The Heart Center, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
Eur J Cardiothorac Surg. 2014 Jan;45(1):77-82. doi: 10.1093/ejcts/ezt251. Epub 2013 May 9.
Children with various single ventricle anomalies are at risk of developing systemic ventricular outflow tract obstruction (SVOTO) following volume unloading with cavopulmonary connection (CPC). We aim to evaluate the value of Damus-Kaye-Stansel (DKS) anastomosis at the time of CPC in eliminating late SVOTO risk.
Retrospective review of single ventricle patients who underwent DKS concurrent with CPC between 1997 and 2012 was performed. Clinical, echocardiographic and angiographic outcomes were analysed.
Thirty-six children with single ventricle underwent DKS at the time of Glenn bidirectional CPC (n = 29) or Fontan total CPC (n = 7). The underlying anatomy was double inlet left ventricle (n = 18), double outlet right ventricle (n = 8), unbalanced atrioventricular septal defect (n = 4) and other (n = 6). Prior palliation included pulmonary artery band (n = 35), coarctation/arch repair (n = 11) and atrial septectomy (n = 8). Median age at the time of DKS was 8.9 months (range 3.6 months-9.1 years) and the median weight was 6.7 kg (range 5-27 kg). At the time of DKS, 17 patients (47%) had no SVOT gradient and 19 (53%) had SVOT gradient (mean 23.4 ± 18.7 mmHg). Overall survival was 89 and 83% at 1 month and 5 years, respectively. None of the deaths were related to SVOTO or DKS complications. When present, SVOT gradient decreased from 23.4 ± 18.7 mmHg preoperatively to 0 after DKS (P < 0.001). At the last follow-up, none of the patients developed any SVOT gradient; 78% of them had zero or trivial aortic/neoaortic valve regurgitation while 22% had mild regurgitation. None of the patients had evidence of compression of the left pulmonary artery or bronchus. Eighty-one percent of patients have reached or are suitable candidates awaiting final palliative surgery.
DKS can be safely performed in conjunction with CPC without added mortality risk. It is very effective in mitigating SVOTO risk, with sustainable good semilunar valves function. Our data support an aggressive approach to performing DKS concurrent with CPC in children with single ventricle pathologies at risk of developing SVOTO.
在腔静脉-肺动脉连接(CPC)后,各种单心室畸形的儿童由于容量卸载会发生体循环流出道梗阻(SVOTO)。我们旨在评估 Damus-Kaye-Stansel(DKS)吻合术在 CPC 时消除晚期 SVOTO 风险的价值。
回顾性分析了 1997 年至 2012 年间接受 DKS 与 CPC 同期手术的单心室患者。分析了临床、超声心动图和血管造影结果。
36 例单心室患者行 Glenn 双向 CPC(n = 29)或 Fontan 全 CPC(n = 7)时行 DKS。基础解剖结构为左心室双入口(n = 18)、右心室双出口(n = 8)、房室间隔缺损不平衡(n = 4)和其他(n = 6)。先前的姑息治疗包括肺动脉带(n = 35)、缩窄/弓修复(n = 11)和房间隔切除术(n = 8)。DKS 时的中位年龄为 8.9 个月(范围 3.6 个月至 9.1 年),中位体重为 6.7kg(范围 5-27kg)。DKS 时,17 例(47%)患者无 SVOT 梯度,19 例(53%)患者有 SVOT 梯度(平均 23.4 ± 18.7mmHg)。术后 1 个月和 5 年的总体生存率分别为 89%和 83%。无死亡与 SVOTO 或 DKS 并发症有关。SVOT 梯度术前为 23.4 ± 18.7mmHg,术后降为 0(P<0.001)。末次随访时,所有患者均无 SVOT 梯度;78%患者主动脉/新主动脉瓣反流为零或轻微,22%患者为轻度反流。无患者出现左肺动脉或支气管受压证据。81%的患者已达到或适合接受最终姑息性手术。
DKS 可与 CPC 安全联合进行,无额外死亡率风险。它在减轻 SVOTO 风险方面非常有效,可持续维持良好的半月瓣功能。我们的数据支持在有发生 SVOTO 风险的单心室病变患儿中积极行 DKS 与 CPC 同期手术。