Moss L E, Neppe V M, Drevets W C
Washington University School of Medicine, Department of Psychiatry, St. Louis, MO 63110.
J Clin Psychopharmacol. 1993 Jun;13(3):204-9.
Eight patients with mild to severe tardive dyskinesia (TD) were treated for 12 weeks with buspirone in dosages of up to 180 mg/day in an open-label study. Changes in TD severity were assessed by the Abnormal Involuntary Movement Scale. The rater was blind to buspirone dosage. Buspirone was well tolerated by most subjects. A within-subjects comparison of pretreatment and post-treatment Abnormal Involuntary Movement Scale scores revealed a mean improvement of 4.4 (p < 0.01). Improvement was also observed in neuroleptic-induced extrapyramidal side effects such as parkinsonism and akathisia. Scores on the Hamilton Rating Scale for Anxiety and the Brief Psychiatric Rating Scale did not change during the 12-week study. The results of this open-label pilot study suggest that relatively high doses of buspirone may be efficacious in the treatment of TD.
在一项开放标签研究中,8例轻至重度迟发性运动障碍(TD)患者接受了为期12周的丁螺环酮治疗,剂量最高达180毫克/天。通过异常不自主运动量表评估TD严重程度的变化。评估者对丁螺环酮剂量不知情。大多数受试者对丁螺环酮耐受性良好。对治疗前和治疗后异常不自主运动量表评分进行受试者内比较,结果显示平均改善了4.4(p < 0.01)。在抗精神病药物引起的锥体外系副作用如帕金森症和静坐不能方面也观察到了改善。在为期12周的研究中,汉密尔顿焦虑量表评分和简明精神病评定量表评分没有变化。这项开放标签的初步研究结果表明,相对高剂量的丁螺环酮可能对TD治疗有效。