Idiopathic Pulmonary Fibrosis
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Idiopathic Pulmonary Fibrosis
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Author : Keith C. Meyer
language : en
Publisher: Springer Science & Business Media
Release Date : 2013-10-16
Idiopathic Pulmonary Fibrosis written by Keith C. Meyer and has been published by Springer Science & Business Media this book supported file pdf, txt, epub, kindle and other format this book has been release on 2013-10-16 with Medical categories.
Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide delivers a concise review of our current understanding of disease pathogenesis and provides current evidence in the medical literature regarding its diagnosis and management. Each chapter includes key points and a summary aiming to update clinicians about various issues concerning the diagnosis and management of IPF. In addition to outlining the current state of knowledge, each chapter also provides a summary of ongoing research and identifies the needs for future research in the field. Idiopathic Pulmonary Fibrosis: A Comprehensive Clinical Guide is an important new text that provides its readers with a better understanding of the pathobiology and natural history of IPF as it continues to evolve.
Idiopathic Pulmonary Fibrosis
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Author : Jeffrey Swigris
language : en
Publisher: Elsevier Health Sciences
Release Date : 2018-07-25
Idiopathic Pulmonary Fibrosis written by Jeffrey Swigris and has been published by Elsevier Health Sciences this book supported file pdf, txt, epub, kindle and other format this book has been release on 2018-07-25 with Medical categories.
Designed with the practicing clinician in mind, Idiopathic Pulmonary Fibrosis provides a succinct, easy-to-digest overview of this challenging condition in which the cause of thickening lung tissue is unknown. This concise resource by Drs. Kevin K. Brown and Jeff Swigris provides essential information for the physician who sees pulmonary fibrosis patients, including epidemiology, genetics and biomarkers, pathology, diagnosis, disease monitoring, and therapeutics intended to improve the patient’s lifespan and quality of life.
Idiopathic Pulmonary Fibrosis
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Author : Ulrich Costabel
language : en
Publisher: European Respiratory Society
Release Date : 2016-03-01
Idiopathic Pulmonary Fibrosis written by Ulrich Costabel and has been published by European Respiratory Society this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-03-01 with Medical categories.
Idiopathic pulmonary fibrosis (IPF) is a steadily progressive and ultimately fatal disease of unknown origin. Recent years have seen advances in our understanding of IPF and a number of guidelines have been published. But many questions remain unanswered, particularly surrounding probable versus definite IPF. This Monograph aims to discuss the latest achievements in IPF, and covers key diagnostic issues, staging of the disease, complications and comorbidities, treatment, unmet patient needs and perspectives for the future. This book will be of interest to all clinicians and researchers in this area.
Idiopathic Pulmonary Fibrosis
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Author : Joseph P. Lynch
language : en
Publisher: CRC Press
Release Date : 2003-12-18
Idiopathic Pulmonary Fibrosis written by Joseph P. Lynch and has been published by CRC Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2003-12-18 with Medical categories.
A discussion of the epidemiology, clinical features, and differential diagnoses of idiopathic pulmonary fibrosis (IPF). Key topics include the role of polymorphonuclear leukocytes in the pathogenesis of pulmonary fibrosis, and current treatment options, including medical therapy and lung transplantation.
Guide To Clinical Management Of Idiopathic Pulmonary Fibrosis
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Author : Steven D Nathan
language : en
Publisher: Springer
Release Date : 2016-07-27
Guide To Clinical Management Of Idiopathic Pulmonary Fibrosis written by Steven D Nathan and has been published by Springer this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-07-27 with Medical categories.
This clinically focused pocket guide offers a concise yet complete overview of idiopathic pulmonary fibrosis, covering the most recent information on aspects such as pathophysiology, management, treatment, and clinical trials. The text is easily accessible and offers pulmonologists and other health care professionals with an excellent quick reference tool. Full color images and figures enhance and summarize key aspects of the text. Idiopathic pulmonary fibrosis is a condition that affects the alveoli and leads to serious lung damage, and the idiopathic nature of this disease means that the origin or cause is unknown. This disease is relatively rare, affecting 3 in 10,000 people, but it is becoming more common. Physicians should be aware of the early stages and symptoms of this disease so management strategies can be implemented quickly, and the best treatment can be administered.
Idiopathic Pulmonary Fibrosis
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Author : Hiroyuki Nakamura
language : en
Publisher: Springer
Release Date : 2015-09-28
Idiopathic Pulmonary Fibrosis written by Hiroyuki Nakamura and has been published by Springer this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-09-28 with Medical categories.
From epidemiology and pathogenesis to disease management, this book reviews our current understanding of and provides up-to-date information of Idiopathic Pulmonary Fibrosis (IPF). A subtype of Idiopathic Interstitial Pneumonias (IIP), IPF is one of the most elusive and intractable respiratory disease to date and its triggering factors remain unclear. However, new developments such as serum markers that are highly specific to IPF (i.e. KL-6, SP-A, and SP-D), the establishment of systematic diagnostic imaging (HRCT) and accumulated reports of treatment using an antifibrotic agent (pirfenidone) are slowly improving our understanding of the disease. Edited by an established authority in the field and written by experts, this book will be valuable to not only to beginning learners but also to physicians, instructors and researchers whose work involves IIPs. With each chapter exploring critical questions, with unresolved issues and future prospects, the book offers a valuable resource for understanding issues such as the newly proposed entity of interstitial pneumonia with emphysema (combined pulmonary fibrosis and emphysema: CPFE) and the mechanism of how so many IIP sufferers develop lung cancer.
