Evidence map›Paper›PMID 34518603›Full record

ArticleScientific reports2021

Nested pool testing strategy for the diagnosis of infectious diseases.

Inés Armendáriz, Pablo A Ferrari, Daniel Fraiman, José M Martínez, Hugo G Menzella, Silvina Ponce Dawson

Abstract read
In one paragraph

Article in Scientific reports, 2021. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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.

Inés ArmendárizDepartamento de Matemática & IMAS, FCEN-UBA & CONICET, C1428EGA, Buenos Aires, Argentina.
Pablo A FerrariDepartamento de Matemática & IMAS, FCEN-UBA & CONICET, C1428EGA, Buenos Aires, Argentina.
Daniel FraimanDepartamento de Matemática y Ciencias, Universidad de San Andrés & CONICET, B1644BID, Victoria, Argentina.
José M MartínezDepartment of Applied Mathematics, IMECC-UNICAMP, Campinas, 13083-859, Brazil.
Hugo G MenzellaDepartamento de Tecnología & IPROByQ, FBIOyF-UNR & CONICET, S2002LRK, Rosario, Argentina.
Silvina Ponce DawsonDepartamento de Física & IFIBA, FCEN-UBA & CONICET, C1428EGA, Buenos Aires, Argentina. silvina@df.uba.ar.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 302538/2019-4Conselho Nacional de Desenvolvimento Científico e Tecnológico 302682/2019-8Fondo para la Investigación Científica y Tecnológica PICT 2015-3583Fondo para la Investigación Científica y Tecnológica PICT 2015-3824Fondo para la Investigación Científica y Tecnológica PICT 2018-02026Fondo para la Investigación Científica y Tecnológica PICT 2018-02842Fundação de Amparo à Pesquisa do Estado de São Paulo 2013/07375-0Fundação de Amparo à Pesquisa do Estado de São Paulo 2016/01860-1Fundação de Amparo à Pesquisa do Estado de São Paulo 2018/24293-0Universidad de Buenos Aires UBACYT 20020160100155BAUniversidad de Buenos Aires UBACyT 20020170100482BA
6 · The paper itself

Abstract

The progress of the SARS-CoV-2 pandemic requires the design of large-scale, cost-effective testing programs. Pooling samples provides a solution if the tests are sensitive enough. In this regard, the use of the gold standard, RT-qPCR, raises some concerns. Recently, droplet digital PCR (ddPCR) was shown to be 10-100 times more sensitive than RT-qPCR, making it more suitable for pooling. Furthermore, ddPCR quantifies the RNA content directly, a feature that, as we show, can be used to identify nonviable samples in pools. Cost-effective strategies require the definition of efficient deconvolution and re-testing procedures. In this paper we analyze the practical implementation of an efficient hierarchical pooling strategy for which we have recently derived the optimal, determining the best ways to proceed when there are impediments for the use of the absolute optimum or when multiple pools are tested simultaneously and there are restrictions on the throughput time. We also show how the ddPCR RNA quantification and the nested nature of the strategy can be combined to perform self-consistency tests for a better identification of infected individuals and nonviable samples. The studies are useful to those considering pool testing for the identification of infected individuals.

Indexed as

AlgorithmsCommunicable DiseasesCOVID-19COVID-19 Nucleic Acid TestingDiagnostic Tests, RoutineHumansModels, GeneticPandemicsReal-Time Polymerase Chain ReactionReproducibility of ResultsRNA, ViralSARS-CoV-2Sensitivity and SpecificitySpecimen HandlingRNA, Viral

Identifiers

PMID34518603
PMCPMC8438083

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.