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抗抑郁药物之争与平衡安慰剂试验设计:一项伦理学分析

The antidepressant debate and the balanced placebo trial design: an ethical analysis.

作者信息

Waring Duff R

机构信息

York University, 4700 Keele Street, Toronto, Ontario, Canada.

出版信息

Int J Law Psychiatry. 2008 Dec;31(6):453-62. doi: 10.1016/j.ijlp.2008.09.001. Epub 2008 Oct 26.

Abstract

There is ongoing debate about whether randomized, placebo-controlled trials under a double-blind have reliably established the pharmacological efficacy of antidepressants. Numerous meta-analyses of antidepressant efficacy trials, e.g., Kirsch et al. [Kirsch, I., Moore, T. J., Scoboria, A., & Nicholls, S. (2002). The emperor's new drugs: An analysis of antidepressant medication data submitted to the U.S. food and drug administration. Prevention and Treatment, 5, Article 23. (Retrieved July 19, 2007 from http://journals.apa.org/prevention/volume5)], have shown a modest drug-placebo difference but methodological problems with standard trial design preclude a definitive conclusion that this difference results from specific biological effects of antidepressants or the nonspecific factors that have not been adequately excluded. Standard trial design assumes the additivity thesis of pharmacological efficacy, being the assumption that the specific or "true" magnitude of the pharmacological effect is limited to the difference between the drug and placebo responses in a standard trial. If the drug effects are as small as these meta-analyses suggest, then their clinical effectiveness is questionable. If the drug effects are actually larger but masked by placebo effects, then the additivity thesis is not valid and we risk false negative results with standard trial design. Kirsch et al. propose an alternative, four arm balanced placebo trial design (BPTD) that can accurately test the additivity thesis. The BPTD uses antidepressants, active placebos and the intentional deception of research subjects. My focal question is whether the BPTD is ethically defensible. I will explore two objections that can be raised against it: 1) lying to BPTD research subjects violates their autonomy and exploits their illness and 2) the BPTD may not enable us to test the additivity thesis with accuracy, i.e., it may contribute to the masking of drug effects that it aims to avoid. I argue that these objections support the conclusion that the BPTD is ethically indefensible.

摘要

关于双盲随机安慰剂对照试验是否可靠地确立了抗抑郁药的药理疗效,目前仍存在争议。对抗抑郁药疗效试验的大量荟萃分析,例如基尔希等人的研究[基尔希,I.,摩尔,T. J.,斯科博里亚,A.,& 尼科尔斯,S.(2002年)。皇帝的新药:对提交给美国食品药品监督管理局的抗抑郁药数据的分析。《预防与治疗》,第5卷,第23篇文章。(2007年7月19日从http://journals.apa.org/prevention/volume5获取)],显示出药物与安慰剂之间存在适度差异,但标准试验设计存在方法学问题,妨碍了得出明确结论,即这种差异是由抗抑郁药的特定生物学效应还是未被充分排除的非特异性因素导致的。标准试验设计假定药理疗效的可加性论点,即假定药理效应的特定或“真实”大小仅限于标准试验中药物与安慰剂反应之间的差异。如果药物效应如这些荟萃分析所表明的那么小,那么它们的临床有效性就值得怀疑。如果药物效应实际上更大,但被安慰剂效应掩盖,那么可加性论点就不成立,我们使用标准试验设计就可能面临假阴性结果的风险。基尔希等人提出了一种替代的四臂平衡安慰剂试验设计(BPTD),它可以准确地检验可加性论点。BPTD使用抗抑郁药、活性安慰剂以及对研究对象的故意欺骗。我的核心问题是BPTD在伦理上是否站得住脚。我将探讨可以针对它提出的两个反对意见:1)对BPTD研究对象说谎侵犯了他们的自主权并利用了他们的疾病;2)BPTD可能无法使我们准确地检验可加性论点,即它可能导致掩盖其旨在避免的药物效应。我认为这些反对意见支持了BPTD在伦理上站不住脚的结论。

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