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. 2020 Nov 13;27(3):458–466. doi: 10.1016/j.cmi.2020.11.005

Table 3.

Neurologic assessment in COVID-19 patients with acute ischaemic cerebrovascular syndrome, encephalitis, encephalopathy and GBS

Characteristic Acute ischaemic cerebrovascular syndrome (n = 57) Encephalitis (n = 21) Encephalopathy (n = 67) GBS (n = 15)
Brain imaging 57 (100) 21 (100) 57 (85.1) 5 (33.3)
CT scan 9 (15.8) 0 12 (17.9) 0
MRI 48 (84.2) 21 (100) 45 (67.2) 5 (33.3)
 Acute ischaemic lesion 52 (91.7) 2 (9.5) 6 (9) 2 (13.3)
Unifocal ischaemic lesion 39 (68.4) 1 (4.8) 1 (1.5) 1 (6.7)
Multifocal ischaemic lesions 13 (22.8) 1 (4.8) 5 (7.5) 1 (6.7)
Large vessel infarct 46 (88.4)a 0 0 1 (6.7)
Small vessel infarct 6 (11.5) 2 (9.5) 6 (9) 1 (6.7)
 Microhemorrhages 0 2 (9.5) 2 (3) 0
 Other lesion 0 14 (66.7)b 1 (1.5)c 0
Spine MRI 0 0 2 (3) 3 (20)
 Any lesion 0 0
Cerebrospinal fluid examination 3 (5.2) 21 (100) 36 (53.7) 14 (93.3)
 Normal 3 (5.2) 3 (14.3) 28 (41.8) 5 (33.3)
 WBC count >5/mm³ 14 (66.7) 0 1 (6.7)
 Proteins >0.45 g/L 12 (57.1) 8 (11.9) 8 (53.3)
 Isolated elevated proteins 4 (19.0) 8 (11.9) 8 (53.3)
 Positive SARS-CoV-2 PCR 0 2 (9.5) 0 0
Electroencephalogram 4 (7.0) 15 (71.4) 32 (47.8) 2 (14.3)
 Normal 0 1 (4.8) 6 (9) 0
 Diffuse slowing 3 (5.3) 9 (42.9) 17 (25.4) 1 (6.7)
 Anterior slowing 0 2 (9.5) 5 (7.5) 1 (6.7)
 Focal lateralized slowing and/or paroxysm 1 (1.8) 4 (19) 8 (11.9) 0
 Periodic pattern 0 1 (4.8) 3 (4.5) 0
 Status epilepticus 0 1 (4.8) 1 (1.5) 0
Electroneuromyography 1 (1.8) 1 (4.8) 3 (4.5) 14 (93.3)
 Abnormal findings 1 (1.8) 1 (4.8) 3 (4.5) 13 (86.7)
 Axonal injury 1 (1.8) 1 (4.8) 1 (1.5) 0
 Demyelination 1 (1.8) 0 2 (3) 13 (86.7)

Data are presented as n (%). COVID-19, coronavirus disease 2019; CT, computed tomography; FLAIR, fluid-attenuated inversion recovery; GBS, Guillain-Barré syndrome; MRI, magnetic resonance imaging; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; WBC, white blood cell count.

a

Among 46 patients with large vessel infarct, 16 had a persisting thrombosis located in internal carotid artery (n = 9) and/or proximal segment of middle cerebral artery (n = 6) or in basilar artery (n = 1).

b

Basal ganglia FLAIR hyperintensity (n = 3), acute diffuse hemispheric white matter lesions (n = 2), FLAIR hyperintensity of genu of corpus callosum (n = 1), mesiotemporal FLAIR hyperintensity (n = 3) with frontoinsular extension in 2, brainstem and cerebellar peduncular FLAIR hyperintensity (n = 2), cranial nerve FLAIR hyperintensity (n = 1), focal leptomeningeal FLAIR hyperintensity (n = 2).

c

Lesion in splenium of corpus callosum typical of mild encephalopathy with reversible splenial lesion syndrome.