Diagnosis of IPF
Document Type
Book Chapter
ISBN
978-1-83969-241-3
Editor
Salim Surani
Publication (Name of Journal)
Idiopathic Pulmonary Fibrosis
Department
Internal Medicine (East Africa)
Publisher
IntechOpen
Abstract
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive interstitial lung fibrosis with an unknown cause commonly seen in the elderly. Obtaining histories such as past medical history, exposure history, occupational history, and family history can be crucial parts to help to find other pulmonary fibrosis causes. Not only that, but thorough physical examination can rule out pulmonary fibrosis related to other diseases. Several diagnostic modalities have helped to improve the IPF assessment, including computer tomographic scan, histopathology, bronchoscopy lavage, serological testing, and serum biomarkers. Diagnostic of exclusion is required. The consensus from multidisciplinary IPF experts’ discussion from various societies recommends the clinical practice for IPF diagnosis to help define this condition. In this book chapter, we will discuss the evidence for each of the diagnostic techniques for IPF.
Recommended Citation
Taweesedt, P. T.,
Gandhi, K.,
Shah, R.,
Surani, S.
(2022). Diagnosis of IPF. Idiopathic Pulmonary Fibrosis.
Available at:
https://ecommons.aku.edu/book_chapters/418