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Epidemiology of Epileptic Spasm and Affecting Factors on One-Year Prognosis: A Study in Tabriz Children's Hospital
Shahram Sadeghvand1, Ali Kamali1, Mirhadi Mousavi1
1Pediatric Health Research Center, Tabriz university of Medical Sciences, Tabriz, Iran.
Insights
Epileptic spasms (ES) in infants are often resistant to standard treatments. This study found prenatal insults and CNS malformations are common causes, with high rates of recurrence and complications within one year.
Area of Science:
- Pediatric Neurology
- Clinical Epidemiology
Background:
- Epileptic Spasm (ES) is a distinct convulsive disorder predominantly affecting infants, often proving refractory to conventional anticonvulsant therapies.
- Understanding the epidemiology and prognostic factors of ES is crucial for improving patient outcomes.
Purpose of the Study:
- To investigate the epidemiology of Epileptic Spasm (ES) in infants.
- To identify factors influencing the one-year prognosis of ES patients.
- To analyze clinical characteristics, causes, and treatment responses in ES patients.
Main Methods:
- A descriptive-analytical cross-sectional study was conducted on 37 ES patients at Tabriz Children's Hospital (2015-2019).
- Data collection involved a census sampling method using a checklist for demographic, clinical, and treatment histories.
- Statistical analysis was employed to report findings on seizure types, causes, EEG, imaging, treatments, and one-year prognosis.
Main Results:
- Flexor seizures were most common (40.5%), followed by mixed (37.8%) and extensor (21.7%).
- Leading causes included prenatal insult (27.0%), cryptogenic factors (24.3%), and CNS malformations (16.2%).
- High rates of disease recurrence (67.6%) and recovery with complications (18.9%) were observed within one year, with two deaths (5.4%).
Conclusions:
- Prenatal insults, cryptogenic origins, and CNS malformations are significant contributors to ES.
- Disease recurrence and complications represent key challenges in the one-year prognosis of infantile ES.
- Effective management strategies are needed to address the high recurrence and complication rates in ES.
Objectives:
Epileptic Spasm (ES) is a special type of convulsive disorder that primarily occurs in infants, typically within the first year of life. This disorder is usually resistant to routine anticonvulsant drugs. This study aims to evaluate the epidemiology and factors affecting one-year prognosis in patients with ES in Tabriz Children's Hospital.
Materials & Methods:
This descriptive-analytical cross-sectional study focused on patients diagnosed with ES who were referred to the neurology department of Tabriz Children's Hospital between 2015 and 2019. Data was collected using a census sampling method and a checklist that included demographic information and clinical and treatment histories. The results were then reported statistically.
Results:
Thirty-seven patients were studied, with 15 (40.5%) exhibiting flexor seizures, eight (21.7%) extensor seizures, and 14 (37.8%) mixed seizures. The most common causes were prenatal insult (10 cases, 27.0%), cryptogenic (9 cases, 24.3%), and Central Nervous System (CNS) malformations (6 cases, 16.2%). Electroencephalography findings included modified hypsarrhythmia in 12 cases (30.8%), hypsarrhythmia in 16 (41.0%), and frequent epileptiform discharge in nine (23.1%). MRI and CT scans showed abnormalities in three cases (8.1%) and 16 cases (43.2%), respectively. Treatment involved Phenobarbital in 35 patients (94.6%), Vigabatrin in 29 (78.4%), and ACTH in 11 (29.7%). The one-year prognosis indicated 25 patients (67.6%) experienced disease recurrence, seven (18.9%) recovered with complications, and two (5.4%) died.
Conclusion:
The most common causes of ES are prenatal insults, cryptogenic factors, and CNS malformations. The key one-year prognoses include disease recurrence and recovery with complications.
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