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具有新型治疗特性的新药。它们是否经过随机对照试验?

New drugs with novel therapeutic characteristics. Have they been subject to randomized controlled trials?

作者信息

Lexchin Joel

机构信息

School of Health Policy and Management at York University, Toronto, Ont.

出版信息

Can Fam Physician. 2002 Sep;48:1487-92.

Abstract

OBJECTIVE

To determine how many randomized controlled trials on the safety or efficacy of new drugs are published when these drugs are first marketed in Canada, and to determine the quality of the information in those trials.

DESIGN

A MEDLINE search was conducted on each drug identified as having novel therapeutic characteristics and first marketed between 1990 and 2000.

MAIN OUTCOME MEASURES

Number of trials dealing with the safety or efficacy of each drug published at the time the drug was marketed. Number of patients taking the study drug, length of the trial, and type of control.

RESULTS

The number of trials varied substantially. For some drugs, there were more than 20 studies; for others only a single study. Many trials were small and short-term, and used placebo controls.

CONCLUSION

Too few trials or inadequate trials on the safety and efficacy of new drugs are published when these drugs are first marketed in Canada. The lack of published trials means that physicians do not know whether results are generalizable to their patients, how to position the drug in relation to other treatments, or whether the drugs have long-term safety and efficacy.

摘要

目的

确定新药在加拿大首次上市时,有多少关于其安全性或有效性的随机对照试验被发表,并确定这些试验中信息的质量。

设计

对每一种被确定具有新型治疗特性且于1990年至2000年间首次上市的药物进行了医学索引数据库(MEDLINE)检索。

主要观察指标

药物上市时发表的涉及每种药物安全性或有效性的试验数量。服用研究药物的患者数量、试验时长以及对照类型。

结果

试验数量差异很大。对于一些药物,有20多项研究;而对于其他药物,只有一项研究。许多试验规模小、持续时间短,且使用安慰剂对照。

结论

新药在加拿大首次上市时,发表的关于其安全性和有效性的试验太少或不够充分。缺乏已发表的试验意味着医生不知道试验结果是否能推广到他们的患者身上,不知道如何将该药物与其他治疗方法相比较,也不知道这些药物是否具有长期安全性和有效性。

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