首页> 外文期刊>Transfusion and apheresis science: official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis >Can the nucleic acid amplification test (NAT) be an alternative to the serologic tests? A prospective study, the results of 18,200 blood donors from the Turkish Red Crescent.
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Can the nucleic acid amplification test (NAT) be an alternative to the serologic tests? A prospective study, the results of 18,200 blood donors from the Turkish Red Crescent.

机译:核酸扩增测试(NAT)可以替代血清学测试吗?一项前瞻性研究,来自土耳其红新月会的18200名献血者的结果。

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AIM: Serologic tests having high sensitivity and specificity are used in order to prevent contamination with infectious agents from blood and blood products for transfusion safety. The present serologic tests have problems such as low sensitivity and weak detection capacity of infectious agents in the "window period". We aimed to test the use of NAT (Nucleic Acid Amplification Test) in routine blood screening in the Blood Bank. METHOD: We used the Procleix Ultrio (Chiron Ltd., USA) test kit based TMA (Transcription Mediated Amplification) for the NAT study of serum samples from 18,200 donors who came to the Turkish Red Crescent between February 2007 and September 2008. The NAT positive samples were studied twice. The discrimination of HIV, HCV and HBV NAT positive samples was performed by the Procleix Discrimination (Chiron Ltd., USA) test. Otherwise, Micro ELISA were used in parallel for routine serological screening of Anti-HIV, Anti-HCV, and HBsAg with Vironoste HIV Uni-form, AG/Ab innotest HCV Ab and Hepanostika Ultra HBsAg test kits. RESULTS: The results of serum samples with serology (+) and NAT (+) (13/18,200 and 0.05%) for anti-HIV, anti-HCV and HBsAg were higher than in other NAT studies; we also detected that a transfusion risk can occur in every 1400 transfusions.
机译:目的:使用具有高灵敏度和特异性的血清学检测方法,以防止血液和血液制品中的传染原污染,以确保输血安全。当前的血清学检查存在诸如“窗期”中的敏感性低和传染剂的检测能力弱的问题。我们旨在测试NAT(核酸扩增测试)在血库中常规血液筛查中的使用。方法:我们使用基于TMA(转录介导扩增)的Procleix Ultrio(美国Chiron Ltd.)测试试剂盒对2007年2月至2008年9月间来自土耳其红新月会的18,200个供体的血清样品进行NAT研究。NAT阳性样品进行了两次研究。通过Procleix Discrimination(美国Chiron Ltd.)测试对HIV,HCV和HBV NAT阳性样本进行区分。否则,将Micro ELISA平行用于Vironoste HIV Uni-form,AG / Ab innotest HCV Ab和Hepanostika Ultra HBsAg测试试剂盒的抗HIV,抗HCV和HBsAg的常规血清学筛查。结果:血清样本中血清(+)和NAT(+)的抗HIV,抗HCV和HBsAg含量分别高于其他NAT研究,分别为13 / 18,200和0.05%。我们还检测到每1400次输血可能发生输血风险。

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