Evidence map›Paper›PMID 36240599›Full record

ArticleComputers in biology and medicine2022

Dynamic feature learning for COVID-19 segmentation and classification.

Xiaoqin Zhang, Runhua Jiang, Pengcheng Huang, Tao Wang, Mingjun Hu, Andrew F Scarsbrook, Alejandro F Frangi

Open access · greenAbstract read
In one paragraph

Article in Computers in biology and medicine, 2022. 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
0.9field-weighted citation impact, top 28% of its field
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

1 citing paper in PubMed, 6 citations in OpenAlex.

  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

7 authors at 3 institutions in 2 countries.

Xiaoqin ZhangCollege of Computer Science and Artificial Intelligence, Wenzhou University, China. Electronic address: zhangxiaoqinnan@gmail.com.
Runhua JiangCollege of Computer Science and Artificial Intelligence, Wenzhou University, China.
Pengcheng HuangCollege of Computer Science and Artificial Intelligence, Wenzhou University, China.
Tao WangCollege of Computer Science and Artificial Intelligence, Wenzhou University, China.
Mingjun HuCollege of Computer Science and Artificial Intelligence, Wenzhou University, China.
Andrew F ScarsbrookRadiology Department, Leeds Teaching Hospitals NHS Trust, UK; Leeds Institute of Medical Research, University of Leeds, UK.
Alejandro F FrangiCentre for Computational Imaging and Simulation Technologies in Biomedicine, Leeds Institute for Cardiovascular and Metabolic Medicine, University of Leeds, Leeds, UK; Department of Electrical Engineering, Department of Cardiovascular Sciences, KU Leuven, Belgium.
Wenzhou University · CNLeeds Teaching Hospitals NHS Trust · GBUniversity of Leeds · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since December 2019, coronavirus SARS-CoV-2 (COVID-19) has rapidly developed into a global epidemic, with millions of patients affected worldwide. As part of the diagnostic pathway, computed tomography (CT) scans are used to help patient management. However, parenchymal imaging findings in COVID-19 are non-specific and can be seen in other diseases. In this work, we propose to first segment lesions from CT images, and further, classify COVID-19 patients from healthy persons and common pneumonia patients. In detail, a novel Dynamic Fusion Segmentation Network (DFSN) that automatically segments infection-related pixels is first proposed. Within this network, low-level features are aggregated to high-level ones to effectively capture context characteristics of infection regions, and high-level features are dynamically fused to model multi-scale semantic information of lesions. Based on DFSN, Dynamic Transfer-learning Classification Network (DTCN) is proposed to distinguish COVID-19 patients. Within DTCN, a pre-trained DFSN is transferred and used as the backbone to extract pixel-level information. Then the pixel-level information is dynamically selected and used to make a diagnosis. In this way, the pre-trained DFSN is utilized through transfer learning, and clinical significance of segmentation results is comprehensively considered. Thus DTCN becomes more sensitive to typical signs of COVID-19. Extensive experiments are conducted to demonstrate effectiveness of the proposed DFSN and DTCN frameworks. The corresponding results indicate that these two models achieve state-of-the-art performance in terms of segmentation and classification.

Indexed as

COVID-19Deep LearningPneumoniaHumansSARS-CoV-2Tomography, X-Ray ComputedComputed tomographyCOVID-19Dynamical fusionTransfer learning

Identifiers

PMID36240599
PMCPMC9523910
OpenAlexW4298149760

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.