Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis
Author: Keith C. Meyer,Steven D. Nathan
Publsiher: Springer Science & Business Media
Total Pages: 451
Release: 2013-10-16
Genre: Medical
ISBN: 9781627036825

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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
Publsiher: European Respiratory Society
Total Pages: 287
Release: 2016-03-01
Genre: Medical
ISBN: 9781849840682

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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.

Respiratory Health

Respiratory Health
Author: Mieczyslaw Pokorski
Publsiher: Springer
Total Pages: 114
Release: 2015-07-29
Genre: Medical
ISBN: 9783319187938

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The tracheobronchial tree is open to the environment surrounding the body. Respiration has thus the essential bearing on general morbidity, vulnerability to disease and immunity. Further, respiratory function shapes the neuropsychological responses to succumbing to disease, controls the mind-to-body interaction and sets the perception of quality of life. The chapters of this book deal with the preventable drivers of poor respiratory health, the role of health information technology, the improvement in health care delivery and the integration of respiratory health and behavioral health services. Innovative strategies to promote prevention, care coordination and care integration as well as to align disease acceptance and quality of life measures also are tackled. Maintaining respiratory health is of rising research interest as a way of preventing a disease or a non pharmacological therapeutic succor. The book will be of interest to clinicians, family practitioners and medical researchers.

Interstitial Lung Disease E Book

Interstitial Lung Disease E Book
Author: Harold R Collard,Luca Richeldi
Publsiher: Elsevier Health Sciences
Total Pages: 204
Release: 2017-02-18
Genre: Medical
ISBN: 9780323480253

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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.

Guide to Clinical Management of Idiopathic Pulmonary Fibrosis

Guide to Clinical Management of Idiopathic Pulmonary Fibrosis
Author: Steven D Nathan,A Whitney Brown,Christopher S King
Publsiher: Springer
Total Pages: 123
Release: 2016-07-27
Genre: Medical
ISBN: 9783319327945

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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.

Evidence Based Critical Care

Evidence Based Critical Care
Author: Robert C. Hyzy
Publsiher: Springer
Total Pages: 805
Release: 2017-05-30
Genre: Medical
ISBN: 9783319433417

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This book provides learners with a unique opportunity by virtue of the format outlined above. Each case presentation has a case vignette, which leads up to an important clinical question, and is followed by additional discussion which resolves the question posed. This is a new way to present knowledge in a medical book and should help critical care practitioners, fellows, residents, allied health professionals and students expand their critical care knowledge in an efficient and effective manner. This approach should also benefit those preparing for board examinations.

Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis
Author: Joseph P. Lynch
Publsiher: CRC Press
Total Pages: 800
Release: 2003-12-18
Genre: Medical
ISBN: 9780203913444

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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.

Diffuse Lung Disease

Diffuse Lung Disease
Author: Robert P. Baughman,Roland M. du Bois
Publsiher: Springer Science & Business Media
Total Pages: 400
Release: 2011-11-04
Genre: Medical
ISBN: 9781441997715

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Interstitial lung diseases comprise a significant part of any respiratory medicine practice. This timely second edition of Diffuse Lung Disease is a practical clinically-oriented resource, covering all the major advances in diagnostic techniques and therapies. Authored by world authorities in the field, this book provides clear and specific recommendations for the management of all forms of interstitial lung diseases. This book is divided into two sections. The first section addresses the general aspects of diagnosis and management, including clinical approach, radiographic approach, physiological changes, and classification. The second section details each individual form of interstitial lung disease. Organized in an easy to follow format, each disease specific chapter includes tables outlining diagnostic approach, differential diagnosis, disease monitoring, and treatment. Illustrative cases, replete with high quality HRCT images, bring an added dimension to this outstanding book.

Cystic and Idiopathic Pulmonary Fibrosis

Cystic and Idiopathic Pulmonary Fibrosis
Author: Lorenzo Robertson
Publsiher: Unknown
Total Pages: 175
Release: 2016-09-01
Genre: Electronic Book
ISBN: 1634855086

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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.

Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis
Author: Jeffrey Swigris,Kevin K Brown
Publsiher: Elsevier Health Sciences
Total Pages: 350
Release: 2018-07-25
Genre: Medical
ISBN: 9780323544320

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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 New Insights for the Healthcare Professional 2011 Edition

Idiopathic Pulmonary Fibrosis  New Insights for the Healthcare Professional  2011 Edition
Author: Anonim
Publsiher: ScholarlyEditions
Total Pages: 22
Release: 2012-01-09
Genre: Medical
ISBN: 9781464911170

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Idiopathic Pulmonary Fibrosis: New Insights for the Healthcare Professional: 2011 Edition is a ScholarlyPaper™ that delivers timely, authoritative, and intensively focused information about Idiopathic Pulmonary Fibrosis in a compact format. The editors have built Idiopathic Pulmonary Fibrosis: New Insights for the Healthcare Professional: 2011 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Idiopathic Pulmonary Fibrosis in this eBook 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: 2011 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/.

Difficult to Diagnose Rare Diffuse Lung Disease

Difficult to Diagnose Rare Diffuse Lung Disease
Author: Alexander V. Averyanov
Publsiher: Academic Press
Total Pages: 430
Release: 2019-08-24
Genre: Science
ISBN: 9780128153765

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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

Clinical Handbook of Interstitial Lung Disease

Clinical Handbook of Interstitial Lung Disease
Author: Muhunthan Thillai,David R. Moller,Keith C. Meyer
Publsiher: CRC Press
Total Pages: 529
Release: 2017-11-03
Genre: Medical
ISBN: 9781351650083

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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.

Diseases of the Chest Breast Heart and Vessels 2019 2022

Diseases of the Chest  Breast  Heart and Vessels 2019 2022
Author: Juerg Hodler,Rahel A. Kubik-Huch,Gustav K. von Schulthess
Publsiher: Springer
Total Pages: 238
Release: 2019-02-19
Genre: Medical
ISBN: 9783030111496

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This open access book focuses on diagnostic and interventional imaging of the chest, breast, heart, and vessels. It consists of a remarkable collection of contributions authored by internationally respected experts, featuring the most recent diagnostic developments and technological advances with a highly didactical approach. The chapters are disease-oriented and cover all the relevant imaging modalities, including standard radiography, CT, nuclear medicine with PET, ultrasound and magnetic resonance imaging, as well as imaging-guided interventions. As such, it presents a comprehensive review of current knowledge on imaging of the heart and chest, as well as thoracic interventions and a selection of "hot topics". The book is intended for radiologists, however, it is also of interest to clinicians in oncology, cardiology, and pulmonology.

Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis
Author: Hiroyuki Nakamura,Kazutetsu Aoshiba
Publsiher: Springer
Total Pages: 259
Release: 2015-09-28
Genre: Medical
ISBN: 9784431555827

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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.