29PMyological evaluation of patients with post-acute COVID-19 syndrome

IF 2.8 4区 医学 Q2 CLINICAL NEUROLOGY
F. Authier , M. Aoun Sebaiti , S. Souvannanorath , E. Malfatti , E. Itti , G. Severa
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Abstract

Post-acute COVID-19 syndrome (PACS) is a highly multifaceted condition, mimicking myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) in patients with the most prolonged evolution. Due to the frequency of muscle pain and exertion intolerance, these patients are often suspected of having a muscular disease. Here we present the results of the neuromuscular evaluation of patients with a clinically defined PACS. Twenty-two consecutive PACS patients (17F, 5M; median age 47 yrs) were included. All had at least one Covid-infection, confirmed by PCR, with mild respiratory symptoms, only one having required hospitalization and transfer to intensive care unit at acute stage. After a variable period between weeks to few months, patients developed chronic fatigue (duration > 6 months; n=22, 100%), post-exertional malaise (n=22, 100%), cognitive impairment including short-term memory loss or “brain fog” (n=22, 100%), muscle pain (n=18, 82%). No other specific neuromuscular clinical sign were found. 100% of patients fulfilled diagnostic criteria for ME/CSF: CDC1994/Fukuda, International Consensus Criteria 2011, US Inst Medicine 2015, UK National Institute for health and Care Excellence, 2021. Nineteen (86%) didn’t show any recovery period after the onset of symptoms. ENMG examination was normal, without myogenic pattern; CK levels were normal; and muscle MRI available in five patients did not present any changes including fibro-fatty replacement. Brain 18FDG -PET/MRI showed a pattern of hypometabolism compatible with ME/CSF in half of patients. Muscle biopsy was performed in 3 patients and disclosed mild myopathic features in 2/3. In conclusion, our long-lasting PACS patients with muscular symptoms fulfilled criteria for ME/CSF and may present myopathological changes at muscle biopsy.
29急性后COVID-19综合征患者的肌电学评价
急性后COVID-19综合征(PACS)是一种高度多面性疾病,与肌痛性脑脊髓炎/慢性疲劳综合征(ME/CFS)相似,病程演变时间最长。由于频繁出现肌肉疼痛和运动不耐受,这些患者常被怀疑患有肌肉疾病。在这里,我们提出了临床定义的PACS患者的神经肌肉评估结果。纳入22例连续PACS患者(17F, 5M,中位年龄47岁)。所有人都至少有一次经聚合酶链反应确诊的covid - 19感染,并出现轻度呼吸道症状,只有一人需要住院并在急性期转入重症监护病房。在几周到几个月不等的时间后,患者出现慢性疲劳(持续时间>; 6个月;n= 22,100 %),运动后不适(n= 22,100 %),认知障碍包括短期记忆丧失或“脑雾”(n= 22,100 %),肌肉疼痛(n= 18,82 %)。未发现其他特殊的神经肌肉临床体征。100%的患者符合ME/CSF的诊断标准:CDC1994/Fukuda, 2011年国际共识标准,美国医学研究所2015年,英国国家健康与护理卓越研究所,2021年。19例(86%)在出现症状后没有任何恢复期。ENMG检查正常,未见肌原型;CK水平正常;5名患者的肌肉MRI没有显示任何变化,包括纤维脂肪替代。脑18FDG -PET/MRI显示一半患者的低代谢模式与ME/CSF相容。3例患者行肌肉活检,2/3患者有轻度肌病特征。总之,我们的长期PACS患者有肌肉症状,符合ME/CSF的标准,并且在肌肉活检中可能出现肌肉病理改变。
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来源期刊
Neuromuscular Disorders
Neuromuscular Disorders 医学-临床神经学
CiteScore
4.60
自引率
3.60%
发文量
543
审稿时长
53 days
期刊介绍: This international, multidisciplinary journal covers all aspects of neuromuscular disorders in childhood and adult life (including the muscular dystrophies, spinal muscular atrophies, hereditary neuropathies, congenital myopathies, myasthenias, myotonic syndromes, metabolic myopathies and inflammatory myopathies). The Editors welcome original articles from all areas of the field: • Clinical aspects, such as new clinical entities, case studies of interest, treatment, management and rehabilitation (including biomechanics, orthotic design and surgery). • Basic scientific studies of relevance to the clinical syndromes, including advances in the fields of molecular biology and genetics. • Studies of animal models relevant to the human diseases. The journal is aimed at a wide range of clinicians, pathologists, associated paramedical professionals and clinical and basic scientists with an interest in the study of neuromuscular disorders.
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