Literature DB >> 17665467

Development and validation of a disease-specific health-related quality of life measure, the LupusQol, for adults with systemic lupus erythematosus.

Kathleen McElhone1, Janice Abbott, Joanna Shelmerdine, Ian N Bruce, Yasmeen Ahmad, Caroline Gordon, Kate Peers, David Isenberg, Ada Ferenkeh-Koroma, Bridget Griffiths, Mohamed Akil, Peter Maddison, Lee-Suan Teh.   

Abstract

OBJECTIVE: To develop and validate a disease-specific health-related quality of life (HRQOL) instrument for adults with systemic lupus erythematosus (SLE).
METHODS: The work consisted of 6 stages. Stage 1 included item generation for questionnaire content from semistructured interviews with SLE patients. In stage 2 item selection for the draft questionnaire was performed by thematic analysis of the patient interview transcripts and expert panel agreement. In stage 3 the content validity of the draft questionnaire was assessed by patients completing the questionnaire and providing critical feedback. In stages 4 and 5 construct validity and internal reliability of the 3 versions of the LupusQoL were evaluated using principal component analysis with varimax rotation and Cronbach's alpha coefficients, respectively. In stage 6 discriminatory validity, concurrent validity, and test-retest reliability were evaluated.
RESULTS: Stages 1, 2, and 3 resulted in a preliminary instrument containing 63 items. In stage 4, 8 domains were identified. This factor structure, accounting for 82% of the variance, was confirmed in stage 5. The domains and Cronbach's alpha coefficients were physical health (0.94), emotional health (0.94), body image (0.89), pain (0.92), planning (0.93), fatigue (0.88), intimate relationships (0.96), and burden to others (0.94). Discriminant validity was demonstrated for different levels of disease activity (British Isles Lupus Assessment Group Index) and damage (Systemic Lupus International Collaborating Clinics/American College of Rheumatology Damage Index). High correlations (r = 0.71-0.79) between comparable domains of the Short Form 36 and the LupusQoL assured acceptable concurrent validity. Good test-retest reliability (r = 0.72-0.93) was demonstrated.
CONCLUSION: The LupusQoL is a validated SLE-specific HRQOL instrument with 34 items across 8 domains defined by patients as being important.

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Year:  2007        PMID: 17665467     DOI: 10.1002/art.22881

Source DB:  PubMed          Journal:  Arthritis Rheum        ISSN: 0004-3591


  67 in total

Review 1.  Top 10 recent developments in health-related quality of life in patients with systemic lupus erythematosus.

Authors:  Anisha B Dua; Zahi Touma; Sergio Toloza; Meenakshi Jolly
Journal:  Curr Rheumatol Rep       Date:  2013-12       Impact factor: 4.592

2.  Health-related quality of life assessed by LupusQoL questionnaire and SF-36 in Turkish patients with systemic lupus erythematosus.

Authors:  Sibel Yilmaz-Oner; Can Oner; Fatih Mert Dogukan; Toklong Filam Moses; Kubra Demir; Nazar Tekayev; Pamir Atagunduz; Serhan Tuglular; Haner Direskeneli
Journal:  Clin Rheumatol       Date:  2015-04-07       Impact factor: 2.980

3.  [Possibilities and limits of patient-reported outcome exemplified by systemic lupus erythematosus and the LuLa study].

Authors:  G Chehab; J Richter; M Schneider
Journal:  Z Rheumatol       Date:  2014-10       Impact factor: 1.372

4.  Components of quality of life in a sample of patients with lupus: a confirmatory factor analysis and Rasch modeling of the LupusQoL.

Authors:  Ana-Belén Meseguer-Henarejos; Juan-José Gascón-Cánovas; José-Antonio López-Pina
Journal:  Clin Rheumatol       Date:  2017-05-02       Impact factor: 2.980

5.  Development and validity of the DyNaChron questionnaire for chronic nasal dysfunction.

Authors:  Sophie Kacha; Francis Guillemin; Roger Jankowski
Journal:  Eur Arch Otorhinolaryngol       Date:  2011-07-08       Impact factor: 2.503

6.  Systemic lupus erythematosus: The promise of PROMIS - is it ready for prime time in SLE?

Authors:  Meenakshi Jolly; Patricia Katz
Journal:  Nat Rev Rheumatol       Date:  2017-06-22       Impact factor: 20.543

Review 7.  The humanistic and economic burden of systemic lupus erythematosus : a systematic review.

Authors:  Rachel Meacock; Nicola Dale; Mark J Harrison
Journal:  Pharmacoeconomics       Date:  2013-01       Impact factor: 4.981

Review 8.  Patient-Reported Outcomes in Systemic Lupus Erythematosus.

Authors:  Mary Mahieu; Susan Yount; Rosalind Ramsey-Goldman
Journal:  Rheum Dis Clin North Am       Date:  2016-03-17       Impact factor: 2.670

9.  Fatigue in systemic lupus erythematosus : Association with disease activity, quality of life and psychosocial factors.

Authors:  S Yilmaz-Oner; B Ilhan; M Can; F Alibaz-Oner; O Polat-Korkmaz; G Ozen; G Mumcu; H M Kremers; S Tuglular; H Direskeneli
Journal:  Z Rheumatol       Date:  2017-12       Impact factor: 1.372

10.  The Chinese version of the SLEQOL is a reliable assessment of health-related quality of life in Han Chinese patients with systemic lupus erythematosus.

Authors:  Hai-Zhi Jiang; Zhi-Guo Lin; Hong-Juan Li; Qing -Du; Wei -Tian; Shu-Ya Wang; Shang-Qi Guan; Yi-Fang Mei
Journal:  Clin Rheumatol       Date:  2017-11-22       Impact factor: 2.980

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