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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 |
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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 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3153607013</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3153607013</sourcerecordid><originalsourceid>FETCH-LOGICAL-c359t-4a0f9531ffcddf623066695d20fa72762aad5a7ec0a98657e50bb4a85fbe1d773</originalsourceid><addsrcrecordid>eNqFkstu1TAQhi0EoofCC7BAltiwSRnHcRyzQwUKUiXEbR35OJPWVRIHjwOcXd-BFS_CA_VJcDgFJBawsaXR98_1Z-y-gCMBoB9TfmtdQFkVUBsFhbzBNqKSVWFMZW6yDWidg8I0B-wO0QUAlI0Rt9mBbJSWlTYb9v2Z_4TxDKfEZ4w0o0s5QE84fpmHEP10xtM58oiDTT5MdO5n4ltMnxEn_i4d8RMMWX51-Y34W6TZR5tC3PE3C9IqmKyPyO3U8bAkF0bkI1paIhL3E6cdJRy94-QGjIE8XV1-tUTBeZuwy0jKTSWfvB34sORmOk9Zj3fZrd4OhPeu_0P24cXz98cvi9PXJ6-On54WTiqTispCb5QUfe-6rq9LCXWdN9WV0Ftd6rq0tlNWowNrmlppVLDdVrZR_RZFp7U8ZI_2eecYPq4jtaMnh8NgJwwLtVIoWYMGIf-PgpT5XrlORh_-hV6EJU55kJVqqropQWWq3FMub4Yi9u0c_WjjrhXQrgZo9wZoswHanwZo1y4eXKdetiN2vyW_Lp4BuQdoXq-L8U_tf6T9AV3Kws4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3038468205</pqid></control><display><type>article</type><title>Divergent perspectives: exploring the relationships between St. George’s Respiratory Questionnaire and outcome measures in systemic sclerosis–associated interstitial lung disease</title><source>Springer Link</source><creator>Basaran, Enes ; Temiz Karadag, Duygu ; Cakir, Ozgur ; Gokcen, Neslihan ; Yazici, Ayten ; Cefle, Ayse</creator><creatorcontrib>Basaran, Enes ; Temiz Karadag, Duygu ; Cakir, Ozgur ; Gokcen, Neslihan ; Yazici, Ayten ; Cefle, Ayse</creatorcontrib><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. 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 & 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. The investigation delves into the compatibility of these measures with each other.</description><subject>Clinical outcomes</subject><subject>Clinical trials</subject><subject>Computed tomography</subject><subject>Cross-Sectional Studies</subject><subject>Fibrosis</subject><subject>health effects assessments</subject><subject>Humans</subject><subject>Lung - diagnostic imaging</subject><subject>Lung diseases</subject><subject>Lung Diseases, Interstitial - complications</subject><subject>Lung Diseases, Interstitial - diagnosis</subject><subject>lung function</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Original Article</subject><subject>Outcome Assessment, Health Care</subject><subject>Patients</subject><subject>pulmonary fibrosis</subject><subject>Questionnaires</subject><subject>radiography</subject><subject>Respiratory function</subject><subject>Rheumatology</subject><subject>Scleroderma</subject><subject>Scleroderma, Systemic</subject><subject>Social interactions</subject><subject>Surveys and Questionnaires</subject><subject>Systemic sclerosis</subject><subject>tomography</subject><subject>Vital Capacity</subject><subject>Well being</subject><issn>0770-3198</issn><issn>1434-9949</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkstu1TAQhi0EoofCC7BAltiwSRnHcRyzQwUKUiXEbR35OJPWVRIHjwOcXd-BFS_CA_VJcDgFJBawsaXR98_1Z-y-gCMBoB9TfmtdQFkVUBsFhbzBNqKSVWFMZW6yDWidg8I0B-wO0QUAlI0Rt9mBbJSWlTYb9v2Z_4TxDKfEZ4w0o0s5QE84fpmHEP10xtM58oiDTT5MdO5n4ltMnxEn_i4d8RMMWX51-Y34W6TZR5tC3PE3C9IqmKyPyO3U8bAkF0bkI1paIhL3E6cdJRy94-QGjIE8XV1-tUTBeZuwy0jKTSWfvB34sORmOk9Zj3fZrd4OhPeu_0P24cXz98cvi9PXJ6-On54WTiqTispCb5QUfe-6rq9LCXWdN9WV0Ftd6rq0tlNWowNrmlppVLDdVrZR_RZFp7U8ZI_2eecYPq4jtaMnh8NgJwwLtVIoWYMGIf-PgpT5XrlORh_-hV6EJU55kJVqqropQWWq3FMub4Yi9u0c_WjjrhXQrgZo9wZoswHanwZo1y4eXKdetiN2vyW_Lp4BuQdoXq-L8U_tf6T9AV3Kws4</recordid><startdate>20240501</startdate><enddate>20240501</enddate><creator>Basaran, Enes</creator><creator>Temiz