Intravenous pantoprazole as an adjuvant therapy following successful endoscopic treatment for peptic ulcer bleeding

Categoría Revisión sistemática
RevistaCanadian journal of gastroenterology = Journal canadien de gastroenterologie
Año 2009
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Background: Several studies have suggested that proton pump inhibitions are efficacious in preventing rebleeding when administered immediately after endoscopic treatments. However, there are limited clinical outcome data on the use of intravenous pantoprazole. Objective: To evaluate the efficacy of intravenous pantoprazole after succesful endoscopic treatment for peptic ulcer bleeding using evidence from ramdomized controlled trials (RCTs). Methods: The Cochrane Library, MEDLINE, EMBASE and several Chinese databases up to July 2008 were searched. RCTs that compared the relative effectiveness of intravenous pantoprazole with placebo, H2,receptor antagonist or other agents for patients with peptic ulcer bleeding who were pretreated with successful endoscopic therapies were retrieved. Results: Five RCTs comprising a total of 821 participants were included in the final meta-analysis. Overall, there were significant differences in ulcer rebleeding, (RR 0.31; 95% Cl 0.18 to 0.53; pooled rates were 4.7% for pantoprazole and 15.0% for control), surgical intervention (RR 0.28, 95% Cl 0.09 to 0.83; pooled rates were 1.4% in pantoprazole group versus 6.5% in control) and total length of hospital stay (weighted mean difference -1.53; 95% Cl -1.91 to -1.16), but not on mortality (RR 0.72, 95% Cl 0.29 to 1.81; pooled mortality rates were 1.9% for pantoprazole versus 2.8% for control) and btcod transfusion requirements (weighted mean difference -0,53; 95% Cl for random effects -1.04 to -0.02) when compared with control treatments. A series of subgroup analyses supported the results from the main analysis. Conclusions: Intravenous administration of pantoprazole After endoscopic therapy for peptic ulcer bleeding reduces rates of ulcer rebleeding, surgical intervention and overall duration of hospital stay, but not mortality and blood transfusion requirements compared with placebo, H2 receptor antagonist or somatostatin. © 2009 Pulsus Group Inc. All rights reserved.
Epistemonikos ID: bab2757664a2bf5ad6627ff07c3d6736fd4a8fc0
First added on: Jun 07, 2012