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Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis
Author: Keith C. Meyer
Publisher: Springer Science & Business Media
Total Pages: 457
Release: 2013-10-16
Genre: Medical
ISBN: 1627036822

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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

Idiopathic Pulmonary Fibrosis
Author: Jeffrey Swigris
Publisher: Elsevier Health Sciences
Total Pages: 350
Release: 2018-07-25
Genre: Medical
ISBN: 0323544320

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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

Idiopathic Pulmonary Fibrosis
Author: Ulrich Costabel
Publisher: European Respiratory Society
Total Pages: 292
Release: 2016-03-01
Genre: Medical
ISBN: 1849840687

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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.


Guide to Clinical Management of Idiopathic Pulmonary Fibrosis

Guide to Clinical Management of Idiopathic Pulmonary Fibrosis
Author: Steven D Nathan
Publisher: Springer
Total Pages: 135
Release: 2016-07-27
Genre: Medical
ISBN: 3319327941

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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

Idiopathic Pulmonary Fibrosis
Author: Hiroyuki Nakamura
Publisher: Springer
Total Pages: 260
Release: 2015-09-28
Genre: Medical
ISBN: 443155582X

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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.


Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis
Author: Salim Surani
Publisher: BoD – Books on Demand
Total Pages: 220
Release: 2022-10-19
Genre: Medical
ISBN: 1839692391

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Idiopathic pulmonary fibrosis (IPF) affects 13–20 people per 100,000 population worldwide. In the United States, approximately 100,000 people have IPF with 30,000–40,000 new cases diagnosed annually. Diagnosis remains a challenge with a significant lag between symptoms onset and diagnosis. Delayed diagnosis and treatment can carry high morbidity and mortality. This book provides concise, easy-to-read, and up-to-date information as it relates to clinical presentation, diagnosis, and treatment of IPF. Despite, adequate treatment, the disease progresses, and a lung transplant is necessary in some cases. This book also discusses the role of lung transplants for IPF and its complications. It is a useful resource for primary care physicians, allied health professionals, hospitalists, and pulmonary physicians who take care of patients with IPF.


Teaching Pearls in Noninvasive Mechanical Ventilation

Teaching Pearls in Noninvasive Mechanical Ventilation
Author: Antonio M. Esquinas
Publisher: Springer Nature
Total Pages: 537
Release: 2022-02-01
Genre: Medical
ISBN: 3030712982

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This book uses real-world clinical case analyses of hot topics to provide insights into noninvasive mechanical ventilation (NIV). Written by leading international teachers and experts, it features a selection of “major controversial topics in clinical practice” and demonstrates how these cases can be used to teach about NIV. It then presents a discussion of the topics in various scenarios (anesthesiology, critical care, emergency, pneumology and sleep medicine, as well). The chapters allow readers to develop a case-by-case understanding of NIV in acute and chronic respiratory disorders, and perioperative and in intensive care patients, also thanks to Electronic Supplementary Materials. Lastly the authors summarize five key points / recommendations. This book is an attractive resource also for universities / educational seminars / national and international postgraduate courses and hot-topics sessions at national/international congresses.


Fibrosis

Fibrosis
Author: Laure Rittié
Publisher: Humana Press
Total Pages: 531
Release: 2017-07-27
Genre: Science
ISBN: 9781493971121

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This volume describes state-of-the-art protocols that serve as “recipes” for scientists concentrating on fibrosis research. This book is divided into four sections. Part I focuses on animal models of fibrosis and covers topics such as mimicking fibrosis in the lungs, skin, liver and heart, and generating transgenic mouse models. Part II discusses cell culture systems, where the chapters explore cell types important for the development of fibrosis. Part III looks at the purification, quantification, and analysis of the ECM proteins, and Part IV describes computer-assisted methods such as quantifying fibrillar collagen alignment and exploring the nano-surface of collagen with atomic force microscopy (AFM). Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. Cutting-edge and practical, Fibrosis: Methods and Protocols is a valuable resource aimed at outstanding quality and repeatability of research experiments in the fibrosis field.


Specialty Imaging: HRCT of the Lung E-Book

Specialty Imaging: HRCT of the Lung E-Book
Author: Santiago Martínez-Jiménez
Publisher: Elsevier Health Sciences
Total Pages: 600
Release: 2017-07-22
Genre: Medical
ISBN: 0323524958

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Part of the highly regarded Specialty Imaging series, this fully updated second edition by Drs. Santiago Martínez-Jiménez, Melissa L. Rosado-de-Christenson, and Brett W. Carter, reflects the many recent changes in HRCT diagnostic interpretation. An easy-to-read bulleted format and state of the art imaging examples guide you step-by-step through every aspect of thin-section CT and HRCT in the evaluation of patients with suspected lung disease. This book is an ideal resource for radiologists who need an easily accessible tool to help them understand the indications, strengths, and limitations of HRCT in their practice. Superb illustrations with comprehensive captions display both typical and variant findings on HRCT scans Introductory sections are specifically designed to lead the general radiologist to differential diagnoses from specific imaging findings, pathologic patterns, or from the disease/pathology itself Time-saving bulleted format distills essential information for fast and easy comprehension Updated content includes changes in HRCT interpretation and novel disease processes such as DIPNECH, new classification of idiopathic interstitial pneumonias, airway-centered interstitial fibrosis, light-chain deposition disease, and interstitial pneumonia with autoimmune features (IPAF) Fully revised throughout with new references, images, and histopathologic correlations