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Pulmonary Arterial Hypertension and Interstitial Lung Diseases

Pulmonary Arterial Hypertension and Interstitial Lung Diseases
Author: Robert P. Baughman
Publisher: Springer Science & Business Media
Total Pages: 255
Release: 2009-01-01
Genre: Medical
ISBN: 1603270744

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Interstitial lung disease (ILD) is a broad category of lung diseases that includes more than 150 disorders characterized by scarring or fibrosis of the lungs. In Pulmonary Arterial Hypertension and Interstitial Lung Disease: A Clinical Guide, renowned experts provide a state-of-the-art overview of the problems seen by physicians in the clinical management of ILDs. Divided into two sections, the first part provides and update on general issues and introduces both interstitial lung disease and associated pulmonary hypertension. A detailed analysis of the pathology of the various interstitial lung diseases is also provided. The second part addresses specific categories of disease. Bronchiolitis, hypersensitivity pneumonitis, and other conditions are covered, and the use of inspiratory and expiratory high resolution CT scan is discussed as well. This important new text is an invaluable resource for the practicing physician who must be aware of the broad and troubling manifestations of interstitial lung disease.


Pulmonary Hypertension and Interstitial Lung Disease

Pulmonary Hypertension and Interstitial Lung Disease
Author: Robert P. Baughman
Publisher: Springer
Total Pages: 216
Release: 2017-08-17
Genre: Medical
ISBN: 3319499181

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The first edition of this book, published in 2009, was the only book of its kind dedicated exclusively to the diagnosis and management of pulmonary arterial hypertension (PAH) in patients with interstitial lung disease (ILD). Over the past few years, new diagnostic tests and treatments of pulmonary arterial hypertension have been developed and tested. Diagnostic testing has led to more frequent and specific diagnosis in PAH patients, leading to the more widespread use of effective treatment and improved quality of life and reduction of mortality for PAH patients. Pulmonary Hypertension and Interstitial Lung Disease: A Clinical Guide, Second Edition provides an updated and expanded state-of-the-art overview of the problems seen by physicians in the clinical management of ILDs. The first section of the book discusses general features and includes an overview of clinical features, diagnosis and pathology of ILD. The second part discusses specific disorders such as idiopathic pulmonary fibrosis, sarcoidosis, and hypersensitivity pneumonia. Pulmonary Hypertension and Interstitial Lung Disease, Second Edition is an invaluable resource for all physicians whose practice involves the care and treatment of patients with interstitial lung disease.


Pulmonary Arterial Hypertension and Interstitial Lung Diseases

Pulmonary Arterial Hypertension and Interstitial Lung Diseases
Author: Robert P. Baughman
Publisher: Humana Press
Total Pages: 248
Release: 2009-03-02
Genre: Medical
ISBN: 9781603278904

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Interstitial lung disease (ILD) is a broad category of lung diseases that includes more than 150 disorders characterized by scarring or fibrosis of the lungs. In Pulmonary Arterial Hypertension and Interstitial Lung Disease: A Clinical Guide, renowned experts provide a state-of-the-art overview of the problems seen by physicians in the clinical management of ILDs. Divided into two sections, the first part provides and update on general issues and introduces both interstitial lung disease and associated pulmonary hypertension. A detailed analysis of the pathology of the various interstitial lung diseases is also provided. The second part addresses specific categories of disease. Bronchiolitis, hypersensitivity pneumonitis, and other conditions are covered, and the use of inspiratory and expiratory high resolution CT scan is discussed as well. This important new text is an invaluable resource for the practicing physician who must be aware of the broad and troubling manifestations of interstitial lung disease.


Cardiovascular Disability

Cardiovascular Disability
Author: Institute of Medicine
Publisher: National Academies Press
Total Pages: 304
Release: 2010-12-04
Genre: Medical
ISBN: 030915698X

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The Social Security Administration (SSA) uses a screening tool called the Listing of Impairments to identify claimants who are so severely impaired that they cannot work at all and thus immediately qualify for benefits. In this report, the IOM makes several recommendations for improving SSA's capacity to determine disability benefits more quickly and efficiently using the Listings.


Pulmonary Hypertension: Mechanisms and Management, History and Future

Pulmonary Hypertension: Mechanisms and Management, History and Future
Author: A. A. Roger Thompson
Publisher: Frontiers Media SA
Total Pages: 92
Release: 2020-06-15
Genre:
ISBN: 2889637905

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We are grateful for the support of Actelion – a sponsor of this Research Topic – whose cooperation has contributed to fostering scientific discovery by reducing article publishing costs for some authors. We hereby state publicly that Actelion has had no editorial input in articles included in this research topic, thus ensuring that all aspects of this Research Topic were evaluated objectively, unbiased by any specific policy or opinion of Actelion. Actelion is part of the Johnson & Johnson Family of Companies. We are leaders in the science and medicine of pulmonary arterial hypertension (PAH), with over 15 years of experience in this devastating cardiovascular disorder.


