齐拉西酮治疗精神分裂症和双相情感障碍:临床试验综述

William M. Greenberg, Leslie Citrome
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引用次数: 82

摘要

齐拉西酮是一种较新的“非典型”或“第二代”抗精神病药。口服齐拉西酮(盐酸齐拉西酮)被美国食品和药物管理局(FDA)批准用于治疗精神分裂症,以及与双相情感障碍相关的急性躁狂或混合性发作(伴有或不伴有精神病性特征)。肌注齐拉西酮(甲磺酸齐拉西酮)被fda批准用于精神分裂症患者的急性躁动。口服齐拉西酮似乎是有效的,并且在改善精神分裂症阴性症状方面比氯丙嗪和氟哌啶醇有一些有限的临床优势。在精神分裂症临床抗精神病药物干预有效性试验(CATIE)的二期试验中,齐拉西酮的临床表现与奥氮平和利培酮不匹配,总体有效性更接近奎硫平。剂量滴定率和达到的剂量可能对齐拉西酮的疗效概况有重要影响。在精神分裂症患者急性躁动的使用研究中,肌注齐拉西酮已被证明是有效的,并且耐受性相对较好。关于耐受性,齐拉西酮具有重要的优势,因为它与临床显著的体重增加或胆固醇,甘油三酯或血糖控制的不良变化无关,并且当患者从其他抗精神病药物切换到齐拉西酮时,这些指标可能会有中度改善。它对催乳素水平也没有显著的持久影响,不是抗胆碱能药物,而且偶尔会引起锥体外系副作用或体位性低血压,尽管它可能与嗜睡有关。这种耐受性在某些患者的治疗中可能很有价值。齐拉西酮可能会延长心电图(ECG) QTc间期(通过标准算法校正心率的QT间期),但经过5年的临床可用性后,齐拉西酮(本身)似乎不会在这方面造成实质性的临床问题。因此,齐拉西酮可作为治疗精神分裂症或躁狂发作的一线药物选择,但鉴于抗精神病药物之间的差异,应根据患者的个体特点和情况进行药物选择。
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Ziprasidone for Schizophrenia and Bipolar Disorder: A Review of the Clinical Trials

Ziprasidone is a newer “atypical” or “second-generation” antipsychotic. Oral ziprasidone (ziprasidone hydrochloride) is approved by the U.S. Food and Drug Administration (FDA) for the treatment of schizophrenia, and acute manic or mixed episodes associated with bipolar disorder (with or without psychotic features). Ziprasidone intramuscular (ziprasidone mesylate) is FDA-approved for acute agitation in patients with schizophrenia. Oral ziprasidone appears efficacious, and has been shown to have some limited clinical advantages over chlorpromazine and haloperidol in ameliorating negative symptoms of schizophrenia. In Phase 2 of the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) for schizophrenia, ziprasidone did not match the clinical performance of olanzapine and risperidone, appearing closer in overall effectiveness to quetiapine. The rate of dose titration and the dose achieved may have an important bearing on ziprasidone's efficacy profile. In studies of usage for acute agitation in individuals with schizophrenia, intramuscular ziprasidone has been shown to be efficacious and relatively well tolerated. Regarding tolerability, ziprasidone, has important advantages in that it is not associated with clinically significant weight gain or adverse changes in cholesterol, triglycerides, or glycemic control, and patients may experience moderate improvement in these measures when switching to ziprasidone from a different antipsychotic agent. It also lacks significant persistent effects on prolactin levels, is not anticholinergic, and only infrequently causes extrapyramidal side effects or postural hypotension, although it can be associated with somnolence. This tolerability profile may be quite valuable in the treatment of some patients. Ziprasidone may prolong the electrocardiogram (ECG) QTc interval (QT interval corrected for heart rate by a standard algorithm), but after 5 years' clinical availability ziprasidone (by itself) does not appear to pose a substantial clinical problem in this regard. Therefore, ziprasidone may be considered a first-line drug option in the treatment of schizophrenia or manic episodes, but, in view of the differences among antipsychotic medications, drug selection should be guided by the patient's individual characteristics and situation.

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