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中度和高度复杂先天性心脏病患者的妊娠

Pregnancy in Patients with Moderate and Highly Complex Congenital Heart Disease.

作者信息

Panebianco Mario, Perrone Marco Alfonso, Gagliardi Maria Giulia, Galletti Lorenzo, Bassareo Pier Paolo

机构信息

Department of Cardiac Surgery, Cardiology, Heart and Lung Transplantation Bambino Gesu' Children's Hospital, IRCCS, 71013 Rome, Italy.

Division of Cardiology and CardioLab, Department of Clinical Sciences and Translational Medicine, University of Rome Tor Vergata, 00133 Rome, Italy.

出版信息

Healthcare (Basel). 2023 May 30;11(11):1592. doi: 10.3390/healthcare11111592.

DOI:10.3390/healthcare11111592
PMID:37297732
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10253212/
Abstract

Although not completely devoid of risk, pregnancy can be managed in virtually all patients affected by even the most complex forms of congenital heart disease. It is not however advisable in patients with any form of pulmonary arterial hypertension. Pregnancy is even manageable in patients with univentricular heart converted to Fontan circulation. A personalised risk stratification should be performed, and patients affected by advanced NYHA functional class appropriately warned of the potential risks. In this setting, metabolomics might represent a novel tool for use in conducting personalised risk stratification. All pregnancies, particularly those at higher risk, should be managed in a tertiary care centre capable of providing the necessary assistance to both the mother and infant. With a few rare exceptions, vaginal delivery is to be preferred over caesarean section due to the lower degree of maternal and foetal complications. The desire for motherhood, at times extreme in women with congenital heart disease, may often be accomplished, thus providing a ray of hope in the lives of these patients.

摘要

尽管并非完全没有风险,但即使是患有最复杂形式先天性心脏病的几乎所有患者,怀孕也可以得到妥善管理。然而,对于任何形式的肺动脉高压患者,怀孕并不适宜。对于已转换为Fontan循环的单心室心脏患者,怀孕也是可以控制的。应进行个性化的风险分层,并适当地警告纽约心脏协会(NYHA)功能分级较高的患者潜在风险。在这种情况下,代谢组学可能是用于进行个性化风险分层的一种新工具。所有怀孕,尤其是那些风险较高的怀孕,都应在能够为母婴提供必要帮助的三级护理中心进行管理。除了少数罕见的例外情况,由于母婴并发症程度较低,阴道分娩优于剖宫产。先天性心脏病女性有时对为人母的渴望极为强烈,这种愿望往往可以实现,从而为这些患者的生活带来一线希望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ffe/10253212/b92700b17dc4/healthcare-11-01592-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ffe/10253212/34fcda5607d2/healthcare-11-01592-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ffe/10253212/b92700b17dc4/healthcare-11-01592-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ffe/10253212/34fcda5607d2/healthcare-11-01592-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ffe/10253212/b92700b17dc4/healthcare-11-01592-g002.jpg

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1
Pregnancy in Patients with Moderate and Highly Complex Congenital Heart Disease.中度和高度复杂先天性心脏病患者的妊娠
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本文引用的文献

1
Metabolomics: A New Tool in Our Understanding of Congenital Heart Disease.代谢组学:我们理解先天性心脏病的新工具。
Children (Basel). 2022 Nov 24;9(12):1803. doi: 10.3390/children9121803.
2
The Effects of Exercise Training on Cardiopulmonary Exercise Testing and Cardiac Biomarkers in Adult Patients with Hypoplastic Left Heart Syndrome and Fontan Circulation.运动训练对成人左心发育不全综合征及Fontan循环患者心肺运动试验和心脏生物标志物的影响
J Cardiovasc Dev Dis. 2022 May 27;9(6):171. doi: 10.3390/jcdd9060171.
3
Reproductive Issues in Patients With the Fontan Operation.
法洛四联症术后患者的生殖问题。
Can J Cardiol. 2022 Jul;38(7):921-929. doi: 10.1016/j.cjca.2022.04.020. Epub 2022 Apr 28.
4
Ebstein's Anomaly: From Fetus to Adult-Literature Review and Pathway for Patient Care.Ebstein 畸形:从胎儿到成人——文献综述及患者治疗路径。
Pediatr Cardiol. 2022 Oct;43(7):1409-1428. doi: 10.1007/s00246-022-02908-x. Epub 2022 Apr 23.
5
Urine metabolomic biomarkers for prediction of isolated fetal congenital heart defect.尿液代谢组学生物标志物预测孤立性胎儿先天性心脏缺陷
J Matern Fetal Neonatal Med. 2022 Dec;35(25):6380-6387. doi: 10.1080/14767058.2021.1914572. Epub 2021 May 4.
6
Tricuspid valve in congenital heart disease: multimodality imaging and electrophysiological considerations.先天性心脏病的三尖瓣:多模态影像学和电生理学考虑因素。
Minerva Cardiol Angiol. 2022 Aug;70(4):491-501. doi: 10.23736/S2724-5683.21.05656-8. Epub 2021 May 4.
7
Pregnancy outcomes in women with a systemic right ventricle and transposition of the great arteries results from the ESC-EORP Registry of Pregnancy and Cardiac disease (ROPAC).来自 ESC-EORP 妊娠与心脏疾病注册研究(ROPAC)的研究显示,患有系统性右心室和大动脉转位的女性的妊娠结局。
Heart. 2022 Jan;108(2):117-123. doi: 10.1136/heartjnl-2020-318685. Epub 2021 Apr 28.
8
Association of maternal gut microbiota and plasma metabolism with congenital heart disease in offspring: a multi-omic analysis.母体肠道微生物群和血浆代谢物与子代先天性心脏病的关联:多组学分析。
Sci Rep. 2021 Mar 5;11(1):5339. doi: 10.1038/s41598-021-84901-7.
9
Noninvasive screening for congenital heart defects using a serum metabolomics approach.使用血清代谢组学方法进行先天性心脏病的无创性筛查。
Prenat Diagn. 2021 May;41(6):743-753. doi: 10.1002/pd.5893. Epub 2021 Feb 13.
10
2020 ESC Guidelines for the management of adult congenital heart disease.2020年欧洲心脏病学会成人先天性心脏病管理指南。
Eur Heart J. 2021 Feb 11;42(6):563-645. doi: 10.1093/eurheartj/ehaa554.