Evidence map›Paper›PMID 33534723›Full record

ArticleJMIR medical informatics2021

Development and Validation of a Machine Learning Approach for Automated Severity Assessment of COVID-19 Based on Clinical and Imaging Data: Retrospective Study.

Juan Carlos Quiroz, You-Zhen Feng, Zhong-Yuan Cheng, Dana Rezazadegan, Ping-Kang Chen, Qi-Ting Lin, Long Qian, Xiao-Fang Liu, Shlomo Berkovsky, Enrico Coiera and 4 more

Abstract read
In one paragraph

Article in JMIR medical informatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

  1. Article
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  3. Observational
  4. Review
  5. Artificial Intelligence Methods.Advances in experimental medicine and biology · 2024
    Review
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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

14 authors.

Juan Carlos Quiroz *Centre for Health Informatics, Australian Institute of Health Innovation, Faculty of Medicine, Health and Human Sciences, Macquarie University, Macquarie Park, Australia.ORCID https://orcid.org/0000-0003-0241-5376
You-Zhen Feng *Medical Imaging Centre, The First Affiliated Hospital of Jinan University, Guangzhou, China.ORCID https://orcid.org/0000-0002-9123-6988
Zhong-Yuan Cheng *Medical Imaging Centre, The First Affiliated Hospital of Jinan University, Guangzhou, China.ORCID https://orcid.org/0000-0003-4810-1129
Dana RezazadeganCentre for Health Informatics, Australian Institute of Health Innovation, Faculty of Medicine, Health and Human Sciences, Macquarie University, Macquarie Park, Australia.ORCID https://orcid.org/0000-0002-0097-3801
Ping-Kang ChenMedical Imaging Centre, The First Affiliated Hospital of Jinan University, Guangzhou, China.ORCID https://orcid.org/0000-0002-2193-756X
Qi-Ting LinMedical Imaging Centre, The First Affiliated Hospital of Jinan University, Guangzhou, China.ORCID https://orcid.org/0000-0003-4205-7745
Long QianDepartment of Biomedical Engineering, Peking University, Beijing, China.ORCID https://orcid.org/0000-0002-9707-1096
Xiao-Fang LiuInstitute of Robotics and Automatic Information System, College of Artificial Intelligence, Nankai University, Tianjin, China.ORCID https://orcid.org/0000-0002-8137-4201
Shlomo BerkovskyCentre for Health Informatics, Australian Institute of Health Innovation, Faculty of Medicine, Health and Human Sciences, Macquarie University, Macquarie Park, Australia.ORCID https://orcid.org/0000-0003-2638-4121
Enrico CoieraCentre for Health Informatics, Australian Institute of Health Innovation, Faculty of Medicine, Health and Human Sciences, Macquarie University, Macquarie Park, Australia.ORCID https://orcid.org/0000-0002-6444-6584
Lei SongDepartment of Radiology, Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Science, Xiangyang, China.ORCID https://orcid.org/0000-0001-8975-5060
Xiaoming QiuDepartment of Radiology, Huangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Edong Healthcare Group, Huangshi, China.ORCID https://orcid.org/0000-0002-0789-6247
Sidong LiuCentre for Health Informatics, Australian Institute of Health Innovation, Faculty of Medicine, Health and Human Sciences, Macquarie University, Macquarie Park, Australia.ORCID https://orcid.org/0000-0002-2371-0713
Xiang-Ran CaiMedical Imaging Centre, The First Affiliated Hospital of Jinan University, Guangzhou, China.ORCID https://orcid.org/0000-0003-4010-7577

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCOVID-19 has overwhelmed health systems worldwide. It is important to identify severe cases as early as possible, such that resources can be mobilized and treatment can be escalated.

objectiveThis study aims to develop a machine learning approach for automated severity assessment of COVID-19 based on clinical and imaging data.

methodsClinical data-including demographics, signs, symptoms, comorbidities, and blood test results-and chest computed tomography scans of 346 patients from 2 hospitals in the Hubei Province, China, were used to develop machine learning models for automated severity assessment in diagnosed COVID-19 cases. We compared the predictive power of the clinical and imaging data from multiple machine learning models and further explored the use of four oversampling methods to address the imbalanced classification issue. Features with the highest predictive power were identified using the Shapley Additive Explanations framework.

resultsImaging features had the strongest impact on the model output, while a combination of clinical and imaging features yielded the best performance overall. The identified predictive features were consistent with those reported previously. Although oversampling yielded mixed results, it achieved the best model performance in our study. Logistic regression models differentiating between mild and severe cases achieved the best performance for clinical features (area under the curve [AUC] 0.848; sensitivity 0.455; specificity 0.906), imaging features (AUC 0.926; sensitivity 0.818; specificity 0.901), and a combination of clinical and imaging features (AUC 0.950; sensitivity 0.764; specificity 0.919). The synthetic minority oversampling method further improved the performance of the model using combined features (AUC 0.960; sensitivity 0.845; specificity 0.929).

conclusionsClinical and imaging features can be used for automated severity assessment of COVID-19 and can potentially help triage patients with COVID-19 and prioritize care delivery to those at a higher risk of severe disease.

Indexed as

algorithmclinical dataclinical featuresCOVID-19CT scansdevelopmentimagingimbalanced datamachine learningoversamplingseverity assessmentvalidation

Identifiers

PMID33534723
PMCPMC7879715

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.