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In this CE/CME activity, Steven D. Nathan, MD, discusses how idiopathic pulmonary fibrosis (IPF) differentiates from other interstitial lung diseases. Dr. Nathan presents the impact of an early and accurate diagnosis of IPF, common symptoms, and the diagnostic tools and criteria used for an accurate diagnosis. In addition, Dr. Nathan reviews the significance of high-resolution computed tomography (HRCT) and what IPF looks like on HRCT scans. Dr. Nathan provides his insights on current treatment options and therapeutic strategies for IPF, which include dosing, monitoring, and common side effects from agents used to treat IPF.
