Author: Palaiodimou, Lina; Stefanou, Mariaâ€Ioanna; Katsanos, Aristeidis H.; Fragkou, Paraskevi C.; Papadopoulou, Marianna; Moschovos, Christos; Michopoulos, Ioannis; Kokotis, Panagiotis; Bakirtzis, Christos; Naska, Androniki; Vassilakopoulos, Theodoros I.; Chroni, Elisabeth; Tsiodras, Sotirios; Tsivgoulis, Georgios
Title: Prevalence, clinical characteristics and outcomes of Guillain−Barré syndrome spectrum associated with COVIDâ€19: A systematic review and metaâ€analysis Cord-id: 3y2j8bej Document date: 2021_4_28
ID: 3y2j8bej
Snippet: BACKGROUND AND PURPOSE: Mounting evidence supports an association between Guillain−Barré syndrome spectrum (GBSs) and severe acute respiratory syndrome coronavirus 2 (SARSâ€CoVâ€2) infection. However, GBSs in the setting of coronavirus disease 2019 (COVIDâ€19) remains poorly characterized, whilst GBSs prevalence amongst COVIDâ€19 patients has not been previously systematically evaluated using a metaâ€analytical approach. METHODS: A systematic review and metaâ€analysis of observational c
Document: BACKGROUND AND PURPOSE: Mounting evidence supports an association between Guillain−Barré syndrome spectrum (GBSs) and severe acute respiratory syndrome coronavirus 2 (SARSâ€CoVâ€2) infection. However, GBSs in the setting of coronavirus disease 2019 (COVIDâ€19) remains poorly characterized, whilst GBSs prevalence amongst COVIDâ€19 patients has not been previously systematically evaluated using a metaâ€analytical approach. METHODS: A systematic review and metaâ€analysis of observational cohort and case series studies reporting on the occurrence, clinical characteristics and outcomes of patients with COVIDâ€19â€associated GBSs was performed. A randomâ€effects model was used to calculate pooled estimates and odds ratios (ORs) with corresponding 95% confidence intervals (CIs), compared to nonâ€COVIDâ€19, contemporary or historical GBSs patients. RESULTS: Eighteen eligible studies (11 cohorts, seven case series) were identified including a total of 136,746 COVIDâ€19 patients. Amongst COVIDâ€19 patients, including hospitalized and nonâ€hospitalized cases, the pooled GBSs prevalence was 0.15‰ (95% CI 0%–0.49‰; I (2) = 96%). Compared with nonâ€infected contemporary or historical controls, patients with SARSâ€CoVâ€2 infection had increased odds for demyelinating GBSs subtypes (OR 3.27, 95% CI 1.32%–8.09%; I (2) = 0%). In SARSâ€CoVâ€2â€infected patients, olfactory or concomitant cranial nerve involvement was noted in 41.4% (95% CI 3.5%–60.4%; I (2) = 46%) and 42.8% (95% CI 32.8%–53%; I (2) = 0%) of the patients, respectively. Clinical outcomes including inâ€hospital mortality were comparable between COVIDâ€19 GBSs patients and nonâ€infected contemporary or historical GBSs controls. CONCLUSION: GBSs prevalence was estimated at 15 cases per 100,000 SARSâ€CoVâ€2 infections. COVIDâ€19 appears to be associated with an increased likelihood of GBSs and with demyelinating GBSs variants in particular.
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