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A biodegradable non-covered self-expandable stent to treat pancreatic duct strictures in chronic pancreatitis: a proof of principle
In chronic pancreatitis (CP), fibrotic pancreatic duct (PD) strictures pose a therapeutic challenge, because endoscopic dilatation requires multiple procedures with suboptimal results. Biodegradable self-expandable stents (BD-SESs) may serve as an alternative in this setting. Patients with CP were e...
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Published in: | Gastrointestinal endoscopy 2018-02, Vol.87 (2), p.486-491 |
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creator | Cahen, Djuna L. van der Merwe, Schalk W. Laleman, Wim Poley, Jan-Werner Bruno, Marco J. |
description | In chronic pancreatitis (CP), fibrotic pancreatic duct (PD) strictures pose a therapeutic challenge, because endoscopic dilatation requires multiple procedures with suboptimal results. Biodegradable self-expandable stents (BD-SESs) may serve as an alternative in this setting.
Patients with CP were eligible for this proof-of-principle study if at least 6 months of endoscopic dilatation with plastic stents had failed to resolve their PD stricture. The non-covered BD-SESs were expected to degrade within 3 to 6 months. Patients were followed at 3-monthly intervals for 1 year. Placement success and safety were the primary outcome parameters. Stricture resolution was assessed by ERCP after 6 months.
BD-SESs were successfully placed in all 19 patients without adverse events. In 2 cases, stent occlusion with sludge and stones was treated by a balloon swipe. One stent disintegrated during this procedure, after which placement of the plastic stent was resumed. A hyperplastic response was observed in 2 patients but did not result in functional obstruction. Stricture resolution was accomplished in 11 patients (technical success rate 58%). Six patients required further treatment of their PD stricture, 4 endoscopically and 2 surgically. Three additional patients underwent surgery for other reasons: 2 Whipple procedures for CP-related adverse events and one tail resection for an intraductal papillary mucinous neoplasm. The remaining 10 patients did not require further PD drainage (clinical success rate 52%).
These preliminary results show that BD-SESs are safe to use and able to resolve fibrotic PD strictures in CP. These encouraging outcomes warrant further testing. |
doi_str_mv | 10.1016/j.gie.2017.08.018 |
format | article |
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Patients with CP were eligible for this proof-of-principle study if at least 6 months of endoscopic dilatation with plastic stents had failed to resolve their PD stricture. The non-covered BD-SESs were expected to degrade within 3 to 6 months. Patients were followed at 3-monthly intervals for 1 year. Placement success and safety were the primary outcome parameters. Stricture resolution was assessed by ERCP after 6 months.
BD-SESs were successfully placed in all 19 patients without adverse events. In 2 cases, stent occlusion with sludge and stones was treated by a balloon swipe. One stent disintegrated during this procedure, after which placement of the plastic stent was resumed. A hyperplastic response was observed in 2 patients but did not result in functional obstruction. Stricture resolution was accomplished in 11 patients (technical success rate 58%). Six patients required further treatment of their PD stricture, 4 endoscopically and 2 surgically. Three additional patients underwent surgery for other reasons: 2 Whipple procedures for CP-related adverse events and one tail resection for an intraductal papillary mucinous neoplasm. The remaining 10 patients did not require further PD drainage (clinical success rate 52%).
These preliminary results show that BD-SESs are safe to use and able to resolve fibrotic PD strictures in CP. These encouraging outcomes warrant further testing.</description><identifier>ISSN: 0016-5107</identifier><identifier>EISSN: 1097-6779</identifier><identifier>DOI: 10.1016/j.gie.2017.08.018</identifier><identifier>PMID: 28843580</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><ispartof>Gastrointestinal endoscopy, 2018-02, Vol.87 (2), p.486-491</ispartof><rights>2018 American Society for Gastrointestinal Endoscopy</rights><rights>Copyright © 2018 American Society for Gastrointestinal Endoscopy. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-178f877630e40c52e9591a43b11a804f2e5f6963b6aba93093a8fd2b8572bd323</citedby><cites>FETCH-LOGICAL-c396t-178f877630e40c52e9591a43b11a804f2e5f6963b6aba93093a8fd2b8572bd323</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28843580$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cahen, Djuna L.</creatorcontrib><creatorcontrib>van der Merwe, Schalk W.</creatorcontrib><creatorcontrib>Laleman, Wim</creatorcontrib><creatorcontrib>Poley, Jan-Werner</creatorcontrib><creatorcontrib>Bruno, Marco J.</creatorcontrib><title>A biodegradable non-covered self-expandable stent to treat pancreatic duct strictures in chronic pancreatitis: a proof of principle</title><title>Gastrointestinal endoscopy</title><addtitle>Gastrointest Endosc</addtitle><description>In chronic pancreatitis (CP), fibrotic pancreatic duct (PD) strictures pose a therapeutic challenge, because endoscopic dilatation requires multiple procedures with suboptimal results. Biodegradable self-expandable stents (BD-SESs) may serve as an alternative in this setting.
Patients with CP were eligible for this proof-of-principle study if at least 6 months of endoscopic dilatation with plastic stents had failed to resolve their PD stricture. The non-covered BD-SESs were expected to degrade within 3 to 6 months. Patients were followed at 3-monthly intervals for 1 year. Placement success and safety were the primary outcome parameters. Stricture resolution was assessed by ERCP after 6 months.
