Key result
Celecoxib use was not associated with a significantly different risk of hospitalization for acute myocardial infarction compared to rofecoxib (HR 0.90; 95% CI 0.79-1.01).
Why the study?
The association between rofecoxib, celecoxib, diclofenac, ibuprofen and risk of hospitalization for AMI in elderly patients was unclear.
Cohort (n=283,784)
No difference in AMI risk supports similar profiles but does not change practice; leaves open need for randomized NSAID safety trials.
PURPOSE: To evaluate the association between rofecoxib, celecoxib, diclofenac, and ibuprofen and the risk of hospitalization for acute myocardial infarction (AMI) in an elderly population. METHODS: We conducted a retrospective cohort study, using data from the government of Quebec health insurance agency databases, among patients 65-80 years of age who filled a prescription for any of the study drugs during 1999-2002. Cox regression models with time-dependent exposure were used to compare the incidence rates of hospitalization for AMI adjusting for patients' baseline characteristics. Analyses stratified by dose and number of supplied days were also conducted. RESULTS: At the index date, a total of 91 062 patients were taking rofecoxib, 127 928 celecoxib, 49 193 diclofenac, and 15 601 ibuprofen. The adjusted hazard ratio (HR) (95%CI) of hospitalization for AMI were: celecoxib versus rofecoxib: 0.90 (0.79, 1.01); ibuprofen versus rofecoxib: 0.95 (0.65, 1.37); diclofenac versus rofecoxib: 1.01 (0.84, 1.22). In secondary analyses based on intended duration of use, neither COX-2 selective inhibitor was associated with a higher risk than ibuprofen or diclofenac. The unadjusted risk of AMI for all NSAIDs increased with dose. In the direct two way adjusted comparison of each NSAID stratified by dose, the only statistically significant difference was with rofecoxib >25 mg/day versus celecoxib >200 mg/day. CONCLUSION: In this study there was no difference between AMI occurrence in elderly patients taking rofecoxib or celecoxib at recommended doses for chronic indications versus those taking ibuprofen/diclofenac. However, the risk of AMI was higher among patients using higher doses of rofecoxib (>25 mg/day) compared to patients using higher doses of celecoxib (>200 mg/day).
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Rahme et al. (2006) conducted a cohort in Acute myocardial infarction risk among NSAID users (n=283,784). Celecoxib vs. Rofecoxib was evaluated on Hospitalization for acute myocardial infarction (AMI) (HR 0.90, 95% CI 0.79-1.01). Celecoxib use was not associated with a significantly different risk of hospitalization for acute myocardial infarction compared to rofecoxib (HR 0.90; 95% CI 0.79-1.01).
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