Evidence map›Paper›PMID 35274327›Full record

ArticleJournal of medical virology2022

Comparison of extraction-based and elution-based polymerase chain reaction testing, and automated and rapid antigen testing for the diagnosis of severe acute respiratory syndrome coronavirus 2.

Nori Yoshioka, Matsuo Deguchi, Hideharu Hagiya, Masanori Kagita, Hiroko Tsukamoto, Miyuki Takao, Hisao Yoshida, Shigeto Hamaguchi, Ikuhiro Maeda, Yoh Hidaka and 1 more

Open access · bronzeAbstract 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 46% 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, 3 citations in OpenAlex.

  1. Article
  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

11 authors at 2 institutions in 1 country.

Nori YoshiokaDivision of Infection Control and Prevention, Osaka University Hospital, Suita, Japan.ORCID 0000-0003-3395-9712
Matsuo DeguchiDivision of Infection Control and Prevention, Osaka University Hospital, Suita, Japan.
Hideharu HagiyaDivision of Infection Control and Prevention, Osaka University Hospital, Suita, Japan.
Masanori KagitaDivision of Infection Control and Prevention, Osaka University Hospital, Suita, Japan.
Hiroko TsukamotoDivision of Infection Control and Prevention, Osaka University Hospital, Suita, Japan.
Miyuki TakaoDivision of Infection Control and Prevention, Osaka University Hospital, Suita, Japan.
Hisao YoshidaDivision of Infection Control and Prevention, Osaka University Hospital, Suita, Japan.
Shigeto HamaguchiDivision of Infection Control and Prevention, Osaka University Hospital, Suita, Japan.
Ikuhiro MaedaLaboratory for Clinical Investigation, Osaka University Hospital, Suita, Japan.
Yoh HidakaLaboratory for Clinical Investigation, Osaka University Hospital, Suita, Japan.
Kazunori TomonoDivision of Infection Control and Prevention, Osaka University Hospital, Suita, Japan.
Osaka University Hospital · JPOkayama University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to compare the differences in testing performance of extraction-based polymerase chain reaction (PCR) assays, elution-based direct PCR assay, and rapid antigen detection tests for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We used nasopharyngeal swab samples of patients with coronavirus disease 2019 (COVID-19). We used the MagNA Pure 24 System (Roche Diagnostics K.K.) or magLEAD 12gC (Precision System Science Co., Ltd.) for RNA extraction, mixed the concentrates with either the LightMix Modular SARS-CoV PCR mixture (Roche Diagnostics K.K.) or Takara SARS-CoV-2 direct PCR detection kit (Takara Bio Inc.), and amplified it using COBAS® z480 (Roche Diagnostics K.K.). For elution-based PCR, we directly applied clinical samples to the Takara SARS-CoV-2 direct PCR detection kit before the same amplification step. Additionally, we performed Espline SARS-CoV-2 (Fuji Rebio Co., Ltd.) for rapid diagnostic test (RDT), and used Lumipulse SARS-CoV-2 antigen (Fuji Rebio Co., Ltd.) and Elecsys SARS-CoV-2 antigen (Roche Diagnostics K.K.) for automated antigen tests (ATs). Extraction-based and elution-based PCR tests detected the virus up to 214-216 and 210 times dilution, respectively. ATs remained positive up to 24-26 times dilution, while RDT became negative after 22 dilutions. For 153 positive samples, positivity rates of the extraction-based PCR assay were 85.6% to 98.0%, while that of the elution-based PCR assay was 73.2%. Based on the RNA concentration process, extraction-based PCR assays were superior to elution-based direct PCR assays for detecting SARS-CoV-2.

Indexed as

COVID-19SARS-CoV-2HumansPolymerase Chain ReactionRNASensitivity and SpecificityRNAnovel coronavirus disease 2019 (COVID-19)polymerase chain reactionrapid diagnostic testsevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)

Identifiers

PMID35274327
PMCPMC9088563
OpenAlexW4220895310

What OpenQuestion holds

Textmetadata
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.