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Divergent perspectives: exploring the relationships between St. George’s Respiratory Questionnaire and outcome measures in systemic sclerosis–associated interstitial lung disease

Introduction/objectives Controversy exists regarding the concordance of patient-reported outcome measures (PROMs) with other assessment parameters in systemic sclerosis–associated interstitial lung disease (SSc-ILD). This study aims to explore the association between the St. George’s Respiratory Que...

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Published in:Clinical rheumatology 2024-05, Vol.43 (5), p.1647-1656
Main Authors: Basaran, Enes, Temiz Karadag, Duygu, Cakir, Ozgur, Gokcen, Neslihan, Yazici, Ayten, Cefle, Ayse
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container_title Clinical rheumatology
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creator Basaran, Enes
Temiz Karadag, Duygu
Cakir, Ozgur
Gokcen, Neslihan
Yazici, Ayten
Cefle, Ayse
description Introduction/objectives Controversy exists regarding the concordance of patient-reported outcome measures (PROMs) with other assessment parameters in systemic sclerosis–associated interstitial lung disease (SSc-ILD). This study aims to explore the association between the St. George’s Respiratory Questionnaire (SGRQ) and various outcome measures in patients with SSc-ILD within a real-world cross-sectional setting. Method Patients with SSc-ILD were consecutively recruited from our SSc cohort. Simultaneous administration of SGRQ, scleroderma Health Assessment Questionnaire (sHAQ), respiratory visual analog scale (R-VAS), pulmonary function tests (PFTs), and the 6-min walking test (6-MWT) was conducted. The total extent of lung fibrosis was quantified using high-resolution computed tomography (HRCT) images. Relationships between SGRQ and functional, radiographic, and other patient-reported outcome measures were analyzed. Results The total SGRQ score demonstrated correlations with forced vital capacity (FVC) and R-VAS ( r  =  − 0.397, p  = 0.016 and r  = 0.418, p  = 0.027, respectively). Symptom score correlated with ILD-extension ( r  = 0.430, p  = 0.005); activity score correlated with FVC and R-VAS ( r  =  − 0.502, p  = 0.002 and r  = 0.395, p  = 0.038, respectively); impact score correlated with R-VAS ( r  = 0.386, p  = 0.043). In patients with fibrosis extent exceeding 20%, total SGRQ score was associated with sHAQ and R-VAS ( r  = 0.398, p  = 0.049; r  = 0.524, p  = 0.021, respectively), activity score with R-VAS ( r  = 0.478, p  = 0.038), and impact score with 6-MWT-D and R-VAS ( r  =  − 0.489, p  = 0.034; r  = 0.545, p  = 0.016, respectively). The symptom score and activity score demonstrated optimal performance in identifying patients with interstitial lung disease (ILD) extent exceeding 20% and forced vital capacity (FVC) less than 70% (area under the curve [AUC] 0.799, p  = 0.002, and AUC 0.792, p  = 0.03, respectively). Conclusions Our study reveals varying degrees of correlation between SGRQ and distinct outcome measures. Given the incomplete alignment of SGRQ with other outcome measures, an integrative approach utilizing existing criteria as complementary tools is recommended. Key Points • Patient-reported outcome measures (PROMs) derive from patients’ subjective evaluations of the impact of the disease on their daily activities, social interactions, and psychological well-being. • PROMs frequently serve as outcome measures in randomized controlle
doi_str_mv 10.1007/s10067-024-06950-3
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This study aims to explore the association between the St. George’s Respiratory Questionnaire (SGRQ) and various outcome measures in patients with SSc-ILD within a real-world cross-sectional setting. Method Patients with SSc-ILD were consecutively recruited from our SSc cohort. Simultaneous administration of SGRQ, scleroderma Health Assessment Questionnaire (sHAQ), respiratory visual analog scale (R-VAS), pulmonary function tests (PFTs), and the 6-min walking test (6-MWT) was conducted. The total extent of lung fibrosis was quantified using high-resolution computed tomography (HRCT) images. Relationships between SGRQ and functional, radiographic, and other patient-reported outcome measures were analyzed. Results The total SGRQ score demonstrated correlations with forced vital capacity (FVC) and R-VAS ( r  =  − 0.397, p  = 0.016 and r  = 0.418, p  = 0.027, respectively). Symptom score correlated with ILD-extension ( r  = 0.430, p  = 0.005); activity score correlated with FVC and R-VAS ( r  =  − 0.502, p  = 0.002 and r  = 0.395, p  = 0.038, respectively); impact score correlated with R-VAS ( r  = 0.386, p  = 0.043). In patients with fibrosis extent exceeding 20%, total SGRQ score was associated with sHAQ and R-VAS ( r  = 0.398, p  = 0.049; r  = 0.524, p  = 0.021, respectively), activity score with R-VAS ( r  = 0.478, p  = 0.038), and impact score with 6-MWT-D and R-VAS ( r  =  − 0.489, p  = 0.034; r  = 0.545, p  = 0.016, respectively). The