East London NHS Foundation Trust, 9 Rush Court, Bedford, MK40 3JT, UK.
University College London, London, UK.
Drug Saf. 2024 Nov;47(11):1095-1126. doi: 10.1007/s40264-024-01446-0. Epub 2024 Jun 11.
Tardive dyskinesia (TD) is a persisting, and potentially irreversible, movement disorder associated with treatment with dopamine receptor antagonists. Few data are available on the risk of TD in children and adolescents treated with antipsychotic medication.
To review the literature on incidence, risk factors, and treatment options for antipsychotic-associated TD in children and adolescents (aged < 18 years).
Relevant articles were identified through a systematic search of Embase and Medline performed in January 2024. Methodological quality was assessed using the Newcastle-Ottawa Scale and Joanna Briggs Institute Critical Appraisal tools.
Thirteen studies were identified. The reported TD point prevalence was 5-20%, with higher rates in studies involving typical antipsychotics. Lower estimates (around 1%) emerged from analyses of clinical database data suggesting underdiagnosis in clinical practice. Risk factors included treatment with typical antipsychotics, higher doses, longer duration of exposure, older age, female gender, higher baseline Abnormal Involuntary Movements Scale (AIMS) scores, intellectual impairment, and perinatal complications.
Although relatively few cases have been reported in children and adolescents, TD remains a risk in this population. Individuals receiving antipsychotics should be monitored carefully for the emergence of abnormal movements. Other than dose reduction, discontinuation, or switch to a lower-risk antipsychotic, few interventions have demonstrated efficacy. The strongest evidence for pharmacological treatment is for VMAT-2 inhibitors (valbenazine and deutetrabenazine), but these drugs are not licensed for use in children. To reduce risk, antipsychotics should be prescribed only if necessary, at the minimum effective dose and for the minimum necessary duration.
迟发性运动障碍(TD)是一种持续存在的、潜在不可逆转的运动障碍,与多巴胺受体拮抗剂的治疗有关。关于接受抗精神病药物治疗的儿童和青少年发生 TD 的风险,数据有限。
综述儿童和青少年(<18 岁)接受抗精神病药物治疗时与 TD 相关的发病率、风险因素和治疗选择的文献。
通过 2024 年 1 月对 Embase 和 Medline 进行的系统检索,确定了相关文章。使用纽卡斯尔-渥太华量表和 Joanna Briggs 研究所批判性评估工具评估方法学质量。
确定了 13 项研究。报告的 TD 时点患病率为 5-20%,涉及典型抗精神病药的研究中患病率更高。从临床数据库数据分析中得出的较低估计值(约 1%)表明临床实践中的诊断不足。风险因素包括使用典型抗精神病药、较高剂量、较长暴露时间、年龄较大、女性、较高的基线异常不自主运动量表(AIMS)评分、智力障碍和围产期并发症。
尽管在儿童和青少年中报告的病例相对较少,但该人群仍存在 TD 的风险。接受抗精神病药物治疗的个体应密切监测异常运动的出现。除了减少剂量、停药或改用风险较低的抗精神病药外,很少有干预措施显示出疗效。VMAT-2 抑制剂(valbenazine 和 deutetrabenazine)在药物治疗方面的证据最强,但这些药物未获准用于儿童。为了降低风险,抗精神病药物仅在必要时、以最低有效剂量和最短必要时间开具。