Title of article :
The Impact of Multidisciplinary Discussion (MDD) in the Diagnosis and Management of Fibrotic Interstitial Lung Diseases
Author/Authors :
Ageely, Ghofran Division of Thoracic Imaging - Department of Medical Imaging - Ottawa Hospital Research Institute - University of Ottawa, Canada , Souza, Carolina Division of Thoracic Imaging - Department of Medical Imaging - Ottawa Hospital Research Institute - University of Ottawa, Canada , De Boer, Kaissa Division of Respirology - Department of Internal Medicine - Ottawa Hospital Research Institute - University of Ottawa, Canada , Zahra, Saly Division of Thoracic Imaging - Department of Medical Imaging - Ottawa Hospital Research Institute - University of Ottawa, Canada , Gomes, Marcio Department of Pathology and Laboratory Medicine - Ottawa Hospital Research Institute - University of Ottawa, Canada
Abstract :
Accurate diagnosis of interstitial lung disease (ILD) is crucial for management and prognosis but can be challenging even for
experienced clinicians. Expert multidisciplinary discussion (MDD) is considered the reference standard for ILD diagnosis;
however, there remain concerns regarding lack of validation studies and relative limited information on the impact of MDD in
real-life clinical practice. The goal of this study was to assess the effect of MDD in providing a specific ILD diagnosis, changing the
diagnosis provided upon referral, and to determine how often and in which way MDD altered management. Material and
Methods. Retrospective observational study in an ILD referral tertiary academic center. MDD diagnoses were categorized as
specific, provisional, and unclassifiable ILD. Pre-MDD and MDD diagnoses were compared for change in diagnosis and
concordance rates for specific diagnoses. Relevant change in management including initiation or change in pharmacological
treatment, referral to surgical biopsy, and nonpharmacological management were recorded. Results. 126 cases were included
(79M, 47F, 36–93 years, mean 70 y). Specific MDD diagnosis was provided in 62% (78/126); 12% (15/126) had provisional
diagnosis, and 21% (27/126) was unclassifiable. Overall agreement for specific pre-MDD and MDD diagnosis was 41% (52/126)
and 80% for idiopathic pulmonary fibrosis (IPF) diagnosis. MDD altered diagnosis in 37% (47/126) and changed management in
39% (50/126). Amongst concordant diagnoses, management was altered in 46% (24/52). In summary, MDD provided a specific
diagnosis discordant with pre-MDD diagnosis in a significant proportion of cases and was particularly valuable in the diagnosis of
non-IPF ILD. MDD often altered management and had relevant impact on management even in cases with concordant preMDD diagnosis.
Keywords :
Multidisciplinary Discussion , Lung Diseases , Fibrotic Interstitial
Journal title :
Canadian Respiratory Journal