Global disparities in the treatment of idiopathic inflammatory myopathies: results from an international online survey study
We aimed to explore current practice and interregional differences in the treatment of idiopathic inflammatory myopathies (IIMs). We triangulated these observations considering countries' gross national income (GNI), disease subtypes, and symptoms using patient-reported information. A cross-sec...
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Veröffentlicht in: | Rheumatology (Oxford, England) England), 2024-03, Vol.63 (3), p.657-664 |
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creator | Ziade, Nelly Aoude, Marc Hmamouchi, Ihsane R, Naveen Lilleker, James B Sen, Parikshit Joshi, Mrudula Agarwal, Vishwesh Kardes, Sinan Day, Jessica Makol, Ashima Milchert, Marcin Gheita, Tamer Salim, Babur Velikova, Tsvetelina Edgar Gracia-Ramos, Abraham Parodis, Ioannis Nikiphorou, Elena Chatterjee, Tulika Tan, Ai Lyn Saavedra, Miguel A Shinjo, Samuel Katsuyuki Knitza, Johannes Kuwana, Masataka Nune, Arvind Cavagna, Lorenzo Distler, Oliver Chinoy, Hector Agarwal, Vikas Aggarwal, Rohit Gupta, Latika |
description | We aimed to explore current practice and interregional differences in the treatment of idiopathic inflammatory myopathies (IIMs). We triangulated these observations considering countries' gross national income (GNI), disease subtypes, and symptoms using patient-reported information.
A cross-sectional ancillary analysis of the 'COVID-19 vaccination in auto-immune disease' (COVAD) e-survey containing demographic characteristics, IIM subtypes (DM, PM, IBM, anti-synthetase syndrome [ASSD], immune-mediated necrotizing myopathy [IMNM], overlap myopathies [OM]), current symptoms (surrogate for organ involvement) and treatments (corticosteroids [CS], immunomodulators [IM], i.e. antimalarials, immunosuppressants [IS], IVIG, biologic treatments and targeted-synthetic small molecules). Treatments were presented descriptively according to continents, GNI, IIM and organ involvement, and associated factors were analysed using multivariable binary logistic regressions.
Of 18 851 respondents from 94 countries, 1418 with IIM were analysed (age 61 years, 62.5% females). DM (32.4%), IBM (24.5%) and OM (15.8%) were the most common subtypes. Treatment categories included IS (49.4%), CS (38.5%), IM (13.8%) and IVIG (9.4%). Notably, treatments varied across regions, GNI categories (IS mostly used in higher-middle income, IM in lower-middle income, IVIG and biologics largely limited to high-income countries), IIM subtypes (IS and CS associated with ASSD, IM with OM and DM, IVIG with IMNM, and biologic treatments with OM and ASSD) and disease manifestations (IS and CS with dyspnoea). Most inter-regional treatment disparities persisted after multivariable analysis.
We identified marked regional treatment disparities in a global cohort of IIM. These observations highlight the need for international consensus-driven management guidelines considering patient-centred care and available resources. |
doi_str_mv | 10.1093/rheumatology/kead250 |
format | Article |
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A cross-sectional ancillary analysis of the 'COVID-19 vaccination in auto-immune disease' (COVAD) e-survey containing demographic characteristics, IIM subtypes (DM, PM, IBM, anti-synthetase syndrome [ASSD], immune-mediated necrotizing myopathy [IMNM], overlap myopathies [OM]), current symptoms (surrogate for organ involvement) and treatments (corticosteroids [CS], immunomodulators [IM], i.e. antimalarials, immunosuppressants [IS], IVIG, biologic treatments and targeted-synthetic small molecules). Treatments were presented descriptively according to continents, GNI, IIM and organ involvement, and associated factors were analysed using multivariable binary logistic regressions.
Of 18 851 respondents from 94 countries, 1418 with IIM were analysed (age 61 years, 62.5% females). DM (32.4%), IBM (24.5%) and OM (15.8%) were the most common subtypes. Treatment categories included IS (49.4%), CS (38.5%), IM (13.8%) and IVIG (9.4%). Notably, treatments varied across regions, GNI categories (IS mostly used in higher-middle income, IM in lower-middle income, IVIG and biologics largely limited to high-income countries), IIM subtypes (IS and CS associated with ASSD, IM with OM and DM, IVIG with IMNM, and biologic treatments with OM and ASSD) and disease manifestations (IS and CS with dyspnoea). Most inter-regional treatment disparities persisted after multivariable analysis.