symptom score and activity score demonstrated optimal performance in identifying patients with interstitial lung disease (ILD) extent exceeding 20% and forced vital capacity (FVC) less than 70% (area under the curve [AUC] 0.799, p  = 0.002, and AUC 0.792, p  = 0.03, respectively). Conclusions Our study reveals varying degrees of correlation between SGRQ and distinct outcome measures. Given the incomplete alignment of SGRQ with other outcome measures, an integrative approach utilizing existing criteria as complementary tools is recommended. Key Points • Patient-reported outcome measures (PROMs) derive from patients’ subjective evaluations of the impact of the disease on their daily activities, social interactions, and psychological well-being. • PROMs frequently serve as outcome measures in randomized controlled trials, yet conflicting findings have emerged in relation to primary outcomes. • This study aims to assess the appropriateness and interrelation of PROMs with both radiological and functional outcome measures, providing insight into the current state of our patients in a real-life context. The investigation delves into the compatibility of these measures with each other.</description><identifier>ISSN: 0770-3198</identifier><identifier>EISSN: 1434-9949</identifier><identifier>DOI: 10.1007/s10067-024-06950-3</identifier><identifier>PMID: 38573479</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Clinical outcomes ; Clinical trials ; Computed tomography ; Cross-Sectional Studies ; Fibrosis ; health effects assessments ; Humans ; Lung - diagnostic imaging ; Lung diseases ; Lung Diseases, Interstitial - complications ; Lung Diseases, Interstitial - diagnosis ; lung function ; Medicine ; Medicine &amp; Public Health ; Original Article ; Outcome Assessment, Health Care ; Patients ; pulmonary fibrosis ; Questionnaires ; radiography ; Respiratory function ; Rheumatology ; Scleroderma ; Scleroderma, Systemic ; Social interactions ; Surveys and Questionnaires ; Systemic sclerosis ; tomography ; Vital Capacity ; Well being</subject><ispartof>Clinical rheumatology, 2024-05, Vol.43 (5), p.1647-1656</ispartof><rights>The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR) 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR).</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c359t-4a0f9531ffcddf623066695d20fa72762aad5a7ec0a98657e50bb4a85fbe1d773</cites><orcidid>0000-0001-6565-9488 ; 0000-0003-2167-4509 ; 0000-0002-7576-3972 ; 0000-0002-5891-2032 ; 0000-0003-3022-493X ; 0000-0002-3273-7969</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38573479$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Basaran, Enes</creatorcontrib><creatorcontrib>Temiz Karadag, Duygu</creatorcontrib><creatorcontrib>Cakir, Ozgur</creatorcontrib><creatorcontrib>Gokcen, Neslihan</creatorcontrib><creatorcontrib>Yazici, Ayten</creatorcontrib><creatorcontrib>Cefle, Ayse</creatorcontrib><title>Divergent perspectives: exploring the relationships between St. George’s Respiratory Questionnaire and outcome measures in systemic sclerosis–associated interstitial lung disease</title><title>Clinical rheumatology</title><addtitle>Clin Rheumatol</addtitle><addtitle>Clin Rheumatol</addtitle><description>Introduction/objectives Controversy exists regarding the concordance of patient-reported outcome measures (PROMs) with other assessment parameters in systemic sclerosis–associated interstitial lung disease (SSc-ILD). This study aims to explore the association between the St. George’s Respiratory Questionnaire (SGRQ) and various outcome measures in patients with SSc-ILD within a real-world cross-sectional setting. Method Patients with SSc-ILD were consecutively recruited from our SSc cohort. Simultaneous administration of SGRQ, scleroderma Health Assessment Questionnaire (sHAQ), respiratory visual analog scale (R-VAS), pulmonary function tests (PFTs), and the 6-min walking test (6-MWT) was conducted. The total extent of lung fibrosis was quantified using high-resolution computed tomography (HRCT) images. Relationships between SGRQ and functional, radiographic, and other patient-reported outcome measures were analyzed. Results The total SGRQ score demonstrated correlations with forced vital capacity (FVC) and R-VAS ( r  =  − 0.397, p  = 0.016 and r  = 0.418, p  = 0.027, respectively). Symptom score correlated with ILD-extension ( r  = 0.430, p  = 0.005); activity score correlated with FVC and R-VAS ( r  =  − 0.502, p  = 0.002 and r  = 0.395, p  = 0.038, respectively); impact score correlated with R-VAS ( r  = 0.386, p  = 0.043). In patients with fibrosis extent exceeding 20%, total SGRQ score was associated with sHAQ and R-VAS ( r  = 0.398, p  = 0.049; r  = 0.524, p  = 0.021, respectively), activity score with R-VAS ( r  = 0.478, p  = 0.038), and impact score with 6-MWT-D and R-VAS ( r  =  − 0.489, p  = 0.034; r  = 0.545, p  = 0.016, respectively). The symptom score and activity score demonstrated optimal performance in identifying patients with interstitial lung disease (ILD) extent exceeding 20% and forced