PMID- 28791317 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220310 IS - 2364-3722 (Print) IS - 2196-9736 (Electronic) IS - 2196-9736 (Linking) VI - 5 IP - 8 DP - 2017 Aug TI - New approach to decrease post-ERCP adverse events in patients with primary sclerosing cholangitis. PG - E710-E717 LID - 10.1055/s-0043-102398 [doi] AB - BACKGROUND AND STUDY AIMS: Endoscopic retrograde cholangiopancreatography (ERCP) is often performed in patients with primary sclerosing cholangitis (PSC). Our aim was to validate a treatment approach with the objective of decreasing ERCP related adverse events (AEs). PATIENTS AND METHODS: All patients who had undergone ERCP for PSC during the period from 2002 - 2012 were identified (group I). This group had traditional ERCP (no bile aspiration prior to contrast injection with balloon dilation and stent placement for treatment of dominant strictures). To decrease ERCP-related AEs, we changed the ERCP approach in which bile aspiration was performed prior to contrast injection and balloon dilation alone was performed for treatment of dominant strictures. This was tested prospectively in all patients undergoing ERCP for PSC from 2012 - 2014 (group II). RESULTS: The risk of overall AEs and cholangitis was relatively less in group II compared with group I [(2.1 % vs. 10.3 %; P = .38) and (0 % vs. 4.4 %; P = .68)]. On bivariate analysis, change in ERCP approach was associated with decreased risk of post-procedure cholangitis (0 % vs. 10.2 %, P = .03) and overall AE (0 % vs. 18.6 %, P = .03). There were no AEs in 22/46 patients in group II who had bile aspiration with balloon dilation. On multivariate analysis, only biliary stent placement was associated with increased risk of AEs (OR 4.10 (1.32 - 12.71); P = .02) and cholangitis (OR 5.43, 1.38 - 21.38; P = .02) respectively. CONCLUSION: Biliary aspiration and avoidance of stenting approach after dilation of strictures during ERCP in PSC patients appears to be associated with decreased risk of cholangitis and overall AEs. Future prospective randomized controlled trials are needed to validate our observation. FAU - Navaneethan, Udayakumar AU - Navaneethan U AD - Center for Interventional Endoscopy, Orlando, Florida, United States. AD - Department of Gastroenterology and Hepatology, Digestive Disease Institute, Cleveland Clinic, Cleveland, Ohio, United States. FAU - Lourdusamy, Dennisdhilak AU - Lourdusamy D AD - Department of Gastroenterology and Hepatology, Digestive Disease Institute, Cleveland Clinic, Cleveland, Ohio, United States. FAU - Gutierrez, Norma G AU - Gutierrez NG AD - Department of Gastroenterology and Hepatology, Digestive Disease Institute, Cleveland Clinic, Cleveland, Ohio, United States. FAU - Zhu, Xiang AU - Zhu X AD - Center for Interventional Endoscopy, Orlando, Florida, United States. FAU - Vargo, John J AU - Vargo JJ AD - Department of Gastroenterology and Hepatology, Digestive Disease Institute, Cleveland Clinic, Cleveland, Ohio, United States. FAU - Parsi, Mansour A AU - Parsi MA AD - Department of Gastroenterology and Hepatology, Digestive Disease Institute, Cleveland Clinic, Cleveland, Ohio, United States. LA - eng PT - Journal Article DEP - 20170807 PL - Germany TA - Endosc Int Open JT - Endoscopy international open JID - 101639919 PMC - PMC5546902 COIS- Competing interests Dr. Navaneethan is a consultant for AbbVie, Janssen and Takeda. Dr. Parsi is a consultant for Boston Scientific. Dr. Vargo is a consultant for Olympus. EDAT- 2017/08/10 06:00 MHDA- 2017/08/10 06:01 PMCR- 2017/08/01 CRDT- 2017/08/10 06:00 PHST- 2016/04/27 00:00 [received] PHST- 2016/12/30 00:00 [accepted] PHST- 2017/08/10 06:00 [entrez] PHST- 2017/08/10 06:00 [pubmed] PHST- 2017/08/10 06:01 [medline] PHST- 2017/08/01 00:00 [pmc-release] AID - 10.1055/s-0043-102398 [doi] PST - ppublish SO - Endosc Int Open. 2017 Aug;5(8):E710-E717. doi: 10.1055/s-0043-102398. Epub 2017 Aug 7.