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机构地区:[1]中山大学附属第三医院检验科,广州510630
出 处:《国际医药卫生导报》2014年第19期3003-3006,共4页International Medicine and Health Guidance News
摘 要:目的探讨三种检测方法作为临床筛选和诊断丙型肝炎的的优缺点。方法随机收集71例丙肝患者血清作为阳性组,63例非丙肝患者血清作为阴性组,采用PCR-荧光探针法检测HCV RNA,同时采用CMIA法和ELISA法检测Anti—HCV。结果阳性组中,PCR-荧光探针法灵敏度为87.32%,CMIA为100%,ELISA为97.18%;经卡方检验分析,χ^2=4.95,两种Anti—HCV检测方法均与PCR-荧光探针法检测结果的差异有统计学意义(P〈0.05);而两种Anti—HCV检测方法之间差异无统计学意义(P〉0.05);阴性组中,HCV RNA特异度为100%,CMIA为95.23%,ELISA为98.41%;经χ^2检验分析,χ^2=3.84,三种诊断方法特异度的差异无统计学意义(P〉0.05)。结论三种方法各有利弊,在诊断丙型肝炎方面,本文推荐采用其中一种抗体检测方法与PCR-荧光探针法联合检测;在疗效观察方面,本文推荐PCR-荧光探针法;在大规模体检时,考虑经济因素,本文推荐ELISA;在Anti—HCV检测结果为阳性,或者两种Anti—HCV检测方法结果不一致时,需联合HCV RNA检测。Objective To explore the advantages and disadvantages of three methods for clinical screening and diagnosis in Hepatitis C. Methods 71 cases of Hepatitis C patients for experimental group , while 63 negative samples excluding Hepatitis C as control group. Antibody Hepatitis C Virus (Anti-HCV) was detected by PCR-fluorescent probe ,chemiluminesent microparticle immunoassay(CMIA) and enzyme linked immunosorbent assay(ELISA) respectively. Results In the positive group, the sensitivity of PCR-fluorescent probe was 87.32%, CMIA was 100%, ELISA was 97.18%; Analyzed by chi-square test, χ^2=4-95, the difference between PCR-fluorescent probe and other kinds of methods was statistically significant (P 〈0.05), while no significant difference between CMIA and ELISA (P〉 0.05). In control group, the specificity of PCR- fluorescent probe was 100%, CMIA 95.23%, ELISA 98.41%, respectively; Analyzed hy χ^2 test, the specificity of three methods had no statistically significant (P〉 0.05), χ^2=3.84. Conclusions There were advantages and disadvantages for three methods in the diagnosis of Hepatitis C. One of the methods in CMIA and ELISA combined with PCR-fluoreseence probe was recommended for diagnosing Hepatitis C. If you are going to monitor the treatment effect, PCR-fluorescence probe must be used; However, ELISA is widely used in most of the hospitals for the economic reasan. When the result of Anti-HCV was suspicious or positive, PCR was needed to be detected to conform its authenticity.
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