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...
Gespeichert in:
| Weitere Verfasser: | , |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
London
InTechOpen
2022
|
| Online-Zugang: | URL des Erstveröffentlichers |
| Zusammenfassung: | 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. |
| Beschreibung: | 1 Online-Ressource (218 Seiten) |
| ISBN: | 9781839692406 9781839692413 |
| DOI: | 10.5772/intechopen.87624 |
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| 520 | |a 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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| illustrated | Not Illustrated |
| index_date | 2024-07-03T21:08:48Z |
| indexdate | 2025-01-22T04:01:17Z |
| institution | BVB |
| isbn | 9781839692406 9781839692413 |
| language | English |
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| spellingShingle | Idiopathic Pulmonary Fibrosis |
| title | Idiopathic Pulmonary Fibrosis |
| title_auth | Idiopathic Pulmonary Fibrosis |
| title_exact_search | Idiopathic Pulmonary Fibrosis |
| title_exact_search_txtP | Idiopathic Pulmonary Fibrosis |
| title_full | Idiopathic Pulmonary Fibrosis edited by Salim Surani, Venkat Rajasurya |
| title_fullStr | Idiopathic Pulmonary Fibrosis edited by Salim Surani, Venkat Rajasurya |
| title_full_unstemmed | Idiopathic Pulmonary Fibrosis edited by Salim Surani, Venkat Rajasurya |
| title_short | Idiopathic Pulmonary Fibrosis |
| title_sort | idiopathic pulmonary fibrosis |
| url | https://doi.org/10.5772/intechopen.87624 |
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