Guidewire with perfusion capability

• US 20070129682A1
• Filed: 12/02/2005
• Published: 06/07/2007
• Est. Priority Date: 12/02/2005
• Status: Abandoned Application

• Current Assignee: Boston Scientific Scimed, Inc. (Boston Scientific Corporation)
• Original Assignee: Boston Scientific Scimed, Inc. (Boston Scientific Corporation)
• Inventors: Eidenschink, Tracee
• Application Number:
  US11/292,538
• Publication Number:
  US 20070129682A1
• Time in Patent Office: Days
• US Class Current: 604/164.130
• CPC Class Codes: A61M 2025/0057 Catheters delivering medicament other than through a conventional lumen, e.g. porous walls or hydrogel coatings
• CPC Class Codes: A61M 2025/0058 having an electroactive polymer material, e.g. for steering purposes, for control of flexibility, for locking, for opening or closing
• CPC Class Codes: A61M 2025/0073 Tip designed for influencing the flow or the flow velocity of the fluid, e.g. inserts for twisted or vortex flow
• CPC Class Codes: A61M 2025/09008 having a balloon
• CPC Class Codes: A61M 2025/091 having a lumen for drug delivery or suction
• CPC Class Codes: A61M 25/007 Side holes, e.g. their profiles or arrangements; Provisions to keep side holes unblocked
• CPC Class Codes: A61M 25/09 Guide wires

Abstract

A guidewire is described which includes an elongate member shaped for insertion into a body vessel such that a catheter can be guided over the elongate member and into the body vessel, the elongate member having a perfusion lumen extending therethrough from a proximal end of the elongate member to exit openings included in a distal portion of the elongate member, the distal portion of the elongate member being constructed so that it is has a retracted state that facilitates introduction of the elongate member into and through the body vessel and an expanded state where the area of the exit openings in the distal portion of the elongate member is increased. A method of performing a balloon catheter procedure using the described guidewire, and a system for performing a balloon catheter procedure using the described guidewire are also described.

Claims

1. A guidewire for use with a therapeutic device, the guidewire comprising an elongate member shaped for insertion into a body vessel such that a therapeutic device can be guided over the elongate member and into the body vessel, the elongate member having a perfusion lumen extending therethrough from a fluid entry port to exit openings included in a distal portion of the elongate member, the distal portion of the elongate member being constructed to have a retracted state that facilitates introduction of the elongate member into and through the body vessel and an expanded state where the area of the exit openings in the distal portion of the elongate member is increased.

2. The guidewire of claim 1, wherein the guidewire is used with a balloon catheter, and is sized such that a balloon catheter can be guided over the elongate member.

3. The guidewire of claim 1, wherein the elongate member distal portion includes a plurality of longitudinally extending ribs and expandable mesh material included between each of the ribs, each of the ribs extending for a distance from near the distal tip of the elongate member, wherein the mesh material covers the exit openings.

4. The guidewire of claim 3, wherein the longitudially extending ribs extend generally straight in the retracted state and generally bow outward in the expanded state.

5. The guidewire of claim 3, wherein the longitudinally extending ribs comprise bending rods which extend generally straight in the retracted state and generally bow outward in the expanded state.

6. The guidewire of claim 4, further comprising a elongate structure attached to the elongate member distal tip, wherein pulling the elongate structure proximally causes a distal end of the elongate member distal portion to be pulled nearer to a proximal end of the elongate member distal portion, which causes the longitudinally extending ribs to bow outwardly.

7. The guidewire of claim 6, wherein the elongate structure extends proximally from an attachment point at the elongate member distal tip, within the elongate member perfusion lumen, and out of the perfusion lumen near the elongate member proximal end.

8. The guidewire of claim 3, wherein the longitudinally extending ribs are formed from a composition comprising a shape memory material.

9. The guidewire of claim 3, wherein the expandable mesh material is formed from a composition comprising a shape memory material.

