Patent US5728131A successfully refreshed from Google Patents.
US5728131A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Coupling device and method of use
Assignee: Boston Scientific Scimed Inc
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Filing: 1995-06-12
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Granted: 1998-03-17
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Expires: 2015-06-12
Abstract
Abstract A coupler is provided for connecting a stent and a vascular graft for repairing aneurysms. An intravascular stent is connected to a vascular graft by a coupler having a high degree of elasticity so that the stent-coupler-graft assembly can be implanted to repair a body passageway, including aortic aneurysms.
Inventors
- 👤 John J. Frantzen
- 👤 Geoffrey A. Orth
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-23 11:54
CPC Classifications
A; A61; A61F; A61F2/00; A61F2/02; A61F2/04; A61F2/06; A61F2/07; A61F2/95; A61F2/9522; A61F2/9525; A61B; A61B17/00; A61B17/04; A61B17/06; A61B17/06166; A61B17/11; A61B2017/1107; A61F2/30; A61F2/3094; A61F2/30965; A61F2/82; A61F2/848; A61F2/86; A61F2/90; A61F2/91; A61F2/915; A61F2/958; A61F2002/075; A61F2002/30001; A61F2002/30108; A61F2002/3011; A61F2002/30159; A61F2002/30172; A61F2002/30199; A61F2002/30205; A61F2002/30217; A61F2002/30224; A61F2002/30233; A61F2002/30235; A61F2002/30316; A61F2002/30329; A61F2002/30331; A61F2002/30354; A61F2002/30461; A61F2002/30535; A61F2002/30589; A61F2220/00; A61F2220/0025; A61F2220/0033; A61F2220/0075; A61F2230/00; A61F2230/0002; A61F2230/0028; A61F2230/0052; A61F2230/0063; A61F2230/0067; A61F2230/0069; A61F2240/00; A61F2240/001; A61F2250/00; A61F2250/0058; A61F2250/0069
Claims Analysis
Total Claims: 20
Claim 1
Independent Claim
140 words
An assembly for connecting a stent and a vascular graft, comprising: an intravascular stent that is expandable from a delivery diameter to an implanted diameter; a vascular graft having a folded diameter approximating said delivery diameter of said stent, and having an unfolded diameter approximating said implanted diameter of said stent; a flexible coupler having a first end attached to said stent and a second end attached to said graft, said stent, said graft and said coupler forming a stent-coupler graft assembly that remains connected during delivery through a body lumen, wherein said stent-coupler-graft assembly has a substantially uniform reduced profile formed by contracting said stent and folding said graft, said stent-coupler-graft assembly remaining connected after deployment of said stent to said implanted diameter and said graft to said unfolded diameter, with no portion of said graft overlapping said stent.
Claim 2
Dependent Claim
140 words
An assembly for connecting a stent and a vascular graft, comprising: an intravascular stent that is expandable from a delivery diameter to an implanted diameter; a vascular graft having a folded diameter approximating said delivery diameter of said stent, and having an unfolded diameter approximating said implanted diameter of said stent; a flexible coupler having a first end attached to said stent and a second end attached to said graft, said stent, said graft and said coupler forming a stent-coupler graft assembly that remains connected during delivery through a body lumen, wherein said stent-coupler-graft assembly has a substantially uniform reduced profile formed by contracting said stent and folding said graft, said stent-coupler-graft assembly remaining connected after deployment of said stent to said implanted diameter and said graft to said unfolded diameter, with no portion of said graft overlapping said stent.
Claim 3
Dependent Claim
10 words
The assembly of claim 1, wherein said coupler is funnel-shaped.
Claim 4
Dependent Claim
41 words
The assembly of claim 2, wherein said first end of said coupler is expandable up to a diameter of approximately 0.800 inches, and said second end of said coupler is unexpanded and at rest at a diameter of approximately 0.800 inches.
Claim 5
Dependent Claim
14 words
The assembly of claim 1, wherein said coupler material can elongate up to 500%.
Claim 6
Dependent Claim
14 words
The assembly of claim 1, wherein said coupler is made from a biocompatible material.
