King Faisal Heart Institute, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.
J Thorac Cardiovasc Surg. 2011 Jul;142(1):142-147.e2. doi: 10.1016/j.jtcvs.2011.01.064. Epub 2011 Apr 7.
Delayed first-stage palliation of children with hypoplastic left heart syndrome and related pathologies can be associated with poor outcomes because of development of progressive pulmonary vascular disease and volume load effects on the systemic ventricle and atrioventricular valve. We examine the current era's survival in this subgroup.
Fifty-five infants older than 2 weeks underwent the Norwood operation (2003-2007). Separate competing risk analyses were performed to model outcomes (death and transition to the next stage) after the Norwood operation and after bidirectional cavopulmonary connection.
Median age was 32 days (range, 15-118 days). Forty-seven percent had hypoplastic left heart syndrome, and 53% had other complex univentricular variants. Mean ascending aortic size was 4.4 ± 1.9 mm, 10% had impaired ventricular function, 11% had moderate atrioventricular valve regurgitation, and 32% had restrictive pulmonary venous return. Pulmonary blood flow was established through an aortopulmonary shunt (n = 30) or Sano shunt (n = 25). After the Norwood operation, patients required longer ventilation and more oxygen and nitric oxide and had higher inotropic scores compared with those undergoing the traditional management protocol. Competing risks analysis showed that 2 years after the Norwood operation, 39% had died, and 57% underwent bidirectional cavopulmonary connection. Four years after bidirectional cavopulmonary connection, 15% had died, and 85% underwent the Fontan operation. Overall 3-year survival after the Norwood operation was 53%. Factors associated with mortality were age, lower weight at the time of the Norwood operation, impaired ventricular function, longer circulatory arrest, and lower pre-bidirectional cavopulmonary connection saturation.
Children older than 2 weeks undergoing the Norwood operation frequently require postoperative pulmonary vasodilatation and high inotropic support. A significant hazard of death persists through all steps of multistage palliation. Increased pulmonary vascular resistance and volume load effects, such as systemic ventricular impairment and atrioventricular valve regurgitation, are commonly evident in patients in whom treatment fails or who do not qualify to proceed to the next stage of palliation. Those patients should be closely monitored for timely referral for heart transplantation when indicated.
患有左心发育不全综合征和相关病变的儿童延迟进行一期姑息性治疗可能会导致不良结局,因为会发生进行性肺血管疾病以及容量负荷对体循环心室和房室瓣的影响。我们研究了当前这一分组的生存情况。
55 名年龄大于 2 周的婴儿接受了 Norwood 手术(2003-2007 年)。分别进行了竞争风险分析,以对 Norwood 手术后和双向腔肺连接后的结局(死亡和过渡到下一阶段)进行建模。
中位年龄为 32 天(范围 15-118 天)。47%患有左心发育不全综合征,53%患有其他复杂的单心室变体。升主动脉直径平均为 4.4 ± 1.9mm,10%存在心室功能障碍,11%存在中度房室瓣反流,32%存在限制性肺静脉回流。通过主动脉-肺动脉分流(n = 30)或 Sano 分流(n = 25)建立肺血流。与接受传统管理方案的患者相比,Norwood 手术后的患者需要更长时间的通气、更多的氧气和一氧化氮,并且需要更高的正性肌力评分。竞争风险分析显示,Norwood 手术后 2 年,39%的患者死亡,57%的患者进行了双向腔肺连接。双向腔肺连接后 4 年,15%的患者死亡,85%的患者进行了 Fontan 手术。Norwood 手术后的 3 年总生存率为 53%。死亡的相关因素包括年龄、Norwood 手术时的体重较低、心室功能障碍、更长的体外循环时间以及双向腔肺连接前的饱和度较低。
年龄大于 2 周的儿童接受 Norwood 手术后,经常需要术后肺血管扩张和高正性肌力支持。在多阶段姑息治疗的所有步骤中,死亡的风险仍然很大。在治疗失败或不符合下一阶段姑息治疗条件的患者中,通常会出现明显的肺血管阻力增加和容量负荷效应,例如体循环心室功能障碍和房室瓣反流。这些患者应密切监测,以便在需要时及时转介进行心脏移植。