Evidence map›Paper›PMID 31383693›Full record

ArticleBMJ open2019

Performance evaluation of three rapid antigen tests for the diagnosis of group A

Ha-Nui Kim, Jeeyong Kim, Woong Sik Jang, Jeonghun Nam, Chae Seung Lim

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

5 authors at 1 institution in 1 country.

Ha-Nui KimLaboratory Medicine, College of Medicine, Korea University, Seongbuk-gu, Seoul, Republic of Korea.
Jeeyong KimLaboratory Medicine, College of Medicine, Korea University, Seongbuk-gu, Seoul, Republic of Korea.
Woong Sik JangLaboratory Medicine, College of Medicine, Korea University, Seongbuk-gu, Seoul, Republic of Korea.
Jeonghun NamLaboratory Medicine, College of Medicine, Korea University, Seongbuk-gu, Seoul, Republic of Korea.
Chae Seung LimLaboratory Medicine, College of Medicine, Korea University, Seongbuk-gu, Seoul, Republic of Korea.
Korea University · KR

Funding

PROVIDE RABBITS, RATS MICE, HAMSTERS GERBILS, GUINEA PIGS27307C0012 · NIEHS · PI BOLEN, WAYNE · 2007 to 2007
$1.0M
NIEHS NIH HHS 27307C0012
6 · The paper itself

Abstract

objectiveTo compare the diagnostic performance of three rapid antigen detection tests (RADTs) for group A

designA hospital-based, cross-sectional, retrospective study.

settingA comparative study of rapid diagnostic tests for GAS using clinical specimens in a single institute.

participants225 children in the outpatient clinics ofKorea University Guro Hospitalwith suspicious symptoms were subjected to throat swab sampling. A dual-swab applicator was used. Samples were stored at below -70°C in a 10 mL transport tube containing 1 mL liquid Stuart's transport medium. OUTCOME MEASURES: All tests were performed in the laboratory by trained clinical laboratory scientists. Sensitivity, specificity, accuracy and kappa index of three RADTs were compared with the reference PCR test and culture results.

resultsOf the 225 patients suspected of having GAS, 67 and 90 were positive for GAS in the culture and PCR tests, respectively. Compared with the reference culture, the sensitivity for GAS was 92.5% (CI 83.4 to 97.5), 71.6% (CI 59.3 to 81.9) and 74.63% (CI 62.5 to 84.4) for careUS Strep A Plus, SD Bioline and BD Veritor, respectively, and the specificity was 97.0% (CI 93.1 to 99.0), 94.6% (CI 90.1 to 97.5) and 92.9% (CI 87.8 to 96.2) for careUS Strep A Plus, SD Bioline and BD Veritor, respectively. Compared with the reference GAS real-time PCR, the sensitivity was 73.3% (CI 62.9 to 82.1), 63.3% (CI 52.5 to 73.2) and 67.8% (CI 57.1 to 77.2) for careUS Strep A Plus, SD Bioline and BD Veritor, respectively, and the specificity was 99.3% (CI 95.9 to 99.9), 100.0% (CI 97.3 to 100.0) and 99.3% (CI 95.9 to 99.9) for careUS Strep A Plus, SD Bioline and BD Veritor, respectively.

conclusionsThe careUS Strep A Plus is a useful test that showed highly comparable results with those of the culture test and superior performances among the three RADTs. The use of RADTs should be encouraged to provide acceptable and fast results using simple equipment.

Indexed as

AdolescentAntigens, BacterialChildChild, PreschoolCross-Sectional StudiesFemaleHumansMaleReagent Kits, DiagnosticReproducibility of ResultsRetrospective StudiesSensitivity and SpecificityStreptococcal InfectionsStreptococcus pyogenesAntigens, BacterialReagent Kits, Diagnosticgroup A streptococcuspharyngitisrapid antigen detection test

Identifiers

PMID31383693
PMCPMC6687028
OpenAlexW2965132354

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.