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利培酮与氟哌啶醇治疗首发精神病:一项长期随机试验

Risperidone and haloperidol in first-episode psychosis: a long-term randomized trial.

作者信息

Schooler Nina, Rabinowitz Jonathan, Davidson Michael, Emsley Robin, Harvey Philip D, Kopala Lili, McGorry Patrick D, Van Hove Ilse, Eerdekens Marielle, Swyzen Wim, De Smedt Goedele

机构信息

Hurwich Professor, Bar Ilan University, Ramat Gan, Israel.

出版信息

Am J Psychiatry. 2005 May;162(5):947-53. doi: 10.1176/appi.ajp.162.5.947.

Abstract

OBJECTIVE

The first episode of psychotic illness is a key intervention point. The initial experience with medication can affect willingness to accept treatment. Further, relapse prevention is a treatment cornerstone during the first years of illness because active psychotic illness may affect lifetime outcomes. Thus, initial treatment of active symptoms and subsequent relapse prevention are central goals of pharmacotherapy. This study compared long-term effectiveness of risperidone versus haloperidol in first-episode psychosis patients.

METHOD

First-episode psychosis patients (N=555, mean age=25.4 years) participated in a double-blind, randomized, controlled flexible-dose trial that compared risperidone (mean modal dose=3.3 mg) and haloperidol (mean modal dose=2.9 mg). The median treatment length was 206 days (maximum=1,514).

RESULTS

Positive and Negative Syndrome Scale scores and Clinical Global Impression ratings improved significantly relative to baseline, with no significant differences between groups. Three-quarters of the patients achieved initial clinical improvement, defined as >20% reduction in total Positive and Negative Syndrome Scale score. However, among those who achieved clinical improvement, 42% of the risperidone group experienced a relapse compared with 55% of the haloperidol group. The median time to relapse was 466 days for risperidone-treated subjects and 205 days for those given haloperidol. These differences were statistically significant based on Kaplan-Meier survival analysis. Adverse effects distinguished the treatments: there were significantly more extrapyramidal signs and symptoms and adjunctive medication use in the haloperidol group and greater prolactin elevation in the risperidone group. There was less weight gain with haloperidol initially but no significant differences between groups at endpoint.

CONCLUSIONS

Relatively low doses of antipsychotic drugs lead to significant symptom amelioration in the majority of first-episode psychosis patients. In the long term, risperidone prevents relapse in more patients and for a longer time and also induces less abnormal movements than haloperidol.

摘要

目的

精神病性疾病的首次发作是一个关键的干预点。药物治疗的初始体验会影响接受治疗的意愿。此外,在疾病的最初几年,预防复发是治疗的基石,因为活跃的精神病性疾病可能会影响终生预后。因此,积极症状的初始治疗和随后的复发预防是药物治疗的核心目标。本研究比较了利培酮与氟哌啶醇在首发精神病患者中的长期疗效。

方法

首发精神病患者(N = 555,平均年龄 = 25.4岁)参与了一项双盲、随机、对照的灵活剂量试验,该试验比较了利培酮(平均模式剂量 = 3.3毫克)和氟哌啶醇(平均模式剂量 = 2.9毫克)。中位治疗时长为206天(最长 = 1514天)。

结果

阳性和阴性症状量表评分及临床总体印象评分相对于基线有显著改善,组间无显著差异。四分之三的患者实现了初始临床改善,定义为阳性和阴性症状量表总分降低超过20%。然而,在实现临床改善的患者中,利培酮组42%的患者复发,而氟哌啶醇组为55%。利培酮治疗的受试者复发的中位时间为466天,给予氟哌啶醇的受试者为205天。基于Kaplan-Meier生存分析,这些差异具有统计学意义。不良反应区分了这两种治疗方法:氟哌啶醇组的锥体外系体征和症状及辅助药物使用显著更多,而利培酮组的催乳素升高更明显。最初氟哌啶醇导致的体重增加较少,但在终点时组间无显著差异。

结论

相对低剂量的抗精神病药物可使大多数首发精神病患者的症状得到显著改善。从长期来看,与氟哌啶醇相比,利培酮能预防更多患者复发且复发时间更长,还能减少异常运动的发生。

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