Sky-Net: A Deep Learning Approach to Predicting Lung Function Decline in Sufferers of Idiopathic Pulmonary Fibrosis

Arjun Taneja, Anju Yadav
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Abstract

Idiopathic Pulmonary Fibrosis (IPF) is a kind of Interstitial Lung Disease (ILD) that can be recognized by observing an atypical formation and accumulation of fibrotic tissue in the lungs. The lung's alveolar structure is damaged; as a result, people afflicted with IPF experience increasingly restricted lung capacity as time progresses. Diagnosis of this disease is typically performed by analyzing the patient's computed tomography (CT) scans and measuring their Forced Vital Capacity (FVC) using a Spirometer. However, the absence of an apparent cause of IPF restricts the ability of doctors to accurately diagnose the patient. Furthermore, IPF progression in patients is highly volatile and unpredictable, which means that one patient's health could deteriorate significantly quicker compared to another. Taking the problems mentioned above into account, in this paper a 3-layer ResNet machine learning model is proposed that determines the rate of lung function decline of sufferers from IPF. Proposed model is applied on the “OSIC Pulmonary Fibrosis Progression” dataset publicly available on Kaggle, and compare it against various state-of-the-art models and winning Kaggle entries.
Sky-Net:预测特发性肺纤维化患者肺功能下降的深度学习方法
特发性肺纤维化(Idiopathic Pulmonary Fibrosis, IPF)是一种间质性肺疾病(ILD),可通过观察肺内纤维化组织的非典型形成和积聚来识别。肺的肺泡结构受损;因此,随着时间的推移,患有IPF的人的肺活量越来越受限。这种疾病的诊断通常是通过分析患者的计算机断层扫描(CT)和使用肺活量计测量其用力肺活量(FVC)来进行的。然而,缺乏明显的IPF病因限制了医生准确诊断患者的能力。此外,患者的IPF进展是高度不稳定和不可预测的,这意味着一个患者的健康状况可能比另一个患者恶化得快得多。考虑到上述问题,本文提出了一种确定IPF患者肺功能下降速率的3层ResNet机器学习模型。提出的模型应用于Kaggle上公开的“OSIC肺纤维化进展”数据集,并将其与各种最先进的模型和获奖的Kaggle条目进行比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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