Acute coronary syndromes in women: Is treatment different? Should it be?

被引:23
作者
Bennett S.K. [1 ]
Redberg R.F. [1 ]
机构
[1] Women's Heart Program, George Washington Univ. Hospital, Washington, DC 20037
关键词
Acute Coronary Syndrome; Clopidogrel; Acute Myocardial Infarction; Enoxaparin; Abciximab;
D O I
10.1007/s11886-004-0071-2
中图分类号
学科分类号
摘要
The vast majority of acute coronary syndrome (ACS) trials conducted over the past two decades support the view that women have persistently higher mortality and morbidity despite the introduction of new medical therapies and devices. Even after adjustment for older age, higher prevalence of diabetes, hypertension, heart failure, smaller vessel size, and late presentation, some studies still point to a persistent sex disadvantage. Even in contemporary practice, women continue to have longer delays in presentation and treatment. Selection bias in unstable angina/non-ST-elevation myocardial infarction (UA/NSTEMI) trials allows inclusion of large numbers of women with clinically insignificant coronary disease and may mistakenly shift results toward apparent benefit of a less aggressive approach. This bias causes further difficulty in determining efficacy and safety of new antithrombotic agents such as direct thrombin inhibitors and glycoprotein IIb/IIa inhibitors across the spectrum of ACS. In trials of UA/NSTEMI, use of objective evidence of ischemia such as elevated troponin levels, would greatly assist the determination of efficacy and benefit in women. Enrollment of more women in clinical trials and timely sex-specific analysis would promote a better understanding of the role of female gender in ACS and would facilitate better care of all patients. Copyright © 2004 by Current Science Inc.
引用
收藏
页码:243 / 252
页数:9
相关论文
共 65 条
  • [1] Wizemann T., Pardue M., Exploring the Biological Contributions to Human Health: Does Sex Matter?, (2001)
  • [2] Heart Disease and Stroke Statistics - 2004 Update, (2003)
  • [3] Mosca L., Appel L., Benjamin E., Et al., Evidence-based guidelines for cardiovascular disease prevention in women, Circulation, 109, pp. 672-692, (2004)
  • [4] Collaborative overview of randomized trials of antiplatelet therapy prevention of death, myocardial infarction, and stroke by prolonged antiplatelet therapy in various categories of patients, Br. Med. J., 308, pp. 81-106, (1994)
  • [5] Randomised trial of intravenous streptokinase, oral aspirin, both, or neither among 17 187 cases of suspected myocardial infarction (ISIS-2), Lancet, 2, pp. 349-360, (1988)
  • [6] Freemantle N., Cleland J., Young P., Et al., Beta-blockade after myocardial infarction: Systematic review and meta regression analysis, Br. Med. J., 318, pp. 1730-1737, (1999)
  • [7] The Beta-Blocker Pooling Project (BBPP): Subgroup findings for randomized trials in post infarction patients, Eur. Heart J., 9, pp. 8-16, (1988)
  • [8] Sleight P., Beta-blockade early in acute myocardial infarction, Am. J. Cardiol., 60, (1987)
  • [9] Roberts R., Rogers W., Mueller H., Lambrew A., Et al., Immediate versus deferred beta-blockade following thrombolytic therapy in patients with acute myocardial infarction, Circulation, 83, pp. 422-437, (1991)
  • [10] Silvet H., Spencer F., Yarzebski J., Et al., Communitywide trends in the use and outcomes associated with beta-blockers in patients with acute myocardial infarction, Arch. Intern. Med., 163, pp. 2175-2183, (2003)