PMID- 19523620 OWN - NLM STAT- MEDLINE DCOM- 20091002 LR - 20090727 IS - 1097-6779 (Electronic) IS - 0016-5107 (Linking) VI - 70 IP - 2 DP - 2009 Aug TI - Temporary placement of fully covered self-expandable metal stents in benign biliary strictures: midterm evaluation (with video). PG - 303-9 LID - 10.1016/j.gie.2008.11.029 [doi] AB - BACKGROUND: Benign biliary strictures (BBS) have been endoscopically managed with placement of multiple plastic stents. Uncovered metal stents have been associated with mucosal hyperplasia and partially covered self-expandable metal stents with migration. Recently, fully covered self-expandable metal stents (CSEMSs) with anchoring fins have become available. OBJECTIVE: Our purpose was to analyze the efficacy and complication rates of CSEMSs in the treatment of BBS. DESIGN: CSEMSs (10-mm diameter) were placed in 44 patients with BBS. CSEMSs were left in place until adequate biliary drainage was achieved, confirmed by resolution of symptoms, normalization of liver function tests, and imaging. SETTING: Tertiary care center with long-standing experience with metal stents. PATIENTS: A total of 44 patients with BBS (28 men, median age 53.5 years) were included. The preprocedure diagnoses included chronic pancreatitis (n = 19), gallstone-related strictures (n = 14), post liver transplant (n = 9), autoimmune pancreatitis (n = 1), and primary sclerosing cholangitis (n = 1). INTERVENTION: ERCP with temporary CSEMS placement. Removal of CSEMSs was performed with a snare or rat tooth. MAIN OUTCOME MEASUREMENTS: Stricture resolution and morbidity. RESULTS: The median time of CSEMS placement was 3.3 months (interquartile range 3.0-4.8). Resolution of the BBS was confirmed in 34 of 41 patients (83%) after a median postremoval follow-up time of 3.8 months (interquartile range 1.2-7.7). Complications were observed in 6 (14%) patients after CSEMS placement and in 4 (9%) after CSEMS removal. LIMITATION: Pilot study from a single center. CONCLUSION: Temporary placement of CSEMSs for BBS may offer an alternative to plastic stenting. Further investigation is required to further assess safety and long-term efficacy. FAU - Mahajan, Anshu AU - Mahajan A AD - Digestive Health Center, University of Virginia Health System, Charlottesville, Virginia 22908-0708, USA. FAU - Ho, Henry AU - Ho H FAU - Sauer, Bryan AU - Sauer B FAU - Phillips, Melissa S AU - Phillips MS FAU - Shami, Vanessa M AU - Shami VM FAU - Ellen, Kristi AU - Ellen K FAU - Rehan, Michele AU - Rehan M FAU - Schmitt, Timothy M AU - Schmitt TM FAU - Kahaleh, Michel AU - Kahaleh M LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20090611 PL - United States TA - Gastrointest Endosc JT - Gastrointestinal endoscopy JID - 0010505 SB - IM MH - Cholestasis/*surgery MH - Constriction, Pathologic MH - Female MH - Humans MH - Male MH - Middle Aged MH - Prosthesis Design MH - *Stents MH - Time Factors MH - Video Recording EDAT- 2009/06/16 09:00 MHDA- 2009/10/03 06:00 CRDT- 2009/06/16 09:00 PHST- 2008/09/10 00:00 [received] PHST- 2008/11/12 00:00 [accepted] PHST- 2009/06/16 09:00 [entrez] PHST- 2009/06/16 09:00 [pubmed] PHST- 2009/10/03 06:00 [medline] AID - S0016-5107(08)02951-9 [pii] AID - 10.1016/j.gie.2008.11.029 [doi] PST - ppublish SO - Gastrointest Endosc. 2009 Aug;70(2):303-9. doi: 10.1016/j.gie.2008.11.029. Epub 2009 Jun 11.