Evidence map›Paper›PMID 34926297›Full record

ArticleFrontiers in oncology2021

Automatic Sequence-Based Network for Lung Diseases Detection in Chest CT.

Jinkui Hao, Jianyang Xie, Ri Liu, Huaying Hao, Yuhui Ma, Kun Yan, Ruirui Liu, Yalin Zheng, Jianjun Zheng, Jiang Liu and 2 more

Abstract read
In one paragraph

Article in Frontiers in oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Jinkui HaoCixi Institute of Biomedical Engineering, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, China.
Jianyang XieCixi Institute of Biomedical Engineering, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, China.
Ri LiuHwa Mei Hospital, University of Chinese Academy of Sciences, Ningbo, China.
Huaying HaoCixi Institute of Biomedical Engineering, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, China.
Yuhui MaCixi Institute of Biomedical Engineering, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, China.
Kun YanHwa Mei Hospital, University of Chinese Academy of Sciences, Ningbo, China.
Ruirui LiuSchool of Medicine, Ningbo University, Ningbo, China.
Yalin ZhengDepartment of Eye and Vision Science, University of Liverpool, Liverpool, United Kingdom.
Jianjun ZhengSchool of Medicine, Ningbo University, Ningbo, China.
Jiang LiuCixi Institute of Biomedical Engineering, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, China.
Jingfeng ZhangHwa Mei Hospital, University of Chinese Academy of Sciences, Ningbo, China.
Yitian ZhaoCixi Institute of Biomedical Engineering, Ningbo Institute of Material Technology and Engineering, Chinese Academy of Sciences, Ningbo, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

CNNConvLSTMCTdeep learninglung diseases

Identifiers

PMID34926297
PMCPMC8674429

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