University of Iowa Health Care, Department of Pediatrics, 200 Hawkins Dr, Iowa City, IA 52242, USA.
Pediatrics. 2010 Dec;126(6):1132-40. doi: 10.1542/peds.2010-1824. Epub 2010 Nov 22.
Our objective was to compare survival and neonatal morbidity rates between very low birth weight (VLBW) infants with Down syndrome (DS) and VLBW infants with non-DS chromosomal anomalies, nonchromosomal birth defects (BDs), and no chromosomal anomaly or major BD.
Data were collected prospectively for infants weighing 401 to 1500 g who were born and/or cared for at one of the study centers participating in the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network in 1994-2008. Risk of death and morbidities, including patent ductus arteriosus (PDA), necrotizing enterocolitis (NEC), late-onset sepsis (LOS), retinopathy of prematurity, and bronchopulmonary dysplasia (BPD), were compared between VLBW infants with DS and infants in the other groups.
Infants with DS were at increased risk of death (adjusted relative risk: 2.47 [95% confidence interval: 2.00-3.07]), PDA, NEC, LOS, and BPD, relative to infants with no BDs. Decreased risk of death (relative risk: 0.40 [95% confidence interval: 0.31-0.52]) and increased risks of NEC and LOS were observed when infants with DS were compared with infants with other non-DS chromosomal anomalies. Relative to infants with nonchromosomal BDs, infants with DS were at increased risk of PDA and NEC.
The increased risk of morbidities among VLBW infants with DS provides useful information for counseling parents and for anticipating the need for enhanced surveillance for prevention of these morbidities.
本研究旨在比较唐氏综合征(DS)合并极低出生体重儿(VLBW)与非 DS 染色体异常、非染色体性出生缺陷(BD)以及无染色体异常或重大 BD 的 VLBW 儿的存活率和新生儿发病率。
本研究数据来自 1994 年至 2008 年期间,在 Eunice Kennedy Shriver 国家儿童健康与人类发育研究所新生儿研究网络参与研究的中心出生和/或接受治疗的体重为 401-1500g 的婴儿。比较了 DS 合并 VLBW 儿与其他各组婴儿的死亡风险和包括动脉导管未闭(PDA)、坏死性小肠结肠炎(NEC)、晚发性败血症(LOS)、早产儿视网膜病变和支气管肺发育不良(BPD)等并发症的发病率。
与无 BD 的婴儿相比,DS 合并 VLBW 儿的死亡风险(校正相对风险:2.47[95%置信区间:2.00-3.07])、PDA、NEC、LOS 和 BPD 的发病率更高。与其他非 DS 染色体异常儿相比,DS 合并 VLBW 儿的死亡风险(相对风险:0.40[95%置信区间:0.31-0.52])降低,NEC 和 LOS 的发病风险增加。与非染色体性 BD 儿相比,DS 合并 VLBW 儿更易发生 PDA 和 NEC。
DS 合并 VLBW 儿的发病率较高,这为向家长提供咨询以及预测这些疾病的发生风险并进行针对性监测提供了有用的信息。