Literature DB >> 8243442

Measuring the impact of epilepsy: the development of a novel scale.

A Jacoby1, G Baker, D Smith, M Dewey, D Chadwick.   

Abstract

The impact of a chronic illness is experienced not only through its physical symptoms, but also as a result of its effect on psychosocial functioning. In the case of an illness such as epilepsy, where the physical manifestations are transient, the psychosocial consequences may, with time, come to be of greater concern. We have been involved in developing a quality of life model for epilepsy. As part of the refinement of the initial model, we have devised a novel scale to measure the impact of the condition on a number of different aspects of daily life. The scale was administered to 75 patients attending an epilepsy out-patient clinic. Initial analysis of its psychometric properties is encouraging, although the inclusion of an item relating to employment reduced the scale's reliability. As a result, the wording of the existing item has been amended and an additional item has been incorporated. We hope the scale will be useful in investigations of treatment for epilepsy and of its psychosocial aspects.

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Year:  1993        PMID: 8243442     DOI: 10.1016/0920-1211(93)90042-6

Source DB:  PubMed          Journal:  Epilepsy Res        ISSN: 0920-1211            Impact factor:   3.045


  35 in total

1.  The SF-36 as a health status measure for epilepsy: a psychometric assessment.

Authors:  A Jacoby; G A Baker; N Steen; D Buck
Journal:  Qual Life Res       Date:  1999-06       Impact factor: 4.147

2.  Quality of life after epilepsy surgery.

Authors:  M W Kellett; D F Smith; G A Baker; D W Chadwick
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-07       Impact factor: 10.154

Review 3.  The problem of quality of life.

Authors:  S M Hunt
Journal:  Qual Life Res       Date:  1997-04       Impact factor: 4.147

Review 4.  Assessing quality of life in patients with epilepsy.

Authors:  A Jacoby
Journal:  Pharmacoeconomics       Date:  1996-05       Impact factor: 4.981

5.  The contribution of the measurement of seizure severity to quality of life research.

Authors:  D Smith; G A Baker; A Jacoby; D W Chadwick
Journal:  Qual Life Res       Date:  1995-04       Impact factor: 4.147

Review 6.  Quality of life as an outcome measure for epilepsy clinical trials.

Authors:  J A Cramer
Journal:  Pharm World Sci       Date:  1997-10

7.  Epilepsy and quality of life: what does really matter?

Authors:  Mario Tombini; Giovanni Assenza; Livia Quintiliani; Lorenzo Ricci; Jacopo Lanzone; Vincenzo Di Lazzaro
Journal:  Neurol Sci       Date:  2021-01-15       Impact factor: 3.307

8.  Reliability and Validity of the Korean Version of QOLIE-10 in Epilepsy.

Authors:  Sang-Ahm Lee; Sung-Cheol Yun; Byung-In Lee
Journal:  J Clin Neurol       Date:  2006-12-20       Impact factor: 3.077

9.  Measuring stigma across neurological conditions: the development of the stigma scale for chronic illness (SSCI).

Authors:  Deepa Rao; Seung W Choi; David Victorson; Rita Bode; Amy Peterman; Allen Heinemann; David Cella
Journal:  Qual Life Res       Date:  2009-04-25       Impact factor: 4.147

10.  Adaptation and evaluation of the Liverpool Seizure Severity Scale and Liverpool Quality of Life battery for American epilepsy patients.

Authors:  S Rapp; S Shumaker; T Smith; P Gibson; R Berzon; R Hoffman
Journal:  Qual Life Res       Date:  1998-05       Impact factor: 4.147

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