Prevention of nonsteroidal anti-inflammatory drug-induced small-intestinal injury by prostaglandin: a pilot randomized controlled trial evaluated by capsule endoscopy

Gastrointest Endosc. 2009 Jun;69(7):1339-46. doi: 10.1016/j.gie.2008.08.017. Epub 2009 Feb 24.

Abstract

Background: There is no known preventive agent against nonsteroidal anti-inflammatory drug (NSAID) induced small-intestinal injury.

Objective: To evaluate by capsule endoscopy whether coadministration of prostaglandin (PG) can prevent small-intestinal damage induced by short-term NSAID treatment.

Design: Single-blind, randomized, controlled trial.

Setting: All procedures were performed at Nippon Medical School.

Subjects: Thirty-four healthy male volunteers.

Methods: All subjects were randomly assigned to 2 groups: an NSAID-control group, who underwent NSAID (diclofenac sodium, 25 mg 3 times daily) and omeprazole (20 mg once daily) treatment, and an NSAID-PG group, who received PG (misoprostol, 200 microg 3 times daily) in addition to the same NSAID-omeprazole treatment. Eligible subjects, 15 per group, underwent capsule endoscopy before and 14 days after treatment.

Main outcome measurements: The number of mucosal breaks at capsule endoscopy.

Results: NSAID treatment significantly increased the mean (SD) number of mucosal breaks per subject, from a basal level of 0.1 +/- 0.3 up to 2.9 +/- 6.3 lesions in the NSAID-control group (P = .012). In contrast, there was no significant change in the mean number of mucosal breaks before and after PG cotreatment (P = 0.42). Thus, the mean number of posttreatment mucosal breaks per subject was significantly higher in the NSAID-control group than in the NSAID-PG group (P = .028). There was a significant increase in the percentage of subjects in the NSAID-control group, with at least 1 mucosal break after treatment (from 6.7% to 53.3%), whereas there was no change in the incidence of mucosal breaks in the NSAID-PG group, which remained at 13.3%. (P = .002).

Limitations: Single-center, open-label study.

Conclusions: PG cotherapy reduced the incidence of small-intestinal lesions induced by a 2-week administration of diclofenac sodium.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects*
  • Capsule Endoscopy
  • Diclofenac / adverse effects*
  • Humans
  • Intestinal Diseases / chemically induced*
  • Intestinal Diseases / prevention & control
  • Intestinal Mucosa / drug effects
  • Intestinal Mucosa / injuries
  • Intestine, Small / drug effects
  • Intestine, Small / injuries
  • Male
  • Middle Aged
  • Misoprostol / therapeutic use*
  • Omeprazole / administration & dosage
  • Prostaglandins E, Synthetic / therapeutic use*
  • Proton Pump Inhibitors / administration & dosage
  • Single-Blind Method
  • Young Adult

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Prostaglandins E, Synthetic
  • Proton Pump Inhibitors
  • Misoprostol
  • Diclofenac
  • Omeprazole