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奥氮平用于儿童/青少年广泛性发育障碍的双盲安慰剂对照试验性研究。

A double-blind placebo-controlled pilot study of olanzapine in childhood/adolescent pervasive developmental disorder.

作者信息

Hollander Eric, Wasserman Stacey, Swanson Erika N, Chaplin William, Schapiro Melissa L, Zagursky Karen, Novotny Sherie

机构信息

Seaver and NY Autism Center of Excellence, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1230, New York, New York 10029, USA.

出版信息

J Child Adolesc Psychopharmacol. 2006 Oct;16(5):541-8. doi: 10.1089/cap.2006.16.541.

Abstract

Atypical antipsychotics have been shown to improve disruptive and repetitive behaviors in pervasive developmental disorders (PDDs), but they require assessment of potential side effects. This is the first placebo-controlled trial of olanzapine in the treatment of children and adolescents with PDD. Eleven patients with a diagnosis of either autism, Asperger's syndrome, or PDD not otherwise specified (PDD-NOS) and aged 6-14 years were randomized into an 8-week double-blind, placebo-controlled, parallel treatment study with olanzapine. There was a significant linear trend x group interaction on the Clinical Global Impressions- Improvement (CGI-I) and 50% on olanzapine versus 20% on placebo were responders. Olanzapine was associated with significant weight gain (7.5 +/- 4.8 lbs vs. 1.5 +/- 1.5 lbs on placebo). Olanzapine may be a promising treatment for improving global functioning of PDDs, but the risk of significant weight gain remains a concern. Additional studies are needed to determine the efficacy and safety of olanzapine in the treatment of children with PDD.

摘要

非典型抗精神病药物已被证明可改善广泛性发育障碍(PDD)中的破坏性行为和重复行为,但需要评估其潜在副作用。这是第一项关于奥氮平治疗PDD儿童和青少年的安慰剂对照试验。11名年龄在6至14岁、诊断为自闭症、阿斯伯格综合征或未特定的PDD(PDD-NOS)的患者被随机纳入一项为期8周的双盲、安慰剂对照、奥氮平平行治疗研究。在临床总体印象改善量表(CGI-I)上存在显著的线性趋势×组间交互作用,奥氮平组的有效率为50%,而安慰剂组为20%。奥氮平与显著体重增加相关(奥氮平组体重增加7.5±4.8磅,安慰剂组为1.5±1.5磅)。奥氮平可能是改善PDD整体功能的一种有前景的治疗方法,但显著体重增加的风险仍然令人担忧。需要进一步研究以确定奥氮平治疗PDD儿童的疗效和安全性。

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