No Benefit of Oral Diclofenac on Post-Endoscopic Retrograde Cholangiopancreatography Pancreatitis

Dig Dis Sci. 2016 Nov;61(11):3292-3301. doi: 10.1007/s10620-016-4251-x. Epub 2016 Jul 22.

Abstract

Background: Pancreatitis following endoscopic retrograde cholangiopancreatography (ERCP) is a serious complication. Rectal diclofenac (100 mg) has been shown to reduce the incidence of pancreatitis; however, this dosage form is unavailable in several countries.

Aims: We aimed to investigate the preventive effect of oral diclofenac on pancreatitis after ERCP in a multicenter, randomized, prospective, placebo-controlled, double-blind trial.

Methods: Patients undergoing a first ERCP in seven high-volume centers between July 2012 and August 2014 were considered eligible. Participants were administered oral diclofenac (50 mg) or placebo before and after ERCP. The primary endpoint was the incidence of pancreatitis. A subgroup analysis was performed for patients at high or low risk of pancreatitis. Secondary endpoints were pancreatic enzyme levels (amylase and lipase).

Results: We initially enrolled 430 patients (216 in the diclofenac and 214 in the placebo group), and 23 were excluded after randomization. The overall incidence of pancreatitis was 9.8 % (20/205) and 9.4 % (19/202) in the diclofenac and placebo groups, respectively (p = 0.90). The incidence of pancreatitis was 20.3 % (13/64) and 21.3 % (13/61) in patients at high risk of pancreatitis (p = 0.78) and 5.0 % (7/141) and 4.3 % (6/141) in patients at low risk of pancreatitis in the diclofenac and placebo groups (p = 0.94), respectively. There were no significant differences in serum amylase and lipase levels between the two groups before and 24 h after ERCP.

Conclusions: Oral administration of diclofenac before and after ERCP showed no benefit in the prevention of pancreatitis.

Clinical trials registry no: UMIN000008109.

Keywords: Diclofenac; Endoscopic retrograde cholangiopancreatography; Pancreaticobiliary disease; Pancreatitis.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial

MeSH terms

  • Administration, Oral
  • Aged
  • Aged, 80 and over
  • Amylases / blood
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Autoimmune Diseases / diagnosis
  • Autoimmune Diseases / immunology
  • Bile Duct Neoplasms / diagnosis
  • Cholangiopancreatography, Endoscopic Retrograde / adverse effects*
  • Cholangitis / diagnosis
  • Cholangitis / immunology
  • Cholelithiasis / diagnosis
  • Cholelithiasis / surgery
  • Diclofenac / therapeutic use*
  • Double-Blind Method
  • Female
  • Hospitals, University
  • Humans
  • Immunoglobulin G
  • Lipase / blood
  • Logistic Models
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Pancreatic Neoplasms / diagnosis
  • Pancreatitis / blood
  • Pancreatitis / diagnosis
  • Pancreatitis / etiology
  • Pancreatitis / prevention & control*
  • Postoperative Complications / blood
  • Postoperative Complications / etiology
  • Postoperative Complications / prevention & control*

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Immunoglobulin G
  • Diclofenac
  • Lipase
  • Amylases