Claim 7
Dependent Claim
33 words
The assembly of claim 5, wherein said coupler is made from highly elastic materials, taken from the group of elastic materials of polyurethane, silicone copolymers, latex, and polyseloxane modified ethylene/butylene-styrene block copylymers (SEB's).
Claim 8
Dependent Claim
21 words
The assembly of claim 1, wherein said coupler has a wall thickness in the range of 0.0003 inches to 0.010 inches.
Claim 9
Dependent Claim
18 words
The assembly of claim 1, wherein said coupler provides a fluid-tight seal between said stent and said graft.
Claim 10
Dependent Claim
17 words
The assembly of claim 1, wherein said graft is bonded to said second end of said coupler.
Claim 11
Dependent Claim
17 words
The assembly of claim 1, wherein said stent is bonded to said first end of said coupler.
Claim 12
Dependent Claim
30 words
The assembly of claim 1, wherein said stent has a plurality of T-members extending from one end, said T-members being adapted for attachment to said first end of said graft.
Claim 13
Dependent Claim
33 words
The assembly of claim 1, wherein said first end of said coupler is sutured to said stent, and said second end of said coupler is attached to said graft by a dipping process.
Claim 14
Dependent Claim
56 words
The assembly of claim 1, wherein a plurality of fibers are woven into said coupler, said fibers extending from said first end and from said second end of said coupler, wherein said fibers extending from said first end are attached to said stent, and said fibers extending from said second end are attached to said graft.
Claim 15
Dependent Claim
14 words
The assembly of claim 13, wherein said fibers are made from a suture material.
Claim 16
Dependent Claim
16 words
The assembly of claim 14, wherein said fibers are bonded to said stent and said graft.
Claim 17
Independent Claim
176 words
A method of repairing a body passageway, including an intravascular stent that is expandable from a first, delivery diameter to a second, implanted diameter, a vascular graft having a diameter approximating said implanted diameter of said stent, and a flexible coupler adapted to attach said intravascular stent and said vascular graft to form a stent-coupler-graft assembly, the method comprising: attaching said stent to one end of said coupler and attaching said graft to the opposite end of said coupler; mounting the stent-coupler-graft assembly on a balloon catheter; reducing the profile of the stent-coupler-graft assembly to a first diameter by crimping said stent onto the balloon portion of said catheter, and folding said graft onto said catheter, to reduce the overall profile so that said stent-coupler-graft assembly has a substantially uniform first delivery diameter; inserting said stent-coupler-graft assembly on said balloon catheter assembly percutaneously and transporting through the body passageway; deploying said stent-coupler-graft assembly by expanding said stent to an enlarged, second diameter and unfolding said graft; and withdrawing said balloon catheter assembly from the body passageway.
Claim 18
Independent Claim
176 words
A method of repairing a body passageway, including an intravascular stent that is expandable from a first, delivery diameter to a second, implanted diameter, a vascular graft having a diameter approximating said implanted diameter of said stent, and a flexible coupler adapted to attach said intravascular stent and said vascular graft to form a stent-coupler-graft assembly, the method comprising: attaching said stent to one end of said coupler and attaching said graft to the opposite end of said coupler; mounting the stent-coupler-graft assembly on a balloon catheter; reducing the profile of the stent-coupler-graft assembly to a first diameter by crimping said stent onto the balloon portion of said catheter, and folding said graft onto said catheter, to reduce the overall profile so that said stent-coupler-graft assembly has a substantially uniform first delivery diameter; inserting said stent-coupler-graft assembly on said balloon catheter assembly percutaneously and transporting through the body passageway; deploying said stent-coupler-graft assembly by expanding said stent to an enlarged, second diameter and unfolding said graft; and withdrawing said balloon catheter assembly from the body passageway.
Claim 19
Dependent Claim
17 words
The method of claim 16, wherein said coupler expands up to 500% when said stent is expanded.
Claim 20
Dependent Claim
22 words
The method of claim 16, wherein said stent and said graft remain spaced apart during delivery and implanting of said stent-coupler-graft assembly.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 2001-03-16 | 2001-09-15 | 2002-03-17 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 2005-03-16 | 2005-09-15 | 2006-03-17 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 2009-03-16 | 2009-09-15 | 2010-03-17 | $7700.00 | Window Closed / Lapsed |