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Disability and Mortality in Convulsive Status Epilepticus in Children at 3 Months' Follow-Up: A Prospective Study
Vansha Pathania1, Vishal Guglani1, Chandrika Azad1
1Department of Paediatrics, Government Medical College and Hospital, Chandigarh, India.
Insights
Convulsive status epilepticus (CSE) in children has a high immediate mortality and risk of new disabilities. Proper follow-up is crucial as poor outcomes persist after hospital discharge.
Area of Science:
- Neurology
- Pediatrics
- Emergency Medicine
Background:
- Convulsive status epilepticus (CSE) is a critical neurological emergency.
- High mortality, morbidity, and reduced quality of life are associated with CSE.
- Limited follow-up data exist for pediatric CSE in developing nations.
Purpose of the Study:
- To investigate the clinico-etiological profile of pediatric CSE.
- To estimate immediate and short-term mortality in children with CSE.
- To identify predictive factors for poor outcomes in pediatric CSE.
Main Methods:
- Prospective longitudinal study conducted at a tertiary care institute in Northern India.
- Enrolled 200 children (ages 1-16) with CSE after informed consent.
- Patients were observed during hospitalization and followed for 3 months post-discharge.
Main Results:
- Acute symptomatic etiology was most common (63.5%).
- 12.5% of patients died during hospitalization; 80% had good recovery at discharge.
- Predictors of poor outcome included female gender, prolonged seizures (>1 hour), low GCS (<8), refractory SE, critical care need, and acute symptomatic etiology.
Conclusions:
- Pediatric CSE is linked to immediate poor outcomes.
- Risks of death and new disabilities continue post-discharge.
- Essential to implement proper and sustained follow-up care for pediatric CSE survivors.
Abstract:
Background Convulsive status epilepticus (CSE) is a common neurological emergency with high mortality, morbidity, and poor quality of life. There is a paucity of follow-up studies from developing nations in pediatric age group. Objectives This article looks for clinico-etiological profile of CSE and estimates the immediate and short-term mortality in children with CSE and its predictive factors. Methodology This prospective longitudinal study was done at a tertiary care institute of Northern India. The patients between the ages of 1 and 16 years with CSE were enrolled after informed consent, they were observed in the hospital, and survived patients were followed till 3 months after discharge. Results A total of 200 patients (58% males) were enrolled. Acute symptomatic (63.5%) was the most common etiology. Twenty-five (12.5%) patients died during hospital stay; at discharge, 160 (80%) had good recovery and rest had a varying range of disability. The predictive factors for poor outcome were female gender, duration of CSE > 1 hour at presentation, generalized seizures, Glasgow Coma Scale < 8 at presentation, refractory status epilepticus, need for critical care support, and acute symptomatic etiology. On follow-up, two patients died at 1-month and one at 3-month follow-up, the cause of death was probably seizures in two patients and feed aspiration in one patient. Seven patients deteriorated from good recovery scoring to moderate disability during the time interval between first and second follow-up, none of them reported apparent repeat seizures. Conclusion Pediatric CSE is associated with immediate poor outcome; risk of death and new disabilities persist after discharge thus proper follow-up is essential.
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