Composite elongate medical device including distal tubular member

• US 8,409,114 B2
• Filed: 08/02/2007
• Issued: 04/02/2013
• Est. Priority Date: 08/02/2007
• Status: Active Grant

• Current Assignee: Boston Scientific Scimed, Inc. (Boston Scientific Corporation)
• Original Assignee: Boston Scientific Scimed, Inc. (Boston Scientific Corporation)
• Inventors: Parins, David J.
• Primary Examiner(s): DOUGHERTY, SEAN PATRICK
• Application Number:
  US11/833,117
• Publication Number:
  US 20090036833A1
• Time in Patent Office: 2,070 Days
• Field of Search: 600/585, 604/525, 604/164.13
• US Class Current: 600/585
• CPC Class Codes: A61M 2025/09175 having specific characteristics at the distal tip
• CPC Class Codes: A61M 25/00 Catheters; Hollow probes dilators A61M29/00; peritoneal catheters A61M1/285; tracheal tubes A61M16/04; for drainage A61M27/00; for uterus, vagina or rectum A61M31/00 ; for measuring or testing A61B; materials for catheters A61L29/00
• CPC Class Codes: A61M 25/09 Guide wires

Abstract

An intracorporeal device includes a shaft having a proximal section including a first elongate member and a distal section including a tubular member and a second elongate member. A proximal region of the tubular member is attached to the distal region of the first elongate member. The second elongate member is disposed within the lumen of the tubular member, and a proximal region of the second elongate member is attached to the proximal region of the elongate tubular member. As such, in some embodiments, the tubular member can function both as a member joining the first and second elongate members, and as a structural element in the distal section of the shaft providing for desired flexibility, torqueability, and/or pushability characteristics.

Claims

1. An intracorporeal medical device comprising:

a first elongate member having a proximal region, a distal region and a distal end;

wherein the proximal region of the first elongate member has a circular cross section defining an outer diameter;

an elongate tubular member comprising a metallic material and defining a lumen there through, the tubular member having a proximal region, a proximal end, a distal region, and a distal end, the proximal region of the tubular member attached to the distal region of the first elongate member at a first attachment region, the tubular member extending in a distal direction away from the first elongate member from the proximal end of the tubular member to the distal end of the tubular member;

wherein the elongate tubular member has a circular cross section defining an outer diameter;

wherein the outer diameter of the elongate tubular member is the same length as the outer diameter of the first elongate member; and

a second elongate member having a proximal region, a proximal end, a distal region, and a distal end, the second elongate member disposed within the lumen of the tubular member, an outer surface of the proximal region of the second elongate member attached to an inner surface of the proximal region of the elongate metallic tubular member at a second attachment region.

2. The intracorporeal device according to claim 1, wherein the first elongate member and the second elongate member are not directly attached to one another.

3. The intracorporeal device according to claim 1, wherein a distal end of the first elongate member is attached to the tubular member.

4. The intracorporeal device according to claim 1, wherein a proximal end of the tubular member is attached to the first elongate member.

5. The intracorporeal medical device according to claim 1, wherein the tubular member extends distally such that at least a portion of the distal region of the tubular member is disposed adjacent to or distally of the distal region of the second elongate member.

6. The intracorporeal medical device according to claim 1, wherein the distal end of the tubular member is disposed adjacent to or distally of the distal end of the second elongate member.

7. The intracorporeal medical device according to claim 1, wherein the tubular member has a length, and the second elongate member extends within the lumen of the tubular member along at least about 50% of the length thereof.

8. The intracorporeal medical device according to claim 1, further including a distal tip, and wherein the tubular member extends distally to a point adjacent the distal tip and is attached to the distal tip.

9. The intracorporeal medical device according to claim 1, further including a distal tip, and wherein the second elongate member extends distally to a point adjacent the distal tip and is attached to the distal tip.

10. The intracorporeal device according to claim 1, wherein a distal end of the first elongate member extends into the lumen of the tubular member.

11. The intracorporeal device according to claim 1, wherein at least a portion of the distal region of the first elongate member is tapered.

12. The intracorporeal device according to claim 1, wherein at least a portion of the proximal region of the tubular member is tapered.

13. The intracorporeal device according to claim 1, wherein the first elongate member has a solid cross-section and the second elongate member has a solid cross-section.

14. The intracorporeal device according to claim 1, wherein the first elongate member comprises a first metallic material and the second elongate member comprises a second metallic material different from the first metallic material.

15. The intracorporeal device according to claim 1, wherein the second elongate member comprises a nickel titanium alloy.

16. The intracorporeal device according to claim 1, wherein the tubular member comprises a nickel titanium alloy.

17. The intracorporeal device according to claim 1, wherein the tubular member comprises a tubular wall defining a plurality of cuts or slots formed therein.

18. The intracorporeal device according to claim 17, wherein the tubular member extends along a longitudinal axis, and the cuts or slots include a length extending about the longitudinal axis, and the length of the cuts or slots is oriented substantially perpendicular to the longitudinal axis.

