This activity has been designed to meet the educational needs of pulmonologists, radiologists, and pathologists. It may also be of benefit to primary care physicians, rheumatologists, PAs, nurse practitioners, nurses, pharmacists, fellows, residents, and other healthcare professionals who care for patients with chronic progressive fibrosing interstitial lung disease (PF-ILD).
There are 2 forms of hypersensitivity pneumonitis (HP), nonfibrotic and fibrotic. Early diagnosis, antigen avoidance, and treatment are key minimize progression to fibrotic HP.
Upon completion of this activity, participants should be better able to: