Examination of the utility of the COVID-19 detection kit, TRC Ready® SARS-CoV-2 i for nasopharyngeal swabs.

IF 1.9 Q3 PHARMACOLOGY & PHARMACY Drug Discoveries and Therapeutics Pub Date : 2023-05-15 DOI:10.5582/ddt.2022.01106
Satoru Ishii, Moto Kimura, Tohru Miyoshi-Akiyama, Ataru Moriya, Masami Kurokawa, Erina Isaka, Junko Terada-Hirashima, Jin Takasaki, Shinyu Izumi, Masayuki Hojo, Haruhito Sugiyama
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Abstract

The reverse transcription polymerase chain reaction (RT-PCR) offers high sensitivity, but has some drawbacks, such as the time required for the RNA extraction. Transcription reverse-transcription concerted reaction (TRC) Ready® SARS-CoV-2 i is easy to use and can be performed in about 40 minutes. TRC Ready® SARS-CoV-2 i and real-time one-step RT-PCR using the TaqMan probe tests of cryopreserved nasopharyngeal swab samples from patients diagnosed with COVID-19 were compared. The primary objective was to examine the positive and negative concordance rates. A total of 69 samples cryopreserved at -80° C were examined. Of the 37 frozen samples that were expected to be RT-PCR positive, 35 were positive by the RT-PCR method. TRC Ready® SARS-CoV-2 i detected 33 positive cases and 2 negative cases. One frozen sample that was expected to be RT-PCR positive was negative on both TRC Ready® SARS-CoV-2 i and RT-PCR. In addition, one frozen sample that was expected to be RT-PCR positive was positive by the RT-PCR method and negative by TRC Ready® SARS-CoV-2 i. Of the 32 frozen samples that were expected to be RT-PCR negative, both the RT-PCR method and TRC Ready® SARS-CoV-2 i yielded negative results for all 32 samples. Compared with RT-PCR, TRC Ready® SARS-CoV-2 i had a positive concordance rate of 94.3% and a negative concordance rate of 97.1%. TRC Ready® SARS-CoV-2 i can be utilized in a wide range of medical sites such as clinics and community hospitals due to its ease of operability, and is expected to be useful in infection control.

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检验COVID-19检测试剂盒TRC Ready®SARS-CoV-2 i用于鼻咽拭子的实用性。
逆转录聚合酶链反应(RT-PCR)具有高灵敏度,但也存在一些缺点,如RNA提取所需的时间。转录逆转录协同反应(TRC) Ready®SARS-CoV-2 i易于使用,可在约40分钟内完成。比较了诊断为COVID-19的患者冷冻保存的鼻咽拭子样本的TRC Ready®SARS-CoV-2 i和使用TaqMan探针检测的实时一步RT-PCR。主要目的是检查阳性和阴性的一致性率。在-80°C低温保存的样品共69个。在预期为RT-PCR阳性的37个冷冻样本中,35个通过RT-PCR方法呈阳性。TRC Ready®SARS-CoV-2 i检测到33例阳性病例和2例阴性病例。一份预计RT-PCR阳性的冷冻样本在TRC Ready®SARS-CoV-2 i和RT-PCR上均呈阴性。此外,一份预计为RT-PCR阳性的冷冻样本经RT-PCR方法检测为阳性,而经TRC Ready®SARS-CoV-2 i检测为阴性。在32份预计为RT-PCR阴性的冷冻样本中,RT-PCR方法和TRC Ready®SARS-CoV-2 i检测均为阴性。与RT-PCR相比,TRC Ready®SARS-CoV-2 i阳性符合率为94.3%,阴性符合率为97.1%。TRC Ready®SARS-CoV-2 i由于易于操作,可广泛用于诊所和社区医院等医疗场所,并有望在感染控制方面发挥作用。
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来源期刊
Drug Discoveries and Therapeutics
Drug Discoveries and Therapeutics PHARMACOLOGY & PHARMACY-
CiteScore
3.20
自引率
3.20%
发文量
51
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