Removable sheath for device protection

• US 20060200048A1
• Filed: 02/07/2006
• Published: 09/07/2006
• Est. Priority Date: 03/03/2005
• Status: Abandoned Application

• Current Assignee: Icon Medical Corp. (ICON Interventional Systems, Inc.)
• Original Assignee: Icon Medical Corp. (ICON Interventional Systems, Inc.)
• Inventors: Furst, Joseph G., Sachar, Ravish
• Application Number:
  US11/349,296
• Publication Number:
  US 20060200048A1
• Time in Patent Office: Days
• US Class Current: 600/585
• CPC Class Codes: A61M 2025/0681 Systems with catheter and outer tubing, e.g. sheath, sleeve or guide tube
• CPC Class Codes: A61M 25/0662 Guide tubes

Abstract

A medical device designed to be used with a guide catheter. The medical device has a body and cross-sectional shape and size that enables the guide catheter to be at least partially fed through a guide catheter. The body of the medical device has a longitudinal length that is at least about 10% of a longitudinal length of the guide catheter. The body of the medical device is at least partially formed of a flexible material.

Claims

1. A medical device designed to be used with a guide catheter, said medical device including a body having a cross-sectional area that is less than a cross-sectional area of an inner passageway of the guide catheter, said body including an internal passageway having a cross-sectional area that is adapted to be large enough to enable a treatment device to at least partially move within said internal passageway, said body having a longitudinal length that is at least about 10% of a longitudinal length of the guide catheter, said body at least partially formed of a flexible material.

2. The medical device as defined in claim 1, wherein said cross-section shape of said body is generally tubular.

3. The medical device as defined in claim 1, where said body has a longitudinal length that is greater than a longitudinal length of the guide catheter.

4. The medical device as defined in claim 2, where said body has a longitudinal length that is greater than a longitudinal length of the guide catheter.

5. The medical device as defined in claim 1, wherein said body includes at least one slit along a longitudinal length of said body.

6. The medical device as defined in claim 4, wherein said body includes at least one slit along a longitudinal length of said body.

7. The medical device as defined in claim 5, wherein said at least one slit is at least about 1% of said longitudinal length of said body.

8. The medical device as defined in claim 7, wherein said at least one slit is at least about 90% of said longitudinal length of said body.

9. The medical device as defined in claim 6, wherein said at least one slit is at least about 90% of said longitudinal length of said body.

10. The medical device as defined in claim 1, wherein said treatment device includes a device selected from the group consisting of a guide wire, an angioplasty balloon, a stent or combinations thereof.

11. The medical device as defined in claim 9, wherein said treatment device includes a device selected from the group consisting of a guide wire, an angioplasty balloon, a stent or combinations thereof.

12. The medical device as defined in claim 1, wherein said body includes at least one location marker.

13. The medical device as defined in claim 11, wherein said body includes at least one location marker.

14. The medical device as defined in claim 1, wherein at least a portion of said body includes at least one coating to reduce the roughness or surface friction of said coated body portion.

15. The medical device as defined in claim 11, wherein at least a portion of said body includes at least one coating to reduce the roughness or surface friction of said coated body portion.

16. The medical device as defined in claim 1, wherein at least a portion of said body includes at least one coating that includes at least one biological agent.

17. The medical device as defined in claim 11, wherein at least a portion of said body includes at least one coating that includes at least one biological agent.

18. The medical device as defined in claim 1, wherein at least a portion of said body includes at least one reinforcing, stiffening and/or strengthening components.

19. The medical device as defined in claim 11, wherein at least a portion of said body includes at least one reinforcing, stiffening and/or strengthening components.

20. The medical device as defined in claim 1, wherein said body includes one or more perforations.

21. The medical device as defined in claim 11, wherein said body includes one or more perforations.

22. The medical device as defined in claim 1, wherein said body includes a gripping surface at at least one proximal end of said body.

23. The medical device as defined in claim 11, wherein said body includes a gripping surface at at least one proximal end of said body.

24. The medical device as defined in claims 22, wherein said gripping surface includes a guide hub that is releasably connected to at least one proximal end of said body.

25. The medical device as defined in claims 23, wherein said gripping surface includes a guide hub that is releasably connected to at least one proximal end of said body.

