A randomized trial of rectal indomethacin and sublingual nitrates to prevent post-ERCP pancreatitis

dc.contributor.authorSotudehmanesh, Rasool
dc.contributor.authorEloubeidi, Mohamad Ali S.
dc.contributor.authorAliasgari, Ali
dc.contributor.authorFarsinejad, Maryam
dc.contributor.authorKhatibian, Morteza
dc.contributor.departmentInternal Medicine
dc.contributor.departmentDivision of Gastroenterology and Hepatology
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:42:49Z
dc.date.available2025-01-24T11:42:49Z
dc.date.issued2014
dc.description.abstractOBJECTIVES:Acute pancreatitis is the most common adverse event of endoscopic retrograde cholangiopancreatography (ERCP). Recent data suggest that indomethacin can reduce the risk of post-ERCP pancreatitis (PEP) in high-risk individuals. However, whether the combination of indomethacin and sublingual nitrates is superior to indomethacin alone is unknown. Therefore, we aimed to evaluate the efficacy of rectally administered indomethacin plus sublingual nitrate compared with indomethacin alone to prevent PEP.METHODS:During a 17-month period, all eligible patients who underwent ERCP were enrolled in this study. We excluded patients who had undergone a prior endoscopic sphincterotomy. In a double-blind controlled randomized trial, patients received a suppository containing 100 mg of indomethacin, plus 5 mg of sublingual nitrate (group A), or a suppository containing 100 mg of indomethacin, plus sublingual placebo (group B), before ERCP. Serum amylase levels and clinically pertinent evaluations were measured in all patients after ERCP.RESULTS:Of the 300 enrolled patients, 150 received indomethacin plus nitrate. Thirty-three patients developed pancreatitis: 10 (6.7%) in group A and 23 (15.3%) in group B (P=0.016, risk ratio=0.39, 95% confidence intervals (CI): 0.18-0.86). More than 80% of the patients were at high risk of developing pancreatitis after ERCP. Absolute risk reduction, relative risk reduction, and number needed to treat for the prevention of PEP were 8.6% (95% CI: 4.7-14.5), 56.2% (95% CI: 50.6-60.8), and 12 (95% CI: 7-22), respectively.CONCLUSIONS:Combination of rectal indomethacin and sublingual nitrate given before ERCP was significantly more likely to reduce the incidence of PEP than indomethacin suppository alone. Multicenter trials to confirm these promising findings are needed. © 2014 by the American College of Gastroenterology.
dc.identifier.doihttps://doi.org/10.1038/ajg.2014.9
dc.identifier.eid2-s2.0-84902081486
dc.identifier.pmid24513806
dc.identifier.urihttp://hdl.handle.net/10938/30087
dc.language.isoen
dc.publisherNature Publishing Group
dc.relation.ispartofAmerican Journal of Gastroenterology
dc.sourceScopus
dc.subjectCholangiopancreatography, endoscopic retrograde
dc.subjectHumans
dc.subjectIndomethacin
dc.subjectNitrates
dc.subjectPancreatitis
dc.subjectAmylase
dc.subjectIndometacin
dc.subjectIsosorbide dinitrate
dc.subjectPlacebo
dc.subjectAbdominal pain
dc.subjectAcute pancreatitis
dc.subjectAdult
dc.subjectAged
dc.subjectAmylase blood level
dc.subjectArticle
dc.subjectBleeding
dc.subjectChemoprophylaxis
dc.subjectCholangitis
dc.subjectClinical evaluation
dc.subjectCombination chemotherapy
dc.subjectComparative effectiveness
dc.subjectControlled study
dc.subjectDizziness
dc.subjectDouble blind procedure
dc.subjectDrug efficacy
dc.subjectDrug induced headache
dc.subjectDrug safety
dc.subjectEndoscopic retrograde cholangiopancreatography
dc.subjectFemale
dc.subjectHigh risk patient
dc.subjectHuman
dc.subjectMajor clinical study
dc.subjectMale
dc.subjectMiddle aged
dc.subjectMonotherapy
dc.subjectPerforation
dc.subjectPriority journal
dc.subjectRandomized controlled trial
dc.subjectRisk reduction
dc.subjectSuppository
dc.subjectTreatment outcome
dc.titleA randomized trial of rectal indomethacin and sublingual nitrates to prevent post-ERCP pancreatitis
dc.typeArticle

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