COVID-19 and Myasthenia Gravis Exacerbation in an Elderly Patient: a Case Report

I. Kaidashev, A. V. Lavrenko, Y. Avramenko, L.P. Ozarchuk
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Abstract

Treatment of COVID-19 in elderly patients with myasthenia gravis (MG), an autoimmune disease characterized by increased dynamic muscle weakness, is associated with a number of challenges, such as chronic immunosuppression, exacerbation of MG, and polymorbidity.We present the case of an elderly patient with generalized seropositive MG who contracted COVID-19. Aggravating factors are the patient’s age, the duration of myasthenia gravis, COVID-19, and comorbidity (chronic coronary heart disease, diffuse cardiosclerosis, atrial fibrillation, NYHA class I heart failure, hyper­tension). The patient had a favorable outcome despite the exacerbation. The patient required intravenous injections of immunoglobulin (1 mg/kg) for 2 days, non-invasive ventilatory support, and treatment of respira­tory and urogenital nosocomial infections (Pseudomonas aeruginosa and Klebsiella oxytoca).COVID-19 led to exacerbation of MG, progression of muscle weakness, development of respiratory failure, and hypoxia in an elderly patient. Intravenous immunoglobulin is a possible effective medication in the treatment of this comorbid pathology.During the COVID-19 pandemic patients with MG may be at greater risk of worse outcomes than healthy individuals due to an immunodeficient state associated with immunotherapy and possible respiratory and bulbar muscle weakness. The examination of patients with MG and a COVID-19 may reveal new pathogenetic patterns and change the therapeutic strategy.Knowledge of the essence of the disease, the main links of its pathogenesis, the spectrum of modern therapeutic agents, and algorithms for their use allow us to improve the quality of medical care for patients with MG. The implementation of a comprehensive multidisciplinary approach in the treatment of these patients allows us to significantly reduce the mortality rate, prolong the life of patients, and improve its quality.
COVID-19 与一名老年患者的肌无力加重:病例报告
肌无力(MG)是一种以动态肌无力加重为特征的自身免疫性疾病,对患有肌无力的老年患者进行 COVID-19 治疗会面临一系列挑战,如慢性免疫抑制、MG 病情加重和多病症等。我们介绍了一例全身血清反应阳性的老年 MG 患者感染 COVID-19 的病例。加重病情的因素包括患者的年龄、重症肌无力的病程、COVID-19 和合并症(慢性冠心病、弥漫性心脏硬化、心房颤动、NYHA I 级心力衰竭、高血压)。尽管病情恶化,但患者的预后良好。患者需要连续两天静脉注射免疫球蛋白(1 毫克/千克),接受无创呼吸机支持治疗,并治疗呼吸道和泌尿道感染(铜绿假单胞菌和氧合克雷伯菌)。COVID-19 导致一名老年患者的 MG 病情加重、肌无力恶化、呼吸衰竭和缺氧。在 COVID-19 大流行期间,由于与免疫疗法相关的免疫缺陷状态以及可能出现的呼吸和球部肌无力,MG 患者可能比健康人面临更严重的后果风险。对 MG 和 COVID-19 患者进行检查可能会发现新的发病模式,并改变治疗策略。了解疾病的本质、发病的主要环节、现代治疗药物的范围以及使用这些药物的算法,有助于提高 MG 患者的医疗质量。在治疗这些患者时采用多学科综合方法,可以大大降低死亡率,延长患者的生命并提高其质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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