Literature DB >> 9972963

Quality of life in systemic lupus erythematosus: a controlled study.

M Abu-Shakra1, R Mader, P Langevitz, M Friger, S Codish, L Neumann, D Buskila.   

Abstract

OBJECTIVE: To assess the quality of life (QOL) of patients with systemic lupus erythematosus (SLE) and to compare it with that of healthy women and patients with primary fibromyalgia (FM).
METHODS: QOL was evaluated using the QOL scale, which includes 16 items, each scored on a 7 point scale. Healthy controls were chosen from hospital personnel.
RESULTS: The study population comprised 75 female patients with SLE, 50 healthy women, and 30 women with primary FM. Compared to controls, patients with SLE had significantly lower scores for the health, work, active recreation, and independence items. The QOL scores were not associated with disease activity. Patients with SLE and FM had significantly lower scores for the health related items compared with patients with SLE without FM.
CONCLUSION: The QOL of patients with SLE was found to be impaired compared with controls. FM adversely affects the QOL of patients with SLE.

Entities:  

Mesh:

Year:  1999        PMID: 9972963

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


  17 in total

Review 1.  Epidemiology of fibromyalgia.

Authors:  Lily Neumann; Dan Buskila
Journal:  Curr Pain Headache Rep       Date:  2003-10

2.  The evaluation of anxiety, depression and quality of life scores of children and adolescents with familial Mediterranean fever.

Authors:  Arzu Önal Sönmez; Hafize Emine Sönmez; Mustafa Çakan; Mesut Yavuz; Gonca Keskindemirci; Nuray Aktay Ayaz
Journal:  Rheumatol Int       Date:  2020-01-25       Impact factor: 2.631

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.  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

5.  Depression, medication adherence, and service utilization in systemic lupus erythematosus.

Authors:  Laura J Julian; Edward Yelin; Jinoos Yazdany; Pantelis Panopalis; Laura Trupin; Lindsey A Criswell; Patricia Katz
Journal:  Arthritis Rheum       Date:  2009-02-15

6.  Health-related quality of life in patients with systemic lupus erythematosus: development and validation of a lupus specific symptom checklist.

Authors:  C Grootscholten; G Ligtenberg; R H W M Derksen; K M G Schreurs; J W de Glas-Vos; E C Hagen; A W L van den Wall Bake; T W J Huizinga; F H J van den Hoogen; M Bijl; J C van Houwelingen; F J Snoek; J H M Berden
Journal:  Qual Life Res       Date:  2003-09       Impact factor: 4.147

7.  Disability in valued life activities among individuals with systemic lupus erythematosus.

Authors:  Patricia Katz; Anne Morris; Laura Trupin; Jinoos Yazdany; Edward Yelin
Journal:  Arthritis Rheum       Date:  2008-04-15

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

Review 9.  The socioeconomic burden of SLE.

Authors:  Chak Sing Lau; Anselm Mak
Journal:  Nat Rev Rheumatol       Date:  2009-06-09       Impact factor: 20.543

10.  Urinary tract infections and lupus erythematosus.

Authors:  C Hidalgo-Tenorio; J Jiménez-Alonso; J de Dios Luna; M Tallada; A Martínez-Brocal; J Mario Sabio
Journal:  Ann Rheum Dis       Date:  2004-04       Impact factor: 19.103

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