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喹硫平治疗老年精神病的疗效与安全性。

The efficacy and safety of quetiapine for treatment of geriatric psychosis.

作者信息

Yang Cheng-Hung, Tsai Shih-Jen, Hwang Jen-Ping

机构信息

Department of Psychiatry, Taipei Veterans General Hospital and Division of Psychiatry, School of Medicine, National Yang-Ming University, Taipei, Taiwan, PR China.

出版信息

J Psychopharmacol. 2005 Nov;19(6):661-6. doi: 10.1177/0269881105056669.

Abstract

Quetiapine, an atypical antipsychotic, is effective for psychosis in younger patients, with limited adverse effects reported. This open-label naturalistic study was conducted to assess the 4-week efficacy and safety of quetiapine for treatment of geriatric psychosis. Clinical efficacy was evaluated using the Brief Psychiatric Rating Scale (BPRS) and Clinical Global Impression Improvement (CGI-I) instruments before and after 4 weeks of quetiapine treatment. The sample population consisted of 100 geropsychiatric inpatients with psychosis, with the therapeutic evaluation completed by 91. Eighty-one of these 91 patients (89.0%) experienced mild-to-substantial improvement, as determined from the CGI-I. Further, a mean reduction in BPRS score of 39.5% (from baseline) was also determined. The mean daily dose of quetiapine for the fourth week was 276.1 177.2mg/day (range 50-800). Higher quetiapine dosages were administered for patients with functional psychoses compared to an analogous group with organic mental disorders. The most common adverse effects were somnolence (30.0%), lower-limb weakness (28.0%) and dizziness (27.0%). Body weight and fasting triglyceride were significantly elevated after quetiapine treatment (2.2% and 8.9% from baseline, respectively). Based on the results of this study, it appears that quetiapine is an efficacious and safe treatment for geriatric inpatients with psychosis, however, there is a wide dosing range and optimal dosage is diagnosis-dependent.

摘要

喹硫平是一种非典型抗精神病药物,对年轻患者的精神病有效,且报道的不良反应有限。本开放性自然主义研究旨在评估喹硫平治疗老年精神病4周的疗效和安全性。在喹硫平治疗4周前后,使用简明精神病评定量表(BPRS)和临床总体印象改善量表(CGI-I)评估临床疗效。样本群体包括100名患有精神病的老年精神科住院患者,其中91人完成了治疗评估。根据CGI-I量表判定,这91名患者中有81人(89.0%)病情有轻度至显著改善。此外,还确定BPRS评分平均降低了39.5%(相对于基线)。第四周喹硫平的平均日剂量为276.1±177.2mg/天(范围50 - 800mg)。与患有器质性精神障碍的类似组相比,功能性精神病患者服用的喹硫平剂量更高。最常见的不良反应是嗜睡(30.0%)、下肢无力(28.0%)和头晕(27.0%)。喹硫平治疗后体重和空腹甘油三酯显著升高(分别比基线升高2.

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