首页> 外文期刊>The journal of clinical psychiatry >Effectiveness of switching from long-acting injectable fluphenazine or haloperidol decanoate to long-acting injectable risperidone microspheres: An open-label, randomized controlled trial
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Effectiveness of switching from long-acting injectable fluphenazine or haloperidol decanoate to long-acting injectable risperidone microspheres: An open-label, randomized controlled trial

机译:从长效可注射氟奋乃静或癸酸氟哌啶醇切换为长效可注射利培酮微球的有效性:一项开放标签,随机对照试验

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Objective: This multisite randomized trial addressed risks and benefits of staying on long-acting injectable haloperidol or fluphenazine versus switching to long-acting injectable risperidone microspheres. Method: From December 2004 through March 2008, adult outpatients with a Structured Clinical Interview for DSM-IV Axis I Disorders-Patient Edition diagnosis of schizophrenia or schizoaffective disorder who were taking haloperidol decanoate (n = 40) or fluphenazine decanoate (n = 22) were randomly assigned to stay on current long-acting injectable medication or switch to risperidone microspheres and followed for 6 months under study protocol and an additional 6 months naturalistic follow-up. Kaplan-Meier and Cox regression analyses were used to examine the primary outcome (time to treatment discontinuation), and random regression models were used to examine secondary outcomes. Results: Groups did not differ significantly in time to treatment discontinuation through 6 months of protocol-driven treatment. When the 6-month naturalistic follow-up period was included, time to treatment discontinuation was significantly shorter for individuals assigned to switch than for individuals assigned to stay (10% of stayers discontinued versus 31% of switchers; P = .01). Groups did not differ with respect to psychopathology, hospitalizations, sexual side effects, new-onset tardive dyskinesia, or new-onset extrapyramidal symptoms. However, those randomized to switch to long-acting injectable risperidone microspheres had greater increases in body mass (increase of 1.0 body mass index [BMI] versus decrease of -0.3 BMI; P = .00) and prolactin (maximum increase to 23.4 ng/mL versus decrease to 15.2 ng/mL, P = .01) compared to those randomized to stay. Conclusion: Switching from haloperidol decanoate or fluphenazine decanoate to risperidone microspheres resulted in more frequent treatment discontinuation as well as significant weight gain and increases in prolactin.
机译:目的:这项多点随机试验探讨了长期使用氟哌啶醇或氟哌嗪注射液与使用长效注射利培酮微球相比的风险和益处。方法:从2004年12月至2008年3月,接受DSM-IV轴I障碍-患者版结构性临床访谈的成人门诊患者正在服用氟哌啶醇癸酸酯(n = 40)或氟哌嗪癸酸酯(n = 22),对精神分裂症或精神分裂症进行诊断。被随机分配以继续使用长效注射药物或转用利培酮微球,并按照研究方案随访6个月,并进行6个月的自然随访。 Kaplan-Meier和Cox回归分析用于检查主要结局(停药时间),随机回归模型用于检查次要结局。结果:经过6个月的方案驱动治疗,各组在停药时间上无显着差异。如果包括6个月的自然随访期,则被终止转诊的患者的治疗中止时间明显短于被分配为转诊的个体(10%的停业者与31%的转业者; P = 0.01)。在心理病理学,住院,性副作用,新发迟发性运动障碍或新发锥体外系症状方面,各组没有差异。但是,那些随机转用长效注射利培酮微球的人的体重增加更大(增加1.0体重指数[BMI],而减少了-0.3 BMI; P = .00)和催乳激素(最大增加到23.4 ng /与随机分组的样本相比,mL样本减少至15.2 ng / mL,P = 0.01)。结论:从氟哌啶醇癸酸酯或氟奋乃静癸酸酯转换为利培酮微球体会导致更频繁的治疗中断,显着的体重增加和催乳素增加。

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