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Infantile spasms : electroclinical syndrome
G N Dakshinamurty1, P Satishchandra1
1Department of Neurology, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bangalore - 560 029, India.
Insights
This study investigated infantile spasms in 29 Indian children, finding birth asphyxia a common cause. Treatment with anticonvulsants and steroids showed varied responses, highlighting the need for more research on this infant seizure disorder.
Area of Science:
- Neurology
- Pediatrics
- Epileptology
Background:
- Infantile spasms (IS) is an age-specific seizure disorder in infancy/early childhood.
- IS can be part of an epileptic syndrome with hypsarrhythmia or chronic spasms with mental retardation.
- Limited information on IS exists in Indian medical literature.
Purpose of the Study:
- To evaluate infantile spasms cases in India.
- To analyze clinical characteristics, EEG findings, and treatment responses.
- To identify common causes and therapeutic outcomes in Indian infants with IS.
Main Methods:
- Retrospective study of 29 patients with infantile spasms over 5 years at NIMHANS.
- EEG evaluation for all patients; hypsarrhythmia pattern noted in 5.
- Analysis of patient data including etiology, treatment (anticonvulsants, ACTH/Steroids), and follow-up.
Main Results:
- All 29 patients had abnormal EEGs; 5 showed hypsarrhythmia.
- 14 cases were cryptogenic; the rest were symptomatic, with birth asphyxia being the most frequent cause.
- Mean follow-up was 18 months; treatment responses varied based on etiology and therapy.
Conclusions:
- Infantile spasms present unique challenges in the Indian context.
- Birth asphyxia is a significant etiological factor in symptomatic IS.
- Further research is needed to optimize management and understand outcomes for infantile spasms in India.
Abstract:
Infantile spasms is an age specific seizure disorder which occurs in infancy or early childhood either as a part of an epileptic syndrome accompanied by hypsarrhythmia or as chronic spasms involving the axial musculature with mental retardation. Information about infantile spasms in the Indian literature is very sparse. 29 patients of infantile spasms seen over a period of 5 years at NIMHANS were evaluated in this study. EEG was abnormal in all, with classical/modified hypsarrhythmia pattern in 5.14 were cryptogenic and the rest were symptomatic with birth asphyxia as the commonest underlying cause. All were treated with anticonvulsants and in addition 20 children received ACTH/Steroids. They were followed for a mean period of 18 months. The clinical status at the end of the follow-up, serial EEG findings and response in relation to the underlying cause and mode of therapy are discussed.
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