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海拔≥2500米地区的埃布斯坦畸形修复术:来自玻利维亚的首例经验

Ebstein Repair in a High-Altitude Setting ≥2,500 m: First Experience from Bolivia.

作者信息

Weber Sven C, Alvensleben Inge von, Vadiunec Valentin, Iben Andre, Berger Felix, Sallmon Hannes, Photiadis Joachim

机构信息

Department of Congenital Heart Disease-Pediatric Cardiology, Deutsches Herzzentrum der Charité (DHZC), Berlin, Germany.

Kardiozentrum, La Paz, Bolivia.

出版信息

Thorac Cardiovasc Surg. 2025 Jan;73(S 03):e31-e38. doi: 10.1055/a-2620-3643. Epub 2025 May 26.

Abstract

Contemporary surgical approaches for Ebstein anomaly are based on a paradigm shift towards earlier surgery in order to avoid the deleterious effects of chronic right ventricular (RV) volume overload. In addition, RV dysfunction may worsen in the setting of high altitude, and to date, no results on Ebstein anomaly surgery have been reported from a high-altitude setting.We herein present first postoperative results from Ebstein anomaly patients who underwent cone reconstruction (with or without bidirectional Glenn anastomosis) in Cochabamba, Bolivia (>2,500 m above sea level) using a specific high-altitude protocol for prophylactic medical treatment of presumed pulmonary hypertension (PH), including sildenafil, iloprost, and higher FiO.Four patients underwent surgical correction of Ebstein anomaly (median age 9 years, range 4-12 years, all female). Ebstein anomaly was classified as Carpentier type C in three and as Carpentier Type B in one patient. All patients showed some degree of atrial shunting while one patient exhibited an additional perimembranous ventricular septal defect. All underwent cone reconstruction of the tricuspid valve. Due to massive intraoperative bleeding, which required rethoracotomy, subsequently causing impaired RV function, one patient underwent concomitant "one and a half ventricle" repair. All other patients showed an uncomplicated postoperative course and all were alive with a good and/or improved RV function and only minimal-to-mild tricuspid regurgitation after 1 year.Cone reconstruction in children with Ebstein anomaly is feasible in a high-altitude setting when using a dedicated protocol to prophylactically manage PH.

摘要

当代治疗埃布斯坦畸形的手术方法基于一种向早期手术的范式转变,以避免慢性右心室容量超负荷的有害影响。此外,在高海拔环境中右心室功能障碍可能会恶化,迄今为止,尚无来自高海拔地区的埃布斯坦畸形手术结果报告。我们在此展示了在玻利维亚科恰班巴(海拔超过2500米)接受圆锥重建(伴或不伴双向格林吻合术)的埃布斯坦畸形患者的首次术后结果,手术采用了针对假定的肺动脉高压(PH)进行预防性药物治疗的特定高海拔方案,包括西地那非、伊洛前列素和更高的吸氧浓度。4例患者接受了埃布斯坦畸形的手术矫正(中位年龄9岁,范围4 - 12岁,均为女性)。3例埃布斯坦畸形被分类为Carpentier C型,1例为Carpentier B型。所有患者均有一定程度的心房分流,1例患者还伴有膜周部室间隔缺损。所有患者均接受了三尖瓣圆锥重建。由于术中大量出血,需要再次开胸,随后导致右心室功能受损,1例患者同时接受了“一个半心室”修复。所有其他患者术后过程均无并发症,1年后所有患者均存活,右心室功能良好和/或改善,仅有轻微至轻度三尖瓣反流。在高海拔环境中,当使用专门方案预防性管理肺动脉高压时,对患有埃布斯坦畸形的儿童进行圆锥重建是可行的。

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