Risk of Adverse Outcomes Associated With Concomitant Use of Clopidogrel and Proton Pump Inhibitors Following Acute Coronary Syndrome

被引:780
作者
Ho, P. Michael [1 ,2 ]
Maddox, Thomas M. [1 ,2 ]
Wang, Li [3 ]
Fihn, Stephan D. [3 ,4 ]
Jesse, Robert L. [4 ,5 ]
Peterson, Eric D. [6 ]
Rumsfeld, John S. [1 ,2 ]
机构
[1] Denver VA Med Ctr, Denver, CO USA
[2] Univ Colorado, Hlth Sci Ctr, Denver, CO USA
[3] VA Puget Sound Hlth Care Syst, Seattle, WA USA
[4] VA Cent Off, Washington, DC USA
[5] Richmond VA Med Ctr, Richmond, VA USA
[6] Duke Clin Res Inst, Durham, NC USA
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2009年 / 301卷 / 09期
基金
美国医疗保健研究与质量局;
关键词
ACUTE MYOCARDIAL-INFARCTION; OF-FUNCTION POLYMORPHISM; MEDICATION NONADHERENCE; ANTIPLATELET ACTION; TRIAL; ATORVASTATIN; THERAPY; ASPIRIN; RESISTANCE; REGRESSION;
D O I
10.1001/jama.2009.261
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Prior mechanistic studies reported that omeprazole decreases the platelet inhibitory effects of clopidogrel, yet the clinical significance of these findings is not clear. Objective To assess outcomes of patients taking clopidogrel with or without a proton pump inhibitor (PPI) after hospitalization for acute coronary syndrome (ACS). Design, Setting, and Patients Retrospective cohort study of 8205 patients with ACS taking clopidogrel after discharge from 127 Veterans Affairs hospitals between October 1, 2003, and January 31, 2006. Vital status information was available for all patients through September 30, 2006. Main Outcome Measures All-cause mortality or rehospitalization for ACS. Results Of 8205 patients taking clopidogrel after discharge, 63.9% (n = 5244) were prescribed PPI at discharge, during follow-up, or both and 36.1% (n = 2961) were not prescribed PPI. Death or rehospitalization for ACS occurred in 20.8% (n = 615) of patients taking clopidogrel without PPI and 29.8% (n = 1561) of patients taking clopidogrel plus PPI. In multivariable analyses, use of clopidogrel plus PPI was associated with an increased risk of death or rehospitalization for ACS compared with use of clopidogrel without PPI ( adjusted odds ratio [AOR], 1.25; 95% confidence interval [CI], 1.11-1.41). Among patients taking clopidogrel after hospital discharge and prescribed PPI at any point during follow-up (n = 5244), periods of use of clopidogrel plus PPI ( compared with periods of use of clopidogrel without PPI) were associated with a higher risk of death or rehospitalization for ACS (adjusted hazard ratio, 1.27; 95% CI, 1.10-1.46). In analyses of secondary outcomes, patients taking clopidogrel plus PPI had a higher risk of hospitalizations for recurrent ACS compared with patients taking clopidogrel without PPI (14.6% vs 6.9%; AOR, 1.86 [ 95% CI, 1.57-2.20]) and revascularization procedures (15.5% vs 11.9%; AOR, 1.49 [ 95% CI, 1.30-1.71]), but not for all-cause mortality (19.9% vs 16.6%; AOR, 0.91 [ 95% CI, 0.80-1.05]). The association between use of clopidogrel plus PPI and increased risk of adverse outcomes also was consistent using a nested case-control study design (AOR, 1.32; 95% CI, 1.14-1.54). In addition, use of PPI without clopidogrel was not associated with death or rehospitalization for ACS among patients not taking clopidogrel after hospital discharge (n = 6450) ( AOR, 0.98; 95% CI, 0.85-1.13). Conclusion Concomitant use of clopidogrel and PPI after hospital discharge for ACS was associated with an increased risk of adverse outcomes than use of clopidogrel without PPI, suggesting that use of PPI may be associated with attenuation of benefits of clopidogrel after ACS.
引用
收藏
页码:937 / 944
页数:8
相关论文
共 34 条
[1]   NONPARAMETRIC ESTIMATION OF PARTIAL TRANSITION-PROBABILITIES IN MULTIPLE DECREMENT MODELS [J].
AALEN, O .
ANNALS OF STATISTICS, 1978, 6 (03) :534-545
[2]  
*AM COLL CARD CV N, FDA INV INT PLAV HEA
[3]   ACC/AHA 2007 guide lines for the management of patients with unstable Angina/Non-ST-Elevation myocardial infraction - Executive summary [J].
Anderson, Jeffrey L. ;
Adams, Cynthia D. ;
Antman, Elliott M. ;
Bridges, Charles R. ;
Califf, Robert M. ;
Casey, Donald E., Jr. ;
Chavey, William E., II ;
Fesmire, Francis M. ;
Hochman, Judith S. ;
Levin, Thomas N. ;
Lincoff, A. Michael ;
Peterson, Eric D. ;
Theroux, Pierre ;
Wenger, Nanette Kass ;
Wright, R. Scott ;
Smith, Sidney C., Jr. ;
Jacobs, Alice K. ;
Adams, Cynthia D. ;
Riegel, Barbara .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2007, 50 (07) :652-726
[4]  
Aubert RE, 2008, CIRCULATION, V118, pS815
[5]   Resistance to thienopyridines: Clinical detection of coronary stent thrombosis by monitoring of vasodilator-stimulated phosphoprotein phosphorylation [J].
Barragan, P ;
Bouvier, JL ;
Roquebert, PO ;
Macaluso, G ;
Commeau, P ;
Comet, B ;
Lafont, A ;
Camoin, L ;
Walter, U ;
Eigenthaler, M .
CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS, 2003, 59 (03) :295-302
[6]   The metabolism of clopidogrel is catalyzed by human cytochrome P450 3A and is inhibited by atorvastatin [J].
Clarke, TA ;
Waskell, LA .
DRUG METABOLISM AND DISPOSITION, 2003, 31 (01) :53-59
[7]   A primer and comparative review of major US mortality databases [J].
Cowper, DC ;
Kubal, JD ;
Maynard, C ;
Hynes, DM .
ANNALS OF EPIDEMIOLOGY, 2002, 12 (07) :462-468
[8]  
*FOOD DRUS ADM, EARL COMM ONG SAF RE
[9]   Effect of cytochrome P450 polymorphisms on platelet reactivity after treatment with Clopidogrel in acute coronary syndrome [J].
Frere, Corinne ;
Cuisset, Thomas ;
Morange, Pierre-Emmanuel ;
Qpilici, Jacques ;
Camoin-Jaumd, Laurence ;
Saut, Noemie ;
Faille, Dorothee ;
Lambert, Marc ;
Juhan-Vague, Irene ;
Bonnet, Jean-Louis ;
Alessi, Marie-Christine .
AMERICAN JOURNAL OF CARDIOLOGY, 2008, 101 (08) :1088-1093
[10]   CYP2C19 pharmacogenomics associated with therapy of Helicobacter pylori infection and gastro-esophageal reflux diseases with a proton pump inhibitor [J].
Furuta, Takahisa ;
Sugimoto, Mitsushige ;
Shirai, Naohito ;
Ishizaki, Takashi .
PHARMACOGENOMICS, 2007, 8 (09) :1199-1210