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Guide to Clinical Management of Idiopathic Pulmonary Fibrosis

2016-07-27 Medical
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Release : 2016-07-27
Genre : Medical
Kind : eBook
Book Rating : 941/5 ( reviews)

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Book Synopsis Guide to Clinical Management of Idiopathic Pulmonary Fibrosis by : Steven D Nathan

Download or read book Guide to Clinical Management of Idiopathic Pulmonary Fibrosis written by Steven D Nathan. This book was released on 2016-07-27. Available in PDF, EPUB and Kindle. Book excerpt: 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

2013-10-16 Medical
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Release : 2013-10-16
Genre : Medical
Kind : eBook
Book Rating : 822/5 ( reviews)

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Book Synopsis Idiopathic Pulmonary Fibrosis by : Keith C. Meyer

Download or read book Idiopathic Pulmonary Fibrosis written by Keith C. Meyer. This book was released on 2013-10-16. Available in PDF, EPUB and Kindle. Book excerpt: 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.

Clinical Handbook of Interstitial Lung Disease

2017-11-03 Medical
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Release : 2017-11-03
Genre : Medical
Kind : eBook
Book Rating : 084/5 ( reviews)

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Book Synopsis Clinical Handbook of Interstitial Lung Disease by : Muhunthan Thillai

Download or read book Clinical Handbook of Interstitial Lung Disease written by Muhunthan Thillai. This book was released on 2017-11-03. Available in PDF, EPUB and Kindle. Book excerpt: 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.

Idiopathic Pulmonary Fibrosis

2016-03-01 Medical
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Release : 2016-03-01
Genre : Medical
Kind : eBook
Book Rating : 687/5 ( reviews)

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Book Synopsis Idiopathic Pulmonary Fibrosis by : Ulrich Costabel

Download or read book Idiopathic Pulmonary Fibrosis written by Ulrich Costabel. This book was released on 2016-03-01. Available in PDF, EPUB and Kindle. Book excerpt: 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.

Diagnosis and Management of Suspected

2013
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Release : 2013
Genre :
Kind : eBook
Book Rating : /5 ( reviews)

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Book Synopsis Diagnosis and Management of Suspected by : National Clinical Guideline Centre for Acute and Chronic Conditions (Great Britain)

Download or read book Diagnosis and Management of Suspected written by National Clinical Guideline Centre for Acute and Chronic Conditions (Great Britain). This book was released on 2013. Available in PDF, EPUB and Kindle. Book excerpt: Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive fibrotic interstitial lung disease (ILD) of unknown origin. It is a difficult disease to diagnose and often requires the collaborative expertise of a chest physician, radiologist and histopathologist to reach a consensus diagnosis. Most people with idiopathic pulmonary fibrosis experience symptoms of breathlessness, which may initially be only on exertion. Cough, with or without sputum is a common symptom. Over time, these symptoms are associated with a decline in lung function, reduced quality of life and ultimately death. Specific pharmacological therapies for IPF are limited but the last decade has seen more trials of new drugs which have had a variable impact on clinical practice. A number of difficulties arise when undertaking clinical trials in IPF in terms of defining precise, diagnostic inclusion criteria and clinically meaningful end-points. However, such trials are the only way by which promising new treatments will come to benefit patients. Furthermore, it is only by performing rigorous clinical trials, we have learned that drugs once widely used to treat IPF may in fact have been harmful. The limitations of current pharmacological therapies for IPF highlight the importance of other forms of treatment including lung transplantation and best supportive care such as oxygen therapy, pulmonary rehabilitation and palliation of symptoms. These are interventions which justifiably require scrutiny in the context of healthcare delivery by the modern NHS. Despite the significant burden of disease caused by IPF, there is currently no established framework within the NHS for its diagnosis and management thus creating an environment in which significant variations in clinical care may occur. In recognition of this, the Department of Health commissioned the National Institute of Health and Care Excellence (NICE) to produce a guideline aimed at improving the care of people with IPF.

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