Correll Christoph U
Department of Psychiatry, The Zucker Hillside Hospital, Glen Oaks, NY 11004, USA.
J Clin Psychiatry. 2008;69 Suppl 4:26-36.
When taking antipsychotic medications, children and adolescents seem to have a higher risk than adults for experiencing adverse events such as extrapyramidal symptoms, prolactin elevation, sedation, weight gain, and metabolic effects. Side effects may be predicted by the pharmacologic binding profiles of antipsychotics to certain neuroreceptors. Data from 7 recently completed randomized placebo-controlled trials in adolescent schizophrenia and pediatric bipolar disorder that included a total of 1480 patients extend prior results and provide numbers-needed-to-harm as a clinically useful measure of risk. Results from these pediatric studies indicate that adverse effect profiles differ among commonly used antipsychotics. However, more detailed data are needed, as information is lacking regarding carryover or withdrawal effects from prior medications and regarding the masking of effects by adjunctive treatments used to treat agitation, insomnia, or extrapyramidal symptoms and akathisia in these studies. Moreover, randomized head-to-head trials and large-scale studies that investigate predictors of adverse effects as well as the safety and efficacy of interventions aimed at preventing and reversing negative effects of antipsychotics with relevant impact on psychological, psychiatric, and physical functioning are lacking. When choosing an antipsychotic treatment, patients and their families should be included in a careful risk-benefit assessment. Consideration of adverse effects, as well as dietary and lifestyle counseling, should be part of any antipsychotic treatment initiation and continuation. Routine, proactive monitoring of side effects is essential to optimize patient outcomes. In all treatment decisions, the benefits of improving often severe and debilitating manic, psychotic, and aggressive symptomatology must be balanced against the varying risks of adverse effects associated with specific antipsychotic agents in child and adolescent patients.
在服用抗精神病药物时,儿童和青少年似乎比成年人更容易出现锥体外系症状、催乳素升高、镇静、体重增加和代谢影响等不良事件。副作用可能由抗精神病药物与某些神经受体的药理结合特性预测。最近完成的7项针对青少年精神分裂症和儿童双相情感障碍的随机安慰剂对照试验的数据,涉及总共1480名患者,扩展了先前的结果,并提供了伤害所需人数这一临床有用的风险衡量指标。这些儿科研究的结果表明,常用抗精神病药物的不良反应情况有所不同。然而,由于缺乏关于先前用药的残留或撤药效应以及这些研究中用于治疗激越、失眠、锥体外系症状和静坐不能的辅助治疗对效应的掩盖情况的信息,因此需要更详细的数据。此外,还缺乏随机的头对头试验以及大规模研究,这些研究旨在调查不良反应的预测因素以及旨在预防和逆转抗精神病药物对心理、精神和身体功能产生相关负面影响的干预措施的安全性和有效性。在选择抗精神病药物治疗时,应让患者及其家属参与仔细的风险效益评估。考虑不良反应以及饮食和生活方式咨询,应成为任何抗精神病药物治疗开始和持续过程的一部分。对副作用进行常规、主动监测对于优化患者治疗效果至关重要。在所有治疗决策中,改善通常严重且使人衰弱的躁狂、精神病性和攻击症状的益处,必须与儿童和青少年患者使用特定抗精神病药物相关的不同不良反应风险相权衡。