Diagnosis and Classification of Pediatric Epilepsy in Sub-Saharan Africa: A Comprehensive Review

Sofia Di Noia1,2, Linda Bonezzi3,4,5, Ilaria Accorinti4,5

  • 1Neuropediatric Unit, Woman and Child Department, Polyclinic of Foggia, 71122 Foggia, Italy.

PubMed

Insights

Pediatric epilepsy in Sub-Saharan Africa faces significant challenges due to limited resources and stigma, leading to underdiagnosis and undertreatment. Culturally sensitive interventions are crucial for improving care and quality of life for affected children.

Area of Science:

  • Neurology
  • Public Health
  • Pediatrics

Background:

  • Epilepsy is a critical public health concern in Sub-Saharan Africa, disproportionately affecting children.
  • Limited healthcare, socioeconomic disparities, and cultural stigma contribute to underdiagnosis and undertreatment.

Purpose of the Study:

  • To review the diagnosis, classification, and management of pediatric epilepsy in Sub-Saharan Africa.
  • To identify challenges and propose culturally appropriate interventions for improving care quality.

Main Methods:

  • A comprehensive literature review was conducted using major scientific databases (MEDLINE, Embase, Scopus, Web of Science).
  • Studies published between 2013 and 2024 focusing on pediatric epilepsy epidemiology, seizure classification, and etiologies in Sub-Saharan Africa were included.

Main Results:

  • Sub-Saharan Africa exhibits higher epilepsy incidence and prevalence compared to high-income nations, driven by infectious diseases and perinatal injuries.
  • Generalized and focal seizures are common, with structural and infectious causes (e.g., nodding syndrome, HIV-related epilepsy) being significant contributors.
  • A substantial treatment gap exists, with up to 80% of children lacking access to appropriate antiseizure medications.

Conclusions:

  • Pediatric epilepsy diagnosis and treatment in Sub-Saharan Africa are hindered by cultural stigma and inadequate healthcare infrastructure.
  • There is an urgent need for culturally adapted diagnostic tools, affordable treatments, and public health initiatives to reduce stigma.
  • Improving care requires enhanced research, better healthcare access, and targeted educational campaigns to improve the quality of life for children with epilepsy.