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    <IdentifierDoi>10.3205/25rhk135</IdentifierDoi>
    <IdentifierUrn>urn:nbn:de:0183-25rhk1356</IdentifierUrn>
    <ArticleType>Meeting Abstract</ArticleType>
    <TitleGroup>
      <Title language="en">A novel screening protocol for early detection of pulmonary involvement in patients with Rheumafactor- and ACPA positive Rheumatoid Arthritis (RA-ILD)</Title>
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        <PersonNames>
          <Lastname>Fischinger</Lastname>
          <LastnameHeading>Fischinger</LastnameHeading>
          <Firstname>Carina</Firstname>
          <Initials>C</Initials>
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        <Address>
          <Affiliation>LMU University Hospital Munich, Department of Pneumology, Munich</Affiliation>
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        <PersonNames>
          <Lastname>Popp</Lastname>
          <LastnameHeading>Popp</LastnameHeading>
          <Firstname>Florian</Firstname>
          <Initials>F</Initials>
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        <Address>
          <Affiliation>MVZ f&#252;r Rheumatologie Dr. M. Welcker, Planegg</Affiliation>
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          <Lastname>Reichenberger</Lastname>
          <LastnameHeading>Reichenberger</LastnameHeading>
          <Firstname>Frank</Firstname>
          <Initials>F</Initials>
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          <Affiliation>Augustinum Hospital Munich, Department of Pneumology, Munich</Affiliation>
          <Affiliation>Clinic of Pulmonary Medicine, Seefeld-Hechendorf</Affiliation>
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          <Lastname>Kneidinger</Lastname>
          <LastnameHeading>Kneidinger</LastnameHeading>
          <Firstname>Nikolaus</Firstname>
          <Initials>N</Initials>
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        <Address>
          <Affiliation>LMU University Hospital Munich, Department of Pneumology, Munich</Affiliation>
          <Affiliation>Medical University Graz, Department of Pneumology, Graz</Affiliation>
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      <Creator>
        <PersonNames>
          <Lastname>Tiede</Lastname>
          <LastnameHeading>Tiede</LastnameHeading>
          <Firstname>Robin</Firstname>
          <Initials>R</Initials>
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        <Address>
          <Affiliation>LMU University Hospital Munich, Department of Pneumology, Munich</Affiliation>
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        <PersonNames>
          <Lastname>von Wulffen</Lastname>
          <LastnameHeading>von Wulffen</LastnameHeading>
          <Firstname>Werner</Firstname>
          <Initials>W</Initials>
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        <Address>
          <Affiliation>Augustinum Hospital Munich, Department of Pneumology, Munich</Affiliation>
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      <Creator>
        <PersonNames>
          <Lastname>Welcker</Lastname>
          <LastnameHeading>Welcker</LastnameHeading>
          <Firstname>Martin</Firstname>
          <Initials>M</Initials>
        </PersonNames>
        <Address>
          <Affiliation>MVZ f&#252;r Rheumatologie Dr. M. Welcker, Planegg</Affiliation>
          <Affiliation>M.B.W.-Welcker GbR, Rheumatologie, Planegg</Affiliation>
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          <Corporatename>German Medical Science GMS Publishing House</Corporatename>
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        <Address>D&#252;sseldorf</Address>
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    <SubjectGroup>
      <SubjectheadingDDB>610</SubjectheadingDDB>
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    <DatePublishedList>
      <DatePublished>20250917</DatePublished>
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    <Language>engl</Language>
    <License license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
      <AltText language="en">This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License.</AltText>
      <AltText language="de">Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung).</AltText>
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    <SourceGroup>
