Ifakara Health Institute, Ifakara Branch, Ifakara, United Republic of Tanzania.
Swiss Tropical and Public Health Institute, Basel, Switzerland.
BMC Infect Dis. 2023 Apr 7;23(1):222. doi: 10.1186/s12879-023-08155-6.
Monitoring HIV viral load (HVL) in people living with HIV (PLHIV) on antiretroviral therapy (ART) is recommended by the World Health Organization. Implementation of HVL testing programs have been affected by logistic and organizational challenges. Here we describe the HVL monitoring cascade in a rural setting in Tanzania and compare turnaround times (TAT) between an on-site and a referral laboratory.
In a nested study of the prospective Kilombero and Ulanga Antiretroviral Cohort (KIULARCO) we included PLHIV aged ≥ 15 years, on ART for ≥ 6 months after implementation of routine HVL monitoring in 2017. We assessed proportions of PLHIV with a blood sample taken for HVL, whose results came back, and who were virally suppressed (HVL < 1000 copies/mL) or unsuppressed (HVL ≥ 1000 copies/mL). We described the proportion of PLHIV with unsuppressed HVL and adequate measures taken as per national guidelines and outcomes among those with low-level viremia (LLV; 100-999 copies/mL). We compare TAT between on-site and referral laboratories by Wilcoxon rank sum tests.
From 2017 to 2020, among 4,454 PLHIV, 4,238 (95%) had a blood sample taken and 4,177 (99%) of those had a result. Of those, 3,683 (88%) were virally suppressed. In the 494 (12%) unsuppressed PLHIV, 425 (86%) had a follow-up HVL (102 (24%) within 4 months and 158 (37%) had virologic failure. Of these, 103 (65%) were already on second-line ART and 32/55 (58%) switched from first- to second-line ART after a median of 7.7 months (IQR 4.7-12.7). In the 371 (9%) PLHIV with LLV, 327 (88%) had a follow-up HVL. Of these, 267 (82%) resuppressed to < 100 copies/ml, 41 (13%) had persistent LLV and 19 (6%) had unsuppressed HVL. The median TAT for return of HVL results was 21 days (IQR 13-39) at the on-site versus 59 days (IQR 27-99) at the referral laboratory (p < 0.001) with PLHIV receiving the HVL results after a median of 91 days (IQR 36-94; similar for both laboratories).
Robust HVL monitoring is achievable in remote resource-limited settings. More focus is needed on care models for PLHIV with high viral loads to timely address results from routine HVL monitoring.
世界卫生组织建议对接受抗逆转录病毒疗法(ART)的艾滋病毒感染者(PLHIV)进行 HIV 病毒载量(HVL)监测。HVL 检测项目的实施受到后勤和组织方面挑战的影响。在此,我们描述了坦桑尼亚农村地区的 HVL 监测级联,并比较了现场和转介实验室之间的周转时间(TAT)。
在 2017 年常规 HVL 监测实施后,我们对前瞻性 Kilombero 和 Ulanga 抗逆转录病毒队列(KIULARCO)进行了嵌套研究,纳入了年龄≥15 岁、接受 ART 治疗≥6 个月的 PLHIV。我们评估了有血液样本进行 HVL 检测的 PLHIV 的比例、其结果返回的比例以及病毒抑制(HVL<1000 拷贝/ml)或未抑制(HVL≥1000 拷贝/ml)的比例。我们描述了根据国家指南,未抑制 HVL 的 PLHIV 的比例和采取的适当措施,以及低病毒载量(LLV;100-999 拷贝/ml)患者的结果。我们通过 Wilcoxon 秩和检验比较现场和转介实验室之间的 TAT。
在 2017 年至 2020 年期间,在 4454 名 PLHIV 中,有 4238 名(95%)接受了血液样本采集,其中 4177 名(99%)有检测结果。在这些患者中,有 3683 名(88%)病毒抑制。在 494 名(12%)未抑制的 PLHIV 中,有 425 名(86%)进行了 HVL 随访(102 名[24%]在 4 个月内,158 名[37%]发生病毒学失败)。其中,有 103 名(65%)已经在接受二线 ART,32 名/55 名(58%)在中位 7.7 个月(IQR 4.7-12.7)后从一线转为二线 ART。在 371 名(9%)有 LLV 的 PLHIV 中,有 327 名(88%)进行了 HVL 随访。其中,有 267 名(82%)重新抑制至<100 拷贝/ml,有 41 名(13%)持续存在 LLV,有 19 名(6%)未抑制 HVL。现场实验室 HVL 结果返回的中位 TAT 为 21 天(IQR 13-39),转介实验室为 59 天(IQR 27-99)(p<0.001),PLHIV 收到 HVL 结果的中位时间为 91 天(IQR 36-94;两个实验室相似)。
在偏远的资源有限的环境中,可以实现稳健的 HVL 监测。需要更加关注 HIV 载量高的 PLHIV 的护理模式,以便及时处理常规 HVL 监测的结果。