Real-World Experiences with VMAT2 Inhibitors in Pediatric Hyperkinetic Movement Disorders.

IF 2.1 Q2 CLINICAL NEUROLOGY
Tremor and Other Hyperkinetic Movements Pub Date : 2025-06-16 eCollection Date: 2025-01-01 DOI:10.5334/tohm.1023
Sujal Manohar, Jennifer Jacobe, Rebecca Berger, Joseph Jankovic, Mariam Hull
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引用次数: 0

Abstract

Background: Vesicular monoamine transporter 2 (VMAT2) inhibitors are often prescribed for the treatment of hyperkinetic movement disorders such as tics, stereotypy, tardive dyskinesia and chorea. These dopamine depleters have been FDA approved in adults for the treatment of chorea in Huntington's disease and tardive dyskinesia. Use of VMAT2 inhibitors in pediatric hyperkinetic movement disorders, however, is limited due to lack of pediatric FDA approval. We review the real-world prescribing practices and patient experiences with VMAT2 inhibitors in children.

Methods: We performed a retrospective chart review of patients treated with VMAT2 inhibitors at a pediatric movement disorders clinic from 2011 to 2023. Demographics, indication, medical history, and clinical notes were reviewed.

Results: We identified 340 pediatric patients (65.3% male, average age 11.9 years) who had been prescribed a VMAT2 inhibitor for a variety of hyperkinetic movement disorders (359 total prescriptions) at our large pediatric movement disorders center. Of the 359 prescriptions for VMAT2 inhibitors, 94% included tetrabenazine, 4.6% deutetrabenazine, and 1.4% valbenazine. Most common clinical indication was tics (73.5%), followed by chorea (9.1%) and self-injurious stereotypy (7.1%). Of these prescriptions, 75.8% (N = 275) successfully commenced treatment. Most patients (62.8%) had clinical improvement with an average Clinical Global Impression-Improvement of 1.8 (±1.2), indicating "very much" or "much" improved, but 11.5% experienced no improvement in symptoms. Most patients (63.9%) reported some side effects, most commonly drowsiness; however, only 35 (10.1%) necessitated discontinuation due to side effects. Seven patients were transitioned from tetrabenazine to deutetrabenazine with resolution of side effects, and one to valbenazine with similar effect. Of the 359 prescriptions, 194 (54%) experienced at least one denial from insurance companies; 24.2% were unable to initiate treatment due to barriers such as insurance denials and 19.6% expressed financial concerns regarding medication affordability.

Discussion: Our study suggests that VMAT2 inhibitors are effective for treating pediatric hyperkinetic movement disorders. Furthermore, this study provides insights into barriers to access to these drugs by pediatric patients.

VMAT2抑制剂治疗小儿多动运动障碍的实际经验
背景:水疱单胺转运蛋白2 (VMAT2)抑制剂常用于治疗多动运动障碍,如抽搐、刻板、迟发性运动障碍和舞蹈病。这些多巴胺消耗剂已被FDA批准用于治疗亨廷顿舞蹈病和迟发性运动障碍的成人舞蹈病。然而,由于缺乏儿科FDA批准,VMAT2抑制剂在儿童多动运动障碍中的应用受到限制。我们回顾了现实世界中儿童使用VMAT2抑制剂的处方实践和患者经验。方法:我们对2011年至2023年在儿科运动障碍诊所接受VMAT2抑制剂治疗的患者进行了回顾性图表回顾。回顾了人口统计学、适应症、病史和临床记录。结果:我们确定了340名儿童患者(65.3%男性,平均年龄11.9岁),他们在我们的大型儿童运动障碍中心开了VMAT2抑制剂治疗各种多动运动障碍(总共359张处方)。在359份VMAT2抑制剂处方中,94%包括丁苯那嗪,4.6%包括二苯那嗪,1.4%包括缬苯那嗪。最常见的临床指征是抽搐(73.5%),其次是舞蹈病(9.1%)和自残刻板印象(7.1%)。在这些处方中,75.8% (N = 275)成功开始治疗。大多数患者(62.8%)临床改善,平均临床总体印象改善为1.8(±1.2),表明“非常”或“非常”改善,但11.5%的患者症状没有改善。大多数患者(63.9%)报告了一些副作用,最常见的是嗜睡;然而,只有35人(10.1%)因副作用需要停药。7例患者从四苯那嗪转为二苯那嗪,副作用得到缓解,1例患者改用丙苯那嗪,效果相似。在359张处方中,194张(54%)至少被保险公司拒绝过一次;由于保险拒绝等障碍,24.2%的人无法开始治疗,19.6%的人表达了对药物负担能力的经济担忧。讨论:我们的研究表明VMAT2抑制剂对治疗儿童多动运动障碍是有效的。此外,本研究还提供了对儿科患者获得这些药物的障碍的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.00
自引率
4.50%
发文量
31
审稿时长
6 weeks
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