We identified marked regional treatment disparities in a global cohort of IIM. These observations highlight the need for international consensus-driven management guidelines considering patient-centred care and available resources.</description><identifier>ISSN: 1462-0324</identifier><identifier>ISSN: 1462-0332</identifier><identifier>EISSN: 1462-0332</identifier><identifier>DOI: 10.1093/rheumatology/kead250</identifier><identifier>PMID: 37228012</identifier><language>eng</language><publisher>England</publisher><subject>Adjuvants, Immunologic ; Autoimmune Diseases ; COVID-19 Vaccines ; Cross-Sectional Studies ; Equity ; Female ; Humans ; Immunoglobulins, Intravenous - therapeutic use ; Immunosuppressive Agents - therapeutic use ; inflammatory myopathies ; Male ; Middle Aged ; myositis ; Myositis - drug therapy ; rheumatic disease ; survey ; treatment</subject><ispartof>Rheumatology (Oxford, England), 2024-03, Vol.63 (3), p.657-664</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c429t-76d083b5d918eb4887a1d070dab99ec8afae54661f73c92f0772e7370cfc70c43</citedby><cites>FETCH-LOGICAL-c429t-76d083b5d918eb4887a1d070dab99ec8afae54661f73c92f0772e7370cfc70c43</cites><orcidid>0000-0003-2014-3925 ; 0000-0002-2089-027X ; 0000-0001-7531-8038 ; 0000-0002-9230-4137 ; 0000-0001-8430-9299 ; 0000-0002-3849-614X ; 0000-0001-9695-0657 ; 0000-0002-3682-4517 ; 0000-0001-8352-6136 ; 0000-0002-0546-8310 ; 0000-0001-8844-851X ; 0000-0002-6311-8634 ; 0000-0002-9158-7243 ; 0000-0002-1630-6026 ; 0000-0002-4875-5395 ; 0000-0001-6492-1288 ; 0000-0002-0943-8768 ; 0000-0001-7312-351X ; 0000-0003-4402-5034 ; 0000-0003-1842-2554 ; 0000-0003-0687-9944 ; 0000-0002-4479-7678 ; 0000-0002-0986-8354 ; 0000-0002-8748-898X ; 0000-0002-4508-1233 ; 0000-0001-8528-4361 ; 0000-0001-6847-3726 ; 0000-0003-2753-2990 ; 0000-0002-1155-9729 ; 0000-0002-0593-1272 ; 0000-0003-3292-1528</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,550,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37228012$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-106048$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:153264791$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Ziade, Nelly</creatorcontrib><creatorcontrib>Aoude, Marc</creatorcontrib><creatorcontrib>Hmamouchi, Ihsane</creatorcontrib><creatorcontrib>R, Naveen</creatorcontrib><creatorcontrib>Lilleker, James B</creatorcontrib><creatorcontrib>Sen, Parikshit</creatorcontrib><creatorcontrib>Joshi, Mrudula</creatorcontrib><creatorcontrib>Agarwal, Vishwesh</creatorcontrib><creatorcontrib>Kardes, Sinan</creatorcontrib><creatorcontrib>Day, Jessica</creatorcontrib><creatorcontrib>Makol, Ashima</creatorcontrib><creatorcontrib>Milchert, Marcin</creatorcontrib><creatorcontrib>Gheita, Tamer</creatorcontrib><creatorcontrib>Salim, Babur</creatorcontrib><creatorcontrib>Velikova, Tsvetelina</creatorcontrib><creatorcontrib>Edgar Gracia-Ramos, Abraham</creatorcontrib><creatorcontrib>Parodis, Ioannis</creatorcontrib><creatorcontrib>Nikiphorou, Elena</creatorcontrib><creatorcontrib>Chatterjee, Tulika</creatorcontrib><creatorcontrib>Tan, Ai Lyn</creatorcontrib><creatorcontrib>Saavedra, Miguel A</creatorcontrib><creatorcontrib>Shinjo, Samuel Katsuyuki</creatorcontrib><creatorcontrib>Knitza, Johannes</creatorcontrib><creatorcontrib>Kuwana, Masataka</creatorcontrib><creatorcontrib>Nune, Arvind</creatorcontrib><creatorcontrib>Cavagna, Lorenzo</creatorcontrib><creatorcontrib>Distler, Oliver</creatorcontrib><creatorcontrib>Chinoy, Hector</creatorcontrib><creatorcontrib>Agarwal, Vikas</creatorcontrib><creatorcontrib>Aggarwal, Rohit</creatorcontrib><creatorcontrib>Gupta, Latika</creatorcontrib><creatorcontrib>COVAD Study Group</creatorcontrib><creatorcontrib>the COVAD Study Group</creatorcontrib><title>Global disparities in the treatment of idiopathic inflammatory myopathies: results from an international online survey study</title><title>Rheumatology (Oxford, England)</title><addtitle>Rheumatology (Oxford)</addtitle><description>We aimed to explore current practice and interregional differences in the treatment of idiopathic inflammatory myopathies (IIMs). We triangulated these observations considering countries' gross national income (GNI), disease subtypes, and symptoms using patient-reported information.
