ISSN 1308-8734 | E-ISSN 1308-8742
Review
Acute Exacerbation of Idiopathic Pulmonary Fibrosis
1 Department of Respiratory Medicine, Okinawa Chubu Hospital, Okinawa, Japan  
Eurasian J Med 2017; 49: 204-206
DOI: 10.5152/eurasianjmed.2017.17219
Key Words: Acute exacerbation, idiopathic pulmonary fibrosis, new criteria, idiopathic, triggered
Abstract

Idiopathic pulmonary fibrosis (IPF) is the most common cause of chronic diffuse parenchymal disease of unknown cause. However, IPF patients sometimes develop acute exacerbation (AE), which is a life-threatening condition. The cause of AE of IPF remains unknown. The new criteria for AE of IPF have been proposed last year, wherein both idiopathic and triggered AE were proposed. Triggered AE includes infection, post-procedure and post-operation, drug toxicity, and aspiration. Therefore, detailed history taking is crucial. In this review, the definition, clinical symptoms, chest imaging, management, and prognosis for AE of IPF are described.

 

Cite this article as: Kishaba T. Acute Exacerbation of Idiopathic Pulmonary Fibrosis. Eurasian J Med 2017; 49: 204-6.

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