Evidence map›Paper›PMID 33747257›Full record

ArticleDisease markers2021

Validation of a One-Step Reverse Transcription-Droplet Digital PCR (RT-ddPCR) Approach to Detect and Quantify SARS-CoV-2 RNA in Nasopharyngeal Swabs.

Catia Mio, Adriana Cifù, Stefania Marzinotto, Barbara Marcon, Corrado Pipan, Giuseppe Damante, Francesco Curcio

Open access · hybridAbstract readValidation Study
In one paragraph

Article in Disease markers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Catia MioDepartment of Medicine (DAME), University of Udine, Udine, Italy.ORCID https://orcid.org/0000-0002-6245-8266
Adriana CifùDepartment of Medicine (DAME), University of Udine, Udine, Italy.ORCID https://orcid.org/0000-0002-6794-8838
Stefania MarzinottoDepartment of Laboratory Medicine, University Hospital of Udine, Udine, Italy.
Barbara MarconDepartment of Laboratory Medicine, University Hospital of Udine, Udine, Italy.
Corrado PipanDepartment of Medicine (DAME), University of Udine, Udine, Italy.
Giuseppe DamanteDepartment of Medicine (DAME), University of Udine, Udine, Italy.
Francesco CurcioDepartment of Medicine (DAME), University of Udine, Udine, Italy.ORCID https://orcid.org/0000-0002-9070-4807
University of Udine · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has rapidly spread worldwide from the beginning of 2020. Quantitative reverse transcription-PCR (RT-qPCR) is, to this day, the preferred methodology for viral RNA detection, even if not without problems. To overcome some of the limitations still existing for the detection and quantification of nucleic acids in various applications, the use of one-step reverse transcription-droplet digital PCR (RT-ddPCR) has been established. The purpose of this study was, then, to evaluate the efficacy of ddPCR for the detection of SARS-CoV-2 RNA in nasopharyngeal swabs, optimizing the detection of low-viral load-burdened samples.

methodsThe RT-ddPCR workflow was validated for sensitivity, specificity, linearity, reproducibility, and precision using samples from 90 COVID-19-infected patients referred to the Department of Laboratory Medicine of the University Hospital of Udine (Italy).

resultsThe present study shows that RT-ddPCR allows the detection of as low as 10.3 copies of a SARS-COV-2

conclusionDuring the postpeak phase of the SARS-CoV-2 pandemic, it is essential to rely on a highly robust molecular biology method to identify infected subjects, whether they have symptoms or not, in order to prepare appropriate containment measures.

Indexed as

Carrier StateCOVID-19 Nucleic Acid TestingHumansLimit of DetectionNasopharynxReverse Transcriptase Polymerase Chain ReactionRNA, ViralSARS-CoV-2Viral LoadWorkflowRNA, Viral

Identifiers

PMID33747257
PMCPMC7934789
OpenAlexW3135648011

What OpenQuestion holds

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LicenceCC BY
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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.