26. A medical device designed to be used with a guide catheter, said medical device including a body having a cross-sectional area that is at least 5% less than a cross-sectional area of an inner passageway of the guide catheter, a majority of said body having a generally circular cross-sectional shape, said body including an internal passageway having a cross-sectional area that is adapted to be large enough to enable a treatment device to at least partially move within said internal passageway, a majority of said inner passageway of said body having a generally circular cross-sectional shape, said body having a longitudinal length that is at least about 10 cm and that is at least about 10% longer than a longitudinal length of the guide catheter, said body at least partially formed of a flexible polymer material, said treatment device includes a device selected from the group consisting of a guide wire, an angioplasty balloon, a stent or combinations thereof.

27. The medical device as defined in claim 26, wherein said body includes at least one slit along at least about 50% of a longitudinal length of said body.

28. The medical device as defined in claim 26, wherein said body includes at least one location marker.

29. The medical device as defined in claim 26, wherein at least a portion of said body includes at least one coating to reduce the roughness or surface friction of said coated body portion.

30. The medical device as defined in claim 26, wherein at least a portion of said body includes at least one coating that includes at least one biological agent.

31. The medical device as defined in claim 26, wherein at least a portion of said body includes at least one reinforcing, stiffening and/or strengthening components.

32. The medical device as defined in claim 26, wherein said body includes one or more perforations.

33. The medical device as defined in claim 26, wherein said body includes a gripping surface at at least one proximal end of said body, said gripping surface includes a guide hub that is releasably connected to said at least one proximal end of said body.

34. A method of treating a diseased area of a body passageway comprising:

a. inserting a guide catheter at least partially through a body passageway until one end of said guide catheter is within about 18 inches or less from the diseased area, said guide catheter having an inner passageway; and

,

b. inserting a medical device into at least a majority longitudinal length of said inner passageway of said guide catheter, said medical device including a body having a cross-sectional area that is at least 5% less than a cross-sectional area of said inner passageway of the guide catheter, said body including an internal passageway having a cross-sectional area that is adapted to be large enough to enable a treatment device to at least partially move within said internal passageway, said body having a longitudinal length that is at least about 10 cm.

35. The method as defined in claim 34, including the step of moving a treatment device at least partially through said internal passageway of said body of said medical device when said medical device is at least partially positioned in said inner passageway of said guide catheter, said treatment device including a device selected from the group consisting of a guide wire, an angioplasty balloon, a stent or combinations thereof.

36. The method as defined in claim 34, wherein said medical device has a longitudinal length that is greater than a longitudinal length of said guide catheter and including the step of inserting said medical device in said inner passageway of said guide catheter until as one end of said medical device extends from a first end of said guide catheter and another end of said medical device extends from a second end of said guide catheter.

37. The method as defined in claim 34, wherein said body of said medical device includes at least one slit along at least about 50% of a longitudinal length of said body.

38. The method as defined in claim 34, wherein said body of said medical device includes at least one location marker.

39. The method as defined in claim 34, wherein at least a portion of said body of said medical device includes at least one coating to reduce the roughness or surface friction of said coated body portion.

40. The method as defined in claim 34, wherein at least a portion of said body of said medical device includes at least one coating that includes at least one biological agent.

41. The method as defined in claim 34, wherein at least a portion of said body of said medical device includes at least one reinforcing, stiffening and/or strengthening components.

42. The method as defined in claim 34, wherein said body of said medical device includes one or more perforations.

43. The method as defined in claim 34, wherein said body of said medical device includes a gripping surface at at least one proximal end of said body, said gripping surface includes a guide hub that is releasably connected to at least one proximal end of said body.

44. The method as defined in claim 34, including the step of directing an end of said medical device to close proximity to a portion of an angioplasty balloon that has at least partially adhered to another treatment device and withdrawing said balloon until said balloon releases from said treatment device.

45. The method as defined in claim 34, including the steps of moving a portion of said medical device to a treatment site, at least partially withdrawing an end of said guide catheter from said treatment site, and subsequently sliding said guide catheter on said medical device until the end of said guide catheter is again positioned at or closely to the treatment site.

46. The method as defined in claim 34, including the steps of positioning on end of said medical device at or closely to said diseased area in said body passageway and then moving at least one of said treatment devices at least partially through said internal passageway of said body of said medical device to at least partially protect said treatment device from said body passageway until said treatment device is positioned at or closely to said diseased area.

47. The method as defined in claim 34, including the steps of positioning on end of said medical device at or closely to at least of said treatment devices and then at least partially drawing said treatment device into and through said internal passageway of said body of said medical device so as to at least partially protect an inner surface of the body passageway.