The Success of a New Protocol for Early Diagnosis and Management of Congenital Atrioventricular Block: A Follow-up Study of 15 Fetuses from November 2007 to August 2022

Q3 Medicine
M. Shahidi, A. Afkhamzadeh
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Abstract

Background: Congenital atrioventricular heart block (CAVB) is a relatively rare condition that can lead to long-term complications. Early diagnosis and management of CAVB is currently the ideal goal, particularly in high-risk pregnancies. Methods: The Fetal Heart Center at Kurdistan University serves as the primary referral center for pregnant mothers residing in the western region of Iran. Fifteen fetuses with CAVB were admitted between November 2007 and August 2022. They were referred for one or more of the following reasons: fetal bradycardia or arrhythmia, abnormal ultrasound findings, and previous maternal or fetal risk factors. After obtaining a complete medical history, we conducted fetal echocardiography and ordered testing for maternal Lo/Ra autoantibodies. Our therapeutic approach was based on the type of atrioventricular block (AVB), serum titer of Lo/Ra antibodies, and specific risk factors associated with each type of AVB. Consequently, we used a combination of different medications, including dexamethasone, Hydroxychloroquine (HCQ), IVIG, beta-agonists, and inotropes. Results: We admitted 15 fetuses with CAVB, including seven females (47%) and eight males (53%). Most of our cases had positive tests for Lo and Ra autoantibodies, with varying degrees of AVB. A previous fetal death was common in our case series, accounting for 47% of cases. Moderate and high antibody titers were present in 80% of our cases. Mild bradycardia was a relatively common finding in our cases of first and second-degree atrioventricular block (AVB), occurring in 33% of patients. All of the above-mentioned findings, commonly referred to as major risk factors, were used for either early evaluation or therapeutic goals. No cases with first-degree AVB developed a higher grade of AVB after our therapeutic approach. One fetus with second-degree AVB developed CCHB, and another with mixed second/third-degree AVB reverted to second-degree AVB with the use of appropriate medications. Conclusions: Our therapeutic approach for the current cases yielded satisfactory results. Subsequently, we attempted to develop a rudimentary approach for early managing and treating fetuses with various types of CAVB. We are looking forward to future multicenter studies.
先天性房室传导阻滞早期诊断和治疗新方案的成功:2007年11月至2022年8月对15例胎儿的随访研究
背景:先天性房室传导阻滞(CAVB)是一种相对罕见的可导致长期并发症的疾病。早期诊断和治疗CAVB是目前的理想目标,特别是在高危妊娠中。方法:库尔德斯坦大学的胎儿心脏中心是居住在伊朗西部地区的孕妇的主要转诊中心。2007年11月至2022年8月期间,收治了15名患有CAVB的胎儿。他们是由于以下一个或多个原因转诊的:胎儿心动过缓或心律失常,超声检查异常,以及既往的母体或胎儿危险因素。在获得完整的病史后,我们进行了胎儿超声心动图检查,并要求检测母体的Lo/Ra自身抗体。我们的治疗方法基于房室传导阻滞(AVB)的类型、Lo/Ra抗体的血清滴度以及与每种类型AVB相关的特定危险因素。因此,我们使用了不同药物的组合,包括地塞米松、羟氯喹(HCQ)、IVIG、受体激动剂和肌力药物。结果:我们收治了15例CAVB胎儿,其中女性7例(47%),男性8例(53%)。大多数病例的Lo和Ra自身抗体检测呈阳性,伴有不同程度的AVB。先前的胎儿死亡在我们的病例系列中很常见,占病例的47%。在80%的病例中存在中高抗体滴度。在我们的一、二度房室传导阻滞(AVB)病例中,轻度心动过缓是相对常见的发现,发生在33%的患者中。所有上述发现,通常被称为主要危险因素,用于早期评估或治疗目标。在我们的治疗方法后,没有一例一级AVB发展为更高级别的AVB。二度AVB 1例发展为CCHB,二度/三度混合AVB 1例经适当药物治疗后恢复为二度AVB。结论:我们的治疗方法取得了满意的效果。随后,我们试图开发一种早期管理和治疗各种类型CAVB胎儿的基本方法。我们期待未来的多中心研究。
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来源期刊
Shiraz E Medical Journal
Shiraz E Medical Journal Medicine-Medicine (all)
CiteScore
1.00
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0.00%
发文量
63
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