Speaker:
Lisa H. Lancaster, MD 
Medical Director, Interstitial Lung Disease Program 
Professor of Medicine 
Division of Allergy, Pulmonary and Critical Care Medicine 
Vanderbilt University Medical Center 
Nashville, TN 

Learning Objectives
Upon completion of this activity, participants should be able to:

• Differentiate idiopathic pulmonary fibrosis (IPF) from other common ILDs, such as connective tissue disease-associated ILD (CTD-ILD), accurately and efficiently using recommended clinical evaluation, radiologic testing, and pathologic testing as needed
• Apply evidence informing the use of antifibrotic therapy, nonpharmacologic strategies, and management of risk factors and comorbidities in patients with IPF to formulate treatment plans
• Individualize treatment of IPF based on patient characteristics and preferences, using shared decision-making

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This activity is provided by Paradigm Medical Communications, LLC.
Held in collaboration with the Pulmonary Fibrosis Foundation.