Department of Public Health, Faculté de Medicine, University of Bunia, Bunia P.O. Box 292, Congo.
Department of Biostatistics and Epidemiology, Kinshasa School of Public Health, University of Kinshasa, Kinshasa P.O. Box 11850, Congo.
Int J Environ Res Public Health. 2022 Jan 19;19(3):1085. doi: 10.3390/ijerph19031085.
The Democratic Republic of the Congo adopted the integrase inhibitor dolutegravir (DTG) as part of its preferred first-line HIV treatment regimen in 2019. This study aimed to identify predictors of viral non-suppression among HIV-infected patients under a DTG-based regimen in the context of ongoing armed conflict since 2017 in the city of Bunia in the DRC. We conducted a cohort study of 468 patients living with HIV under DTG in all health facilities in Bunia. We calculated the proportion of participants with an HIV RNA of below 50 copies per milliliter. About three in four patients (72.8%) in this cohort had a viral load (VL) of <50 copies/mL after 6-12 months. After controlling for the effect of other covariates, the likelihood of having non-suppression remained significantly lower among the 25-34 age group and self-reported naïve patients with a baseline VL of ≥50 copies/mL. The likelihood of having non-suppression remained significantly higher among those who were at advanced stages of the disease, those with abnormal serum creatinine, those with high baseline HIV viremia over 1000 copies/mL, and the Sudanese ethnic group compared to the reference groups. This study suggests that we should better evaluate adherence, especially among adolescents and economically vulnerable populations, such as the Sudanese ethnic group in the city of Bunia. This suggests that an awareness of the potential effects of DTG and tenofovir is important for providers who take care of HIV-positive patients using antiretroviral therapy (ART), especially those with abnormal serum creatinine levels before starting treatment.
刚果民主共和国于 2019 年将整合酶抑制剂多替拉韦(DTG)纳入其首选的一线 HIV 治疗方案中。本研究旨在确定在刚果民主共和国布尼亚市自 2017 年以来持续武装冲突背景下,接受 DTG 为基础方案治疗的 HIV 感染患者病毒未抑制的预测因素。我们对布尼亚市所有卫生机构中接受 DTG 治疗的 468 名 HIV 感染者进行了队列研究。我们计算了 HIV RNA 低于 50 拷贝/毫升的参与者比例。在该队列中,约四分之三的患者(72.8%)在 6-12 个月后病毒载量(VL)<50 拷贝/mL。在控制了其他协变量的影响后,年龄在 25-34 岁之间且基线 VL≥50 拷贝/mL 的自报初治患者以及报告基线 HIV 病毒载量超过 1000 拷贝/mL 的患者,其未抑制的可能性仍显著较低。在疾病晚期、血清肌酐异常、基线 HIV 病毒载量高(超过 1000 拷贝/mL)的患者以及与参考组相比,苏丹族患者中,未抑制的可能性显著更高。本研究表明,我们应该更好地评估依从性,特别是在青少年和经济弱势群体中,如布尼亚市的苏丹族。这表明,对于使用抗逆转录病毒疗法(ART)治疗 HIV 阳性患者的提供者来说,了解 DTG 和替诺福韦的潜在影响很重要,尤其是那些在开始治疗前血清肌酐水平异常的患者。