Medication use patterns of antiepileptics and epileptic events

dc.contributor.advisorRascati, Karen L.en
dc.contributor.committeeMemberBrown, Carolynen
dc.contributor.committeeMemberLawson, Kennethen
dc.contributor.committeeMemberNovak, Suzanneen
dc.contributor.committeeMemberRichards, Kristinen
dc.contributor.committeeMemberYoder, Lindaen
dc.creatorShcherbakova, Natalia G., 1982-en
dc.date.accessioned2012-10-23T14:03:28Zen
dc.date.accessioned2017-05-11T22:28:56Z
dc.date.available2012-10-23T14:03:28Zen
dc.date.available2017-05-11T22:28:56Z
dc.date.issued2012-08en
dc.date.submittedAugust 2012en
dc.date.updated2012-10-23T14:03:39Zen
dc.descriptiontexten
dc.description.abstractThe purpose of this study was to identify clinical and demographic predictors of seizure recurrence in medically-treated patients with epilepsy. Innovus Invision™ Data Mart insurance claims from January 1, 2007 to September 30, 2010 were retrospectively analyzed. Patients aged 18-64 years with a primary or secondary diagnosis of epilepsy and >1 prescription claim for an antiepileptic drug (AED) pre-index were included. The primary outcome was incidence of seizures defined as an occurrence of an emergency room visit, ambulance service use or hospitalization with a primary or secondary diagnosis of epilepsy during the 1-year follow-up period. Predictor variables included antiepileptic drug (AED) adherence (Proportion of Days Covered ≥ 80 %), general comorbidity (Charlson’s Comorbidity Index ≥ 1), any mental health comorbidity, evidence of a prior seizure, type of epilepsy diagnosis (intractable versus non-intractable), presence of AED-interacting medications and any bioequivalent AED switch. The covariates included age, gender and geographic region of residence. The overall incidence of post-index seizures in the 1-year follow-up period for all four monotherapy cohorts combined was 5.3 % (n=166/3140), but was higher for the Keppra®/levetiracetam cohort (7.9%; n=88/1114) compared to the other cohorts [Lamictal®/lamotrigine (3.9%; n=45/1143), Trileptal®/oxcarbazepine (4.0%; n=18/456) and Topamax®/topiramate (3.5%; n=15/427)]. The combined cohort analysis demonstrated that pre-index seizures (odds ratio [OR] = 4.28; 95% CI, 2.81-6.53), any mental health comorbidity ([OR] = 3.41; 95% CI, 2.10-5.54), Charlson comorbidity Index ≥1 ([OR] = 2.88; 95% CI, 1.96-4.24) and monotherapy with Keppra®/levetiracetam ([OR] = 1.54; 95% CI, 1.03-2.31) were significant predictors of seizure recurrence. Among covariates, only geographic region was a significant predictor, with patients residing in the Northeast U.S. having higher odds of post-index seizure ([OR] = 1.92; 95% CI, 1.19-3.10), while controlling for clinical, medication and demographic characteristics. A bioequivalent AED switch, type of epilepsy diagnosis, AED adherence and the presence of interacting medications were not significant predictors of seizure recurrence in the combined cohort (p>0.05). Results indicate that epilepsy patients with comorbid conditions (both mental and somatic diseases), as well as patients who may have initially been unstable (with previous seizure occurrences) were more likely to experience seizures during the follow-up period.en
dc.description.departmentPharmacyen
dc.format.mimetypeapplication/pdfen
dc.identifier.slug2152/ETD-UT-2012-08-6127en
dc.identifier.urihttp://hdl.handle.net/2152/ETD-UT-2012-08-6127en
dc.language.isoengen
dc.subjectAntiepilepticsen
dc.subjectEpilepsyen
dc.subjectSeizure predictorsen
dc.subjectMonotherapyen
dc.titleMedication use patterns of antiepileptics and epileptic eventsen
dc.type.genrethesisen

Files