19. The intracorporeal device according to claim 17, wherein the cuts or slots are formed in groups of two defined at generally corresponding points along the length of the tubular member, and wherein the two cuts or slots within each group are located on opposite sides of the tubular member.

20. The intracorporeal device according to claim 19, wherein each of the groups of cuts or slots is disposed at a 90 degree rotation around the axis with respect to the adjacent groups.

21. The intracorporeal device according to claim 17, wherein the cuts or slots have a density and wherein the density of cuts or slots per unit length of the tubular member increases in the distal direction along the tubular member.

22. The intracorporeal device according to claim 17, wherein the cuts or slots have a depth and wherein the depth or size of the cuts or slots increases in the distal direction along the tubular member.

23. The intracorporeal device according to claim 1, wherein a proximal end of the second elongate member is spaced from the distal end of the first elongate member.

24. The intracorporeal device according to claim 1, wherein a proximal end of the second elongate member is in contact with a distal end of the first elongate member.

25. The intracorporeal device according to claim 1, wherein the second elongate member includes a taper.

26. A medical guidewire comprising:

an elongated proximal core member including a proximal region and a distal region;

an elongated tubular member comprising a metallic material and defining a lumen there through and having a distal end, a distal region and a proximal region, the proximal region of the tubular member being connected to the distal region of the proximal core member at a first attachment region such that the tubular member extends in a distal direction away from the distal region of first elongate member from the proximal region of the tubular member toward distal region of the tubular member;

wherein the proximal core member has a circular cross section defining an outer diameter;

wherein the elongate tubular member has a circular cross section defining an outer diameter;

wherein the outer diameter of the proximal core member is the same length as the outer diameter of the elongate tubular member;

an elongated distal core member having a distal end, a proximal region and a distal region, the distal core member disposed within and extending along at least a portion of the lumen of the elongated metallic tubular member, and an outer surface of the proximal region of the distal core member connected to an inner surface of the proximal region of the tubular member at a second attachment region; and

wherein the distal end of the elongated tubular member and the distal end of the elongated distal core member are longitudinally aligned.

27. The medical guidewire according to claim 26, wherein the proximal core member and the distal core member are not directly attached to one another.

28. The medical guidewire according to claim 26, further including a distal tip, and wherein the tubular member extends distally to a point adjacent the distal tip and is attached to the distal tip.

29. The medical guidewire according to claim 26, wherein the proximal core member comprises a metallic material, the tubular member comprises a nickel titanium alloy, and the distal core member comprises a nickel-titanium alloy.

30. The medical guidewire according to claim 26, wherein the tubular member comprises a tubular wall defining a plurality of cuts or slots formed therein.

31. The medical guidewire according to claim 26, wherein the distal core member includes a proximal end, and the proximal core member includes a distal end, and the proximal end of the distal core member is spaced from the distal end of the proximal core member.

32. The medical guidewire according to claim 26, wherein a proximal end of the distal core member is in contact with a distal end of the proximal core member.

33. A method of manufacturing an intracorporeal medical device, the method comprising:

providing a first elongate member having a proximal region, a distal region and a distal end;

wherein the proximal region of the first elongate member has a circular cross section defining an outer diameter;

providing an elongate tubular member comprising a metallic material and defining a lumen there through, the tubular member having a proximal region, a proximal end, a distal region, and a distal end;

wherein the elongate tubular member has a circular cross section defining an outer diameter;

wherein the outer diameter of the elongate tubular member is the same length as the outer diameter of the proximal region of the first elongate member;

providing a second elongate member having a proximal region, a proximal end, a distal region, and a distal end;

disposing the second elongate member within the lumen of the tubular member;

attaching an outer surface of the proximal region of the second elongate member to an inner surface of the proximal region of the elongate metallic tubular member; and

attaching the proximal region of the tubular member to the distal region of the first elongate member such that the tubular member extends in a distal direction away from the distal region of the first elongate member from the proximal region of the tubular member toward distal region of the tubular member.

34. The method according to claim 33, wherein the proximal region of the second elongate member is attached to the proximal region of the elongate metallic tubular member by welding, soldering, adhesive bonding, or mechanical interlocking.

35. The method according to claim 33, wherein the proximal region of the tubular member is attached to the distal region of the first elongate member by welding, soldering, adhesive bonding, or mechanical interlocking.

36. The method according to claim 33, further comprising providing a distal tip, and attaching the distal tip to the tubular member.

37. The method according to claim 33, further comprising providing a distal tip, and attaching the distal tip to the second elongate member.

38. The method according to claim 33, wherein the intracorporeal medical device comprises a guidewire, the first elongate member comprises a proximal core member, the second elongate member comprises a distal core member, and the elongate tubular member comprising a structure that interconnects the distal region of the proximal core member and the proximal region of the distal core member, and also extends distally about the distal region of the distal core member.