Clopidogrel with or without Omeprazole in Coronary Artery Disease

Клопидогрел с омепразолом или без него при ишемической болезни сердца
Pablo Lapuerta, Marc Cohen, Sabina A. Murphy, Deepak L. Bhatt, Christopher P. Cannon, Benjamin M. Scirica, Thomas J. Schnitzer, Loren Laine, Charles F. Contant, Thomas Shook, Byron Cryer, Angel Lanas, Mark A. Goldsmith
2010-10-06

ClopidogrelDual antiplatelet therapyOmeprazoleProton-pump inhibitorsUpper gastrointestinal bleeding
BACKGROUND: Gastrointestinal complications are an important problem of antithrombotic therapy. Proton-pump inhibitors (PPIs) are believed to decrease the risk of such complications, though no randomized trial has proved this in patients receiving dual antiplatelet therapy. Recently, concerns have been raised about the potential for PPIs to blunt the efficacy of clopidogrel. METHODS: We randomly assigned patients with an indication for dual antiplatelet therapy to receive clopidogrel in combination with either omeprazole or placebo, in addition to aspirin. The primary gastrointestinal end point was a composite of overt or occult bleeding, symptomatic gastroduodenal ulcers or erosions, obstruction, or perforation. The primary cardiovascular end point was a composite of death from cardiovascular causes, nonfatal myocardial infarction, revascularization, or stroke. The trial was terminated prematurely when the sponsor lost financing. RESULTS: We planned to enroll about 5000 patients; a total of 3873 were randomly assigned and 3761 were included in analyses. In all, 51 patients had a gastrointestinal event; the event rate was 1.1% with omeprazole and 2.9% with placebo at 180 days (hazard ratio with omeprazole, 0.34, 95% confidence interval [CI], 0.18 to 0.63; P<0.001). The rate of overt upper gastrointestinal bleeding was also reduced with omeprazole as compared with placebo (hazard ratio, 0.13; 95% CI, 0.03 to 0.56; P = 0.001). A total of 109 patients had a cardiovascular event, with event rates of 4.9% with omeprazole and 5.7% with placebo (hazard ratio with omeprazole, 0.99; 95% CI, 0.68 to 1.44; P = 0.96); high-risk subgroups did not show significant heterogeneity. The two groups did not differ significantly in the rate of serious adverse events, though the risk of diarrhea was increased with omeprazole. CONCLUSIONS: Among patients receiving aspirin and clopidogrel, prophylactic use of a PPI reduced the rate of upper gastrointestinal bleeding. There was no apparent cardiovascular interaction between clopidogrel and omeprazole, but our results do not rule out a clinically meaningful difference in cardiovascular events due to use of a PPI. (Funded by Cogentus Pharmaceuticals; ClinicalTrials.gov number, NCT00557921.).
1
Cardiovascular event rates were similar with omeprazole and placebo (4.9% versus 5.7%; hazard ratio, 0.99; P=0.96), showing no apparent attenuation of clopidogrel efficacy.
2
In patients receiving aspirin and clopidogrel, omeprazole reduced gastrointestinal events at 180 days from 2.9% to 1.1% versus placebo.
3
Omeprazole significantly reduced overt upper gastrointestinal bleeding compared with placebo (hazard ratio, 0.13; 95% CI, 0.03–0.56).
4
Serious adverse events did not differ significantly, although diarrhea occurred more frequently with omeprazole.
5
The prematurely terminated trial randomized 3873 patients, with 3761 included in the analyses, fewer than the planned approximately 5000 participants.

Patients with coronary artery disease receiving aspirin and clopidogrel dual antiplatelet therapy

The effects of prophylactic omeprazole on gastrointestinal and cardiovascular clinical outcomes, including bleeding and cardiovascular events

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2010-10-06
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Pablo Lapuerta
Marc Cohen
Sabina A. Murphy
Deepak L. Bhatt
Christopher P. Cannon
Benjamin M. Scirica
Thomas J. Schnitzer
Loren Laine
Charles F. Contant
Thomas Shook
Byron Cryer
Angel Lanas
Mark A. Goldsmith
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