首页> 外文期刊>European archives of psychiatry and clinical neuroscience >The effect of atypical versus typical antipsychotics on tardive dyskinesia : A naturalistic study.
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The effect of atypical versus typical antipsychotics on tardive dyskinesia : A naturalistic study.

机译:非典型抗精神病药与典型抗精神病药对迟发性运动障碍的影响:一项自然研究。

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OBJECTIVE: The aim was testing whether atypical antipsychotics (versus typicals) were associated with less risk of tardive dyskinesia (TD) in 516 severely mentally ill patients. METHODS: The sample included 11% (57/516) with no exposure before current treatment with atypicals; 9% (48/516) with prior and current treatment with atypicals but no exposure to typicals; 18% (94/516) with lifetime exposure to typicals for <5 years (plus atypicals); and 62% (317/516) with lifetime exposure to typicals for >/=5 years (plus atypicals). The Abnormal Involuntary Movement Scale (AIMS) was used to assess dyskinetic movements. Following Schooler and Kane's criteria TD was considered present when mild movements were present in at least two body areas or moderate movements were present in at least one body area. RESULTS: TD prevalences were 5% (3/57) in previously naive patients, 19% (9/48) after exposure only to atypicals, 19% (18/94) after typical exposure of <5 years, and 42% (132/317) after typical exposure of >/=5years. There was no significant effect comparing those taking only atypicals to those exposed to typicals for <5 years (OR = 1.0, CI 0.42-2.5). CONCLUSION: This study is limited by the naturalistic design, the relatively small samples in the first two groups, the lack of information on the duration of the atypicals and their relatively recent introduction to the market (ziprasidone and aripiprazole were introduced to the market in the middle of the study). This study raises the question that new TD studies need to establish whether decades of treatment with atypical antipsychotics make a difference.
机译:目的:目的是测试516例重度精神病患者中非典型抗精神病药(相对于典型药物)与迟发性运动障碍(TD)风险是否相关。方法:样本中有11%(57/516)在当前非典型药物治疗前没有暴露;先前和目前使用非典型药物治疗的患者为9%(48/516),但未接触典型患者; 18%(94/516)的终身暴露水平低于5年(不典型);以及62%(317/516)的终身暴露于> / = 5年的典型经历(加上非典型)。异常非自愿运动量表(AIMS)用于评估运动障碍运动。遵循Schooler和Kane的标准,当至少两个身体区域出现轻度运动或至少一个身体区域出现中度运动时,就认为存在TD。结果:以前未接受过治疗的患者的TD患病率为5%(3/57),仅暴露于非典型患者后TD患病率为19%(9/48),典型的暴露时间小于5年的TD患病率为19%(18/94),42%(132 / 317),通常暴露> / = 5年。将仅服用非典型药物的患者与暴露于典型时间<5年的患者(OR = 1.0,CI 0.42-2.5)相比,没有显着影响。结论:该研究受到自然主义设计的限制,前两组样本相对较少,缺乏关于非典型药物持续时间的信息以及它们相对较新的市场介绍(齐拉西酮和阿立哌唑已在市场上引入)。研究的中间阶段)。这项研究提出了一个问题,即新的TD研究需要确定数十年的非典型抗精神病药治疗是否会有所作为。

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