Extension for iliac branch delivery device and methods of using the same

• US 9,439,793 B2
• Filed: 03/12/2013
• Issued: 09/13/2016
• Est. Priority Date: 03/12/2013
• Status: Active Grant

• Current Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Original Assignee: Cook Medical Incorporated (Cook Group Incorporated)
• Inventors: Roeder, Blayne A.
• Primary Examiner(s): Severson, Ryan J
• Assistant Examiner(s): DANG, ANH TIEU
• Application Number:
  US13/795,923
• Publication Number:
  US 20140277355A1
• Time in Patent Office: 1,281 Days
• US Class Current: 1/1
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/954 for placing stents or stent-grafts in a bifurcation
• CPC Class Codes: A61F 2/966 with relative longitudinal movement between outer sleeve and prosthesis, e.g. using a push rod
• CPC Class Codes: A61F 2002/061 provided with means for allowing access to secondary lumens
• CPC Class Codes: A61F 2002/067 modular

Abstract

Methods for accessing the common and internal iliac arteries and delivering and deploying an endovascular graft therein are disclosed. A system including a pre-loaded delivery and deployment device with an extension sheath is described which enables such a method to be practiced is also disclosed.

Claims

1. A system for the delivery and deployment of an endovascular graft comprising:

a. a delivery device comprising;

i. a pusher catheter having a proximal end portion a distal end portion and a lumen extending there between, and a proximal end opening;

ii. a cannula having a proximal end portion and a distal end portion extending longitudinally within the lumen of the pusher catheter;

iii. a nose cone dilator proximal of the proximal end portion of the cannula, the nose cone dilator having a proximal tip;

iv. an extension sheath extending from the proximal tip of the nose cone dilator, the extension sheath having a lumen extending there through, wherein a portion of the extension sheath has a U-shaped configuration;

b. a stent graft carried on the delivery device, the stent graft comprising;

i. a main tubular body of a biocompatible graft material defining a main lumen having a proximal end portion, a distal end portion, a distal end opening;

ii. a side branch extending from the main tubular body, the side branch defining a lumen and being in fluid communication with the main lumen, whereby the stent graft is configured to be deployed into the vasculature of a patient with the main tubular body being located in the ipsilateral common iliac artery and the side branch being directed towards an internal iliac artery of the common iliac artery;

c. a pre-loaded guide wire extending through the lumen of the pusher catheter, exiting the proximal end opening of the pusher catheter distal to the distal end opening of the main tubular body, extending entirely outside of the distal portion of the main tubular body along side the main tubular body and entering the main lumen of the main tubular body through the lumen of the side branch and extending out of the proximal end portion of the main tubular body, the pre-loaded guide wire further extending at least partially through the lumen of the extension sheath.

2. The system of claim 1 wherein the extension sheath is flexible and adapted to be manipulated though the contours of a vessel lumen.

3. The system of claim 1 wherein the stent graft is secured to the proximal end portion of the cannula.

4. The system of claim 1 wherein the delivery device further comprises a mechanism for manipulating the extension sheath.

5. The system of claim 1 further comprising a second delivery device, the second delivery device comprising a second stent graft carried on a proximal end portion of the second delivery device, the second stent graft comprising a tubular body of a biocompatible graft material defining a main lumen.

6. The system of claim 5 wherein the second delivery device is sized and configured to be advanced through the proximal end portion of the main tubular graft body and into the lumen of the side branch.

7. The system of claim 5 wherein the second stent graft carried by the second delivery device is configured to be positioned within the internal iliac artery.

8. The system of claim 5 further comprising a sheath mounted coaxially over at least a portion of the second stent graft.

9. The system of claim 1, wherein the greatest diameter of the extension sheath is less than the diameter of the proximal tip of the nose cone dilator.

10. A method for treating a diseased vessel, the method comprising:

a. introducing a delivery device into an ipsilateral common iliac artery, the delivery device comprising;

i. a pusher catheter having a proximal end portion, a distal end portion and a lumen extending there between, and a proximal end opening;

ii. a cannula having a proximal end portion and a distal end portion extending longitudinally within the lumen of the pusher catheter;

iii. a nose cone dilator proximal of the proximal end portion of the cannula, the nose cone dilator having a proximal tip;

iv. an extension sheath extending from the proximal tip of the nose cone dilator, the extension sheath having a lumen extending there through, wherein a portion of the extension sheath has a U-shaped configuration;

v. a stent graft carried on the delivery device, the stent graft comprising a main tubular body of a biocompatible graft material defining a main lumen having a proximal end portion, a distal end portion, a distal end opening, a side branch extending from the main tubular body, the side branch defining a lumen and being in fluid communication with the main lumen, whereby the stent graft is configured to be deployed into the vasculature of a patient with the main tubular body being located in the ipsilateral common iliac artery and the side branch being directed towards an internal iliac artery of the common iliac artery;

vi. a pre-loaded guide wire extending through the lumen of the pusher catheter, exiting the proximal end opening of the pusher catheter distal to the distal end opening of the main tubular body, extending entirely outside of the distal portion of the main tubular body along side the main tubular body and entering the main lumen of the main tubular body through the side branch lumen and extending out of the proximal end portion of the main tubular body, the pre-loaded guide wire having a proximal end portion extending at least partially through the lumen of the extension sheath,

b. extending the extension sheath and proximal end portion of the pre-loaded guide wire over the aortic bifurcation and in a distal direction down the contralateral common iliac artery.

11. The method of claim 10 further comprising at least partially deploying the stent graft in the ipsilateral common iliac artery.

12. The method of claim 11 further comprising withdrawing the extension sheath from the patient'"'"'s vasculature.

13. The method of claim 12 wherein the extension sheath is withdrawn from the contralateral side.

14. The method of claim 11 further comprising:

a. introducing an auxiliary sheath having a lumen into the contralateral common iliac artery, and

b. tracking the auxiliary sheath over the pre-loaded guidewire such that the sheath lumen provides a pathway that extends from the contralateral common iliac artery, over the aortic bifurcation, through the proximal end portion of the main graft and through the lumen of the side branch.

15. The method of claim 14 further comprising:

a. introducing a second delivery device through the pathway defined by the auxiliary sheath lumen, the second delivery device comprising a second stent graft carried on a proximal end portion thereof, the second stent graft comprising a tubular body of biocompatible graft material,

b. positioning, the second stent graft within the ipsilateral internal iliac artery,

c. at least partially deploying the second stent graft in the ipsilateral internal iliac artery.

16. The method of claim 15 further comprising removing the auxiliary sheath and second delivery device from the patient'"'"'s vasculature.