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. 2022 Jun 22;134:108808. doi: 10.1016/j.yebeh.2022.108808

Table 1.

Demographic characteristics of PWE.

Increase >50% seizure frequency during the first month after vaccination No increase in seizure frequency during the first month after vaccination p p
univariate multivariate
N (%) 26 (6.2%) 392 (93.8%)



Sex Man 15 (57.7%) 202 (51.5%) 0.543
Woman 11 (42.3%) 190 (48.5%)



Age Mean (SD) 49.73 (12.3) 48.12 (10.2) 0.675



Epilepsy type Generalized 3 (11.5%) 62 (15.8%) 0.810
IGE with GTCS only 1 (33.3%) 10 (16.4%)
JME 0 18 (29.5%)
Childhood absence 1 (33.3%) 9 (14.8%)
Juvenile absence 0 4 (6.6%)
Epileptic encephalopathy 1 (33.3%) 11 (18.0%)
Other genetic generalized epilepsies# 0 4 (6.6%)
Others 0 5 (8.2%)
Focal 20 (76.9%) 299 (76.3%) 0.773
Frontal 4 (20.0%) 71 (23.7%)
Temporal 9 (45.0%) 100 (33.4%)
Posterior quadrant 2 (10.0%) 35 (11.7%)
Unknown 5 (25.0%) 93 (31.1%)
Unknown 3 (11.5%) 31 (7.9%) 0.711



Etiology Unknown 9 (34.6%) 148 (37.8%) 0.815
Genetic 1 (3.8%) 23 (5.9%)
MCD 4 (15.4%) 21 (5.4%)
Perinatal 1 (3.8%) 20 (5.1%)
Vascular 4 (15.4%) 49 (12.5%)
Infectious 0 12 (3.1%)
TBI 1 (3.8%) 15 (3.8%)
Autoimmune 0 5 (1.3%)
Tumoral 2 (7.7%) 34 (8.7%)
Others 2 (7.7%) 24 (6.1%)
IGE 2 (7.7%) 41 (10.5%)



Pre-vaccination seizure frequency No seizure >1 year 7 (26.9%) 199 (50.8%) 0.018 0.859
Annual 6 (23.1%) 81 (20.7%) 0.771
Monthly 13 (50.0%) 66 (16.8%) 0.001 0.007
Weekly 0 28 (7.1%) 0.158
Daily 0 18 (4.6%) 0.262



ASM 0 1 (3.8%) 19 (4.9%) 0.093 0.185
1 10 (38.5%) 180 (46.2%)
2 11 (42.3%) 104 (26.7%)
>2 4 (15.3%) 87 (22.4%)



Intellectual disability 2 (7.7%) 77 (19.6%) 0.194 0.179



Active epilepsy 24 (92.3%) 307 (78.3%) 0.131 0.452



Drug-refractory epilepsy 13 (50.0%) 132 (33.7%) 0.090 0.116



Epilepsy surgery 1 (3.8%) 24 (6.1%) 0.999

ASM: anti-seizure medication; GTCS: generalized tonic-clonic seizure; IGE: idiopathic generalized epilepsy; JME: juvenile myoclonic epilepsy; MCD: malformation of cortical development; TBI: traumatic brain injury.

#

Including generalized epilepsies with genetic confirmation different than IGE and epileptic encephalopathies.