Centers for Disease Control and Prevention, Division of Healthcare Quality Promotion, Atlanta, GA, USA.
Am J Transplant. 2011 Jun;11(6):1201-8. doi: 10.1111/j.1600-6143.2011.03518.x.
To prevent unintentional transmission of bloodborne pathogens through organ transplantation, organ procurement organizations (OPOs) screen potential donors by serologic testing to identify human immunodeficiency virus (HIV) and hepatitis C virus (HCV) infection. Newly acquired infection, however, may be undetectable by serologic testing. Our objective was to estimate the incidence of undetected infection among potential organ donors and to assess the significance of risk reductions conferred by nucleic acid testing (NAT) versus serology alone. We calculated prevalence of HIV and HCV-stratified by OPO risk designation-in 13,667 potential organ donors managed by 17 OPOs from 1/1/2004 to 7/1/2008. We calculated incidence of undetected infection using the incidence-window period approach. The prevalence of HIV was 0.10% for normal risk potential donors and 0.50% for high risk potential donors; HCV prevalence was 3.45% and 18.20%, respectively. For HIV, the estimated incidence of undetected infection by serologic screening was 1 in 50,000 for normal risk potential donors and 1 in 11,000 for high risk potential donors; for HCV, undetected incidence by serologic screening was 1 in 5000 and 1 in 1000, respectively. Projected estimates of undetected infection with NAT screening versus serology alone suggest that NAT screening could significantly reduce the rate of undetected HCV for all donor risk strata.
为了防止通过器官移植传播血源性病原体,器官获取组织(OPO)通过血清学检测来筛选潜在供体,以确定人类免疫缺陷病毒(HIV)和丙型肝炎病毒(HCV)感染。然而,新获得的感染可能无法通过血清学检测检测到。我们的目的是估计潜在器官供体中未检测到的感染发生率,并评估核酸检测(NAT)与单独血清学相比降低风险的意义。我们计算了在 2004 年 1 月 1 日至 2008 年 7 月 1 日期间,由 17 个 OPO 管理的 13667 名潜在器官供体中,按 OPO 风险分类划分的 HIV 和 HCV 分层的流行率。我们使用发病率-窗口期方法计算未检测到感染的发生率。正常风险潜在供体的 HIV 流行率为 0.10%,高风险潜在供体为 0.50%;HCV 的流行率分别为 3.45%和 18.20%。对于 HIV,通过血清学筛查未检测到的感染发生率在正常风险潜在供体中为每 50000 例 1 例,在高风险潜在供体中为每 11000 例 1 例;对于 HCV,通过血清学筛查未检测到的感染发生率分别为每 5000 例和每 1000 例 1 例。与单独使用血清学筛查相比,NAT 筛查对未检测到的感染的预测估计表明,NAT 筛查可以显著降低所有供体风险分层的未检测到的 HCV 发生率。