Complex Motor Disorder Service, Children's Neurosciences, Evelina London Children's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, UK; Perinatal Imaging, Imaging Sciences and Biomedical Engineering, King's College London, UK.
Department of Neurosurgery, University Hospital Montpellier, France.
Parkinsonism Relat Disord. 2023 Jul;112:105438. doi: 10.1016/j.parkreldis.2023.105438. Epub 2023 May 18.
Status Dystonicus (SD) represents the most severe end of the spectrum of dystonia. We aimed to explore whether reported features of cases of SD have changed over time.
A systematic review of cases of SD reported from 2017 to 2023 and comparison of features to data extracted from 2 previous literature reviews (epochs 2012-2017 and pre-2012).
From 53 papers, a total 206 SD episodes in 168 patients were identified from 2017 to 2023. Combining data from all 3 epochs, a total of 339 SD episodes were reported from 277 patients. SD episodes occurred mostly in children, with a trigger identified in 63.4% of episodes, most commonly infection/inflammation. Most reported underlying aetiologies were genetic (e.g. 49.5% between 2017 and 2023), including new associated aetiologies in each epoch. Deep Brain Stimulation (DBS)-related SD increased over time. Neurosurgical interventions were more frequently reported in later epochs. Across the epochs, return to or improvement post SD episode, compared to baseline was reported above 70%. Reported mortality was 4.9% most recently, compared to 11.4% and 7.9%, previously.
SD episodes reported have more than doubled in the last 5 years. Reports of medication change-induced SD have become less frequent, whilst episodes of DBS-related SD have become more frequent. More dystonia aetiologies, including novel aetiologies have been reported in recent cohorts, reflecting advances in genetic diagnosis. Neurosurgical interventions are increasingly reported in the management of SD episodes, including novel use of intraventricular baclofen. Overall outcomes from SD remain largely unchanged over time. No prospective epidemiological studies of SD were identified.
扭转痉挛状态(Status Dystonicus,SD)代表了痉挛谱中最严重的一端。我们旨在探讨报告的 SD 病例的特征是否随时间发生了变化。
对 2017 年至 2023 年报告的 SD 病例进行系统回顾,并将特征与之前两次文献回顾(2012-2017 年和 2012 年前)中提取的数据进行比较。
从 53 篇论文中,共确定了 2017 年至 2023 年期间 168 名患者的 206 例 SD 发作,将所有 3 个时期的数据合并,共报告了 277 名患者的 339 例 SD 发作。SD 发作主要发生在儿童中,63.4%的发作有明确的诱因,最常见的是感染/炎症。报告的大多数潜在病因是遗传的(例如,2017 年至 2023 年期间为 49.5%),每个时期都有新的相关病因。随着时间的推移,与深部脑刺激(Deep Brain Stimulation,DBS)相关的 SD 发作增加。神经外科干预在后期更频繁地报告。在所有时期中,与基线相比,SD 发作后恢复或改善的比例均高于 70%。最近报告的死亡率为 4.9%,而之前分别为 11.4%和 7.9%。
在过去的 5 年中,报告的 SD 发作增加了一倍以上。药物改变引起的 SD 报告频率降低,而与 DBS 相关的 SD 发作变得更加频繁。在最近的队列中报告了更多的肌张力障碍病因,包括新的病因,这反映了遗传诊断的进展。神经外科干预在 SD 发作的治疗中越来越多地被报告,包括新型脑室注射巴氯芬的应用。SD 的总体结果随时间变化不大。没有发现 SD 的前瞻性流行病学研究。