Status epilepticus and tiagabine therapy: Review of safety data and epidemiologic comparisons

Citation
S. Shinnar et al., Status epilepticus and tiagabine therapy: Review of safety data and epidemiologic comparisons, EPILEPSIA, 42(3), 2001, pp. 372-379
Citations number
39
Categorie Soggetti
Neurosciences & Behavoir
Journal title
EPILEPSIA
ISSN journal
00139580 → ACNP
Volume
42
Issue
3
Year of publication
2001
Pages
372 - 379
Database
ISI
SICI code
0013-9580(200103)42:3<372:SEATTR>2.0.ZU;2-Z
Abstract
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 disch arges (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, Br onx, New York, and New Haven, Connecticut was analyzed as an external compa rison. 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 ha ve electrographic evidence of SE. There was no difference in the frequency of SE or CPSE in the placebo-controlled clinical trials between the TGB-tre ated (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 coho rts. 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 e pisode of SE. Treatment with TGB in recommended doses does not increase the risk of SE in patients with partial seizures.