DRAVET SYNDROME
Comprehensive care of children with Dravet syndrome
Article first published online: 4 APR 2011
DOI: 10.1111/j.1528-1167.2011.03011.x
Wiley Periodicals, Inc. © 2011 International League Against Epilepsy
Issue

Epilepsia
Special Issue: Severe Myoclonic Epilepsy – Dravet Syndrome: Thirty Years Later
Volume 52, Issue Supplement s2, pages 90–94, April 2011
Additional Information
How to Cite
Granata, T. (2011), Comprehensive care of children with Dravet syndrome. Epilepsia, 52: 90–94. doi: 10.1111/j.1528-1167.2011.03011.x
Publication History
- Issue published online: 4 APR 2011
- Article first published online: 4 APR 2011
- Abstract
- Article
- References
- Cited By
Keywords:
- Severe myoclonic epilepsy of infancy;
- Management;
- Cognitive development;
- Social problems;
- Treatment;
- Comorbidities
Summary
The comprehensive care of a patient with Dravet syndrome encompasses both the “care” and the “cure” of the patient, and requires cooperation among family, doctors, and several other specialized caregivers to search for the attainment of the best quality of life for the patients and their families. Several issues peculiar to the disease to be faced while dealing with the patient are: (1) SMEI is an “evolving” disease that appears in an otherwise healthy child with symptoms that appear and mutate throughout the course of the disease; (2) the severity of the disease is not fully predictable at onset and appears to be individual-specific; (3) the seizures are invariably drug resistant and seizure freedom is not a realistic goal; and (4) in addition to seizures many other invalidating clinical problems, including cognitive impairment, behavior disorders, and a number of comorbidities characterize the disease course. The comprehensive caring must be physician-guided and patient-centered and implies a multidisciplinary approach to be built around the children and caregivers, who need to be guided through the steps of the diagnosis, treatments, and managements of the various comorbidities.

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