基于dolutegravvir的抗逆转录病毒治疗在埃塞俄比亚亚的斯亚贝巴预防母婴传播诊所的妇女中实现无法检测到的HIV-1病毒载量方面的作用。

IF 2.3 Q2 MEDICINE, GENERAL & INTERNAL
SAGE Open Medicine Pub Date : 2025-02-12 eCollection Date: 2025-01-01 DOI:10.1177/20503121251320460
Belete Woldesemayat, Yimam Getaneh, Sisay Adane, Ajanaw Yizengaw, Amelework Yilma, Shambel Araya Haile, Kidist Zealiyas
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引用次数: 0

摘要

目的:本研究旨在确定孕妇和哺乳期妇女中基于和不基于dolutegravil方案的可检测HIV-1病毒载量及其相关因素的流行情况。方法:hiv阳性孕妇和哺乳期妇女纳入横断面研究设计,将Dolutegravir组与非Dolutegravir组进行比较,研究于2022年9月至2023年3月进行。共有684名妇女在16个预防母婴传播诊所接受抗逆转录病毒治疗(456名妇女接受基于dolutegravvir的治疗,228名妇女接受非基于dolutegravvir的治疗)。未检测到的病毒载量被定义为:结果:在不基于dolutegravvir的方案组中可检测到的病毒载量为32.9%,在基于dolutegravvir的方案组中为19.7%。总患病率为24.1% (95% CI: 20.9-27.6)。与非dolutegravir方案相比,dolutegravir方案与69%的相关性(AOR: 0.31;95% CI: 0.16-0.61)具有可检测病毒载量的风险较低。基于dolutegravvir方案的女性的中位病毒载量(1.66 log copies/mL)显著低于非基于dolutegravvir方案的女性(2.11 log copies/mL;结论:尽管基于dolutegravite的方案的规模扩大,但可检测到的病毒血症的总体患病率为24.1%,而非基于dolutegravite的方案的妇女患病率更高,为32.9%,这表明可能影响母婴传播结果的规划挑战。加强依从性监测和维持世界卫生组织的临床I期对于实现孕妇和哺乳期妇女无法检测到的病毒载量水平至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of Dolutegravir-based antiretroviral treatment in achieving an undetectable HIV-1 viral load among women attending prevention of mother-to-child transmission clinics in Addis Ababa, Ethiopia.

Objectives: This study aimed to determine the prevalence of detectable HIV-1 viral load and associated factors among pregnant and lactating women on Dolutegravir-based and non-Dolutegravir-based regimens.

Methods: HIV-positive pregnant and breastfeeding women enrolled in a cross-sectional study design incorporating Dolutegravir versus non-Dolutegravir group for comparison purposes, and the study was conducted from September 2022 to March 2023. In total, 684 women receiving antiretroviral treatment (456 on Dolutegravir-based and 228 on non-Dolutegravir-based regimens) were enrolled across 16 prevention of mother-to-child transmission clinics. An undetectable viral load was defined as <20 RNA copies/mL. Univariable and multivariable regression models were used to determine the associations of the detectable viral load with factors such as sociodemographic, clinical, obstetric, and laboratory parameters.

Results: The prevalence of detectable viral load on a non-Dolutegravir-based regimen was 32.9% and on a Dolutegravir-based regimen group was 19.7%. The overall prevalence was 24.1% (95% CI: 20.9-27.6). Compared with non-Dolutegravir-based regimens, Dolutegravir-based regimens were associated with 69% (AOR: 0.31; 95% CI: 0.16-0.61) lower risk of having a detectable viral load. The median viral load was significantly lower in women on a Dolutegravir-based regimen (1.66 log copies/mL) compared to those on a non-Dolutegravir-based regimen (2.11 log copies/mL; p < 0.001). A lower level of adherence was associated with 2.33 times (AOR: 2.33; 95% CI: 1.06-5.12) higher odds of having a detectable viral load and women who had a WHO clinical stage II and above were 2.71 times (AOR: 2.71: 95% CI: 1.30-5.64) more vulnerable to developing a detectable viremia than their counterparts.

Conclusion: Despite the scale-up of Dolutegravir-based regimens, the overall prevalence of detectable viremia was 24.1%, with a higher prevalence of 32.9% among women on non-Dolutegravir-based regimens indicating a programmatic challenge that could affect mother-to-child transmission outcomes. Strengthening adherence monitoring and maintaining World Health Organization clinical stage I is crucial for achieving undetectable viral load levels in pregnant and breastfeeding women.

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SAGE Open Medicine
SAGE Open Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
3.50
自引率
4.30%
发文量
289
审稿时长
12 weeks
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