Literature DB >> 9610219

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

S Rapp1, S Shumaker, T Smith, P Gibson, R Berzon, R Hoffman.   

Abstract

The Liverpool Seizure Severity Scale (LSSS) and the Liverpool Quality of Life (LQOL) battery were developed in Great Britain to assess the severity of seizure symptoms and the impact of epilepsy on patients' quality of life. The scales have been validated on British patients, but have not been validated for use with American patients. The objectives of this study were to adapt the scales to the American population and to evaluate their reliability and validity. After modifications recommended by focus groups with patients and epilepsy specialists, the scales were administered to a sample of 90 epilepsy patients who had experienced seizures within the previous 4 weeks. Comparisons of patients with generalized tonic-clonic seizures (n = 58) and partial seizures (n = 32) revealed significant differences on 12 of the 20 items on the LSSS as well as the total score. None of the six LQOL subscales (negative drug effects, positive drug effects, affect balance, sense of mastery, life fulfillment and impact of epilepsy) distinguished patients with different seizure types but five of the six subscales were significantly correlated with seizure severity. The internal consistency and test-retest reliability were adequate for both the LSSS and LQOL. Finally, five of the six LQOL scales were significantly correlated with independent measures of mental health, physical health and role functioning.

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Year:  1998        PMID: 9610219     DOI: 10.1023/a:1024942215515

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  19 in total

1.  The development of a seizure severity scale as an outcome measure in epilepsy.

Authors:  G A Baker; D F Smith; M Dewey; J Morrow; P M Crawford; D W Chadwick
Journal:  Epilepsy Res       Date:  1991-04       Impact factor: 3.045

2.  The MOS 36-item short-form health survey (SF-36). I. Conceptual framework and item selection.

Authors:  J E Ware; C D Sherbourne
Journal:  Med Care       Date:  1992-06       Impact factor: 2.983

3.  The structure of coping.

Authors:  L I Pearlin; C Schooler
Journal:  J Health Soc Behav       Date:  1978-03

4.  A health-related quality of life instrument for patients evaluated for epilepsy surgery.

Authors:  B G Vickrey; R D Hays; J Graber; R Rausch; J Engel; R H Brook
Journal:  Med Care       Date:  1992-04       Impact factor: 2.983

Review 5.  Epidemiology and genetics of epilepsy.

Authors:  J F Annegers
Journal:  Neurol Clin       Date:  1994-02       Impact factor: 3.806

6.  Development of the quality of life in epilepsy inventory.

Authors:  O Devinsky; B G Vickrey; J Cramer; K Perrine; B Hermann; K Meador; R D Hays
Journal:  Epilepsia       Date:  1995-11       Impact factor: 5.864

7.  The stigma of epilepsy as a self-concept.

Authors:  R Ryan; K Kempner; A C Emlen
Journal:  Epilepsia       Date:  1980-08       Impact factor: 5.864

8.  The initial development of a health-related quality of life model as an outcome measure in epilepsy.

Authors:  G A Baker; D F Smith; M Dewey; A Jacoby; D W Chadwick
Journal:  Epilepsy Res       Date:  1993-09       Impact factor: 3.045

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

Authors:  A Jacoby; G Baker; D Smith; M Dewey; D Chadwick
Journal:  Epilepsy Res       Date:  1993-09       Impact factor: 3.045

10.  Agreement between self reports and proxy reports of quality of life in epilepsy patients.

Authors:  R D Hays; B G Vickrey; B P Hermann; K Perrine; J Cramer; K Meador; K Spritzer; O Devinsky
Journal:  Qual Life Res       Date:  1995-04       Impact factor: 4.147

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  2 in total

1.  Validity of the Neurology Quality-of-Life (Neuro-QoL) measurement system in adult epilepsy.

Authors:  David Victorson; Jose E Cavazos; Gregory L Holmes; Anthony T Reder; Valerie Wojna; Cindy Nowinski; Deborah Miller; Sarah Buono; Allison Mueller; Claudia Moy; David Cella
Journal:  Epilepsy Behav       Date:  2013-12-20       Impact factor: 2.937

Review 2.  Patient Reported Outcome (PRO) assessment in epilepsy: a review of epilepsy-specific PROs according to the Food and Drug Administration (FDA) regulatory requirements.

Authors:  Annabel Nixon; Cicely Kerr; Katie Breheny; Diane Wild
Journal:  Health Qual Life Outcomes       Date:  2013-03-11       Impact factor: 3.186

  2 in total

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