Long Term Outcome of Quality of Life in Newly Diagnosed Epilepsy
Abstract number :
3.131
Submission category :
Clinical Epilepsy-Adult
Year :
2006
Submission ID :
6816
Source :
www.aesnet.org
Presentation date :
12/1/2006 12:00:00 AM
Published date :
Nov 30, 2006, 06:00 AM
Authors :
1David M. Ficker, 1Cynthia Hughes, 1Michael D. Privitera, and 2Rakesh Shukla
To determine which components of quality of life (HRQOL) are different between subjects who were seizure free and not seizure free at last follow up in a cohort of newly diagnosed epilepsy., We prospectively measure the QOLIE-89, Profile of Mood States (POMS) and Adverse Events Profile in patients within three months of a new diagnosis of epilepsy. Serial measures are performed every four months. Inclusion criteria are: age between 18-64, able to read and speak English and a minimum tenth grade education. Exclusion criteria are: inability to complete forms, presence of other neurologic or medical disorders that may affect HRQOL, prior craniotomy and use of medications that can affect the central nervous system (other than AEDs).
A t-test was performed comparing QOL measures at last follow up between subjects who were seizure free and those not seizure free., We enrolled 53 subjects with newly diagnosed epilepsy (22 males, 32 females). Follow-up data was available on 40 patients (mean duration of follow-up 1.3 years). At last follow-up, 65% were seizure free and 35% were not seizure free. Table 1 summarizes differences on QOL measures between these groups., These results suggest that a seizure free state is associated with a higher QOL and improved anxiety symptoms. We found non-significant trends toward superior scores on other POMS subscales in the seizure free group.[table1], (Supported by NINDS 5K23NS002170.)
Clinical Epilepsy