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Please select the option that best describes you:
Topics:
General Internal Medicine
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Rheumatology
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Rheumatoid Arthritis
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Interstitial lung disease
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Pulmonology
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Diffuse Parenchymal Lung Disease
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Pulmonary
How do you manage pleuroparenchymal fibroelastosis in a patient with seronegative RA that is progressing on Rituxan and DMARD therapy?
Is there a role for antifibrotics in these patients?
Related Questions
How would you approach management of a patient with seropositive RA and UIP-ILD, with concern for active lung disease?
Do you seek pathologic confirmation before proceeding with empiric immunosuppressive therapy in symptomatic patients with radiographic NSIP?
Do you always get a baseline chest xray in patients who will be starting methotrexate?
Is it still significant to denote the etiology of ILD in a patient with PPF?
What are your thoughts on using abatacept for RA-associated ILD in a patient undergoing treatment for CLL with zanubrutinib, and how would you assess the potential increased risk of infection in this context?
How frequently do you monitor CT scans, PFTs, and TTEs in patients with ILA or mild ILD?
Are there benefits to adding IL5/IL5 receptor blockade in patients with vasculitic manifestations of EGPA?
When would you consider referring a patient with suspected cardiac sarcoidosis based on PET and MRI for endomyocardial biopsy given degree of patchy involvement, as opposed to initiating empiric immunosuppressive therapies?
For patients who do not have access to biologic therapies, what are some csDMARD combination pearls or tips that you have that have particular efficacy in different rheumatologic diseases?
How often are you performing CT screening in CVID patients to screen for ILD?