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重症肌无力与2019冠状病毒病:病例系列及与文献对比

Myasthenia gravis and COVID-19: A case series and comparison with literature.

作者信息

Saied Zakaria, Rachdi Amine, Thamlaoui Saber, Nabli Fatma, Jeridi Cyrine, Baffoun Nader, Kaddour Chokri, Belal Samir, Ben Sassi Samia

机构信息

Neurology Department, National Institute Mongi Ben Hamida of Neurology, Tunis, Tunisia.

Intensive Care Unit, National Institute Mongi Ben Hamida of Neurology, Tunis, Tunisia.

出版信息

Acta Neurol Scand. 2021 Sep;144(3):334-340. doi: 10.1111/ane.13440. Epub 2021 Apr 29.

Abstract

OBJECTIVE

To describe presenting symptoms, clinical outcomes, and therapeutic management of concurrent Coronavirus disease 2019 (COVID-19) infections in patients with a pre-existing myasthenia gravis (MG).

METHODS

We conducted a retrospective study in patients with preexisting MG presenting with concurrent COVID-19 between September 21st and November 4th, 2020 when attending the emergency department or routine neurology consultation at the National Institute Mongi Ben Hamida of Neurology of Tunis, Tunisia.

RESULTS

Five patients were identified. The Myasthenia Gravis Foundation of America scores (MGFA) prior to COVID-19 infection were class I in one patient, class II (IIa, IIb) in two patients, and class IIIb in one patient. Four patients had mild to moderate courses of COVID-19 infection. One patient presented a critical infection with acute respiratory disease syndrome (ARDS) requiring mechanical ventilation. Two of them also demonstrated signs of MG exacerbation requiring the use of intravenous immunoglobulin in one case. We maintained immunosuppressant therapy to MG in all our patients. All our patients received Azithromycin (AZM) as a part of specific drug treatment of COVID-19 infection. Outcome was favorable in 4 patients and rapidly fatal evolution was observed in the patient with ADRS.

DISCUSSIONS AND CONCLUSION

The results from our study suggest that prior MG activity could partially influence the subsequent clinical outcomes. It emerged also that ongoing long-term immunosuppressive immunotherapy to MG should be maintained during the COVID-19 pandemic and that AZM can be used safely in MG patients and concurrent COVID-19 infection.

摘要

目的

描述合并新型冠状病毒肺炎(COVID-19)感染的重症肌无力(MG)患者的症状表现、临床结局及治疗管理。

方法

我们对2020年9月21日至11月4日期间在突尼斯突尼斯市蒙吉·本·哈米达国家神经病学研究所急诊科就诊或进行常规神经科会诊时合并COVID-19感染的既往MG患者进行了一项回顾性研究。

结果

共确定5例患者。COVID-19感染前美国重症肌无力基金会评分(MGFA),1例为I级,2例为II级(IIa、IIb),1例为IIIb级。4例患者COVID-19感染病程为轻至中度。1例患者出现严重感染伴急性呼吸窘迫综合征(ARDS),需要机械通气。其中2例还表现出MG加重迹象,1例需要使用静脉注射免疫球蛋白。我们对所有患者维持MG免疫抑制治疗。所有患者均接受阿奇霉素(AZM)作为COVID-19感染特异性药物治疗的一部分。4例患者预后良好,ARDS患者观察到快速死亡进展。

讨论与结论

我们的研究结果表明,既往MG活动可能部分影响随后的临床结局。还发现,在COVID-19大流行期间应维持对MG的长期免疫抑制免疫治疗,并且AZM可安全用于MG患者合并COVID-19感染。

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