Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
New England Research Institutes, Boston, Massachusetts.
J Am Soc Echocardiogr. 2018 Oct;31(10):1151-1157. doi: 10.1016/j.echo.2018.05.003. Epub 2018 Jul 3.
Children with single-right ventricle anomalies such as hypoplastic left heart syndrome (HLHS) have left ventricles of variable size and function. The impact of the left ventricle on the performance of the right ventricle and on survival remains unclear. The aim of this study was to identify whether left ventricular (LV) size and function influence right ventricular (RV) function and clinical outcome after staged palliation for single-right ventricle anomalies.
In the Single Ventricle Reconstruction trial, echocardiography-derived measures of LV size and function were compared with measures of RV systolic and diastolic function, tricuspid regurgitation, and outcomes (death and/or heart transplantation) at baseline (preoperatively), early after Norwood palliation, before stage 2 palliation, and at 14 months of age.
Of the 522 subjects who met the study inclusion criteria, 381 (73%) had measurable left ventricles. The HLHS subtype of aortic atresia/mitral atresia was significantly less likely to have a measurable left ventricle (41%) compared with the other HLHS subtypes: aortic stenosis/mitral stenosis (100%), aortic atresia/mitral stenosis (96%), and those without HLHS (83%). RV end-diastolic and end-systolic volumes were significantly larger, while diastolic indices suggested better diastolic properties in those subjects with no left ventricles compared with those with measurable left ventricles. However, RV ejection fraction was not different on the basis of LV size and function after staged palliation. Moreover, there was no difference in transplantation-free survival to Norwood discharge, through the interstage period, or at 14 months of age between those subjects who had measurable left ventricles compared with those who did not.
LV size varies by anatomic subtype in infants with single-right ventricle anomalies. Although indices of RV size and diastolic function were influenced by the presence of a left ventricle, there was no difference in RV systolic function or transplantation-free survival on the basis of LV measures.
患有单右心室畸形(如左心发育不全综合征,HLHS)的儿童的左心室大小和功能各不相同。左心室对右心室功能以及生存的影响仍不清楚。本研究旨在确定左心室(LV)大小和功能是否会影响单右心室畸形分期姑息治疗后的右心室(RV)功能和临床结局。
在单心室重建试验中,在基线(术前)、Norwood 姑息手术后早期、进行 2 期姑息手术前和 14 月龄时,将 LV 大小和功能的超声心动图测量值与 RV 收缩和舒张功能、三尖瓣反流以及结局(死亡和/或心脏移植)进行比较。
在符合研究纳入标准的 522 名受试者中,有 381 名(73%)的左心室可测量。主动脉瓣闭锁/二尖瓣闭锁的 HLHS 亚型发生左心室不可测量的可能性明显低于其他 HLHS 亚型:主动脉瓣狭窄/二尖瓣狭窄(100%)、主动脉瓣闭锁/二尖瓣闭锁(96%)和无 HLHS 者(83%)。那些无左心室的受试者的 RV 舒张末期和收缩末期容积明显较大,而舒张指数表明与可测量的左心室相比,这些受试者的舒张功能更好。然而,基于分期姑息治疗后的 LV 大小和功能,RV 射血分数并无差异。此外,与可测量的左心室相比,在 Norwood 出院期间、间期或 14 月龄时,那些有可测量的左心室的受试者与那些没有的受试者之间在无移植存活率方面没有差异。
在患有单右心室畸形的婴儿中,LV 大小因解剖亚型而异。尽管 RV 大小和舒张功能指数受左心室存在的影响,但根据 LV 测量值,RV 收缩功能或无移植存活率并无差异。