Evidence map›Paper›PMID 33349261›Full record

ArticleJournal of translational medicine2020

Evaluation of the diagnostic accuracy of a new point-of-care rapid test for SARS-CoV-2 virus detection.

Leonardo Miscio, Antonio Olivieri, Francesco Labonia, Gianfranco De Feo, Paolo Chiodini, Giuseppe Portella, Luigi Atripaldi, Roberto Parrella, Rodolfo Conenna, Franco Maria Buonaguro and 4 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in Journal of translational medicine, 2020. 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
0.2field-weighted citation impact, top 38% 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, 6 citations in OpenAlex.

  1. Recent progress on rapid diagnosis of COVID-19 by point-of-care testing platforms.Chinese chemical letters = Zhongguo hua xue kuai bao · 2023
    Review
  2. 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

14 authors at 4 institutions in 1 country.

Leonardo MiscioIstituto Nazionale Tumori Di Napoli, IRCCS "G. Pascale", Naples, Italy. leonardo.miscio@istitutotumori.na.it.
Antonio OlivieriGaboservice, Caserta, Italy.
Francesco LaboniaIstituto Nazionale Tumori Di Napoli, IRCCS "G. Pascale", Naples, Italy.
Gianfranco De FeoIstituto Nazionale Tumori Di Napoli, IRCCS "G. Pascale", Naples, Italy.
Paolo ChiodiniUniversità Degli Studi Della Campania Luigi Vanvitelli, Naples, Italy.
Giuseppe PortellaAzienda Ospedaliera Universitaria "Federico II", Naples, Italy.
Luigi AtripaldiAzienda Ospedaliera dei Colli - PO Cotugno, Naples, Italy.
Roberto ParrellaAzienda Ospedaliera dei Colli - PO Cotugno, Naples, Italy.
Rodolfo ConennaAzienda Ospedaliera dei Colli - PO Cotugno, Naples, Italy.
Franco Maria BuonaguroIstituto Nazionale Tumori Di Napoli, IRCCS "G. Pascale", Naples, Italy.
Ernesta CavalcantiIstituto Nazionale Tumori Di Napoli, IRCCS "G. Pascale", Naples, Italy.
Paolo AsciertoIstituto Nazionale Tumori Di Napoli, IRCCS "G. Pascale", Naples, Italy.
Gerardo BottiIstituto Nazionale Tumori Di Napoli, IRCCS "G. Pascale", Naples, Italy.
Attilio BianchiIstituto Nazionale Tumori Di Napoli, IRCCS "G. Pascale", Naples, Italy.
Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITOspedale D. Cotugno · ITAzienda Ospedaliera Universitaria Università degli Studi della Campania Luigi Vanvitelli · ITFederico II University Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe easy access to a quick diagnosis of coronavirus disease 2019 (COVID-19) is a key point to improve the management of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and to contain its spread. Up to now, laboratory real-time PCR is the standard of care, but requires a fully equipped laboratory and significant infrastructure. Consequently, new diagnostic tools are required.

methodsIn the present work, the diagnostic accuracy of the point-of-care rapid test "bKIT Virus Finder COVID-19" (Hyris

resultsResults obtained with the Hyris Kit are the same as that of standard laboratory-based real time PCR methods for all the analyzed samples. In addition, the Hyris Kit provides the test results in less than 2 h, a significantly shorter time compared to the reference methods, without the need of a fully equipped laboratory.

conclusionsTo conclude, the Hyris kit represents a promising tool to improve the health surveillance and to increase the capacity of SARS-CoV-2 testing.

Indexed as

Point-of-Care SystemsCOVID-19COVID-19 Nucleic Acid TestingEarly DiagnosisHumansItalyLimit of DetectionPandemicsProspective StudiesReference StandardsRetrospective StudiesSARS-CoV-2Sensitivity and SpecificityTranslational Research, BiomedicalCOVID-19Health surveillancePoint-of-care rapid testSARS-CoV-2

Identifiers

PMID33349261
PMCPMC7752099
OpenAlexW3117023831

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.