Neurology Unit, "Azienda Provinciale per i Servizi Sanitari", Trento "Santa Chiara" Hospital, Largo Medaglie d'oro 9, 38122 Trento, Italy.
Section of Neurophysiology, Neurology Unit, "Azienda Ospedaliera Universitaria Integrata Verona", Verona "Borgo Trento" Hospital, Piazzale Aristide Stefani 1, 37126 Verona, Italy.
Toxins (Basel). 2024 Jun 26;16(7):289. doi: 10.3390/toxins16070289.
Botulinum toxin (BT), a first-line treatment for focal dystonias in adults, has gained USA Food and Drug Administration approval for pediatric upper and lower extremity spasticity and sialorrhea, though its use in children younger than 2 years old is still considered off-label treatment for all pathologies. Dosing, treatment strategies and outcome measures lack international consensus, and they are often extrapolated from adult or spasticity guidelines. This review aims to evaluate the best available evidence on the efficacy and safety of BT therapy in pediatric dystonia (age under 21 years old), isolated or associated with other medical conditions. A comprehensive search in PubMed, Scopus and Web of Science was conducted, including only articles in English. Although no randomized controlled trials are still present, 12 articles were included with an overall of 57 patients. All the papers demonstrate that BT can improve motor function, decrease pain and ameliorate quality of life, with minimal adverse effects in pediatric patients affected by pure or mixed dystonic motor disorders. Despite the low level of evidence, our review shows that BT could be an efficacious treatment for these pediatric patients. The frequent generalized involvement, together with the heterogeneous nature of childhood dystonic forms, sometimes intermingled with spasticity, prompts further multicenter clinical trials or prospective studies with a higher level of evidence to shed light on the efficacy and safety profile of BT in pediatric dystonia.
肉毒毒素(BT)是成人局灶性肌张力障碍的一线治疗药物,已获得美国食品和药物管理局(FDA)批准,用于治疗小儿上下肢痉挛和流涎症,但对于所有疾病,其在 2 岁以下儿童中的使用仍被视为超适应证治疗。剂量、治疗策略和结局评估缺乏国际共识,且常从成人或痉挛指南中推断而来。本综述旨在评估 BT 治疗儿科肌张力障碍(21 岁以下),包括单独或合并其他医学病症的有效性和安全性的最佳现有证据。我们在 PubMed、Scopus 和 Web of Science 中进行了全面检索,仅纳入英文文章。尽管目前仍无随机对照试验,但纳入了 12 篇文章,共计 57 例患者。所有研究均表明,BT 可改善运动功能、减轻疼痛并改善生活质量,且在纯或混合性运动障碍性肌张力障碍的儿科患者中,不良反应最小。尽管证据水平较低,但本综述表明 BT 可能是这些儿科患者的有效治疗方法。频繁的全身性受累,以及儿童期肌张力障碍的异质性性质,有时与痉挛相混合,促使进一步开展多中心临床试验或具有更高证据水平的前瞻性研究,以阐明 BT 在儿科肌张力障碍中的疗效和安全性特征。