Literature DB >> 25367348

Wolf-living with SLE in a novel.

Ad A Kaptein1, Joshua M Smyth, Richard S Panush.   

Abstract

Living with SLE is a major task for the patients and their social environment. In modern health care, quality of life is increasingly incorporated as an important outcome. Studying novels about illness is a new method of exploring quality of life in patients with an illness. In this paper, we use the novel A tribe of women by Hervé Bazin as data to explore how a patient with SLE gives meaning to her illness and how her social environment reacts toward the illness and its treatment. We find that the novel-probably the only one where SLE is a major subject-offers a rich set of data on "living with SLE". Our findings may be instrumental in encouraging health care providers to explore quality of life in patients with SLE, incorporating self-management in order to improve their quality of life, and in teaching medical students about "medical humanities".

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Year:  2014        PMID: 25367348     DOI: 10.1007/s10067-014-2814-9

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  24 in total

1.  What constitutes uncertainty in systemic lupus erythematosus and rheumatoid arthritis?

Authors:  S Cleanthous; S P Newman; M Shipley; D A Isenberg; S J Cano
Journal:  Psychol Health       Date:  2012-07-10

2.  Effects of writing about stressful experiences on symptom reduction in patients with asthma or rheumatoid arthritis: a randomized trial.

Authors:  J M Smyth; A A Stone; A Hurewitz; A Kaell
Journal:  JAMA       Date:  1999-04-14       Impact factor: 56.272

3.  The needs of persons with lupus and health care providers: a qualitative study aimed toward the development of the Lupus Interactive Navigator™.

Authors:  C Neville; D Da Costa; C Mill; M Rochon; J A Aviña-Zubieta; C A Pineau; D Eng; P R Fortin
Journal:  Lupus       Date:  2013-12-13       Impact factor: 2.911

4.  Do art lovers make better doctors?

Authors:  Ad A Kaptein; Frans Meulenberg; Joshua M Smyth
Journal:  Lancet Respir Med       Date:  2013-12-02       Impact factor: 30.700

5.  Fatigue in patients with spondyloarthritis associates with disease activity, quality of life and inflammatory bowel symptoms.

Authors:  Simon M Stebbings; Gareth J Treharne; Katey Jenks; John Highton
Journal:  Clin Rheumatol       Date:  2013-12-10       Impact factor: 2.980

6.  Predictors of self-reported health-related quality of life in systemic lupus erythematosus.

Authors:  Adnan N Kiani; Vibeke Strand; Hong Fang; Jawali Jaranilla; Michelle Petri
Journal:  Rheumatology (Oxford)       Date:  2013-05-16       Impact factor: 7.580

Review 7.  Experiences and perspectives of adults living with systemic lupus erythematosus: thematic synthesis of qualitative studies.

Authors:  Bernadet Sutanto; Davinder Singh-Grewal; H Patrick McNeil; Sean O'Neill; Jonathan C Craig; Julie Jones; Allison Tong
Journal:  Arthritis Care Res (Hoboken)       Date:  2013-11       Impact factor: 4.794

8.  Depression and pain in night time and daytime functioning of individuals with lupus.

Authors:  Leah F Lederman; Helen Lindner; Kenneth M Greenwood; Errol J Philip
Journal:  Psychol Health       Date:  2008

9.  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

10.  Problematic social support from patients' perspective: the case of systemic lupus erythematosus.

Authors:  Davide Mazzoni; Elvira Cicognani
Journal:  Soc Work Health Care       Date:  2014
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  1 in total

1.  Interaction between self-perceived disease control and self-management behaviours among Chinese middle-aged and older hypertensive patients: the role of subjective life expectancy.

Authors:  Jiao Lu; Linhui Liu; Jiaming Zheng; Zhongliang Zhou
Journal:  BMC Public Health       Date:  2022-04-13       Impact factor: 3.295

  1 in total

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