January 25, 2021

Download Ebook Free Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis
Author : Jeffrey Swigris,Kevin K Brown
Publisher : Elsevier Health Sciences
Release Date : 2018-07-25
Category : Medical
Total pages :350
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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 : Keith C. Meyer,Steven D. Nathan
Publisher : Springer Science & Business Media
Release Date : 2013-10-16
Category : Medical
Total pages :451
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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 : Ulrich Costabel,Bruno Crestani,Athol U. Wells
Publisher : European Respiratory Society
Release Date : 2016-03-01
Category : Medical
Total pages :287
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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.

Clinical Handbook of Interstitial Lung Disease

Clinical Handbook of Interstitial Lung Disease
Author : Muhunthan Thillai,David R. Moller,Keith C. Meyer
Publisher : CRC Press
Release Date : 2017-11-03
Category : Medical
Total pages :529
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This handbook provides clinical guidance to the practicing physician on the diagnosis and treatment of Interstitial Lung Diseases (ILD). A contributed work with invited chapters which draw on the knowledge and experience of recognised global leaders in respiratory medicine, it is authoritative, concise and portable and is intended for use in a fast-paced clinical setting. The book: offers practical tips and clear guidance for clinicians provides detailed explanations of the main therapeutic options for each individual ILD contains high-quality visuals, including radiology and histopathology of the most common as well as some of the rarer ILDs discusses individual ILDs and has topics common to all including critical care, lung transplantation and palliative care navigates clinicians through cases with decision making guidelines and algorithms includes appendices with international practice guidelines, sample patient information sheets and other helpful resources. Emphasizing how to perform a thorough assessment of an ILD patient for accurate diagnosis and their subsequent effective management, this is both a gold standard text as well as a daily companion for physicians caring for ILD patients. A first-of-its-kind, it will become the go-to guide for all clinicians who manage patients with ILD.

Interstitial Lung Disease

Interstitial Lung Disease
Author : Marvin I. Schwarz,Talmadge E. King
Publisher : PMPH-USA
Release Date : 2011
Category : Medical
Total pages :1161
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Deals with interstitial lung diseases and includes clinical, pathologic, radiologic and physiologic evaluation of the patient with ILD. This book covers a wide array of disorders, sarcoidosis, asbestosis, hypersensitivity pneumonitis, drug induced lung disease, connective tissue disease and pulmonary vasculitis, to name but a few.

Idiopathic pulmonary fibrosis

Idiopathic pulmonary fibrosis
Author : Sics Editore
Publisher : SICS Editore
Release Date : 2014-10-01
Category : Medical
Total pages :129
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Cystic and Idiopathic Pulmonary Fibrosis

Cystic and Idiopathic Pulmonary Fibrosis
Author : Lorenzo Robertson
Publisher : Unknown
Release Date : 2016-09-01
Category :
Total pages :175
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Cystic fibrosis (CF) is one of the most common autosomal recessive disorders in the Caucasian population with an estimated incidence of 1 in 2,500 childbirths. While this disease affects several organ systems of the body, morbidity and mortality is chiefly related to the extent of pulmonary involvement. Idiopathic pulmonary fibrosis (IPF) is the most common idiopathic interstitial disease of the lung of unknown etiology with a median survival time of about 3 years. IPF occurs mainly in men older than 60 years who have comorbidities such as pulmonary hypertension, COPD, lung cancer, gastro-esophageal reflux, ischemic heart disease and obstructive sleep apnoea. This book provides current research on risk factors of CF and IPF, as well as management options and long-term health outcomes of the disorders.

Acoustic Measures in Idiopathic Pulmonary Fibrosis

Acoustic Measures in Idiopathic Pulmonary Fibrosis
Author : Angela Lucy Key
Publisher : Unknown
Release Date : 2014
Category :
Total pages :129
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Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis
Author : Joseph P. Lynch
Publisher : CRC Press
Release Date : 2003-12-18
Category : Medical
Total pages :800
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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.

Treatment of Cystic Fibrosis and Other Rare Lung Diseases

Treatment of Cystic Fibrosis and Other Rare Lung Diseases
Author : Arata Azuma,Michael S. Schechter
Publisher : Springer
Release Date : 2017-01-28
Category : Medical
Total pages :263
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This volume describes the pathogenesis and pathophysiology of several pulmonary diseases as well as their treatment. It also discusses the underlying genetic and molecular biological basis, which opens the way for new treatments for these conditions. It focuses on the treatment of cystic fibrosis including CFTR (cystic fibrosis transmembrane-conductance regulator) modulator therapies, drug therapies that augment airway surface liquid as well as anti-inflammatory and anti-infective therapies. Further topics include long-term, low-dose macrolide therapy for diffuse panbronchiolitis; novel agents for previously untreatable idiopathic pulmonary fibrosis; possible new treatments for pulmonary alveolar proteinosis (PAP); and multiple novel therapeutic targets for treating lymphangiomyomatosis. Research into these conditions has led to major advances in our understanding of the underlying genetic and molecular basis of this disease, and to dramatic improvements in survival and quality of life for affected individuals.

