Abstract | BACKGROUND: METHODS: In this randomized, double-blind study involving 10 days of treatment and 30 days of follow-up, 1671 patients were randomly assigned to receive intravenous parecoxib for at least 3 days, followed by oral valdecoxib through day 10; intravenous placebo followed by oral valdecoxib; or placebo for 10 days. All patients had access to standard opioid medications. The primary end point was the frequency of predefined adverse events, including cardiovascular events, renal failure or dysfunction, gastroduodenal ulceration, and wound-healing complications. RESULTS: As compared with the group given placebo alone, both the group given parecoxib and valdecoxib and the group given placebo and valdecoxib had a higher proportion of patients with at least one confirmed adverse event (7.4 percent in each of these two groups vs. 4.0 percent in the placebo group; risk ratio for each comparison, 1.9; 95 percent confidence interval, 1.1 to 3.2; P=0.02 for each comparison with the placebo group). In particular, cardiovascular events (including myocardial infarction, cardiac arrest, stroke, and pulmonary embolism) were more frequent among the patients given parecoxib and valdecoxib than among those given placebo (2.0 percent vs. 0.5 percent; risk ratio, 3.7; 95 percent confidence interval, 1.0 to 13.5; P=0.03). CONCLUSIONS: The use of parecoxib and valdecoxib after CABG was associated with an increased incidence of cardiovascular events, arousing serious concern about the use of these drugs in such circumstances.
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Authors | Nancy A Nussmeier, Andrew A Whelton, Mark T Brown, Richard M Langford, Andreas Hoeft, Joel L Parlow, Steven W Boyce, Kenneth M Verburg |
Journal | The New England journal of medicine
(N Engl J Med)
Vol. 352
Issue 11
Pg. 1081-91
(Mar 17 2005)
ISSN: 1533-4406 [Electronic] United States |
PMID | 15713945
(Publication Type: Clinical Trial, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | Copyright 2005 Massachusetts Medical Society. |
Chemical References |
- Cyclooxygenase Inhibitors
- Isoxazoles
- Sulfonamides
- valdecoxib
- parecoxib
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Topics |
- Administration, Oral
- Adult
- Aged
- Cardiovascular Diseases
(chemically induced, epidemiology, mortality)
- Coronary Artery Bypass
(mortality)
- Cyclooxygenase Inhibitors
(adverse effects, therapeutic use)
- Double-Blind Method
- Female
- Humans
- Infusions, Intravenous
- Isoxazoles
(adverse effects, therapeutic use)
- Male
- Middle Aged
- Pain, Postoperative
(drug therapy)
- Sulfonamides
(adverse effects, therapeutic use)
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