Greenberg Benjamin, Plumb Patricia, Cutter Gary, Dean Janet, Desena Allen, Hopkins Sarah, Krishnan Chitra, Pardo Carlos, Recio Albert, Schreiner Teri, Yeh E Ann, McCreary Morgan
Neurology, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Biostatistics, The University of Alabama at Birmingham, Birmingham, Alabama, USA.
BMJ Neurol Open. 2021 May 19;3(1):e000127. doi: 10.1136/bmjno-2021-000127. eCollection 2021.
Since 2014, the USA has documented three outbreaks of acute flaccid myelitis (AFM). Unique features and treatment responses of this myelitis variant have not been prospectively studied. This study prospectively measured outcomes in paediatric myelitis patients relative to treatments.
This was a prospective, multicentre, non-randomised, observational cohort study. The study duration was 5 years and the length of follow-up was 1 year. This study collected data from children and families in North America. Patients were enrolled at academic centres with expertise in myelitis or online via a web portal. Paediatric patients diagnosed with myelitis were eligible for enrolment in the study within 6 months of onset of symptoms. Patients were characterised as transverse myelitis (TM) or the AFM variant based on clinical and radiographic findings.
The cohort of 90 patients included patients with AFM and TM. Of the 51 patients with AFM there was evidence of two clinically relevant patterns. This included a grey matter restricted form of AFM and a cohort with concomitant white matter that could explain lower extremity motor deficits in patients with lesions restricted to the cervical spine. The improvement in deficits with the use of corticosteroids was similar to what was observed in the TM cohort (p=0.97).
Clinicians should consider on a case by case basis the approach to therapy for AFM patients. Prospective controlled studies of long-term outcomes would be useful in this growing patient population.
自2014年以来,美国已记录了三起急性弛缓性脊髓炎(AFM)疫情。这种脊髓炎变体的独特特征和治疗反应尚未得到前瞻性研究。本研究前瞻性地测量了小儿脊髓炎患者相对于治疗的结局。
这是一项前瞻性、多中心、非随机、观察性队列研究。研究持续时间为5年,随访时间为1年。本研究收集了北美儿童及其家庭的数据。患者在具有脊髓炎专业知识的学术中心或通过网络门户在线入组。确诊为脊髓炎的小儿患者在症状出现后6个月内有资格参加本研究。根据临床和影像学检查结果,将患者分为横贯性脊髓炎(TM)或AFM变体。
90名患者的队列包括AFM和TM患者。在51名AFM患者中,有证据表明存在两种临床相关模式。这包括灰质受限型AFM和伴有白质的队列,这可以解释病变局限于颈椎的患者的下肢运动缺陷。使用皮质类固醇后缺陷的改善与TM队列中观察到的相似(p=0.97)。
临床医生应根据具体情况考虑AFM患者的治疗方法。对这一不断增长的患者群体进行长期结局的前瞻性对照研究将是有用的。