PUBLISHER: DelveInsight | PRODUCT CODE: 1129044
PUBLISHER: DelveInsight | PRODUCT CODE: 1129044
DelveInsight's 'Progressive pulmonary fibrosis (PPF)- Epidemiology Forecast-2032' report delivers an in-depth understanding of the Progressive pulmonary fibrosis (PPF), historical and forecasted epidemiology as well as the PPF trends in the United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan.
Progressive pulmonary fibrosis (PPF) Disease Understanding
Progressive pulmonary fibrosis (PPF) consists of a diverse group of interstitial lung diseases (ILDs) characterized by a similar clinical phenotype of accelerated respiratory failure, frequent disease exacerbation and earlier mortality.
Interstitial lung disease is believed to be caused by long-term exposure to hazardous materials, such as asbestos or coal dust, or it can be caused by an auto-immune disease such as rheumatoid arthritis. Once lung scarring occurs, it is generally irreversible.
Progressive pulmonary fibrosis (PPF) are composed of Idiopathic Interstitial Pneumonias such as non-specific interstitial pneumonia and unclassifiable interstitial pneumonia, and inhalation lung diseases such as chronic hypersensitivity pneumonia, and connective tissue disease-associated ILD such as rheumatoid arthritis-related ILD and SSc-related ILD, and sarcoidosis and so on. Many interstitial lung diseases (ILDs) are characterized by chronic progressive fibrosis. The type-specific segmentation majorly includes, Idiopathic Interstitial Pneumonias (IIPs), Autoimmune ILDs, Hypersensitivity Pneumonitis, Sarcoidosis, and other ILDs.
Progressive pulmonary fibrosis (PPF) Diagnosis
Imaging tests such as X-ray and a high-resolution computed tomography (CT scan), is key to, and sometimes the first step in, the diagnosis of interstitial lung disease. The severity level of Progressive pulmonary fibrosis (PPF) is calculated on the basis of FVC score. However, identifying and determining the cause of interstitial lung disease can be challenging, as a large number of disorders fall into this broad category. Hence differential diagnosis is needed.
The differential diagnosis of Interstitial Lung Diseases requires a multidisciplinary approach, usually involving pulmonologist, radiologist, and pathologist. The evaluations include clinical presentation, specific history assessment, smoking status, lung function evaluation, serological test results, imaging and if required, lung biopsy.
Continued in the report…..
Progressive pulmonary fibrosis (PPF) Epidemiology Perspective by DelveInsight
The disease epidemiology covered in the report provides historical as well as forecasted epidemiology segmented by Total Diagnosed Total Prevalent Cases of Interstitial Lung Disease (ILD), Total Diagnosed Prevalent Cases of ILD, Type-specific Diagnosed Prevalent Cases of ILD, and Total Diagnosed Prevalent Cases of Progressive pulmonary fibrosis (PPF), in the 7MM covering the United States, EU5 countries (Germany, France, Italy, Spain, and the United Kingdom), and Japan, from 2019 to 2032.
Key Questions Answered
The Progressive pulmonary fibrosis (PPF) report will allow the user to -
Geographies Covered
Study Period: 2019-2032