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  • © 2019

Idiopathic Pulmonary Fibrosis

A Comprehensive Clinical Guide

  • Fully updated information on diagnosis and management of IPF, including six new chapters
  • Includes new coverage of interstitial lung disease classification, biomarkers in IPF, new concepts in disease pathogenesis, and the genetic underpinnings of the disease
  • Written by an international group of expert authors

Part of the book series: Respiratory Medicine (RM)

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Table of contents (20 chapters)

  1. Front Matter

    Pages i-xvii
  2. Idiopathic Pulmonary Fibrosis: The Epidemiology and Natural History of Disease

    • Michael P. Mohning, Jeffrey J. Swigris, Amy L. Olson
    Pages 11-35
  3. Histopathology of IPF and Related Disorders

    • Amir Lagstein, Jeffrey L. Myers
    Pages 37-60
  4. Imaging of Idiopathic Pulmonary Fibrosis

    • Jonathan H. Chung, Jeffrey P. Kanne
    Pages 61-83
  5. Pulmonary Function Tests in Idiopathic Pulmonary Fibrosis

    • Francesco Bonella, Fabiano di Marco, Paolo Spagnolo
    Pages 85-95
  6. The Role of Immunity and Inflammation in IPF Pathogenesis

    • Marcus W. Butler, Michael P. Keane
    Pages 97-131
  7. Mechanisms of Fibrosis in IPF

    • Nathan Sandbo
    Pages 133-182
  8. Genetics of Pulmonary Fibrosis

    • Traci N. Adams, Christine Kim Garcia
    Pages 183-206
  9. Evolving Genomics of Pulmonary Fibrosis

    • Gabriel Ibarra, Jose D. Herazo-Maya, Naftali Kaminski
    Pages 207-239
  10. Biomarkers in Idiopathic Pulmonary Fibrosis

    • Shweta Sood, Tonya D. Russell, Adrian Shifren
    Pages 241-271
  11. Idiopathic Pulmonary Fibrosis: Phenotypes and Comorbidities

    • Christopher S. King, Shambhu Aryal, Steven D. Nathan
    Pages 273-297
  12. The Keys to Making a Confident Diagnosis of IPF

    • Jamie Sheth, Anish Wadhwa, Kevin R. Flaherty
    Pages 299-323
  13. Pharmacologic Treatment of IPF

    • Andrea Smargiassi, Giuliana Pasciuto, Emanuele Giovanni Conte, Mariarita Andreani, Roberta Marra, Luca Richeldi
    Pages 325-364
  14. Mimics of Idiopathic Pulmonary Fibrosis

    • Keith C. Meyer, Steven D. Nathan
    Pages 365-378
  15. Gastroesophageal Reflux and IPF

    • Joyce S. Lee
    Pages 379-387
  16. Acute Exacerbation of Idiopathic Pulmonary Fibrosis

    • Joyce S. Lee, Harold R. Collard
    Pages 401-417
  17. Lung Transplantation for Idiopathic Pulmonary Fibrosis

    • Daniela J. Lamas, David J. Lederer
    Pages 419-432
  18. Clinical Trials in IPF: What Are the Best Endpoints?

    • Paolo Spagnolo, Elisabetta Cocconcelli, Vincent Cottin
    Pages 433-453

About this book

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.

Reviews

“This is likely one of the most comprehensive and complete books on idiopathic pulmonary fibrosis currently available, and it should be extremely useful to pulmonologists and researchers who are interested in the pathogenesis, diagnosis, and treatment of this fatal disease.” (Santosh Dhungana, Doody's Book Reviews, April 26, 2019)

Editors and Affiliations

  • Department of Internal Medicine, Section of Allergy, Pulmonary and Critical Care Medicine, University of Wisconsin School of Medicine & Public Health, Madison, USA

    Keith C. Meyer

  • Advanced Lung Disease and Lung Transplant Program, Inova Fairfax Hospital, Falls Church, USA

    Steven D. Nathan

About the editors

Keith C. Meyer, MD is a professor of pulmonary and critical care medicine at the University of Wisconsin School of Medicine and Public Health. He is volume editor of three successful Springer books: Idiopathic Pulmonary Fibrosis, Gastroesophageal Reflux and the Lung, and Bronchiolitis Obliterans Syndrome in Lung Transplantation

Steven D. Nathan, MD is professor of medicine at Virginia Commonwealth University Inova Campus and director of the Lung Transplant and Advanced Lung Disease programs. He is also volume editor of Idiopathic Pulmonary Fibrosis and the upcoming Guide to Clinical Management of Idiopathic Pulmonary Fibrosis (with Springer Healthcare)

Bibliographic Information

  • Book Title: Idiopathic Pulmonary Fibrosis

  • Book Subtitle: A Comprehensive Clinical Guide

  • Editors: Keith C. Meyer, Steven D. Nathan

  • Series Title: Respiratory Medicine

  • DOI: https://doi.org/10.1007/978-3-319-99975-3

  • Publisher: Humana Cham

  • eBook Packages: Medicine, Medicine (R0)

  • Copyright Information: Springer Nature Switzerland AG 2019

  • Hardcover ISBN: 978-3-319-99974-6Published: 04 January 2019

  • eBook ISBN: 978-3-319-99975-3Published: 14 December 2018

  • Series ISSN: 2197-7372

  • Series E-ISSN: 2197-7380

  • Edition Number: 2

  • Number of Pages: XVII, 475

  • Number of Illustrations: 29 b/w illustrations, 50 illustrations in colour

  • Topics: Pneumology/Respiratory System, Primary Care Medicine

Buy it now

Buying options

eBook USD 149.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book USD 199.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Other ways to access