Apparatus and method for deploying an implantable device within the body

• US 8,287,583 B2
• Filed: 09/30/2005
• Issued: 10/16/2012
• Est. Priority Date: 01/10/2005
• Status: Active Grant

• Current Assignee: Taheri Laduca LLC
• Original Assignee: Taheri Laduca LLC
• Inventors: LaDuca, Robert, LaDuca, Paul
• Primary Examiner(s): Jackson, Gary
• Assistant Examiner(s): BACHMAN, LINDSEY MICHELE
• Application Number:
  US11/241,242
• Publication Number:
  US 20060155363A1
• Time in Patent Office: 2,573 Days
• Field of Search: 623/1.11, 623/1.23, 623/1.35, 623/1.12, 606/108, 606/194
• US Class Current: 623/1.11
• CPC Class Codes: A61F 2/06 Blood vessels
• CPC Class Codes: A61F 2/2418 Scaffolds therefor, e.g. support stents
• CPC Class Codes: A61F 2/844 folded prior to deployment
• CPC Class Codes: A61F 2/856 Single tubular stent with a side portal passage
• CPC Class Codes: A61F 2/90 characterised by a net-like or mesh-like structure
• CPC Class Codes: A61F 2/95 Instruments specially adapted for placement or removal of stents or stent-grafts
• CPC Class Codes: A61F 2/9517 handle assemblies therefor
• CPC Class Codes: A61F 2/954 for placing stents or stent-grafts in a bifurcation
• CPC Class Codes: A61F 2002/075 the stent being loosely attached to the graft material, e.g. by stitching
• CPC Class Codes: A61F 2002/9511 the retaining means being filaments or wires
• CPC Class Codes: A61F 2220/0008 Fixation appliances for connecting prostheses to the body
• CPC Class Codes: A61F 2220/0016 with sharp anchoring protrusions, e.g. barbs, pins, spikes
• CPC Class Codes: A61F 2220/0041 using additional screws, bolts, dowels or rivets, e.g. connecting screws
• CPC Class Codes: A61F 2220/0066 stapled
• CPC Class Codes: A61F 2220/0075 sutured, ligatured or stitched, retained or tied with a rope, string, thread, wire or cable
• CPC Class Codes: A61F 2250/0039 differing in diameter

Abstract

The present invention provides devices and methods for fabricating and deploying an implantable device within the body. The invention is particularly suitable for delivering and deploying a stent, graft or stent graft device within a vessel or tubular structure within the body, particularly where the implant site involves two or more interconnecting vessels. The delivery and deployment system utilizes a plurality of strings which are releasably attached to the luminal ends of the implantable device.

Claims

1. A method of implanting a device having a main lumen and at least one side-branch lumen extending therefrom to a target location within a vessel or tubular structure within the body having a main vessel and at least one side branch vessel in fluid communication with the main vessel, the method comprising:

creating first and second incisions within the body;

advancing a first member through the vasculature from the first incision to the second incision until a first end of the member is exposed from the second incision;

tethering the first member to a first end of a catheter;

retracting the first member from the first incision until the first end of the catheter is positioned at the target location;

advancing the device with the catheter, where the device is in a stretched or tensioned state such that a diameter of the device is reduced;

partially deploying the device from the first end of the catheter at the target location to position the main lumen of the device in the main vessel, wherein during partial deployment the device is selectively tensioned while maintained in the stretched or tensioned state, such that selectively tensioning the device can reposition the device by expanding and reducing the diameter of the device during delivery so that it can be repositioned, subsequently withdrawing the catheter relative to the device to expose the at least one side-branch lumen;

guiding the respective side-branch lumen into at least one side branch vessel while the side-branch lumen is in the stretched or tensioned state; and

fully deploying the device from the first end of the catheter by releasing the device from the stretched or tensioned state so that the device expands against the main branch vessel and side branch vessel to form a seal with the wall of the vessel.

2. The method of claim 1, wherein the tethering of the first member to the catheter comprises attaching the ends of a string to the catheter wherein the string is releasably attached to the device.

3. The method of claim 2, wherein the main lumen comprises a proximal end and a distal end defining a length therebetween and the side branch lumen comprises a distal end and defining a length, and wherein the string is releasably attached to the distal end of the at least one side branch lumen.

4. The method of claim 1, wherein the first and second incisions are made locations on the body to provide access to at least one of the innominate artery, the left carotid artery and the left subclavian artery.

5. The method of claim 4, wherein the first incision is made into the brachiocephalic artery and the second incision is made a femoral artery.

6. The method of claim 1, where fully deploying the device by releasing the device from the stretched or tensioned state so that the device expands against the main branch vessel and side branch vessel comprises first expanding the main branch vessel against the main lumen while the at least one side-branch lumen remains in the stretched or tensioned state.

7. The method of claim 6, wherein fully deploying the device comprises relaxing tension on the device causing foreshortening of the device and increasing the diameter of the device thus securing the device against vessel lumen walls.

8. The method of claim 7 wherein the device is in the stretched or tensioned state using a plurality of attachment strings and, further comprising withdrawing the attachment strings.

9. The method of claim 6, further comprising removing the catheters.

10. The method of claim 1, where partially deploying the device from the first end of the catheter at the target location comprises first positioning the main lumen of the device in the main vessel while in the stretched or tensioned state and subsequently positioning at least one side-branch lumen extending from the main lumen of the device in the at least one side branch vessel while in the stretched or tensioned state.

11. The method of claim 10, where the device further includes at least one additional side branch lumen, and where the partially deploying the device further comprises extending the at least one additional side-branch lumen in an additional side branch vessel while the additional side-branch lumen is in the stretched or tensioned state.

12. The method of claim 11, wherein partially deploying the device comprises extending each side-branch lumen of the device in each of the respective side branch vessels one at a time.

13. The method of claim 11, wherein partially deploying the device comprises extending each side-branch lumen of the device in each of the respective side branch vessels simultaneously.

14. The method of claim 11, wherein the side-branch lumens are deployed serially or simultaneously.

15. The method of claim 1, wherein the device comprises a wire stent structure where the side branch lumen is adjustable relative to the main lumen until the device expands against the main branch vessel and side vessel.

16. The method of claim 1, wherein the device comprises a wire stent structure where an angular orientation of the side branch lumen is adjustable on the device until the device expands against the main branch vessel and side vessel.

17. The method of claim 1, wherein the main vessel is selected from an aortic arch and a thoracic abdominal artery.

18. The method of claim 1, wherein the side branch vessel is selected from the innominant artery, the left common carotid artery, and the left subclavian artery.

19. The method of claim 1, further comprising maintaining continuous blood flow around the device during placement.

20. The method of claim 1, further comprising maintaining patency of arched branches during and following placement of the device.

21. The method of claim 1, further comprising repositioning the device before fully deploying the device by withdrawing at least a portion the device into the catheter and relocating the portion.