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首页> 外文期刊>The Lancet >Effectiveness of antipsychotic drugs in first-episode schizophrenia and schizophreniform disorder: an open randomised clinical trial.
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Effectiveness of antipsychotic drugs in first-episode schizophrenia and schizophreniform disorder: an open randomised clinical trial.

机译:抗精神病药在首发精神分裂症和精神分裂症患者中的有效性:一项开放的随机临床试验。

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BACKGROUND: Second-generation antipsychotic drugs were introduced over a decade ago for the treatment of schizophrenia; however, their purported clinical effectiveness compared with first-generation antipsychotic drugs is still debated. We aimed to compare the effectiveness of second-generation antipsychotic drugs with that of a low dose of haloperidol, in first-episode schizophrenia. METHODS: We did an open randomised controlled trial of haloperidol versus second-generation antipsychotic drugs in 50 sites, in 14 countries. Eligible patients were aged 18-40 years, and met diagnostic criteria for schizophrenia, schizophreniform disorder, or schizoaffective disorder. 498 patients were randomly assigned by a web-based online system to haloperidol (1-4 mg per day; n=103), amisulpride (200-800 mg per day; n=104), olanzapine (5-20 mg per day; n=105), quetiapine (200-750 mg per day; n=104), or ziprasidone (40-160 mg per day; n=82); follow-up was at 1 year. The primary outcome measure was all-cause treatment discontinuation. Patients and their treating physicians were not blinded to the assigned treatment. Analysis was by intention to treat. This study is registered as an International Standard Randomised Controlled Trial, number ISRCTN68736636. FINDINGS: The number of patients who discontinued treatment for any cause within 12 months was 63 (Kaplan-Meier estimate 72%) for haloperidol, 32 (40%) for amisulpride, 30 (33%) for olanzapine, 51 (53%) for quetiapine, and 31 (45%) for ziprasidone. Comparisons with haloperidol showed lower risks for any-cause discontinuation with amisulpride (hazard ratio [HR] 0.37, [95% CI 0.24-0.57]), olanzapine (HR 0.28 [0.18-0.43]), quetiapine (HR 0.52 [0.35-0.76]), and ziprasidone (HR 0.51 [0.32-0.81]). However, symptom reductions were virtually the same in all the groups, at around 60%. INTERPRETATION: This pragmatic trial suggests that clinically meaningful antipsychotic treatment of first-episode of schizophrenia is achievable, for at least 1 year. However, we cannot conclude that second-generation drugs are more efficacious than is haloperidol, since discontinuation rates are not necessarily consistent with symptomatic improvement.
机译:背景:第二代抗精神病药是十年前引入的,用于治疗精神分裂症。然而,与第一代抗精神病药相比,它们声称的临床有效性仍存在争议。我们的目的是比较第二代抗精神病药与低剂量氟哌啶醇在首发精神分裂症中的疗效。方法:我们在14个国家/地区的50个地点进行了氟哌啶醇与第二代抗精神病药的开放性随机对照试验。符合条件的患者年龄为18-40岁,并且符合精神分裂症,精神分裂症样疾病或精神分裂症的诊断标准。 498名患者通过基于网络的在线系统随机分配给氟哌啶醇(1-4 mg /天; n = 103),氨磺必利(200-800 mg /天; n = 104),奥氮平(5-20​​ mg /天; n = 105),喹硫平(每天200-750 mg; n = 104)或齐拉西酮(每天40-160 mg; n = 82);随访时间为1年。主要结局指标是全因治疗中断。患者及其治疗医师对指定的治疗没有盲目性。分析是按意向进行的。该研究已注册为国际标准随机对照试验,编号为ISRCTN68736636。结果:在12个月内因任何原因停药的患者中,氟哌啶醇为63(Kaplan-Meier估计为72%),氨磺必利为32(40%),奥氮平为30(33%),奥沙平为51(53%)。喹硫平,齐拉西酮为31(45%)。与氟哌啶醇的比较显示,因氨磺必利(危险比[HR] 0.37,[95%CI 0.24-0.57]),奥氮平(HR 0.28 [0.18-0.43]),喹硫平(HR 0.52 [0.35-0.76] ])和齐拉西酮(HR 0.51 [0.32-0.81])。但是,所有组的症状减轻幅度几乎相同,约为60%。解释:这项实用的试验表明,精神分裂症首发的临床意义上的抗精神病药物治疗至少可达到一年。但是,我们不能得出结论,第二代药物比氟哌啶醇更有效,因为停药率不一定与症状改善一致。

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