Department of Brain and Behavioural Sciences, University of Pavia, Pavia, Italy.
IRCCS Mondino Foundation, Pavia, Italy.
Muscle Nerve. 2021 Aug;64(2):206-211. doi: 10.1002/mus.27324. Epub 2021 Jun 12.
INTRODUCTION/AIMS: Coronavirus disease 2019 (COVID-19), a disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, has become a global pandemic. Patients with myasthenia gravis (MG), often treated with immunosuppressants, might be at higher risk of developing COVID-19 and of demonstrating a severe disease course. We aimed to study prevalence and describe features of COVID-19 in MG patients.
In May 2020, we conducted telephonic interviews with MG patients followed at our referral center. We collected structured data regarding MG and COVID-19, which was diagnosed as probable or confirmed according to the European Centre for Disease Prevention and Control case definition. We compared confirmed-COVID-19 prevalence calculated from the beginning of the pandemic in MG patients with that of the overall Pavia district.
We interviewed 162 MG patients (median age, 66 y; interquartile range 41-77; males 59.9%), 88 from the Pavia district. Three patients had SARS-CoV-2-confirmed by polymerase chain reaction and eight had probable-COVID-19. In the Pavia district, the prevalence of confirmed-COVID-19 among MG patients (1/88, 1.14%) and overall population (4777/546 515, 0.87%) did not differ (P = .538). Higher Myasthenia Gravis Foundation of America clinicalclass and the need for recent rescue treatment, but not ongoing immunosuppressive treatments, were associated with COVID-19 risk. Of 11 MG patients with probable/confirmed-COVID-19, 3 required ventilator support, and 2 elderly patients died of COVID-19 respiratory insufficiency. Only 1 of11 patients experienced worsening MG symptoms, which improved after increasing their steroid dose.
The risk of COVID-19 in MG patients seems to be no higher than that of the general population, regardless of immunosuppressive therapies. In our cohort, COVID-19 barely affected MG course.
简介/目的:由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)感染引起的 2019 年冠状病毒病(COVID-19)已成为全球大流行。经常接受免疫抑制剂治疗的重症肌无力(MG)患者可能面临更高的 COVID-19 发病风险和更严重的疾病进程。我们旨在研究 MG 患者 COVID-19 的患病率并描述其特征。
2020 年 5 月,我们对在我们的转诊中心接受治疗的 MG 患者进行了电话访谈。我们收集了关于 MG 和 COVID-19 的结构化数据,这些数据是根据欧洲疾病预防控制中心的病例定义,诊断为疑似或确诊病例。我们比较了 MG 患者从大流行开始到 COVID-19 确诊的患病率,并与帕维亚地区的整体患病率进行了比较。
我们共访谈了 162 例 MG 患者(中位年龄 66 岁,四分位间距为 41-77 岁;男性占 59.9%),其中 88 例来自帕维亚地区。3 例患者通过聚合酶链反应检测到 SARS-CoV-2 确诊,8 例为疑似 COVID-19。在帕维亚地区,MG 患者中确诊 COVID-19 的患病率(1/88,1.14%)与总体人群(4777/546515,0.87%)没有差异(P=0.538)。更高的美国重症肌无力基金会临床分类和近期需要抢救治疗,但不是持续的免疫抑制治疗,与 COVID-19 风险相关。在 11 例疑似/确诊 COVID-19 的 MG 患者中,有 3 例需要呼吸机支持,2 例老年患者死于 COVID-19 呼吸衰竭。仅有 11 例患者中 1 例出现 MG 症状恶化,增加类固醇剂量后症状改善。
MG 患者感染 COVID-19 的风险似乎并不高于普通人群,无论是否接受免疫抑制治疗。在我们的队列中,COVID-19 对 MG 病程的影响很小。