Evidence map›Paper›PMID 34931760›Full record

ArticleThe Kaohsiung journal of medical sciences2022

Evaluation of a new NS1 rapid diagnostic test using a single acute-phase serum panel collected during the largest dengue outbreak in Taiwan history in 2015.

Li-Teh Liu, Chun-Hong Chen, Ping-Chang Lin, Ching-Yi Tsai, Miao-Chen Hsu, Bo-Yi Huang, Yan-Yi Tsai, Jih-Jin Tsai

Open access · goldAbstract read
In one paragraph

Article in The Kaohsiung journal of medical sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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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

8 authors at 3 institutions in 1 country.

Li-Teh LiuDepartment of Medical Laboratory Science and Biotechnology, College of Medical Technology, Chung-Hwa University of Medical Technology, Tainan City, Taiwan.
Chun-Hong ChenNational Mosquito-Borne Diseases Control Research Center, National Health Research Institutes, Zhunan, Taiwan.
Ping-Chang LinTropical Medicine Center, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Ching-Yi TsaiTropical Medicine Center, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Miao-Chen HsuTropical Medicine Center, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Bo-Yi HuangTropical Medicine Center, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Yan-Yi TsaiTropical Medicine Center, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Jih-Jin TsaiTropical Medicine Center, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.ORCID https://orcid.org/0000-0003-2226-8916
Kaohsiung Medical University · TWChung Hwa University of Medical Technology · TWNational Health Research Institutes · TW

Funding

National Health Research Institutes NHRI-110A1-MRCO-03212101
6 · The paper itself

Abstract

Dengue virus (DENV) infection results mostly from the bites of virus-carrying Aedes mosquitoes, which results in dengue fever (DF) with or without warning signs, severe dengue, or asymptomatic infections in humans. For point-of care identification of DENV-infected patients, a rapid diagnostic test (RDT) for DENV nonstructural protein 1 (NS1) has been developed to achieve early diagnosis and timely clinical management. We evaluated the performance of a new commercially available dengue NS1 RDT AsiaGen Dengue NS1 Antigen Rapid Diagnosis Test using real-time qRT-PCR as a reference method and compared the results with SD BIOLINE Dengue NS1 Ag using a single acute-phase serum panel collected during the largest dengue outbreak in the history of Taiwan in 2015. The results suggested that the sensitivity and specificity of AsiaGen Dengue NS1 Antigen RDT (96.9% and 100%) were similar to those of SD BIOLINE Dengue NS1 RDT (100% and 100%) for detection in the acute phase of DENV-2 infection. The results suggested that the sensitivity of both RDTs was similar (95.4% ~ 100%) for the sera collected at less than or equal to three days postsymptom onset (PSO). Our results suggested that the two DENV NS1 RDTs used in this study were promising for the timely diagnosis of DENV infection during dengue outbreaks, at least for DENV-2 in areas where authorized medical laboratories are not available or medical resources are limited. However, the performance of AsiaGen DENV NS1 RDTs in the detection of primary/secondary infections and infection by serotypes of DENV other than DENV-2 requires further investigation.

Indexed as

DengueDengue VirusAnimalsAntibodies, ViralAntigens, ViralDiagnostic Tests, RoutineDisease OutbreaksEnzyme-Linked Immunosorbent AssayHumansReagent Kits, DiagnosticSensitivity and SpecificityTaiwanViral Nonstructural ProteinsAntibodies, ViralAntigens, ViralReagent Kits, DiagnosticViral Nonstructural Proteinsdengue feverdengue virusDENV-2NS1rapid diagnosis test

Identifiers

PMID34931760
PMCPMC11896572
OpenAlexW4200187523

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.