RECONFIGURABLE STENT-GRAFT DELIVERY SYSTEM AND METHOD OF USE

• US 20130289692A1
• Filed: 04/27/2012
• Published: 10/31/2013
• Est. Priority Date: 04/27/2012
• Status: Abandoned Application

• Current Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Original Assignee: Medtronic Vascular, Inc. (Medtronic Plc)
• Inventors: Argentine, Jeffery, Haggard, Mathew, Maggard, Jason, Simmons, Emilie
• Application Number:
  US13/457,541
• Publication Number:
  US 20130289692A1
• Time in Patent Office: Days
• US Class Current: 623/1.11
• 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 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
• CPC Class Codes: A61F 2250/006 modular

Abstract

A reconfigurable delivery system is disclosed having a multi-lumen delivery catheter configuration that permits the delivery and staged release of a self-expanding main vessel stent-graft and a delivery sheath configuration that permits the introduction of various medical devices for the delivery and implantation of various branch vessel stent-grafts that are to be mated with the main vessel stent-graft. A method is disclosed wherein the delivery system is first used in the multi-lumen delivery catheter configuration to deliver and release a main vessel stent-graft that is configured for placement in the abdominal aorta for treatment of short-neck infrarenal, juxtarenal, and/or suprarenal aneurysms and then used in the delivery sheath configuration to facilitate the delivery of branch vessel stent-grafts that are configured to extend from the main vessel stent-graft into a respective renal artery.

Claims

1. A reconfigurable stent-graft delivery system comprising:

a tubular sheath component defining a lumen from a proximal end to distal end thereof that is reconfigurable from a multi-lumen delivery catheter configuration to a delivery sheath configuration,

wherein in the multi-lumen delivery catheter configuration a proximal portion of the sheath component lumen is divided into a plurality of working lumens and a distal portion of the sheath component lumen includes a stent-graft delivery area for compressing a main stent-graft prosthesis in a delivery configuration therein, and

wherein in the delivery sheath configuration the proximal portion of the sheath component lumen is not divided into the plurality of working lumens.

2. The delivery system of claim 1, further comprising:

a middle member component removably coupled to the delivery system, the middle member component having a middle member shaft that extends within and divides the sheath component lumen into the plurality of working lumens when the delivery system is in the multi-lumen delivery catheter configuration.

3. The delivery system of claim 2, wherein the middle member component is removed from the delivery system when the delivery system is in the delivery sheath configuration.

4. The delivery system of claim 2, wherein a plurality of grooves longitudinally extend within an exterior surface of the middle member shaft with each groove at least partially defining one of the plurality of working lumens.

5. The delivery system of claim 4, wherein each groove is a U-shaped channel.

6. The delivery system of claim 3, further comprising:

a handle component operably attached to the proximal end of the tubular sheath component that includes an access port through which the middle member shaft passes when the middle member component is coupled to and removed from the delivery system.

7. The delivery system of claim 6, wherein the access port includes a hemostasis seal through which the middle member shaft passes when the middle member component is coupled to and removed from the delivery system.

8. The delivery system of claim 7, wherein the middle member component includes a middle member handle attached to a proximal end of the middle member shaft and wherein the middle member handle includes a distal tubular segment that is inserted within the hemostasis seal when the middle member component is coupled to the delivery system in its multi-lumen delivery catheter configuration.

9. The delivery system of claim 8, wherein the middle member handle has a head portion for gripping by an operator that radially extends from the distal tubular segment and sits against a rim of the handle component access port when the middle member component is coupled to the delivery system in its multi-lumen delivery catheter configuration.

10. The delivery system of claim 1, wherein in the delivery sheath configuration the sheath component lumen is sized for introducing one or more delivery systems therethrough with each of the one or more delivery systems being used to deliver a stent-graft prosthesis that mates with the main stent-graft prosthesis in vivo to form an implant.

11. A stent-graft delivery system comprising:

a handle component;

a tubular sheath component having a proximal end operably attached to the handle component and defining a lumen from the proximal end to distal end thereof; and

a middle member component removably coupled to the delivery system, the middle member component having a middle member shaft that extends within and divides at least a proximal portion of the sheath component lumen into a plurality of working lumens when the delivery system is in a multi-lumen delivery catheter configuration.

12. The delivery system of claim 11, wherein a plurality of grooves longitudinally extend within an exterior surface of the middle member shaft with each groove at least partially defining one of the plurality of working lumens.

13. The delivery system of claim 12, wherein each groove is a U-shaped channel.

14. The delivery system of claim 11, wherein the middle member component is removed from the delivery system when the delivery system is in a delivery sheath configuration

15. The delivery system of claim 14, wherein the handle component includes an access port through which the middle member shaft passes when the middle member component is coupled to and removed from the delivery system.

16. The delivery system of claim 15, wherein the access port includes a hemostasis seal through which the middle member shaft passes when the middle member component is coupled to and removed from the delivery system.

17. The delivery system of claim 16, wherein the middle member component includes a middle member handle attached to a proximal end of the middle member shaft and wherein the middle member handle includes a distal tubular segment that is inserted within the hemostasis seal when the middle member component is coupled to the delivery system in its multi-lumen delivery catheter configuration.

18. The delivery system of claim 17, wherein the middle member handle has a head portion for gripping by an operator that radially extends from the distal tubular segment and sits against a rim of the handle component access port when the middle member component is coupled to the delivery system in its multi-lumen delivery catheter configuration.

19. The delivery system of claim 14, wherein in the delivery sheath configuration the sheath component lumen is sized for introducing one or more delivery systems therethrough with each of the one or more delivery systems having a stent-graft prosthesis in a delivery configuration therein.

20. The delivery system of claim 11, wherein in the multi-lumen delivery catheter configuration the proximal portion of the sheath component lumen is divided into the plurality of working lumens and a distal portion of the sheath component lumen includes a stent-graft delivery area for compressing a main stent-graft prosthesis in a delivery configuration therein.