Mayo Clinic Guide to Arthritis

Mayo Clinic Guide to Arthritis
Author : Lynne S. Peterson
Publisher : Rosetta Books
Release Date : 2020-09-08
Category : Health & Fitness
Total pages :543
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From the doctors at Mayo Clinic, the top-ranked hospital in the U.S., this book is a complete guide to understanding and living with arthritis. Find the latest expertise on various forms of arthritis, medications and other treatment options, and self care to successfully manage joint pain and continue an active life. If you have joint pain, you know it can lead to frustrating limitations in daily life. In fact, arthritis is the most common cause of disability in the United States. This complex group of joint diseases _x2014_ osteoarthritis, rheumatoid arthritis and many other forms _x2014_ affects at least 54 million Americans. But living with arthritis doesn’t have to mean sitting on the sidelines. Understanding the cause of your joint pain is key to finding relief. This book offers the same expert knowledge that Mayo Clinic doctors, nurses and therapists use in caring for patients. Gain a better grasp of how arthritis works, discover the latest advances in treatment options, and find out how activity, your diet, work and daily habits play a role in managing the disease. These tools can help you take control of joint pain to live more comfortably and get back to the activities you love. Mayo Clinic Guide to Arthritis is divided into three parts: Part 1 breaks down different forms of arthritis and joint pain to help you understand their causes, their signs and symptoms, and what each may mean for your health. Part 2 explores the latest in arthritis treatments, including new medications to slow or stop the disease, improved options for joint surgery, joint injections, and evidence-based guidance on pain control and integrative medicine. Part 3 provides practical tips for living with arthritis. Chapters focus on staying active, eating a healthy diet, caring for your mental health, protecting your joints, traveling and working.

Difficult to Diagnose Rare Diffuse Lung Disease

Difficult to Diagnose Rare Diffuse Lung Disease
Author : Alexander V. Averyanov
Publisher : Academic Press
Release Date : 2019-08-24
Category : Science
Total pages :430
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Difficult to Diagnose Rare Diffuse Lung Disease presents the theoretical basis and practical aspects of differential diagnoses of rare lung diseases with the use of new method of probe-based confocal laser endomicroscopy (alveoscopy) of the distal respiratory region. Each chapter describes signs and symptoms of the disease and its typical and atypical manifestations. The book contains full color illustrations, including high-resolution histological microphotographs, CT-scans and confocal laser endomicroscopy images. In combination, these elements make this book an invaluable reference and guide for pulmonary researchers, pulmonologists, radiologists, and pathologists who wish to broaden their spectrum of knowledge in rare lung diseases. Highlights the new method of probe-based confocal laser endomicroscopy (alveoscopy) of the distal respiratory region, opening new horizons in the minimally invasive diagnosis of lung diseases Discusses current treatment strategies in accordance with clinical guidelines, including data from the latest clinical trials Presented in tabular format to aid in the diagnostic process

Diffuse Parenchymal Lung Disease

Diffuse Parenchymal Lung Disease
Author : Ulrich Costabel,Roland M. Du Bois,Jim J. Egan
Publisher : Karger Medical and Scientific Publishers
Release Date : 2007-01-01
Category : Medical
Total pages :348
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Diffuse parenchymal lung disease (DPLD) represents a large and heterogeneous group of disorders. Although new insights into the pathogenesis and new techniques such as high-resolution-CT have led to a better understanding of DPLD, clinical management remains a challenge. This volume is designed to become a valuable aid in the diagnosis and management of DPLD. It starts with general topics such as a new classification system for DPLD, the general diagnostic approach, and clinical evaluation of the patient by radiology, histological patterns and bronchoalveolar lavage. This is followed by consideration of some basic aspects such as the genetics of DPLD, the principles of granuloma formation, pulmonary fibrogenesis and vasculitis, as well as novel treatment approaches. A large part of the book consists of disease-specific chapters, which discuss granulomatous disorders, idiopathic pulmonary fibrosis and other entities of idiopathic interstitial pneumonia, the collagen vascular diseases, drug-induced infiltrative lung disease as well as orphan diffuse lung diseases including Langerhans' cell histiocytosis, lymphangioleiomyomatosis and pulmonary alveolar proteinosis. Special chapters on DPLD in children and lung transplantation for end-stage fibrosis complete this comprehensive publication. Written by internationally known experts, this well-organized volume is recommended to a wide audience including respiratory physicians in training, practice and research as well as radiologists and pulmonary pathologists.

Pulmonary Manifestations of Systemic Diseases

Pulmonary Manifestations of Systemic Diseases
Author : Wim A. Wuyts,Vincent Cottin,Paolo Spagnolo,Athol U. Wells
Publisher : European Respiratory Society
Release Date : 2019-12-01
Category : Medical
Total pages :432
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This Monograph provides expert clinical guidance on these difficult diseases, which will be helpful to both respiratory and nonrespiratory physicians alike. The initial chapters consider diagnostic issues, pulmonary function tests and techniques that are currently in development. The book then goes on to cover a variety of pulmonary manifestations of very different disease entities, such as connective tissue diseases, systemic vasculitis and much more.

Specialty Imaging: HRCT of the Lung E-Book

Specialty Imaging: HRCT of the Lung E-Book
Author : Santiago Martínez-Jiménez,Melissa L. Rosado-de-Christenson,Brett W. Carter
Publisher : Elsevier Health Sciences
Release Date : 2017-07-22
Category : Medical
Total pages :600
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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