Rudorfer M V
Clinical Treatment Research Branch, National Institute of Mental Health, Rockville, MD 20857.
Psychopharmacol Bull. 1993;29(1):35-44.
The keystone of pharmacological therapy is the medication clinical trial. Beyond the straightforward administration of an adequate amount of medication for a sufficient duration of time, attention to a variety of methodologic issues is necessary to ensure a successful study. These include diagnostic and severity criteria for entry into the trial and a host of potentially confounding biological and psychosocial factors. Adequacy of treatment must be insured, aided by continued refinement of plasma drug concentration monitoring and understanding of the role of active metabolites. Outcome measures must be valid and reliable. These principles are being applied to the still-new field of child and adolescent psychopharmacology. Results thus far have indicated the importance of placebo control in young populations. The equivocal efficacy demonstrated to date for pharmacotherapy in controlled antidepressant trials in children and adolescents has limited understanding of dose (or plasma level)/response relationships which could serve to optimize further studies.
药物治疗的关键在于药物临床试验。除了在足够长的时间内直接给予足够剂量的药物外,还需要关注各种方法学问题以确保研究成功。这些问题包括进入试验的诊断和严重程度标准以及一系列可能产生混淆的生物学和社会心理因素。必须确保治疗的充分性,这得益于血浆药物浓度监测的不断完善以及对活性代谢物作用的理解。结果测量必须有效且可靠。这些原则正应用于儿童和青少年精神药理学这个仍属新兴的领域。迄今为止的结果表明了在年轻人群中进行安慰剂对照的重要性。目前在儿童和青少年抗抑郁药物对照试验中所显示的药物治疗疗效不明确,这限制了我们对剂量(或血浆水平)/反应关系的理解,而这种关系有助于优化进一步的研究。