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除左心发育不全综合征外的单心室畸形患者接受诺伍德手术的当前疗效。

Current outcomes of the Norwood operation in patients with single-ventricle malformations other than hypoplastic left heart syndrome.

作者信息

Alsoufi Bahaaldin, Slesnick Timothy, McCracken Courtney, Ehrlich Alexandra, Kanter Kirk, Schlosser Brian, Maher Kevin, Sachdeva Ritu, Kogon Brian

机构信息

Division of Cardiothoracic Surgery, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA, USA

Department of Pediatrics, Division of Cardiology, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA, USA.

出版信息

World J Pediatr Congenit Heart Surg. 2015 Jan;6(1):46-52. doi: 10.1177/2150135114558069.

Abstract

BACKGROUND

Subsequent to increased experience with the Norwood operation in children with hypoplastic left heart syndrome (HLHS), its application has expanded to allow palliation of single-ventricle (SV) malformations other than HLHS. We describe current palliation outcomes in this group of SV patients.

METHODS

Between 2002 and 2012, 65 of the 303 Norwood operations were performed in non-HLHS SV patients. Competing risk analysis modeled events after Norwood and after subsequent Glenn and examined risk factors affecting outcomes.

RESULTS

Competing risk analysis showed that one year following Norwood, 24% of patients had died or received transplantation, 72% had undergone Glenn, and 4% were alive awaiting Glenn/Kawashima. Five years following Glenn, 9% of patients had died, 68% had undergone Fontan, and 23% were alive awaiting Fontan. Overall seven-year survival following Norwood was 68%. On multivariable analysis, mortality risk factors were unplanned cardiac reoperation (hazard ratio [HR]: 4.0 [1.5-10.6], P = .006), right dominant ventricle morphology (HR: 3.3 [1.3-8.3], P = .012), and postoperative extracorporeal membrane oxygenation (HR: 3.1 [1.1-9.0], P = .035).

CONCLUSIONS

Operative death and interstage mortality continue to be problematic following Norwood palliation for non-HLHS SV variants. Outcomes seem comparable to those reported for HLHS, however they are influenced by underlying pathology; children with dominant left ventricle morphology (tricuspid atresia and double inlet left ventricle) have superior survival compared to those with dominant right ventricle morphology (mitral atresia, unbalanced atrioventricular septal defect, and most patients with atrial isomerism). Unplanned reoperations for technical imperfections diminish survival. Large multicenter studies might be warranted to better identify high-risk patients and provide guidance toward improving their survival.

摘要

背景

随着对左心发育不全综合征(HLHS)患儿实施诺伍德手术的经验增加,该手术的应用范围已扩大到可用于除HLHS之外的单心室(SV)畸形的姑息治疗。我们描述了这组SV患者当前的姑息治疗结果。

方法

2002年至2012年期间,303例诺伍德手术中有65例是在非HLHS的SV患者中进行的。竞争风险分析对诺伍德手术后以及随后的格林手术之后的事件进行建模,并检查了影响结果的风险因素。

结果

竞争风险分析显示,诺伍德手术后一年,24%的患者死亡或接受了移植,72%的患者接受了格林手术,4%的患者存活等待格林/川岛手术。格林手术后五年,9%的患者死亡,68%的患者接受了丰坦手术,23%的患者存活等待丰坦手术。诺伍德手术后总体七年生存率为68%。多变量分析显示,死亡风险因素包括非计划心脏再次手术(风险比[HR]:4.0[1.5 - 10.6],P = 0.006)、右优势心室形态(HR:3.3[1.3 - 8.3],P = 0.012)和术后体外膜肺氧合(HR:3.1[1.1 - 9.0],P = 0.035)。

结论

对于非HLHS的SV变异型进行诺伍德姑息治疗后,手术死亡和过渡期死亡率仍然是问题。结果似乎与HLHS报道的结果相当,然而它们受到基础病理的影响;左优势心室形态(三尖瓣闭锁和双入口左心室)的儿童比右优势心室形态(二尖瓣闭锁、不平衡房室间隔缺损以及大多数心房异构患者)的儿童生存率更高。因技术缺陷进行的非计划再次手术会降低生存率。可能需要进行大型多中心研究,以更好地识别高危患者并为提高其生存率提供指导。

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