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US5876450A Expired / Lapsed US ⏱️ 0.0 years remaining

Stent for draining the pancreatic and biliary ducts and instrumentation for the placement thereof

Assignee: Cook Medical Technologies LLC
•
Filing: 1997-05-09
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Granted: 1999-03-02
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Expires: 2017-05-09
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Abstract

Abstract A stent is disclosed for placement within the pancreatic or biliary duct to facilitate drainage therethough, and related instrumentation which facilitates the atraumatic placement of the stent within the duct. The stent is atraumatically placed by means of an instrumentation system which draws or pulls the stent into position and wedges the distal end portion of the stent into the terminating portion of the duct to maintain the stent in place within the duct. As described herein, the stent is made of a soft biocompatible material which is resiliently compliant so as to allow the stent to readily conform to the curvature of the ductal passageway in which it has been placed. When placed, the stent extends along the length of the duct, with the proximal end extending into the duodenum. Perforations in the stent further faciliate drainage along the length of the stent.

Inventors

  • 👤 Frederick C. Johlin, Jr.

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 07:59
CPC Classifications
A; A61; A61M; A61M27/00; A61M27/002; A61M27/008; A61F; A61F2/00; A61F2/02; A61F2/04; A61M25/00; A61M25/01; A61M2025/018

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 310 words
A stent for placement in a desired duct in a patient, the duct including a proximal end and a terminating distal end portion, and an introduction system for the placement of said stent into the desired duct, comprising: a wire guide, said wire guide being sized and shaped for advancement to the terminating distal end portion of the duct; a stent made of a biocompatible material, said stent being formed in a generally tubular shape and having a proximal end portion with an open proximal end thereat, and an distal end portion with an open distal end thereat, and having an internal lumen with an inner diameter greater than the diameter of said wire guide; said internal lumen extending along the length of said stent from said open proximal end to said open distal end, said stent being deployable onto said wire guide with said distal end of said stent towards the duct and with said wire guide passing through said internal lumen of said stent; said stent further defining an interior shoulder within the distal end portion thereof; and an introducer catheter, said introducer catheter defining an inner lumen therethrough sized to receive said wire guide, said introducer catheter having a distal end portion with a terminating distal end thereof, said distal end portion of said introducer catheter being sized to be received into the internal lumen of said stent with the terminating distal end thereof abutting against the interior shoulder within the distal end portion of said stent; and wherein said introducer catheter is advanceable to press the terminating distal end thereof against the interior shoulder of the distal end portion of said stent and to thereby wedge the distal end portion of said stent into the terminating distal end portion of the duct, and whereby the stable placement of said stent into the duct is effectively accomplished.
Claim 2
Dependent Claim 310 words
A stent for placement in a desired duct in a patient, the duct including a proximal end and a terminating distal end portion, and an introduction system for the placement of said stent into the desired duct, comprising: a wire guide, said wire guide being sized and shaped for advancement to the terminating distal end portion of the duct; a stent made of a biocompatible material, said stent being formed in a generally tubular shape and having a proximal end portion with an open proximal end thereat, and an distal end portion with an open distal end thereat, and having an internal lumen with an inner diameter greater than the diameter of said wire guide; said internal lumen extending along the length of said stent from said open proximal end to said open distal end, said stent being deployable onto said wire guide with said distal end of said stent towards the duct and with said wire guide passing through said internal lumen of said stent; said stent further defining an interior shoulder within the distal end portion thereof; and an introducer catheter, said introducer catheter defining an inner lumen therethrough sized to receive said wire guide, said introducer catheter having a distal end portion with a terminating distal end thereof, said distal end portion of said introducer catheter being sized to be received into the internal lumen of said stent with the terminating distal end thereof abutting against the interior shoulder within the distal end portion of said stent; and wherein said introducer catheter is advanceable to press the terminating distal end thereof against the interior shoulder of the distal end portion of said stent and to thereby wedge the distal end portion of said stent into the terminating distal end portion of the duct, and whereby the stable placement of said stent into the duct is effectively accomplished.

References Cited (Backward Citations)

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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) 2002-03-01 2002-08-31 2003-03-02 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2006-03-01 2006-08-31 2007-03-02 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2010-03-01 2010-08-31 2011-03-02 $7700.00 Window Closed / Lapsed

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