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Evaluation of a commercial Real Time PCR for clinical samples without RNA extraction for detection of SARS-CoV-2.
- Source :
-
Diagnostic microbiology and infectious disease [Diagn Microbiol Infect Dis] 2024 Nov; Vol. 110 (3), pp. 116441. Date of Electronic Publication: 2024 Jul 25. - Publication Year :
- 2024
-
Abstract
- RT-PCR is the gold standard for diagnosis of COVID-19. All RT-PCR kits are based on RNA extraction from the clinical sample. There was a sudden increase in demand of these kits, both RNA extraction and COVID-19 RT-PCR kits during the pandemic. This sudden spurt in global demand created a situation of shortage of consumables, especially the RNA extraction kits. Hence, this study was carried out to evaluate and compare COVID-19 RT-PCR without RNA extraction step using buffer R3. Sensitivity, specificity and accuracy of RT-PCR kit without RNA extraction were 89.16 %, 100% and 89.6% respectively. This approach saved more than 50 % time compared to the RT-PCR kit with RNA extraction approach allowing enhanced daily sample processing capability. RT-PCR kit without RNA extraction help in managing a greater number of samples, reduces cost and turnaround time.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024. Published by Elsevier Inc.)
- Subjects :
- Humans
Reagent Kits, Diagnostic standards
COVID-19 Nucleic Acid Testing methods
Specimen Handling methods
SARS-CoV-2 genetics
SARS-CoV-2 isolation & purification
COVID-19 diagnosis
COVID-19 virology
RNA, Viral genetics
RNA, Viral isolation & purification
Sensitivity and Specificity
Real-Time Polymerase Chain Reaction methods
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0070
- Volume :
- 110
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Diagnostic microbiology and infectious disease
- Publication Type :
- Academic Journal
- Accession number :
- 39128205
- Full Text :
- https://doi.org/10.1016/j.diagmicrobio.2024.116441