Lack of aspirin effect: Aspirin resistance or resistance to taking aspirin?

被引:140
作者
Cotter, G
Shemesh, E
Zehavi, M
Dinur, I
Rudnick, A
Milo, O
Vered, Z
Krakover, R
Kaluski, E
Kornberg, A
机构
[1] Mt Sinai Med Ctr, Dept Psychiat, New York, NY 10029 USA
[2] Mt Sinai Med Ctr, Dept Pediat, New York, NY 10029 USA
[3] Tel Aviv Univ, Sch Med, Dept Behav Sci, IL-69978 Tel Aviv, Israel
[4] Assaf Harofeh Med Ctr, Inst Hematol, IL-70300 Zerifin, Israel
[5] Assaf Harofeh Med Ctr, Cardiol Inst, Clin Pharmacol Res Unit, IL-70300 Zerifin, Israel
关键词
D O I
10.1016/j.ahj.2003.07.011
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background A lack of aspirin effect on platelets after a myocardial infarction (MI) is associated with poor health outcome. This lack of effect may be due to biological resistance to aspirin or due to nonadherence (the patient is not taking the aspirin, hence it has no effect). Determining which of these factors predicts poor outcome would inform potential intervention strategies. Method's Aspirin effect on platelets was assessed in a cohort of MI survivors who were divided into three groups: group A ("adherent"), patients whose platelets were affected by aspirin; group B ("nonadherent"), patients whose platelets showed no aspirin effect and who admitted in an interview that they were not taking their medications; and group C (potentially biologically resistant to aspirin), patients whose platelets showed no aspirin effect but maintained that they were taking their, aspirin. Two health outcome measures (death, reinfarction, or rehospitalization for unstable angina; or admission for any cardiovascular causes) were assessed 12 months after enrollment. Results Seventy-three patients were enrolled and classified into groups A ("adherent," 52 patients), B ("nonadherent," 12 patients), and C ("potentially aspirin resistant," 9 patients). Adverse events and readmission were more common in the nonadherent group (B)- 42% and 67%, respectively, when compared with the adherent group (A)- 6% and 11%, and with the potentially biologically resistant group (C)-11% and 11%. Conclusions Nonadherence is a significant mediator of poor outcome. It is important to evaluate whether or not patients are taking their medications in clinical settings and in studies that evaluate the effect of prescribed medications.
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页码:293 / 300
页数:8
相关论文
共 19 条
[1]   COLLABORATIVE OVERVIEW OF RANDOMIZED TRIALS OF ANTIPLATELET THERAPY .1. PREVENTION OF DEATH, MYOCARDIAL-INFARCTION, AND STROKE BY PROLONGED ANTIPLATELET THERAPY IN VARIOUS CATEGORIES OF PATIENTS [J].
ALTMAN, R ;
CARRERAS, L ;
DIAZ, R ;
FIGUEROA, E ;
PAOLASSO, E ;
PARODI, JC ;
CADE, JF ;
DONNAN, G ;
EADIE, MJ ;
GAVAGHAN, TP ;
OSULLIVAN, EF ;
PARKIN, D ;
RENNY, JTG ;
SILAGY, C ;
VINAZZER, H ;
ZEKERT, F ;
ADRIAENSEN, H ;
BERTRANDHARDY, JM ;
BRAN, M ;
DAVID, JL ;
DRICOT, J ;
LAVENNEPARDONGE, E ;
LIMET, R ;
LOWENTHAL, A ;
MORIAU, M ;
SCHAPIRA, S ;
SMETS, P ;
SYMOENS, J ;
VERHAEGHE, R ;
VERSTRAETE, M ;
ATALLAH, A ;
BARNETT, H ;
BATISTA, R ;
BLAKELY, J ;
CAIRNS, JA ;
COTE, R ;
CROUCH, J ;
EVANS, G ;
FINDLAY, JM ;
GENT, M ;
LANGLOIS, Y ;
LECLERC, J ;
NORRIS, J ;
PINEO, GF ;
POWERS, PJ ;
ROBERTS, R ;
SCHWARTZ, L ;
SICURELLA, J ;
TAYLOR, W ;
THEROUX, P .
BMJ-BRITISH MEDICAL JOURNAL, 1994, 308 (6921) :81-100
[2]   Adherence to single daily dose of aspirin in a chemoprevention trial - An evaluation of self-report and microelectronic monitoring [J].
Burney, KD ;
Krishnan, K ;
Ruffin, MT ;
Zhang, DW ;
Brenner, DE .
ARCHIVES OF FAMILY MEDICINE, 1996, 5 (05) :297-300
[3]  
CANNER PL, 1980, NEW ENGL J MED, V303, P1038
[4]   Economic implications of non-compliance in health care [J].
Cleemput, I ;
Kesteloot, K .
LANCET, 2002, 359 (9324) :2129-2130
[5]   Prior peripheral arterial disease and cerebrovascular disease are independent predictors of adverse outcome in patients with acute coronary syndromes: Are we doing enough? Results from the Orbofiban in Patients with Unstable Coronary Syndromes-Thrombolysis In Myocardial Infarction (OPUS-TIMI) 16 study [J].
Cotter, G ;
Cannon, CP ;
McCabe, CH ;
Michowitz, Y ;
Kaluski, E ;
Charlesworth, A ;
Milo, O ;
Bentley, J ;
Blatt, A ;
Krakover, R ;
Zimlichman, R ;
Reisin, L ;
Marmor, A ;
Lewis, B ;
Vered, Z ;
Caspi, A ;
Braunwald, E .
AMERICAN HEART JOURNAL, 2003, 145 (04) :622-627
[6]   Effect of carvedilol on outcome after myocardial infarction in patients with left-ventricular dysfunction: the CAPRICORN randomised trial [J].
Dargie, HJ ;
Colucci, Y ;
Ford, I ;
Sendon, JLL ;
Remme, W ;
Sharpe, N ;
Blank, A ;
Holcslaw, TL .
LANCET, 2001, 357 (9266) :1385-1390
[7]  
Dew MA, 1996, J HEART LUNG TRANSPL, V15, P631
[8]   Aspirin-resistant thromboxane biosynthesis and the risk of myocardial infarction, stroke, or cardiovascular death in patients at high risk for cardiovascular events [J].
Eikelboom, JW ;
Hirsh, J ;
Weitz, JI ;
Johnston, M ;
Yi, Q ;
Yusuf, S .
CIRCULATION, 2002, 105 (14) :1650-1655
[9]   Aspirin absorption rates and platelet inhibition times with 325-mg buffered aspirin tablets (chewed or swallowed intact) and with buffered aspirin solution [J].
Feldman, M ;
Cryer, B .
AMERICAN JOURNAL OF CARDIOLOGY, 1999, 84 (04) :404-409
[10]   Effects of low-dose aspirin on serum C-reactive protein and thromboxane B2 concentrations:: A placebo-controlled study using a highly sensitive C-reactive protein assay [J].
Feldman, M ;
Jialal, I ;
Devaraj, S ;
Cryer, B .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2001, 37 (08) :2036-2041