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Journal of Child Neurology
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Efficacy and Tolerability of Topiramate in Children Younger Than 2 Years Old

Ignacio Valencia

Section of Neurology Department of Pediatrics, St. Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA Ignacio.Valencia{at}drexel.edu.

Carmen Fons, MD

Section of Neurology Department of Pediatrics, St. Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA

Sanjeev V. Kothare, MD

Section of Neurology Department of Pediatrics, St. Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA

Divya S. Khurana, MD

Section of Neurology Department of Pediatrics, St. Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA

Sabrina Yum, MD

Section of Neurology Department of Pediatrics, St. Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA

H. Huntley Hardison, MD

Section of Neurology Department of Pediatrics, St. Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA

Agustin Legido, MD, PhD

Section of Neurology Department of Pediatrics, St. Christopher's Hospital for Children, Drexel University College of Medicine, Philadelphia, PA

To evaluate the efficacy and tolerability of topiramate in children with epilepsy younger than 2 years of age, we retrospectively reviewed the records of patients treated at our institution between 2001 and 2003. Thirteen children ages 5 to 23 months, five boys and eight girls, were identified. Seizure types were partial (five), generalized tonic-clonic (three), myoclonic (one), and infantile spasms (four). The mean age at seizure onset was 9.7 months. Topiramate was started at a mean age of 11.4 months (4—23 months). The number of antiepileptic drugs prior to topiramate therapy ranged from zero to four. One patient had been on the ketogenic diet. Topiramate was used as monotherapy in seven children and as poly-therapy in six children. Mean follow-up was 14 months. The mean dose of topiramate was 8.8 mg/kg/day (2.5—18 mg/kg/day). The degree of seizure reduction was as follows: > 75% in five (38.5%) children, 50% to 75% in three (23%) children, and 0 to 25% in five (38.5%) children. Three of four (75%) patients with infantile spasms had a > 75% reduction in seizures. Adverse effects occurred in two children, including lethargy, hyperthermia, and anorexia. In children younger than 2 years of age, for whom the antiepileptic drug armamentarium is limited, topiramate appears to be an efficacious and safe therapeutic alternative for a variety of seizure types. (J Child Neurol 2005;20:667—670).

Journal of Child Neurology, Vol. 20, No. 8, 667-670 (2005)
DOI: 10.1177/08830738050200080601


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This article has been cited by other articles:


Home page
J Child NeurolHome page
R. Korinthenberg and A. Schreiner
Topiramate in Children With West Syndrome: A Retrospective Multicenter Evaluation of 100 Patients
J Child Neurol, March 1, 2007; 22(3): 302 - 306.
[Abstract] [PDF]