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胎儿先天性完全性心脏传导阻滞:6例患者的血流动力学特征、产前治疗及结局

Congenital complete heart block in the fetus: hemodynamic features, antenatal treatment, and outcome in six cases.

作者信息

Eronen M, Heikkilä P, Teramo K

机构信息

The Hospital for Children and Adolescents, Helsinki University Hospital, Stenbäckinkatu 11, 00290 Helsinki, Finland.

出版信息

Pediatr Cardiol. 2001 Sep-Oct;22(5):385-92. doi: 10.1007/s002460010256.

DOI:10.1007/s002460010256
PMID:11526412
Abstract

Congenital heart block (CHB) can result in intrauterine cardiac failure leading to fetal or neonatal loss. To establish perinatal hemodynamic factors which might predict adverse outcome, six fetuses with CHB diagnosed between 20 and 30 gestational weeks were examined by echocardiography at 2-week intervals. Neonatal morbidity and outcome in infancy are detailed. The fetuses showed a significant decrease in ventricular rate (VR) with advancing gestation (60 +/- 7 vs 51 +/- 4 beats/min, p = 0.03). Cardiac decompensation defined as hydrops or pericardial effusion was associated with VR of lower than 55 beats/min in two fetuses. Three mothers had a therapeutic trial with a sympathomimetic and digoxin. Salbutamol increased VR 10% in one of three fetuses treated. Digoxin decreased pericardial effusion in one hydropic fetus with autoimmune myocarditis. In this fetus, poor left ventricular fractional shortening (LVFS) was accompanied with high umbilical artery resistance index (RI). High amniotic fluid erythropoietin indicated severe hypoxia preceding death. Pacemaker was indicated in all the newborns. At the age of 2 weeks all the surviving infants had tricuspid regurgitation and a shunt through foramen ovale due to asynchronized atrioventricular contraction. During the 12-month follow-up two of five surviving infants had no symptoms. One had symptomatic neonatal lupus. Two infants had patent ductus arteriosus, one with dilated cardiomyopathy. In conclusion, poor fetal outcome was associated with low VR, low LVFS, and high RI. Despite early pacing, morbidity was high in infancy due to cardiomyopathy and associated heart defects. Regular echocardiographic monitoring during pregnancy and after delivery is required in order to optimize care and timing of any interventions.

摘要

先天性心脏传导阻滞(CHB)可导致宫内心力衰竭,进而导致胎儿或新生儿死亡。为了确定可能预测不良结局的围产期血流动力学因素,对6例在孕20至30周期间诊断为CHB的胎儿每隔2周进行一次超声心动图检查。详细记录了新生儿发病率和婴儿期结局。随着孕周增加,胎儿的心室率(VR)显著下降(60±7次/分钟对51±4次/分钟,p = 0.03)。定义为水肿或心包积液的心脏失代偿与2例胎儿VR低于55次/分钟有关。3名母亲接受了拟交感神经药和地高辛的治疗试验。沙丁胺醇使3例接受治疗的胎儿中的1例VR增加了10%。地高辛使1例患有自身免疫性心肌炎的水肿胎儿的心包积液减少。在该胎儿中,左心室缩短分数(LVFS)降低伴有高脐动脉阻力指数(RI)。高羊水促红细胞生成素表明死亡前存在严重缺氧。所有新生儿均需植入起搏器。在2周龄时,所有存活婴儿均因房室收缩不同步而出现三尖瓣反流和卵圆孔分流。在12个月的随访中,5例存活婴儿中有2例无症状。1例有症状性新生儿狼疮。2例婴儿有动脉导管未闭,1例伴有扩张型心肌病。总之,不良胎儿结局与低VR、低LVFS和高RI有关。尽管早期起搏,但由于心肌病和相关心脏缺陷,婴儿期发病率仍很高。孕期和产后需要定期进行超声心动图监测,以优化护理和任何干预措施的时机。

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引用本文的文献

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Fetal Congenital Complete Heart Block: A Rare Case with an Extremely Low Ventricular Rate and Review of Current Management Strategies.胎儿先天性完全性心脏传导阻滞:1例心室率极低的罕见病例及当前管理策略综述
Children (Basel). 2023 Jun 29;10(7):1132. doi: 10.3390/children10071132.
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Fetal Situs, Isomerism, Heterotaxy Syndrome: Diagnostic Evaluation and Implication for Postnatal Management.胎儿体位、异构、内脏异位综合征:诊断评估及对产后管理的意义
Curr Treat Options Cardiovasc Med. 2016 Dec;18(12):77. doi: 10.1007/s11936-016-0494-2.
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Perinatal outcome in fetuses with heterotaxy syndrome and atrioventricular block or bradycardia.
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Pediatr Cardiol. 2014 Aug;35(6):906-13. doi: 10.1007/s00246-014-0874-x. Epub 2014 Feb 9.
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Congenital heart block maternal sera autoantibodies target an extracellular epitope on the α1G T-type calcium channel in human fetal hearts.先天性心脏传导阻滞母体血清自身抗体针对人类胎儿心脏α1G T 型钙通道的细胞外表位。
PLoS One. 2013 Sep 9;8(9):e72668. doi: 10.1371/journal.pone.0072668. eCollection 2013.
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