迟发性运动障碍的治疗试验。

A Villeneuve
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引用次数: 7

摘要

寻找治疗迟发性运动障碍的方法通常以锥体外系疾病的假定生化机制为指导,但尚未发现明显有效的治疗方法。目前推测迟发性运动障碍的机制涉及中枢多巴胺-乙酰胆碱系统之间的失衡,其平衡也可能受到神经内分泌因素的影响。据报道,这些药物对这些系统的神经系统并发症有一定的临床疗效。治疗迟发性运动障碍的临床研究是艰苦的,并提出了几个问题,可以解释结果的不可预测性和差异。这些问题可以分为三大类:患者变量、实验治疗变量和方法变量。对这些变量进行了讨论,并提出了一些建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Therapeutic trials in tardive dyskinesia.

The search for a treatment of tardive dyskinesia has generally been guided by the putative biochemical mechanisms underlying the extrapyramidal disorders, but no markedly effective treatment has yet been found. The currently postulated mechanism in tardive dyskinesia involves namely an imbalance between the central dopamine-acetylcholine systems whose balance may also be influenced by neuroendocrine factors. The agents reported having some clinical efficacy in the management of this neurological complication act on these systems. The clinical investigation for the treatment of tardive dyskinesia is laborious and raises several problems that could account for the unpredictability and the discrepancies in results. These problems can be divided into three broad categories: patient variables, experimental treatment variables and methodological variables. These variables are discussed and some suggestions made.

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