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• W2103377881 abstract "Background The efficacy of many pharmacological agents for preventing post-ERCP pancreatitis (PEP) has been evaluated in randomised controlled trials (RCTs), but it is unclear which agent(s) should be used in clinical practice. Network meta-analyses of RCTs are used to simultaneously compare several agents to determine their relative efficacy and identify priority agents for comparison in future RCTs. Aim To evaluate pharmacological agents for the prevention of PEP by conducting a network meta-analysis of RCTs. Methods We searched MEDLINE, EMBASE and Cochrane Library databases for RCTs that evaluated the efficacy of agents for preventing PEP. RCTs were simultaneously analysed using random-effects network meta-analysis under the Bayesian framework to identify the best agents. The efficacy of agents was ordered according to the probability of being ranked as any of the top three best performing agents. Results The network meta-analysis included 99 RCTs evaluating 16 agents in 25 313 patients. Topical epinephrine (adrenaline) was the most efficacious agent with 85.9% probability of ranking among the top three agents, followed by nafamostat (51.4%), antibiotics (44.5%) and NSAIDs (42.8%). However, in a sensitivity analysis including only rectal NSAIDs, NSAIDs moved from fourth rank to second (58.1%). Patients receiving topical epinephrine, compared with placebo, had a 75% reduced risk of PEP (OR 0.25, 95% probability interval 0.06–0.66). Conclusions Topical epinephrine and rectal NSAIDs are the most efficacious agents for preventing post-ERCP pancreatitis, based on existing RCTs. Combinations of these agents, which act on different steps in the pathogenesis of post-ERCP pancreatitis, should be evaluated in future trials." @default.
• W2103377881 created "2016-06-24" @default.
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• W2103377881 date "2013-10-20" @default.
• W2103377881 modified "2023-10-17" @default.
• W2103377881 title "Systematic review with network meta-analysis: pharmacological prophylaxis against post-ERCP pancreatitis" @default.
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• W2103377881 doi "https://doi.org/10.1111/apt.12534" @default.
• W2103377881 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24138390" @default.
• W2103377881 hasPublicationYear "2013" @default.
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