4.2 Article

Non-aspirin NSAIDs, cyclooxygenase-2 inhibitors and risk for cardiovascular events-stroke, acute myocardial infarction, and death from coronary heart disease

Journal

PHARMACOEPIDEMIOLOGY AND DRUG SAFETY
Volume 18, Issue 11, Pages 1053-1063

Publisher

WILEY
DOI: 10.1002/pds.1820

Keywords

cardiovascular disease; stroke; myocardial infarction; epidemiology; NSAIDs

Funding

  1. Department of Veterans Affairs Clinical Research Center of Excellence
  2. VA Career Development [04-342-2]
  3. VA Geriatric Research, Education and Clinical Center (GRECC)
  4. Targeted Research Enhancement Program (TREP)
  5. Center for Patient Healthcare Behavior [TRP 03-073]
  6. Vanderbilt Center for Education and Research
  7. Vanderbilt Center for Education and Research on Therapeutics
  8. Vanderbilt University School of Medicine
  9. Pfizer

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Purpose To determine if certain non-steroidal anti-inflammatory drugs (NSAIDs) are associated with increased risk of cardiovascular events: acute myocardial infarction (AMI), stroke, and death from coronary heart disease (CHD). Methods We conducted a retrospective cohort study of Tennessee Medicaid enrollees aged 35-94 years between 1 January 1999 and 31 December 2005. Eligible persons were non-institutionalized, had continuous enrollment, and had no serious illness prior to cohort entry. Exposure to celecoxib, rofecoxib, valdecoxib, ibuprofen, naproxen, diclofenac, and indomethacin was studied. The outcome was hospitalization for AMI, stroke, or death from CHD among those with and without a history of cardiovascular disease (CVD). Adjusted hazard ratios (aHR) and 95% confidence intervals (95% CI) are reported. Results There were 610001 persons in the final cohort and 14% had a baseline history of CVD. In those without CVD (N=525 249) there were 1566678 person-years of follow-up and 12 184 events. In this group, non-users had 7.90 events/1000 person-years. Events/1000 person-years were 10.41 for current use of celecoxib (aHR 1.00, 95% CI 0.89-1.13), 10.91 for rofecoxib (aHR 1.21, 95% CI 1.07-1.37), 12.46 for valdecoxib(aHR 1.3095% CI 1.04-1.61), and 13.25 for indomethacin (aHR 1.36,95% CI 1.11-1.66) compared to non-users. Among patients with a past history of CVD (N=84752) there were 397977 person-years of follow-up and 10248 events. Non-users had 28.30 events/1000 person-years. Among those with CVD, rofecoxib use was associated with increased event rate (30.28 events/1000 person-years [aHR 1.21, 95% CI 1.08-1.37]) and naproxen was associated with a decreased event rate (22.66 events/1000 person-years [aHR 0.88, 95% CI 0.79-0.99]). Among new users, the results were similar except risk among naproxen users was no longer different than non-users. Conclusions We found an increased risk of cardiovascular events among all and new current users of rofecoxib, valdecoxib, and indomethacin in patients with no history of CVD. Among patients with CVD, all and new current rofecoxib use was associated with an increased risk of a cardiovascular event. Copyright (C) 2009 John Wiley & Sons, Ltd.

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