Kupka Roland, Kassaye Tarik, Saathoff Elmar, Hertzmark Ellen, Msamanga Gernard I, Fawzi Wafaie W
Department of Nutrition, Harvard School of Public Health, Boston, MA, USA.
Acta Obstet Gynecol Scand. 2009;88(5):584-92. doi: 10.1080/00016340902835901.
To determine maternal risk factors for stillbirth among pregnant HIV-infected women in sub-Saharan Africa.
Prospective cohort study nested within a micronutrient trial. At enrollment, maternal sociodemographic, obstetric, immunologic, clinical, and nutritional variables were measured. Women were followed through monthly clinic visits until delivery. Multivariate predictors of stillbirth were identified in Poisson regression models.
Antenatal clinic in a tertiary care hospital in urban Dar es Salaam, Tanzania.
N=1,078 women enrolled between 12 and 27 weeks of gestation.
Stillbirth (delivery of dead baby > or = 28 weeks' gestation), fresh stillbirth, and macerated stillbirth.
Among 1,017 singleton pregnancies, there were 49 stillbirths, yielding a stillbirth risk of 50.0 per 1,000 deliveries (95% Confidence Interval(CI) = 37.2, 65.6). Of stillbirths with known type, 53.7% were fresh and 46.3% macerated. In multivariate analyses, baseline measures of late (> or = 21 weeks' gestation) study entry (Relative Risk (RR) = 2.13, 95% CI = 1.17, 3.87), CD3 count > or = 1,179 cells/ml (RR = 2.15, 95% CI = 1.16, 4.01), stillbirth history (RR = 3.53, 95% CI = 1.30, 9.59), primiparity (RR = 3.65, 95% CI = 1.83, 7.29), and syphilis infection (RR = 2.06, 95% CI = 1.09, 3.88) predicted increased stillbirth risk. Late study entry, illiteracy, stillbirth history, primiparity, CD3 count > or = 1,179 cells/ml, gonorrhea infection, and previous hospitalization predicted increased risk of fresh stillbirth, while living alone and syphilis infection predicted increased risk of macerated stillbirth.
Applying antenatal screening and preventive tools for the socioeconomic, obstetric, immunologic, and clinical risk factors identified may assist in reducing the high incidence of stillbirth among HIV-infected women in urban sub-Saharan Africa.
确定撒哈拉以南非洲地区感染艾滋病毒的孕妇中死产的孕产妇风险因素。
嵌套在一项微量营养素试验中的前瞻性队列研究。在入组时,测量孕产妇的社会人口统计学、产科、免疫学、临床和营养变量。通过每月门诊随访直至分娩来跟踪这些妇女。在泊松回归模型中确定死产的多变量预测因素。
坦桑尼亚达累斯萨拉姆市一家三级护理医院的产前诊所。
N = 1078名在妊娠12至27周之间入组的妇女。
死产(妊娠≥28周分娩出死胎)、新鲜死产和浸软死产。
在1017例单胎妊娠中,有49例死产,死产风险为每1000例分娩中有50.0例(95%置信区间(CI)=37.2, 65.6)。在已知类型的死产中,53.7%为新鲜死产,46.3%为浸软死产。在多变量分析中,妊娠晚期(≥21周)入组的基线测量值(相对风险(RR)=2.13,95%CI = 1.17, 3.87)、CD3计数≥1179个细胞/毫升(RR = 2.15,95%CI = 1.16, 4.01)、死产史(RR = 3.53,95%CI = 1.30, 9.59)、初产(RR = 3.65,95%CI = 1.83, 7.29)和梅毒感染(RR = 2.06,95%CI = 1.09, 3.88)预测死产风险增加。妊娠晚期入组、文盲、死产史、初产、CD3计数≥1179个细胞/毫升、淋病感染和既往住院史预测新鲜死产风险增加,而独居和梅毒感染预测浸软死产风险增加。
应用针对已确定的社会经济、产科、免疫和临床风险因素的产前筛查和预防工具,可能有助于降低撒哈拉以南非洲城市地区感染艾滋病毒妇女的高死产发生率。