Evidence map›Paper›PMID 39347447›Full record

ArticleChina CDC weekly2024

Development and Diagnosis Performance of IgM-Based Rapid Antigen Test for Early Detection of SARS-CoV-2 Infection in a Large Cohort of Suspected COVID-19 Cases - USA, Poland, and Sweden, 2021-2022.

Yihua Huang, Yiyi Pu, Youhong Weng, Yahan Wu, Qing He, Sofia Litchev, Longyou Zhao, Haojie Ding, Yunru Lai, Jie Li and 7 more

Abstract read
In one paragraph

Article in China CDC weekly, 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

17 authors.

Yihua HuangDepartment of Laboratory Medicine, Lishui Second People's Hospital Affiliated to Wenzhou Medical University, Lishui City, Zhejiang Province, China.
Yiyi PuKey Laboratory of Biomarkers and In Vitro Diagnosis Translation of Zhejiang province, School of Laboratory Medicine and Bioengineering, Hangzhou Medical College, Hangzhou City, Zhejiang Province, China.
Youhong WengSchool of Basic Medicine and Forensics, Key Laboratory of Bio-tech Vaccine of Zhejiang Province, Engineering Research Center of Novel Vaccine of Zhejiang Province, Hangzhou Medical College, Hangzhou City, Zhejiang Province, China.
Yahan WuSchool of Basic Medicine and Forensics, Key Laboratory of Bio-tech Vaccine of Zhejiang Province, Engineering Research Center of Novel Vaccine of Zhejiang Province, Hangzhou Medical College, Hangzhou City, Zhejiang Province, China.
Qing HeSchool of Basic Medicine and Forensics, Key Laboratory of Bio-tech Vaccine of Zhejiang Province, Engineering Research Center of Novel Vaccine of Zhejiang Province, Hangzhou Medical College, Hangzhou City, Zhejiang Province, China.
Sofia LitchevBaylor College of Medicine, Houston, TX, USA.
Longyou ZhaoDepartment of Laboratory Medicine, Lishui Second People's Hospital Affiliated to Wenzhou Medical University, Lishui City, Zhejiang Province, China.
Haojie DingSchool of Basic Medicine and Forensics, Key Laboratory of Bio-tech Vaccine of Zhejiang Province, Engineering Research Center of Novel Vaccine of Zhejiang Province, Hangzhou Medical College, Hangzhou City, Zhejiang Province, China.
Yunru LaiDepartment of Laboratory Medicine, Lishui Second People's Hospital Affiliated to Wenzhou Medical University, Lishui City, Zhejiang Province, China.
Jie LiDepartment of Laboratory Medicine, Lishui Second People's Hospital Affiliated to Wenzhou Medical University, Lishui City, Zhejiang Province, China.
Xiaojun ZhengDepartment of Research and Development, Hangzhou AllTest Biotech Co., Ltd, Hangzhou City, Zhejiang Province, China.
Jinshu ChenDepartment of Research and Development, Hangzhou AllTest Biotech Co., Ltd, Hangzhou City, Zhejiang Province, China.
Xianqin XiongDepartment of Research and Development, Hangzhou AllTest Biotech Co., Ltd, Hangzhou City, Zhejiang Province, China.
Shaohong LuSchool of Basic Medicine and Forensics, Key Laboratory of Bio-tech Vaccine of Zhejiang Province, Engineering Research Center of Novel Vaccine of Zhejiang Province, Hangzhou Medical College, Hangzhou City, Zhejiang Province, China.
Fei GaoDepartment of Research and Development, Hangzhou AllTest Biotech Co., Ltd, Hangzhou City, Zhejiang Province, China.
Meng GaoSchool of Basic Medicine and Forensics, Key Laboratory of Bio-tech Vaccine of Zhejiang Province, Engineering Research Center of Novel Vaccine of Zhejiang Province, Hangzhou Medical College, Hangzhou City, Zhejiang Province, China.
Qingming KongKey Laboratory of Biomarkers and In Vitro Diagnosis Translation of Zhejiang province, School of Laboratory Medicine and Bioengineering, Hangzhou Medical College, Hangzhou City, Zhejiang Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Antigen testing has been crucial in effectively managing the coronavirus disease 2019 (COVID-19) pandemic. This study evaluated the clinical performance of a nasopharyngeal swab (NPS)-based antigen rapid diagnostic test (Ag-RDT) compared to the gold standard real-time reverse transcription-polymerase chain reaction (RT-PCR) for early detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Methods: We developed an IgM-based rapid antigen test for early detection of SARS-CoV-2 infection. Between July 2021 and January 2022, we analyzed 1,030 NPS samples from participants at three centers in different countries, using both antigen rapid diagnostic tests (Ag-RDT) and RT-PCR. Results: The Ag-RDT demonstrated minimal detection limits as low as 0.1 ng/mL for recombinant N antigen and 100 TCID50/mL for heat-inactivated SARS-CoV-2 virus. Specificity assessments involving four human coronaviruses and 13 other respiratory viruses showed no cross-reactivity. The Ag-RDT assay (ALLtest) exhibited high sensitivity (93.18%-100%) and specificity (99.67%-100%) across all centers. Factors such as cycle threshold (Ct) values and the timing of symptoms since onset were influential, with sensitivity increasing at lower Ct values (<30) and within the first week of symptoms. Conclusion: The ALLtest Ag-RDT demonstrated high reliability and significant potential for diagnosing suspected COVID-19 cases.

Indexed as

antigenearly rapid diagnostic testIgMlateral flow chromatographic immunoassaynasopharyngeal swabSARS-CoV-2

Identifiers

PMID39347447
PMCPMC11427342

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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.