Complete Heart Block In Pregnancy : A Case Report

Dhanang Ali Yafi, Cloudia Noviani, R. E. Saputri, A. Purnawarman, Mohd. Andalas, Yusmalinda Yusmalinda
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引用次数: 3

Abstract

Background: Complete heart block occurs due to various pathological conditions that cause an infiltration, fibrosis, or lose the connection from a part of the cardiac conduction system. Complete heart  block in pregnancy is often caused by congenital anomalies. Around 30% cases, complete heart block remain asymptomatic and not detected until adulthood and may present in pregnancy state and puerperium. When the reversible cause of the AV Block cannot be found, the permanent pacemaker or temporary pacemaker may be indicated when the patients show the symptoms. Case Illusration: A-21 year old female, G2P0A1 preterm pregnancy (27-28 weeks) with bradycardia. From electrocardiograph examination revealed Total AV Block with junctional escape rhytym. Transthoracic echocardiogram shows massive tricuspid regurgitation, early phase of peripartum cardiomyopathy and ejection fraction 36-40%. Caesarean section was peformed due to PPROM. A male baby was born with birth weight of 1100 grams, 32 centimeters of body length and APGAR score of 7/9. The baby was died in NICU on day care 4th, with suspected respiratory problem. Conclusion: Complete heart block in pregnancy is a rare condition. This condition could remain asymptomatic and not detected until pregnancy. Multidisciplinary approach, close monitoring of the symptoms and cardiac functions are needed for patients with CHB.
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妊娠期完全性心脏传导阻滞1例报告
背景:完全性心脏传导阻滞的发生是由于各种病理情况引起浸润、纤维化或心脏传导系统的一部分失去连接。妊娠期完全性心脏传导阻滞常由先天性异常引起。约30%的完全性心脏传导阻滞患者直到成年后才被发现,并可能在妊娠期和产褥期出现。当无法找到可逆的房室传导阻滞原因时,当患者出现症状时,可能需要使用永久起搏器或临时起搏器。病例说明:A-21岁女性,G2P0A1早产(27-28周)伴心动过缓。心电图检查显示全房室传导阻滞伴交界性逃逸节律。经胸超声心动图显示大量三尖瓣反流,围产期早期心肌病,射血分数36-40%。因PPROM行剖宫产。男婴出生体重1100克,体长32厘米,APGAR评分7/9。该婴儿于4日在新生儿重症监护室死亡,疑似呼吸问题。结论:妊娠期完全性心脏传导阻滞罕见。这种情况可能没有症状,直到怀孕才被发现。多学科联合治疗,密切监测慢性乙型肝炎患者的症状和心功能。
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8 weeks
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