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先天性完全性心脏传导阻滞早产儿队列研究:15 年单中心经验。

Cohort study of congenital complete heart block among preterm neonates: a single-center experience over a 15-year period.

机构信息

Department of Neonatology, Evelina London Children's Hospital, London, UK.

Department of Paediatrics, Monash University, Melbourne, VIC, Australia.

出版信息

Eur J Pediatr. 2022 Mar;181(3):1047-1054. doi: 10.1007/s00431-021-04293-8. Epub 2021 Oct 27.

Abstract

Congenital complete heart block (CCHB) is a very rare condition, with high risk of mortality. Prematurity is associated with immaturity of the cardiovascular system. Morbidity related to CCHB and prematurity has never been described. We describe a tertiary perinatal center experience over a 15-year period on CCHB management and complications in preterm infants. This is a single-center observational cohort study. All neonates admitted to neonatal intensive care unit with a diagnosis of isolated CCHB between January 2006 and January 2021 were identified. All preterm neonates (< 37 weeks) were compared with a control cohort of term neonates (≥ 37 weeks). Antenatal data, complications of prematurity, medical, and surgical management of CCHB were recorded. Twenty-four neonates with isolated CCHB (16 preterm and 8 term) were born during the study period, including 5 very preterm (< 32 weeks) and 11 preterm (32 to 37 weeks). All very preterm were born via emergency caesarian section without antenatal steroid administration. They had multiple severe morbidities including chronic lung disease, necrotizing enterocolitis, grades 3-4 intraventricular hemorrhage, cystic periventricular leukomalacia, and longer periods of mechanical and non-invasive ventilatory support than preterm. Thirteen out of sixteen preterm infants had permanent pacemakers inserted, compared to 1/8 for term newborns. All babies born before 35-week gestation were either paced or died.Conclusion: Premature neonates with CCHB have high risk of mortality and morbidity especially if undiagnosed and born by unnecessary emergency caesarian section without antenatal steroids. Prematurity below 35 weeks may be associated with death or pacemaker insertion. This supports better antenatal screening to avoid induced prematurity. What is Known: • Congenital complete heart block is a very rare condition associated with high morbidity and mortality. • Antenatal risk factors for poor outcome include fetal hydrops, low ventricular rate (HR <55 beats per minute), and congenital heart defect. What is New: • Infants born <32 weeks with CCHB had no antenatal steroid administration, and sustained high burden of morbidity (chronic lung disease, intraventricular hemorrhage, and cystic periventricular leukomalacia). • Birth <35 weeks is strongly associated with requiring pacing prior to discharge or death.

摘要

先天性完全性心脏传导阻滞(CCHB)是一种非常罕见的疾病,死亡率很高。早产与心血管系统不成熟有关。与 CCHB 和早产相关的发病率从未被描述过。我们描述了一个 15 年期间在三级围产期中心对 CCHB 管理和早产儿并发症的经验。这是一项单中心观察性队列研究。所有 2006 年 1 月至 2021 年 1 月期间因孤立性 CCHB 被收入新生儿重症监护病房的新生儿均被确定为研究对象。所有早产儿(<37 周)均与足月新生儿(≥37 周)对照组进行比较。记录了围产期数据、早产并发症、CCHB 的医疗和手术管理。在研究期间,共有 24 例孤立性 CCHB 新生儿(16 例早产儿和 8 例足月儿)出生,其中包括 5 例极早产儿(<32 周)和 11 例早产儿(32-37 周)。所有极早产儿均未经产前类固醇治疗而行紧急剖宫产分娩。他们患有多种严重疾病,包括慢性肺病、坏死性小肠结肠炎、3-4 级脑室内出血、囊性脑室周围白质软化症和较长时间的机械通气和无创通气支持。16 例早产儿中有 13 例植入了永久性起搏器,而足月儿只有 1/8 例。所有在 35 周前出生的婴儿要么起搏要么死亡。结论:患有 CCHB 的早产儿死亡率和发病率很高,尤其是如果未经诊断且未经产前类固醇治疗而由不必要的紧急剖宫产分娩,则风险更高。<35 周的早产可能与死亡或起搏器植入有关。这支持更好的产前筛查以避免诱导性早产。已知情况:先天性完全性心脏传导阻滞是一种非常罕见的疾病,与高发病率和死亡率相关。不良结局的产前危险因素包括胎儿水肿、心室率低(<55 次/分钟)和先天性心脏病。新情况:患有 CCHB 的<32 周婴儿未接受产前类固醇治疗,且发病率高(慢性肺病、脑室内出血和囊性脑室周围白质软化症)。出生<35 周与出院前或死亡前需要起搏强烈相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aac/8548064/6840bb2c404f/431_2021_4293_Fig1_HTML.jpg

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