Cheung Po-Yin, Hajihosseini Morteza, Dinu Irina A, Switzer Heather, Joffe Ari R, Bond Gwen Y, Robertson Charlene M T
Department of Pediatrics, University of Alberta, Edmonton, AB, Canada.
NICU, Northern Alberta Neonatal Program of Alberta Health Services, Edmonton, AB, Canada.
Front Pediatr. 2021 Jan 28;8:616659. doi: 10.3389/fped.2020.616659. eCollection 2020.
Compared with those born at term gestation, infants with complex congenital heart defects (CCHD) who were delivered before 37 weeks gestational age and received neonatal open-heart surgery (OHS) have poorer neurodevelopmental outcomes in early childhood. We aimed to describe the growth, disability, functional, and neurodevelopmental outcomes in early childhood of preterm infants with CCHD after neonatal OHS. Prediction models were evaluated at various timepoints during hospitalization which could be useful in the management of these infants. We studied all preterm infants with CCHD who received OHS within 6 weeks of corrected age between 1996 and 2016. The Western Canadian Complex Pediatric Therapies Follow-up Program completed multidisciplinary comprehensive neurodevelopmental assessments at 2-year corrected age at the referral-site follow-up clinics. We collected demographic and acute-care clinical data, standardized age-appropriate outcome measures including physical growth with calculated scores; disabilities including cerebral palsy, visual impairment, permanent hearing loss; adaptive function (Adaptive Behavior Assessment System-II); and cognitive, language, and motor skills (Bayley Scales of Infant and Toddler Development-III). Multiple variable logistic or linear regressions determined predictors displayed as Odds Ratio (OR) or Effect Size (ES) with 95% confidence intervals. Of 115 preterm infants (34 ± 2 weeks gestation, 2,339 ± 637 g, 64% males) with CCHD and OHS, there were 11(10%) deaths before first discharge and 21(18%) deaths by 2-years. Seven (6%) neonates had cerebral injuries, 7 had necrotizing enterocolitis; none had retinopathy of prematurity. Among 94 survivors, 9% had cerebral palsy and 6% had permanent hearing loss, with worse outcomes in those with syndromic diagnoses. Significant predictors of mortality included birth weight score [OR 0.28(0.11,0.72), = 0.008], single-ventricle anatomy [OR 5.92(1.31,26.80), = 0.021], post-operative ventilation days [OR 1.06(1.02,1.09), = 0.007], and cardiopulmonary resuscitation [OR 11.58 (1.97,68.24), = 0.007]; for adverse functional outcome in those without syndromic diagnoses, birth weight 2,000-2,499 g [ES -11.60(-18.67, -4.53), = 0.002], post-conceptual age [ES -0.11(-0.22,0.00), = 0.044], post-operative lowest pH [ES 6.75(1.25,12.25), = 0.017], and sepsis [ES -9.70(-17.74, -1.66), = 0.050]. Our findings suggest preterm neonates with CCHD and early OHS had significant mortality and morbidity at 2-years and were at risk for cerebral palsy and adverse neurodevelopment. This information may be important for management, parental counseling and the decision-making process.
与足月出生的婴儿相比,孕龄小于37周且接受新生儿心脏直视手术(OHS)的复杂先天性心脏病(CCHD)婴儿在幼儿期的神经发育结局较差。我们旨在描述新生儿OHS后CCHD早产儿在幼儿期的生长、残疾、功能和神经发育结局。在住院期间的不同时间点对预测模型进行了评估,这可能有助于这些婴儿的管理。我们研究了1996年至2016年间所有在矫正年龄6周内接受OHS的CCHD早产儿。加拿大西部复杂儿科治疗随访项目在转诊点随访诊所对矫正年龄2岁的患儿进行了多学科综合神经发育评估。我们收集了人口统计学和急性护理临床数据、标准化的适合年龄的结局指标,包括计算得分的身体生长情况;残疾情况,包括脑瘫、视力障碍、永久性听力损失;适应功能(《适应行为评估系统-II》);以及认知、语言和运动技能(《贝利婴幼儿发展量表-III》)。多元变量逻辑回归或线性回归确定的预测因素以比值比(OR)或效应量(ES)表示,并带有95%置信区间。在115例接受OHS的CCHD早产儿中(孕龄34±2周,体重2339±637g,64%为男性),11例(10%)在首次出院前死亡,21例(18%)在2岁时死亡。7例(6%)新生儿有脑损伤,7例有坏死性小肠结肠炎;无早产儿视网膜病变。在94名幸存者中,9%有脑瘫,6%有永久性听力损失,综合征诊断患儿的结局更差。死亡率的显著预测因素包括出生体重评分[OR 0.28(0.11,0.72),P = 0.008]、单心室解剖结构[OR 5.92(1.31,26.80),P = 0.021]、术后通气天数[OR 1.06(1.02,1.09),P = 0.007]和心肺复苏[OR 11.58(1.97,68.24),P = 0.007];对于无综合征诊断的患儿出现不良功能结局的情况,出生体重2000 - 2499g[ES -11.60(-18.67,-4.53),P = 0.002]、孕龄[ES -0.11(-0.22,0.00),P = 0.044]、术后最低pH值[ES 6.75(1.25,12.25),P = 0.017]和败血症[ES -9.70(-17.74,-1.66),P = 0.050]。我们的研究结果表明,患有CCHD且早期接受OHS的早产儿在2岁时存在显著的死亡率和发病率,并有患脑瘫和不良神经发育的风险。这些信息对于管理、家长咨询和决策过程可能很重要。