Burden and determinants of developmental disability in epilepsy: Insights from primary healthcare in Palestine
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1Department of Physiology, Pharmacology, and Toxicology, Faculty of Medicine and Allied Health Sciences, An-Najah National University, Nablus, Palestine; Clinical Research Center, An-Najah National University Hospital, Nablus, Palestine.
Insights
Developmental disability affects nearly a quarter of epilepsy patients in Palestine’s primary care. Younger age, family history of epilepsy, postictal state, and polytherapy are associated factors, highlighting the need for integrated care.
Area of Science:
- Neurology
- Developmental Pediatrics
- Public Health
Background:
- Epilepsy is a common neurological disorder.
- Developmental disability is a significant concern in pediatric populations.
- Understanding the co-occurrence of epilepsy and developmental disability is crucial for effective healthcare planning.
Purpose of the Study:
- To determine the prevalence of developmental disability in individuals with epilepsy attending primary healthcare clinics in the West Bank, Palestine.
- To identify demographic, clinical, and treatment-related factors associated with developmental disability in this population.
Main Methods:
- A retrospective cross-sectional study was conducted.
- Medical records of 256 patients with epilepsy from primary care clinics in the West Bank were reviewed.
- Data collected included demographics, medical history, seizure characteristics, and antiseizure medication use.
Main Results:
- The prevalence of developmental disability among epilepsy patients was 23.0%.
- Younger age (OR=0.91), family history of epilepsy (OR=4.36), postictal state (OR=15.15), and polytherapy (OR=2.95) were significantly associated with developmental disability.
- Younger age and family history of epilepsy were key predictors.
Conclusions:
- A substantial burden of developmental disability exists among people with epilepsy in Palestinian primary care.
- Integrated care pathways incorporating seizure management, developmental screening, and early intervention are recommended.
- Targeted risk-reduction strategies are essential for improving outcomes.
Objective:
To estimate the prevalence of developmental disability among people with epilepsy attending primary healthcare clinics in the West Bank of Palestine, and to identify demographic, clinical, and treatment‑related associated factors.
Methods:
A retrospective cross‑sectional review was conducted of medical records for all patients with a confirmed diagnosis of epilepsy who attended outpatient primary healthcare clinics in the West Bank between November 2023 and June 2024. Data on demographic characteristics, medical and family history, seizure type and manifestations, and current antiseizure medication use were extracted.
Results:
A total of 256 patients with a mean age of 12.7 years (SD = 5.8) were included in the analysis, of whom 59 (23.0%) had a documented developmental disability. In the multivariable logistic regression model, younger age remained significantly associated with developmental disability (OR = 0.91, 95% CI: 0.85-0.97, p = 0.003). In addition, a family history of epilepsy was also strongly associated with developmental disability (OR = 4.36, 95% CI: 1.52-12.55, p = 0.006). The presence of a postictal state emerged as a prominent clinical correlate (OR = 15.15, 95% CI: 3.33-68.89, p < 0.001). In terms of treatment patterns, polytherapy was significantly associated with developmental disability (OR = 2.95, 95% CI: 1.04-8.35, p = 0.042).
Conclusions:
This first national‑level analysis in Palestine highlights a considerable burden of developmental disability among people with epilepsy in the primary care setting. The findings underscore the need for integrated care pathways that combine seizure management with systematic developmental screening, early intervention, and targeted risk‑reduction strategies.
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