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作 者:赵年丰[1] 张伟红[1] 赵允文[1] 马亦林[1]
机构地区:[1]浙江医科大学附属第一医院传染病科
出 处:《浙江医科大学学报》1998年第6期252-253,270,共3页
摘 要:目的:对UGA作为药物性肝病诊断检测指标的价值作出评估。方法:以UGA检测、临床综合诊断及药物再投试验作联合平行或前后重叠试验,以药物再投试验作金标准,评估UGA的诊断价值。结果:药肝108例和各型病毒性肝炎150例中,UGA真阳性85例、假阳性23例,假阴性23例,真阴性127例。敏感性78.70%、特异性84.67%、漏诊率21.29%、误诊率15.33%,拟然比5.14,阳性符合率64.89%,阴性符合率73.41%,总符合率82.17,正确诊断指数0.64,可用度0.63。结论:UGA作为药物性肝病诊断检测指标,方法灵敏书异,结果较满意。Objective: To assess the value of UGA(urine glucaric acid) as a biochemical marker to diagnose drug-induced hepatitis. Methods =UGA measurement,clinical diagnosis and drug regiving test were performed in parallel or overlaping tests, with drug regiving test as the gold standard to assess the value of UGA measurement.Results: 108 cases of drug-induced hepatitis, 150 cases of viral hepatitis were included in the study. There were85 patients with true-positive result, 23 false-positive, 23 false-negative and 127 true negative. The sensitivitywas 78. 70%,specificity 84. 67 %,rate of missed diagnosis 21. 29 %, misdiagnosis rate 15. 33 %, likelihood rate is5. 14, positive-coincident rate 64. 89%, negative-coincident rate 73. 41 and total coincident rate 82. 17%,Youden's index 0. 64,and availability 0. 63. Conclusion:The method is sensitive,specific and satisfactory in diagnosing drug-induced hepatitis.
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