Evidence map›Paper›PMID 35614569›Full record

ArticleJournal of medical virology2022

COVID salivary diagnostics: A comparative technical study.

Hanh Nguyen-Kim, Christiane Beckmann, Maurice Redondo, Jérémy Ziliox, Virginie Vallet, Karin Berger-Sturm, Jan Von Overbeck, Lavinia Alberi Auber

Abstract read
In one paragraph

Article in Journal of medical virology, 2022. 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.

  1. Article
  2. Article
  3. Salivary Biomarkers to Differentiate betweenDiagnostics (Basel, Switzerland) · 2023
    Article
  4. Article
  5. Review
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

8 authors.

Hanh Nguyen-KimSwiss Integrative Center for Human Health, Fribourg, Switzerland.ORCID 0000-0003-0703-2171
Christiane BeckmannViollier, Baselland, Switzerland.ORCID 0000-0001-9030-083X
Maurice RedondoViollier, Baselland, Switzerland.
Jérémy ZilioxViollier, Baselland, Switzerland.
Virginie ValletViollier, Baselland, Switzerland.
Karin Berger-SturmRed Cross Switzerland, Bern, Switzerland.
Jan Von OverbeckTask Force COVID, Canton of Bern, Bern, Switzerland.
Lavinia Alberi AuberSwiss Integrative Center for Human Health, Fribourg, Switzerland.ORCID 0000-0002-0446-5337

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since the beginning of the coronavirus disease 2019 (COVID-19) pandemic, molecular diagnostics of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have taken center stage in the detection of infected individuals for isolation purposes but also in the mass surveillance as a preventive strategy to contain the virus spread. While nasopharyngeal swabs (NPS) have remained the golden standard substrate, salivary diagnostic for SARS-CoV-2 has been proposed as an alternative and noninvasive measure in vulnerable individuals. Nevertheless, there is a widespread assumption that salivary reverse-transcription polymerase chain reaction (RT-PCR) does not match the quality of testing using NPS and particular care should be taken in respect to food or beverage intake, when sampling saliva. Our study indicates that without any precaution in the selection of 190 patients, nor restriction over the time window of sampling, there is 99% match in the COVID-19 positivity between NPS and saliva when using RT-PCR, with a reported Delta in thermal cycles (Cts) values for the viral genes Envelope (E) and Open reading frame 1ab (Orf1ab) between 0 and 2, a 98.7% sensitivity and 100% specificity. This high accuracy is maintained in pooling configurations that can be used for mass-testing purposes in professional and educational settings. The further advantage to using crude saliva as compared to NPS or mouthwash is that direct methods yield robust results. Overall, our study validates and promotes the use of salivary diagnostic for COVID-19 eliminating the need of a medical practitioner for the sampling, resolving the unpleasantness of the NPS intervention and empowering the patient to do self-testing in times of need.

Indexed as

COVID-19SARS-CoV-2COVID-19 TestingHumansNasopharynxPandemicsRNA, ViralSalivaSpecimen HandlingRNA, Viralheat-released RNAnasopharyngeal swabsRNA extractionsalivaSARS-CoV-2

Identifiers

PMID35614569
PMCPMC9347777

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.