Evidence map›Paper›PMID 37202367›Full record

ArticleEpidemiology and infection2023

Development and external validation of a prognostic tool for nonsevere COVID-19 inpatients.

Ensi Luo, Qingyang Zhong, Yongtao Wen, Jie Cai, Xia Xie, Lingjuan Zhou

Abstract read
In one paragraph

Article in Epidemiology and infection, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

6 authors.

Ensi LuoDepartment of Endocrinology, Binhaiwan Central Hospital of Dongguan, Dongguan, China.ORCID 0000-0002-4127-9760
Qingyang ZhongMedical Department, The Ninth People's Hospital of Dongguan, Dongguan, China.
Yongtao WenDepartment of Respiratory Medicine, Binhaiwan Central Hospital of Dongguan, Dongguan, China.
Jie CaiDepartment of Respiratory Medicine, Binhaiwan Central Hospital of Dongguan, Dongguan, China.
Xia XiePain Department, Binhaiwan Central Hospital of Dongguan, Dongguan, China.
Lingjuan ZhouNursing Department, Binhaiwan Central Hospital of Dongguan, Dongguan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To develop a machine learning model and nomogram to predict the probability of persistent virus shedding (PVS) in hospitalized patients with coronavirus disease 2019 (COVID-19), the clinical symptoms and signs, laboratory parameters, cytokines, and immune cell data of 429 patients with nonsevere COVID-19 were retrospectively reviewed. Two models were developed using the Akaike information criterion (AIC). The performance of these two models was analyzed and compared by the receiver operating characteristic (ROC) curve, calibration curve, net reclassification index (NRI), and integrated discrimination improvement (IDI). The final model included the following independent predictors of PVS: sex, C-reactive protein (CRP) level, interleukin-6 (IL-6) level, the neutrophil-lymphocyte ratio (NLR), monocyte count (MC), albumin (ALB) level, and serum potassium level. The model performed well in both the internal validation (corrected C-statistic = 0.748, corrected Brier score = 0.201) and external validation datasets (corrected C-statistic = 0.793, corrected Brier score = 0.190). The internal calibration was very good (corrected slope = 0.910). The model developed in this study showed high discriminant performance in predicting PVS in nonsevere COVID-19 patients. Because of the availability and accessibility of the model, the nomogram designed in this study could provide a useful prognostic tool for clinicians and medical decision-makers.

Indexed as

COVID-19InpatientsClinical Decision RulesHumansMachine LearningNomogramsCOVID-19developmentduration of viral sheddingexternal validationprediction model

Identifiers

PMID37202367
PMCPMC10540186

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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.