@article{3c79c96d1dc641e9bc1e4111922f1c4e,
title = "Prescription trends and psychiatric symptoms following first receipt of one of seven common antiepileptic drugs in general practice",
abstract = "We sought to examine the risk of psychiatric symptoms associated with a first prescription for specific antiepileptic drugs (AEDs) used in monotherapy in a general cohort of patients with epilepsy. We used The Health Improvement Network database (comprising the years 2000–2012) to identify incident patients with epilepsy. The index date was that on which they met the case definition for epilepsy, and analyses only included patients who remained on monotherapy or received no AED therapy following diagnosis to avoid confounding by polytherapy. Psychiatric symptoms were defined using mental health clinical or treatment (medical or therapeutic) code. We analyzed the AED of interest as a time-varying covariate in multivariate Cox proportional hazard regression models controlling for confounding factors. We identified 9595 patients with incident epilepsy, 7400 of whom (77%) received a first-recorded AED prescription. Prescriptions for newer generation AEDs (lamotrigine and levetiracetam) steadily increased (constituting over 30% of all AED prescriptions by 2012) while valproate use significantly declined in females (~ 40% in 2002 to just over 20% by 2012). A total of 2190 patients were first exposed to carbamazepine (29.3%) and 222 to lamotrigine (3%), both of which were associated with a lower hazard of any coded psychiatric symptom or disorder in multivariate analyses (hazard ratio [HR]: 0.84, 95% confidence interval [95% CI]: 0.73–0.97; p = 0.02 and HR: 0.83, 95% CI: 0.70–0.99; p = 0.03, respectively, for carbamazepine and lamotrigine). Carbamazepine was also associated with a lower hazard for depression (HR: 0.81; 95% CI: 0.69–0.96; p = 0.013) and anxiety (HR: 0.77; 95% CI: 0.63–0.95; p = 0.013) in secondary analyses. This study provides evidence that carbamazepine and lamotrigine are associated with lower hazards for psychiatric symptoms following a diagnosis of epilepsy. These estimates can be used in clinical settings, and the precision should improve with more contemporary data that include larger proportions of newer generation AEDs.",
keywords = "Antiepileptic drugs, Cohort studies, Epilepsy/seizures, Medication adverse effects, Psychiatric disorders",
author = "Josephson, {Colin B.} and Engbers, {Jordan D.T.} and Nathalie Jette and Patten, {Scott B.} and Sajobi, {Tolulope T.} and Deborah Marshall and Mark Lowerison and Samuel Wiebe",
note = "Funding Information: All authors (except if noted below) declare that they have no conflicts of interest. NJ holds operating grants (paid to the University of Calgary) from the Canadian Institutes of Health Research, NIH/NINDS, Alberta Health, the University of Calgary Cumming School of Medicine, and Hotchkiss Brain Institute for work unrelated to this study. DM holds operating grants (paid to the University of Calgary) from the Canadian Institutes of Health Research, Alberta Innovates Health Solutions, EuroQoL Foundation, Colorectal Cancer Association of Canada, Genome Canada, Canadian Initiative for Outcomes in Rheumatology Care, and the University of Calgary Cumming School of Medicine for work unrelated to this study. Funding Information: The Health Improvement Network has been used for scientific research since approval from the NHS South-East Multi-Centre Research Ethics Committee in 2003. Ethics approval for this study was obtained both through the University of Calgary's Conjoint Health Research Ethics Board (REB15-0203) and the CMD Medical Research's Scientific Review Committee in December 2015 (SRC Reference number 15THIN087). 3 Funding Information: • CBJ was the holder of the American Brain Foundation/American Epilepsy Society/Epilepsy Foundation/American Academy of Neurology Susan S. Spencer Clinical Research Training Fellowship in Epilepsy and an Alberta Innovates Health Solutions Clinician Fellowship during the completion of this project. • JDTE was supported by an Alberta Innovates Health Solutions Postdoctoral Fellowship during the completion of this project. • NJ was the holder of a Canada Research Chair Tier 2 in Neurological Health Services Research during the research period. • SBP has no declarations. • TTS is supported by the MSI Foundation New Investigator Grant. • DM is supported by a Canada Research Chair (Health Services and Systems Research) and the Arthur J.E. Child Chair in Rheumatology Outcomes Research. • ML has no declarations. • SW is the holder of the Hopewell Professorship of Clinical Neurosciences Research at the University of Calgary. Publisher Copyright: {\textcopyright} 2018 Elsevier Inc.",
year = "2018",
month = jul,
doi = "10.1016/j.yebeh.2018.04.012",
language = "English",
volume = "84",
pages = "49--55",
journal = "Epilepsy and Behavior",
issn = "1525-5050",
publisher = "Academic Press Inc.",
}