Somatostatin or octreotide for acute bleeding oesophageal varices
- PMID: 10796699
- DOI: 10.1002/14651858.CD000193
Somatostatin or octreotide for acute bleeding oesophageal varices
Update in
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Somatostatin analogues for acute bleeding oesophageal varices.Cochrane Database Syst Rev. 2002;(1):CD000193. doi: 10.1002/14651858.CD000193. Cochrane Database Syst Rev. 2002. Update in: Cochrane Database Syst Rev. 2005 Jan 25;(1):CD000193. doi: 10.1002/14651858.CD000193.pub2. PMID: 11869569 Updated.
Abstract
Background: Somatostatin and its derivative, octreotide, are often used for emergency treatment of bleeding oesophageal varices in patients with cirrhosis of the liver. The placebo controlled trials have shown varying results, however, and their power has been quite low. An updated systematic review of a previously published meta-analysis was therefore performed.
Objectives: To study whether somatostatin or octreotide improve survival or reduce the number of blood transfusions in patients with suspected or verified acute or recently bleeding oesophageal varices.
Search strategy: MEDLINE and The Cochrane Library are searched every three months. Reference lists of articles and authors.
Selection criteria: All randomised trials comparing somatostatin or octreotide with placebo or no treatment in patients suspected of acute bleeding from oesophageal varices.
Data collection and analysis: The effect variables extracted were: mortality, number of blood transfusions, number with balloon tamponade, number with initial haemostasis and number with rebleeding. Intention to treat analyses were conducted; a random effects analysis was preferred if there was significant heterogeneity between the trials (p<0.10).
Main results: The meta-analysis comprised 820 patients. The active drugs had no effect on survival; a total of 91 patients died in the experimental groups vs 85 patients in the control groups (odds ratio 1.04, 95% confidence interval (CI) 0.74 to 1.46). The number of transfusions was less with drugs, the difference between experimental and control therapy was 1.2 units of blood products saved per patient (95% CI 0. 8 to 1.6). There were no significant differences in use of balloon tamponade (odds ratio 0.59, 95% CI 0.21 to 1.70), number of patients failing initial haemostasis (odds ratio 0.66, 95% CI 0.32 to 1.37) or number with rebleeding (odds ratio 0.73, 95% CI 0.30 to 1.79). It should be noted, however, that the trials were heterogeneous with respect to these secondary variables.
Reviewer's conclusions: The effect corresponded to one unit of blood saved per patient. This effect is small and treatment with these drugs in acute bleeding oesophageal varices is therefore of doubtful value. This does not suggest a need for further studies. On the other hand, the confidence interval for the effect on mortality was wide. Hence, a large placebo controlled trial is needed if one wishes to rule out the possibility that a worthwhile effect on mortality may have been overlooked.
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