【實用醫療app】Idiopathic Pulmonary Fibrosis (IPF) @Point of Care™ Edition|最夯免費app-綠色工廠好玩App

Idiopathic Pulmonary Fibrosis @Point of Care, featuring Maria L. Padilla, MD as Editor-in-Chief, is an interactive resource to support learning in the field of idiopathic pulmonary fibrosis.Within each chapter, you will find supportive multimedia hyperlinks that provide access to illustrations, journal articles, websites, and other resources to enhance understanding of relevant issues.Chapter 1 provides an overview of the prevalence, incidence, and natural history of idiopathic pulmonary fibrosis, demographic factors related to prevalence and incidence, and risk prediction.Chapter 2 reviews the etiology and pathophysiology of IPF; genetic factors and their underpinnings; environmental and other risk factors that contribute to disease onset and progression; and current hypotheses concerning pathophysiology in terms of wound healing, inflammation, and other factors.Chapter 3 discusses current consensus guideline recommendations, diagnostic modalities, differential diagnoses, common comorbid conditions, and the importance of multidisciplinary collaboration in the diagnosis of idiopathic pulmonary fibrosis.Chapter 4 focuses on current consensus guideline recommendations, previous unsuccessful therapies, investigational therapies, nonpharmacologic treatment strategies, and management of idiopathic pulmonary fibrosis patients.Chapter 5 describes the evaluation and management of comorbidities and lifestyle factors that may influence idiopathic pulmonary fibrosis disease presentation and management.Chapter 6 presents two real-life idiopathic pulmonary fibrosis case scenarios: the first focuses on the typical presentation of idiopathic pulmonary fibrosis, and the second describes the diagnosis of “atypical” idiopathic pulmonary fibrosis in patients that do not present with typical findings.