Evidence map›Paper›PMID 38082318›Full record

ArticleVirology journal2023

Development and evaluation of serological screening based on one dried plasma spot for HIV, syphilis, and HCV.

Jie-Qiong Ma, Ya-Nan Ren, Shi-Yuan Wen, Ao-Bo Dong, Wen-Ge Xing, Yan Jiang

Open access · goldAbstract read
In one paragraph

Article in Virology journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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 at 2 institutions in 1 country.

Jie-Qiong MaCollege of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China. maxiaoqiong1122@163.com.
Ya-Nan RenFangshan Center for Disease Control and Prevention, Fangshan, Beijing, China.
Shi-Yuan WenCollege of Basic Medical Sciences, Shanxi Medical University, Taiyuan, China.
Ao-Bo DongThird Hospital of Baotou City, Baotou, 014040, China.
Wen-Ge XingNational HIV/HCV Reference Laboratory, National Center for AIDS/STD Control and Prevention, China CDC, Beijing, China.
Yan JiangNational HIV/HCV Reference Laboratory, National Center for AIDS/STD Control and Prevention, China CDC, Beijing, China. jiangyan03@263.net.
National Center for AIDS/STD Control and Prevention,China CDC · CNShanxi Medical University · CN

Funding

Natural Science Foundation of Shanxi Province for Youths No. 202103021223240Science Research Start-up Fund of Shanxi Medical University for Doctor No.XD2014Science Research Start-up Fund of Shanxi Province for Doctor No. SD2009Scientific and Technological Innovation Programs of Higher Education Institutions in Shanxi No. 2021L217the National Science and Technology Major Project of China in the 13th Five-Year 2017ZX10201101-002- 003
6 · The paper itself

Abstract

backgroundIn the effort to prevent and control HIV/AIDS, China has established a national sentinel surveillance system. However, some sentinel sites face limitations in environmental resources and accessibility, prompting the exploration of alternative sample strategies. Dried plasma spots (DPS) samples are viewed as promising alternatives to traditional plasma samples due to their advantages, including sample stability, easy storage, and convenient transport. This study aims to develop a method for screening HIV, Treponema pallidum (TP), and Hepatitis C Virus (HCV) using DPS samples and assess their performance.

methodsBased on existing commercial assay kits, a detection method was established through the optimization of experimental parameters, including the amount of plasma on filter paper, the volume of elution solution applied to dried plasma spots, the size of dried plasma spots, elution solution volume, elution solution components, elution temperature, and elution time. A series of laboratory evaluation panels were constructed for laboratory assessments, including the laboratory basic panel, laboratory interference panel, and laboratory precision panel. Additionally, clinical samples were used for evaluation.

resultsOptimal conditions for DPS sample extraction were: plasma volume, 100 µL; DPS size, whole spot; eluent volume, 500 µL; eluent, PBS with 1‰ Tween20; elution time, 2 h; elution temperature, room temperature. A total of 619 paired plasma/DPS samples were tested by both methods. The DPS-based ELISA method exhibited 100% sensitivity/specificity for HIV, 98.6%/100% for TP, and 99.6%/100% for HCV. Kappa values between the plasma samples and DPS samples were 100% for HIV, 99% for TP, and 100% for HCV. The DPS-based ELISA method failed to detect 1 HCV mono-infected sample and TP in 1 HIV/HCV/TP co-infected sample. For the HIV/HCV/TP co-infected sample, the S/CO in the plasma sample was 2.143 and in the DPS sample was 0.5. For HCV, the S/CO (sample OD/cut-off) was 3.049 in the plasma sample and 0.878 in the DPS sample.

conclusionsA single DPS, following one-time standardized processing, can be used to detect HIV, HCV, and TP. Researching and establishing laboratory testing methods better suited for China's sentinel surveillance have significant practical applications in improving HIV testing in resource-constrained environments.

Indexed as

Hepatitis CHIV InfectionsSyphilisDried Blood Spot TestingHepacivirusHumansPlasmaSensitivity and SpecificityDried plasma spotsELISAHepatitis C virusHuman immunodeficiency virusTreponema pallidum

Identifiers

PMID38082318
PMCPMC10712157
OpenAlexW4389574620

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LicenceCC BY
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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.