Patient selection for urgent endoscopic retrograde cholangio-pancreatography by endoscopic ultrasound in predicted severe acute biliary pancreatitis (APEC-2): a multicentre prospective study

医学 内镜逆行胰胆管造影术 胆结石 急性胰腺炎 胰腺炎 内镜超声 胆总管 临床终点 前瞻性队列研究 外科 内科学 胃肠病学 随机对照试验
作者
Nora D. Hallensleben,Pauline M. C. Stassen,Nicolien J. Schepers,Marc G. Besselink,Marie-Paule Anten,Olaf J. Bakker,Thomas L. Bollen,David W. da Costa,Sven M. van Dijk,Hendrik M. van Dullemen,Marcel G. W. Dijkgraaf,Brechje C van Eijck,Casper H.J. van Eijck,Willemien Erkelens,Nicole S. Erler,Paul Fockens,Erwin-Jan M. van Geenen,Janneke van Grinsven,Wouter L. Hazen,Robbert A. Hollemans
出处
期刊:Gut [BMJ]
卷期号:72 (8): 1534-1542 被引量:29
标识
DOI:10.1136/gutjnl-2022-328258
摘要

OBJECTIVE: Routine urgent endoscopic retrograde cholangiopancreatography (ERCP) with endoscopic biliary sphincterotomy (ES) does not improve outcome in patients with predicted severe acute biliary pancreatitis. Improved patient selection for ERCP by means of endoscopic ultrasonography (EUS) for stone/sludge detection may challenge these findings. DESIGN: A multicentre, prospective cohort study included patients with predicted severe acute biliary pancreatitis without cholangitis. Patients underwent urgent EUS, followed by ERCP with ES in case of common bile duct stones/sludge, within 24 hours after hospital presentation and within 72 hours after symptom onset. The primary endpoint was a composite of major complications or mortality within 6 months after inclusion. The historical control group was the conservative treatment arm (n=113) of the randomised APEC trial (Acute biliary Pancreatitis: urgent ERCP with sphincterotomy versus conservative treatment, patient inclusion 2013-2017) applying the same study design. RESULTS: Overall, 83 patients underwent urgent EUS at a median of 21 hours (IQR 17-23) after hospital presentation and at a median of 29 hours (IQR 23-41) after start of symptoms. Gallstones/sludge in the bile ducts were detected by EUS in 48/83 patients (58%), all of whom underwent immediate ERCP with ES. The primary endpoint occurred in 34/83 patients (41%) in the urgent EUS-guided ERCP group. This was not different from the 44% rate (50/113 patients) in the historical conservative treatment group (risk ratio (RR) 0.93, 95% CI 0.67 to 1.29; p=0.65). Sensitivity analysis to correct for baseline differences using a logistic regression model also showed no significant beneficial effect of the intervention on the primary outcome (adjusted OR 1.03, 95% CI 0.56 to 1.90, p=0.92). CONCLUSION: In patients with predicted severe acute biliary pancreatitis without cholangitis, urgent EUS-guided ERCP with ES did not reduce the composite endpoint of major complications or mortality, as compared with conservative treatment in a historical control group. TRIAL REGISTRATION NUMBER: ISRCTN15545919.
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