TY - JOUR
T1 - Cognitive and psychosocial effects of oxcarbazepine monotherapy in newly diagnosed partial epilepsy
AU - Kim, Daeyoung
AU - Seo, Ji Hye
AU - Joo, Eun Yeon
AU - Lee, Hyang Woon
AU - Shin, Won Chul
AU - Hong, Seung Bong
PY - 2014
Y1 - 2014
N2 - Objectives: The aim of this study was to assess the effects of oxcarbazepine (OXC) on cognition and psychosocial difficulties in patients with new-onset partial epilepsy. Methods: Cognitive and psychosocial assessments were performed before and after 6 to 12 months of OXC monotherapy in 52 drug-naive patients (25 women; mean age, 31.1 years; SD, 12.1 years). Cognitive functions were evaluated with well-structured and validated tools. Mood, psychological distress, subjective handicap, and quality of life were also evaluated. Differences between baseline and after-treatment evaluation were compared and adjusted for possible confounders such as age, sex, seizure control, duration of epilepsy, assessment interval, and epileptogenic region. Results: Mean assessment interval was 231.8 (range, 182-348) days, and mean (SD) OXC dose at retest was 693.8 (208.9) mg. The OXC was found to have no significant adverse effect on cognition. Furthermore, OXC monotherapy was not found to affect psychosocial difficulties, including psychological distress and subjective handicap. Conclusions: The results suggest that OXC monotherapy could be used to treat newly diagnosed partial epilepsy without adversely affecting cognitive and psychosocial functions.
AB - Objectives: The aim of this study was to assess the effects of oxcarbazepine (OXC) on cognition and psychosocial difficulties in patients with new-onset partial epilepsy. Methods: Cognitive and psychosocial assessments were performed before and after 6 to 12 months of OXC monotherapy in 52 drug-naive patients (25 women; mean age, 31.1 years; SD, 12.1 years). Cognitive functions were evaluated with well-structured and validated tools. Mood, psychological distress, subjective handicap, and quality of life were also evaluated. Differences between baseline and after-treatment evaluation were compared and adjusted for possible confounders such as age, sex, seizure control, duration of epilepsy, assessment interval, and epileptogenic region. Results: Mean assessment interval was 231.8 (range, 182-348) days, and mean (SD) OXC dose at retest was 693.8 (208.9) mg. The OXC was found to have no significant adverse effect on cognition. Furthermore, OXC monotherapy was not found to affect psychosocial difficulties, including psychological distress and subjective handicap. Conclusions: The results suggest that OXC monotherapy could be used to treat newly diagnosed partial epilepsy without adversely affecting cognitive and psychosocial functions.
KW - anticonvulsants
KW - cognition
KW - epilepsy
KW - oxcarbazepine
KW - psychosocial difficulties (PSD)
UR - http://www.scopus.com/inward/record.url?scp=84925351523&partnerID=8YFLogxK
U2 - 10.1097/WNF.0000000000000038
DO - 10.1097/WNF.0000000000000038
M3 - Article
C2 - 24992084
AN - SCOPUS:84925351523
SN - 0362-5664
VL - 37
SP - 100
EP - 107
JO - Clinical Neuropharmacology
JF - Clinical Neuropharmacology
IS - 4
ER -