How do you approach screening for ILD in patients with a diagnosis of MCTD given the recommendation discrepancies between the most recent EULAR and ACR/CHEST guidelines?
How do you use PFTs and/or HRCT to screen for ILD in patients newly diagnosed with MCTD?
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Another excellent question! While the EULAR guidelines treat MCTD as SSc-equivalent and suggest universal screening, ACR/CHEST guidelines suggest risk-stratified screening with emphasis on symptoms, PFT abnormalities, and high-risk phenotypes.
Prevalence of ILD in MCTD can be high, in the range of 30...
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As I go through the ACR/Chest and EULAR ILD guidelines, I do not see a significant discrepancy IF we consider MCTD in general a high-risk disease for ILD. Patients with MCTD are considered high-risk for ILD if they have scleroderma features, which are defined as Raynaud’s phenomenon, puffy fingers, ...
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I do CT at baseline in all high-risk patients - MCTD is high risk for ILD. If abnormal CT, then do PFT.
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