Dilatation/centering catheter used for the treatment of stenosis or other constriction in a bodily passageway and method thereof

• US 5,947,924 A
• Filed: 09/13/1996
• Issued: 09/07/1999
• Est. Priority Date: 09/13/1996
• Status: Expired due to Fees

• Current Assignee: Interventional Therapies L L C
• Original Assignee: Angiorad, LLC
• Inventors: Liprie, Samuel F.
• Primary Examiner(s): Yasko, John D.
• Assistant Examiner(s): Blyveis, Deborah
• Application Number:
  US08/713,696
• Time in Patent Office: 1,089 Days
• Field of Search: 604/96-102, 606/192, 606/194, 600/3-5
• US Class Current: 604/103.07
• CPC Class Codes: A61M 2025/1047 having centering means, e.g. balloons having an appropriate shape
• CPC Class Codes: A61M 2025/1072 having balloons with two or more compartments
• CPC Class Codes: A61M 2025/1093 having particular tip characteristics
• CPC Class Codes: A61M 25/1002 characterised by balloon shape A61M25/1006, A61M25/1009 take precedence
• CPC Class Codes: A61M 25/1011 Multiple balloon catheters
• CPC Class Codes: A61M 25/104 used for angioplasty
• CPC Class Codes: A61N 2005/1003 having means for centering a radioactive source within the lumen, e.g. balloons
• CPC Class Codes: A61N 5/1002 Intraluminal radiation therapy

Abstract

An apparatus and method for treating an occlusion or constriction, such as a stenosis in a blood vessel or other conduit in the body, as well as an apparatus and method for treating a tumor or cancerous area occurring around a conduit or duct in the body. The apparatus includes a catheter provided with a centering balloon including a catheter centering balloon encircling a portion of the catheter near its distal end. This centering balloon contains a plurality of thin spoke-like members. A second dilatation balloon attached to the surface of the catheter is used to treat the stenosed area. A radioactive source of material is included for treating the stenosis or cancer.

Claims

1. A device for treating an occlusion or a constriction in a bodily conduit passageway having an inner surface in the body, comprising:

a flexible, elongated catheter having a distal end and a proximal end, said catheter provided with a first hollow treatment lumen extending within said catheter and provided with an exterior surface;

a centering balloon attached to said exterior surface proximate to said distal end of said catheter, said centering balloon provided with at least two inflatable thin spokes which are dimensioned and configured to extend from said exterior surface of said catheter to the inner surface of the passageway when said centering balloon is inflated, said spokes encircling said distal end around a first particular point, said at least two inflatable thin spokes surrounded by a flexible membrane attached to said centering balloon; and

a source for inflating and deflating said centering balloon in communication with said centering balloon;

wherein when inflated, said centering balloon would allow a significant amount of perfusion of bodily fluids around said spokes.

2. The device in accordance with claim 1, wherein said flexible membrane abuts the inner surface of the passageway to ensure a greater flow of bodily fluids past the occlusion or constriction when said centering balloon is inflated.

3. The device in accordance with claim 2, wherein said centering balloon includes at least one additional set of inflatable thin spokes encircling a portion of said outer surface of said catheter, each of said additional sets of inflatable thin spokes encircling said outer surface at a point removed from said first particular point, each of said thin spokes of a particular set of thin spokes symmetrically spaced from one another.

4. The device in accordance with claim 1, further including a source of radiation maneuvered to the occlusion or constriction through said hollow treatment lumen.

5. The device in accordance with claim 4 further including a flexible membrane attached to said centering balloon, said flexible membrane abutting the inner surface of the passageway to ensure a greater flow of bodily fluids past the occlusion or constriction when said centering balloon is inflated.

6. The device in accordance with claim 5, wherein said centering balloon includes at least one additional set of inflatable thin spokes encircling a portion of said outer surface of said catheter, each of said additional sets of inflatable thin spokes encircling said outer surface at a point removed from said first particular point, each of said thin spokes of a particular set of thin spokes symmetrically spaced from one another.

