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机构地区:[1]佳木斯大学临床医学院检验系,黑龙江佳木斯154003 [2]佳木斯大学附属第一医院检验科,黑龙江佳木斯154003
出 处:《黑龙江医药科学》2008年第3期17-18,共2页Heilongjiang Medicine and Pharmacy
摘 要:目的:探讨荧光定量逆转录聚合酶链反应(FQ-PCR)、酶联免疫吸附试验(ELISA)联合检测丙型肝炎病毒的临床意义。方法:用FQ-PCR联合ELISA方法检测117例临床已确诊为丙型肝炎患者的血清,同时检测它们的丙氨酸氨基转移酶(AAT)。结果:1抗-HCV阳性率随着HCV-RNA含量的升高而增高,其阳性率与HCV-RNA含量呈正相关。287例HCV-RNA阳性标本中,有50例ALT异常,其异常率随着HCV-RNA含量的升高而增高,ALT异常率与HCV-RNA含量呈正相关,ALT水平和HCV-RNA含量之间呈正相关。3FQ-PCR检测敏感性为74.4%(87/117),漏检率为25.6%(30/117)。ELISA法检测敏感性为76.9%(90/117),漏检率为23.1%(27/117)。两种方法联合检测敏感性为92.3%(108/117),漏检率为7.7%(9/117)。结论:两种方法联合检测,互相补充,大大提高了丙型肝炎病毒的检出率,为临床早期,准确诊断丙型病毒肝炎、监测病情、观察疗效提供了有力的依据,为献血人员筛选和血制品安全提供了有力保障。Objective : To discuss the clinical significance of detection of hepatitis C virus by FQ--PCR and ELISA. Methods:We detected of 117 sera of clinical patients who had been diagnosed as hepatitis C, and at the same time tested their atanine aminotransferase(AAT). Results :(1) Anti -- HCV's positive rate rose with HCV--RNA content increase. By using correlation analysis,anti--HCV positive rate and HCV-- RNA content showed positive correlation. (2)There were 50 AAT abnormal ones in 87 HCV--RNA positive samples. AAT abnormal rate rose with HCV--RNA content increase,showing positive correlation by using correlation analysis, and there was a positive correlation between the AAT level and HCV--RNA content. (3)FQ--PCR detection sensitivity was 74.4%(87/117),and omission factor was 25.6%(30/117). ELISA detection sensitivity was 76.9%(90/117),and omission factor was 23. 1%(27/117). Combined detection sensitivity of two kinds of methods was 92. 3%(108/117), and omission factor was 7. 7%(9/117). Combined detection sensitivity was higher than that of separate. Conclusion:The combined detection is complementary,and greatly improves the hepatitis C virus detection rate,providing a powerful basis for clinical early and accurate diagnosis of hepatitis C virus ,condition monitoring,and clinical observation, and providing a strong support for screening blood donors and safety of blood products.
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