Volume 42, Issue 3 pp. 372-379

Status Epilepticus and Tiagabine Therapy: Review of Safety Data and Epidemiologic Comparisons

Shlomo Shinnar

Shlomo Shinnar

Departments of Neurology and Pediatrics and Comprehensive Epilepsy Management Center, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York;

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Anne T. Berg

Anne T. Berg

Department of Biological Sciences, Northern Illinois University, DeKalb, Illinois;

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David M. Treiman

David M. Treiman

Department of Neurology, University of Medicine and Dentistry of New Jersey–Robert Wood Johnson Medical School, New Brunswick, New Jersey;

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W. Allen Hauser

W. Allen Hauser

Department of Neurology

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Dale C. Hesdorffer

Dale C. Hesdorffer

Department of Neurology

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J. Chris Sackellares

J. Chris Sackellares

Departments of Neurology and Neuroscience, University of Florida and Gainesville VA Medical Center, Gainesville, Florida;

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Ilo Leppik

Ilo Leppik

MINCEP Epilepsy Care and University of Minnesota, Minneapolis, Minnesota, U.S.A.;

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Matti Sillanpaa

Matti Sillanpaa

Department of Child Neurology, University Hospital, TYKS, Turku, Finland; and

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Kenneth W. Sommerville

Kenneth W. Sommerville

Neuroscience Franchise, Abbott Laboratories, North Chicago, Illinois, U.S.A.

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First published: 01 May 2002
Citations: 54
Address correspondence and reprint requests to Dr. S. Shinnar at Comprehensive Epilepsy Management Center, Montefiore Medical Center, 111 E. 210th St., Bronx, NY 10467, U.S.A. Presented in part at the American Academy of Neurology Meeting, April 1997, and the International Epilepsy Congress, June 1997, Dublin, Ireland.

Abstract

Summary: Purpose: To determine whether an increased risk of status epilepticus (SE) and complex partial status epilepticus (CPSE) is associated with tiagabine (TGB) therapy.

Methods: Thirteen cases in which an EEG, performed on patients with altered mental status taking TGB, was reported to demonstrate spike-and-wave discharges (SWDs) were reviewed by a panel of experts. In addition, all cases of suspected SE from TGB clinical trials were reviewed. The occurrence of SE in four epidemiologic cohorts from Rochester, Minnesota, Turku, Finland, Bronx, New York, and New Haven, Connecticut was analyzed as an external comparison.

Results: Review of the 13 cases with reported SWDs found that the majority had had prior EEGs with similar findings, and only three were thought to have electrographic evidence of SE. There was no difference in the frequency of SE or CPSE in the placebo-controlled clinical trials between the TGB-treated (1.0% SE, 0.8% CPSE) and placebo-treated (1.5% SE, 1.5% CPSE) groups. The 5% frequency of SE and 3% frequency of CPSE in the TGB-treated patients in the long-term safety studies, which included 2,248 patients, were very similar to the rates of occurrence of SE and CPSE in the four external cohorts. The major risk factor for the occurrence of SE and CPSE in all groups was a prior episode of SE (p < 0.0001).

Conclusions: Over a 3-year period, SE will occur in 5–10% of patients with epilepsy not in remission. At highest risk are those who have had a prior episode of SE. Treatment with TGB in recommended doses does not increase the risk of SE in patients with partial seizures.

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