de Beaurepaire R, Labelle A, Naber D, Jones B D, Barnes T R
INSERM U.320, Hôpital du Bon-Sauveur, Caen, France.
Psychopharmacology (Berl). 1995 Oct;121(3):323-7. doi: 10.1007/BF02246070.
Six psychotic patients were included in a four-week study of the effects of the D1 selective antagonist SCH 39166 given as monotherapy. Four had a diagnosis of schizophrenia, and two suffered from a schizoaffective disorder. All presented with an acute psychotic exacerbation at the beginning of the trial. SCH 39166 was progressively increased from 50 mg/day to 600 mg/day. In the four schizophrenic patients, the BPRS worsened, and three out of the four failed to complete the study because of this. Three schizophrenic patients were aggressive or violent after abrupt discontinuation of treatment. In the two patients with schizoaffective disorder the BPRS improved during the trial, but they had an acute relapse immediately after treatment discontinuation. Extrapyramidal symptoms improved in three of the six patients, and worsened in one.
六名精神病患者参与了一项为期四周的研究,该研究旨在探讨D1选择性拮抗剂SCH 39166作为单一疗法的效果。其中四名被诊断为精神分裂症,两名患有分裂情感性障碍。所有患者在试验开始时均出现急性精神病性发作。SCH 39166的剂量从每天50毫克逐渐增加至600毫克。在四名精神分裂症患者中,简明精神病评定量表(BPRS)评分恶化,其中四人中有三人因此未能完成研究。三名精神分裂症患者在突然停药后出现攻击或暴力行为。在两名分裂情感性障碍患者中,BPRS评分在试验期间有所改善,但在停药后立即出现急性复发。六名患者中有三名锥体外系症状改善,一名恶化。