Literature DB >> 33811590

Evaluation of rheumatoid arthritis and connective tissue disease-related interstitial lung disease with pulmonary physiologic test, HRCT, and patient-based measures of dyspnea and functional disability.

Atakan Topcu1, H Hakan Mursaloglu2, Yasemin Yalcinkaya3, Sait Karakurt4, Burcu Yagiz5, Zeynep Alaca1, Meryem Demir1, Belkis Nihan Coskun5, Ediz Dalkilic5, Nevsun Inanc6.   

Abstract

OBJECTIVES: We aim to investigate the relationship between pulmonary function and imaging parameters with symptom-related patient-reported outcome measures (PROs).
METHOD: We included 65 patients of rheumatoid arthritis (RA) and connective tissue disease (CTD) with and without interstitial lung disease (ILD) into this cross-sectional study. We evaluated the relationship between FVC, DLco, and PROs and compared to HRCT findings. PROs included visual analogue scale for breathing, modified Borg scale, medical research council dyspnea scale, St. George's respiratory questionnaire (SGRQ), Leicester cough questionnaire, and Short Form 36 quality of life (SF-36 QoL).
RESULTS: The mean age was 57.4 ± 9.7 and 61.9% (39/65) of patients had an established ILD. In RA-ILD group, SGRQ score was higher (p < 0.001) and SF-36 physical functioning score was lower (p = 0.02) than CTD-ILD group. In RA group, there was a significant correlation between FVC and SF-36 role functioning/physical score (r = 0.724, p = 0.012). In CTD group, SF-36 general health score was correlated with both FVC (r = 0.441, p = 0.045) and DLco (r = 0.485, p = 0.035), and also SF-36 physical functioning score was correlated with FVC (r = 0.441, p = 0.040). PROs were found to be similar between ILD and non-ILD patients. SF-36 QoL total and SGRQ outcomes were worse in non-ILD group.
CONCLUSIONS: We concluded that PROs could be used to evaluate health-related quality of life (HRQoL) in RA- or CTD-related ILD. The physical health determinants of HRQoL are measurably worse in RA-ILD patients than in CTD patients. But, PROs may not be very helpful in differentiating patients with cough and/or shortness of breath due to ILD or non-ILD causes in RA/CTD. KEY POINTS: • HRQoL may be affected differently among specific subtypes of ILD. • PROs can be used to evaluate dyspnea and function of patients with RA- or CTD-related ILD but are not distinguished from patients with cough and/or shortness of breath due to non-ILD causes in RA/CTD.

Entities:  

Keywords:  Connective tissue disease; Interstitial lung disease; Patient-reported outcome measures; Rheumatoid arthritis; Warrick score

Year:  2021        PMID: 33811590     DOI: 10.1007/s10067-021-05693-9

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


  28 in total

1.  Connective tissue disease related fibrotic lung disease: high resolution computed tomographic and pulmonary function indices as prognostic determinants.

Authors:  Simon L F Walsh; Nicola Sverzellati; Anand Devaraj; Gregory J Keir; Athol U Wells; David M Hansell
Journal:  Thorax       Date:  2013-10-14       Impact factor: 9.139

Review 2.  Six-minute walk test in systemic sclerosis: A systematic review and meta-analysis.

Authors:  Els Vandecasteele; Michel De Pauw; Filip De Keyser; Saskia Decuman; Ellen Deschepper; Yves Piette; Guy Brusselle; Vanessa Smith
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3.  The evidence of benefits of exercise training in interstitial lung disease: a randomised controlled trial.

Authors:  Leona M Dowman; Christine F McDonald; Catherine J Hill; Annemarie L Lee; Kathryn Barker; Claire Boote; Ian Glaspole; Nicole S L Goh; Anne M Southcott; Angela T Burge; Rebecca Gillies; Alicia Martin; Anne E Holland
Journal:  Thorax       Date:  2017-02-17       Impact factor: 9.139

4.  Thin-section CT findings in rheumatoid arthritis-associated lung disease: CT patterns and their courses.

Authors:  M Akira; M Sakatani; H Hara
Journal:  J Comput Assist Tomogr       Date:  1999 Nov-Dec       Impact factor: 1.826

5.  Connective tissue disease-associated interstitial pneumonia and idiopathic interstitial pneumonia: similarity and difference.

Authors:  Thomas Bryson; Baskaran Sundaram; Dinesh Khanna; Ella A Kazerooni
Journal:  Semin Ultrasound CT MR       Date:  2013-10-24       Impact factor: 1.875

Review 6.  Review series: Aspects of interstitial lung disease: connective tissue disease-associated interstitial lung disease: how does it differ from IPF? How should the clinical approach differ?

Authors:  Angelo de Lauretis; Srihari Veeraraghavan; Elisabetta Renzoni
Journal:  Chron Respir Dis       Date:  2011       Impact factor: 2.444

7.  Interstitial lung disease in systemic sclerosis: a simple staging system.

Authors:  Nicole S L Goh; Sujal R Desai; Srihari Veeraraghavan; David M Hansell; Susan J Copley; Toby M Maher; Tamera J Corte; Clare R Sander; Jonathan Ratoff; Anand Devaraj; Gracijela Bozovic; Christopher P Denton; Carol M Black; Roland M du Bois; Athol U Wells
Journal:  Am J Respir Crit Care Med       Date:  2008-03-27       Impact factor: 21.405

8.  Limitations to the 6-minute walk test in interstitial lung disease and pulmonary hypertension in scleroderma.

Authors:  Margaret C Garin; Kristin B Highland; Richard M Silver; Charlie Strange
Journal:  J Rheumatol       Date:  2009-01-22       Impact factor: 4.666

Review 9.  Management of connective tissue diseases associated interstitial lung disease: a review of the published literature.

Authors:  Beth Wallace; Dharshan Vummidi; Dinesh Khanna
Journal:  Curr Opin Rheumatol       Date:  2016-05       Impact factor: 5.006

10.  Idiopathic nonspecific interstitial pneumonia: lung manifestation of undifferentiated connective tissue disease?

Authors:  Brent W Kinder; Harold R Collard; Laura Koth; David I Daikh; Paul J Wolters; Brett Elicker; Kirk D Jones; Talmadge E King
Journal:  Am J Respir Crit Care Med       Date:  2007-06-07       Impact factor: 21.405

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