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EP0536164B1 Expired / Lapsed EP ⏱️ 0.0 years remaining

Self-expanding prosthesis having stable axial length

Assignee: Schneider USA Inc
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Filing: 1991-04-25
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Granted: 1994-03-09
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Expires: 2011-04-25
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Abstract

Abstract A body implantable stent consists of two or more generally tubular, coaxial and slidably connected stent segments. Each of the stent segments is of open weave construction, formed of multiple braided, helically wound strands of resilient material. The stent is elastically deformed to a reduced radius when deployed. When released after positioning, the stent self-expands radially into contact with a tissue wall segment defining a blood vessel or other body cavity. As each stent segment expands radially, it contracts in the axial direction. To preserve a consistent length of the stent in spite of axial contraction of the segments, the axially outward and non-overlapping portions of the stent can be designed for secure fixation to the tissue wall segment, for example as radially outward flares. Accordingly, axial contraction occurs as a reduction in the length of the medial regions where adjacent stent segments overlap. Alternative approaches to maintain axial length include the addition of reinforcing filaments near the stent opposite ends to increase the restoring force, the provision of fixation hooks at opposite ends of the stent, and securing an elongate, axially directed, flexible and inextensible wire to the opposite ends of the stent.

Inventors

  • 👤 Christopher H. Porter

Bibliographic Details

Application Number —
Jurisdiction EP
Data Source google_patents
Last Synchronized 2026-10-23 05:13
CPC Classifications
A; A61; A61F; A61F2/00; A61F2/82; A61F2/86; A61F2/90; A61F2/852; A61F2002/826; A61F2/848; A61F2002/8486; A61F2220/00; A61F2220/0008; A61F2220/0016; A61F2230/00; A61F2230/0063; A61F2230/0073; A61F2230/0078; A61F2250/00; A61F2250/0014; A61F2250/0023; A61F2250/0058; A61F2250/006; A61F2250/0063

Claims Analysis

Total Claims: 10
Claim 1
Independent Claim 245 words
A device for fixation in a body cavity, comprising: a stent (16) including generally tubular and coaxial first and second open weave stent segments (20, 22) slidably engaged along respective first and second axially inward portions overlapping one another to form a medial region (24) of the stent (16), said stent segments (20, 22) further including respective non-overlapping first and second axially outward regions (30, 32) including respective and opposite first and second ends (34, 36) of the stent (16); said stent segments (20, 22), at least along said axially inward portions, having a predetermined first diameter and a predetermined first axial length, said stent segments (20, 22) being radially compressible to a second diameter less than said first diameter and to a second axial length longer than said first axial length, to facilitate an axial insertion of said stent (16) into a body cavity for delivery to a selected location therealong and subsequent fixation of the stent (16) within the cavity by effecting an engagement of the stent segments (20, 22) with a tissue wall segment defining said body cavity; and wherein said first and second axially inward portions are capable of sliding relative to one another to reduce the axial length of said medial region (24) as said stent segments (20, 22) radially expand into said engagement under positive fixation of said first and second ends (34,36), thus to maintain a substantially constant axial length of said stent (16) during said radial expansion.
Claim 2
Dependent Claim 28 words
The device of Claim 1 wherein: each of said stent segments (20, 22) is an open weave construction of helically wound filaments (18) of a resilient, body-compatible material.
Claim 3
Dependent Claim 23 words
The device of Claim 2 further including: a means for fixing said first and second ends (34, 36) to said tissue wall segment.
Claim 4
Dependent Claim 37 words
The device of Claim 3 wherein: said stent segments (20, 22) are flexible and have said predetermined first diameter and first axial length when not subject to external force, and are elastically compressible to said second diameter.
Claim 5
Dependent Claim 52 words
The device of Claim 4 wherein: said fixing means comprises first and second flared outer end portions of said first and second axially outward regions (30, 32), respectively, whereby said first and second ends (34, 36) have diameters greater than said first diameter when the stent (16) is in the relaxed state.
Claim 6
Dependent Claim 27 words
The device of Claim 5 wherein: the diameters of said first and second ends (34, 36) are greater than said first diameter by at least five percent.
Claim 7
Dependent Claim 35 words
The device of Claim 6 wherein: the axial length of each of said flared outer end portions is less than one-third of the axial length of its associated one of said stent segments (20, 22).
Claim 8
Dependent Claim 33 words
The device of Claim 4 wherein: said fixing means comprises elastic reinforcing strands connected to said filaments along first and second outer end portions including said first and second ends (34, 36), respectively.
Claim 9
Dependent Claim 31 words
The device of Claim 3 wherein: said fixing means comprises first and second pluralities of fixation hooks mounted to the stent (16) at said first and second ends (34, 36), respectively.
Claim 10
Dependent Claim 49 words
The device of Claim 1 further including: an elongate, flexible and substantially inextensible member running axially and connected to said first and second stent segments (20, 22) proximate said first and second ends (34, 36), for maintaining the axial length of the stent (16) constant during said radial expansion.

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