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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?
In a patient with low titer +anti-SAE antibody and known ILD, but no other clinical features of dermatomyositis, how would you approach further testing or would you treat the patient as dermatomyositis associated ILD?
Do you seek pathologic confirmation before proceeding with empiric immunosuppressive therapy in symptomatic patients with radiographic NSIP?
Does the pattern on chest CT help determine which patients with RA-ILD will respond to immunosuppression?
What factors would encourage you to choose abatacept vs tocilizumab in a patient with RA-ILD with a UIP pattern of pulmonary fibrosis?
What is your approach to differentiating RA-ILD from medication toxicity (I.e. from methotrexate)?
Do you always get a baseline chest xray in patients who will be starting methotrexate?
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 do you approach a patient with sarcoidosis who cannot tolerate steroids and who is developing ILD?
How frequently do you monitor CT scans, PFTs, and TTEs in patients with ILA or mild ILD?