Melaku Abebe Yehualaw, Cherie Niguss, Birhanu Tarikua Afework, Wudu Muluken Amare
CDC Monitoring and Evaluation Officer at Dessie Comprehensive Specialized Hospital, Dessie, Ethiopia.
Reproductive and Family Health Department, School of Public Health, College of Medicine and Health Sciences, Wollo University, Dessie, Ethiopia.
Front Med (Lausanne). 2025 Mar 10;12:1496144. doi: 10.3389/fmed.2025.1496144. eCollection 2025.
Despite the increasing number of patients on second-line antiretroviral therapy in low-income countries such as Ethiopia, there is limited evidence regarding the time to viral re-suppression. Therefore, this study aimed to assess the time to viral load re-suppression and its predictors among adult patients on second-line antiretroviral therapy in northeastern Ethiopia.
A multi-center, institution-based prospective follow-up study was conducted over 48 months, from February 2022 to February 2024, involving 526 adults living with human immunodeficiency virus (HIV) who were receiving second-line antiretroviral therapy in northeastern Ethiopia. Data were collected through face-to-face interviews and chart reviews. A Weibull proportional hazards model was fitted to identify the predictors of viral re-suppression.
The median time to viral re-suppression was 9 months (IQR = 3-15 months). The rate of viral re-suppression was 44.3 per 1,000 person-months (95% CI: 40.4-49). Predictors of viral re-suppression included disclosure of Human Immunodeficiency Virus (HIV) status [AHR 2.24 (95% CI: 1.4-3.7)], classification in World Health Organization (WHO) clinical stages I and II [AHR 6.9 (95% CI: 4.4-9.6)], receipt of tuberculosis (TB) preventive treatment [AHR 3.7 (95% CI: 2.3-5.93)], absence of first-line drug substitution history [AHR 1.44 (95% CI: 1.2-1.8)], and good adherence to treatment [AHR 1.9 (95% CI: 1.4-2.54)].
In this study, the time to viral load re-suppression was longer than expected. Disclosure status, WHO clinical stage I or II, receiving tuberculosis preventive treatment, and the absence of first-line drug substitution history were predictors of viral load re-suppression. Health managers and antiretroviral therapy care providers must improve the timing and effectiveness of early disclosure, encourage the early use of tuberculosis prophylaxis, and maintain good adherence through various strategies.
尽管在埃塞俄比亚等低收入国家接受二线抗逆转录病毒治疗的患者数量不断增加,但关于病毒重新抑制时间的证据有限。因此,本研究旨在评估埃塞俄比亚东北部接受二线抗逆转录病毒治疗的成年患者的病毒载量重新抑制时间及其预测因素。
从2022年2月至2024年2月进行了一项为期48个月的多中心、基于机构的前瞻性随访研究,涉及526名在埃塞俄比亚东北部接受二线抗逆转录病毒治疗的成人艾滋病病毒(HIV)感染者。数据通过面对面访谈和病历审查收集。采用威布尔比例风险模型来确定病毒重新抑制的预测因素。
病毒重新抑制的中位时间为9个月(四分位间距=3-15个月)。病毒重新抑制率为每1000人月44.3例(95%置信区间:40.4-49)。病毒重新抑制的预测因素包括艾滋病病毒(HIV)感染状况的披露[AHR 2.24(95%置信区间:1.4-3.7)]、世界卫生组织(WHO)临床I期和II期分类[AHR 6.9(95%置信区间:4.4-9.6)]、接受结核病(TB)预防性治疗[AHR 3.7(95%置信区间:2.3-5.93)]、无一线药物替代史[AHR 1.44(95%置信区间:1.2-1.8)]以及良好的治疗依从性[AHR 1.9(95%置信区间:1.4-2.54)]。
在本研究中,病毒载量重新抑制的时间比预期的要长。感染状况的披露、WHO临床I期或II期、接受结核病预防性治疗以及无一线药物替代史是病毒载量重新抑制的预测因素。卫生管理人员和抗逆转录病毒治疗护理提供者必须改善早期披露的时机和效果,鼓励早期使用结核病预防措施,并通过各种策略保持良好的依从性。