Discovery of a Generalization Gap of Convolutional Neural Networks on COVID-19 X-Rays Classification

被引:0
作者
Ben Ahmed, Kaoutar [1 ]
Goldgof, Gregory M. [2 ]
Paul, Rahul [3 ,4 ]
Goldgof, Dmitry B. [1 ]
Hall, Lawrence O. [1 ]
机构
[1] Univ S Florida, Dept Comp Sci & Engn, Tampa, FL 33620 USA
[2] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
[3] Massachusetts Gen Hosp, Dept Radiat Oncol, Boston, MA 02115 USA
[4] Harvard Med Sch, Dept Radiat Oncol, Boston, MA 02115 USA
关键词
COVID-19; Biomedical imaging; X-rays; Pulmonary diseases; X-ray imaging; Data models; Medical diagnostic imaging; Coronavirus (COVID-19); pneumonia; chest X-ray images; deep learning; confounder; CHEST; IMAGES; IDENTIFICATION;
D O I
10.1109/ACCESS.2021.3079716
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
A number of recent papers have shown experimental evidence that suggests it is possible to build highly accurate deep neural network models to detect COVID-19 from chest X-ray images. In this paper, we show that good generalization to unseen sources has not been achieved. Experiments with richer data sets than have previously been used show models have high accuracy on seen sources, but poor accuracy on unseen sources. The reason for the disparity is that the convolutional neural network model, which learns features, can focus on differences in X-ray machines or in positioning within the machines, for example. Any feature that a person would clearly rule out is called a confounding feature. Some of the models were trained on COVID-19 image data taken from publications, which may be different than raw images. Some data sets were of pediatric cases with pneumonia where COVID-19 chest X-rays are almost exclusively from adults, so lung size becomes a spurious feature that can be exploited. In this work, we have eliminated many confounding features by working with as close to raw data as possible. Still, deep learned models may leverage source specific confounders to differentiate COVID-19 from pneumonia preventing generalizing to new data sources (i.e. external sites). Our models have achieved an AUC of 1.00 on seen data sources but in the worst case only scored an AUC of 0.38 on unseen ones. This indicates that such models need further assessment/development before they can be broadly clinically deployed. An example of fine-tuning to improve performance at a new site is given.
引用
收藏
页码:72970 / 72979
页数:10
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