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量化公共卫生服务中高危献血者中未检出的 HIV、乙肝病毒或丙肝病毒感染的风险。

Quantifying the risk of undetected HIV, hepatitis B virus, or hepatitis C virus infection in Public Health Service increased risk donors.

机构信息

Division of Healthcare Quality and Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia.

Office of Science and H. Milton Stewart School of Industrial and Systems Engineering, Georgia Institute of Technology, Centers for Disease Control and Prevention, Atlanta, Georgia.

出版信息

Am J Transplant. 2019 Sep;19(9):2583-2593. doi: 10.1111/ajt.15393. Epub 2019 May 10.

Abstract

To reduce the risk of HIV, hepatitis B virus (HBV), and hepatitis C virus (HCV) transmission through organ transplantation, donors are universally screened for these infections by nucleic acid tests (NAT). Deceased organ donors are classified as "increased risk" if they engaged in specific behaviors during the 12 months before death. We developed a model to estimate the risk of undetected infection for HIV, HBV, and HCV among NAT-negative donors specific to the type and timing of donors' potential risk behavior to guide revisions to the 12-month timeline. Model parameters were estimated, including risk of disease acquisition for increased risk groups, number of virions that multiply to establish infection, virus doubling time, and limit of detection by NAT. Monte Carlo simulation was performed. The risk of undetected infection was <1/1 000 000 for HIV after 14 days, for HBV after 35 days, and for HCV after 7 days from the time of most recent potential exposure to the day of a negative NAT. The period during which reported donor risk behaviors result in an "increased risk" designation can be safely shortened.

摘要

为了降低通过器官移植传播艾滋病毒、乙型肝炎病毒 (HBV) 和丙型肝炎病毒 (HCV) 的风险,供体通过核酸检测 (NAT) 普遍筛查这些感染。如果死者在死亡前 12 个月内有特定行为,则将其归类为“高风险”。我们开发了一种模型,以估算特定于供体潜在风险行为的类型和时间的 NAT 阴性供体中 HIV、HBV 和 HCV 未检测到感染的风险,以指导对 12 个月时间线的修订。估计了模型参数,包括高风险组获得疾病的风险、感染建立所需的病毒数量、病毒倍增时间以及 NAT 的检测下限。进行了蒙特卡罗模拟。从最近一次潜在暴露到 NAT 阴性的那一天起,14 天后 HIV 未检测到感染的风险<1/1 000 000,35 天后 HBV 未检测到感染的风险<1/1 000 000,7 天后 HCV 未检测到感染的风险<1/1 000 000。可以安全地缩短报告供体风险行为导致“高风险”指定的时间。

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