Pulmonary hypertension

Pulmonary hypertension
Author: Sics Editore
Publisher: SICS Editore
Total Pages: 45
Release: 2014-10-01
Genre: Medical
ISBN: 8869300552

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Pulmonary hypertension (PH) denotes a state where the mean pulmonary artery pressure is 25 mmHg or higher (measured invasively via right heart catheterisation in specialist medical care). In clinical practice, echocardiography is used as a screening tool because it provides the means to indirectly estimate the pressure within the pulmonary arteries. The most common causes of increased pulmonary blood pressure are problems related to the left side of the heart (such as ventricular failure and valvular defects) and hypoxaemia caused either by lung disease or other conditions (such as COPD, pulmonary fibrosis and sleep apnoea). In these situations the increase in pulmonary blood pressure is a secondary haemodynamic phenomenon and, according to current understanding, it only plays a minor role as far as the management of the condition is concerned. At present, no evidence exists on the benefit of PH medication in the treatment of these conditions. Pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH) are markedly rarer causes of PH, and in these conditions both pulmonary blood pressure and pulmonary vascular resistance play a major role. The principal mechanism behind PAH is an endothelial dysfunction in the small pulmonary arteries leading to an imbalance between vasoactive mediators (e.g. prostacycline, nitrous oxide and endothelin), which are responsible for the dilatation and constriction of the vessels as well as for enhancing or inhibiting vascular proliferation. Promising new drugs have been introduced during the last few years for the treatment of PAH, which improve the patient’s functional capacity and probably also the prognosis. The investigations of PH are always carried out in specialist medical care, and the diagnosis and treatment of PAH and CTEPH should be concentrated in specialist centres.


Lung Diseases—Advances in Research and Treatment: 2013 Edition

Lung Diseases—Advances in Research and Treatment: 2013 Edition
Author:
Publisher: ScholarlyEditions
Total Pages: 186
Release: 2013-06-21
Genre: Medical
ISBN: 1481677330

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Lung Diseases—Advances in Research and Treatment: 2013 Edition is a ScholarlyEditions™ book that delivers timely, authoritative, and comprehensive information about Pulmonary Fibrosis. The editors have built Lung Diseases—Advances in Research and Treatment: 2013 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Pulmonary Fibrosis 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 Lung Diseases—Advances in Research and Treatment: 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/.


Clinical Focus Series

Clinical Focus Series
Author: Om P. Sharma
Publisher: JAYPEE BROTHERS PUBLISHERS
Total Pages: 514
Release: 2012-12-15
Genre: Medical
ISBN: 9350259796

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The purpose of this book is to provide medical students, postgraduate fellows, general practitioners and specialists a succinct, easy to read, well-illustrated and comprehensive review of interstitial disorders encountered in clinical practice. Authored by a team of internationally recognized experts, the chapters cover different aspects of these complex maladies and suggest plans for effective management of patients with diffuse parenchymal disease. The book opens with a brief historical account followed by physiological and radiological features of interstitial lung diseases. Each concise ch.


Pulmonary Hypertension

Pulmonary Hypertension
Author: H. James Ford
Publisher: Springer Nature
Total Pages: 206
Release: 2020-10-13
Genre: Medical
ISBN: 3030527875

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This book is a clinical guide to controversial and emerging topics in pulmonary hypertension. There are multiple challenges and unanswered questions encountered by clinicians that evaluate, diagnose and treat patients with suspected or confirmed pulmonary vascular disease. This book provides a deep dive into the diagnosis and therapeutics of pulmonary hypertension supported by the literature and balanced with personal clinical experience. Expert authors have chosen these specific topics to address issues where uncertainty and/or controversy exists as well as highlight areas that are just being incorporated into clinical practice. These topics include: exercise pulmonary hypertension, sickle cell disease and pulmonary hypertension, and sarcoid pulmonary hypertension, among many others. Chapters address the diagnostic and treatment dilemmas posed by these various clinical entities through literature review, sharing of expert opinion, and review of recent guidelines and their applicability to the multiple different nuanced presentations of pulmonary hypertension. This is an ideal guide for pulmonologists, cardiologists, and other specialty practitioners caring for patients with pulmonary hypertension.


Palliative Care in Lung Disease

Palliative Care in Lung Disease
Author: Kathleen O. Lindell
Publisher: Humana
Total Pages: 0
Release: 2022-10-16
Genre: Medical
ISBN: 9783030817909

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This book details the benefits of palliative care to improve the lives of patients with serious lung disease and their caregivers. Palliative care is specialized medical care for people living with a serious illness. This type of care is focused on providing relief from the symptoms and stress of a serious illness, and is often described as “an extra layer of support” for patients and their caregivers, as patients with malignant and nonmalignant lung disease experience great symptom burden and have advanced care planning needs. This book has three main objectives: Define the role of palliative care in advanced lung disease Incorporate a patient-centered perspective in describing symptom burden and interventions to improve quality of life Provide current initiatives to expand evidence-based practice and improve access to palliative care Written by leading experts in palliative care and respiratory medicine, the chapters seek to answer those objectives by first defining and describing palliative care, advanced lung disease, and inadequate palliative care in this patient population. Patient reported outcomes, quality of life, and interventions to help deal with the psychological toll of serious illness are then detailed, as well as pharmacological and non-pharmacological interventions for symptom management. Detailed information is additionally provided on current research studies and management for several lung diseases, including COPD, ILD, Lung Cancer, Pulmonary Arterial Hypertension, Neuromuscular disease, and pediatric lung disease. The more administrative aspects of palliative care programs are then covered with an example of a specialty palliative care program for advanced lung disease and advice on how to address policy that promotes palliative care. Finally, palliative care's role during a pandemic is thoughtfully considered. This book is an ideal guide for clinicians, nurses, hospital administrators, teachers, students to help them understand and fill unmet care needs that many patients with serious lung disease experience.