Weber S S, Dufresne R L, Becker R E, Mastrati P
Drug Intell Clin Pharm. 1983 Jul-Aug;17(7-8):523-7. doi: 10.1177/106002808301700705.
Tardive dyskinesia, a syndrome of involuntary motor movements, can be a permanent consequence of the long-term use of antipsychotic drugs. While there is no well-established drug treatment, case reports and the results of a few clinical studies suggest that drugs that facilitate the GABA-ergic system may decrease the abnormal movements. One such class of drugs is the benzodiazepines. We administered diazepam to 13 subjects in a 24-week, crossover design study. Tardive dyskinesia and psychopathology were assessed by blind raters using the Abnormal Involuntary Movement Scale and the Brief Psychiatric Rating Scale (BPRS). The means of all movement measurements improved from the baseline, with orofacial, subtotal, symptom severity, and total reaching significance. However, we were unable to demonstrate a drug effect; the patients improved to a similar degree whether or not they received diazepam. Their psychiatric disorders did not worsen with diazepam administration and, in fact, improved slightly; the activation factor of the BPRS was significantly improved over baseline. Our results suggest that diazepam is not effective in managing the movements of tardive dyskinesia and that behavior modification strategies be investigated to help patients control symptoms.
迟发性运动障碍是一种不自主运动综合征,可能是长期使用抗精神病药物的永久性后果。虽然目前尚无成熟的药物治疗方法,但病例报告和一些临床研究结果表明,促进γ-氨基丁酸(GABA)能系统的药物可能会减少异常运动。苯二氮䓬类药物就是这类药物之一。在一项为期24周的交叉设计研究中,我们对13名受试者使用了地西泮。由盲法评分者使用异常不自主运动量表和简明精神病评定量表(BPRS)对迟发性运动障碍和精神病理学进行评估。所有运动测量指标的均值均较基线有所改善,口面部、部分、症状严重程度和总体指标均达到显著水平。然而,我们未能证明药物有效果;无论是否接受地西泮治疗,患者的改善程度相似。服用地西泮后,他们的精神障碍并未恶化,事实上还有轻微改善;BPRS的激活因子较基线有显著改善。我们的结果表明,地西泮对迟发性运动障碍的运动症状无效,应研究行为矫正策略以帮助患者控制症状。