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Cystic fibrosis, a genetic disorder in children and young adults, is a multisystemic disease that mainly affects the lungs. Advances and improvements in the diagnosis and management of this condition have led to increased overall and symptom-free survival in cystic fibrosis patients. This book examines recent advances in the field and presents an evidence-based approach to the management of cystic fibrosis.
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Cystic fibrosis --- Cystic Fibrosis --- Cystic Fibrosis --- diagnosis --- therapy
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Idiopathic pulmonary fibrosis (IPF) affects 13-20 people per 100,000 population worldwide. In the United States, approximately 100,000 people have IPF with 30,000-40,000 new cases diagnosed annually. Diagnosis remains a challenge with a significant lag between symptoms onset and diagnosis. Delayed diagnosis and treatment can carry high morbidity and mortality. This book provides concise, easy-to-read, and up-to-date information as it relates to clinical presentation, diagnosis, and treatment of IPF. Despite, adequate treatment, the disease progresses, and a lung transplant is necessary in some cases. This book also discusses the role of lung transplants for IPF and its complications. It is a useful resource for primary care physicians, allied health professionals, hospitalists, and pulmonary physicians who take care of patients with IPF.
Pulmonary fibrosis. --- Pulmonary fibrosis --- Immunological aspects.
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