Divisions of Pediatric Cardiac Surgery, 10624Stanford University School of Medicine, Stanford, CA, USA.
Pediatric Cardiology, Lucile Packard Children's Hospital Stanford, Stanford, CA, USA.
World J Pediatr Congenit Heart Surg. 2022 May;13(3):353-360. doi: 10.1177/21501351221085975.
Supravalvar aortic stenosis (SVAS) may be an isolated defect of the proximal ascending aorta. However, more severe cases have extension of the arteriopathy into the transverse and proximal descending aorta. The purpose of this study was to review our experience with SVAS with and without aortic arch arteriopathy.
This was a retrospective review of 58 patients who underwent surgical repair of SVAS. The median age at repair was 18 months. A total of 37 patients had Williams syndrome. A total of 31 (53%) patients had associated peripheral pulmonary artery stenosis and 23 (39%) had coronary artery ostial stenosis (CAOS).
A total of 37 of 58 (64%) patients had surgical repair of SVAS without the need for arch intervention while 21 (36%) patients had repair of the distal aortic arch. There were 3 (5.2%) operative deaths, 2 of whom had aortic arch involvement and one without arch involvement. There were 2 deaths after discharge from the hospital. Patients who needed arch surgery were more likely to have severe arch gradients compared to those without arch involvement (71% vs 30%, < .05), were more likely to undergo concomitant procedures for peripheral pulmonary artery stenosis or CAOS (90% vs 62%, < .05), and to have Williams syndrome (86% vs 51%, < .05).
More than one-third of patients who had SVAS repair at our institution had procedures directed at the transverse or proximal descending aorta. Patients with arch involvement had more severe arch obstruction, required more concomitant procedures, and were more likely to have Williams syndrome.
瓣上型主动脉狭窄(SVAS)可能是近端升主动脉的孤立性缺陷。然而,更严重的病例会导致动脉病变延伸至横弓和升主动脉近端。本研究的目的是回顾我们在伴有和不伴有主动脉弓病变的 SVAS 患者中的治疗经验。
这是一项对 58 例行 SVAS 手术修复的患者的回顾性研究。修复时的中位年龄为 18 个月。共有 37 例患者患有威廉姆斯综合征。共有 31 例(53%)患者存在外周肺动脉狭窄,23 例(39%)存在冠状动脉口狭窄(CAOS)。
共有 37 例(64%)患者行 SVAS 手术修复,无需弓部干预,21 例(36%)患者行主动脉弓部修复。共有 3 例(5.2%)手术死亡,其中 2 例有主动脉弓部受累,1 例无弓部受累。出院后有 2 例死亡。需要弓部手术的患者其弓部压力阶差显著高于无弓部受累者(71% vs 30%, <.05),更可能同时行外周肺动脉狭窄或 CAOS 手术(90% vs 62%, <.05),且更可能患有威廉姆斯综合征(86% vs 51%, <.05)。
在我们的机构中,超过三分之一的行 SVAS 修复的患者需要针对横弓或升主动脉近端的手术。有弓部受累的患者其弓部梗阻更严重,需要更多的同期手术,且更可能患有威廉姆斯综合征。