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  • Time to 12-month remission and treatment failure for generalised and unclassified epilepsy.

Time to 12-month remission and treatment failure for generalised and unclassified epilepsy.

Journal of neurology, neurosurgery, and psychiatry (2013-12-03)
Laura J Bonnett, Catrin Tudur Smith, David Smith, Paula R Williamson, David Chadwick, Anthony G Marson
摘要

To develop prognostic models for time to 12-month remission and time to treatment failure after initiating antiepileptic drug monotherapy for generalised and unclassified epilepsy. We analysed data from the Standard and New Antiepileptic Drug (arm B) study, a randomised trial that compared initiating treatment with lamotrigine, topiramate and valproate in patients diagnosed with generalised or unclassified epilepsy. Multivariable regression modelling was used to investigate how clinical factors affect the probability of achieving 12-month remission and treatment failure. Significant factors in the multivariable model for time to 12-month remission were having a relative with epilepsy, neurological insult, total number of tonic-clonic seizures before randomisation, seizure type and treatment. Significant factors in the multivariable model for time to treatment failure were treatment history (antiepileptic drug treatment prior to randomisation), EEG result, seizure type and treatment. The models described within this paper can be used to identify patients most likely to achieve 12-month remission and most likely to have treatment failure, aiding individual patient risk stratification and the design and analysis of future epilepsy trials.

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Supelco
丙戊酸, Pharmaceutical Secondary Standard; Certified Reference Material
USP
丙戊酸, United States Pharmacopeia (USP) Reference Standard
Supelco
拉莫三嗪, Pharmaceutical Secondary Standard; Certified Reference Material
Sigma-Aldrich
拉莫三嗪, ≥98%, powder
Sigma-Aldrich
2-丙基戊酸
Sigma-Aldrich
托吡酯, ≥98% (HPLC), solid
Supelco
丙戊酸标准液 溶液, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
丙戊酸, European Pharmacopoeia (EP) Reference Standard
Supelco
Topiramate solution, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
Supelco
Lamotrigine solution, 1.0 mg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®
USP
托吡酯, United States Pharmacopeia (USP) Reference Standard
USP
拉莫三嗪, United States Pharmacopeia (USP) Reference Standard
拉莫三嗪, European Pharmacopoeia (EP) Reference Standard
拉莫三嗪, European Pharmacopoeia (EP) Reference Standard
峰鉴别用拉莫三嗪, European Pharmacopoeia (EP) Reference Standard