Literature DB >> 18385276

The development of the L-QoL: a quality-of-life instrument specific to systemic lupus erythematosus.

L C Doward1, S P McKenna, D Whalley, A Tennant, B Griffiths, P Emery, D J Veale.   

Abstract

OBJECTIVES: Complex diseases, such as systemic lupus erythematosus (SLE), present dilemmas over choice of outcome measures. Using a battery of instruments to capture the impact of different impairments or activity limitations experienced does not provide assessment of the wider impact on quality of life (QoL). This paper describes the development and testing of a new instrument to measure QoL in systemic lupus erythematosus (L-QoL).
METHODS: The development combines theoretical strengths of the needs-based QoL model with statistical and diagnostic powers of the Rasch model. Content was derived from in-depth interviews with relevant patients. Cognitive debriefing interviews assessed face and content validity. Rasch analysis was applied to data from an initial postal survey to remove misfitting items. A second postal survey assessed scaling properties, reliability, internal consistency and validity.
RESULTS: A 55-item questionnaire was derived from interview transcripts. Cognitive debriefing confirmed acceptability. Rasch analysis of postal survey data (n = 95) removed misfitting items. A second postal survey (n = 93), produced a 25-item version with good item fit and stability, excellent test-retest reliability (0.92), internal consistency (0.92) and strict unidimensionality.
CONCLUSIONS: It is concluded that the L-QoL should prove a valuable instrument for assessing patient-based outcome in clinical trials and practice.

Entities:  

Mesh:

Year:  2008        PMID: 18385276     DOI: 10.1136/ard.2007.086009

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  27 in total

1.  Adaptation of the osteoarthritis-specific quality of life scale (the OAQoL) for use in Germany, Hungary, Italy, Spain and Turkey.

Authors:  Jeanette Wilburn; Stephen P McKenna; Şehim Kutlay; Tamas Bender; Jürgen Braun; Concepcion Castillo-Gallego; Marta Favero; Pal Geher; Uta Kiltz; Emilio Martin-Mola; Roberta Ramonda; Matthew Rouse; Alan Tennant; Ayşe A Küçükdeveci
Journal:  Rheumatol Int       Date:  2017-02-15       Impact factor: 2.631

Review 2.  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

3.  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

4.  [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

5.  Adaptation and validation of the Rheumatoid Arthritis Quality of Life (RAQoL) questionnaire for use in Serbia.

Authors:  Mirjana Zlatkovic-Svenda; Matthew Rouse; Marija Radak-Perovic; Roksanda Stojanovic; Nada Vujasinovic-Stupar; Biljana Lazovic-Popovic; Jeanette Wilburn; Stephen P McKenna
Journal:  Rheumatol Int       Date:  2016-10-31       Impact factor: 2.631

6.  Development of a patient reported outcome measure for fatigue in motor neurone disease: the Neurological Fatigue Index (NFI-MND).

Authors:  Chris J Gibbons; Roger J Mills; Everard W Thornton; John Ealing; John D Mitchell; Pamela J Shaw; Kevin Talbot; A Tennant; Carolyn A Young
Journal:  Health Qual Life Outcomes       Date:  2011-11-22       Impact factor: 3.186

7.  Health-related quality of life and employment among persons with systemic lupus erythematosus.

Authors:  Jinoos Yazdany; Edward Yelin
Journal:  Rheum Dis Clin North Am       Date:  2010-02       Impact factor: 2.670

Review 8.  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

9.  Patient reported outcomes: looking beyond the label claim.

Authors:  Lynda C Doward; Ari Gnanasakthy; Mary G Baker
Journal:  Health Qual Life Outcomes       Date:  2010-08-20       Impact factor: 3.186

Review 10.  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

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