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首页> 外文期刊>BMC Psychiatry >Early response predicts subsequent response to olanzapine long-acting injection in a randomized, double-blind clinical trial of treatment for schizophrenia
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Early response predicts subsequent response to olanzapine long-acting injection in a randomized, double-blind clinical trial of treatment for schizophrenia

机译:早期反应在一个随机,双盲的精神分裂症临床试验中预测了奥氮平长效注射剂的后续反应

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Background In patients with schizophrenia, early non-response to oral antipsychotic therapy robustly predicts subsequent non-response to continued treatment with the same medication. This study assessed whether early response predicted later response when using a long-acting injection (LAI) antipsychotic. Methods Data were taken from an 8-week, randomized, double-blind, placebo-controlled study of olanzapine LAI in acutely ill patients with schizophrenia (n = 233). Early response was defined as ≥30% improvement from baseline to Week 4 in Positive and Negative Syndrome Scale (PANSS0-6) Total score. Subsequent response was defined as ≥40% baseline-to-endpoint improvement in PANSS0-6 Total score. Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and predictive accuracy were calculated. Clinical and functional outcomes were compared between Early Responders and Early Non-responders. Results Early responseon-response to olanzapine LAI predicted later responseon-response with high sensitivity (85%), specificity (72%), PPV (78%), NPV (80%), and overall accuracy (79%). Compared to Early Non-responders, Early Responders had significantly greater improvement in PANSS0-6 Total scores at all time points and greater baseline-to-endpoint improvement in PANSS subscale scores, Quality of Life Scale scores, and Short Form-36 Health Survey scores (all p ≤ .01). Among Early Non-responders, 20% demonstrated response by Week 8. Patients who lacked early improvement (at Week 4) in Negative Symptoms and Disorganized Thoughts were more likely to continue being non-responders at Week 8. Conclusions Among acutely ill patients with schizophrenia, early response predicted subsequent response to olanzapine LAI. Early Responders experienced significantly better clinical and functional outcomes than Early Non-responders. Findings are consistent with previous research on oral antipsychotics. Clinical Trials Registry F1D-MC-HGJZ: Comparison of Intramuscular Olanzapine Depot With Placebo in the Treatment of Patients With Schizophrenia http://clinicaltrials.gov/ct2/show/NCT00088478?term=olanzapine+depot&rank=3 webcite Registry identifier - NCT00088478
机译:背景在精神分裂症患者中,对口服抗精神病药物治疗的早期无反应有力地预测了随后对相同药物继续治疗的无反应。这项研究评估了使用长效注射剂(LAI)抗精神病药时,早期反应是否可预测晚期反应。方法数据来自奥氮平LAI在急性精神分裂症患者(n = 233)中进行的为期8周,随机,双盲,安慰剂对照的研究。早期反应的定义为:从基线到第4周,阳性和阴性综合征评分(PANSS 0-6 )总分提高≥30%。随后的反应定义为PANSS 0-6 总分基线到终点的改善≥40%。计算敏感性,特异性,阳性预测值(PPV),阴性预测值(NPV)和预测准确性。比较早期反应者和早期非反应者的临床和功能结局。结果对奥氮平LAI的早期应答/无应答预测了晚期应答/无应答,具有高敏感性(85%),特异性(72%),PPV(78%),NPV(80%)和总体准确性(79%) 。与早期无反应者相比,早期反应者在所有时间点的PANSS 0-6 总分都有显着提高,并且PANSS子量表得分,生活质量量表得分,和简短的36型健康调查得分(所有p≤.01)。在早期无反应者中,有20%的人在第8周时表现出反应。在阴性症状和思想混乱方面缺乏早期改善(在第4周)的患者更有可能在第8周继续无反应。结论精神分裂症急性病患者,早期反应可预测对奥氮平LAI的后续反应。早期响应者的临床和功能结局明显优于早期非响应者。研究结果与先前对口服抗精神病药的研究一致。 F1D-MC-HGJZ临床试验注册管理机构:肌肉注射奥氮平储存库与安慰剂治疗精神分裂症的比较http://clinicaltrials.gov/ct2/show/NCT00088478?term=olanzapine+depot&rank=3 webcite注册簿标识符-NCT00088478

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