Multidisciplinary Care Approach to Asymptomatic Brugada Syndrome in Pregnancy: A Case Report.

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Isabella Marechal-Ross, Kathryn Austin
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引用次数: 0

Abstract

Background and Clinical Significance: Brugada syndrome (BrS) is a rare inherited cardiac channelopathy, often associated with SCN5A loss-of-function mutations. Clinical presentations range from asymptomatic to malignant arrhythmias and sudden cardiac death. Physiological and pharmacological stressors affecting sodium channel function-such as pyrexia, certain medications, and possibly pregnancy-may unmask or exacerbate arrhythmic risk. However, there is limited information regarding pregnancy and obstetric outcomes. Obstetric management remains largely informed by isolated case reports and small case series. A literature review was conducted using OVID Medline and Embase, identifying case reports, case series, and one retrospective cohort study reporting clinical presentation, obstetric management, and outcomes in maternal BrS. A case is presented detailing coordinated multidisciplinary input, antenatal surveillance, and intrapartum and postpartum care to contribute to the growing evidence base guiding obstetric care in this complex setting. Case Presentation: A 30-year-old G2P0 woman with asymptomatic BrS (SCN5A-positive) was referred at 31 + 5 weeks' gestation for multidisciplinary antenatal care. Regular review and collaborative planning involving cardiology, anaesthetics, maternal-fetal medicine, and obstetrics guided a plan for vaginal delivery with continuous cardiac and fetal monitoring. At 38 + 0 weeks, the woman presented with spontaneous rupture of membranes and underwent induction of labour. A normal vaginal delivery was achieved without arrhythmic events. Epidural block with ropivacaine and local anaesthesia with lignocaine were well tolerated, and 24 h postpartum monitoring revealed no abnormalities. Conclusions: This case adds to the limited but growing literature suggesting that with individualised planning and multidisciplinary care, pregnancies in women with BrS can proceed safely and without complication. Ongoing case reporting is essential to inform future guidelines and optimise maternal and fetal outcomes.

妊娠无症状Brugada综合征的多学科护理方法:1例报告。
背景和临床意义:Brugada综合征(BrS)是一种罕见的遗传性心脏通道病变,通常与SCN5A功能缺失突变相关。临床表现从无症状到恶性心律失常和心源性猝死不等。影响钠通道功能的生理和药理学应激因素——如发热、某些药物和可能的妊娠——可能暴露或加剧心律失常的风险。然而,关于妊娠和产科结果的信息有限。产科管理在很大程度上仍然是通过孤立病例报告和小病例系列来了解的。使用OVID Medline和Embase进行文献综述,确定病例报告、病例系列和一项回顾性队列研究,报告了产妇BrS的临床表现、产科管理和结局。一个案例提出了详细的协调多学科投入,产前监测,产中和产后护理,以促进日益增长的证据基础指导产科护理在这种复杂的设置。病例介绍:一名30岁G2P0女性无症状BrS (scn5a阳性)在妊娠31 + 5周时进行多学科产前护理。包括心脏病学、麻醉学、母胎医学和产科在内的定期审查和协作计划指导了阴道分娩计划,并进行了持续的心脏和胎儿监测。在38 + 0周时,妇女出现自发性胎膜破裂并引产。正常阴道分娩,无心律失常。罗哌卡因硬膜外阻滞和利多卡因局部麻醉耐受良好,产后24 h监测未见异常。结论:该病例增加了有限但越来越多的文献,表明通过个性化计划和多学科护理,BrS妇女的妊娠可以安全进行且无并发症。持续的病例报告对于告知未来的指南和优化孕产妇和胎儿结局至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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