Lucile Packard Children's Hospital Heart Center, Department of Cardiothoracic Surgery, Stanford University School of Medicine, Palo Alto, Calif.
Lucile Packard Children's Hospital Heart Center, Department of Pediatrics, Stanford University School of Medicine, Palo Alto, Calif.
J Thorac Cardiovasc Surg. 2018 Apr;155(4):1747-1755.e1. doi: 10.1016/j.jtcvs.2017.11.001. Epub 2017 Nov 8.
Palliation of hypoplastic left heart syndrome with a standard nonvalved right ventricle to pulmonary artery conduit results in an inefficient circulation in part due to diastolic regurgitation. A composite right ventricle pulmonary artery conduit with a homograft valve has a hypothetical advantage of reducing regurgitation, but may differ in the propensity for stenosis because of valve remodeling.
This retrospective cohort study included 130 patients with hypoplastic left heart syndrome who underwent a modified stage 1 procedure with a right ventricle to pulmonary artery conduit from 2002 to 2015. A composite valved conduit (cryopreserved homograft valve anastomosed to a polytetrafluoroethylene tube) was placed in 100 patients (47 aortic, 32 pulmonary, 13 femoral/saphenous vein, 8 unknown), and a nonvalved conduit was used in 30 patients. Echocardiographic functional parameters were evaluated before and after stage 1 palliation and before the bidirectional Glenn procedure, and interstage interventions were assessed.
On competing risk analysis, survival over time was better in the valved conduit group (P = .040), but this difference was no longer significant after adjustment for surgical era. There was no significant difference between groups in the cumulative incidence of bidirectional Glenn completion (P = .15). Patients with a valved conduit underwent more interventions for conduit obstruction in the interstage period, but this difference did not reach significance (P = .16). There were no differences between groups in echocardiographic parameters of right ventricle function at baseline or pre-Glenn.
In this cohort of patients with hypoplastic left heart syndrome, inclusion of a valved right ventricle to pulmonary artery conduit was not associated with any difference in survival on adjusted analysis and did not confer an identifiable benefit on right ventricle function.
由于舒张期反流,标准无瓣右心室至肺动脉通道姑息性治疗左心发育不全综合征会导致循环效率低下。带同种异体瓣膜的复合右心室肺动脉通道具有减少反流的假设优势,但由于瓣膜重塑,其狭窄倾向可能不同。
本回顾性队列研究纳入了 2002 年至 2015 年间接受改良一期手术的 130 例左心发育不全综合征患者,手术中使用右心室至肺动脉通道。100 例患者(47 例主动脉,32 例肺动脉,13 例股静脉/大隐静脉,8 例不详)采用带瓣复合管道(冷冻同种异体瓣膜与聚四氟乙烯管吻合),30 例患者采用无瓣管道。在一期姑息治疗前后及双向 Glenn 手术前评估超声心动图功能参数,并评估中间期干预。
在竞争风险分析中,带瓣组的生存时间随时间推移更好(P=0.040),但在调整手术时代后,这种差异不再显著。两组双向 Glenn 术完成的累积发生率无显著差异(P=0.15)。带瓣组患者在中间期需要更多的干预来治疗管道阻塞,但差异无统计学意义(P=0.16)。两组基线或 Glenn 术前右心室功能的超声心动图参数无差异。
在本左心发育不全综合征患者队列中,调整分析显示,带瓣右心室至肺动脉通道的纳入与生存率无差异,也未对右心室功能产生可识别的益处。