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Comparative stroke risk of antiepileptic drugs in patients with epilepsy
Author(s) -
Hsieh ChengYang,
Lai Edward ChiaCheng,
Yang YeaHuei Kao,
Lin SwuJane
Publication year - 2013
Publication title -
epilepsia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.687
H-Index - 191
eISSN - 1528-1167
pISSN - 0013-9580
DOI - 10.1111/j.1528-1167.2012.03693.x
Subject(s) - medicine , stroke (engine) , epilepsy , hazard ratio , retrospective cohort study , cohort study , proportional hazards model , phenytoin , cohort , confidence interval , population , carbamazepine , pediatrics , psychiatry , mechanical engineering , environmental health , engineering
Summary Purpose: Patients with epilepsy have higher stroke‐related morbidity and mortality, leading to the suspicion that the increased stroke events may be associated with antiepileptic drug (AED) exposure. We evaluated the comparative risk of stroke in adult patients with epilepsy receiving phenytoin (PHT), valproic acid (VPA), or carbamazepine (CBZ) to help determine the stroke risk for Asian patients with specific AED exposure. Methods: We conducted a population‐based, retrospective cohort study using the Taiwan National Health Insurance Research Database (NHIRD). The cohort consists of adult patients with epilepsy who were new to PHT, CBZ, or VPA monotherapy and without prior stroke history. Patients were followed for 5 years. The event of interest was a hospitalization or emergency visit due to stroke. Cox proportional hazard models were used to estimate the comparative risk of AEDs. Subanalyses included an evaluation of different subtypes of stroke, the propensity score matched technique, the intention‐to‐treat approach, and stratification analyses. Key Findings: Patients receiving PHT had a significantly higher stroke risk (adjusted hazard ratio [HR] 1.72; 95% confidence interval [CI] 1.20–2.47), followed by VPA (adjusted HR 1.27; 95% CI 0.78–2.07), when compared with CBZ. The results of all subanalyses showed a consistent trend of higher stroke risk with PHT use. In addition, there appeared to be a dose–response relationship between stroke risk and PHT prescriptions. Significance: The stroke risk was higher in PHT but not significantly different in VPA as compared to CBZ. Physicians should reconsider using PHT for patients with epilepsy who already have a higher risk of stroke.