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Idiopathic Pulmonary Fibrosis A Comprehensive Clinical Guide [electronic resource]
Meyer, Keith C
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| 자료유형 | 단행본 |
|---|---|
| 개인저자 | Meyer, Keith C.,editor. Nathan, Steven D.,editor. |
| 단체저자명 | SpringerLink (Online service). |
| 서명/저자사항 | Idiopathic Pulmonary Fibrosis [electronic resource] : A Comprehensive Clinical Guide / edited by Keith C. Meyer, Steven D. Nathan. |
| 판사항 | 2nd ed. 2019. |
| 형태사항 | XVII, 475 p. 79 illus., 50 illus. in color:online resource. |
| 총서사항 | Respiratory Medicine=2197-7380 |
| 총서부출표목 | Respiratory Medicine, |
| 기본자료 저록 | Springer Nature eBook |
| 기타형태 저록 | Printed edition:9783319999746Printed edition:9783319999760 |
| ISBN | 9783319999753 |
| 기타표준부호 | 10.1007/978-3-319-99975-3 |
| 내용주기 | Classification and Nomenclature of Interstitial Lung Disease -- Epidemiology and Natural History of IPF -- Histopathology of IPF and Related Disorders -- Imaging of IPF -- Pulmonary Function Tests in Idiopathic Pulmonary Fibrosis -- The Role of Immunity and Inflammation in IPF Pathogenesis -- Mechanisms of Fibrosis in IPF -- The Genetics of Pulmonary Fibrosis -- Genomics and Epigenetics of Pulmonary Fibrosis -- Biomarkers and IPF -- Clinical Phenotypes and Co-morbidities in IPF -- The Keys to Making a Confident Diagnosis of IPF -- Pharmacologic Treatment of IPF -- Mimics of IPF -- Gastroesophageal Reflux and IPF -- The Role of Pulmonary Rehabilitation and Oxygen Therapy -- Acute Exacerbations of IPF -- Lung Transplantation for IPF -- Clinical Trials in IFP: What are the Best Endpoints? -- Future Directions for IPF Research. |
| 요약 | This book is a comprehensive guide to our current understanding of idiopathic pulmonary fibrosis (IPF), its disease pathogenesis, genetic underpinnings, diagnosis, and management. Since the first edition, many new developments have occurred in the understanding and management of this serious disease, revising our understanding of how it presents, manifests, and reacts to certain treatments. This second edition is fully updated with six new chapters by our team of international, expert authors. New topics include: classification of interstitial lung disease, pulmonary function tests in IPF, biomarkers, clinical phenotypes, mimics, and a discussion of clinical trials. Each chapter additionally includes a brief summary of ongoing research and potential future directions. Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide, Second Edition is an invaluable resource for clinicians who desire a deeper understanding of IPF in order to better help their patients. |
| 일반주제명 | Respiratory organs—Diseases. Primary care (Medicine). Pneumology. Primary Care Medicine. |
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