Evidence map›Paper›PMID 38776299›Full record

ArticlePloS one2024

Big data analysis for Covid-19 in hospital information systems.

Xinpa Ying, Haiyang Peng, Jun Xie

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Xinpa YingHospital of Chengdu University of TCM, Chengdu, Sichuan, China.
Haiyang PengHospital of Chengdu University of TCM, Chengdu, Sichuan, China.
Jun XieHospital of Chengdu University of TCM, Chengdu, Sichuan, China.ORCID 0009-0007-1061-5470

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The COVID-19 pandemic has triggered a global public health crisis, affecting hundreds of countries. With the increasing number of infected cases, developing automated COVID-19 identification tools based on CT images can effectively assist clinical diagnosis and reduce the tedious workload of image interpretation. To expand the dataset for machine learning methods, it is necessary to aggregate cases from different medical systems to learn robust and generalizable models. This paper proposes a novel deep learning joint framework that can effectively handle heterogeneous datasets with distribution discrepancies for accurate COVID-19 identification. We address the cross-site domain shift by redesigning the COVID-Net's network architecture and learning strategy, and independent feature normalization in latent space to improve prediction accuracy and learning efficiency. Additionally, we propose using a contrastive training objective to enhance the domain invariance of semantic embeddings and boost classification performance on each dataset. We develop and evaluate our method with two large-scale public COVID-19 diagnosis datasets containing CT images. Extensive experiments show that our method consistently improves the performance both datasets, outperforming the original COVID-Net trained on each dataset by 13.27% and 15.15% in AUC respectively, also exceeding existing state-of-the-art multi-site learning methods.

Indexed as

Big DataCOVID-19Deep LearningHospitalsHumansInformation SystemsMachine LearningPandemicsSARS-CoV-2Tomography, X-Ray Computed

Identifiers

PMID38776299
PMCPMC11111070

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.