Phanjoo A L, Link C
Department of Geriatric Psychiatry, Royal Edinburgh Hospital, United Kingdom.
Acta Psychiatr Scand Suppl. 1990;358:181-5. doi: 10.1111/j.1600-0447.1990.tb05314.x.
A total of 18 hospitalized elderly psychotic patients in need of antipsychotic treatment took part in a double-blind exploratory study concerning the safety, tolerability and efficacy of remoxipride and thioridazine. Their median age was 78 years (range 66-90 years). Over the study period of 6 weeks, 9 patients received remoxipride and 9 thioridazine. Both drugs were given in a dosage range of 50-200 mg/day. The median total score on the Brief Psychiatric Rating Scale at the start of active treatment was 18 in the remoxipride group and 24 in the thioridazine group. The scores were reduced to 6 and 7, respectively, at the last rating. The Clinical Global Impression at last rating showed 4 of the 9 remoxipride patients to be very much improved compared to 1 of the 9 thioridazine patients. Apart from three reports of severe drowsiness in the thioridazine group, the incidence of treatment-emergent adverse effects was low in both groups. No clinically significant aberrations were seen in laboratory tests or cardiovascular data. In conclusion, remoxipride seemed to be well tolerated in this group of patients and its antipsychotic efficacy in the doses used is promising.
共有18名需要接受抗精神病药物治疗的住院老年精神病患者参与了一项关于瑞莫必利和硫利达嗪安全性、耐受性及疗效的双盲探索性研究。他们的年龄中位数为78岁(范围66 - 90岁)。在为期6周的研究期间,9名患者接受瑞莫必利治疗,9名患者接受硫利达嗪治疗。两种药物的给药剂量范围均为50 - 200毫克/天。主动治疗开始时,瑞莫必利组简明精神病评定量表的总得分中位数为18分,硫利达嗪组为24分。在最后一次评定时,两组得分分别降至6分和7分。最后一次评定时的临床总体印象显示,9名接受瑞莫必利治疗的患者中有4名病情显著改善,而9名接受硫利达嗪治疗的患者中只有1名病情显著改善。除了硫利达嗪组有3例严重嗜睡报告外,两组治疗中出现的不良反应发生率均较低。实验室检查或心血管数据未发现具有临床意义的异常。总之,在这组患者中,瑞莫必利似乎耐受性良好,且其所用剂量的抗精神病疗效很有前景。