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卢旺达B+预防母婴传播项目中晚期妊娠妇女的可检测病毒载量:卡贝霍研究的入组结果

Detectable Viral Load in Late Pregnancy among Women in the Rwanda Option B+ PMTCT Program: Enrollment Results from the Kabeho Study.

作者信息

Gill Michelle M, Hoffman Heather J, Bobrow Emily A, Mugwaneza Placidie, Ndatimana Dieudonne, Ndayisaba Gilles F, Baribwira Cyprien, Guay Laura, Asiimwe Anita

机构信息

Elizabeth Glaser Pediatric AIDS Foundation, Washington, District of Columbia, United States of America.

Department of Epidemiology and Biostatistics, Milken Institute School of Public Health, The George Washington University, Washington, District of Columbia, United States of America.

出版信息

PLoS One. 2016 Dec 22;11(12):e0168671. doi: 10.1371/journal.pone.0168671. eCollection 2016.

Abstract

There are limited viral load (VL) data available from programs implementing "Option B+," lifelong antiretroviral treatment (ART) to all HIV-positive pregnant and postpartum women, in resource-limited settings. Extent of viral suppression from a prevention of mother-to-child transmission of HIV program in Rwanda was assessed among women enrolled in the Kigali Antiretroviral and Breastfeeding Assessment for the Elimination of HIV (Kabeho) Study. ARV drug resistance testing was conducted on women with VL>2000 copies/ml. In April 2013-January 2014, 608 pregnant or early postpartum HIV-positive women were enrolled in 14 facilities. Factors associated with detectable enrollment VL (>20 copies/ml) were examined using generalized estimating equations. The most common antiretroviral regimen (56.7%, 344/607) was tenofovir/lamivudine/efavirenz. Median ART duration was 13.5 months (IQR 3.0-48.8); 76.1% of women were on ART at first antenatal visit. Half of women (315/603) had undetectable RNA-PCR VL and 84.6% (510) had <1,000 copies/ml. Detectable VL increased among those on ART > 36 months compared to those on ART 4-36 months (72/191, 37.7% versus 56/187, 29.9%), though the difference was not significant. The odds of having detectable enrollment VL decreased significantly as duration on ART at enrollment increased (AOR = 0.99, 95% CI: 0.9857, 0.9998, p = 0.043). There was a higher likelihood of detectable VL for women with lower gravidity (AOR = 0.90, 95% CI: 0.84, 0.97, p = 0.0039), no education (AOR = 2.25, (95% CI: 1.37, 3.70, p = 0.0004), nondisclosure to partner (AOR = 1.97, 95% CI: 1.21, 3.21, p = 0.0063) and side effects (AOR = 2.63, 95% CI: 1.72, 4.03, p<0.0001). ARV drug resistance mutations were detected in all of the eleven women on ART > 36 months with genotyping available. Most women were receiving ART at first antenatal visit, with relatively high viral suppression rates. Shorter ART duration was associated with higher VL, with a concerning increasing trend for higher viremia and drug resistance among women on ART for >3 years.

摘要

在资源有限的环境中,实施“B+方案”(即对所有感染艾滋病毒的孕妇和产后妇女进行终身抗逆转录病毒治疗)的项目所提供的病毒载量(VL)数据有限。在参与基加利消除艾滋病毒抗逆转录病毒治疗与母乳喂养评估(Kabeho)研究的妇女中,评估了卢旺达预防母婴传播艾滋病毒项目的病毒抑制程度。对病毒载量>2000拷贝/毫升的妇女进行了抗逆转录病毒药物耐药性检测。2013年4月至2014年1月,608名怀孕或产后早期感染艾滋病毒的妇女在14个机构登记入组。使用广义估计方程研究了与可检测到的入组病毒载量(>20拷贝/毫升)相关的因素。最常见的抗逆转录病毒治疗方案(56.7%,344/607)是替诺福韦/拉米夫定/依非韦伦。抗逆转录病毒治疗的中位持续时间为13.5个月(四分位间距3.0 - 48.8);76.1%的妇女在首次产前检查时正在接受抗逆转录病毒治疗。一半的妇女(315/603)RNA-PCR病毒载量检测不到,84.6%(510)的妇女病毒载量<1000拷贝/毫升。与接受抗逆转录病毒治疗4 - 36个月的妇女相比,接受抗逆转录病毒治疗>36个月的妇女中可检测到的病毒载量有所增加(72/191,37.7%对56/187,29.9%),尽管差异不显著。随着入组时抗逆转录病毒治疗持续时间的增加,可检测到入组病毒载量的几率显著降低(调整后比值比 = 0.99,95%置信区间:0.9857,0.9998,p = 0.043)。妊娠次数较少的妇女可检测到病毒载量的可能性更高(调整后比值比 = 0.90,95%置信区间:0.84,0.97,p = 0.0039),未受过教育的妇女(调整后比值比 = 2.25,95%置信区间:1.37,3.70,p = 0.0004),未向伴侣透露感染情况的妇女(调整后比值比 = 1.97,95%置信区间:1.21,3.21,p = 0.0063)以及出现副作用的妇女(调整后比值比 = 2.63,95%置信区间:1.72,4.03,p<0.0001)。在所有11名接受抗逆转录病毒治疗>36个月且进行了基因分型的妇女中均检测到了抗逆转录病毒药物耐药性突变。大多数妇女在首次产前检查时正在接受抗逆转录病毒治疗,病毒抑制率相对较高。抗逆转录病毒治疗持续时间较短与病毒载量较高相关,对于接受抗逆转录病毒治疗超过3年的妇女,病毒血症和耐药性呈令人担忧的上升趋势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/89ca/5179044/56fd22814ce9/pone.0168671.g001.jpg

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