Ravichandran Briyanth, Henriksen Tine B, Hjortdal Vibeke E, Ostergaard John R, Matthiesen Niels B
Department of Paediatrics and Adolescent Medicine Aarhus University Hospital Aarhus Denmark.
Department of Gastroenterology and Hepatology Herlev and Gentofte Hospital Herlev Denmark.
J Am Heart Assoc. 2025 Apr 15;14(8):e038798. doi: 10.1161/JAHA.124.038798. Epub 2025 Apr 10.
Low Apgar scores have been associated with an increased risk of brain injury and neurodevelopmental disorders in newborns with congenital heart defects (CHDs). However, the relation between CHD subtypes and low Apgar scores remains unknown. This study aimed to assess the association between major subtypes of CHD and low (<7) Apgar scores at 5 minutes.
This population-based study included 1 040 474 liveborn singletons in Denmark from 1997 to 2013. The association between CHD and low Apgar scores was estimated by confounder-adjusted, multivariable logistic regression. In mediation analyses, the underlying mechanisms were examined. Low Apgar scores were present in 3.0% of newborns with CHD and in 0.7% of newborns without CHD. Overall, CHD was associated with an increased risk of a low Apgar score (adjusted odds ratio, 2.5 [95% CI, 2.1-3.0]). CHD subtypes associated with the highest risks were anomalous pulmonary venous return (adjusted odds ratio, 5.7 [95% CI, 2.2-14.9]), hypoplastic left heart syndrome (adjusted odds ratio, 5.1 [95% CI, 2.2-11.8]), and transposition of the great arteries (adjusted odds ratio, 3.5 [95% CI, 1.7-7.4]). In mediation analyses, preterm birth explained 25.2% (95% CI, 11.8-38.6) of the association between CHD and low Apgar scores.
Nearly all CHD subtypes were associated with an increased risk of a low Apgar score. The association was most pronounced in severe and potentially cyanotic types of CHD. These findings suggest that CHD is associated with a complicated fetal-to-neonatal transition and highlight the potential for improvements of this process in infants with CHD.
低Apgar评分与先天性心脏病(CHD)新生儿脑损伤和神经发育障碍风险增加有关。然而,CHD亚型与低Apgar评分之间的关系尚不清楚。本研究旨在评估CHD主要亚型与5分钟时低(<7)Apgar评分之间的关联。
这项基于人群的研究纳入了1997年至2013年丹麦1040474例单胎活产儿。通过调整混杂因素的多变量逻辑回归估计CHD与低Apgar评分之间的关联。在中介分析中,研究了潜在机制。患有CHD的新生儿中有3.0%出现低Apgar评分,而没有CHD的新生儿中这一比例为0.7%。总体而言,CHD与低Apgar评分风险增加相关(调整后的优势比为2.5 [95% CI,2.1 - 3.0])。与最高风险相关的CHD亚型是肺静脉异位引流(调整后的优势比为5.7 [95% CI,2.2 - 14.9])、左心发育不全综合征(调整后的优势比为5.1 [95% CI,2.2 - 11.8])和大动脉转位(调整后的优势比为3.5 [95% CI,1.7 - 7.4])。在中介分析中,早产解释了CHD与低Apgar评分之间关联的25.2%(95% CI,11.8 - 38.6)。
几乎所有CHD亚型都与低Apgar评分风险增加有关。这种关联在严重且可能出现青紫型的CHD中最为明显。这些发现表明CHD与复杂的胎儿到新生儿过渡有关,并突出了改善CHD婴儿这一过程的潜力。