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Infantile spasms: outcome and prognostic factors of cryptogenic and symptomatic groups
1Department of Paediatrics, Hospital for Sick Children, Toronto, ON, Canada.
Insights
Infantile spasms impact development and neurologic outcomes. Symptomatic cases show poorer outcomes than cryptogenic ones, influenced by factors like other seizures and treatment delays.
Area of Science:
- Pediatric Neurology
- Developmental Neuroscience
Background:
- Infantile spasms are a severe epilepsy syndrome in infants.
- Distinguishing between cryptogenic and symptomatic causes is crucial for prognosis.
Purpose of the Study:
- To analyze developmental, neurologic, and seizure outcomes in infantile spasms.
- To identify prognostic factors influencing outcomes in both cryptogenic and symptomatic cases.
Main Methods:
- Retrospective review of 57 infantile spasms cases.
- Assessment using Griffith Mental Developmental Scale and clinical evaluation.
- Analysis of prognostic factors including seizure type, neurologic deficits, and treatment response.
Main Results:
- Symptomatic infantile spasms had significantly lower developmental scores than cryptogenic cases.
- Neurologic deficits were more prevalent in the symptomatic group (75%) compared to cryptogenic (23.5%).
- Outcome was negatively affected by coexisting seizures, neurologic deficits, delayed treatment, poor ACTH response, and persistent EEG abnormalities.
Conclusions:
- Symptomatic infantile spasms carry a poorer prognosis than cryptogenic forms.
- Early intervention and management of associated factors are critical for improving outcomes in infantile spasms.
Abstract:
We reviewed the outcome (developmental, neurologic, and seizure) and prognostic factors of 57 cases of infantile spasms (17 cryptogenic, 40 symptomatic). The mean developmental score of the cryptogenic group (71.2 +/- 24.2) was significantly higher than that of the symptomatic group (48.4 +/- 24.5), as assessed by the Griffith Mental Developmental Scale. A resultant neurologic deficit was present in 23.5% of the cryptogenic group and 75.0% of the symptomatic group. Coexistence of other forms of seizures was observed in 35.3% of the cryptogenic group and 57.5% of the symptomatic group. Outcome was affected by the coexistence of other seizures, presence of neurologic deficit, time lag in initiation of treatment (cognitive outcome only), poor response to ACTH treatment, and persistent EEG abnormality. Character of spasms and time lag in initiation of treatment (seizure outcome only) did not have any significant effect on outcome.
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