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• W2948365890 abstract "Idiopathic pulmonary fibrosis (IPF) is a lung disorder where there is scarring of the lungs from an unknown cause. It is usually a progressive disease with a poor long-term prognosis. The classic features of the disorder include progressive dyspnea and a nonproductive cough. Pulmonary function tests usually reveal restrictive impairment and diminished carbon monoxide diffusing capacity. The diagnosis can be made without biopsy if there are compatible imaging tests, appropriate clinical history, and exclusion of other conditions. The classic pattern of imaging on computed tomography (CT) scan will show a peripheral distribution of bilateral fibrosis, more pronounced at the bases. If there is diagnostic uncertainty, IPF can also be diagnosed by lung biopsy. The treatment includes supportive measures, oxygen supplementation when needed, anti-fibrotic drugs, and lung transplant for severe disease." @default.
• W2948365890 created "2019-06-14" @default.
• W2948365890 creator A5004942377 @default.
• W2948365890 creator A5008951215 @default.
• W2948365890 creator A5070878726 @default.
• W2948365890 date "2019-01-11" @default.
• W2948365890 modified "2023-09-26" @default.
• W2948365890 title "Idiopathic Pulmonary Fibrosis" @default.
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