BD-SESs were successfully placed in all 19 patients without adverse events. In 2 cases, stent occlusion with sludge and stones was treated by a balloon swipe. One stent disintegrated during this procedure, after which placement of the plastic stent was resumed. A hyperplastic response was observed in 2 patients but did not result in functional obstruction. Stricture resolution was accomplished in 11 patients (technical success rate 58%). Six patients required further treatment of their PD stricture, 4 endoscopically and 2 surgically. Three additional patients underwent surgery for other reasons: 2 Whipple procedures for CP-related adverse events and one tail resection for an intraductal papillary mucinous neoplasm. The remaining 10 patients did not require further PD drainage (clinical success rate 52%).
These preliminary results show that BD-SESs are safe to use and able to resolve fibrotic PD strictures in CP. These encouraging outcomes warrant further testing.</description><issn>0016-5107</issn><issn>1097-6779</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kE1uFDEQhS0EIkPCAdggL9l045_utg2rKOJPisSGrC23XQ4e9diD7Y6SC-QcOUtOhkcTsmRVJb3vPVU9hN5R0lNCp4_b_jpAzwgVPZE9ofIF2lCiRDcJoV6iDWlQN1IiTtCbUraEEMk4fY1OmJQDHyXZoPtzPIfk4DobZ-YFcEyxs-kGMjhcYPEd3O5NPGqlQqy4JlwzmPr40AR72ILFbrW16TnYumYoOERsf-cUm_RM1VA-YdNsOSX_-JA83ucQbdgvcIZeebMUePs0T9HV1y-_Lr53lz-__bg4v-wsV1PtqJBeCjFxAgOxIwM1KmoGPlNqJBk8g9FPauLzZGajOFHcSO_YLEfBZscZP0Ufjrnthj8rlKp3oVhYFhMhrUVTxTljSg1jQ-kRtTmVksHrdu3O5DtNiT7Ur7e61a8P9Wsidau_ed4_xa_zDtyz41_fDfh8BKA9eRMg62IDRAsuZLBVuxT-E_8XrCiZ7g</recordid><startdate>201802</startdate><enddate>201802</enddate><creator>Cahen, Djuna L.</creator><creator>van der Merwe, Schalk W.</creator><creator>Laleman, Wim</creator><creator>Poley, Jan-Werner</creator><creator>Bruno, Marco J.</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201802</creationdate><title>A biodegradable non-covered self-expandable stent to treat pancreatic duct strictures in chronic pancreatitis: a proof of principle</title><author>Cahen, Djuna L. ; van der Merwe, Schalk W. ; Laleman, Wim ; Poley, Jan-Werner ; Bruno, Marco J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-178f877630e40c52e9591a43b11a804f2e5f6963b6aba93093a8fd2b8572bd323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cahen, Djuna L.</creatorcontrib><creatorcontrib>van der Merwe, Schalk W.</creatorcontrib><creatorcontrib>Laleman, Wim</creatorcontrib><creatorcontrib>Poley, Jan-Werner</creatorcontrib><creatorcontrib>Bruno, Marco J.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Gastrointestinal endoscopy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cahen, Djuna L.</au><au>van der Merwe, Schalk W.</au><au>Laleman, Wim</au><au>Poley, Jan-Werner</au><au>Bruno, Marco J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A biodegradable non-covered self-expandable stent to treat pancreatic duct strictures in chronic pancreatitis: a proof of principle</atitle><jtitle>Gastrointestinal endoscopy</jtitle><addtitle>Gastrointest Endosc</addtitle><date>2018-02</date><risdate>2018</risdate><volume>87</volume><issue>2</issue><spage>486</spage><epage>491</epage><pages>486-491</pages><issn>0016-5107</issn><eissn>1097-6779</eissn><abstract>In chronic pancreatitis (CP), fibrotic pancreatic duct (PD) strictures pose a therapeutic challenge, because endoscopic dilatation requires multiple procedures with suboptimal results. Biodegradable self-expandable stents (BD-SESs) may serve as an alternative in this setting.
Patients with CP were eligible for this proof-of-principle study if at least 6 months of endoscopic dilatation with plastic stents had failed to resolve their PD stricture. The non-covered BD-SESs were expected to degrade within 3 to 6 months. Patients were followed at 3-monthly intervals for 1 year. Placement success and safety were the primary outcome parameters. Stricture resolution was assessed by ERCP after 6 months.
BD-SESs were successfully placed in all 19 patients without adverse events. In 2 cases, stent occlusion with sludge and stones was treated by a balloon swipe. One stent disintegrated during this procedure, after which placement of the plastic stent was resumed. A hyperplastic response was observed in 2 patients but did not result in functional obstruction. Stricture resolution was accomplished in 11 patients (technical success rate 58%). Six patients required further treatment of their PD stricture, 4 endoscopically and 2 surgically. Three additional patients underwent surgery for other reasons: 2 Whipple procedures for CP-related adverse events and one tail resection for an intraductal papillary mucinous neoplasm. The remaining 10 patients did not require further PD drainage (clinical success rate 52%).
These preliminary results show that BD-SESs are safe to use and able to resolve fibrotic PD strictures in CP. These encouraging outcomes warrant further testing.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>28843580</pmid><doi>10.1016/j.gie.2017.08.018</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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title | A biodegradable non-covered self-expandable stent to treat pancreatic duct strictures in chronic pancreatitis: a proof of principle |
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