McEvoy J P
Department of Psychiatry, Duke University Medical Center, Durham, N.C.
J Clin Psychiatry. 1994 May;55 Suppl:18-21.
Dopaminergic hyperactivity mediated via D2 receptors is implicated in the etiology of positive symptoms of schizophrenia, but selective D2 antagonists provide imperfect therapy. This article describes a subanalysis of a trial of risperidone, a combined 5-HT2A/D2 antagonist, in 513 patients with DSM-III-R chronic schizophrenia. Risperidone at 2, 6, 10, and 16 mg/day was compared with placebo and haloperidol 20 mg/day. All doses of risperidone and the 20-mg dose of haloperidol were superior to placebo (mean change from baseline on the PANSS positive and general psychopathology subscales). The 6-mg dose of risperidone also produced significantly more improvement than haloperidol 20 mg. We conclude that risperidone is an effective drug for patients with positive features of schizophrenia.
通过D2受体介导的多巴胺能亢进与精神分裂症阳性症状的病因有关,但选择性D2拮抗剂的治疗效果并不理想。本文描述了一项对513例DSM-III-R慢性精神分裂症患者使用利培酮(一种5-HT2A/D2联合拮抗剂)进行试验的亚组分析。将利培酮2、6、10和16mg/天的剂量与安慰剂和氟哌啶醇20mg/天进行比较。所有剂量的利培酮和20mg剂量的氟哌啶醇均优于安慰剂(PANSS阳性和总体精神病理学分量表相对于基线的平均变化)。利培酮6mg剂量组的改善也明显多于氟哌啶醇20mg剂量组。我们得出结论,利培酮对具有精神分裂症阳性特征的患者是一种有效的药物。