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Idiopathic pulmonary fibrosis (IPF) is a restrictive interstitial lung disease that causes lung function decline by lung tissue scarring. Although lung function decline is assessed by the forced vital capacity (FVC), determining the accurate progression of IPF remains a challenge. To address this challenge, we proposed Fibro-CoSANet, a novel end…
In this competition, we’ll predict a patient’s severity of decline in lung function based on a CT scan of their lungs. We’ll determine lung function based on output from a spirometer, which measures the volume of air inhaled and exhaled.