A cross-sectional ancillary analysis of the 'COVID-19 vaccination in auto-immune disease' (COVAD) e-survey containing demographic characteristics, IIM subtypes (DM, PM, IBM, anti-synthetase syndrome [ASSD], immune-mediated necrotizing myopathy [IMNM], overlap myopathies [OM]), current symptoms (surrogate for organ involvement) and treatments (corticosteroids [CS], immunomodulators [IM], i.e. antimalarials, immunosuppressants [IS], IVIG, biologic treatments and targeted-synthetic small molecules). Treatments were presented descriptively according to continents, GNI, IIM and organ involvement, and associated factors were analysed using multivariable binary logistic regressions.
Of 18 851 respondents from 94 countries, 1418 with IIM were analysed (age 61 years, 62.5% females). DM (32.4%), IBM (24.5%) and OM (15.8%) were the most common subtypes. Treatment categories included IS (49.4%), CS (38.5%), IM (13.8%) and IVIG (9.4%). Notably, treatments varied across regions, GNI categories (IS mostly used in higher-middle income, IM in lower-middle income, IVIG and biologics largely limited to high-income countries), IIM subtypes (IS and CS associated with ASSD, IM with OM and DM, IVIG with IMNM, and biologic treatments with OM and ASSD) and disease manifestations (IS and CS with dyspnoea). Most inter-regional treatment disparities persisted after multivariable analysis.
We identified marked regional treatment disparities in a global cohort of IIM. 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disparities in the treatment of idiopathic inflammatory myopathies: results from an international online survey study</title><author>Ziade, Nelly ; Aoude, Marc ; Hmamouchi, Ihsane ; R, Naveen ; Lilleker, James B ; Sen, Parikshit ; Joshi, Mrudula ; Agarwal, Vishwesh ; Kardes, Sinan ; Day, Jessica ; Makol, Ashima ; Milchert, Marcin ; Gheita, Tamer ; Salim, Babur ; Velikova, Tsvetelina ; Edgar Gracia-Ramos, Abraham ; Parodis, Ioannis ; Nikiphorou, Elena ; Chatterjee, Tulika ; Tan, Ai Lyn ; Saavedra, Miguel A ; Shinjo, Samuel Katsuyuki ; Knitza, Johannes ; Kuwana, Masataka ; Nune, Arvind ; Cavagna, Lorenzo ; Distler, Oliver ; Chinoy, Hector ; Agarwal, Vikas ; Aggarwal, Rohit ; Gupta, Latika</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c429t-76d083b5d918eb4887a1d070dab99ec8afae54661f73c92f0772e7370cfc70c43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adjuvants, 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B</au><au>Sen, Parikshit</au><au>Joshi, Mrudula</au><au>Agarwal, Vishwesh</au><au>Kardes, Sinan</au><au>Day, Jessica</au><au>Makol, Ashima</au><au>Milchert, Marcin</au><au>Gheita, Tamer</au><au>Salim, Babur</au><au>Velikova, Tsvetelina</au><au>Edgar Gracia-Ramos, Abraham</au><au>Parodis, Ioannis</au><au>Nikiphorou, Elena</au><au>Chatterjee, Tulika</au><au>Tan, Ai Lyn</au><au>Saavedra, Miguel A</au><au>Shinjo, Samuel Katsuyuki</au><au>Knitza, Johannes</au><au>Kuwana, Masataka</au><au>Nune, Arvind</au><au>Cavagna, Lorenzo</au><au>Distler, Oliver</au><au>Chinoy, Hector</au><au>Agarwal, Vikas</au><au>Aggarwal, Rohit</au><au>Gupta, Latika</au><aucorp>COVAD Study Group</aucorp><aucorp>the COVAD Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Global disparities in the treatment of idiopathic inflammatory myopathies: results from an international online survey study</atitle><jtitle>Rheumatology (Oxford, England)</jtitle><addtitle>Rheumatology (Oxford)</addtitle><date>2024-03-01</date><risdate>2024</risdate><volume>63</volume><issue>3</issue><spage>657</spage><epage>664</epage><pages>657-664</pages><issn>1462-0324</issn><issn>1462-0332</issn><eissn>1462-0332</eissn><abstract>We aimed to explore current practice and interregional differences in the treatment of idiopathic inflammatory myopathies (IIMs). We triangulated these observations considering countries' gross national income (GNI), disease subtypes, and symptoms using patient-reported information.
