Literature DB >> 31129711

Quality of life among female patients with systemic lupus erythematosus in remission.

Rudra Prosad Goswami1, Rudrani Chatterjee2, Parasar Ghosh3, Geetabali Sircar1, Alakendu Ghosh1.   

Abstract

The objective is to assess quality-of-life (QoL) parameters among Indian female systemic lupus erythematosus (SLE) patients with durable remission. Indian female SLE patients in remission determined by the European consensus criteria and age-matched female control participants were included in the study. All included participants underwent measurements of QoL [Medical Outcomes Study Short-Form-12 (SF12)], Fatigue Severity Scale, and structured interview with a clinical psychologist. The population comprised of 126 female SLE patients [median age: 27.5 years [interquartile range (IQR): 11]; median disease duration: 36 months (IQR 26)] and 110 female controls [median age 30 years (IQR 9)]. Clinical remission was seen in 65.9% (83/126) and complete remission in 34.1% (43/126). Significant fatigue was present in 18.3% (23/126). Both SF-12 physical component summary (PCS) and mental component summary (MCS) were similar between SLE patients and controls [median PCS: 50.3 (IQR: 16.2) vs. 48.6 (IQR: 11.6); median MCS: 57.2 (IQR: 4.8) vs. 57.9 (IQR: 7.6)]. In generalised linear modelling, PCS was associated with fatigue [odd's ratio (OR) 0.012, 95% confidence interval (CI) 0.006-0.025, p < 0.001], disease duration ≥ 5 years (OR 23.16, 95% CI 1.548-346.58, p = 0.023), and complete remission (OR 33.16, 95% CI 4.43-248.15, p = 0.001); MCS with fatigue (OR 0.53, 95% CI 0.34-0.84, p = 0.007) and absence of depression (OR 3.65, 95% CI 1.07-12.44, p = 0.038). Patients with SLE in remission report significant fatigue in 18.3% of subjects. Both PCS and MCS scores are similar to healthy controls. Better PCS was associated with less fatigue, longer disease duration, and complete remission. Better MCS was associated with less fatigue and absence of depression.

Entities:  

Keywords:  Clinical remission; Complete remission; Depression; Fatigue; Quality of life; Remission; Systemic lupus erythematosus

Mesh:

Substances:

Year:  2019        PMID: 31129711     DOI: 10.1007/s00296-019-04329-1

Source DB:  PubMed          Journal:  Rheumatol Int        ISSN: 0172-8172            Impact factor:   3.580


  33 in total

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3.  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
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Authors:  J Calderón; P Flores; J M Aguirre; G Valdivia; O Padilla; I Barra; L Scoriels; S Herrera; A González; L Massardo
Journal:  Scand J Rheumatol       Date:  2016-10-05       Impact factor: 3.641

Review 7.  A framework for remission in SLE: consensus findings from a large international task force on definitions of remission in SLE (DORIS).

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Journal:  Ann Rheum Dis       Date:  2016-11-24       Impact factor: 19.103

Review 8.  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

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Authors:  L B Krupp; N G LaRocca; J Muir-Nash; A D Steinberg
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10.  EQ-5D and SF-36 quality of life measures in systemic lupus erythematosus: comparisons with rheumatoid arthritis, noninflammatory rheumatic disorders, and fibromyalgia.

Authors:  Frederick Wolfe; Kaleb Michaud; Tracy Li; Robert S Katz
Journal:  J Rheumatol       Date:  2009-12-23       Impact factor: 4.666

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  5 in total

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2.  The patient's perspective: are quality of life and disease burden a possible treatment target in systemic lupus erythematosus?

Authors:  Anna Kernder; Elena Elefante; Gamal Chehab; Chiara Tani; Marta Mosca; Matthias Schneider
Journal:  Rheumatology (Oxford)       Date:  2020-12-05       Impact factor: 7.580

3.  Impact of demographic, clinical, and treatment compliance characteristics on quality of life of Venezuelan patients with systemic lupus erythematosus.

Authors:  Fhabián S Carrión-Nessi; María V Marcano-Rojas; Sinibaldo R Romero Arocha; Daniela L Mendoza Millán; David A Forero-Peña; Allen W Antuarez-Magallanes; Soham Al Snih; Martín A Rodríguez; Yurilís J Fuentes-Silva
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4.  Severe flares are associated with a poorer health-related quality of life (HRQoL) in patients with SLE: data from the Almenara Lupus Cohort.

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5.  The impact of distress disclosure and anxiety on the association between social support and quality of life among Chinese women with systemic lupus erythematosus.

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