Case Report: Angiography-guided transvenous single-chamber pacemaker implantation in mirror-image dextrocardia with congenitally corrected transposition of the great arteries.

IF 3 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Frontiers in Cardiovascular Medicine Pub Date : 2026-10-05 eCollection Date: 2026-01-01 DOI:10.3389/fcvm.2026.1956397
Junda Cao, Qin Ao, Jin Ma, Ji Sun
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引用次数: 0

Abstract

Background: Mirror-image dextrocardia with situs inversus is uncommon. Transvenous permanent pacemaker implantation is technically demanding when it coexists with congenitally corrected transposition of the great arteries (ccTGA), because venous access, atrioventricular valve crossing, and fluoroscopic lead orientation may differ from usual anatomy.

Case presentation: A 61-year-old man was admitted with recurrent dizziness and palpitations for 5 years; his symptoms had worsened during the preceding 2 weeks. Preoperative 12-lead electrocardiography showed atrial fibrillation with a slow ventricular response. Twenty-four-hour Holter monitoring documented 707 pauses longer than 2.0 s, with a longest R-R interval of 6.13 s. Echocardiography confirmed mirror-image dextrocardia, situs inversus, and ccTGA. A single-chamber permanent pacemaker was implanted through the right axillary vein. Posteroanterior fluoroscopy defined the right-sided cardiac silhouette; right axillary venography guided venous puncture; right atrial angiography identified the morphologic mitral annular plane; and multi-projection fluoroscopy was used to confirm the final ventricular lead position in the high mid-septal region of the morphologic left ventricle. The procedure lasted 56 min and had no acute complications. At 6-month outpatient follow-up, standard 12-lead electrocardiography, 24-hour Holter monitoring, formal device interrogation, and transthoracic echocardiography showed stable pacing, preserved ventricular performance, and no device-related complication; the paced QRS duration was 144 ms and the pacing burden was 99.8%. During telephone follow-up in June 2026, approximately 1 year after implantation, the patient reported no discomfort.

Conclusion: This case describes a structured approach to conventional transvenous pacemaker implantation in mirror-image dextrocardia with ccTGA. In this patient, venography, chamber angiography, and targeted fluoroscopic views reduced procedural uncertainty, and follow-up through 1 year showed clinical stability without recognized complications.

病例报告:血管造影引导下经静脉单室起搏器植入先天性纠正大动脉转位的镜像右心。
背景:镜像右心并心逆位并不常见。经静脉永久性起搏器植入与先天性纠正性大动脉转位(ccTGA)共存时,在技术上要求很高,因为静脉通路、房室瓣膜交叉和透视导联定向可能与通常的解剖结构不同。病例介绍:男性,61岁,因反复头晕心悸5年入院;他的症状在前两周恶化。术前12导联心电图显示心房颤动伴心室反应缓慢。24小时动态心电图监测记录了707次超过2.0秒的停顿,最长的R-R间隔为6.13秒。超声心动图证实镜像右心、逆位和ccTGA。通过右腋窝静脉植入单腔永久性起搏器。后前方透视确定右侧心脏轮廓;右腋窝静脉造影引导静脉穿刺;右心房血管造影显示二尖瓣环平面;采用多投影透视法确定最终心室导联位置在形态学左心室中隔高区。手术持续56分钟,无急性并发症。在6个月的门诊随访中,标准的12导联心电图、24小时动态心电图监测、正式的器械询问和经胸超声心动图显示起搏稳定,心室功能保留,无器械相关并发症;节律QRS持续时间为144 ms,起搏负荷为99.8%。在2026年6月,植入后大约1年的电话随访中,患者报告没有不适。结论:本病例描述了一种结构化的方法,用于镜像右心ccTGA的常规经静脉起搏器植入。在该患者中,静脉造影、腔室血管造影和靶向透视减少了手术的不确定性,随访1年,临床稳定,无明显并发症。
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来源期刊
Frontiers in Cardiovascular Medicine
Frontiers in Cardiovascular Medicine Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.80
自引率
11.10%
发文量
3529
审稿时长
14 weeks
期刊介绍: Frontiers? Which frontiers? Where exactly are the frontiers of cardiovascular medicine? And who should be defining these frontiers? At Frontiers in Cardiovascular Medicine we believe it is worth being curious to foresee and explore beyond the current frontiers. In other words, we would like, through the articles published by our community journal Frontiers in Cardiovascular Medicine, to anticipate the future of cardiovascular medicine, and thus better prevent cardiovascular disorders and improve therapeutic options and outcomes of our patients.
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