Evidence map›Paper›PMID 41810307›Full record

ArticleFrontiers in public health2026

Preemptive rapid antigen test as an emergency measure during coronavirus disease 2019 outbreaks.

Yaping Pan, Yong Liu, Ye Jiang, Jin Cai

Abstract read
In one paragraph

Article in Frontiers in public health, 2026. 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

4 authors.

Yaping PanNaval Medical Center, Naval Medical University, Shanghai, China.
Yong LiuNaval Medical Center, Naval Medical University, Shanghai, China.
Ye JiangNaval Medical Center, Naval Medical University, Shanghai, China.
Jin CaiNaval Medical Center, Naval Medical University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: We acknowledge that the rapid antigen test (RAT) has several advantages, including faster results, cost-effectiveness, and suitability for on-site self-testing. However, there is still controversy regarding the performance of the RAT for coronavirus disease 2019 (COVID-19). The aim of this study was to evaluate RAT screening in a COVID-19 outbreak situation. Methods: In this study, we developed a preemptive testing model in which a RAT was immediately followed by reverse transcriptase polymerase chain reaction (RT-PCR) during a single screening in a high-density community outbreak to rapidly prevent transmission. The RAT and RT-PCR were performed using the Flowflex Results: Our study showed that the sensitivity and specificity of the RAT were 0.82 and 1.00, respectively. We found a slightly higher false-negative rate, corresponding to decreased sensitivity, in our data compared to the previous study; however, the difference was not statistically significant. In addition, there was no statistically significant difference in the false-positive rate, corresponding to specificity, between the two studies. Conclusion: The current results indicate that a RAT with a single screening does not pose an additional risk of inaccurate diagnosis of COVID-19 compared to serial screening. The strategy of a preemptive RAT might be an effective emergency measure to prevent COVID-19 transmission at an early stage of an outbreak.

Indexed as

COVID-19COVID-19 Serological TestingDisease OutbreaksAdultAntigens, ViralFemaleHumansMaleMiddle AgedRapid Diagnostic TestsRetrospective StudiesReverse Transcriptase Polymerase Chain ReactionSARS-CoV-2Sensitivity and SpecificityAntigens, Viralacute respiratory infectious diseasescoronavirus disease 2019emergency measuresoutbreaksrapid antigen testreverse transcriptase polymerase chain reaction

Identifiers

PMID41810307
PMCPMC12968284

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Registered trials

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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.