Adachi Kristina, Klausner Jeffrey D, Xu Jiahong, Ank Bonnie, Bristow Claire C, Morgado Mariza G, Watts D Heather, Weir Fred, Persing David, Mofenson Lynne M, Veloso Valdilea G, Pilotto Jose Henrique, Joao Esau, Gray Glenda, Theron Gerhard, Santos Breno, Fonseca Rosana, Kreitchmann Regis, Pinto Jorge, Mussi-Pinhata Marisa M, Ceriotto Mariana, Machado Daisy Maria, Bryson Yvonne J, Grinsztejn Beatriz, Bastos Francisco I, Siberry George, Nielsen-Saines Karin
From the *David Geffen UCLA School of Medicine, Los Angeles, California; †UCLA Fielding School of Public Health, Department of Epidemiology, Los Angeles, California; ‡Westat, Rockville, Maryland; §Fundacao Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil; ¶Office of the Global AIDS Coordinator, US Department of State, Washington DC; ‖Cepheid, Sunnyvale, California; **Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland; ††Hospital Geral de Nova Iguaçu, DST/AIDS, Nova Iguaçu, Rio de Janeiro, Brazil; ‡‡Hospital Federal dos Servidores do Estado, Rio de Janeiro, Brazil; §§SAMRC and Perinatal HIV Research Unit, University of Witwatersrand, Cape Town, South Africa; ¶¶Department of Obstetrics and Gynecology, Stellenbosch University/Tygerberg Hospital, Cape Town, South Africa; ‖‖Serviço de Infectologia, Hospital Conceicao, Porto Alegre, Rio Grande do Sul, Brazil; ***Hospital Femina, Porto Alegre, Rio Grande do Sul, Brazil; †††Irmandade da Santa Casa de Misericordia de Porto Alegre, Rio Grande do Sul, Brazil; ‡‡‡Department of Pediatrics, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil; §§§Department of Pediatrics, Ribeirão Preto Medical School, University of São Paulo, São Paulo, Brazil; ¶¶¶Foundation for Maternal and Infant Health (FUNDASAMIN), Buenos Aires, Argentina; and ‖‖‖Escola Paulista de Medicina-Universidade Federal de São Paulo, São Paulo, Brazil.
Pediatr Infect Dis J. 2016 Aug;35(8):894-900. doi: 10.1097/INF.0000000000001199.
Sexually transmitted infections (STIs) in pregnancy such as Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG) may lead to adverse infant outcomes.
Individual urine specimens from HIV-infected pregnant women diagnosed with HIV during labor were collected at the time of infant birth and tested by polymerase chain reaction for CT and NG. Infant HIV infection was determined at 3 months with morbidity/mortality assessed through 6 months.
Of 1373 maternal urine samples, 277 (20.2%) were positive for CT and/or NG; 249 (18.1%) for CT, 63 (4.6%) for NG and 35 (2.5%) for both CT and NG. HIV infection was diagnosed in 117 (8.5%) infants. Highest rates of adverse outcomes (sepsis, pneumonia, congenital syphilis, septic arthritis, conjunctivitis, low birth weight, preterm delivery and death) were noted in infants of women with CT and NG (23/35, 65.7%) compared with NG (16/28, 57.1%), CT (84/214, 39.3%) and no STI (405/1096, 37%, P = 0.001). Death (11.4% vs. 3%, P = 0.02), low birth weight (42.9% vs. 16.9%, P = 0.001) and preterm delivery (28.6% vs. 10.2%, P = 0.008) were higher among infants of CT and NG-coinfected women. Infants who had any adverse outcome and were born to women with CT and/or NG were 3.5 times more likely to be HIV infected after controlling for maternal syphilis (odds ratio: 3.5, 95% confidence interval: 1.4-8.3). By adjusted multivariate logistic regression, infants born to mothers with any CT and/or NG were 1.35 times more likely to have an adverse outcome (odds ratio, 1.35; 95% confidence interval, 1.03-1.76).
STIs in HIV-infected pregnant women are associated with adverse outcomes in HIV-exposed infected and uninfected infants.
孕期性传播感染(STIs),如沙眼衣原体(CT)和淋病奈瑟菌(NG),可能导致不良的婴儿结局。
在婴儿出生时收集分娩期间诊断为HIV感染的孕妇的个体尿液样本,并通过聚合酶链反应检测CT和NG。在3个月时确定婴儿HIV感染情况,并评估至6个月时的发病率/死亡率。
在1373份母体尿液样本中,277份(20.2%)CT和/或NG检测呈阳性;CT阳性249份(18.1%),NG阳性63份(4.6%),CT和NG均阳性35份(2.5%)。117名(8.5%)婴儿被诊断为HIV感染。与NG(16/28,57.1%)、CT(84/214,39.3%)和无STI(405/1096,37%,P = 0.001)的孕妇相比,CT和NG感染孕妇的婴儿出现不良结局(败血症、肺炎、先天性梅毒、化脓性关节炎、结膜炎、低出生体重、早产和死亡)的发生率最高(23/35,65.7%)。CT和NG合并感染孕妇的婴儿死亡(11.4%对3%,P = 0.02)、低出生体重(42.9%对16.9%,P = 0.001)和早产(28.6%对10.2%,P = 0.008)的发生率更高。在控制母体梅毒后,有任何不良结局且母亲感染CT和/或NG的婴儿感染HIV的可能性是其他婴儿的3.5倍(比值比:3.5,95%置信区间:1.4 - 8.3)。通过调整后的多因素逻辑回归分析,母亲感染任何CT和/或NG的婴儿出现不良结局的可能性是其他婴儿的1.35倍(比值比,1.35;95%置信区间,1.03 - 1.76)。
HIV感染孕妇的性传播感染与暴露于HIV的感染和未感染婴儿的不良结局相关。