Pediatric Neurology, Pediatric University Department, Azienda Ospedaliera Universitaria Pisana, University of Pisa, Pisa, Italy.
Pediatric Clinic, Fondazione IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.
Eur J Paediatr Neurol. 2022 Jan;36:1-6. doi: 10.1016/j.ejpn.2021.11.002. Epub 2021 Nov 6.
Sydenham's Chorea (SC) is a neuropsychiatric disorder and a major manifestation of acute rheumatic fever. The erroneous assumption that SC is a benign and self-limiting disease, has led to a lack of high-quality scientific evidence of the therapeutical and prognostic features of SC.
We retrospectively analyzed the medical records of patients <18-years old with SC in 17 Italian pediatric centers. Recorded data included clinical, instrumental and laboratory parameters. Prognostic risk factors including treatment regimens were assessed with univariate and multivariate sub-analysis.
We included 171 patients with SC. 66% had generalized chorea, and 34% hemichorea. 81% had carditis (subclinical in 65%). Additional neurological symptoms were reported in 60% of the patients, mainly dysarthria and dysgraphia. 51% had neuropsychiatric symptoms at onset, which persisted after 12 months in 10%. Among psychiatric manifestations, the most common was anxiety disorder/depression (77%). Neurological remission was reached by 93% of the patients at 6 months; 9% relapsed. Patients were treated as follows: 11% penicillin alone, 37% immunomodulatory therapy, 16% symptomatic drugs (i.e. anti-seizure medication, dopamine antagonists) and 37% both symptomatic and immunomodulatory treatment. Neurological outcome did not differ between groups. Patients receiving symptomatic drugs had a higher risk of relapse on multivariate analysis (p = 0.045).
Treatment of SC was largely heterogeneous. Based on our results, immunomodulatory therapy did not show higher efficacy at medium term, although it was associated to a slightly lower risk of relapse compared to symptomatic therapy. Longitudinal studies are needed to assess specific risk factors and best treatment options.
风湿性舞蹈病(SC)是一种神经精神疾病,也是急性风湿热的主要表现。人们错误地认为 SC 是一种良性和自限性疾病,这导致缺乏关于 SC 治疗和预后特征的高质量科学证据。
我们回顾性分析了 17 家意大利儿科中心的 171 名年龄<18 岁的 SC 患者的病历。记录的数据包括临床、仪器和实验室参数。使用单变量和多变量亚分析评估预后危险因素,包括治疗方案。
我们纳入了 171 例 SC 患者。66%的患者有全身性舞蹈病,34%的患者有单侧舞蹈病。81%的患者有心脏炎(65%为亚临床)。60%的患者有其他神经系统症状,主要为构音障碍和书写障碍。51%的患者在发病时有神经精神症状,其中 10%的症状持续到 12 个月后。在精神表现中,最常见的是焦虑症/抑郁症(77%)。93%的患者在 6 个月时达到神经学缓解;9%的患者复发。患者接受的治疗如下:11%单独使用青霉素,37%免疫调节治疗,16%对症药物(即抗癫痫药物、多巴胺拮抗剂),37%对症和免疫调节联合治疗。不同治疗组之间的神经学结局没有差异。多变量分析显示,接受对症治疗的患者复发风险较高(p=0.045)。
SC 的治疗方法差异很大。根据我们的结果,免疫调节治疗在中期并没有显示出更高的疗效,尽管与对症治疗相比,复发风险略低。需要进行纵向研究来评估特定的风险因素和最佳治疗方案。