[神经麻醉与复苏中的药物评价]。

E Autret
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引用次数: 0

摘要

对用于神经麻醉的药物的评价是基于对照试验的。此类试验的主要原则与其他药物试验没有区别,但需要强调一些特点。药物开发的第一阶段是在健康志愿者中对其耐受性和动力学进行评估,这必须结合快速和短暂的作用而没有残留效应。第二阶段是对耐受性和动力学的研究,同时也是对其疗效的研究,因为只涉及患者。对大脑循环的作用是非常重要的。在第三阶段,试验必须证明新药比通常用于同一适应症的处方药有“更多的东西”,才能获得上市许可。下一阶段是通过记录许多患者接触新药时观察到的不良反应来评估安全性的最佳时期。法国的上市后监测系统是建立在处方者自发报告不良反应的基础上的。为了正确地进行试验,需要神经麻醉师、药理学家和统计学家的合作。试验需要控制,这意味着对两组患者进行比较,一组服用药物,另一组不服用药物。治疗必须是随机和盲的,以确保两组之间的任何差异实际上是由药物引起的。临床医生必须定义评估标准和测量工具,以计算试验目的所需的患者数量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Drug evaluation in neuroanesthesia and resuscitation].

The evaluation of a drug used in neuroanesthesia is based upon controlled trials. The main principles of such trials are not different from trials of other drugs but some characteristics should be emphasized. The first phase of the development of a drug is an evaluation in healthy volunteers of its tolerance and kinetics, which must combine rapid and short action without residual effect. The second phase is a study of the tolerance and kinetics but also of its efficacy because only patients are involved. Action upon cerebral circulation is of great importance. During the third phase, trials have to prove that the new drug has "something more" than the drug usually prescribed for the same indication to obtain approval for marketing. The next phase is the best period for the evaluation of safety by recording the adverse effects observed when many patients are exposed to the new drug. The french system of post marketing surveillance is based upon spontaneous reports of adverse effects by prescribers To be correctly performed a trial needs the collaboration of a neuroanesthetist, a pharmacologist and a statistician. The trial needs to be controlled which means a comparison of two groups of patients, one with the drug and the other one without the drug. The treatment has to be randomized and blind to be sure that any difference between the two groups is in fact due to the drug. The clinician has to define the evaluation criteria and the tool of measurement to calculate the number of patients needed for the purpose of the trial.

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