Karadag, Duygu</creator><creator>Cakir, Ozgur</creator><creator>Gokcen, Neslihan</creator><creator>Yazici, Ayten</creator><creator>Cefle, Ayse</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><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></search><sort><creationdate>20240501</creationdate><title>Divergent perspectives: exploring the relationships between St. George’s Respiratory Questionnaire and outcome measures in systemic sclerosis–associated interstitial lung disease</title><author>Basaran, Enes ; Temiz Karadag, Duygu ; Cakir, Ozgur ; Gokcen, Neslihan ; Yazici, Ayten ; Cefle, Ayse</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-4a0f9531ffcddf623066695d20fa72762aad5a7ec0a98657e50bb4a85fbe1d773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Clinical outcomes</topic><topic>Clinical trials</topic><topic>Computed tomography</topic><topic>Cross-Sectional Studies</topic><topic>Fibrosis</topic><topic>health effects assessments</topic><topic>Humans</topic><topic>Lung - diagnostic imaging</topic><topic>Lung diseases</topic><topic>Lung Diseases, Interstitial - complications</topic><topic>Lung Diseases, Interstitial - diagnosis</topic><topic>lung function</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Original Article</topic><topic>Outcome Assessment, Health Care</topic><topic>Patients</topic><topic>pulmonary fibrosis</topic><topic>Questionnaires</topic><topic>radiography</topic><topic>Respiratory function</topic><topic>Rheumatology</topic><topic>Scleroderma</topic><topic>Scleroderma, Systemic</topic><topic>Social interactions</topic><topic>Surveys and Questionnaires</topic><topic>Systemic sclerosis</topic><topic>tomography</topic><topic>Vital Capacity</topic><topic>Well being</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Clinical rheumatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Basaran, Enes</au><au>Temiz Karadag, Duygu</au><au>Cakir, Ozgur</au><au>Gokcen, Neslihan</au><au>Yazici, Ayten</au><au>Cefle, Ayse</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Divergent perspectives: exploring the relationships between St. George’s Respiratory Questionnaire and outcome measures in systemic sclerosis–associated interstitial lung disease</atitle><jtitle>Clinical rheumatology</jtitle><stitle>Clin Rheumatol</stitle><addtitle>Clin Rheumatol</addtitle><date>2024-05-01</date><risdate>2024</risdate><volume>43</volume><issue>5</issue><spage>1647</spage><epage>1656</epage><pages>1647-1656</pages><issn>0770-3198</issn><eissn>1434-9949</eissn><abstract>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. 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> |
fulltext | fulltext |
identifier | ISSN: 0770-3198 |
ispartof | Clinical rheumatology, 2024-05, Vol.43 (5), p.1647-1656 |
issn | 0770-3198 1434-9949 |
language | eng |
recordid | cdi_proquest_miscellaneous_3153607013 |
source | Springer Link |
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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