7. The device in accordance with claim 4 further including a second lumen provided within said catheter connected to said centering balloon and said source for inflating and deflating said centering balloon.

8. The device in accordance with claim 7 further including a flexible, elongated guide wire maneuvered to the occlusion or constriction and a third lumen provided within at least a portion of said catheter within which said guide wire will travel.

9. The device in accordance with claim 8 further including a sealing means provided within said distal end of said catheter for preventing contamination or germs inside of said first lumen from coming into contact with bodily fluids.

10. The device in accordance with claim 8 wherein the termination of said distal end is tapered.

11. The device in accordance with claim 4, wherein said source of radiation is cesium 137, cobalt 60, iodine 125, iodine 131, cobalt 57, iridium 192, gold 198, palladium 103, strontium 89, strontium 90, phosphate 32 or yttrium 90.

12. The device in accordance with claim 1, wherein said centering balloon includes at least one additional set of inflatable thin spokes encircling a portion of said outer surface of said catheter, each of said additional sets of inflatable thin spokes encircling said outer surface at a point removed from said first particular point, each of said thin spokes of a particular set of thin spokes symmetrically spaced from one another.

13. The device in accordance with claim 1 further including a second lumen provided within said catheter connected to said centering balloon and said source for inflating and deflating said centering balloon.

14. The device in accordance with claim 13 further including a flexible, elongated guide wire maneuvered to the occlusion or constriction and a third lumen provided within at least a portion of said catheter within which said guide wire will travel.

15. The device in accordance with claim 14 further including a sealing means provided within said distal end of said catheter for preventing contamination or germs inside of said first lumen from coming into contact with bodily fluids.

16. The device in accordance with claim 14 wherein the termination of said distal end is tapered.

17. The device in accordance with claim 1 wherein each of said spokes are equally spaced from one another around said first particular point.

18. A device for treating an occlusion or a constriction in a bodily conduit passageway having an inner surface in the body, comprising:

a flexible, elongated catheter having a distal end and a proximal end, said catheter provided with a first hollow treatment lumen extending within said catheter and provided with an exterior surface;

a dilatation balloon attached to and encircling a portion of said distal end of said catheter;

a centering balloon attached to a portion of said exterior surface of said distal end of said catheter;

a first source for inflating and deflating said dilatation balloon for the purpose of treating the occlusion or constriction; and

a second source for inflating and deflating said centering balloon for the purpose of centering said catheter within the passageway during treatment of the occlusion or constriction, said centering balloon when inflated allowing a significant amount of perfusion of bodily fluids around said centering balloon.

19. The device in accordance with claim 18, wherein said dilatation balloon is provided with a plurality of longitudinally extending lobes whose distance from said exterior surface of said catheter would be relatively constant when said dilatation balloon is inflated.

20. The device in accordance with claim 19, wherein said centering balloon is provided with at least two inflatable thin spokes which would extend from said exterior surface of said catheter to the inner surface of the passageway when said centering balloon is inflated, said spokes encircling said distal end around a first particular point, said centering balloon allowing a significantly greater amount of perfusion of bodily fluids around said spokes than when said centering balloon is deflated and said dilatation balloon is inflated.

21. The device in accordance with claim 20, wherein each of said spokes is equally spaced from one another around said first particular point.

22. The device in accordance with claim 19, wherein said centering balloon is provided with at least two inflatable longitudinal balloons which extend along the exterior surface of said catheter when said centering balloon is inflated, said centering balloon allowing a significantly greater amount of perfusion of bodily fluids around said centering balloon when said centering balloon is deflated and said dilatation balloon is inflated.

23. The device in accordance with claim 18, wherein said centering balloon is provided with at least two inflatable thin spokes which would extend from said exterior surface of said catheter to the inner surface of the passageway when said centering balloon is inflated, said spokes encircling said distal end around a first particular point, said centering balloon allowing a significantly greater amount of perfusion of bodily fluids around said spokes than when said centering balloon is deflated and said dilatation balloon is inflated.

