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Idiopathic Pulmonary Fibrosis

A Comprehensive Clinical Guide

  • Keith C. Meyer
  • Steven D. Nathan

Part of the Respiratory Medicine book series (RM)

Table of contents

  1. Front Matter
    Pages i-xvii
  2. Michael P. Mohning, Jeffrey J. Swigris, Amy L. Olson
    Pages 11-35
  3. Amir Lagstein, Jeffrey L. Myers
    Pages 37-60
  4. Jonathan H. Chung, Jeffrey P. Kanne
    Pages 61-83
  5. Francesco Bonella, Fabiano di Marco, Paolo Spagnolo
    Pages 85-95
  6. Marcus W. Butler, Michael P. Keane
    Pages 97-131
  7. Nathan Sandbo
    Pages 133-182
  8. Traci N. Adams, Christine Kim Garcia
    Pages 183-206
  9. Gabriel Ibarra, Jose D. Herazo-Maya, Naftali Kaminski
    Pages 207-239
  10. Shweta Sood, Tonya D. Russell, Adrian Shifren
    Pages 241-271
  11. Christopher S. King, Shambhu Aryal, Steven D. Nathan
    Pages 273-297
  12. Jamie Sheth, Anish Wadhwa, Kevin R. Flaherty
    Pages 299-323
  13. Andrea Smargiassi, Giuliana Pasciuto, Emanuele Giovanni Conte, Mariarita Andreani, Roberta Marra, Luca Richeldi
    Pages 325-364
  14. Keith C. Meyer, Steven D. Nathan
    Pages 365-378
  15. Joyce S. Lee
    Pages 379-387
  16. Joyce S. Lee, Harold R. Collard
    Pages 401-417
  17. Daniela J. Lamas, David J. Lederer
    Pages 419-432
  18. Paolo Spagnolo, Elisabetta Cocconcelli, Vincent Cottin
    Pages 433-453
  19. J. Matt Craig, Neil R. Aggarwal, James P. Kiley
    Pages 455-467
  20. Back Matter
    Pages 469-475

About this book

Introduction

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.

Keywords

idiopathic pulmonary fibrosis IPF interstitial lung disease pulmonary function test lung transplantation biomarkers clinical phenotypes

Editors and affiliations

  • Keith C. Meyer
    • 1
  • Steven D. Nathan
    • 2
  1. 1.Department of Internal Medicine, Section of Allergy, Pulmonary and Critical Care MedicineUniversity of Wisconsin School of Medicine & Public HealthMadisonUSA
  2. 2.Advanced Lung Disease and Lung Transplant ProgramInova Fairfax HospitalFalls ChurchUSA

Bibliographic information

  • DOI https://doi.org/10.1007/978-3-319-99975-3
  • Copyright Information Springer Nature Switzerland AG 2019
  • Publisher Name Humana Press, Cham
  • eBook Packages Medicine
  • Print ISBN 978-3-319-99974-6
  • Online ISBN 978-3-319-99975-3
  • Series Print ISSN 2197-7372
  • Series Online ISSN 2197-7380
  • Buy this book on publisher's site