Literature DB >> 15802538

Illness representations of systemic lupus erythematosus.

Donna Goodman, Shirley Morrissey, Deborah Graham, David Bossingham.   

Abstract

Systemic lupus erythematosus (SLE) is a chronic illness that usually follows a fluctuating course and, therefore, can be difficult to diagnose. Consequently, individuals with SLE often hold beliefs about the nature and course of the illness that are at odds with medical opinion. Clearly, a shared understanding of the illness would be beneficial to illness management. In this study, the authors used semistructured interviews and interpretative phenomenological analysis to explore the content of the illness representations held by 36 individuals diagnosed with SLE. They also identified the ways in which these illness representations were generated initially and attempted to determine whether changes occurred over time in these illness representations, as predicted by the self-regulatory model.

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Year:  2005        PMID: 15802538     DOI: 10.1177/1049732305275167

Source DB:  PubMed          Journal:  Qual Health Res        ISSN: 1049-7323


  10 in total

1.  "Joining the dots" for patients with systemic lupus erythematosus: personal perspectives of health care from a qualitative study.

Authors:  E D Hale; G J Treharne; A C Lyons; Y Norton; S Mole; D L Mitton; K M J Douglas; N Erb; G D Kitas
Journal:  Ann Rheum Dis       Date:  2005-10-11       Impact factor: 19.103

2.  Musicians' illness perceptions of musculoskeletal complaints.

Authors:  Laura M Kok; Theodora P M Vliet Vlieland; Marta Fiocco; Ad A Kaptein; Rob G H H Nelissen
Journal:  Clin Rheumatol       Date:  2013-02-17       Impact factor: 2.980

Review 3.  Illness perceptions and work participation: a systematic review.

Authors:  J L Hoving; M van der Meer; A Y Volkova; M H W Frings-Dresen
Journal:  Int Arch Occup Environ Health       Date:  2010-02-04       Impact factor: 3.015

4.  Patients' perspective: lupus in patients' drawings. Assessing drawing as a diagnostic and therapeutic method.

Authors:  Katarzyna Nowicka-Sauer
Journal:  Clin Rheumatol       Date:  2007-04-20       Impact factor: 2.980

5.  The influence of 'significant others' on persistent back pain and work participation: a qualitative exploration of illness perceptions.

Authors:  Serena McCluskey; Joanna Brooks; Nigel King; Kim Burton
Journal:  BMC Musculoskelet Disord       Date:  2011-10-14       Impact factor: 2.362

6.  The Lived Experience of Lupus Flares: Features, Triggers, and Management in an Australian Female Cohort.

Authors:  Marline L Squance; Glenn E M Reeves; Howard Bridgman
Journal:  Int J Chronic Dis       Date:  2014-11-20

7.  "Am I carrier?" The patient's lived experience of thrombophilia genetic screening and its outcome.

Authors:  Guendalina Graffigna; Daniela Leone; Elena Vegni
Journal:  Health Psychol Behav Med       Date:  2014-06-04

8.  How do patients with systemic autoimmune rheumatic disease perceive the use of their medications: a systematic review and thematic synthesis of qualitative research.

Authors:  Hans Haag; Tim Liang; J Antonio Avina-Zubieta; Mary A De Vera
Journal:  BMC Rheumatol       Date:  2018-04-02

9.  Exploring the Perceived Impact of the Chronic Disease Self-Management Program on Self-Management Behaviors among African American Women with Lupus: A Qualitative Study.

Authors:  Abena A Twumasi; Anna Shao; Charmayne Dunlop-Thomas; Cristina Drenkard; Hannah L Cooper
Journal:  ACR Open Rheumatol       Date:  2020-02-09

10.  Development and preliminary evaluation of the validity and reliability of a revised illness perception questionnaire for healthcare professionals.

Authors:  Seher Arat; Anke Van den Zegel; Maity Van Rillaer; Philip Moons; Joris Vandenberghe; Ellen De Langhe; René Westhovens
Journal:  BMC Nurs       Date:  2016-06-01
  10 in total

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