A cross-sectional ancillary analysis of the 'COVID-19 vaccination in auto-immune disease' (COVAD) e-survey containing demographic characteristics, IIM subtypes (DM, PM, IBM, anti-synthetase syndrome [ASSD], immune-mediated necrotizing myopathy [IMNM], overlap myopathies [OM]), current symptoms (surrogate for organ involvement) and treatments (corticosteroids [CS], immunomodulators [IM], i.e. antimalarials, immunosuppressants [IS], IVIG, biologic treatments and targeted-synthetic small molecules). Treatments were presented descriptively according to continents, GNI, IIM and organ involvement, and associated factors were analysed using multivariable binary logistic regressions.
Of 18 851 respondents from 94 countries, 1418 with IIM were analysed (age 61 years, 62.5% females). DM (32.4%), IBM (24.5%) and OM (15.8%) were the most common subtypes. Treatment categories included IS (49.4%), CS (38.5%), IM (13.8%) and IVIG (9.4%). Notably, treatments varied across regions, GNI categories (IS mostly used in higher-middle income, IM in lower-middle income, IVIG and biologics largely limited to high-income countries), IIM subtypes (IS and CS associated with ASSD, IM with OM and DM, IVIG with IMNM, and biologic treatments with OM and ASSD) and disease manifestations (IS and CS with dyspnoea). Most inter-regional treatment disparities persisted after multivariable analysis.
We identified marked regional treatment disparities in a global cohort of IIM. These observations highlight the need for international consensus-driven management guidelines considering patient-centred care and available resources.</abstract><cop>England</cop><pmid>37228012</pmid><doi>10.1093/rheumatology/kead250</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-2014-3925</orcidid><orcidid>https://orcid.org/0000-0002-2089-027X</orcidid><orcidid>https://orcid.org/0000-0001-7531-8038</orcidid><orcidid>https://orcid.org/0000-0002-9230-4137</orcidid><orcidid>https://orcid.org/0000-0001-8430-9299</orcidid><orcidid>https://orcid.org/0000-0002-3849-614X</orcidid><orcidid>https://orcid.org/0000-0001-9695-0657</orcidid><orcidid>https://orcid.org/0000-0002-3682-4517</orcidid><orcidid>https://orcid.org/0000-0001-8352-6136</orcidid><orcidid>https://orcid.org/0000-0002-0546-8310</orcidid><orcidid>https://orcid.org/0000-0001-8844-851X</orcidid><orcidid>https://orcid.org/0000-0002-6311-8634</orcidid><orcidid>https://orcid.org/0000-0002-9158-7243</orcidid><orcidid>https://orcid.org/0000-0002-1630-6026</orcidid><orcidid>https://orcid.org/0000-0002-4875-5395</orcidid><orcidid>https://orcid.org/0000-0001-6492-1288</orcidid><orcidid>https://orcid.org/0000-0002-0943-8768</orcidid><orcidid>https://orcid.org/0000-0001-7312-351X</orcidid><orcidid>https://orcid.org/0000-0003-4402-5034</orcidid><orcidid>https://orcid.org/0000-0003-1842-2554</orcidid><orcidid>https://orcid.org/0000-0003-0687-9944</orcidid><orcidid>https://orcid.org/0000-0002-4479-7678</orcidid><orcidid>https://orcid.org/0000-0002-0986-8354</orcidid><orcidid>https://orcid.org/0000-0002-8748-898X</orcidid><orcidid>https://orcid.org/0000-0002-4508-1233</orcidid><orcidid>https://orcid.org/0000-0001-8528-4361</orcidid><orcidid>https://orcid.org/0000-0001-6847-3726</orcidid><orcidid>https://orcid.org/0000-0003-2753-2990</orcidid><orcidid>https://orcid.org/0000-0002-1155-9729</orcidid><orcidid>https://orcid.org/0000-0002-0593-1272</orcidid><orcidid>https://orcid.org/0000-0003-3292-1528</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1462-0324 |
ispartof | Rheumatology (Oxford, England), 2024-03, Vol.63 (3), p.657-664 |
issn | 1462-0324 1462-0332 1462-0332 |
language | eng |
recordid | cdi_swepub_primary_oai_swepub_ki_se_664201 |
source | Oxford University Press Journals All Titles (1996-Current); MEDLINE; SWEPUB Freely available online |
subjects | Adjuvants, Immunologic Autoimmune Diseases COVID-19 Vaccines Cross-Sectional Studies Equity Female Humans Immunoglobulins, Intravenous - therapeutic use Immunosuppressive Agents - therapeutic use inflammatory myopathies Male Middle Aged myositis Myositis - drug therapy rheumatic disease survey treatment |
title | Global disparities in the treatment of idiopathic inflammatory myopathies: results from an international online survey study |
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