Kuhn L, Abrams E J, Matheson P B, Thomas P A, Lambert G, Bamji M, Greenberg B, Steketee R W, Thea D M
Sergievsky Center, Columbia University, New York, NY 10032, USA.
AIDS. 1997 Mar 15;11(4):429-35. doi: 10.1097/00002030-199704000-00005.
To investigate the hypothesis that labour and delivery events, perinatal characteristics, and maternal factors are only associated with intrapartum HIV transmission, and not with intrauterine HIV transmission.
In the New York City Perinatal HIV Transmission Collaborative Study 276 infants of HIV-infected women were followed prospectively and had results of early polymerase chain reaction (PCR) tests available. Among infected children, intrauterine infection was presumed if HIV DNA was detected by PCR in samples collected from children aged < or = 3 days, and intrapartum infection was presumed if HIV DNA was not detected in these early samples. The proportion of infants with presumed intrauterine and intrapartum infections were compared by selected intrapartum, perinatal and maternal characteristics.
Presumed intrapartum infection was found in 7% of infants delivered by Cesarean section and, among infants delivered vaginally, those with longer duration of membrane rupture (> 4 h) were significantly more likely to have presumed intrapartum HIV infection (22%) than those with shorter duration (9%; P = 0.02). There were no differences in presumed intrauterine HIV infection by mode of delivery or longer duration of membrane rupture. Infants born preterm and small for gestational age had significantly higher risks of presumed intrapartum infection, but only those who were small for gestational age had higher risks of intrauterine infection.
Our results support the notion that selected intrapartum conditions, long duration of membrane rupture prior to delivery in particular, are independent risk factors for maternal-infant transmission, and suggest that preterm infants may be especially vulnerable to intrapartum HIV exposure.
探讨分娩事件、围产期特征和母亲因素仅与产时HIV传播相关,而与宫内HIV传播无关这一假设。
在纽约市围产期HIV传播协作研究中,对276名感染HIV的妇女所生婴儿进行前瞻性随访,并可获得早期聚合酶链反应(PCR)检测结果。在受感染儿童中,如果在小于或等于3日龄儿童采集的样本中通过PCR检测到HIV DNA,则推测为宫内感染;如果在这些早期样本中未检测到HIV DNA,则推测为产时感染。通过选定的产时、围产期和母亲特征比较推测为宫内和产时感染的婴儿比例。
剖宫产分娩的婴儿中,7%被推测为产时感染;在阴道分娩的婴儿中,胎膜破裂时间较长(>4小时)的婴儿比胎膜破裂时间较短的婴儿更有可能被推测为产时HIV感染(22%对9%;P=0.02)。产时感染的推测比例在分娩方式或胎膜破裂时间较长的婴儿中没有差异。早产和小于胎龄儿出生的婴儿产时感染的推测风险显著更高,但只有小于胎龄儿有更高的宫内感染风险。
我们的结果支持这样一种观点,即选定的产时条件,特别是分娩前胎膜破裂时间较长,是母婴传播的独立危险因素,并表明早产儿可能特别容易在产时暴露于HIV。