Differential effects of seizure control and affective symptoms on quality of life in people with epilepsy

The purpose of the study was to delineate how affective symptoms (AS) influence quality of life (QOL) for individuals with drug-refractory epilepsy (DRE) and those with well-controlled epilepsy (WCE) independently. All subjects participating in the study were asked to complete reliable and validated...

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Published inEpilepsy & behavior Vol. 18; no. 4; pp. 455 - 459
Main Authors Park, Sung-Pa, Song, Hyun-Seok, Hwang, Yang-Ha, Lee, Ho-Won, Suh, Chung-Kyu, Kwon, Soon-Hak
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.08.2010
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Online AccessGet full text
ISSN1525-5050
1525-5069
1525-5069
DOI10.1016/j.yebeh.2010.05.021

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Abstract The purpose of the study was to delineate how affective symptoms (AS) influence quality of life (QOL) for individuals with drug-refractory epilepsy (DRE) and those with well-controlled epilepsy (WCE) independently. All subjects participating in the study were asked to complete reliable and validated self-report health questionnaires, including AS, measured with the Korean versions of the Beck Depression Inventory, Beck Anxiety Inventory, and Quality of Life in Epilepsy Inventory-31 (QOLIE-31). We examined predictors of QOLIE-31 scores among the various demographic and clinical factors. We compared the effects of AS on QOL between patients with DRE and those with WCE and investigated the differential effects of seizure control and AS on QOL. Two hundred forty-nine patients with DRE or WCE were included in the study. The strongest predictor of QOL was AS, followed by seizure control and MRI abnormality. Affective symptoms had almost two times the effect of seizure control and six times the effect of MRI abnormality. Poorest QOL was noted in patients with DRE with AS, followed by those with WCE with AS, DRE without AS, and WCE without AS. The major determinant of QOL in patients with epilepsy is AS rather than DRE or WCE status.
AbstractList Abstract Objective The purpose of the study was to delineate how affective symptoms (AS) influence quality of life (QOL) for individuals with drug-refractory epilepsy (DRE) and those with well-controlled epilepsy (WCE) independently. Methods All subjects participating in the study were asked to complete reliable and validated self-report health questionnaires, including AS, measured with the Korean versions of the Beck Depression Inventory, Beck Anxiety Inventory, and Quality of Life in Epilepsy Inventory-31 (QOLIE-31). We examined predictors of QOLIE-31 scores among the various demographic and clinical factors. We compared the effects of AS on QOL between patients with DRE and those with WCE and investigated the differential effects of seizure control and AS on QOL. Results Two hundred forty-nine patients with DRE or WCE were included in the study. The strongest predictor of QOL was AS, followed by seizure control and MRI abnormality. Affective symptoms had almost two times the effect of seizure control and six times the effect of MRI abnormality. Poorest QOL was noted in patients with DRE with AS, followed by those with WCE with AS, DRE without AS, and WCE without AS. Conclusion The major determinant of QOL in patients with epilepsy is AS rather than DRE or WCE status.
The purpose of the study was to delineate how affective symptoms (AS) influence quality of life (QOL) for individuals with drug-refractory epilepsy (DRE) and those with well-controlled epilepsy (WCE) independently.OBJECTIVEThe purpose of the study was to delineate how affective symptoms (AS) influence quality of life (QOL) for individuals with drug-refractory epilepsy (DRE) and those with well-controlled epilepsy (WCE) independently.All subjects participating in the study were asked to complete reliable and validated self-report health questionnaires, including AS, measured with the Korean versions of the Beck Depression Inventory, Beck Anxiety Inventory, and Quality of Life in Epilepsy Inventory-31 (QOLIE-31). We examined predictors of QOLIE-31 scores among the various demographic and clinical factors. We compared the effects of AS on QOL between patients with DRE and those with WCE and investigated the differential effects of seizure control and AS on QOL.METHODSAll subjects participating in the study were asked to complete reliable and validated self-report health questionnaires, including AS, measured with the Korean versions of the Beck Depression Inventory, Beck Anxiety Inventory, and Quality of Life in Epilepsy Inventory-31 (QOLIE-31). We examined predictors of QOLIE-31 scores among the various demographic and clinical factors. We compared the effects of AS on QOL between patients with DRE and those with WCE and investigated the differential effects of seizure control and AS on QOL.Two hundred forty-nine patients with DRE or WCE were included in the study. The strongest predictor of QOL was AS, followed by seizure control and MRI abnormality. Affective symptoms had almost two times the effect of seizure control and six times the effect of MRI abnormality. Poorest QOL was noted in patients with DRE with AS, followed by those with WCE with AS, DRE without AS, and WCE without AS.RESULTSTwo hundred forty-nine patients with DRE or WCE were included in the study. The strongest predictor of QOL was AS, followed by seizure control and MRI abnormality. Affective symptoms had almost two times the effect of seizure control and six times the effect of MRI abnormality. Poorest QOL was noted in patients with DRE with AS, followed by those with WCE with AS, DRE without AS, and WCE without AS.The major determinant of QOL in patients with epilepsy is AS rather than DRE or WCE status.CONCLUSIONThe major determinant of QOL in patients with epilepsy is AS rather than DRE or WCE status.
The purpose of the study was to delineate how affective symptoms (AS) influence quality of life (QOL) for individuals with drug-refractory epilepsy (DRE) and those with well-controlled epilepsy (WCE) independently. All subjects participating in the study were asked to complete reliable and validated self-report health questionnaires, including AS, measured with the Korean versions of the Beck Depression Inventory, Beck Anxiety Inventory, and Quality of Life in Epilepsy Inventory-31 (QOLIE-31). We examined predictors of QOLIE-31 scores among the various demographic and clinical factors. We compared the effects of AS on QOL between patients with DRE and those with WCE and investigated the differential effects of seizure control and AS on QOL. Two hundred forty-nine patients with DRE or WCE were included in the study. The strongest predictor of QOL was AS, followed by seizure control and MRI abnormality. Affective symptoms had almost two times the effect of seizure control and six times the effect of MRI abnormality. Poorest QOL was noted in patients with DRE with AS, followed by those with WCE with AS, DRE without AS, and WCE without AS. The major determinant of QOL in patients with epilepsy is AS rather than DRE or WCE status.
Author Lee, Ho-Won
Kwon, Soon-Hak
Park, Sung-Pa
Suh, Chung-Kyu
Song, Hyun-Seok
Hwang, Yang-Ha
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Issue 4
Keywords Depression
Anxiety
Seizure control
Affective symptoms
Epilepsy
Quality of life
Language English
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Snippet The purpose of the study was to delineate how affective symptoms (AS) influence quality of life (QOL) for individuals with drug-refractory epilepsy (DRE) and...
Abstract Objective The purpose of the study was to delineate how affective symptoms (AS) influence quality of life (QOL) for individuals with drug-refractory...
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SubjectTerms Adult
Affective symptoms
Affective Symptoms - diagnosis
Affective Symptoms - etiology
Affective Symptoms - psychology
Anxiety
Depression
Epilepsy
Epilepsy - complications
Epilepsy - pathology
Epilepsy - psychology
Female
Humans
Linear Models
Magnetic Resonance Imaging
Male
Middle Aged
Neurology
Psychiatric Status Rating Scales
Quality of Life
Retrospective Studies
Seizure control
Seizures - diagnosis
Seizures - etiology
Seizures - psychology
Surveys and Questionnaires
Title Differential effects of seizure control and affective symptoms on quality of life in people with epilepsy
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https://www.ncbi.nlm.nih.gov/pubmed/20591744
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