      <Meeting>
        <MeetingId>M0627</MeetingId>
        <MeetingSequence>135</MeetingSequence>
        <MeetingCorporation>Deutsche Gesellschaft f&#252;r Rheumatologie</MeetingCorporation>
        <MeetingCorporation>Deutsche Gesellschaft f&#252;r Orthop&#228;dische Rheumatologie</MeetingCorporation>
        <MeetingName>53. Kongress der Deutschen Gesellschaft f&#252;r Rheumatologie (DGRh), 39. Jahrestagung der Deutschen Gesellschaft f&#252;r Orthop&#228;dische Rheumatologie (DGORh)</MeetingName>
        <MeetingTitle>Deutscher Rheumatologiekongress 2025</MeetingTitle>
        <MeetingSession>Rheumatoide Arthritis</MeetingSession>
        <MeetingCity>Wiesbaden</MeetingCity>
        <MeetingDate>
          <DateFrom>20250917</DateFrom>
          <DateTo>20250920</DateTo>
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    <ArticleNo>RA.08</ArticleNo>
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      <MainHeadline>Text</MainHeadline><Pgraph><Mark1>Introduction: </Mark1>Rheumatoid Arthritis (RA), in particular Rheumafactor- and ACPA-positive RA, is associated with a significantly higher risk for pulmonary and cardiovascular comorbidities <TextLink reference="1"></TextLink>, <TextLink reference="2"></TextLink>.</Pgraph><Pgraph>In order to achieve a better prognosis as well as a better therapeutic outcome early detection of pulmonary comorbidities, in particular of interstitial lung disease (ILD), is crucial. Despite its great relevance, no recommendations for a screening protocol are not yet issued.</Pgraph><Pgraph><Mark1>Methods: </Mark1>In this study, we enrolled 214 consecutive patients with a confirmed diagnosis of seropositive and ACPA-positive RA, who exhibited no symptoms or prior history of cardiopulmonary disease. To screen for pulmonary, pleural, or vascular manifestations of RA, we utilized noninvasive, radiation-free methods, including pulmonary function tests (PFT), cardiopulmonary exercise testing (CPET), echocardiography, and pleuro-pulmonary transthoracic ultrasound (LUS). The study was divided into two phases.</Pgraph><Pgraph><Mark1>Results: </Mark1>203 patients (mean age 59,2 &#177;12,2 years, 76&#37; female, 16,7&#37; current smokers and 26,6&#37; previous smokers) were examined.</Pgraph><Pgraph>The average duration of disease in the overall cohort is 8.3 (&#177;7.1) years, with 32&#37; of patients (n&#61;64) suffering from an erosive course of RA.</Pgraph><Pgraph>In total, the disease activity of the cohort is in remission, regardless of the method used to measure disease activity (DAS28CRP 2.3, CDAI 5.7, SDAI 6.2, BSG 16.4, CRP 4.5).</Pgraph><Pgraph>In the pulmonary function test, 81 patients (42&#37;) showed abnormalities. With a mean FVC of 97.3&#37;, the comparison of the ILD-group vs. non-ILD-group showed differences in DLCOc&#37; (68.2&#37;&#177;13.5 vs. 82.4&#37;&#177;14.9). Sonographic changes were seen in 107 patients (52.7&#37;), with 29&#37; (n&#61;58) showing typical LUS pattern compatible with ILD such as B-lines, comet tail artifacts and pleural irregularities3.With the parallel occurrence of characteristic alterations in LUS as well as additional changes in PFT, ILD was suspected, affecting 15.1&#37; of the patients (n&#61;30).</Pgraph><Pgraph>Secondary findings included pleural consolidation suspected of malignancy and pleural effusion on LUS, severe aortic stenosis in the context of a bicuspid aortic valve, and severely impaired diffusion capacity due to pulmonary emphysema and obstructive lung disease.</Pgraph><Pgraph><Mark1>Conclusion: </Mark1>In conclusion, this novel screening protocol including lung sonography for RA patients enables the early detection of pulmonary manifestation of RA and various other cardiopulmonary comorbidities, revealing a significant number of asymptomatic patients.</Pgraph><Pgraph>Figure 1 <ImgLink imgNo="1" imgType="figure" /></Pgraph><Pgraph>Table 1 <ImgLink imgNo="1" imgType="table" /></Pgraph></TextBlock>
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          <Caption><Pgraph><Mark1>Table 1: Cohort description, first &#38; second part of the study</Mark1></Pgraph></Caption>
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          <Caption><Pgraph><Mark1>Figure 1: Scatterplot RA activity scores vs. FVC (&#37;), first part of the study</Mark1></Pgraph></Caption>
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