Department of Neonatal Medicine Karolinska University Hospital and Karolinska Institutet Stockholm Sweden.
Department of Clinical Sciences/Pediatrics Umeå University and Umeå University Hospital Umeå Sweden.
J Am Heart Assoc. 2020 Mar 3;9(5):e015369. doi: 10.1161/JAHA.119.015369. Epub 2020 Feb 21.
Background Very preterm infants are at high risk of death or severe morbidity. The objective was to determine the significance of severe congenital heart defects (CHDs) for these risks. Methods and Results This cohort study included infants from 10 countries born from 2007-2015 at 24 to 31 weeks' gestation with birth weights <1500 g. Severe CHDs were defined by () and () codes and categorized as those compromising systemic output, causing sustained cyanosis, or resulting in congestive heart failure. The primary outcome was in-hospital mortality. Secondary outcomes were neonatal brain injury, necrotizing enterocolitis, bronchopulmonary dysplasia, and retinopathy of prematurity. Adjusted and propensity score-matched odds ratios (ORs) were calculated. Analyses were stratified by type of CHD, gestational age, and network. A total of 609 (0.77%) infants had severe CHD and 76 371 without any malformation served as controls. The mean gestational age and birth weight were 27.8 weeks and 1018 g, respectively. The mortality rate was 18.6% in infants with CHD and 8.9% in controls (propensity score-matched OR, 2.30; 95% CI, 1.61-3.27). Severe CHD was not associated with neonatal brain injury, necrotizing enterocolitis, or retinopathy of prematurity, whereas the OR for bronchopulmonary dysplasia increased. Mortality was higher in all types, with the highest propensity score-matched OR (4.96; 95% CI, 2.11-11.7) for CHD causing congestive heart failure. While mortality did not differ between groups at <27 weeks' gestational age, adjusted OR for mortality in infants with CHD increased to 10.9 (95% CI, 5.76-20.70) at 31 weeks' gestational age. Rates of CHD and mortality differed significantly between networks. Conclusions Severe CHD is associated with significantly increased mortality in very preterm infants.
极早产儿死亡或发生严重合并症的风险较高。本研究旨在明确严重先天性心脏病(CHD)对这些风险的影响。
本队列研究纳入了 2007 年至 2015 年期间胎龄 24 至 31 周、出生体重<1500g 的 10 个国家的婴儿。严重 CHD 定义为使用()和()编码,包括影响全身输出、导致持续性发绀或引起充血性心力衰竭的 CHD。主要结局为院内死亡率。次要结局为新生儿脑损伤、坏死性小肠结肠炎、支气管肺发育不良和早产儿视网膜病变。计算了校正和倾向评分匹配比值比(OR)。分析根据 CHD 类型、胎龄和网络进行分层。共有 609 例(0.77%)婴儿患有严重 CHD,76371 例无任何畸形的婴儿作为对照。平均胎龄和出生体重分别为 27.8 周和 1018g。CHD 患儿的死亡率为 18.6%,对照组为 8.9%(倾向评分匹配 OR,2.30;95%CI,1.61-3.27)。严重 CHD 与新生儿脑损伤、坏死性小肠结肠炎或早产儿视网膜病变无关,而支气管肺发育不良的 OR 增加。所有类型的死亡率均较高,其中导致充血性心力衰竭的 CHD 的校正后倾向评分匹配 OR 最高(4.96;95%CI,2.11-11.7)。胎龄<27 周时,两组之间的死亡率无差异,但 CHD 患儿的调整后死亡率 OR 增加至 31 周时的 10.9(95%CI,5.76-20.70)。不同网络之间的 CHD 发生率和死亡率存在显著差异。
严重 CHD 与极早产儿的死亡率显著增加相关。