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单心室和房室间隔缺损婴儿的多阶段姑息治疗结果

Outcomes of Multistage Palliation of Infants With Single Ventricle and Atrioventricular Septal Defect.

作者信息

Alsoufi Bahaaldin, McCracken Courtney, Kanter Kirk, Shashidharan Subhadra, Border William, Kogon Brian

机构信息

Department of Cardiothoracic Surgery, University of Louisville and Norton Children's Hospital, Louisville, KY, USA.

Division of Pediatric Cardiology, Emory University and Children's Healthcare of Atlanta, Druid Hills, GA, USA.

出版信息

World J Pediatr Congenit Heart Surg. 2020 Jan;11(1):39-48. doi: 10.1177/2150135119885890.

Abstract

BACKGROUND

Published palliation outcomes of infants with functional single ventricle (SV) and common atrioventricular septal defect (AVSD) are poor due to associated cardiac and extracardiac anomalies and development of atrioventricular valve (AVV) regurgitation. We report current palliation results.

METHODS

From 2002 to 2012, 80 infants with functional SV with AVSD underwent multistage palliation. Competing-risks analyses modeled events after first-stage surgery and Glenn (death/transplantation vs next palliation surgery) and examined factors associated with survival and AVV intervention.

RESULTS

Sixty-eight (80%) patients received neonatal palliation: modified Blalock-Taussig shunt (n = 33, 41%), Norwood (n = 20, 25%), and pulmonary artery band (n = 15, 19%), whereas 12 (15%) received primary Glenn. On competing-risks analysis, one-year following first-stage surgery, 29% of patients had died or received transplantation and 62% had undergone Glenn. Five years following Glenn, 9% of patients had died or received transplantation and 68% had undergone Fontan. Overall eight-year survival was 64% and was lower in patients with genetic syndromes (53% vs 82%), patients requiring concomitant total anomalous pulmonary venous connection repair (53% vs 69%), and those requiring neonatal palliation (48% vs 100%). Factors associated with mortality were unplanned reoperation (hazard ratio [HR]: 3.7 [1.7-8.0], = .001) and extracorporeal membrane oxygenation use (HR: 7.1 [3.0-16.6], < .001). Initial AVV regurgitation ≥ moderate was associated with AVV intervention (HR: 6.2 [2.4-16.1], = .002) with eight-year freedom from death or AVV intervention of 25% in those patients.

CONCLUSIONS

Patients with SV with AVSD are a distinct group and commonly have associated cardiac and extracardiac malformations that complicate care and affect survival. The development of AVV regurgitation requiring intervention is common but does not affect survival.

摘要

背景

由于合并心脏和心外畸形以及房室瓣(AVV)反流的发展,已发表的功能性单心室(SV)和共同房室间隔缺损(AVSD)婴儿的姑息治疗结果较差。我们报告了当前的姑息治疗结果。

方法

2002年至2012年,80例患有功能性SV合并AVSD的婴儿接受了多阶段姑息治疗。竞争风险分析对一期手术后的事件以及格林手术(死亡/移植与下一次姑息手术)进行建模,并检查与生存和AVV干预相关的因素。

结果

68例(80%)患者接受了新生儿姑息治疗:改良布莱洛克-陶西格分流术(n = 33,41%)、诺伍德手术(n = 20,25%)和肺动脉环扎术(n = 15,19%),而12例(15%)接受了一期格林手术。在竞争风险分析中,一期手术后一年,29% 的患者死亡或接受了移植,62% 的患者接受了格林手术。格林手术后五年,9% 的患者死亡或接受了移植,68% 的患者接受了Fontan手术。总体八年生存率为64%,患有遗传综合征的患者(53% 对82%)、需要同时进行完全性肺静脉异位连接修复的患者(53% 对69%)以及需要新生儿姑息治疗的患者(48% 对100%)的生存率较低。与死亡率相关的因素是计划外再次手术(风险比[HR]:3.7[1.7 - 8.0],P = .001)和使用体外膜肺氧合(HR:7.1[3.0 - 16.6],P < .001)。初始AVV反流≥中度与AVV干预相关(HR:6.2[2.4 - 16.1],P = .002),这些患者八年无死亡或AVV干预的生存率为25%。

结论

患有SV合并AVSD的患者是一个独特的群体,通常合并心脏和心外畸形,使治疗复杂化并影响生存。需要干预的AVV反流的发生很常见,但不影响生存。

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