Why Do Patients Get Idiopathic Pulmonary Fibrosis Current Concepts In The Pathogenesis Of Pulmonary Fibrosis
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Author : Newcastle Newcastle Press
language : en
Publisher:
Release Date : 2016-01-18
Why Do Patients Get Idiopathic Pulmonary Fibrosis Current Concepts In The Pathogenesis Of Pulmonary Fibrosis written by Newcastle Newcastle Press and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2016-01-18 with categories.
Idiopathic pulmonary fibrosis (IPF) is a devastating lung disease of unknown origin. Recent findings suggest that IPF results from multiple factors that eventually lead to interstitial lung injury. In the pathogenesis it is likely that complex relationships between genetic predispositions, environmental exposures, and lung infections promote the fibrotic processes causing IPF; it is this complexity and the multiplicity of causes that make the population and clinical course of IPF so heterogeneous. Thus, it is clear that one common factor driving IPF pathogenesis in all patients would be far too simplified of an understanding. In recent years, efforts have been made in finding therapeutic strategies that target disease progression rather than disease onset. The biochemical composition and abnormal stiffness of the matrix might be crucial in controlling the cellular phenotype in fibrotic lungs that promotes disease progression and persistence. Though there has been substantial progress in the IPF field in recent years, much more work is required in order to improve the prognosis associated with this disease.
Idiopathic Pulmonary Fibrosis New Insights For The Healthcare Professional 2013 Edition
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Author :
language : en
Publisher: ScholarlyEditions
Release Date : 2013-07-22
Idiopathic Pulmonary Fibrosis New Insights For The Healthcare Professional 2013 Edition written by and has been published by ScholarlyEditions this book supported file pdf, txt, epub, kindle and other format this book has been release on 2013-07-22 with Medical categories.
Idiopathic Pulmonary Fibrosis: New Insights for the Healthcare Professional: 2013 Edition is a ScholarlyBrief™ that delivers timely, authoritative, comprehensive, and specialized information about Additional Research in a concise format. The editors have built Idiopathic Pulmonary Fibrosis: New Insights for the Healthcare Professional: 2013 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Additional Research in this book to be deeper than what you can access anywhere else, as well as consistently reliable, authoritative, informed, and relevant. The content of Idiopathic Pulmonary Fibrosis: New Insights for the Healthcare Professional: 2013 Edition has been produced by the world’s leading scientists, engineers, analysts, research institutions, and companies. All of the content is from peer-reviewed sources, and all of it is written, assembled, and edited by the editors at ScholarlyEditions™ and available exclusively from us. You now have a source you can cite with authority, confidence, and credibility. More information is available at http://www.ScholarlyEditions.com/.
The Voice Of The Patient
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Author : Humberto Repka
language : en
Publisher:
Release Date : 2021-04-16
The Voice Of The Patient written by Humberto Repka and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2021-04-16 with categories.
Idiopathic pulmonary fibrosis (IPF) is a serious lung disease. When you breathe in, oxygen moves through tiny air sacs in your lungs and into your bloodstream. From there, it travels to your organs. IPF causes scar tissue to grow inside your lungs and makes it hard to breathe. This book is the story of one man's experience with pulmonary fibrosis, from diagnosis to lung transplantation, and life afterward. Here are the introductory comments from the author: "Imagine being told you have a disease you have never heard of, a disease with no known cause, for which there is no known effective medical treatment and no cure. Your future has been instantly shortened to three to five years. I want to share with you my journey with idiopathic pulmonary fibrosis (IPF)." Physicians, others diagnosed with IPF, and their caregivers have endorsed it as an uplifting, hopeful, and forward-looking story.
Interstitial Lung Disease E Book
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Author : Harold R Collard
language : en
Publisher: Elsevier Health Sciences
Release Date : 2017-02-18
Interstitial Lung Disease E Book written by Harold R Collard and has been published by Elsevier Health Sciences this book supported file pdf, txt, epub, kindle and other format this book has been release on 2017-02-18 with Medical categories.
Clinically focused and designed to provide a to-the-point overview, Interstitial Lung Disease, by Drs. Talmadge King, Harold Collard, and Luca Richeldi, bring you up to date with increased understanding, new treatment protocols, and recent advances in the field. Written by contributing specialists who are global experts in their respective areas, this one-stop reference provides pulmonologists, intensivists, internal medicine physicians, and researchers with a dependable source of information on current treatment options and patient care. • Evidence for current treatment options for interstitial pneumonia, idiopathic pulmonary fibrosis, and smoking-related interstitial lung diseases. • Approach to diagnosis of interstitial lung diseases, such as sarcoidosis, hypersensitivity pneumonitis, and Churg-Strauss syndrome. • Genetic markers for inherited interstitial lung diseases such as dyskeratosis congenita, tuberous sclerosis/LAM, and hyper-IgE syndrome.