Centre for the AIDS Programme of Research in South Africa (CAPRISA), Doris Duke Medical Research Institute (2nd floor), Nelson R Mandela School of Medicine, University of KwaZulu-Natal, Private Bag X7, Congella, Durban, 4013, South Africa.
School of Laboratory Medicine and Medical Science, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Durban, South Africa.
BMC Pregnancy Childbirth. 2022 Jul 26;22(1):596. doi: 10.1186/s12884-022-04829-2.
In South Africa, women continue to face a high burden of Human Immunodeficiency Virus (HIV) infection and the possible complications thereof during pregnancy. We assessed pregnancy incidence rates and outcomes in a longitudinal HIV cohort study over a 15-year period.
We evaluated pregnancies among women ≥ 18 years between 2004 and 2019 in the CAPRISA 002 study. We analysed pregnancy rates following HIV acquisition, CD4 counts and HIV viral load dynamics and pregnancy outcomes. We used linear regression to assess if the mean CD4 and log viral load close to delivery increases or decreases linearly across three different timepoints.
In total 245 women enrolled into the HIV negative study phase, 225 into the HIV infection phase and 232 in the antiretroviral therapy (ART) phase. Median follow-up time was 2.0 years [Interquartile Range (IQR) 0.8-2.0] during the HIV negative phase, 2.6 years; (IQR) 1.2-4.8] during HIV infection and 3.7 years (IQR 1.8-5.0) on ART, with maximum follow-up time of 2, 10 and 6 years respectively. Overall, 169 pregnancies occurred in 140 women, of which 16 pregnancies were observed during acute or early HIV infection [Incidence Rate (IR) 8.0 per 100 women-years; 95% confidence interval (CI): 4.6-12.9], 48 during established infection [IR 9.3; (CI 6.8-12.3)] and 68 on ART [IR 8.9; (CI: 7.0 - 11.4)]. Birth outcomes from 155/169 (91.7%) pregnancies were 118 (76.1%) full term live births, 17 (10.9%) premature live births, 9 (5.8%) therapeutic/elective miscarriages, 8 (5.1%) spontaneous miscarriages and 3 (1.9%) spontaneous foetal deaths or stillbirths. Six mother-to-child transmission events occurred, with four documented prior to 2008. Over time, mean CD4 count in pregnant women increased from 395 cells/µL (2004-2009) to 543 cells/µL (2010-2014) and to 696 cells/µL (2015-2019), p < 0.001. Conversely, the viral load declined from 4.2 log copies/ml to 2.5 log copies/ml and to 1.2 log copies/ml (p < 0.001) for the corresponding periods.
Pregnancy rates following HIV acquisition were high, emphasising a need for timeous ART provision and contraception counselling in women recently diagnosed with HIV. CD4 count and HIV viral load trajectories reflect improvements in treatment guidance for pregnant women over time.
在南非,女性仍然面临着艾滋病毒(HIV)感染的高负担,以及在怀孕期间可能出现的并发症。我们评估了在 15 年的纵向 HIV 队列研究中怀孕的发生率和结局。
我们评估了 2004 年至 2019 年期间 CAPRISA 002 研究中≥18 岁的女性的怀孕情况。我们分析了 HIV 感染后怀孕率、CD4 计数和 HIV 病毒载量的动态以及妊娠结局。我们使用线性回归来评估在三个不同时间点,分娩时的平均 CD4 和对数病毒载量是否呈线性增加或减少。
共有 245 名妇女参加了 HIV 阴性研究阶段,225 名参加了 HIV 感染阶段,232 名参加了抗逆转录病毒治疗(ART)阶段。HIV 阴性阶段的中位随访时间为 2.0 年[四分位间距(IQR)0.8-2.0],HIV 感染阶段为 2.6 年[IQR 1.2-4.8],ART 阶段为 3.7 年[IQR 1.8-5.0],最大随访时间分别为 2、10 和 6 年。总的来说,140 名妇女中有 169 次妊娠,其中 16 次妊娠发生在急性或早期 HIV 感染期间[发病率(IR)为 8.0/100 妇女年;95%置信区间(CI):4.6-12.9],48 次妊娠发生在已确立的感染期间[IR 9.3;(CI 6.8-12.3)],68 次妊娠发生在接受 ART 治疗期间[IR 8.9;(CI:7.0-11.4)]。155/169(91.7%)例妊娠的分娩结局为 118(76.1%)足月活产、17(10.9%)早产、9(5.8%)治疗性/选择性流产、8(5.1%)自然流产和 3(1.9%)自然胎儿死亡或死产。有 6 例母婴传播事件,其中 4 例发生在 2008 年之前。随着时间的推移,孕妇的平均 CD4 计数从 2004-2009 年的 395 个细胞/µL 增加到 2010-2014 年的 543 个细胞/µL 和 2015-2019 年的 696 个细胞/µL,p<0.001。相反,病毒载量从 4.2 对数拷贝/ml 下降到 2.5 对数拷贝/ml 和 1.2 对数拷贝/ml(p<0.001)。
HIV 感染后怀孕率较高,这强调了需要及时提供抗逆转录病毒治疗和避孕咨询,以帮助最近诊断为 HIV 的妇女。CD4 计数和 HIV 病毒载量的变化反映了随着时间的推移,孕妇治疗指南的改善。