Facente Consulting, San Francisco, California, United States of America.
PLoS One. 2011;6(7):e21813. doi: 10.1371/journal.pone.0021813. Epub 2011 Jul 6.
Federal guidelines now recommend supplemental HIV RNA testing for persons at high risk for acute HIV infection. However, many rapid HIV testing sites do not include HIV RNA or p24 antigen testing due to concerns about cost, the need for results follow-up, and the impact of expanded venipuncture on clinic flow. We developed criteria to identify patients in a municipal STD clinic in San Francisco who are asymptomatic but may still be likely to have acute infection.
Data were from patients tested with serial HIV antibody and HIV RNA tests to identify acute HIV infection. BED-CEIA results were used to classify non-acute cases as recent or longstanding. Demographics and self-reported risk behaviors were collected at time of testing. Multivariate models were developed and preliminarily evaluated using predictors associated with recent infection in bivariate analyses as a proxy for acute HIV infection. Multivariate models demonstrating ≥70% sensitivity for recent infection while testing ≤60% of patients in this development dataset were then validated by determining their performance in identifying acute infections.
From 2004-2007, 137 of 12,622 testers had recent and 36 had acute infections. A model limiting acute HIV screening to MSM plus any one of a series of other predictors resulted in a sensitivity of 83.3% and only 47.6% of patients requiring testing. A single-factor model testing only patients reporting any receptive anal intercourse resulted in 88.9% sensitivity with only 55.2% of patients requiring testing.
In similar high risk HIV testing sites, acute screening using "supplemental" HIV p24 antigen or RNA tests can be rationally targeted to testers who report particular HIV risk behaviors. By improving the efficiency of acute HIV testing, such criteria could facilitate expanded acute case identification.
联邦指南现在建议对有急性 HIV 感染高危风险的人群进行补充 HIV RNA 检测。然而,由于担心成本、对结果进行随访的需求以及扩大静脉穿刺对诊所流程的影响,许多快速 HIV 检测点不包括 HIV RNA 或 p24 抗原检测。我们制定了标准,以确定旧金山一家市立 STD 诊所中无症状但仍可能发生急性感染的患者。
数据来自接受连续 HIV 抗体和 HIV RNA 检测以确定急性 HIV 感染的患者。BED-CEIA 结果用于将非急性病例归类为近期或长期。在检测时收集人口统计学和自我报告的风险行为数据。使用双变量分析中与近期感染相关的预测因子开发多变量模型,并初步评估其作为急性 HIV 感染替代指标的近期感染相关性。在开发数据集内检测到≥70%的近期感染且仅对≤60%的患者进行检测的多变量模型,然后通过确定其在识别急性感染方面的性能进行验证。
2004-2007 年,137 名测试者中有近期感染,36 名有急性感染。一种将急性 HIV 筛查限制为男男性行为者加一系列其他预测因子的模型导致敏感性为 83.3%,仅需检测 47.6%的患者。仅对报告任何接受性肛交的患者进行测试的单因素模型具有 88.9%的敏感性,仅需检测 55.2%的患者。
在类似的高风险 HIV 检测点,使用“补充”HIV p24 抗原或 RNA 检测进行急性筛查可以合理地针对报告特定 HIV 风险行为的测试者。通过提高急性 HIV 检测的效率,这些标准可以促进急性病例的广泛识别。