Comparison of seven commercial RT-PCR kits with the NIV kit for the diagnosis of Covid-19

Mala Chhabra, K. Nirmal, Ankit Chauhan, A. Athotra, Stuti Kansra, Anuradha Shulania, A. Achra, N. Duggal
{"title":"Comparison of seven commercial RT-PCR kits with the NIV kit for the diagnosis of Covid-19","authors":"Mala Chhabra, K. Nirmal, Ankit Chauhan, A. Athotra, Stuti Kansra, Anuradha Shulania, A. Achra, N. Duggal","doi":"10.25259/anams-2022-12-3-(794)","DOIUrl":null,"url":null,"abstract":"\n\nCoronavirus disease 2019 (COVID-19) caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) spread across the globe in an unprecedented manner and was declared a pandemic on March 11, 2020 by the World Health Organization (WHO). This study was carried out with the aim to compare the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and agreement of the eight different RT-PCR kits for the diagnosis of COVID-19.\n\n\n\nThis observational cross-sectional study was carried out in the Department of Microbiology of a tertiary care hospital in Central Delhi from July to October 2021. A total of 45 nasopharyngeal and/or oropharyngeal swabs in Viral Transport Medium (VTM) from suspected COVID-19 patients were received in the laboratory for RT-PCR. These samples were tested by eight different Indian Council of Medical Research (ICMR)-approved RT-PCR kits with different gene targets. The comparison was made with the National Institute of Virology (NIV), the Pune COVID-19 RT-PCR kit. Statistical analysis: sensitivity, specificity, PPV, and NPV were calculated for each kit and compared using the McNemar test. Agreement of different kits was evaluated using Kappa analysis.\n\n\n\nThe results of the 45 samples of suspected COVID-19 cases were recorded as per the cycle threshold (Ct) provided in the kit insert. Of these, 15 samples detected both E and RdRp genes and 30 were negative for both the genes of SARS CoV-2 by NIV, the Pune COVID-19 RT-PCR kit. All kits showed 100% sensitivity and had 100% NPV when compared with the NIV kit. However, specificity, PPV, and agreement were variable as compared to the NIV kit.\n\n\n\nThe reporting should be carried out as per the manufacturer’s instructions. However, positive results with Ct values ≥ 36 showed variable results with different RT PCR kits and hence should be interpreted with caution.\n","PeriodicalId":517858,"journal":{"name":"Annals of National Academy of Medical Sciences","volume":"30 34","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of National Academy of Medical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25259/anams-2022-12-3-(794)","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Coronavirus disease 2019 (COVID-19) caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) spread across the globe in an unprecedented manner and was declared a pandemic on March 11, 2020 by the World Health Organization (WHO). This study was carried out with the aim to compare the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and agreement of the eight different RT-PCR kits for the diagnosis of COVID-19. This observational cross-sectional study was carried out in the Department of Microbiology of a tertiary care hospital in Central Delhi from July to October 2021. A total of 45 nasopharyngeal and/or oropharyngeal swabs in Viral Transport Medium (VTM) from suspected COVID-19 patients were received in the laboratory for RT-PCR. These samples were tested by eight different Indian Council of Medical Research (ICMR)-approved RT-PCR kits with different gene targets. The comparison was made with the National Institute of Virology (NIV), the Pune COVID-19 RT-PCR kit. Statistical analysis: sensitivity, specificity, PPV, and NPV were calculated for each kit and compared using the McNemar test. Agreement of different kits was evaluated using Kappa analysis. The results of the 45 samples of suspected COVID-19 cases were recorded as per the cycle threshold (Ct) provided in the kit insert. Of these, 15 samples detected both E and RdRp genes and 30 were negative for both the genes of SARS CoV-2 by NIV, the Pune COVID-19 RT-PCR kit. All kits showed 100% sensitivity and had 100% NPV when compared with the NIV kit. However, specificity, PPV, and agreement were variable as compared to the NIV kit. The reporting should be carried out as per the manufacturer’s instructions. However, positive results with Ct values ≥ 36 showed variable results with different RT PCR kits and hence should be interpreted with caution.
七种商用 RT-PCR 试剂盒与 NIV 试剂盒在诊断 Covid-19 方面的比较
由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起的冠状病毒病 2019(COVID-19)以前所未有的方式在全球蔓延,世界卫生组织(WHO)于 2020 年 3 月 11 日宣布其为大流行病。本研究旨在比较八种不同 RT-PCR 试剂盒诊断 COVID-19 的灵敏度、特异性、阳性预测值 (PPV)、阴性预测值 (NPV) 和一致性。这项观察性横断面研究于 2021 年 7 月至 10 月在德里中部一家三甲医院的微生物学系进行。实验室共收到 45 份疑似 COVID-19 患者的鼻咽和/或口咽拭子,并将其置于病毒转运培养基(VTM)中进行 RT-PCR 检测。这些样本由印度医学研究委员会(ICMR)批准的八种不同基因靶向的 RT-PCR 试剂盒进行检测。与国家病毒研究所(NIV)的普纳 COVID-19 RT-PCR 试剂盒进行了比较。统计分析:使用 McNemar 检验计算每种试剂盒的灵敏度、特异性、PPV 和 NPV,并进行比较。根据试剂盒说明书中提供的周期阈值(Ct)记录了 45 份 COVID-19 疑似病例样本的检测结果。普纳 COVID-19 RT-PCR 检测试剂盒 NIV 的检测结果显示,其中 15 份样本检测出 E 和 RdRp 基因,30 份样本检测出 SARS CoV-2 的两个基因均为阴性。与 NIV 试剂盒相比,所有试剂盒的灵敏度均为 100%,NPV 均为 100%。然而,与 NIV 试剂盒相比,特异性、PPV 和一致性则各不相同。然而,Ct 值≥ 36 的阳性结果在不同的 RT PCR 试剂盒中显示出不同的结果,因此应谨慎解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信