Ota Noritaka, Fujimoto Yoshifumi, Hirose Keiichi, Tosaka Yuko, Nakata Tomohiro, Ide Yujiro, Sakamoto Kisaburo
Shizuoka Children's Hospital, 860 Urushiyama, Aoi-ku, Shizuoka City, Shizuoka, 420-8660, Japan.
Cardiol Young. 2010 Feb;20(1):60-5. doi: 10.1017/S1047951109990965. Epub 2010 Mar 4.
Heterotaxy syndrome, which is often associated with atrioventricular valvar regurgitation, has been considered a risk factor for the surgical repair for Fontan candidates. The results of atrioventricular valve repair in this challenging patient population remain largely unknown.
From July, 1994 to January, 2007, 25 patients with the heterotaxy syndrome consisting of 22 right isomerism and three left isomerism presented to the Shizuoka Children's Hospital Japan with significant (3-4+) atrioventricular valvar regurgitation necessitating atrioventricular valve repair. The clinical and Doppler/echocardiographic data were retrospectively reviewed to determine the efficacy of the repair and patient outcome.
Patients were divided into two groups on the basis of atrioventricular valvar regurgitation at the most recent follow-up: those with a successful late outcome, (0-2) and those with a poor outcome (3-4). There were 17 (67%) patients with a successful outcome and 8 (33%) with a poor outcome. The repair technique including leaflet apposition was predictive of a successful outcome (p = 0.003). Overall survival was 64% (16/25). Survival was 88.2% (15/17) for patients with a successful result versus 12.5% (1/8) for those with a poor outcome (p = 0.0007). Of the 15 survivors, 13 have reached final completion of the Fontan circulation, and two currently remain at the bi-directional Glenn shunt stage.
Atrioventricular valve repair can be accomplished in this challenging patient population with excellent results. The combination of the leaflet apposition technique and the Kay suture can be performed with an excellent outcome in the majority of patients with heterotaxy syndrome, even with significant atrioventricular valvar regurgitation.
心脏异构综合征常与房室瓣反流相关,被认为是Fontan手术候选患者的一个危险因素。在这一具有挑战性的患者群体中,房室瓣修复的结果在很大程度上仍不明确。
1994年7月至2007年1月,25例心脏异构综合征患者(22例右位异构和3例左位异构)因严重(3-4+级)房室瓣反流到日本静冈儿童医院就诊,需要进行房室瓣修复。对临床及多普勒/超声心动图数据进行回顾性分析,以确定修复的疗效及患者的预后。
根据最近一次随访时的房室瓣反流情况,将患者分为两组:远期预后良好组(0-2级)和预后不良组(3-4级)。17例(67%)患者预后良好,8例(33%)患者预后不良。包括瓣叶对合在内的修复技术可预测预后良好(p = 0.003)。总体生存率为64%(16/25)。预后良好的患者生存率为88.2%(15/17),而预后不良的患者生存率为12.5%(1/8)(p = 0.0007)。15例存活患者中,13例已完成Fontan循环的最终阶段,2例目前仍处于双向格林分流阶段。
在这一具有挑战性的患者群体中可以完成房室瓣修复,且效果良好。瓣叶对合技术与Kay缝合相结合,在大多数心脏异构综合征患者中,即使存在严重的房室瓣反流,也可取得良好的效果。