Idiopathic Pulmonary Fibrosis

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Idiopathic Pulmonary Fibrosis is a groundbreaking book designed to provide pulmonary and internal medicine clinicians and healthcare professionals with a comprehensive understanding of this complex lung disease. Idiopathic pulmonary fibrosis is a chronic and progressive interstitial lung disease characterized by the scarring of lung tissue, leading to difficulty breathing and decreased lung function. Despite its [...]

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Work TypeMonograph
Internal ReferenceNBL76
Edition1
DOIhttps://doi.org/10.69860/nobel.9786053359517
ISBN978-605-335-951-7 (PAPERBACK)
Page Count152
Print Lenght152
PlaceIstanbul
Copyright HolderNobel Tıp Kitabevleri
Licensehttps://nobelpub.com/publish-with-us/copyright-and-licensing
BICMJL
BISACMED079000
THEMAMJL
Idiopathic Pulmonary Fibrosis is a groundbreaking book designed to provide pulmonary and internal medicine clinicians and healthcare professionals with a comprehensive understanding of this complex lung disease. Idiopathic pulmonary fibrosis is a chronic and progressive interstitial lung disease characterized by the scarring of lung tissue, leading to difficulty breathing and decreased lung function. Despite its significant impact on quality of life and prognosis, idiopathic pulmonary fibrosis remains poorly understood by many. In this book, clinicians will embark on a journey through the intricacies of idiopathic pulmonary fibrosis from its underlying causes to its clinical manifestations, diagnosis, treatment options, complications, and treatment options in special conditions. Written in accessible language, the book aims to demystify the disease while empowering individuals affected by idiopathic pulmonary fibrosis to actively participate in their care journey.
Key topics covered in idiopathic pulmonary fibrosis include Pathophysiology and Etiology: Explore the underlying mechanisms driving the development and progression of IPF, including genetic predispositions, environmental factors, and immune dysregulation. Clinical Presentation: Learn to recognize the signs and symptoms of idiopathic pulmonary fibrosis, including progressive dyspnea, dry cough, fatigue, and unexplained weight loss, and understand the importance of early detection and timely intervention.
Diagnostic Approaches: gain insights into the various diagnostic modalities used to confirm idiopathic pulmonary fibrosis, including high-resolution computed tomography (HRCT), pulmonary function tests (PFTs), bronchoscopy, and surgical lung biopsy, as well as the importance of multidisciplinary collaboration in reaching an accurate diagnosis.
Treatment Strategies: explore the current standards of care for idiopathic pulmonary fibrosis, including pharmacological interventions such as antifibrotic medications and immunosuppressive therapies, as well as non-pharmacological approaches such as pulmonary rehabilitation, supplemental oxygen therapy, and lung transplantation. Disease Management: Receive practical guidance on managing the symptoms and complications of IPF, optimizing respiratory function, promoting physical and emotional well-being, and navigating the challenges of living with a chronic lung condition. The chapter idippathic pulmonary fibrosis in special conditions comprises the treatment approaches in the elderley and the pregnant patinets.
1. Introduction
2. Definition and Overview
3. Epidemiology
4. Etiology and Risk Factors
5. Pathogenesis
6. Pathology
7. Genetic Phenotypes of Idiopathic Pulmonary Fibrosis
8. Clinical Manifestations
9. Physical Examination
10. Radiological Features
11. Laboratory and Pulmonary Function Tests
12. Diagnosis
13. Pharmacological Treatment
14. Non-Pharmacological Treatment
15. Complications and Prognosis
16. Special Considerations in Idiopathic Pulmonary Fibrosis

    Cuneyt Tetikkurt (Author)
    Department of Pulmonary Pulmonary Diseases, Istanbul Cerrahpasa University
    https://orcid.org/0000-0002-4122-2908
    3Doctor of Medicine (MD): Istanbul Medical Faculty, Istanbul University, 1984 Residency in Internal Medicine: Pulmonary Diseases Department, Istanbul Medical Faculty, Istanbul University, 1990 Fellowship in Pulmonary Medicine: Pulmonary Diseases Department, Istanbul Medical Faculty, Istanbul University, 1990-1993 Academic career: Associate Professor 1993, Professor 2000 Professional Memberships: American Thoracic Society (ATS); European Respiratory Society (ERS) Publications: has a toral of 175 publications including 21 national papers, 88 international papers, 20 Turkish books and 5 English books

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