Evidence map›Paper›PMID 37356827›Full record

ArticleIndian journal of medical microbiology

Effect of storage temperatures simulating transport conditions of nasopharyngeal swabs on the results of a chemiluminescence immunoassay (CLIA) to detect severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antigen.

Poonam Kanta, Arnab Ghosh, Kapil Goyal, Ramandeep Kaur, Manjari Baluni, Shubhankar Sircar, Vikas Kumar, Krishan Kumar, Neetu Vijay, Mini P Singh

Open access · goldAbstract read
In one paragraph

Article in Indian journal of medical microbiology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 3 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

10 authors at 2 institutions in 1 country.

Poonam KantaDepartment of Virology, PGIMER, Chandigarh, India.
Arnab GhoshDepartment of Virology, PGIMER, Chandigarh, India.
Kapil GoyalDepartment of Virology, PGIMER, Chandigarh, India.
Ramandeep KaurDepartment of Virology, PGIMER, Chandigarh, India.
Manjari BaluniDepartment of Virology, PGIMER, Chandigarh, India.
Shubhankar SircarDepartment of Virology, PGIMER, Chandigarh, India.
Vikas KumarDepartment of Virology, PGIMER, Chandigarh, India.
Krishan KumarDepartment of Virology, PGIMER, Chandigarh, India.
Neetu VijayIndian Council of Medical Research (ICMR), Department of Health Research, New Delhi, India.
Mini P SinghDepartment of Virology, PGIMER, Chandigarh, India. Electronic address: minipsingh@gmail.com.
Post Graduate Institute of Medical Education and Research · INIndian Council of Medical Research · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeChemiluminescence Immunoassay (CLIA) is high throughput, rapid diagnostic test which has recently come up for the detection of SARS-CoV-2 antigen. The present study evaluated performance of CLIA antigen test in nasopharyngeal swab samples stored at different temperatures for 7 days to simulate the transport conditions and transit time across the country from remote peripheral laboratories to central facilities. MATERIALS AND

methodsLimit of detection (LOD), sensitivity and specificity of VITROS® SARS-CoV-2 antigen assay was determined using Real-time reverse transcriptase PCR (rRT-PCR) confirmed SARS-CoV-2 positive and negative samples. To detect the effect of storage temperatures on VITROS ®SARS-CoV-2 antigen results, samples were stored at 4 ​°C, 25 ​°C & 37 ​°C for 7 days followed by detection of SARS-CoV-2 nucleocapsid antigen and compared with N-gene rRT-PCR.

resultsThe VITROS® SARS-CoV-2 antigen test was found to have a sensitivity and specificity of 78.9% and 100% respectively with high sensitivity of 88.1% for samples with Ct ​< ​30. The LOD of VITROS assay was equivalent to 3800 copies of RNA per reactions as compared to 72 copies per reaction for rRT-PCR. We observed that more than 80% of samples with <30 Ct values could be detected by VITROS SARS-CoV-2 antigen assay at day 7 even when stored at 37 ​°C. For samples with Ct values between 26 and 30, on day 7 the positivity rate of N-antigen at 4 ​°C was 90.9% and 37 ​°C was 63.6%.

conclusionsCLIA testing can be carried out for the detection of SARS-CoV-2 N-protein in NP-swab samples transported in cold chain even with 7 days transit time, particularly for Ct ​< ​30 samples which represents cases with higher transmissibility. As drop in positivity for VITROS assay was lower as compared to rRT-PCR on day 7 in cold chain-maintained samples, the assay can be useful to screen samples received from remote peripheral areas before performing rRT-PCR.

Indexed as

COVID-19HumansImmunoassayLuminescenceNasopharynxSARS-CoV-2Sensitivity and SpecificityTemperatureCLIASARS-CoV-2 antigenStorage temperatureTransport

Identifiers

PMID37356827
PMCPMC10163922
OpenAlexW4372313967

What OpenQuestion holds

Textmetadata
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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.