PMID- 16651060 OWN - NLM STAT- MEDLINE DCOM- 20060516 LR - 20181201 IS - 1555-7162 (Electronic) IS - 0002-9343 (Linking) VI - 119 IP - 5 DP - 2006 May TI - Comparing rates of dyspepsia with Coxibs vs NSAID+PPI: a meta-analysis. PG - 448.e27-36 AB - PURPOSE: Because dyspeptic symptoms are far more prevalent than ulcer complications in users of nonsteroidal anti-inflammatory drugs (NSAIDs), economic models indicate that dyspepsia rates (not ulcer complications) are the major determinant of cost-effectiveness in treating arthritis. We performed a meta-analysis to compare rates of dyspepsia for two common therapies in high-risk patients with arthritis: cyclooxygenase-2 inhibitor (Coxib) alone and combination therapy with a nonselective NSAID and a proton pump inhibitor (PPI) (NSAID+PPI). METHODS: We performed a systematic review to identify trials comparing either a Coxib versus NSAID or NSAID+PPI versus NSAID in chronic arthritis. We selected studies that report incident dyspepsia, defined a priori as "epigastric pain," "dyspepsia," and "nausea." We then performed meta-analysis to compare the relative risk reduction and absolute risk reduction of dyspepsia for Coxib versus NSAID and NSAID+PPI versus NSAID. RESULTS: Meta-analysis of 26 studies comparing dyspepsia between Coxibs and NSAIDs revealed a 12% relative risk reduction for Coxibs with an absolute risk reduction of 3.7%. Meta-analysis of four studies comparing dyspepsia between the NSAID+PPI combination and NSAIDs alone revealed a 66% relative risk reduction for NSAID+PPI with an absolute risk reduction of 9%. Compared with the NSAID strategy, the number needed to treat to prevent dyspepsia was 27 for Coxibs and 11 for NSAID+PPI. CONCLUSION: NSAID+PPI affords greater risk reduction for dyspepsia than Coxibs when compared with the common baseline of NSAIDs. Because there are limited head-to-head data comparing Coxibs versus NSAID+PPI, these data provide the best indirect evidence that NSAID+PPI may be superior to Coxibs in minimizing incident dyspepsia. FAU - Spiegel, Brennan M R AU - Spiegel BM AD - Division of Gastroenterology and Hepatology, Veterans Affairs Greater Los Angeles Healthcare System, Los Angeles, Calif 90073, USA. bspiegel@mednet.ucla.edu FAU - Farid, Mary AU - Farid M FAU - Dulai, Gareth S AU - Dulai GS FAU - Gralnek, Ian M AU - Gralnek IM FAU - Kanwal, Fasiha AU - Kanwal F LA - eng PT - Comparative Study PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, Non-P.H.S. PT - Systematic Review PL - United States TA - Am J Med JT - The American journal of medicine JID - 0267200 RN - 0 (Anti-Inflammatory Agents, Non-Steroidal) RN - 0 (Cyclooxygenase 2 Inhibitors) RN - 0 (Enzyme Inhibitors) RN - 0 (Proton Pump Inhibitors) SB - IM MH - Anti-Inflammatory Agents, Non-Steroidal/*adverse effects/therapeutic use MH - Arthritis/drug therapy MH - Cyclooxygenase 2 Inhibitors/*adverse effects/therapeutic use MH - Drug Therapy, Combination MH - Dyspepsia/*chemically induced/epidemiology MH - Enzyme Inhibitors/*adverse effects/therapeutic use MH - Humans MH - Incidence MH - *Proton Pump Inhibitors MH - Risk Factors EDAT- 2006/05/03 09:00 MHDA- 2006/05/17 09:00 CRDT- 2006/05/03 09:00 PHST- 2005/09/06 00:00 [received] PHST- 2005/11/20 00:00 [revised] PHST- 2005/11/21 00:00 [accepted] PHST- 2006/05/03 09:00 [pubmed] PHST- 2006/05/17 09:00 [medline] PHST- 2006/05/03 09:00 [entrez] AID - S0002-9343(05)01139-3 [pii] AID - 10.1016/j.amjmed.2005.11.020 [doi] PST - ppublish SO - Am J Med. 2006 May;119(5):448.e27-36. doi: 10.1016/j.amjmed.2005.11.020.