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低剂量利培酮治疗首发精神分裂症、分裂样障碍或分裂情感性障碍患者的试验。

A trial of low doses of risperidone in the treatment of patients with first-episode schizophrenia, schizophreniform disorder, or schizoaffective disorder.

作者信息

Huq Zahid-Ul

机构信息

Department of Psychiatry, Park Royal Centre for Mental Health, Central Middlesex Hospital, London, UK.

出版信息

J Clin Psychopharmacol. 2004 Apr;24(2):220-4. doi: 10.1097/01.jcp.0000115663.45074.8a.

Abstract

This UK multicenter, noncomparative, open-trial study assessed risperidone in 74 first-psychotic-episode patients (DSM-IV schizophrenia) treated with flexible doses. Treatment commenced at 1 mg/day, increasing to 2 mg after 3 days; then adjusted to 8 mg/day maximum. Treatment duration was 12 weeks (Phase 1) with follow-up of 62 patients to 1 year on risperidone or another antipsychotic (Phase 2). Superiority over baseline was recorded on all Positive and Negative Syndrome Scale (PANSS) subscale scores at week 12 (P < 0.0001), occurring after 3 days of treatment. Clinical Global Impression of Severity of Illness and Improvement (CGI-Severity) significantly improved over Phase 1 (80% of patients improved, 1% deteriorated). Treatment was considered from being very to quite acceptable in 79% and a success in 77% (P = 0.0001). Only 5 patients switched to another antipsychotic. Significant improvements were maintained to 1 year. Treatment-related adverse events reported by > 10% of patients in Phase 1 were somnolence (23%) and fatigue (10.8%). Five patients stopped risperidone due to adverse events. Nine patients reported that adverse events started in Phase 2, and 3 patients stopped risperidone. Twenty-one patients (28%) in Phase 1 and 4 patients (6%) in Phase 2 (including a patient taking thioridazine) reported extrapyramidal symptoms (EPS); none stopped treatment. There was no significant change in Abnormal Involuntary Movement Scale (AIMS) or Targeting Abnormal Kinetic Effects (TAKE) scale at 12 weeks. No significant change in AIMS and a significant improvement in TAKE scale were found from week 12 to 1 year. There was no significant difference in efficacy and tolerability between 1- to 4-mg/day and 5- to 8-mg/day dose groups in Phase 1 or 2. Low-dose risperidone is concluded to be effective and well tolerated in first episode psychosis. Only 2 patients (3%) required doses of over 6 mg/day.

摘要

这项英国多中心、非对照、开放性试验研究评估了利培酮对74例首次发作精神病患者(DSM-IV精神分裂症)的疗效,采用灵活剂量给药。治疗起始剂量为1毫克/天,3天后增至2毫克;然后根据情况调整,最大剂量为8毫克/天。治疗持续12周(第1阶段),62例患者随访1年,期间服用利培酮或另一种抗精神病药物(第2阶段)。在第12周时,所有阳性与阴性症状量表(PANSS)子量表得分均较基线有显著改善(P < 0.0001),在治疗3天后即出现改善。疾病严重程度和改善情况的临床总体印象(CGI-Severity)在第1阶段有显著改善(80%的患者病情改善,1%病情恶化)。79%的患者认为治疗从非常可接受至相当可接受,77%的患者认为治疗成功(P = 0.0001)。仅5例患者换用了另一种抗精神病药物。显著改善持续至1年。在第1阶段,超过10%的患者报告的与治疗相关的不良事件为嗜睡(23%)和疲劳(10.8%)。5例患者因不良事件停用利培酮。9例患者报告不良事件始于第2阶段,3例患者停用利培酮。第1阶段有21例患者(28%)、第2阶段有4例患者(6%)(包括1例服用硫利达嗪的患者)报告有锥体外系症状(EPS);无人因此停药。在12周时,异常不自主运动量表(AIMS)或靶向异常运动效应(TAKE)量表无显著变化。从第12周到1年,AIMS无显著变化,TAKE量表有显著改善。在第1阶段或第2阶段,1至4毫克/天剂量组和5至8毫克/天剂量组在疗效和耐受性方面无显著差异。得出结论,低剂量利培酮在首次发作精神病中有效且耐受性良好。仅2例患者(3%)需要超过6毫克/天的剂量。

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