Mu Shu-Chi, Lin Cheng-Hui, Chen Yi-Ling, Sung Tseng-Chen, Bai Chyi-Huey, Jow Guey-Mei
Department of Pediatrics, Shin-Kong Wu Ho-Su Memorial Hospital.
Pediatr Neonatol. 2008 Dec;49(6):230-3. doi: 10.1016/S1875-9572(09)60016-4.
Neonates with a single umbilical artery (SUA) are considered at increased risk for chromosomal and structural abnormalities, and an increased adverse perinatal outcome.
The specific aims of our study were to evaluate (1) the association of asymptomatic infants with isolated SUA and perinatal outcomes and (2) whether asymptomatic neonates with isolated SUA at birth need full investigation.
The inclusion criteria for the study were full-term neonates with isolated SUA delivered from January 1996 to December 2006. For a control group, we used the next consecutive two newborns delivered after the SUA case in the same maternity ward with matched gestational age and without phenotypic features suspicious for aneuploidy delivered after each SUA group subject. All prenatal, peripartum and delivery records were reviewed for maternal demographics, associated anomalies, karyotypic analysis, pregnancy complications and perinatal outcomes. All SUA cases had undergone sonogram for renal anomalies.
We enrolled 14 and 28 cases into the SUA and control groups respectively. There was all normal karyotyping for the 14 cases. The placental weight in SUA was significantly Lighter compared to that in the control group (597.1+/-175.4 vs. 709.3+/-95.2 g, p=0.010). All renal sonographic screens and karyotyping in the SUA group were normal. The incidence of small for gestational age (SGA) in SUA group was higher compared to control group (SGA, 5/14, 35.7% vs. 1/28, 3.6%, p=0.011) and less body length (48.7+/-5.0 vs. 50.8+/-1.8 cm, p=0.028).
SUA is a relatively rare finding. When a SUA is identified, the routine check of karyotyping and kidney sonography for possible chromosome and associated renal anomalies may be unnecessary. According to lighter placental weight probably causing the higher incidence of small for gestational age (SGA), pregnancies with isolated SUA should be carefully monitored for evidence of fetal growth restriction.
单脐动脉(SUA)新生儿被认为染色体和结构异常风险增加,围产期不良结局风险也增加。
本研究的具体目的是评估(1)无症状孤立性SUA婴儿与围产期结局的关联,以及(2)出生时无症状孤立性SUA新生儿是否需要全面检查。
研究的纳入标准为1996年1月至2006年12月分娩的足月孤立性SUA新生儿。对于对照组,我们选取同一产科病房中SUA病例之后连续出生的接下来两名新生儿,其孕周匹配且无染色体非整倍体可疑表型特征。回顾所有产前、产时和分娩记录,了解产妇人口统计学信息、相关畸形、核型分析、妊娠并发症和围产期结局。所有SUA病例均接受了肾脏异常超声检查。
SUA组和对照组分别纳入14例和28例。14例核型分析均正常。SUA组胎盘重量明显轻于对照组(597.1±175.4 vs. 709.3±95.2 g,p = 0.010)。SUA组所有肾脏超声检查和核型分析均正常。SUA组小于胎龄儿(SGA)发生率高于对照组(SGA,5/14,35.7% vs. 1/28,3.6%,p = 0.011),且身长较短(48.7±5.0 vs. 50.8±1.8 cm,p = 0.028)。
SUA是一种相对罕见的情况。当发现SUA时,可能无需常规进行核型分析和肾脏超声检查以排查可能的染色体及相关肾脏异常。鉴于胎盘重量较轻可能导致小于胎龄儿(SGA)发生率较高,对于孤立性SUA妊娠应密切监测胎儿生长受限的证据。