Literature DB >> 9738676

Evaluating health-related quality of life outcomes in clinical trials of antiepileptic drug therapy.

N Kline Leidy1, A M Rentz, E M Grace.   

Abstract

PURPOSE: To provide an overview of condition-specific health-related quality of life (HRQL) assessment in clinical trials of antiepileptic drug (AED) therapy in adults. We describe the key measurement issues in HRQL evaluation, identify the instruments that have been used in this population, summarize the psychometric characteristics of these instruments, propose areas of HRQL most likely to change with treatment, and offer recommendations for further research.
METHODS: We conducted a comprehensive review of the literature using repeated searches of the MEDLINE database together with a review of reference lists from published papers. Psychometric information on the instruments was gathered from published literature.
RESULTS: Three epilepsy-specific HRQL measures were identified: the Epilepsy-Surgery Inventory (ESI-55), the Liverpool Assessment Battery, and the Quality of Life in Epilepsy Inventory (QOLIE, the 89-, 31-, and 10-item versions). One new measure, the Epilepsy Foundation of America (EFA) Concerns Index was also found. The psychometric characteristics of these instruments are discussed in relationship to performance or expected performance in a clinical trial setting. A review of descriptive studies and trials to date suggests that subscales reflecting the psychological and social domains of HRQL may be most sensitive to treatment designed to increase seizure-free periods, reduce seizure severity, and minimize undesirable side effects.
CONCLUSIONS: Although evaluation of HRQL outcomes in clinical trials of epilepsy is still in its infancy, several reliable and valid condition-specific measures are available for understanding the impact of disease and treatment on HRQL. Further research is needed to determine minimal clinically important change scores and to assess the psychometric stability of measures across cultures and mode of administration (self, interview, telephone). Studies of patient preferences for health outcomes in the form of utilities will provide needed data for evaluating the cost-effectiveness of new treatments.

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Year:  1998        PMID: 9738676     DOI: 10.1111/j.1528-1157.1998.tb01446.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  4 in total

Review 1.  Evaluation of the methodological quality of systematic reviews of health status measurement instruments.

Authors:  Lidwine B Mokkink; Caroline B Terwee; Paul W Stratford; Jordi Alonso; Donald L Patrick; Ingrid Riphagen; Dirk L Knol; Lex M Bouter; Henrica C W de Vet
Journal:  Qual Life Res       Date:  2009-02-24       Impact factor: 4.147

Review 2.  Quality of life in patients with epilepsy and impact of treatments.

Authors:  Patrizia Berto
Journal:  Pharmacoeconomics       Date:  2002       Impact factor: 4.981

3.  Nonepileptic seizures treatment workshop summary.

Authors:  W Curt LaFrance; Kenneth Alper; Debra Babcock; John J Barry; Selim Benbadis; Rochelle Caplan; John Gates; Margaret Jacobs; Andres Kanner; Roy Martin; Lynn Rundhaugen; Randy Stewart; Christina Vert
Journal:  Epilepsy Behav       Date:  2006-03-15       Impact factor: 2.937

4.  The health-related quality of life of patients with epilepsy compared with angina pectoris, rheumatoid arthritis, asthma and chronic obstructive pulmonary disease.

Authors:  K Stavem; M I Lossius; T K Kvien; B Guldvog
Journal:  Qual Life Res       Date:  2000       Impact factor: 3.440

  4 in total

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