Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
Department of Molecular Microbiology & Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
J Acquir Immune Defic Syndr. 2019 Nov 1;82(3):287-296. doi: 10.1097/QAI.0000000000002155.
To minimize false-positive diagnoses of HIV in exposed infants, the World Health Organization recommends confirmatory testing for all infants initiating antiretroviral therapy (ART). In settings where confirmatory testing is not feasible or intermittently performed, clinical decisions may be aided by semi-quantitative cycle thresholds (Cts) that identify positive results most likely to be false-positive.
We developed a decision analysis model of HIV-exposed infants in sub-Saharan Africa to estimate the clinical consequences of deferring ART for infants with weakly positive ("indeterminate") results. We assessed the degree to which "indeterminate" results may reduce the number of infants starting ART unnecessarily while missing a small number of HIV-infected infants. Our primary outcome was the ratio of averted unnecessary ART regimens to additional HIV-related deaths (due to false-negative diagnosis) at different Ct cutoffs.
The clinical consequences of adopting an indeterminate range varied with the prevalence of HIV and Ct cutoff. Considering a Ct cutoff ≥33, adopting an indeterminate range could prevent a median of 1.4 infants from receiving ART unnecessarily (95% UR: 1.0-2.0) for each additional HIV-related death. This ratio could be improved by prioritizing infants with indeterminate results for confirmatory testing [median 8.8 (95% UR: 6.0-13.3)] and by adopting a higher cutoff [median 82.3 (95% UR: 49.0-155.8) with Ct ≥36].
When implemented in settings where confirmatory testing is not universal, the benefits of classifying weakly positive results as "indeterminate" may outweigh the risks. Accordingly, the World Health Organization has recommended Ct values ≥33 be considered indeterminate for infant HIV diagnosis.
为了尽量减少暴露于 HIV 的婴儿中 HIV 假阳性诊断,世界卫生组织建议对所有开始抗逆转录病毒治疗(ART)的婴儿进行确认性检测。在无法进行或间歇性进行确认性检测的情况下,半定量循环阈值(Ct)可帮助临床决策,确定最有可能为假阳性的阳性结果。
我们开发了撒哈拉以南非洲地区 HIV 暴露婴儿的决策分析模型,以估计对弱阳性(“不确定”)结果的婴儿延迟 ART 的临床后果。我们评估了“不确定”结果在错过少数 HIV 感染婴儿的情况下,减少不必要开始 ART 的婴儿数量的程度。我们的主要结果是不同 Ct 截止值下避免不必要的 ART 方案与因假阴性诊断而导致的额外 HIV 相关死亡(ART)的比值。
采用不确定范围的临床后果因 HIV 流行率和 Ct 截止值而异。考虑到 Ct 截止值≥33,采用不确定范围可以防止中位数为 1.4 名婴儿因每例额外的 HIV 相关死亡而不必要地接受 ART(95% UR:1.0-2.0)。通过优先对不确定结果的婴儿进行确认性检测[中位数 8.8(95% UR:6.0-13.3)],或者通过采用更高的截止值[Ct≥36 时中位数 82.3(95% UR:49.0-155.8)],可以改善该比值。
在无法普遍进行确认性检测的情况下实施时,将弱阳性结果归类为“不确定”的好处可能大于风险。因此,世界卫生组织建议将 Ct 值≥33 视为婴儿 HIV 诊断的不确定值。