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Bronchiectasis

The EMBARC Manual

Format: Hardback
Publisher: Springer International Publishing AG, Cham, Switzerland
Published: 24th Jan 2018
Dimensions: w 155mm h 235mm
Weight: 839g
ISBN-10: 3319614517
ISBN-13: 9783319614519
Barcode No: 9783319614519
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Synopsis
This book presents state of the art knowledge and practice in the rapidly developing field of bronchiectasis not due to cystic fibrosis. The focus is especially on diagnosis and existing and emerging therapies, but the book also covers a wide range of other key topics, from pathophysiology, histopathology, and immunology through to pulmonary rehabilitation, nursing care, and management in primary care and pediatric settings. While non-cystic fibrosis bronchiectasis was formerly regarded as an "orphan" disease, international data reveal an increase in its prevalence in recent years. Accordingly, there has been renewed interest in the disease, resulting in more clinical research and the development of new treatments. The impact of bronchiectasis on healthcare systems is substantial and it has a clear attributable mortality. In covering all aspects of the disease, this book will be of interest to respiratory, internal medicine, and infectious disease fellows as well as specialists, final-year medical students, nurses and physiotherapists. The authors are leading experts and chairs of the steering committee of EMBARC, the first truly international bronchiectasis network.

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"This is excellently written book provides an up-to-date and concise summary of our current understanding of bronchiectasis as well as highlighting gaps in our knowledge and where we should target research efforts in the future. ... This is book will provide a valuable reference for health-care professionals looking for succinct, up-to-date information to help them holistically investigate and manage their patients with bronchiectasis." (J.K. Quin, British Journal of Hospital Medicine, Vol. 79 (6), June, 2018)

"This is a very useful book on the causes, diagnosis, and management of bronchiectasis not due to cystic fibrosis with an emphasis on the role of chronic infections in disease progression. This should be a welcome addition to the library of every pulmonologist who takes care of patients with this difficult disease." (Santosh Dhungana, Doody's Book Reviews, May, 2018)