Steerable device having a corewire within a tube and combination with a functional medical component

• US 8,092,483 B2
• Filed: 03/04/2005
• Issued: 01/10/2012
• Est. Priority Date: 03/06/2004
• Status: Active Grant

• Current Assignee: Medtronic Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Incorporated (Medtronic Plc)
• Inventors: Galdonik, Jason A., Ogle, Matthew F., Pokorney, James, Ganesan, Kavitha, Wlodarski, Grace
• Primary Examiner(s): Lucchesi, Nicholas
• Assistant Examiner(s): PATEL, PRITESH ASHOK
• Application Number:
  US11/072,001
• Publication Number:
  US 20060200047A1
• Time in Patent Office: 2,503 Days
• Field of Search: 138/39, 604/73
• US Class Current: 606/200
• CPC Class Codes: A61M 25/0054 with regions for increasing flexibility
• CPC Class Codes: A61M 25/0133 Tip steering devices
• CPC Class Codes: A61M 25/0138 having flexible regions as a result of weakened outer material, e.g. slots, slits, cuts, joints or coils

Abstract

An integrated guiding device has a tube and a corewire within the tube and a torque coupler. The torque coupler can couple the rotational motion of the tube with the rotational motion of the corewire. The wire can be moved longitudinally at least some amount relative to the tube. The device can further comprise a functional medical structure, such as an embolism protection structure. The device can be used in medical procedures, such as less invasive procedures within the cardiovascular system. Improved fiber based embolism protection devices comprise fiber bundles that are twisted prior to delivery.

Claims

1. A method for using a filter element attached to a guide structure within a vessel of a patient, the method comprising:

inserting the filter element into the vessel wherein the guide structure comprises a corewire and a tube with an inner lumen over at least substantial length of the corewire, the filter element comprises a plurality of polymer fibers in a bundle comprising a first end constrained to the corewire and a second end constrained to the tube;

deploying the filter element by moving the corewire relative to the tube to transition the filter element from a low profile configuration to an extended configuration that extends outward from the axis of the guide structure relative to the low profile configuration to form a three dimensional filtration matrix following insertion of the filter element;

delivering a distinct treatment device into the vessel over the guide structure;

performing a treatment procedure within the vessel using the distinct treatment device after the filter element is deployed to the three dimensional filtration matrix and prior to the application of suction;

transitioning the filter element from the extended configuration to a removal configuration by changing the relative positions of the corewire and the tube; and

applying suction during at least a portion of the process of transitioning of the filter element to the removal configuration through an aspiration catheter that is loaded over the guide structure.

2. The method of claim 1 wherein the removal of the filter element comprises withdrawing the filter element at least part way into an aspiration catheter.

3. The method of claim 2 wherein suction is applied during the transition of the filter element from the extended configuration to a removal configuration and during withdrawal of the filter element at least part way into the aspiration catheter.

4. The method of claim 1 wherein the filter element is inserted to capture emboli generated during an anastomosis procedure.

5. The method of claim 1 wherein the filter element is inserted to capture emboli generated during a carotid endarterectomy.

6. The method of claim 1 wherein the treatment procedure comprises the delivery of a stent.

7. The method of claim 1 wherein the treatment procedure comprises the deployment of a balloon.

8. The method of claim 1 wherein the distinct treatment device is delivered over the guide structure.

9. The method of claim 1 wherein the guide structure comprises a coil connected around a core wire distal end distal to the filter element.

10. The method of claim 1 wherein the corewire is solid.

11. The method of claim 1 wherein the aspiration catheter is loaded over the guide structure in a rapid exchange configuration.

12. The method of claim 1 wherein the fibers are surface capillary fibers.

13. The method of claim 1 wherein the fibers are twisted within the fiber bundle for at least 5 degrees.

14. The method of claim 1 wherein the distal half of the tube comprises a plurality of slots oriented transverse to the axis of the tube.

15. The method of claim 14 wherein the slots penetrate through the tube to the inner lumen.

16. The method of claim 1 wherein the tube comprises a key way within the lumen having a surface with an asymmetrical cross section and the corewire comprises a key having a surface with an asymmetrical cross section complimentary to the asymmetrical cross section of the key way surface.

17. The method of claim 1 wherein the guide structure further comprises a backend tool that controls the relative position of the corewire relative to the tube over a range of motion.

18. The method of claim 17 wherein the corewire within the tube has at least one stable position effectively locking the relative position between the end points of the range of motion.

19. The method of claim 1 wherein the corewire has a bend that provides friction against the tube wherein the friction provides the effective locking of the corewire.

20. The method of claim 1 wherein the guide structure has a length of no more than about 100 centimeters.

21. The method of claim 1 wherein the suction is applied with a syringe that is attached at a port of the aspiration catheter.

22. The method of claim 1 wherein a cannula having a central lumen and a pointed tip is mounted over the guide structure to facilitate insertion of the filter element and guide structure into the patient'"'"'s vessel.

23. The method of claim 22 wherein the cannula has a slit to provide for placement and removal from a position with the guide structure within the central lumen of the cannula.

24. The method of claim 22 wherein the cannula has a range of adjustable outer diameters less than the inner diameter of the aspiration catheter.