Doyle Nora M, Levison Judy E, Gardner Michael O
Department of Obstetrics, Gynecology, and Reproductive Medicine, Division of Maternal-Fetal Medicine, University of Texas-Houston Health Science Center, USA.
Am J Obstet Gynecol. 2005 Sep;193(3 Pt 2):1280-5. doi: 10.1016/j.ajog.2005.07.001.
Mother-to-child transmission of human immunodeficiency virus is the most common cause of pediatric human immunodeficiency virus in the United States; the Centers for Disease Control and Prevention recommendations endorse rapid human immunodeficiency virus testing for women with unknown viral status to quicken antiretroviral therapy. We compared the cost-effectiveness of Oraquick (Orasure Technologies, Bethlehem, Pa) rapid testing versus enzyme-linked immunosorbent assay testing for a low-risk population of Mexican American women who are in labor.
Using decision analysis techniques, we tested 2 strategies: (1) testing with enzyme-linked immunosorbent assay that was confirmed by Western blot and (2) testing with Oraquick rapid testing that was confirmed by Western blot. All seropositive parturients received zidovudine treatment in labor. The baseline assumptions were the incidence of human immunodeficiency virus in Mexican American mothers (0.05%), mother-to-child transmission with no treatment (25%), with treatment in labor (10%), sensitivity of enzyme-linked immunosorbent assay (98%), positive predictive value of enzyme-linked immunosorbent assay (10%), sensitivity/specificity of Oraquick rapid testing (99%/100%), positive predictive value of Oraquick rapid testing (83%-100%), sensitivity/specificity of Western blot (97%/99%), costs (enzyme-linked immunosorbent assay [dollar 5], Oraquick rapid testing [dollar 15], Western blot [dollar 25], zidovudine treatment [dollar 76] for 12 hours labor, neonatal treatment [dollar 2.50], lifetime treatment of human immunodeficiency virus-affected child [dollar 194,250]). Sensitivity analyses were done over a wide range of assumptions that included the costs of tests, the sensitivity of Oraquick rapid testing, the positive predictive value of enzyme-linked immunosorbent assay and Oraquick rapid testing, and the costs of treatments.
Oraquick rapid testing was the preferred strategy at dollar 98 spent per human immunodeficiency virus-negative child versus dollar 491 for enzyme-linked immunosorbent assay testing. Much of the cost of the enzyme-linked immunosorbent assay strategy was due to the treatment of women and infants with false-positive tests. Sensitivity analysis over test costs, test sensitivity, and other variables found the analysis results to be robust. Threshold analysis revealed that, if the cost remained < dollar 409.90, Oraquick rapid testing was the dominant test.
In a low prevalence population, the universal use of Oraquick rapid testing is cost-effective because of the low rate of false-positive results, thus preventing the emotional and economic costs of unnecessary treatment for human immunodeficiency virus to the new mother and her family.
在美国,人类免疫缺陷病毒母婴传播是儿童感染人类免疫缺陷病毒最常见的原因;疾病控制与预防中心的建议支持对病毒感染状况不明的女性进行快速人类免疫缺陷病毒检测,以加快抗逆转录病毒治疗。我们比较了Oraquick(奥瑞捷科技公司,宾夕法尼亚州伯利恒)快速检测与酶联免疫吸附测定法检测对低风险的墨西哥裔美国分娩女性人群的成本效益。
运用决策分析技术,我们测试了两种策略:(1)采用经蛋白印迹法确认的酶联免疫吸附测定法进行检测,(2)采用经蛋白印迹法确认的Oraquick快速检测法进行检测。所有血清学阳性的产妇在分娩时均接受齐多夫定治疗。基线假设为墨西哥裔美国母亲中人类免疫缺陷病毒的发病率(0.05%)、未治疗时的母婴传播率(25%)、分娩时治疗的母婴传播率(10%)、酶联免疫吸附测定法的敏感性(98%)、酶联免疫吸附测定法的阳性预测值(10%)、Oraquick快速检测法的敏感性/特异性(99%/100%)、Oraquick快速检测法的阳性预测值(83%-100%)、蛋白印迹法的敏感性/特异性(97%/99%)、成本(酶联免疫吸附测定法[5美元]、Oraquick快速检测法[15美元]、蛋白印迹法[25美元]、分娩12小时的齐多夫定治疗[76美元]、新生儿治疗[2.50美元]、受人类免疫缺陷病毒感染儿童的终身治疗[194,250美元])。在包括检测成本、Oraquick快速检测法的敏感性、酶联免疫吸附测定法和Oraquick快速检测法的阳性预测值以及治疗成本等广泛的假设范围内进行了敏感性分析。
对于每例人类免疫缺陷病毒阴性儿童,Oraquick快速检测法是首选策略,花费98美元,而酶联免疫吸附测定法检测花费491美元。酶联免疫吸附测定法策略的大部分成本是由于对检测结果为假阳性的女性和婴儿进行治疗所致。对检测成本、检测敏感性和其他变量的敏感性分析发现分析结果具有稳健性。阈值分析表明,如果成本保持在<409.90美元,Oraquick快速检测法是主导检测方法。
在低流行率人群中,普遍使用Oraquick快速检测法具有成本效益,因为假阳性结果率低,从而避免了给新妈妈及其家庭带来不必要的人类免疫缺陷病毒治疗的情感和经济成本。