Abstract
High-dose suppressive therapy (HDST) is used to treat refractory status epilepticus (RSE). Prolonged therapy is required in some cases, and prognosis is important in making therapeutic decisions. The authors therefore studied the long-term outcome in previously normal children who survived prolonged HDST for acute symptomatic RSE. All have intractable epilepsy, and none returned to baseline.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acute Disease
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Adolescent
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Anticonvulsants / therapeutic use*
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Biopsy
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Brain / drug effects
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Brain / pathology
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Child
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Child, Preschool
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Developmental Disabilities / etiology
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Dose-Response Relationship, Drug
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Drug Resistance
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Electroencephalography
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Encephalitis / complications
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Encephalitis / diagnosis
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Encephalitis / pathology
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Female
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Humans
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Male
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Prognosis
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Status Epilepticus / complications
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Status Epilepticus / diagnosis
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Status Epilepticus / drug therapy*
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Time Factors
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Treatment Outcome