Controlled trial of cimetidine in upper gastrointestinal haemorrhage

Gut
|October 1, 1979
PubMed

Insights

Oral cimetidine did not significantly prevent acute upper gastrointestinal bleeding recurrence in a double-blind trial. This study assessed cimetidine

Area of Science:

  • Gastroenterology
  • Clinical Pharmacology

Background:

  • Acute upper gastrointestinal hemorrhage is a significant clinical concern, often stemming from peptic ulcers.
  • Effective preventative strategies for bleeding continuation or recurrence are crucial for patient outcomes.

Purpose of the Study:

  • To evaluate the efficacy of oral cimetidine in preventing the continuation or recurrence of acute upper gastrointestinal hemorrhage.
  • To assess the role of cimetidine in patients with bleeding peptic ulcers and other upper GI sources.

Main Methods:

  • A double-blind, placebo-controlled trial involving 101 patients with acute upper gastrointestinal hemorrhage.
  • Patients received either oral cimetidine (800 mg loading dose, then 400 mg six-hourly) or a placebo.
  • Endoscopic evaluation was used to identify the source of bleeding in 96% of participants.

Main Results:

  • Bleeding continued or recurred in 21.5% of patients receiving cimetidine versus 24% receiving placebo.
  • Peptic ulcer was the primary source of bleeding, identified in 70% of cases.
  • No statistically significant advantage of cimetidine was observed when analyzed by patient age or bleeding severity.

Conclusions:

  • Oral cimetidine demonstrated no significant benefit in preventing the continuation or recurrence of acute upper gastrointestinal hemorrhage in this study population.
  • Further research may be needed to explore alternative or adjunctive therapies for managing upper GI bleeding.

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