To define the risk factors for postencephalitic
epilepsy (PE) and
drug-resistant epilepsy (DRE) in childhood following infectious and
autoimmune encephalitis, we included 147 acute
encephalitis patients with a median follow-up of 7.3 years (range 2-15.8 years). PE was defined as the use of
antiepileptic drugs (AEDs) for ≥24 months, and DRE was defined as the persistence of
seizures despite ≥2 appropriate AEDs at final follow-up. PE and DRE were diagnosed in 31 (21%) and 15 (10%) of patients, respectively. The features during acute
encephalitis predictive of DRE (presented as odds ratio [OR] with confidence intervals [CIs]) were
status epilepticus (OR 10.8, CI 3.4-34.3), visual disturbance (6.4, 1.4-29.9),
focal seizures (6.2, 1.9-20.6), magnetic resonance imaging (MRI) hippocampal/amygdala involvement (5.0, 1.7-15.4),
intensive care admission (4.7, 1.4-15.4), use of >3 AEDs (4.5, 1.2-16.1), MRI
gadolinium enhancement (4.1, 1.2-14.2), any seizure (3.9, 1.1-14.4), and electroencephalography (EEG) epileptiform discharges (3.9, 1.3-12.0). On multivariable regression analysis, only
status epilepticus remained predictive of DRE in all models. DRE was common in herpes simplex virus (3/9, 33%) and unknown (8/40, 20%)
encephalitis, but absent in
acute disseminated encephalomyelitis (ADEM) (0/32, 0%), enterovirus (0/18), and anti-
N-methyl-d-aspartate receptor-NMDAR
encephalitis (0/9). We have identified risk factors for DRE and demonstrated "high-risk," and "low-risk" etiologies.