Department of Neurology and Center for Clinical Neuroscience, Charles University in Prague, First Faculty of Medicine and General University Hospital in Prague, Prague, Czech Republic.
Institute of Biophysics and Informatics of the First Faculty of Medicine, Charles University, Prague, Czech Republic.
Eur J Neurol. 2021 Oct;28(10):3418-3425. doi: 10.1111/ene.14951. Epub 2021 Jun 25.
Myasthenia gravis (MG) patients could be a vulnerable group in the pandemic era of coronavirus 2019 (COVID-19) mainly due to respiratory muscle weakness, older age and long-term immunosuppressive treatment. We aimed to define factors predicting the severity of COVID-19 in MG patients and risk of MG exacerbation during COVID-19.
We evaluated clinical features and outcomes after COVID-19 in 93 MG patients.
Thirty-five patients (38%) had severe pneumonia and we recorded 10 deaths (11%) due to COVID-19. Higher forced vital capacity (FVC) values tested before COVID-19 were shown to be protective against severe infection (95% CI 0.934-0.98) as well as good control of MG measured by the quantified myasthenia gravis score (95% CI 1.047-1.232). Long-term chronic corticosteroid treatment worsened the course of COVID-19 in MG patients (95% CI 1.784-111.43) and this impact was positively associated with dosage (p = 0.005). Treatment using azathioprine (95% CI 0.448-2.935), mycophenolate mofetil (95% CI 0.91-12.515) and ciclosporin (95% CI 0.029-2.212) did not influence the course of COVID-19. MG patients treated with rituximab had a high risk of death caused by COVID-19 (95% CI 3.216-383.971). Exacerbation of MG during infection was relatively rare (15%) and was not caused by remdesivir, convalescent plasma or favipiravir (95% CI 0.885-10.87).
As the most important predictors of severe COVID-19 in MG patients we identified unsatisfied condition of MG with lower FVC, previous long-term corticosteroid treatment especially in higher doses, older age, the presence of cancer, and recent rituximab treatment.
重症肌无力(MG)患者由于呼吸肌无力、年龄较大和长期免疫抑制治疗,可能成为 2019 年冠状病毒(COVID-19)大流行时期的脆弱群体。我们旨在确定预测 COVID-19 中 MG 患者严重程度和 COVID-19 期间 MG 恶化风险的因素。
我们评估了 93 例 MG 患者 COVID-19 后的临床特征和结局。
35 例(38%)患者患有重症肺炎,我们记录了 10 例(11%)COVID-19 死亡病例。COVID-19 前检测到的更高用力肺活量(FVC)值被证明可预防严重感染(95%置信区间 0.934-0.98),以及通过量化肌无力评分(95%置信区间 1.047-1.232)测量的 MG 良好控制。长期慢性皮质类固醇治疗使 MG 患者 COVID-19 病程恶化(95%置信区间 1.784-111.43),且这种影响与剂量呈正相关(p=0.005)。使用硫唑嘌呤(95%置信区间 0.448-2.935)、霉酚酸酯(95%置信区间 0.91-12.515)和环孢素(95%置信区间 0.029-2.212)治疗并未影响 COVID-19 病程。用利妥昔单抗治疗的 MG 患者 COVID-19 死亡风险较高(95%置信区间 3.216-383.971)。MG 在感染期间恶化相对罕见(15%),且与瑞德西韦、恢复期血浆或法匹拉韦无关(95%置信区间 0.885-10.87)。
作为 MG 患者 COVID-19 严重程度的最重要预测因素,我们确定了 FVC 较低、既往长期皮质类固醇治疗(尤其是高剂量)、年龄较大、存在癌症以及近期利妥昔单抗治疗的 MG 状况不佳。