Idiopathic Pulmonary Fibrosis
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 d...
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| Autres auteurs: | , |
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| Format: | Électronique Chapitre de livre |
| Langue: | anglais |
| Publié: |
IntechOpen
2022
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| Sujets: | |
| Accès en ligne: | DOAB: download the publication DOAB: description of the publication |
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| Résumé: | 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. |
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| Description matérielle: | 1 electronic resource (218 p.) |
| ISBN: | intechopen.87624 9781839692406 9781839692390 9781839692413 |
| Accès: | Open Access |