Rheumatological assessment is important for interstitial lung disease diagnosis

Yair Levi, Lilach Israeli-Shani, Michael Kuchuk, Gali Epstein Shochet, Matthew Koslow, David Shitrit*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Pages (from-to)1509-1514
Number of pages6
JournalJournal of Rheumatology
Volume45
Issue number11
DOIs
StatePublished - 1 Nov 2018

Keywords

  • CONNECTIVE TISSUE DISEASES
  • INTERSTITIAL LUNG DISEASE
  • PULMONARY FIBROSIS
  • RHEUMATIC DISEASES

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