COVID-19感染合并格林-巴利综合征:临床特征、致病机制和呼吸衰竭的系统综述

M. Khaki, P. Dehghan, Naghmeh Malekzadeh, M. Khamoushi, Fahimehalsadat Shojaei, Sahar Memar Motazerin, H. Najafi, R. Boostani, G. Malekzadeh, G. Chi
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摘要

背景:世界卫生组织(世卫组织)于2020年3月宣布由严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)引起的大流行。鉴于冠状病毒的神经嗜性特征以及越来越多的COVID-19相关神经系统疾病,包括格林-巴利综合征(GBS),我们对78例COVID-19相关GBS的临床特征、诊断检查和临床结局进行了系统回顾。方法:我们通过在PubMed/MEDLINE和EMBASE数据库中进行检索,确定了与COVID-19相关的GBS病例报告和病例系列。我们使用Cochrane Murad等人提供的评估清单来评估研究的质量。提取的数据包括人口统计学特征、临床表现、诊断检查和结果。结果:系统检索共获得60篇文章,报告了78例诊断为COVID-19相关GBS的患者。患者以男性为主(65.3%),平均年龄57岁。上升对称性轻瘫是最常见的表现(79.4%),脱髓鞘模式54例(79.4%)。脑脊液分析显示48例(75%)患者有白蛋白细胞分离。COVID-19相关GBS的死亡率估计为6.4%,可归因于进行性呼吸衰竭。结论:考虑到COVID-19相关性GBS患者存在呼吸衰竭等相关并发症,及时发现对预防临床预后不良至关重要。另一方面,临床医生必须保持警惕,以确定新诊断的GBS患者的SARS-CoV-2感染的临床表现,因为这可能是亚临床病毒感染的神经系统并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COVID-19 infection complicated by Guillain-Barre Syndrome: a systematic review of clinical features, pathogenic mechanism, and respiratory failure
Background: The World Health Organization (WHO) declared a pandemic in March 2020 caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Given the neurotropism feature of the coronavirus and growing number of COVID-19 associated neurological disorders, including Guillain Barre syndrome (GBS), we conducted a systematic review to thoroughly describe the clinical features, diagnostic workup, and clinical outcome of COVID-19 associated GBS in 78 cases. Methods: We identified case reports and case series of COVID-19 associated GBS by conducting a search in the PubMed/MEDLINE and EMBASE databases. We assessed the quality of studies using an appraisal checklist presented by Cochrane Murad et al. Extracted data included demographic characteristics, clinical presentation, diagnostic workup, and outcome. Results: The systematic search yielded a total of 60 articles reporting 78 patients with a diagnosis of COVID-19 associated GBS. The patients were mainly male (65.3%) with an average age of 57 years. The ascending symmetrical paresis was the most common presentation (79.4%), with demyelinating pattern in 54 patients (79.4%). The CSF analysis showed albuminocytologic dissociation in 48 patients (75%). The mortality of COVID-19 associated GBS was estimated as 6.4% attributable to progressive respiratory failure. Conclusion: Given the associated morbidities such as respiratory failure in patients with COVID-19 associated GBS, its timely detection is crucial to prevent poor clinical outcomes. On the other hand, clinicians must be vigilant to identify the clinical findings of SARS-CoV-2 infection in newly diagnosed GBS patients, as this might be a neurological complication of the subclinical viral infection.
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