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Volume 4, Issue 12, Pages 1452-1458 (December 2006)


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Esomeprazole Versus Other Proton Pump Inhibitors in Erosive Esophagitis: A Meta-Analysis of Randomized Clinical Trials

Ian M. Gralnek§Corresponding Author Informationemail address, Gareth S. Dulai§, M. Brian Fennerty#1, Brennan M.R. Spiegel§

Background & Aims: There are limited data comparing the effectiveness of available proton pump inhibitors (PPIs) in erosive esophagitis (EE). We performed a meta-analysis to calculate the pooled effect of esomeprazole on healing rates, symptom relief, and adverse events versus competing PPIs in EE. Methods: We performed a structured electronic search of MEDLINE and EMBASE and reviewed published abstracts to identify English-language, randomized clinical trials from 1995–2005, comparing rates of endoscopic healing, symptom relief, and adverse events with esomeprazole versus alternative PPIs in the treatment of gastroesophageal reflux disease (GERD)/EE. We then performed meta-analysis to compare the relative risk (RR) of EE healing, symptom relief, and adverse events between study arms and calculated the absolute risk reduction and number needed to treat (NNT) for each outcome. Results: Meta-analysis was performed on 10 studies (n = 15,316). At 8 weeks, there was a 5% (RR, 1.05; 95% confidence interval, 1.02–1.08) relative increase in the probability of healing of EE with esomeprazole, yielding an absolute risk reduction of 4% and NNT of 25. The calculated NNTs by Los Angeles grade of EE (grades A–D) were 50, 33, 14, and 8, respectively. Last, esomeprazole conferred an 8% (RR, 1.08; 95% confidence interval, 1.05–1.11) relative increase in the probability of GERD symptom relief at 4 weeks. Conclusions: As compared with other PPIs, esomeprazole confers a statistically significant improvement, yet, clinically, only a modest overall benefit in 8-week healing and symptom relief in all-comers with EE. The clinical benefit of esomeprazole appears negligible in less severe erosive disease but might be important in more severe disease.

 Rambam Medical Center; Department of Gastroenterology, GI Outcomes Unit, Faculty of Medicine, Technion Institute of Technology, Haifa, Israel

 VA Greater Los Angeles Healthcare System; David Geffen School of Medicine at UCLA, Los Angeles, California

§ UCLA/VA Center for Outcomes Research and Education (CORE), Los Angeles, California

 CURE Digestive Diseases Research Center, Los Angeles, California

# Oregon Health & Sciences University, Portland, Oregon

 Southern California Permanente Medical Group, Bellflower, California

Corresponding Author InformationAddress requests for reprints to: Ian M. Gralnek, MD, MSHS, FASGE, Rappaport Faculty of Medicine, Technion Israel Institute of Technology, GI Outcomes Unit Department of Gastroenterology, Rambam Medical Center, Haifa, Israel. fax: +970-4-854-3058.

 Supported by VA HSR&D Advanced Research Career Development Award and VA HSR&D IIR 01-191-1 (I.M.G.); supported by VA HSR&D Research Career Development Award RCD 03-179-2 and by the CURE Digestive Diseases Research Center (NIH 2P30 DK 041301-17) (B.M.R.S.); and by a grant from EBMed with funding for the grant obtained from AstraZeneca.

1 M.B.F. is a consultant for TAP Pharmaceuticals, Santarus, AstraZeneca, Atlanta, and Axcan.

PII: S1542-3565(06)00941-4

doi:10.1016/j.cgh.2006.09.013


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