COX-2 inhibitors: complex association with lower risk of hospitalization for gastrointestinal events compared to traditional NSAIDs plus proton pump inhibitors
Purpose To compare hospitalization rates for serious upper and lower gastrointestinal (GI) events between chronic and acute users of a traditional non‐steroidal anti‐inflammatory drugs (tNSAID) + proton pump inhibitor (PPI) and users of a COX‐2 selective inhibitor (Coxib). Methods The PHARMO Record...
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Published in: | Pharmacoepidemiology and drug safety Vol. 18; no. 10; pp. 880 - 890 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Chichester, UK
John Wiley & Sons, Ltd
01-10-2009
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Subjects: | |
Online Access: | Get full text |
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Summary: | Purpose
To compare hospitalization rates for serious upper and lower gastrointestinal (GI) events between chronic and acute users of a traditional non‐steroidal anti‐inflammatory drugs (tNSAID) + proton pump inhibitor (PPI) and users of a COX‐2 selective inhibitor (Coxib).
Methods
The PHARMO Record Linkage System, including linked drug‐dispensing and hospital records of approximately 3 million individuals in the Netherlands was used. We selected new Coxib or tNSAID users (01/01/2000–31/12/2004) with ≥1 year history before the first NSAID dispensing and ≥1 year follow‐up ending at the first hospitalization for GI event (the outcome), last dispensing, or end of the study period. Chronic users were patients who used any NSAIDs for ≥60 days during the first year (n = 58 770); others were acute users (n = 538 420). Multivariate analysis was performed by Poisson regression adjusted for gender, age, and duration of follow‐up, tNSAID and Coxib dose, NSAID/PPI adherence, use of other gastroprotective agents, anticoagulants, acetaminophen, corticosteroids, and cardiovascular disease.
Results
The cohort included 23 999 new tNSAIDs + PPI users and 25 977 new Coxib users, with main characteristics: mean ± SD age 58.1 ± 15.5 vs. 56.7 ± 17.5; female 55.3% vs. 62.2%; duration of treatment (days): 137 ± 217 vs. 138 ± 179, respectively. Among acute users, adjusted hazard ratios (95% Confidence Interval) were 0.21 (0.14–0.32) for upper and 0.26 (0.16–0.42) for lower GI events, for Coxib versus tNSAIDs + PPI users. Among chronic users, these were 0.35 (0.22–0.55) for upper GI and 0.43 (0.25–0.75) for lower GI events.
Conclusions
Coxib users had significantly lower rates of GI events. Further research should elucidate the possible impact of selection bias. Copyright © 2009 John Wiley & Sons, Ltd. |
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Bibliography: | ark:/67375/WNG-3W0HXW8K-7 Conflict of interest statements: M.W. van der Linden, M.P.P. van Herk-Sukel, and R.M.C. Herings are employees of the PHARMO Institute. The PHARMO Institute has received financial support for research from various pharmaceutical companies including Merck & Co., Inc., Whitehouse Station, NJ, USA. At the time of preparing the manuscript, S.S. Sen and S. Gaugris were employees of Merck & Co., Inc., Whitehouse Station, NJ, USA. istex:DDFA89EE03A570D37F3C4AF3BF2F07497C6ABFB3 ArticleID:PDS1782 Director. Conflict of interest statements: M.W. van der Linden, M.P.P. van Herk‐Sukel, and R.M.C. Herings are employees of the PHARMO Institute. The PHARMO Institute has received financial support for research from various pharmaceutical companies including Merck & Co., Inc., Whitehouse Station, NJ, USA. At the time of preparing the manuscript, S.S. Sen and S. Gaugris were employees of Merck & Co., Inc., Whitehouse Station, NJ, USA. |
ISSN: | 1053-8569 1099-1557 |
DOI: | 10.1002/pds.1782 |