Methods and systems for bypassing an occlusion in a blood vessel

• US 8,241,311 B2
• Filed: 12/15/2009
• Issued: 08/14/2012
• Est. Priority Date: 12/15/2009
• Status: Active Grant

• Current Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Original Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Inventors: Ward, Sean, Sweeney, Fiachra
• Primary Examiner(s): Houston, Elizabeth
• Assistant Examiner(s): WEBB, SARAH K
• Application Number:
  US12/637,859
• Publication Number:
  US 20110144677A1
• Time in Patent Office: 973 Days
• Field of Search: 606/108, 606/159, 606/185, 606/191, 606/194, 604/164.01, 604/164.04, 604/164.06, 604/164.09, 604/164.1, 604/164.13
• US Class Current: 606/159
• CPC Class Codes: A61B 17/320783 through side-hole, e.g. sliding or rotating cutter inside catheter
• CPC Class Codes: A61B 2017/00292 mounted on or guided by flexible, e.g. catheter-like, means
• CPC Class Codes: A61B 2017/22044 with a pointed tip
• CPC Class Codes: A61B 2017/22077 with a part piercing the tissue A61B2017/22044 takes precedence
• CPC Class Codes: A61B 2017/22095 accessing a blood vessel true lumen from the sub-intimal space

Abstract

Methods and systems for re-entering the true lumen of a vessel after subintimally bypassing an occlusion in a blood vessel. A guidewire is positionable within a subintimal tract in a wall of the blood vessel with a distal end located beyond the occlusion. A hollow lumen of the guidewire includes a retractable blade slidably exposable adjacent a distal end thereof for rotary cutting or scoring the intima layer of the vessel wall to create a transverse cut or line of weakness in the intima. A balloon catheter is subsequently trackable over the guidewire and once inflated tears or otherwise ruptures the transverse cut, thereby creating or enlarging a passageway into the true lumen of the blood vessel beyond the occlusion.

Claims

1. A method for bypassing an occlusion in a blood vessel having a wall and a subintimal tract that has been formed in the wall adjacent to the occlusion, said method comprising the steps of:

transluminally advancing a subintimal reentry guidewire through the subintimal tract from a near side of the occlusion to a position where a distal end of the subintimal reentry guidewire is positioned in the subintimal tract on a far side of the occlusion;

extending a planar, generally triangular cutting blade transversely from a distal side port of the subintimal reentry guidewire to extend beyond an outer surface of the subintimal reentry guidewire;

rotating the subintimal reentry guidewire with the cutting blade exposed to create a transverse cut in an intimal layer of the vessel wall on the far side of the occlusion;

retracting the cutting blade proximally into the distal side port of the subintinial reentry guidewire;

Advancing substantially an entire balloon over the subintimal reentry guidewire to the far side of the occlusion and adjacent the transverse cut in the intimal layer of the vessel wall; and

inflating the balloon to enlarge the transverse cut in the intimal layer of the vessel wall thereby creating a passageway through the intimal layer.

2. The method of claim 1, wherein the transverse cut extends partially through the intimal layer of the wall.

3. The method of claim 1, wherein the transverse cut extends fully through the intimal layer of the wall.

4. The method of claim 1, wherein the step of rotating includes rotating the subintimal reentry guidewire approximately 360 degrees.

5. The method of claim 1, wherein the step of rotating includes rotating the subintimal reentry guidewire between 120 and 180 degrees.

6. The method of claim 1, further comprising the steps of:

following the creation of the passageway through the intimal layer, advancing the subintimal reentry guidewire through the passageway to a position where the distal end of the subintimal reentry guidewire is positioned in a true lumen of the blood vessel on the far side of the occlusion;

tracking a stent delivery catheter with a stent mounted thereon over the subintimal reentry guidewire until the stent extends from the true lumen on the near side of the occlusion through the subintimal tract and passageway and into the true lumen on the far side of the occlusion;

deploying and radially expanding the stent; and

,

removing the stent delivery catheter and leaving the stent in place, such that fluid may flow from the true lumen of the blood vessel on one side of the occlusion through the stent and into the true lumen of the blood vessel on the other side of the occlusion.

7. The method of claim 1, wherein the blood vessel is an artery located in the leg of a human subject.

8. The method of claim 1, wherein the blood vessel is a coronary artery.

9. The method of claim 1, wherein the occlusion is a chronic total occlusion located in an artery.

10. The method of claim 1, wherein an outer diameter of the guidewire is no greater than 0.014 inches.

11. The method of claim 1, wherein the cutting blade is located at a distal end of a core element and the step of exposing the cutting blade includes distally advancing the core element within a lumen of the subintimal reentry guidewire and locking the core element into place relative to the subintimal reentry guidewire after the cutting blade extends out of the lumen of the subintimal reentry guidewire.

12. The method of claim 11, wherein distally advancing the core element includes pushing the cutting blade against an inclined surface formed within the subintimal reentry guidewire that guides the cutting blade to an angled configuration when the cutting blade is exposed.

13. The method of claim 11, wherein the cutting blade is formed of a biocompatible resilient material.