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一项关于利培酮用于治疗难治性精神疾病儿童和青少年的回顾性病历审查。

A retrospective chart review of risperidone use in treatment-resistant children and adolescents with psychiatric disorders.

作者信息

Simeon Jovan, Milin Robert, Walker Selena

机构信息

Royal Ottawa Hospital, Ontario, Canada.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2002 Feb;26(2):267-75. doi: 10.1016/s0278-5846(01)00264-0.

Abstract

Antipsychotic drugs are used to treat a wide variety of child psychiatric disorders characterized by psychotic symptoms, aggression, excitement, tics, stereotypies and hyperactivity nonresponsive to other therapies. Unfortunately, typical antipsychotics have many adverse effects limiting their long-term use. Novel antipsychotics with combined dopaminergic and serotonergic action, such as risperidone, appear to offer better safety and efficacy profiles in controlled studies of adult patients, and therefore appeared as promising pharmacotherapeutic agents in child psychiatry. The purpose of this retrospective chart review was to obtain data on the potential effectiveness and tolerability of risperidone in children and adolescents presenting with a variety of chronic and severe psychiatric disorders who had been unresponsive to previous pharmacological treatments. Charts for 106 children and adolescents (males n = 81 or 76.4%; females n = 25 or 23.6%), presenting with attention deficit and/or hyperactivity disorder (n = 49 or 46.2%), conduct disorder (n = 13 or 12.3%), oppositional-defiant disorder (n = 5 or 4.7%), behavioural problems not otherwise specified (n = 2 or 1.9%), autism (n = 8 or 7.5%), Asperger's syndrome (n = 8 or 7.5%), pervasive developmental disorder (PDD) not otherwise specified (n = 4 or 3.8%), anxiety (n = 6 or 5.7%), depression (n = 2 or 1.9%), dysthymia (n = 2 or 1.9%), schizophrenia (n = 4 or 3.8%), adjustment disorder (n = 1 or 0.9%) and obsessive-compulsive disorder (n = 2 or 1.9%) were reviewed retrospectively to determine the tolerability and potential efficacy of risperidone treatment for a variety of psychiatric disorders. Six subjects also presented with mental retardation. The average length of illness prior to risperidone treatment was 5 years and the average age of risperidone treatment onset was 11 years. The mean daily dose of risperidone was 1.2 mg (range = 0.25 to 8.0 mg). Very few adverse effects were reported. The average length of risperidone treatment was 11 months with the majority (n = 75 or 76%) of patients maintained on risperidone following study termination. Seven cases (6.6%) were missing follow-up data. The majority (n = 78 or 74%) of patients were taking concurrent psychiatric medications, most commonly stimulants for the treatment of ADHD. Clinical global improvements for children and adolescents at the final study visit were marked (n = .37 or 34.9%), moderate (n = .40 or 37.7%), mild (n = 13 or 12.4%), none (n = 12 or 11.3%), or worse (n = 1 or 1%). Three cases (2.9%) were missing clinical improvement data. Results suggest that risperidone may be useful for managing behavioural disturbances and psychotic symptoms associated with a wide variety of childhood psychiatric disorders. For most patients in the study, a combination of risperidone and adjunctive pharmacotherapy was beneficial. Controlled and discontinuation studies of risperidone treatment in children and adolescents with behavioural and psychotic disorders are recommended.

摘要

抗精神病药物用于治疗多种以精神病性症状、攻击性、兴奋、抽动、刻板动作和多动为特征且对其他治疗无反应的儿童精神障碍。不幸的是,传统抗精神病药物有许多不良反应,限制了它们的长期使用。具有多巴胺能和5-羟色胺能联合作用的新型抗精神病药物,如利培酮,在成年患者的对照研究中似乎具有更好的安全性和疗效,因此在儿童精神病学中成为有前景的药物治疗剂。本回顾性病历审查的目的是获取利培酮对患有各种慢性和严重精神障碍且对先前药物治疗无反应的儿童和青少年的潜在有效性和耐受性的数据。回顾了106例儿童和青少年(男性n = 81或76.4%;女性n = 25或23.6%)的病历,这些儿童和青少年患有注意力缺陷和/或多动障碍(n = 49或46.2%)、品行障碍(n = 13或12.3%)、对立违抗障碍(n = 5或4.7%)、未另行说明的行为问题(n = 2或1.9%)、孤独症(n = 8或7.5%)、阿斯伯格综合征(n = 同样为8或7.5%)、未另行说明的广泛性发育障碍(PDD)(n = 4或3.8%)、焦虑症(n = 6或5.7%)、抑郁症(n = 2或1.9%)、心境恶劣(n = 2或1.9%)、精神分裂症(n = 4或3.8%)、适应障碍(n = 1或0.9%)和强迫症(n = 2或1.9%),以确定利培酮治疗各种精神障碍的耐受性和潜在疗效。6名受试者还伴有智力发育迟缓。在开始使用利培酮治疗前,平均患病时长为5年,开始使用利培酮治疗的平均年龄为11岁。利培酮的平均日剂量为1.2毫克(范围 = 0.25至8.0毫克)。报告的不良反应极少。利培酮治疗的平均时长为11个月,在研究结束后,大多数患者(n = 7A或76%)继续使用利培酮。7例(6.6%)缺失随访数据。大多数患者(n = 78或74%)同时服用精神科药物,最常见的是用于治疗多动症的兴奋剂。在最终研究访视时,儿童和青少年的临床整体改善情况为显著改善(n = 37或34.9%)、中度改善(n = 40或37.7%)、轻度改善(n = 13或12.4%)、无改善(n = 12或11.3%)或病情恶化(n = 1或1%)。3例(2.9%)缺失临床改善数据。结果表明,利培酮可能有助于管理与多种儿童精神障碍相关的行为障碍和精神病性症状。对于研究中的大多数患者,利培酮与辅助药物治疗相结合是有益的。建议对患有行为和精神障碍的儿童和青少年进行利培酮治疗的对照和停药研究。

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