Abstract

ObjectiveTo develop an accurate and rapid computed tomography (CT)-based interpretable AI system for the diagnosis of lung diseases.BackgroundMost existing AI systems only focus on viral pneumonia (e.g., COVID-19), specifically, ignoring other similar lung diseases: e.g., bacterial pneumonia (BP), which should also be detected during CT screening. In this paper, we propose a unified sequence-based pneumonia classification network, called SLP-Net, which utilizes consecutiveness information for the differential diagnosis of viral pneumonia (VP), BP, and normal control cases from chest CT volumes.MethodsConsidering consecutive images of a CT volume as a time sequence input, compared with previous 2D slice-based or 3D volume-based methods, our SLP-Net can effectively use the spatial information and does not need a large amount of training data to avoid overfitting. Specifically, sequential convolutional neural networks (CNNs) with multi-scale receptive fields are first utilized to extract a set of higher-level representations, which are then fed into a convolutional long short-term memory (ConvLSTM) module to construct axial dimensional feature maps. A novel adaptive-weighted cross-entropy loss (ACE) is introduced to optimize the output of the SLP-Net with a view to ensuring that as many valid features from the previous images as possible are encoded into the later CT image. In addition, we employ sequence attention maps for auxiliary classification to enhance the confidence level of the results and produce a case-level prediction.ResultsFor evaluation, we constructed a dataset of 258 chest CT volumes with 153 VP, 42 BP, and 63 normal control cases, for a total of 43,421 slices. We implemented a comprehensive comparison between our SLP-Net and several state-of-the-art methods across the dataset. Our proposed method obtained significant performance without a large amount of data, outperformed other slice-based and volume-based approaches. The superior evaluation performance achieved in the classification experiments demonstrated the ability of our model in the differential diagnosis of VP, BP and normal cases.

Highlights

  • COVID-19, the latest in viral pneumonia diseases, is an acute respiratory syndrome that has spread rapidly around the world since the end of 2019, having a devastating effect on the health and well-being of the global population [1, 2]

  • To further verify whether the features containing both axial dimensional and spatial information captured by our model could benefit detection performance, we compared the proposed method to other classic classification models using 2D slices: AlexNet [46], VGG19 [47], InceptionV3 [48], ResNet34 [36], and Xception [49]

  • The motivation of this study was to employ artificial intelligence (AI) techniques to alleviate the problem posed by the fact that even radiologists are hard pressed to distinguish viral pneumonia (VP) from bacterial pneumonia (BP), as they share very similar presentations of infection lesion characteristics in computed tomography (CT) images

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Summary

Introduction

COVID-19, the latest in viral pneumonia diseases, is an acute respiratory syndrome that has spread rapidly around the world since the end of 2019, having a devastating effect on the health and well-being of the global population [1, 2]. To diagnose viral pneumonia (limited to COVID-19 in our work), reverse transcription-polymerase chain reaction (RT-PCR) has widely been accepted as the gold standard. CT is the most widely used imaging technique, due to its high resolution and threedimensional (3D) view, and its relatively high detection sensitivity of around 98% [6]. Most existing AI systems only focus on viral pneumonia (e.g., COVID-19), ignoring other similar lung diseases: e.g., bacterial pneumonia (BP), which should be detected during CT screening. We propose a unified sequence-based pneumonia classification network, called SLP-Net, which utilizes consecutiveness information for the differential diagnosis of viral pneumonia (VP), BP, and normal control cases from chest CT volumes

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