Table 2.
Recognised neuroimmune condition subgroup (n=13) |
Other neurological disorder subgroup (n=14) |
|||||||
---|---|---|---|---|---|---|---|---|
Acute demyelinating syndromes (n=7) | GBS (n=5) | Limbic encephalitis (n=1) | Severe encephalopathy (n=9) | Psychiatric disorder (n=2) | Movement disorder (n=2) | Cerebrovascular disorder (n=1) | ||
Age, years | 5 (1–10) | 6 (1–14) | 4 | 11 (2–16) | 12 (10–14) | 12 (9–14) | 10 | |
Sex | ||||||||
Female | 3 (43%) | 2 (40%) | 0 | 3 (33%) | 1 (50%) | 1 (50%) | 0 | |
Male | 4 (57%) | 3 (60%) | 1 (100%) | 6 (67%) | 1 (50%) | 1 (50%) | 1 (100%) | |
Ethnicity | ||||||||
White | 2 (29%) | 2 (40%) | 1 (100%) | 5 (56%) | 0 | 2 (100%) | 1 (100%) | |
Black | 1 (14%) | 1 (20%) | 0 | 2 (22%) | 2 (100%) | 0 | 0 | |
Asian | 4 (57%) | 2 (40%) | 0 | 2 (22%) | 0 | 0 | 0 | |
Underlying comorbidity | ||||||||
Neurological comorbidities | 1 (14%) | 2 (40%) | 0 | 4 (44%) | 0 | 0 | 1 (100%) | |
Other comorbidities | 1 (14%) | 0 | 0 | 0 | 0 | 0 | 0 | |
Clinical features | ||||||||
Systemic features* | 6 (86%) | 3 (60%) | 0 | 6 (67%) | 0 | 0 | 0 | |
Respiratory involvement at presentation | 2 (29%) | 2 (40%) | 0 | 1 (11%) | 1 (50%) | 0 | 0 | |
Encephalopathy | 4 (57%) | 0 | 1 (100%) | 9 (100%) | 0 | 0 | 0 | |
Seizures | 0 | 0 | 1 (100%) | 7 (78%) | 0 | 0 | 0 | |
Headache or meningism | 2 (29%) | 1 (20%) | 0 | 1 (11%) | 0 | 0 | 0 | |
Peripheral nervous system involvement | 0 | 5 (100%) | 0 | 0 | 0 | 2 (100%) | 0 | |
Focal CNS involvement | 3 (43%) | 0 | 0 | 0 | 0 | 0 | 1 (100%) | |
Behavioural change | 0 | 0 | 1 (100%) | 0 | 2 (100%) | 0 | 0 | |
Hallucinations | 0 | 0 | 0 | 0 | 1 (50%) | 0 | 0 | |
Recognised para-infectious or post-infectious neurological disease | 7 (100%) | 5 (100%) | 1 (100%) | 0 | 0 | 0 | 0 | |
Investigations | ||||||||
SARS-CoV-2 PCR positive | 5 (71%) | 4 (80%) | 1 (100%) | 9 (100%) | 1 (50%) | 0 | 1 (50%) | |
SARS-CoV2- IgG positive | 3 (43%) | 1 (20%) | 1 (100%) | 4 (44%) | 2 (100%) | 2 (100%) | NP | |
C-reactive protein, mg/L | 12 (0–42) | 1 (1–2) | 1 | 1 (0–158) | 9 (5–12) | 0 | NP | |
Elevated acute-phase reactants† | 2 (29%) | 0 | 0 | 1 (11%) | 0 | 0 | NP | |
Plasma white cell count, cells per μL | 10·0 (4·0–27·3) | 11·0 (7·0–18·0) | 7·5 | 9·4 (4·0–11·6) | 7·5 (4·0–10·5) | 6·3 (5·3–7·3) | NP | |
CSF white cell count >5 cells per μL | 5 (71%) | 1 (20%) | 1 (100%) | 1 (11%) | 1 (50%) | NP | NP | |
Abnormal neuroimaging | 7 (100%) | 2 (40%) | 1 (100%) | 2/8 (25%) | 0 | 0 | 0 | |
Treatment | ||||||||
PICU admission | 2 (29%) | 1 (20%) | 0 | 5 (56%) | 0 | 0 | 0 | |
Inotropic support | 0 | 0 | 0 | 0 | 0 | 0 | ||
Immunomodulation | 6 (86%)‡ | 4 (80%) | 1 (100%) | 2 (22%) | 0 | 0 | 0 | |
Outcome | ||||||||
Disability§ | 4 (57%) | 2 (40%) | 0 | 1 (11%) | 1 (50%) | 1 (50%) | 0 | |
Death | 0 | 0 | 0 | 0 | 0 | 0 | 0 |
Data are n (%) or median (range). GBS=Guillain-Barré syndrome. NP=not performed. CSF=cerebrospinal fluid. PICU=paediatric intensive care unit.
Systemic features were fever, shock, hypotension, or rash.
Combined acute-phase reactants were defined as lactate dehydrogenase, ferritin, and D-dimers.
One patient did not receive immunomodulation because of underlying malignancy.
Disability was defined as a modified Rankin scale score of 2–5.