Effect of Concomitant Use of Clopidogrel and Proton Pump Inhibitors After Percutaneous Coronary Intervention

被引:52
作者
Banerjee, Subhash [1 ,2 ]
Weideman, Rick A. [1 ]
Weideman, Mark W. [1 ]
Little, Bertis B. [1 ,3 ]
Kelly, Kevin C. [1 ]
Gunter, Jennifer T. [1 ]
Tortorice, Kathryn L. [4 ]
Shank, Michelle [5 ]
Cryer, Byron [1 ,2 ]
Reilly, Robert F. [1 ,2 ]
Rao, Sunil V. [6 ]
Kastrati, Adnan [7 ]
de Lemos, James A. [2 ]
Brilakis, Emmanouil S. [1 ,2 ]
Bhatt, Deepak L. [8 ]
机构
[1] Vet Affairs N Texas Hlth Care Syst, Dallas, TX USA
[2] Univ Texas SW Med Ctr Dallas, Dallas, TX 75390 USA
[3] Tarleton State Univ, Stephenville, TX USA
[4] Vet Affairs Pharm Benefits Management, Hines, IL USA
[5] Vet Affairs Pharm Benefits Management, VISN 17, Arlington, TX USA
[6] Duke Univ, Med Ctr, Durham Vet Affairs Med Ctr, Durham, NC USA
[7] Deutsch Herzzentrum Munich, Munich, Germany
[8] Harvard Univ, Brigham & Womens Hosp, Sch Med, Vet Affairs Boston Hlth Care Syst, Boston, MA 02115 USA
关键词
GASTROESOPHAGEAL-REFLUX; MYOCARDIAL-INFARCTION; ANTIPLATELET THERAPY; AMERICAN-COLLEGE; TASK-FORCE; IMPACT; RISK; PREVALENCE; OMEPRAZOLE; MANAGEMENT;
D O I
10.1016/j.amjcard.2010.10.073
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of the present study was to analyze the effect of drug exposure patterns of clopidogrel and proton pump inhibitors (PPIs) on the clinical outcomes after percutaneous coronary intervention (PCI). Previous analyses predominantly included discharge medications and did not explore the effect of the drug exposure patterns. We analyzed all-cause death, nonfatal myocardial infarction, repeat revascularization, and major adverse cardiovascular events (MACE) in a cohort of 23,200 post-PCI patients (January 2003 to December 2008) using a multivariate adjusted Cox model and propensity-matched case-control analysis. The adjusted hazard ratio for MACE on PPI according to the exposure patterns of clopidogrel after PCI for 6 years was 1.24(95% confidence interval [CI] 1.11 to 1.38) and 1.12 (95% CI 1.03 to 1.22) for "continuous" (consistent clopidogrel with or without PPIs) and "switched" (clopidogrel with or without varying PPIs) respectively. However, the propensity score adjusted odds ratios for MACE on PPI use was 0.97 (95% CI 0.65 to 1.44) for "continuous" and 1.04 (95% CI 0.87 to 1.25) for "switched." Moreover, in the first year after PCI, the use of "rescue" (<= 30 days before MACE) nitroglycerin was greater in the patients taking clopidogrel and PPIs than in those taking clopidogrel alone, as was the overall use of rescue PPIs (p < 0.001). In conclusion, PPI use in clopidogrel-treated post-PCI patients was not associated with an increased risk of MACE after controlling for the confounding effect of PPI use with propensity matching. A potential for the misdiagnosis of angina symptoms and rescue use of nitroglycerin and PPIs in post-PCI patients exists, a finding that might have confounded previous observational analyses. Published by Elsevier Inc. (Am J Cardiol 2011;107:871-878)
引用
收藏
页码:871 / 878
页数:8
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