Evidence map›Paper›PMID 34003869›Full record

ArticlePloS one2021

Testing of four-sample pools offers resource optimization without compromising diagnostic performance of real time reverse transcriptase-PCR assay for COVID-19.

Anirudh K Singh, Ram Kumar Nema, Ankur Joshi, Prem Shankar, Sudheer Gupta, Ashvini Kumar Yadav, Shashwati Nema, Bijina J Mathew, Arti Shrivas, Chitra Patankar and 8 more

Abstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

18 authors.

Anirudh K SinghDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.ORCID 0000-0001-8625-4447
Ram Kumar NemaRegional Virology Laboratory, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Ankur JoshiDepartment of Community and Family Medicine, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Prem ShankarDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Sudheer GuptaRegional Virology Laboratory, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Ashvini Kumar YadavRegional Virology Laboratory, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Shashwati NemaDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Bijina J MathewDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Arti ShrivasDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Chitra PatankarDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Arun RaghuwanshiRegional Virology Laboratory, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Ritu PandeyDepartment of Biochemistry, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Ranu TripathiDepartment of Pediatrics, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Kudsia AnsariRegional Virology Laboratory, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Kuldeep SinghDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Jogender YadavDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.
Debasis BiswasDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.ORCID 0000-0002-7557-3693
Sarman SinghDepartment of Microbiology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quick identification and isolation of SARS-CoV-2 infected individuals is central to managing the COVID-19 pandemic. Real time reverse transcriptase PCR (rRT-PCR) is the gold standard for COVID-19 diagnosis. However, this resource-intensive and relatively lengthy technique is not ideally suited for mass testing. While pooled testing offers substantial savings in cost and time, the size of the optimum pool that offers complete concordance with results of individualized testing remains elusive. To determine the optimum pool size, we first evaluated the utility of pool testing using simulated 5-sample pools with varying proportions of positive and negative samples. We observed that 5-sample pool testing resulted in false negativity rate of 5% when the pools contained one positive sample. We then examined the diagnostic performance of 4-sample pools in the operational setting of a diagnostic laboratory using 500 consecutive samples in 125 pools. With background prevalence of 2.4%, this 4-sample pool testing showed 100% concordance with individualized testing and resulted in 66% and 59% reduction in resource and turnaround time, respectively. Since the negative predictive value of a diagnostic test varies inversely with prevalence, we re-tested the 4-sample pooling strategy using a fresh batch of 500 samples in 125 pools when the prevalence rose to 12.7% and recorded 100% concordance and reduction in cost and turnaround time by 36% and 30%, respectively. These observations led us to conclude that 4-sample pool testing offers the optimal blend of resource optimization and diagnostic performance across difference disease prevalence settings.

Indexed as

Specimen HandlingCOVID-19COVID-19 Nucleic Acid TestingHumansReal-Time Polymerase Chain ReactionRNA, ViralSARS-CoV-2RNA, Viral

Identifiers

PMID34003869
PMCPMC8130958

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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.