[评价中药上市后临床安全性的证据体]。

中国中西医结合杂志 Pub Date : 2017-01-01
Xing Liao, Yan-Ming Xie
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引用次数: 0

摘要

循证医学早期发展起来的以干预措施疗效评价模型为基础的传统证据评价体系,已推广到整个医学研究和临床实践中。然而,这种等级制度越来越多地被滥用和误解,成为临床决策过程中的障碍。层次模型在有限的有效性问题上是有效的,但在现实世界中对干预措施的评估上是不充分的,特别是对上市后中药的安全性证据。目前国内外对上市后中药安全性的证据分级和分类报道甚少。因此,系统地收集和评价上市后中药安全性的证据具有重要的意义。借鉴循证医学在药物有效性证据分级与分类方面的成功经验,对中药上市后安全性证据评价、分类与分级标准的建立以及安全性证据评价基本框架的形成进行了研究,并从点、线、面三个角度对不同来源的证据进行了综合分析。从而建立中药上市后安全性评价的证据体系,为今后中药上市后安全性评价的证据体系研究提供方法和技术支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Evaluating the Body of Evidence on Postmarketing Clinical Safety of Chinese Herbs].

The traditional evidence evaluating hierarchy developed at the early stage in evidence-based medicine (EBM) , founded on an efficacy evaluation model of intervention, is generalized to whole medical research and clinical practice. However, such a hierarchy system were increasingly abused and misunderstood, which has become an obstacle for clinical decision making process. The hierarchical model is valid for limited questions of efficacy and inadequate for the evaluation of interventions in real world, especially safety evidence for postmarketing Chinese medicines. There are very few studies reporting the evidence grading and classification of postmarketing herbs' safety at home and abroad. Therefore, systematical collection and evaluation of evidence of postmarketing herbs' safety are of important significance. By referring to successful experiences in evidence grading and classification of drug effec- tiveness in EBM, authors studied the establishment of standards for evaluation, classification and grad- ing of safety evidence of postmarketing Chinese herbs, and the formation of basic frameworks of safety evidence evaluation, and comprehensively analyzed different sources of evidence from the perspectives of point, line, and surface, thus establishing the evidence body for safety evaluation of postmarketing Chinese herbs, and providing methodology and technical supports for future studies on evidence system in this field.

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