Literature DB >> 11708416

Living with lupus: a prospective pan-Canadian study.

P L Dobkin1, D Da Costa, P R Fortin, S Edworthy, S Barr, J M Esdaile, J L Senécal, J R Goulet, D Choquette, E Rich, A Beaulieu, A Cividino, S Ensworth, D Smith, M Zummer, D Gladman, A E Clarke.   

Abstract

OBJECTIVE: To portray life with lupus for women affected by this disease and to identify predictors of fatigue, a common symptom that compromises patients' quality of life.
METHODS: A sample of 120 female patients (mean age 42.5 yrs) with systemic lupus erythematosus (SLE) from 9 rheumatology clinics across Canada were followed prospectively for 15 months. Assessments of psychosocial functioning took place at baseline, and at 3, 9, and 15 months. Physician examinations were conducted at baseline and 15 months.
RESULTS: Significant time effects were found for: global psychological distress (p < 0.001), stress (p < 0.01), emotion-oriented coping (p < 0.001), physical health status (p < 0.001), and fatigue (p < 0.001), indicating that patients improved from baseline to 15 months. Disease activity worsened for 40.3%, improved for 50.8%, and remained the same for 8.8% of the patients from baseline to 15 months. Controlling for baseline disease activity and fatigue, and considering sleep problems, decreases in stress and depression predicted less fatigue at 15 months (p < 0.001; adjusted R2 = 0.43).
CONCLUSION: Despite fluctuations in disease activity, patients with SLE, as a group, cope adequately with their disease over time. There is, nonetheless, a subset of patients (about 40%) who remain distressed and who may benefit from psychosocial interventions.

Entities:  

Mesh:

Year:  2001        PMID: 11708416

Source DB:  PubMed          Journal:  J Rheumatol        ISSN: 0315-162X            Impact factor:   4.666


  11 in total

1.  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

2.  Fatigue and depression predict reduced health-related quality of life in childhood-onset lupus.

Authors:  C Donnelly; N Cunningham; J T Jones; L Ji; H I Brunner; S Kashikar-Zuck
Journal:  Lupus       Date:  2017-06-29       Impact factor: 2.911

Review 3.  Quality-of-life measurements versus disease activity in systemic lupus erythematosus.

Authors:  Adnan N Kiani; Michelle Petri
Journal:  Curr Rheumatol Rep       Date:  2010-08       Impact factor: 4.592

4.  The health education for lupus study: a randomized controlled cognitive-behavioral intervention targeting psychosocial adjustment and quality of life in adolescent females with systemic lupus erythematosus.

Authors:  Ronald T Brown; Stephanie R Shaftman; Barbara C Tilley; Kelly K Anthony; Mary C Kral; Bonnie Maxson; Laura Mee; Melanie J Bonner; Larry B Vogler; Laura E Schanberg; Mark A Connelly; Janelle L Wagner; Richard M Silver; Paul J Nietert
Journal:  Am J Med Sci       Date:  2012-10       Impact factor: 2.378

5.  Improvement of coping abilities in patients with systemic lupus erythematosus: a prospective study.

Authors:  M Haupt; S Millen; M Jänner; D Falagan; R Fischer-Betz; M Schneider
Journal:  Ann Rheum Dis       Date:  2005-04-13       Impact factor: 19.103

Review 6.  Optimal management of fatigue in patients with systemic lupus erythematosus: a systematic review.

Authors:  Hon K Yuen; Melissa A Cunningham
Journal:  Ther Clin Risk Manag       Date:  2014-10-01       Impact factor: 2.423

7.  Unmet needs of patients with systemic lupus erythematosus.

Authors:  Sharon Danoff-Burg; Fred Friedberg
Journal:  Behav Med       Date:  2009       Impact factor: 3.104

8.  Understanding systemic lupus erythematosus patients' desired outcomes and their perceptions of the risks and benefits of using corticosteroids.

Authors:  X Ng; S dosReis; R Beardsley; L Magder; C D Mullins; M Petri
Journal:  Lupus       Date:  2017-08-31       Impact factor: 2.911

9.  Obesity is Independently Associated With Worse Patient-Reported Outcomes in Women with Systemic Lupus Erythematosus.

Authors:  Sarah L Patterson; Gabriela Schmajuk; Kashif Jafri; Jinoos Yazdany; Patricia Katz
Journal:  Arthritis Care Res (Hoboken)       Date:  2019-01       Impact factor: 4.794

10.  Psychosocial dimensions of SLE: implications for the health care team.

Authors:  Nancy L Beckerman; Charles Auerbach; Irene Blanco
Journal:  J Multidiscip Healthc       Date:  2011-04-05
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