24. The device in accordance with claim 18, wherein said centering balloon is provided with at least two inflatable thin spokes which would extend from said dilatation balloon to the inner surface of the passageway when said centering balloon is inflated, said spokes encircling said distal end around a first particular point, said centering balloon allowing a significantly greater amount of perfusion of bodily fluids around said spokes than when said centering balloon is deflated and said dilatation balloon is inflated.

25. The device in accordance with claim 18, further including a source of radiation maneuvered to the occlusion or constriction through said hollow treatment lumen.

26. The device in accordance with claim 25 further including a flexible member attached to said centering balloon, said flexible membrane abutting the inner surface of the passage-way to ensure a greater flow of bodily fluids past the occlusion or constriction when said centering balloon is inflated.

27. The device in accordance with claim 25 further including a flexible membrane attached to said dilatation balloon, said flexible membrane abutting the inner surface of the passageway to ensure a greater flow of bodily fluids past the occlusion or constriction when said dilatation balloon is inflated.

28. The device in accordance with claim 25 wherein said centering balloon includes at least one additional set of inflatable thin spokes encircling a portion of said outer surface of said catheter, each of said additional sets of inflatable thin spokes encircling said outer surface at a point removed from said first particular point, each of said thin spokes of a particular set of thin spokes symmetrically spaced from one another.

29. The device in accordance with claim 25, further including a second lumen provided with said catheter connected to said dilatation balloon and said first source for inflating and deflating said dilatation balloon.

30. The device in accordance with claim 29, further including a third lumen provided within said catheter connected to said centering balloon and said second source for inflating and deflating said centering balloon.

31. The device in accordance with claim 30 further including a flexible, elongated guide wire maneuvered to the occlusion or constriction and a fourth lumen provided within at least a portion of said catheter within which said guide wire will travel.

32. The device in accordance with claim 31 wherein the termination of said distal end is tapered.

33. The device in accordance with claim 25, wherein said source of radiation is cesium 137, cobalt 60, iodine 125, iodine 131, cobalt 57, iridium 192, gold 198, palladium 103, strontium 89, strontium 90, phosphate 32 or yttrium 90.

34. The device in accordance with claim 18 further including a flexible member attached to said centering balloon, said flexible membrane abutting the inner surface of the passage-way to ensure a greater flow of bodily fluids past the occlusion or constriction when said centering balloon is inflated.

35. The device in accordance with claim 18 further including a flexible membrane attached to said dilatation balloon, said flexible membrane abutting the inner surface of the passageway to ensure a greater flow of bodily fluids past the occlusion or constriction when said dilatation balloon is inflated.

36. The device in accordance with claim 18 wherein said centering balloon includes at least one additional set of inflatable thin spokes encircling a portion of said outer surface of said catheter, each of said additional sets of inflatable thin spokes encircling said outer surface at a point removed from said first particular point, each of said thin spokes of a particular set of thin spokes symmetrically spaced from one another.

37. The device in accordance with claim 18, further including a second lumen provided with said catheter connected to said dilatation balloon and said first source for inflating and deflating said dilatation balloon.

38. The device in accordance with claim 37, further including a third lumen provided within said catheter connected to said centering balloon and said second source for inflating and deflating said centering balloon.

39. The device in accordance with claim 38 further including a flexible, elongated guide wire maneuvered to the occlusion or constriction and a fourth lumen provided within at least a portion of said catheter within which said guide wire will travel.

40. The device in accordance with claim 39 further including a sealing means provided within said distal end of said catheter for preventing contamination or germs inside of said first lumen from coming into contact with bodily fluids.

41. The device in accordance with claim 39 wherein the termination of said distal end is tapered.

42. The device in accordance with claim 18, wherein said centering balloon is provided with at least two inflatable longitudinal balloons which extend along the exterior surface of said catheter when said centering balloon is inflated, said centering balloon allowing a significantly greater amount of perfusion of bodily fluids around said centering balloon when said centering balloon is deflated and said dilatation balloon is inflated.

43. The device in accordance with claim 31 further including a sealing means provided within said distal end of said catheter for preventing contamination or germs of said first lumen from coming into contact with bodily fluids.