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Sclerotherapy with or without octreotide for acute variceal bleeding
I Besson1, P Ingrand, B Person
1Service d'Hépatogastroentérologie, Centre Hospitalier Universitaire de Poitiers, France.
The New England Journal of Medicine
|August 31, 1995
Summary
Adding octreotide to sclerotherapy significantly reduces rebleeding in patients with esophageal varices. This combination therapy improves survival without rebleeding compared to sclerotherapy alone, though overall mortality remains similar.
Area of Science:
- Gastroenterology
- Hepatology
- Interventional Endoscopy
Background:
- Esophageal varices pose a high risk of bleeding, rebleeding, and mortality despite sclerotherapy.
- Acute variceal bleeding necessitates effective management to prevent severe outcomes.
Purpose of the Study:
- To compare sclerotherapy alone versus sclerotherapy combined with octreotide for controlling acute variceal bleeding.
- To evaluate the efficacy of octreotide in preventing early rebleeding in patients with cirrhosis.
Main Methods:
- A double-blind, prospective trial involving 199 patients with cirrhosis and acute variceal bleeding.
- Patients received emergency sclerotherapy, followed by a continuous infusion of either octreotide (25 mcg/hr) or placebo for five days.
- The primary outcome was survival without rebleeding at five days post-sclerotherapy.
Main Results:
- The octreotide group showed a significantly higher survival rate without rebleeding (87%) compared to the placebo group (71%; P = 0.009).
- Patients receiving octreotide required fewer blood transfusions within 24 hours (1.2 units vs. 2.0 units; P = 0.006).
- Logistic regression identified treatment assignment and pre-treatment blood transfusion volume as independent predictors of survival without rebleeding.
Conclusions:
- Sclerotherapy combined with octreotide is more effective in controlling acute variceal bleeding than sclerotherapy alone.
- While octreotide improves outcomes regarding rebleeding, it does not significantly alter overall 15-day mortality rates.
- Side effects were minor and comparable between the octreotide and placebo groups.