Schlatterer Sarah D, Govindan Rathinaswamy B, Murnick Jonathan, Barnett Scott D, Lopez Catherine, Donofrio Mary T, Mulkey Sarah B, Limperopoulos Catherine, du Plessis Adre J
Prenatal Pediatrics Institute, Children's National Hospital, Washington, DC, USA.
Department of Neurology, The George Washington University School of Medicine and Health Sciences, Washington, DC, USA.
Pediatr Res. 2022 Jun;91(7):1723-1729. doi: 10.1038/s41390-021-01931-7. Epub 2021 Dec 28.
Brain injury is a serious and common complication of critical congenital heart disease (CHD). Impaired autonomic development (assessed by heart rate variability (HRV)) is associated with brain injury in other high-risk neonatal populations.
To determine whether impaired early neonatal HRV is associated with pre-operative brain injury in CHD.
In infants with critical CHD, we evaluated HRV during the first 24 h of cardiac ICU (CICU) admission using time-domain (RMS 1, RMS 2, and alpha 1) and frequency-domain metrics (LF, nLF, HF, nHF). Pre-operative brain magnetic resonance imaging (MRI) was scored for injury using an established system. Spearman's correlation coefficient was used to determine the association between HRV and pre-operative brain injury.
We enrolled 34 infants with median birth gestational age of 38.8 weeks (IQR 38.1-39.1). Median postnatal age at pre-operative brain MRI was 2 days (IQR 1-3 days). Thirteen infants had MRI evidence of brain injury. RMS 1 and RMS 2 were inversely correlated with pre-operative brain injury.
Time-domain metrics of autonomic function measured within the first 24 h of admission to the CICU are associated with pre-operative brain injury, and may perform better than frequency-domain metrics under non-stationary conditions such as critical illness.
Autonomic dysfunction, measured by heart rate variability (HRV), in early transition is associated with pre-operative brain injury in neonates with critical congenital heart disease. These data extend our earlier findings by providing further evidence for (i) autonomic dysfunction in infants with CHD, and (ii) an association between autonomic dysfunction and brain injury in critically ill neonates. These data support the notion that further investigation of HRV as a biomarker for brain injury risk is warranted in infants with critical CHD.
脑损伤是危重型先天性心脏病(CHD)的一种严重且常见的并发症。自主神经发育受损(通过心率变异性(HRV)评估)与其他高危新生儿群体的脑损伤相关。
确定新生儿早期HRV受损是否与CHD术前脑损伤相关。
在患有危重型CHD的婴儿中,我们在心脏重症监护病房(CICU)入院后的头24小时内,使用时域指标(均方根1、均方根2和α1)和频域指标(低频、归一化低频、高频、归一化高频)评估HRV。术前脑磁共振成像(MRI)采用既定系统对损伤进行评分。使用Spearman相关系数确定HRV与术前脑损伤之间的关联。
我们纳入了34例婴儿,中位出生孕周为38.8周(四分位间距38.1 - 39.1)。术前脑MRI检查时的中位出生后年龄为2天(四分位间距1 - 3天)。13例婴儿有MRI脑损伤证据。均方根1和均方根2与术前脑损伤呈负相关。
在入住CICU的头24小时内测量的自主神经功能时域指标与术前脑损伤相关,并且在诸如危重病等非平稳条件下可能比频域指标表现更好。
在早期过渡阶段通过心率变异性(HRV)测量的自主神经功能障碍与患有危重型先天性心脏病的新生儿术前脑损伤相关。这些数据通过为以下两点提供进一步证据扩展了我们早期的发现:(i)CHD婴儿存在自主神经功能障碍,以及(ii)危重新生儿自主神经功能障碍与脑损伤之间的关联。这些数据支持这样一种观点,即有必要对HRV作为危重型CHD婴儿脑损伤风险生物标志物进行进一步研究。