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. 2022 Jan 27;12:820723. doi: 10.3389/fneur.2021.820723

Table 1.

Clinical features of 13 patients with Guillain–Barré syndrome and variants post COVID-19 vaccination.

Case 1 2 3 4 5 6 7 8 9 10 11 12 13
Age 62 73 48 32 38 70 72 84 62 43 18 73 58
Gender M F F F M F M F F M F F F
Time from vaccination to symptom onset (days) 11 29 10 11 29 8 30 8 27 11 12 13 4
Vaccine ChAdOx1-S/nCoV-19 (1st) ChAdOx1-S/nCoV-19 (1st) ChAdOx1-S/nCoV-19 (1st) BNT162b2 (1st) ChAdOx1-S/nCoV-19 (1st) ChAdOx1-S/nCoV-19 (1st) ChAdOx1-S/nCoV-19 (1st) ChAdOx1-S/nCoV-19 (1st) ChAdOx1-S/nCoV-19 (2nd) BNT162b2 (1st) BNT162b2 (1st) BNT162b2 (1st) BNT162b2 (1st)
Clinical phenotype Classic GBS Classic GBS Paraparetic GBS Acute cervicobrachial weakness Classic GBS Classic GBS Classic GBS Classic MFS Classic GBS Classic GBS Paraparetic GBS Paraparetic GBS Classic GBS
Antiganglioside antibody* Negative Negative Negative Negative Negative GM1 IgM(+) NA GQ1b IgG(+) Negative Negative Negative Negative Negative
EDX classification AMAN AIDP AIDP AIDP AMAN AMAN Undetermined Normal Undetermined AIDP Normal Undetermined AIDP
TRF (days from relapse after last day of 1st IVIG) Yes (7) Yes (7) No No No No No No No No No No No
Onset to nadir (days) 10, 22 7, NA 15 12 1 11 10 5 11 21 9 9 4
Severity at nadir
Hughes score 5 4 2 1 2 3 2 1 4 4 2 3 5
MRC sum score 14 28 57 51 56 54 52 60 52 26 56 46 18
Length of hospital stay 139 42 9 6 6 20 2 17 6 20 3 10 44
Treatment First and second IVIG IVIG Steroid IVIG No IVIG No No IVIG IVIG No IVIG IVIG followed by plasmapheresis
Onset to improvement (days) 16, 30 15, 26 18 17 16 18 25 30 43 23 13 15 6
Prognosis at 2 months
Hughes score 4 3 1 1 0 2 1 1 1 3 1 6 3
MRC sum score 26 44 60 60 60 58 60 60 59 48 58 0 35

AIDP, acute inflammatory demyelinating polyradiculoneuropathy; AMAN, acute motor axonal neuropathy; EDX, electrodiagnostic study; F, female; IVIG, intravenous immunoglobulin G; GBS, Guillain–Barré syndrome; M, male; MRC, medical research council; NA, not available; TRF, treatment-related fluctuations.

*

The anti-GM1, GD1b, GQ1b IgG, and IgM panels were checked with ELISA for anti-ganglioside antibody assays.

Electrodiagnostic classification was determined by serial nerve conduction studies according to Uncini's criteria. 11Three patients who did not receive a follow-up nerve conduction study were classified as “undetermined”.

Onset to nadir before and after treatment-related fluctuation, respectively.

Time interval from onset to improvement following the first and second IVIG infusions, respectively.