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首页> 外文期刊>The journal of clinical psychiatry >Orlistat in clozapine- or olanzapine-treated patients with overweight or obesity: a 16-week open-label extension phase and both phases of a randomized controlled trial.
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Orlistat in clozapine- or olanzapine-treated patients with overweight or obesity: a 16-week open-label extension phase and both phases of a randomized controlled trial.

机译:在氯氮平或奥氮平治疗的超重或肥胖患者中使用奥利司他:16周开放标签扩展期以及随机对照试验的两个阶段。

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摘要

OBJECTIVE: To explore long-term effects of orlistat in adult clozapine- or olanzapine-treated patients with DSM-IV-diagnosed schizophrenia and overweight or obesity who tolerate orlistat. METHOD: Orlistat or placebo was added to clozapine or olanzapine in stable doses in a 16-week randomized controlled trial. Open-label orlistat was added to the antipsychotics during a 16-week extension phase for those completing the double-blind phase. No low-calorie diet or participation in behavioral programs was required. Body weight (primary outcome) and some metabolic parameters were measured prospectively. Analyses were performed for those completing both phases (ie, population differing from that reported earlier). The study was conducted from 2004 through 2005. RESULTS: During the open-label phase, the 44 patients experienced mean +/- SD body weight loss of -1.29 +/- 3.04 kg, P = .007. During both phases, men (but not women) showed a weight loss of -2.39 +/- 5.45 kg, P = .023. Some subgroups showed desirable changes in several metabolic parameters. Prolonged (32 weeks) orlistat treatment yielded no additional benefits as compared to short (16 weeks) treatment. CONCLUSIONS: In clozapine- or olanzapine-treated overweight or obese patients able to take orlistat on a long-term basis, the drug, with no concomitant hypocaloric diet or behavioral interventions, caused moderate weight loss only in men. However, some metabolic benefits may be achieved independently of weight changes. In patients who do not respond to orlistat within the first 16 weeks, continuation treatment may provide no additional benefits. TRIAL REGISTRATION: controlled-trials.com Identifier: ISRCTN65731856.
机译:目的:探讨奥利司他对成人氯氮平或奥氮平治疗的DSM-IV诊断为精神分裂症和超重或肥胖的耐受奥利司他的患者的长期疗效。方法:在16周的随机对照试验中,将奥利司他或安慰剂以稳定的剂量加至氯氮平或奥氮平中。对于完成双盲治疗的患者,在16周的延长治疗期中将开放标签的奥利司他加入抗精神病药中。不需要低热量饮食或参加行为计划。前瞻性地测量体重(主要结果)和一些代谢参数。对完成两个阶段的人员(即,与先前报告的人群不同)进行了分析。该研究于2004年至2005年进行。结果:在开放标签阶段,这44例患者的平均+/- SD体重减轻了-1.29 +/- 3.04 kg,P = .007。在这两个阶段中,男性(而非女性)的体重减轻为-2.39 +/- 5.45 kg,P = .023。一些亚组显示了一些代谢参数的理想变化。与短时间(16周)治疗相比,延长(32周)奥利司他治疗无其他益处。结论:在氯氮平或奥氮平治疗的能够长期服用奥利司他的超重或肥胖患者中,该药物无伴随的低热量饮食或行为干预,仅在男性中引起中等程度的体重减轻。但是,一些新陈代谢的益处可能与体重变化无关。对于在头16周内对奥利司他无反应的患者,继续治疗可能没有任何其他益处。试用注册:control-trials.com标识符:ISRCTN65731856。

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