Evidence map›Paper›PMID 33239382›Full record

ArticleJournal of clinical microbiology2021

Clinical Performance of the Point-of-Care cobas Liat for Detection of SARS-CoV-2 in 20 Minutes: a Multicenter Study.

Glen Hansen, Jamie Marino, Zi-Xuan Wang, Kathleen G Beavis, John Rodrigo, Kylie Labog, Lars F Westblade, Run Jin, Nedra Love, Karen Ding and 4 more

Open access · hybridAbstract readEvaluation StudyMulticenter Study
In one paragraph

Article in Journal of clinical microbiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 8% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 106 citations in OpenAlex.

  1. Pooled it
  2. Guidelines and Diagnostic Assays forOpen forum infectious diseases · 2026
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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

14 authors at 6 institutions in 1 country.

Glen Hansen *Department of Pathology and Laboratory Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Jamie MarinoDepartment of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA.
Zi-Xuan Wang *Department of Pathology, Anatomy, and Cell Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Kathleen G Beavis *Department of Pathology, University of Chicago, Chicago, Illinois, USA.ORCID 0000-0002-5611-6809
John RodrigoDepartment of Pathology and Laboratory Medicine, University of California Davis, California, USA.
Kylie LabogDepartment of Pathology and Laboratory Medicine, University of Minnesota, Minneapolis, Minnesota, USA.
Lars F Westblade *Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, New York, USA.
Run JinDepartment of Pathology, Anatomy, and Cell Biology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.
Nedra LoveDepartment of Pathology, University of Chicago, Chicago, Illinois, USA.
Karen DingRoche Molecular Systems, Inc., Pleasanton, California, USA.
Sachin GargRoche Molecular Systems, Inc., Pleasanton, California, USA.
Alan HuangRoche Molecular Systems, Inc., Pleasanton, California, USA.
Joanna SicklerRoche Molecular Systems, Inc., Pleasanton, California, USA.
Nam K Tran *Department of Pathology and Laboratory Medicine, University of California Davis, California, USA nktran@UCDAVIS.EDU.ORCID 0000-0003-1565-0025
Materials Systems (United States) · USCornell University · USThomas Jefferson University · USUniversity of California, Davis · USUniversity of Chicago · USUniversity of Minnesota · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Highly accurate testing for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) at the point of care (POC) is an unmet diagnostic need in emergency care and time-sensitive outpatient care settings. Reverse transcription-PCR (RT-PCR) technology is the gold standard for SARS-CoV-2 diagnostics. We performed a multisite U.S. study comparing the clinical performance of the first U.S. Food and Drug Administration (FDA)-authorized POC RT-PCR for detection of SARS-CoV-2 in 20 min, the cobas Liat SARS-CoV-2 and influenza A/B nucleic acid test, to the most widely used RT-PCR laboratory test, the cobas 68/8800 SARS-CoV-2 test. Clinical nasopharyngeal swab specimens from 444 patients with 357 evaluable specimens at five U.S. clinical laboratories were enrolled from 21 September 2020 to 23 October 2020. The overall agreement between the Liat and 68/8800 systems for SARS-CoV-2 diagnostics was 98.6% (352/357). Using Liat, positive percent agreement for SARS-CoV-2 was 100% (162/162) and the negative percent agreement was 97.4% (190/195). The Liat is an RT-PCR POC test that provides highly accurate SARS-CoV-2 results in 20 min with performance equivalent to that of high-throughput laboratory molecular testing. Rapid RT-PCR testing at the POC can enable more timely infection control and individual care decisions for coronavirus disease 2019.

Indexed as

Point-of-Care SystemsCOVID-19COVID-19 Nucleic Acid TestingHumansNasopharynxSARS-CoV-2Time FactorsUnited Statescobas 68/8800 SARS-CoV-2cobas Liat SARS-CoV-2 and influenza A/Bcoronavirus disease 2019 (COVID-19)Liatpoint-of-care (POC)reverse transcription-polymerase chain reaction (RT-PCR)

Identifiers

PMID33239382
PMCPMC8111162
OpenAlexW3108643339

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.