Catheters with non-removable guide members useable for treatment of sinusitis

• US 8,951,225 B2
• Filed: 05/18/2006
• Issued: 02/10/2015
• Est. Priority Date: 06/10/2005
• Status: Active Grant

• Current Assignee: Acclarent Incorporated (Johnson & Johnson)
• Original Assignee: Acclarent Incorporated (Johnson & Johnson)
• Inventors: Evard, Philip, Muni, Ketan P., Morriss, John, Chang, John
• Primary Examiner(s): MENDEZ, MANUEL A
• Application Number:
  US11/438,090
• Publication Number:
  US 20070208301A1
• Time in Patent Office: 3,190 Days
• Field of Search: 604/96.01, 604/101.01, 60410102-10202, 604/508, 604/514, 604/915, 604/919, 606191-194
• US Class Current: 604/96.01
• CPC Class Codes: A61B 17/24 for use in the oral cavity, larynx, bronchial passages or nose for medical inspection of cavities or tubes in the body A61B1/00; Tongue scrapers
• CPC Class Codes: A61M 2025/1075 having a balloon composed of several layers, e.g. by coating or embedding
• CPC Class Codes: A61M 2025/1079 having radio-opaque markers in the region of the balloon
• CPC Class Codes: A61M 2025/1093 having particular tip characteristics
• CPC Class Codes: A61M 2029/025 characterised by the guiding element
• CPC Class Codes: A61M 2210/0618 Nose
• CPC Class Codes: A61M 2210/0681 Sinus (maxillaris)
• CPC Class Codes: A61M 25/10 Balloon catheters A61M25/0125 takes precedence; embolectomy A61B17/22032; retractors A61B17/02; inflatable balloons for placing stents or stent-grafts A61F2/958 ; stomach balloons for treatment of obesity A61F5/0003; oesophagal tubes A61J15/00
• CPC Class Codes: A61M 29/02 Dilators made of swellable material balloon catheters for angioplasty A61M25/104

Abstract

Balloon catheter, guide catheter and method for dilating openings in paranasal sinuses. A non-removable guide member (e.g., guidewire) extends from the distal end of the balloon catheter. The non-removable guide member initially passes through the opening of the paranasal sinus and is followed by the catheter body on which the balloon is mounted. The balloon is then inflated causing dilation of the opening of the paranasal sinus. In some embodiments, the non-removable guide member may be shapeable so that the operator may place the non-removable guide member in a desired shape prior to insertion of the balloon catheter. In some embodiments, the length of the non-removable guide member may be adjustable such that the operator may adjust the length of the non-removable guide member prior to insertion of the balloon catheter.

Claims

1. A balloon catheter device for dilating an opening of a paranasal sinus in a human or animal subject, said balloon catheter device comprising:

a catheter shaft having a proximal end and a distal end; and

a non-compliant or semi-compliant balloon mounted on the catheter shaft, said balloon being positionable within the opening of the paranasal sinus while in a non-inflated state and thereafter inflatable to an inflated state such that it will cause dilation of the opening of the paranasal sinus;

at least one position indicating element useable to determine when the balloon is positioned within the opening of the paranasal sinus; and

non-removable guide member, at least a portion of which extends from the distal end of the catheter shaft, said non-removable guide member having a limited range of axial movement or no movement relative to the catheter shaft, said non-removable guide member being advanceable through the opening of the paranasal sinus ahead of the catheter shaft, at least a distal portion of said non-removable guide member being more flexible in one plane than another;

wherein the balloon catheter device has a length less than about 20 cm.

2. A catheter device according to claim 1 wherein the non-removable guide member has at least two regions of differing stiffness.

3. A catheter device according to claim 1 wherein a proximal portion of the non-removable guide member resides within the catheter shaft and a distal portion of the guide member extends beyond the distal end of the catheter shaft.

4. A catheter device according to claim 3 wherein the proximal portion of the non-removable guide member extends through the entire length of the catheter shaft.

5. A catheter device according to claim 4 further comprising a hub on the proximal end of the catheter shaft, wherein the proximal portion of the non-removable guide member extends into and is anchored within said hub.

6. A catheter device according to claim 5 wherein the hub comprises a port that is in communication with the balloon to facilitate passage of inflation fluid into and out of the balloon.

7. A catheter device according to claim 6 wherein the hub comprises a fluid infusion port and wherein the crimpable element is crimped in a manner that allows fluid to flow past the location of the crimp.

8. A catheter device according to claim 5 wherein a portion of the hub includes a crimpable element which is crimped so as to engage and hold the proximal portion of the non-removable guide member within the hub.

9. A catheter device according to claim 1 wherein the at least one position indicating element comprises at least one marker on the catheter shaft, said marker being directly or endoscopically visible to the operator when the balloon is positioned within the opening of the paranasal sinus.

10. A catheter device according to claim 1 wherein the at least one position indicating element comprises at least one radiographically visible marker disposed on the non-removable guide member.

11. A catheter device according to claim 10 wherein the non-removable guide member extends through the region of the catheter shaft where the balloon is mounted and wherein radiographic markers are provided on the non-removable guide member to mark the location of the balloon.

12. A catheter device according to claim 11 wherein the balloon has a working length and the non-removable guide member comprises first and second radiographic markers, one of which is at one end of the balloon'"'"'s working length and the other of which is at the other end of the balloon'"'"'s working length.

13. A catheter device according to claim 1 wherein the at least one radiographically visible marker comprises a first marker marking the distal end of a working length of the balloon and a second marker marking the proximal end of the working length of the balloon.

14. A catheter device according to claim 1 wherein the balloon is substantially formed of a material selected from the group consisting of:

polyethylene terephthalateterephthalate, nylon and polyamide.

