莫桑比克儿科多鲁特韦的推广和感染艾滋病毒儿童的病毒学结果。

Southern African journal of HIV medicine Pub Date : 2024-07-31 eCollection Date: 2024-01-01 DOI:10.4102/sajhivmed.v25i1.1578
Ivete Meque, Nicole Herrera, Amâncio Nhangave, Dórcia Mandlate, Rui Guilaze, Ana Tambo, Abdul Mussa, Nilesh Bhatt, Michelle M Gill
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引用次数: 0

摘要

背景:2022年,莫桑比克引入了多罗替拉韦10毫克(pDTG),作为儿童抗逆转录病毒疗法的一部分,用于体重小于20公斤的儿童。了解全国推广过程中的实际挑战可以加强资源有限环境中的卫生系统:我们描述了艾滋病毒感染儿童向 pDTG 过渡的比率和新启动率、pDTG 后的病毒载量抑制(VLS)以及与 VLS 相关的因素:我们对年龄小于 9 岁的儿童进行了一项回顾性队列研究,并从临床资料中提取了数据。我们使用逻辑回归评估了VLS和pDTG启动的预测因素:在 1353 名儿童中,有 1146 名开始使用 pDTG;196 名(14.5%)没有体重记录。转用 pDTG 后,98.9% 的儿童(950/961)保持使用相同的核苷类逆转录酶抑制剂骨架。在开始使用阿巴卡韦/拉米夫定+pDTG后,834名(72.8%)儿童仍在使用该方案,156名(13.6%)儿童停用了该方案(大部分转为使用多罗替韦 50 毫克),22名(1.9%)儿童更换了≥2种锚定药物;134名(11.7%)儿童没有记录后续方案。启动或更换 pDTG 的相关因素是年龄较小(调整后的几率比 [AOR] = 0.71 [0.63-0.80])和有记录的体重(AOR = 55.58 [33.88-91.18])。pDTG后≥5个月后进行病毒载量(VL)检测的294名儿童中,VLS率为75.5%(n = 222/294)。在接受过治疗的儿童中,pDTG 前的 VLS 率为 56.5%(n = 130/230)。与 VLS 相关的因素是年龄较大(AOR = 1.18 [1.03-1.34])和既往 VLS(AOR = 2.27 [1.27-4.06]):结论:大多数符合条件的儿童都按照指南开始了pDTG治疗,改善了pDTG治疗后的VLS。面临的挑战包括:开始使用 pDTG 后出现不明原因的停药、VL 覆盖率低以及诊所记录不足。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The rollout of paediatric dolutegravir and virological outcomes among children living with HIV in Mozambique.

Background: In 2022, Mozambique introduced Dolutegravir 10mg (pDTG), as part of paediatric antiretroviral therapy for children weighing < 20 kg. Understanding real-world challenges during national rollout can strengthen health systems in resource-limited settings.

Objectives: We described the transition rate to, and new initiation of, pDTG, viral load suppression (VLS) post-pDTG, and factors associated with VLS among children living with HIV.

Method: We conducted a retrospective cohort study involving children aged < 9 years and abstracted data from clinical sources. We used logistic regression to assess VLS and pDTG initiation predictors.

Results: Of 1353 children, 1146 initiated pDTG; 196 (14.5%) had no recorded weight. Post-pDTG switch, 98.9% (950/961) of children maintained the same nucleoside reverse transcriptase inhibitor backbone. After initiating Abacavir/Lamivudine+pDTG, 834 (72.8%) children remained on the regimen, 156 (13.6%) switched off (majority to Dolutegravir 50mg), 22 (1.9%) had ≥ 2 anchor drug switches; 134 (11.7%) had no documented follow-up regimen. Factors associated with pDTG initiation or switch were younger age (adjusted odds ratio [AOR] = 0.71 [0.63-0.80]) and a recorded weight (AOR = 55.58 [33.88-91.18]). VLS among the 294 children with a viral load (VL) test after ≥ 5 months post-pDTG was 75.5% (n = 222/294). Pre-pDTG VLS rate among treatment-experienced children was 56.5% (n = 130/230). Factors associated with VLS were older age (AOR = 1.18 [1.03-1.34]) and previous VLS (AOR = 2.27 [1.27-4.06]).

Conclusion: Most eligible children initiated pDTG per guidelines, improving post-pDTG VLS. Challenges included unexplained switches off pDTG after initiation, low VL coverage and inadequate documentation in clinic records.

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