首页> 外文期刊>Transfusion: The Journal of the American Association of Blood Banks >Comparison of the analytical and operational performance of two viral nucleic acid test blood screening systems: Procleix Tigris and cobas s 201.
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Comparison of the analytical and operational performance of two viral nucleic acid test blood screening systems: Procleix Tigris and cobas s 201.

机译:两种病毒核酸试验血液筛查系统的分析和操作性能的比较:Procleix Tigris和Cobas S 201。

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BACKGROUND: The operational and analytical performance of two automated triplex hepatitis B virus (HBV), hepatitis C virus (HCV), and human immunodeficiency virus (HIV) nucleic acid test (NAT) systems were compared in four screening laboratories of the French Blood Service. STUDY DESIGN AND METHODS: Two laboratories evaluated the Procleix Tigris system (Chiron/Gen-Probe) in individual donation (ID) format and two sites used the cobas s 201 system (Roche Molecular Systems) on minipools (MPs) of six donations. The analytical sensitivity, the specificity, and operational performance were compared. RESULTS: The ID to MP-NAT relative sensitivity factors in standard dilution panels of different genotypes varied between 8.7 and 21.9 for HCV RNA, 6.7 and 14.8 for HIV RNA, and 0.71 and 11.6 for HBV DNA. Tigris was 800-fold more sensitive than cobas s 201 (1:6) for a HIV group O sample, but did not detect the HIV-2 sample picked up by cobas s 201 with equal sensitivity as the HIV-1 group M samples. The specificity of both NAT systems after initial screening of 10,520 donations with Tigris and 1444 test pools on s 201 was 99.9 percent for both systems, but reached 100 percent after the repeat and pool resolution test algorithms. A higher throughput of the pool test protocol on cobas s 201 became apparent when the daily workload was more than 400 donations. CONCLUSIONS: Tigris ID-NAT format was significantly more sensitive than cobas s 201 MP-NAT in detecting HCV RNA and HIV RNA dilution panels, but despite the 1:6 dilution factor in s 201 the difference in sensitivity was not significant for some of the HBV genotype panels. Both NAT systems demonstrated acceptable operational performance, but for routine use further improvement in system reliability is desirable.
机译:背景:在法国血液服务的四种筛查实验室比较了两种自动三醇乙型肝炎病毒(HBV),丙型肝炎病毒(HCV),丙型肝炎病毒(HCV)和人免疫缺陷病毒(HIV)核酸试验(NAT)系统的操作和分析性能。研究设计和方法:两位实验室评估了个别捐赠(ID)格式的Procleix Tigris系统(Chiron / Gen-Probe),两种位点在六个捐赠的微型池(MPS)上使用了COBAS S 201系统(Roche分子系统)。比较分析敏感性,特异性和操作性能。结果:不同基因型的标准稀释面板中的MP-NAT相对灵敏度因子的ID在8.7和21.9之间,HCV RNA为6.7和14.8,对于HBV DNA,0.71和11.6。对于HIV族O样品,底格里斯比COIV组201(1:6)更敏感,但没有检测到COBAS S 201拾起的HIV-2样品,与HIV-1组M样品相同的敏感性。对于两种系统初始筛选10,520次捐赠10,520次捐赠的NAT系统的特异性为两种系统的99.9%,但重复和池分辨率测试算法后达到100%。当每日工作量超过400份捐赠时,COBAS 201的池试验协议的较高吞吐量变得明显。结论:TIGRIS ID-NAT格式在检测HCV RNA和HIV RNA稀释面板中的纤维组201 MP-NAT显着敏感,但尽管S 201中的1:6稀释因子,但敏感性的差异对于一些人来说并不重要HBV基因型面板。本土系统都表现出可接受的操作性能,但对于常规使用,可以参与系统可靠性的进一步提升。

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