Staged deployment endograft

• US 7,297,156 B2
• Filed: 06/08/2006
• Issued: 11/20/2007
• Est. Priority Date: 05/27/2003
• Status: Expired due to Fees

• Current Assignee: Lifeport Sciences LLC (Acacia Research Corporation)
• Original Assignee: Boston Scientific Corporation
• Inventors: Nelson, Kristoff
• Primary Examiner(s): GHERBI, SUZETTE JAIME J
• Application Number:
  US11/449,278
• Publication Number:
  US 20060229703A1
• Time in Patent Office: 530 Days
• Field of Search: 623 111- 135, 606/108
• US Class Current: 623/1.12
• CPC Class Codes: A61F 2/07 Stent-grafts
• CPC Class Codes: A61F 2/844 folded prior to deployment
• CPC Class Codes: A61F 2/89 the wire-like elements comprising two or more adjacent rings flexibly connected by separate members
• CPC Class Codes: A61F 2/95 Instruments specially adapted for placement or removal of stents or stent-grafts
• 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 2002/075 the stent being loosely attached to the graft material, e.g. by stitching
• CPC Class Codes: A61F 2002/8483 Barbs
• CPC Class Codes: A61F 2002/9511 the retaining means being filaments or wires
• CPC Class Codes: A61F 2220/005 using adhesives
• 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 2230/001 Figure-8-shaped, e.g. hourglass-shaped
• CPC Class Codes: Y10S 623/903 Blood vessel

Abstract

An apparatus is provided for deploying an endograft that maintains a fluid channel throughout deployment. A method for deploying an endograft maintaining a fluid channel through the deployment is also provided.

Claims

1. A method of deploying an endograft comprising the steps of:

delivering an endograft to a diseased portion of a body lumen, said endograft being radially constrained by a sheath and select longitudinal portions of said endograft being radially constrained by releasable restraining members operatively associated with said select longitudinal portions of said endograft;

withdrawing said sheath to partially deploy said endograft, wherein said releasable restraining members constrain said selected longitudinal portions of said endograft to provide a flow path external said endograft proximate said restraining members while permitting portions of said endograft intermediate said selected longitudinal portions to expand;

releasing said restraining members to further deploy said select longitudinal portions to fully expand said endograft.

2. The method of claim 1 further comprising, prior to the step of releasing said restraining members, the steps of:

determining the position of said endograft; and

repositioning said endograft, as required.

3. The method of claim 2 wherein the position of said endograft is determined using radiography.

4. The method of claim 1 wherein said restraining members are released selectively.

5. The method of claim 4 wherein said restraining members are released sequentially.

6. The method of claim 1 wherein said step of releasing said restraining members comprises severing said restraining members and withdrawing them distally.

7. The method of claim 1 wherein said restraining members are flexible tubes extending longitudinally over said endograft in threaded engagement proximal to said endograft, and said step of releasing said restraining members comprises unscrewing said flexible tubes and withdrawing said flexible tubes distally over said endograft.

8. An endograft delivery system comprising:

a catheter configured to carry said endograft and to be endoluminally advanced through a body lumen;

a nosecone attached to a proximal end of said catheter;

a sheath configured to constrain said endograft in a radially compressed configuration during endoluminal advancement and to be axially withdrawn from said endograft to partially deploy said endograft; and

at least two releasable restraining members extending over and radially constraining lengthwise portions of said endograft.

9. The delivery system of claim 8 wherein said restraining members are releasably attached to said nosecone.

10. The delivery system of claim 8 wherein said restraining members are configured to be released by severing said restraining members.

11. The delivery system of claim 8 wherein said restraining members are absorbable and are configured to be released by absorption.

12. The delivery system of claim 8 wherein said restraining members are individually releasable.

13. The delivery system of claim 12 wherein said restraining members are sequentially releasable.