医学
间质性肺病
抗合成酶综合征
金标准(测试)
肺科医生
体格检查
内科学
寻常性间质性肺炎
类风湿性关节炎
血管炎
肺科医师
肺
结缔组织病
放射科
痹症科
高分辨率计算机断层扫描
皮肌炎
疾病
病理
肺纤维化
DLCO公司
活检
肺功能测试
肺活检
物理疗法
肺病
多发性肌炎
重症监护医学
自身免疫性疾病
作者
Y Levi,Lilach Israeli‐Shani,Michael Kuchuk,Gali Epstein Shochet,Matthew Koslow,David Shitrit
标识
DOI:10.3899/jrheum.171314
摘要
Objective. Interstitial lung diseases (ILD) form a diverse group of parenchymal lung disorders. Currently, a multidisciplinary team (MDT) including pulmonologists, radiologists, and pathologists is the gold standard for ILD diagnosis. Recently, additional subtypes of connective tissue disease (CTD)-ILD with autoimmune features were defined, making the rheumatological assessment increasingly important. We aimed to assess the effect of adding a rheumatologist to the MDT for routine rheumatology assessment. Methods. A prospective study that assessed newly diagnosed ILD patients by 2 parallel blinded arms; all patients were evaluated by both MDT (e.g., history, physical examination, blood tests, pulmonary function tests, and biopsies, if needed) and a rheumatologist (e.g., history, physical examination, blood and serological tests). Results. Sixty patients were assessed with the mean age of 67.3 ± 12 years, 55% male, and 28% smokers. The rheumatological assessment reclassified 21% of the idiopathic pulmonary fibrosis as CTD. Moreover, the number of CTD-ILD with autoimmune features was increased by 77%. These included antineutrophil cytoplasmic antibody–associated vasculitis, antisynthetase syndrome, and IgG4-related ILD. Retrospectively, rheumatological evaluation could have saved 7 bronchoscopies and 1 surgical biopsy. Conclusion. Adding routine rheumatology assessments could significantly increase diagnostic accuracy and reduce invasive procedures.
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