Delivery room and early postnatal management of neonates with congenital heart disease.

IF 2.7 2区 医学 Q2 GENETICS & HEREDITY
Prenatal Diagnosis Pub Date : 2024-07-01 Epub Date: 2024-06-10 DOI:10.1002/pd.6617
Noorjahan Ali, Mary T Donofrio
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引用次数: 0

Abstract

Advancements in prenatal detection have improved postnatal outcomes for patients with congenital heart disease (CHD). Detailed diagnosis during pregnancy allows for preparation for the delivery and immediate postnatal care for the newborns with CHD. Most CHDs do not result in hemodynamic instability at the time of birth and can be stabilized following the guidelines of the neonatal resuscitation program (NRP). Critical CHD that requires intervention immediately after birth is recommended to be delivered in facilities where immediate neonatal and cardiology care can be provided. Postnatal stabilization and resuscitation for these defects warrant deviation from the standardized NRP. For neonatal providers, knowing the diagnosis of fetal CHD allows for preparation for the anticipated instability in the delivery room. Prenatal detection fosters collaboration between fetal cardiology, cardiology specialists, obstetrics, and neonatology, improving outcomes for neonates with critical CHD.

先天性心脏病新生儿的产房和产后早期管理。
产前检测技术的进步改善了先天性心脏病(CHD)患者的产后预后。孕期的详细诊断可为分娩做好准备,并为患有先天性心脏病的新生儿提供及时的产后护理。大多数先天性心脏病不会导致新生儿出生时血流动力学不稳定,可以按照新生儿复苏计划(NRP)的指导方针稳定病情。对于需要在出生后立即进行干预的危重先天性心脏病,建议在可立即提供新生儿和心脏科护理的医疗机构分娩。这些缺陷的产后稳定和复苏需要偏离标准化的 NRP。对于新生儿医疗服务提供者而言,了解胎儿先天性心脏病的诊断有助于为产房中预期的不稳定情况做好准备。产前检测可促进胎儿心脏病学、心脏病学专家、产科和新生儿科之间的合作,从而改善患有严重先天性心脏病的新生儿的预后。
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来源期刊
Prenatal Diagnosis
Prenatal Diagnosis 医学-妇产科学
CiteScore
5.80
自引率
13.30%
发文量
204
审稿时长
2 months
期刊介绍: Prenatal Diagnosis welcomes submissions in all aspects of prenatal diagnosis with a particular focus on areas in which molecular biology and genetics interface with prenatal care and therapy, encompassing: all aspects of fetal imaging, including sonography and magnetic resonance imaging; prenatal cytogenetics, including molecular studies and array CGH; prenatal screening studies; fetal cells and cell-free nucleic acids in maternal blood and other fluids; preimplantation genetic diagnosis (PGD); prenatal diagnosis of single gene disorders, including metabolic disorders; fetal therapy; fetal and placental development and pathology; development and evaluation of laboratory services for prenatal diagnosis; psychosocial, legal, ethical and economic aspects of prenatal diagnosis; prenatal genetic counseling
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