Key result
Drug-resistant pediatric epilepsy linked to lower LV GLS vs responsive epilepsy and healthy controls.
Why the study?
Pediatric epilepsy may adversely affect cardiac function, but cardiac outcomes in children with controlled versus drug-resistant epilepsy needed examination.
Case-Control (n=90)
Blinded assessors
No
Children with drug-resistant epilepsy exhibit significant subclinical left ventricular systolic dysfunction and impaired global longitudinal strain compared to those with drug-responsive epilepsy and healthy controls.
May warrant cardiac surveillance in drug-resistant epilepsy; leaves open whether seizures or medications drive subclinical dysfunction.
Background Pediatric epilepsy may adversely affect cardiac function. This study examined cardiac outcomes in children with controlled and drug-resistant epilepsy (DRE). Methods Sixty children with epilepsy (30 DRE, 30 drug-responsive) and 30 healthy controls underwent 12-lead ECG, M-mode echocardiography, and speckle tracking echocardiography (STE) to assess cardiac electrical activity, left ventricular (LV) volumes, ejection fraction (EF), fractional shortening (FS), and global longitudinal strain (GLS). Results ECG findings were comparable among the three groups. LV end-diastolic (LVEDV) and end-systolic volumes (LVESV), FS, and EF were significantly lower in DRE vs. controls ( p < 0.05). LVEDV and EF were significantly lower in DRE vs. drug-responsive epilepsy ( p < 0.05), while drug-responsive cases had lower LVEDV vs. controls ( p = 0.015). LV GLS was significantly lower in DRE (−19.34 ± 1.80) vs. drug-responsive epilepsy (−20.33 ± 1.45) ( p = 0.023) and controls (−20.58 ± 0.91) ( p = 0.003). LV GLS correlated positively with time since last seizure ( p = 0.007) and negatively with the number of antiseizure medications ( p = 0.007). Conclusions Children with DRE exhibit significant cardiac dysfunction. STE enables early detection of subclinical cardiac abnormalities in DRE, advocating for its integration into routine monitoring. Impact Compares cardiac function in pediatric drug-resistant epilepsy (DRE) and drug-responsive epilepsy, identifying impaired systolic function and global longitudinal strain (GLS) in DRE. Correlates GLS abnormalities with antiseizure medication burden and time since last seizure, linking cardiac dysfunction to treatment intensity and epilepsy disease course. Advocates STE for early cardiac monitoring in DRE and urges longitudinal studies to disentangle epilepsy-related cardiovascular risks from drug-driven effects.
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Noureldeen et al. (2026) conducted a case-control in Pediatric epilepsy (drug-resistant and drug-responsive) (n=90). Drug-resistant epilepsy vs. Drug-responsive epilepsy and healthy controls was evaluated on Left ventricular global longitudinal strain (LV GLS) (p=0.003). Children with drug-resistant epilepsy exhibited significantly lower left ventricular global longitudinal strain (-19.34%) compared to healthy controls (-20.58%) and drug-responsive epilepsy (-20.33%).
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