vital capacity (FVC) less than 70% (area under the curve [AUC] 0.799, p  = 0.002, and AUC 0.792, p  = 0.03, respectively). Conclusions Our study reveals varying degrees of correlation between SGRQ and distinct outcome measures. Given the incomplete alignment of SGRQ with other outcome measures, an integrative approach utilizing existing criteria as complementary tools is recommended. Key Points • Patient-reported outcome measures (PROMs) derive from patients’ subjective evaluations of the impact of the disease on their daily activities, social interactions, and psychological well-being. • PROMs frequently serve as outcome measures in randomized controlled trials, yet conflicting findings have emerged in relation to primary outcomes. • This study aims to assess the appropriateness and interrelation of PROMs with both radiological and functional outcome measures, providing insight into the current state of our patients in a real-life context. 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This study aims to explore the association between the St. George’s Respiratory Questionnaire (SGRQ) and various outcome measures in patients with SSc-ILD within a real-world cross-sectional setting. Method Patients with SSc-ILD were consecutively recruited from our SSc cohort. Simultaneous administration of SGRQ, scleroderma Health Assessment Questionnaire (sHAQ), respiratory visual analog scale (R-VAS), pulmonary function tests (PFTs), and the 6-min walking test (6-MWT) was conducted. The total extent of lung fibrosis was quantified using high-resolution computed tomography (HRCT) images. Relationships between SGRQ and functional, radiographic, and other patient-reported outcome measures were analyzed. Results The total SGRQ score demonstrated correlations with forced vital capacity (FVC) and R-VAS ( r  =  − 0.397, p  = 0.016 and r  = 0.418, p  = 0.027, respectively). Symptom score correlated with ILD-extension ( r  = 0.430, p  = 0.005); activity score correlated with FVC and R-VAS ( r  =  − 0.502, p  = 0.002 and r  = 0.395, p  = 0.038, respectively); impact score correlated with R-VAS ( r  = 0.386, p  = 0.043). In patients with fibrosis extent exceeding 20%, total SGRQ score was associated with sHAQ and R-VAS ( r  = 0.398, p  = 0.049; r  = 0.524, p  = 0.021, respectively), activity score with R-VAS ( r  = 0.478, p  = 0.038), and impact score with 6-MWT-D and R-VAS ( r  =  − 0.489, p  = 0.034; r  = 0.545, p  = 0.016, respectively). The symptom score and activity score demonstrated optimal performance in identifying patients with interstitial lung disease (ILD) extent exceeding 20% and forced vital capacity (FVC) less than 70% (area under the curve [AUC] 0.799, p  = 0.002, and AUC 0.792, p  = 0.03, respectively). Conclusions Our study reveals varying degrees of correlation between SGRQ and distinct outcome measures. Given the incomplete alignment of SGRQ with other outcome measures, an integrative approach utilizing existing criteria as complementary tools is recommended. Key Points • Patient-reported outcome measures (PROMs) derive from patients’ subjective evaluations of the impact of the disease on their daily activities, social interactions, and psychological well-being. • PROMs frequently serve as outcome measures in randomized controlled trials, yet conflicting findings have emerged in relation to primary outcomes. • This study aims to assess the appropriateness and interrelation of PROMs with both radiological and functional outcome measures, providing insight into the current state of our patients in a real-life context. The investigation delves into the compatibility of these measures with each other.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>38573479</pmid><doi>10.1007/s10067-024-06950-3</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-6565-9488</orcidid><orcidid>https://orcid.org/0000-0003-2167-4509</orcidid><orcidid>https://orcid.org/0000-0002-7576-3972</orcidid><orcidid>https://orcid.org/0000-0002-5891-2032</orcidid><orcidid>https://orcid.org/0000-0003-3022-493X</orcidid><orcidid>https://orcid.org/0000-0002-3273-7969</orcidid></addata></record>
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1434-9949
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subjects Clinical outcomes
Clinical trials
Computed tomography
Cross-Sectional Studies
Fibrosis
health effects assessments
Humans
Lung - diagnostic imaging
Lung diseases
Lung Diseases, Interstitial - complications
Lung Diseases, Interstitial - diagnosis
lung function
Medicine
Medicine & Public Health
Original Article
Outcome Assessment, Health Care
Patients
pulmonary fibrosis
Questionnaires
radiography
Respiratory function
Rheumatology
Scleroderma
Scleroderma, Systemic
Social interactions
Surveys and Questionnaires
Systemic sclerosis
tomography
Vital Capacity
Well being
title Divergent perspectives: exploring the relationships between St. George’s Respiratory Questionnaire and outcome measures in systemic sclerosis–associated interstitial lung disease
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