Evidence map›Paper›PMID 35721770›Full record

ArticleIJID regions2021

Detection of SARS-CoV-2 in Clinical Samples: Target-specific Analysis of Qualitative Reverse Transcription-Polymerase Chain Reaction(RT-PCR) Diagnostic Kits.

Ambica Rangaiah, Sathyanarayan Muthur Shankar, Shantala Gowdara Basawarajappa, Pritik A Shah, Aditya Chandrashekar, Asha Munegowda, Shashiraja Padukone

Abstract read
In one paragraph

Article in IJID regions, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

7 authors.

Ambica RangaiahDepartment of Microbiology, Bangalore Medical College and Research Institute, Bangalore, India.
Sathyanarayan Muthur ShankarDepartment of Microbiology, Bangalore Medical College and Research Institute, Bangalore, India.
Shantala Gowdara BasawarajappaDepartment of Microbiology, Bangalore Medical College and Research Institute, Bangalore, India.
Pritik A ShahDepartment of Microbiology, Bangalore Medical College and Research Institute, Bangalore, India.
Aditya ChandrashekarDepartment of Microbiology, Bangalore Medical College and Research Institute, Bangalore, India.
Asha MunegowdaState Level Virus Research & Diagnostic Laboratory, Bangalore Medical College and Research Institute, Karnataka, India.
Shashiraja PadukoneState Level Virus Research & Diagnostic Laboratory, Bangalore Medical College and Research Institute, Karnataka, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe Coronavirus disease 2019 pandemic caused by Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) led to the rise of many available modalities for diagnosis. One such modality is the Reverse Transcription-Polymerase Chain Reaction (RT-PCR) kits which require evaluation amongst the many available commercial kits in the market.

methodsWe conducted a performance evaluation of twelve RT-PCR SARS-CoV-2 commercial kits. A total of 75 nasopharyngeal and oropharyngeal clinical samples were selected with their cycling threshold (Ct) values. Inclusion of 5 gene targets: E gene, N gene, S gene, RdRp and ORF1ab were assessed. Data was analyzed using R software version 4.1.1 and Microsoft Excel.

resultsWe observe that, the positive sample's Ct values differs significantly across the 12 diagnostic kits. However, for gene-specific analysis, we observe that, positive sample's Ct values does not differ significantly across gene targets. There is significant difference in Ct values in Commercial kits targeting all genes except S-gene. All the commercial kits Altona (E and S genes), Thermo (ORF1ab and N genes), Multiplex (E, ORF1ab, RdRdp genes), Meril (N and ORF1ab genes), S D Biosensor (E and ORF1ab genes), Lab Gun (RdRp and N genes) and Lab systems (ORF1ab and E genes) scored a sensitivity of 100%. All other kits scored sensitivity above 95% and lowest sensitivity with the Genes2me (E gene) and Genes2me (RdRp) at 95.08% each. All kits were 100% specific.

conclusionThis study provides an accurate comprehensive assessment of the different kits in the detection of SARS-CoV-2 which may promote standardization of testing across laboratories.

Indexed as

analysisDiagnostic KitsICMR, Indian Council of Medical ResearchRT-PCRRT-PCR, Reverse Transcriptase Polymerase Chain ReactionsSARS-CoV-2SARS-CoV-2, Severe Acute Respiratory Syndrome CoronaVirus-2VRDL, State-Level Virus Research and Diagnostics LaboratoryWHO, World Health Organisation

Identifiers

PMID35721770
PMCPMC8600795

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.