15. A catheter device according to claim 1 wherein the balloon is capable of withstanding pressures of more than 22 atmospheres without bursting.

16. A catheter device according to claim 1 or 15 wherein the balloon is capable of breaking bone located around the opening of the paranasal sinus.

17. A catheter device according to claim 16 wherein the balloon is coated with a polymer coating.

18. A catheter device according to claim 16 wherein the coating is dip applied.

19. A catheter device according to claim 1 wherein the balloon is formed substantially of polyethylene terephthalate that is about 0.002 inch thick having a polyurethane coating disposed thereon, said coating being about 0.002 inch thick.

20. A catheter according to claim 1 wherein the balloon is formed substantially of polyethylene terephthalate that is about 0.002 inch thick having a polyurethane coating disposed thereon, said coating being about 0.002 inch thick.

21. A catheter according to claim 1 having a length of less than about 15 cm.

22. A catheter according to claim 1 having a length of less than about 10 cm.

23. A catheter device according to claim 1 wherein the non-removable guide member is formed substantially of a material selected from the group consisting of nickel-titanium alloy and stainless steel.

24. A catheter device according to claim 1 wherein a region of the non-removable guide member adjacent to its distal end comprises a segment of flattened core wire surrounded by a helical wire coil.

25. A catheter device according to claim 24 wherein the segment of flattened core wire has a height of from about 0.001 inch to about 0.004 inch.

26. A catheter device according to claim 1 wherein the non-removable guide member comprises a wire core having a proximal portion, a middle portion and a distal portion, said proximal portion being of substantially uniform diameter, said middle portion that is smaller in diameter at its distal end than at its proximal end and a distal portion of substantially uniform diameter.

27. A catheter device according to claim 26 wherein the proximal portion of the core wire has a diameter of 0.025 +/−

0.0005 inch.

28. A catheter device according to claim 26 wherein the distal portion of the core wire is flattened.

29. A catheter device according to claim 26 or 28 wherein a helical wire coil surrounds the distal portion and at least some of the middle portion of the core wire.

30. A catheter device according to claim 29 wherein the helical wire coil has an outer diameter of from about 0.014 inch to about 0.038 inch.

31. A catheter device according to claim 28 wherein the flattened distal portion of the core wire has a flattened thickness of 0.001 to 0.006 inches.

32. A catheter device according to claim 1 wherein the non-removable guide member has a substantially radiolucent proximal region, a radiopaque middle region and a substantially radiolucent distal region.

33. A catheter device according to claim 32 wherein said at least one position indicating element comprises the radiopaque middle region of the non-removable guide member.

34. A catheter device according to claim 33 wherein the balloon has a working length and the position of the radiopaque middle region is coterminus with the working length of the balloon.

35. A catheter device according to claim 1 wherein at least a portion of the non-removable guide member extending beyond the distal end of the catheter shaft may be trimmed.

36. A catheter device according to claim 1 wherein the non-removable guide member is secured to the catheter device by adhesive.

37. A catheter device according to claim 1 wherein an outer polymer covering is disposed on at least a portion of the catheter device.

38. A catheter device according to claim 37 wherein the outer covering comprises heat-shrinkable material.

39. A catheter device according to claim 38 wherein the heat shrinkable material comprises polyether block amide.

40. A catheter device according to claim 1 wherein the balloon has a working length of about 12 to about 24 mm.

41. A system comprising a balloon catheter device according to claim 1 in combination with a guide catheter having a lumen through which the balloon catheter device is insertable.

42. A system according to claim 41 wherein the guide catheter has a substantially non-removable shape.

43. A system according to claim 42 wherein the guide catheter has a curve of between 0 degrees to about 135 degrees.

44. A system according to claim 42 further comprising a tubular outer cover having a distal end.

45. A system according to claim 44 wherein the outer cover extends beyond the distal end of the metal tube but terminates short of the distal end of the plastic tube.

46. A system according to claim 45 wherein the outer cover has a distal end that is tapered so as to provide a smooth transition from the outer surface of the plastic tube.

47. A system according to claim 42 or 44 further comprising an inner liner lining the lumen of the plastic tube.

48. A system according to claim 47 wherein a radiopaque marker is captured between the inner liner and the plastic tube.

49. A system according to claim 48 wherein the distal end of the plastic tube stops short of the distal end of the inner liner such that a distal portion of the inner liner protrudes beyond the distal end of the plastic tube, and wherein an atraumatic tip member formed of material that is softer than the plastic tube is disposed about the distal portion of the inner liner.

50. A system according to claim 41 wherein the guide catheter comprises a metal tube having a lumen and a distal end and a plastic tube having a lumen and a distal end, said plastic tube extending coaxially through the lumen of the metal tube with a distal portion of the plastic tube extending out of and beyond the distal end of the metal tube.

51. A system according to claim 50 wherein the distal portion of the plastic tube is curved.

52. A catheter device according to claim 1 wherein the distal portion of the non-removable guide member that extends beyond the end of the catheter shaft is an atraumatic tip.

53. A catheter device according to claim 1 wherein at least a portion of the non-removable guide member is coated.

54. A catheter device according to claim 1 wherein the balloon is coated with a polymer coating and at least a portion of the non-removable guide member is coated with a different coating.

55. A catheter device according to claim 1 wherein the catheter shaft is flexible.

56. A catheter device according to claim 1 wherein the catheter shaft is formed of plastic.

57. A catheter device according to claim 1 wherein the catheter shaft is formed of metal.

58. A catheter device according to claim 57 wherein the catheter shaft is formed of metal hypotube.

59. A catheter device according to claim 57 wherein the catheter shaft is formed of straight metal tube.

60. A catheter device according to claim 57 wherein the catheter shaft is formed of curved metal tube.