TY - JOUR
T1 - Rheumatological assessment is important for interstitial lung disease diagnosis
AU - Levi, Yair
AU - Israeli-Shani, Lilach
AU - Kuchuk, Michael
AU - Shochet, Gali Epstein
AU - Koslow, Matthew
AU - Shitrit, David
N1 - Publisher Copyright:
© 2018. All rights reserved.
PY - 2018/11/1
Y1 - 2018/11/1
N2 - 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.
AB - 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.
KW - CONNECTIVE TISSUE DISEASES
KW - INTERSTITIAL LUNG DISEASE
KW - PULMONARY FIBROSIS
KW - RHEUMATIC DISEASES
UR - http://www.scopus.com/inward/record.url?scp=85055884626&partnerID=8YFLogxK
U2 - 10.3899/jrheum.171314
DO - 10.3899/jrheum.171314
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C2 - 30111640
AN - SCOPUS:85055884626
SN - 0315-162X
VL - 45
SP - 1509
EP - 1514
JO - Journal of Rheumatology
JF - Journal of Rheumatology
IS - 11
ER -