10. The guidewire of claim 9, wherein the shape memory material comprises nitinol.

11. The guidewire of claim 9, wherein the shape memory material comprises polycyclooctane.

12. The guidewire of claim 1, wherein the outer diameter of the elongated member distal portion in a retracted state has a diameter that is less than about 0.02 inches more than the diameter of the elongated member at the longitudinal midpoint between the proximal end and the distal end of the elongated member.

13. The guidewire of claim 1, wherein the outer diameter of the elongated member distal portion in a retracted state has a diameter that is less than about 0.01 inches more than the diameter of the elongated member at the longitudinal midpoint between the proximal end and the distal end of the elongated member.

14. The guidewire of claim 1, wherein the outer diameter of the midpoint of a perfusion section located at the elongated member distal portion in an expanded state has a diameter that is at least about twice the diameter of the same point when the elongated member distal portion is in a retracted state.

15. The guidewire of claim 1, wherein the perfusion lumen has a diameter large enough to allow a cooled fluid to flow therethrough under pressure.

16. The guidewire of claim 1, wherein a distal portion of the elongate member expands upon application of internal fluid pressure from fluid in the perfusion lumen.

17. The guidewire of claim 1, wherein a distal portion of the elongate member expands upon the application of a cooled fluid to the distal portion of the elongate member from the perfusion lumen.

18. The guidewire of claim 1, wherein a distal portion of the elongate member expands following a rotational force applied to the elongate member.

19. The guidewire of claim 1, wherein the outer diameter of any portion of the unexpanded guidewire is equal to or less than 0.035 inches.

20. The guidewire of claim 1, wherein the outer diameter of any portion of the unexpanded guidewire is equal to or less than 0.014 inches.

21. A method of performing a balloon catheter procedure, the method comprising:

introducing a guidewire into a body vessel, the guidewire comprising an elongate member having a perfusion lumen extending therethrough from a proximal end of the elongate member to exit openings included in a distal portion of the elongate member, the introduction of the guidewire being performed while the elongate member distal portion is in a retracted state that facilitates introduction of the elongate member into and through the body vessel;

introducing an expandable balloon catheter over the guidewire and into the body vessel; and

perfusing fluid through the guidewire perfusion lumen and out of the exit openings while the balloon catheter is expanded and while the elongate member distal portion is in an expanded state where the area of the exit openings in the distal portion of the elongate member is increased.

22. The method of claim 21, further comprising perfusing fluid through the guidewire perfusion lumen and out of the exit openings after the balloon catheter has been expanded and deflated and while the elongate member distal portion is in an expanded state.

23. The method of claim 21, further comprising perfusing fluid through the guidewire perfusion lumen and out of the exit openings before the balloon catheter is expanded and while the elongate member distal portion is in an expanded state.

24. The method of claim 21, wherein the fluid comprises a cooled fluid.

25. The method of claim 24, wherein the fluid comprises cooled blood.

26. The method of claim 21, wherein the fluid comprises an effective amount of a drug.

27. The method of claim 21, wherein the method is performed as part of a percutaneous transluminal coronary angioplasty procedure.

28. A system for performing a balloon catheter procedure, the system comprising:

a guidewire comprising an elongate member shaped for insertion into a body vessel such that a balloon catheter can be guided over the elongate member and into the body vessel, the elongate member having a perfusion lumen extending therethrough from a proximal end of the elongate member to exit openings included in a distal portion of the elongate member, the distal portion of the elongate member being constructed so that it is has a retracted state that facilitates introduction of the elongate member into and through the body vessel and an expanded state where the area of the exit openings in the distal portion of the elongate member is increased;

an expandable balloon catheter; and

a control system than controls the perfusion of fluid through the guidewire perfusion lumen and out of the exit openings in the distal portion of the elongate member.

29. The system of claim 28 further comprising a control system that controls the inflation and deflation of the expandable balloon.

30. The system of claim 28, wherein the control system controls an amount of cooled fluid that the guidewire provides to the target region, so as to cool and maintain the target region within a target temperature range below normal body temperature for an extended period of time.