a body of a patient;

introducing a stimulation stylet having a temporary stimulation electrode positioned at its distal end into the catheter;

delivering a test stimulation via the temporary stimulation electrode to produce a patient response;

determining, based on the patient response, whether the catheter is properly positioned with respect to the target tissue; and

removing the temporary stimulation electrode from the catheter when the catheter is properly positioned.

37. The method of claim 36, further comprising delivering a therapeutic substance to the target tissue via the catheter after removing the temporary stimulation electrode.

38. The method of claim 37, wherein delivering a therapeutic substance includes delivering at least one of a pharmaceutical or a biological therapy.