Evaluation of long-term antiepileptic drug use in patients with temporal lobe epilepsy: Assessment of risk factors for drug resistance and polypharmacy. (October 2018)

• Record Type: Journal Article
• Authors: Bjørke, Agnes Balint; Nome, Cecilie Gjessing; Falk, Ragnhild Sørum; Gjerstad, Leif; Taubøll, Erik; Heuser, Kjell
• Is Part Of: Seizure. Volume 61(2018)
• Page Start: 63
• Page End: 70
• Publication Date: 2018-10
• Subjects: TLE temporal lobe epilepsy -- AED antiepileptic drug -- MTS mesial temporal sclerosis -- RCT randomised controlled trial; Temporal lobe epilepsy -- Hippocampal sclerosis -- Antiepileptic drug -- Drug resistance -- Polypharmacy -- Polytherapy; Epilepsy -- Periodicals; Epilepsy -- Periodicals; Seizures -- Periodicals; Épilepsie -- Périodiques; Electronic journals; Electronic journals; 616.853
• DOI: 10.1016/j.seizure.2018.07.011
• Languages: English
• ISSNs: 1059-1311

Abstract

Highlights: Drug resistance and polypharmacy are common in temporal lobe epilepsy. Poor effect on initial pharmacotherapy is an early risk factor of drug resistance. Long disease duration increases the risk of drug resistance and polypharmacy. 2nd generation antiepileptic drugs provide no additional effect. Abstract: Purpose: To evaluate risk factors for drug resistance and polypharmacy in patients with temporal lobe epilepsy. Methods: Patients with temporal lobe epilepsy, treated for more than 5 years, completed questionnaires on antiepileptic drug use and effect. Logistic regression models were used for analysis of risk factors. Results: Of 135 patients included in the study, 65% were classified as drug resistant and 41% identified as using polypharmacy. Poor effects associated with first-choice antiepileptic drug were reported by 59% of the patients, and 70% reported poor effects of second-line treatment. The most frequently used first-generation antiepileptic drugs had a similar mean effect to those of second-generation. Univariate regression analyses showed a significant association between drug resistance and mesial temporal sclerosis, seizure onset below 18 years, and lack of family history of epilepsy. However, multivariate regression analysis showed no association with any demographic or clinical features. Unsuccessful treatment with the first antiepileptic drug increased the risk of drug resistance by 18 times, and the risk of poor effect from the second antiepileptic drug by 9 times. Disease duration was associated with annual risk for drug resistance of 7% and for polypharmacy of 5%. Conclusions: A poor effect from initial pharmacotherapy is the only early risk factor for drug resistance found in this study. Long disease duration increases the risk of drug resistance and polypharmacy. Second-generation antiepileptic drugs provide no additional effect for poor responders to first-generation drugs.