Clopidogrel with or without Omeprazole in Coronary Artery Disease.

被引:875
作者
Bhatt, Deepak L. [1 ,2 ,3 ]
Cryer, Byron L. [4 ,5 ]
Contant, Charles F. [3 ]
Cohen, Marc [6 ]
Lanas, Angel [7 ]
Schnitzer, Thomas J. [8 ,9 ]
Shook, Thomas L. [10 ]
Lapuerta, Pablo [11 ]
Goldsmith, Mark A.
Laine, Loren [12 ]
Scirica, Benjamin M. [3 ]
Murphy, Sabina A. [3 ]
Cannon, Christopher P. [3 ]
机构
[1] VA Boston Healthcare Syst, Boston, MA 02132 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Brigham & Womens Hosp, Thrombolysis Myocardial Infarct TIMI Study Grp, Boston, MA 02115 USA
[4] Univ Texas SW, Dallas, TX USA
[5] VA N Texas Hlth Care Syst, Dallas, TX USA
[6] Newark Beth Israel Med Ctr, Newark, NJ USA
[7] Univ Zaragoza, Inst Aragones Ciencias Salud, Ctr Invest Biomed Red Enfermedades Hepat & Digest, Zaragoza, Spain
[8] Northwestern Univ, Feinberg Sch Med, Dept Phys Med & Rehabil, Chicago, IL 60611 USA
[9] Northwestern Univ, Feinberg Sch Med, Dept Internal Med Rheumatol, Chicago, IL 60611 USA
[10] Parexel Int, Waltham, MA USA
[11] Cogentus Pharmaceut, Menlo Pk, CA USA
[12] Univ So Calif, Los Angeles, CA USA
关键词
LOW-DOSE ASPIRIN; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; PROTON PUMP INHIBITORS; ST-SEGMENT ELEVATION; ANTIPLATELET-THERAPY; MYOCARDIAL-INFARCTION; STATIN-INTERACTION; CONTROLLED TRIAL; RISK; INTERVENTION;
D O I
10.1056/NEJMoa1007964
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.) N Engl J Med 2010;363:1909-17.
引用
收藏
页码:1909 / 1917
页数:9
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