Cystic & Idiopathic Pulmonary Fibrosis : Risk Factors, Management & Long-Term Health Outcomes
Book Details
Format
Hardback or Cased Book
ISBN-10
1634855086
ISBN-13
9781634855082
Publisher
Nova Science Publishers Inc
Imprint
Nova Science Publishers Inc
Country of Manufacture
US
Country of Publication
GB
Publication Date
Sep 1st, 2016
Print length
175 Pages
Weight
406 grams
Dimensions
23.20 x 16.00 x 2.10 cms
Product Classification:
Medical administration & managementRespiratory medicine
Ksh 33,500.00
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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.
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