先天性完全性心脏传导阻滞并发心房扑动的诊断和处理。

IF 0.7 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS

Journal of the Saudi Heart Association Pub Date : 2023-09-07 eCollection Date: 2023-01-01 DOI:10.37616/2212-5043.1347

Ali A Alakhfash, Abdulrahman Almesned, Abdullah Alqwaiee, Hashem D Alqurashi, Waleed Almanea

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引用次数: 0

摘要

17个月大的孩子在子宫内被诊断为先天性完全性心脏传导阻滞。母亲患有干燥综合征，抗Ro抗体较高。婴儿足月分娩时心率为每分钟55-60次。超声心动图显示心脏结构正常，有小房间隔缺损和中度动脉导管未闭。17个月大时，他出现心房扑动，在Cath实验室使用电复律终止。在一年的随访中，心房扑动没有复发。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

Congenital Complete Heart Block Complicated by Atrial Flutter Diagnosis and Management.

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Congenital Complete Heart Block Complicated by Atrial Flutter Diagnosis and Management.

Seventeen-month-old child was diagnosed in utero to have congenital complete heart block. The mother has Sjogren's syndrome with high Anti Ro antibodies. The baby was delivered at term with a heart rate of 55-60 beats per minute. Echocardiography revealed a structurally normal heart with a small atrial septal defect and moderate patent ductus arteriosus. At the age of 17 months, he developed atrial flutter which was aborted using electrical cardioversion in the Cath lab. No recurrence of the atrial flutter during a one-year follow-up.

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来源期刊

Journal of the Saudi Heart Association CARDIAC & CARDIOVASCULAR SYSTEMS-

CiteScore

1.40

自引率

0.00%

发文量

审稿时长

15 weeks