评估生物沙利娃的使用,以检测sars - cov2方法rtpcr

S. Kesuma, Suparno Putera Makkadafi
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引用次数: 0

摘要

自2019年底以来,SARS - CoV-2感染影响了全球,可导致严重的下呼吸道感染,对一些患者可能是致命的。这种感染会导致Covid-19疾病。采用RT-PCR等NAAT(核酸扩增试验)方法诊断SARS-CoV-2感染。鉴定SARS-COV-2所需的样本是鼻咽/口咽拭子。鼻咽/口咽拭子取样需要训练有素的人员。鼻咽/口咽拭子是侵入性的,在实施过程中会引起不适。采样标本的便利性可以作为鉴定SARS-CoV-2的另一种选择,例如使用新开发的生物唾液标本。在检查SARS-CoV-2的鉴定时,使用这种生物唾液样本是一种实用的选择。然而,由于这些标本与临床发现可能存在关系,因此需要首先对这些标本的使用进行评估,以便SARS-CoV-2检查结果有效和可靠。本研究的目的是评价利用生物唾液标本检测SARS-CoV-2感染的RT-PCR方法。生物唾液在鼻咽/口咽拭子配对T检验和金标准诊断法检测SARS-COV-2中的应用评价检测SARS-CoV-2的靶基因为RdRp基因和控制HRP基因的E基因。RT-PCR 40个循环,温度62°C。本研究结果为Sig(双尾)配对T检验为0.106,敏感性为64.86%,特异性为90.92%。本研究的结论是,使用生物唾液标本与鼻咽/口咽拭子的SARS-CoV-2 RT-PCR方法的结果无统计学差异,评价结果表明,在检查SARS-CoV-2感染时,使用可靠的生物唾液标本作为样本。
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Evaluasi Penggunaan Biosaliva Dalam Deteksi Sars-Cov-2 Metode RT-PCR
SARS CoV-2 infection, which has affected the world since late 2019, can cause serious lower respiratory tract infections that may be fatal in some patients. This infection causes the disease Covid-19. The diagnosis of SARS-CoV-2 infection was carried out by NAAT (Nucleic Acid Amplification Test) such as RT-PCR examination. The sample needed for the identification of SARS-COV-2 is a nasopharyngeal/oropharyngeal swab. Nasopharyngeal/oropharyngeal swab sampling requires trained personnel. Taking a nasopharyngeal/oropharyngeal swab is invasive, causing discomfort in its implementation. The convenience of sampling specimens can be an alternative option for the identification of SARS-CoV-2, such as with newly developed biosaliva specimens. The use of this biosaliva sample can be a practical option in the examination of the identification of SARS-CoV-2. However, the use of these specimens needs to be evaluated first because of the possible relationship with clinical findings and so that the results of the SARS-CoV-2 examination are valid and reliable. The purpose of this study was to evaluate the use of biosaliva specimens to detect SARS-CoV-2 infection with the RT-PCR method. Evaluation of the use of biosaliva in the detection of SARS-COV-2 RT-PCR method with paired T test and diagnostic test with the gold standard using nasopharyngeal/oropharyngeal swabs. The target genes for the detection of SARS-CoV-2 are the RdRp gene and the E gene with control of the HRP gene. RT-PCR was carried out with 40 cycles and Tm 62 °C. The results of this study are Sig. (2-tailed) paired T test was 0.106, sensitivity was 64.86% and specificity was 90.92%. The conclusion of this study is that there is no statistical difference in the results of the SARS-CoV-2 RT-PCR method between the use of biosaliva specimens and nasopharyngeal/oropharyngeal swabs, and the evaluation results show that reliable biosaliva specimens are used as samples in the examination of SARS-COV-2 infection.
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