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关于针刺临床疗效的评估

On the evaluation of the clinical effects of acupuncture.

作者信息

Lewith George T, Machin David

机构信息

Primary Medical Care and Community Medicine, University of Southampton, SouthamptonGreat Britain.

出版信息

Pain. 1983 Jun;16(2):111-127. doi: 10.1016/0304-3959(83)90202-6.

Abstract

This paper reviews some of the recent randomised trials on acupuncture published in the literature, with particular reference to the definition of placebo (control), sham acupuncture and real acupuncture. Response rates of 30, 50 and 70% of placebo, sham and real acupuncture respectively, are suggested for the groups of patients studied. The statistical methodology necessary in the design of acupuncture trials, in order to detect differences of this order of magnitude, is discussed. If the postulated response rate had been envisaged at the onset of the trials here reviewed, then the majority of these trials have very low power at a conventional 5% level of significance. It is emphasised that one cannot necessarily conclude from trials which produce statistically non-significant results that acupuncture (when compared with placebo for example) is ineffective. The paper suggests that meaningful comparisons between alternative treatments may be made by using 'pain free intervals' with subsequent analysis using life table techniques. Tables are provided for determining appropriate patient numbers.

摘要

本文回顾了文献中最近发表的一些关于针灸的随机试验,特别提及了安慰剂(对照)、假针灸和真针灸的定义。对于所研究的患者群体,建议安慰剂、假针灸和真针灸的有效率分别为30%、50%和70%。讨论了在针灸试验设计中为检测这种数量级差异所必需的统计方法。如果在本文所回顾的试验开始时就设想了假定的有效率,那么这些试验中的大多数在传统的5%显著性水平下功效很低。需要强调的是,不能仅仅从产生统计学无显著结果的试验中就得出针灸(例如与安慰剂相比)无效的结论。本文建议,可以通过使用“无痛间隔”并随后采用生命表技术进行分析,来对替代疗法进行有意义的比较。还提供了用于确定合适患者数量的表格。

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