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Prenatal assessment of ventriculocoronary connections and ventricular endocardial fibroelastosis in hypoplastic left heart

机译:发育不全的左心室的心室-房室连接和室性心内膜纤维弹性的产前评估

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摘要

Objective: The outlook for newborns with hypoplastic left heart (HLH) has substantially improved over the last decade. However, differences in outcome among various anatomical subgroups have been described. We aimed to describe the incidence of ventriculocoronary communications and endocardial fibroelastosis in HLH and the possible implication on hospital survival (30 d). Methods: We retrospectively reviewed our medical records, still frames and video loops of 72 fetuses with HLH and critical aortic valve stenosis and evolving HLH from 2008 - 2013. The presence of VCAC and EFE were systematically assessed. Outcome parameters were incidence of VCAC and EFE among different anatomical subgroups of HLH and hospital survival (30 d). Results: 72 fetuses were included in this series. The incidence of VCAC was 11.1 % (8 cases) and EFE occurred in 33.3 % (24 cases). 5 fetuses with VCAC occurred in the subgroup of mitral valve stenosis/aortic valve atresia (MS/AA, 62.5 %) and 2 fetuses with VCAC occurred in the group of mitral atresia/aortic valve atresia (MA/AA, 25 %). Further classification was not possible in one case with VCAC (12.5 %). EFE predominantly occurred in the subgroup of MS/AA, MA/AA and in those cases with aortic valve stenosis and evolving HLH. The overall hospital survival on an intention-to-treat basis was 91.2 % (52/57 newborns). Hospital survival was 91 % for the subgroup of cases with MS/AA and for all other anatomical subgroups. Conclusion: The presence of VCAC in HLH can be diagnosed by fetal echocardiography predominantly occurring in cases with obstructed outflow and to some extent patent mitral valve. EFE is a frequent coexisting finding. Hospital survival was comparable among different anatomical subgroups and in cases with VCAC. The presence of VCAC in HLH did not limit the results of surgical palliation within the observation period of 30 days.
机译:目的:过去十年来,患有左心发育不全(HLH)的新生儿的前景得到了显着改善。然而,已经描述了各种解剖亚组之间的结果差异。我们的目的是描述HLH中的心室循环通讯和心内膜纤维弹性增生的发生率,以及对医院生存的可能影响(30天)。方法:我们回顾性回顾了2008年至2013年间72例HLH,严重主动脉瓣狭窄和发展中的HLH胎儿的病历,静止帧和视频循环。系统评估了VCAC和EFE的存在。结果参数是HLH的不同解剖亚组中VCAC和EFE的发生率以及医院生存时间(30天)。结果:该系列中包括72胎。 VCAC的发生率为11.1%(8例),EFE发生率为33.3%(24例)。二尖瓣狭窄/主动脉瓣闭锁(MS / AA,62.5%)亚组中有5例有VCAC胎儿,二尖瓣闭锁/主动脉瓣闭锁(MA / AA,25%)中有2例有VCAC胎儿。对于VCAC(12.5%),不可能进行进一步分类。 EFE主要发生在MS / AA,MA / AA的亚组中,以及那些主动脉瓣狭窄和HLH演变的病例。按意向治疗的总医院生存率为91.2%(52/57新生儿)。 MS / AA病例亚组和所有其他解剖亚组的医院存活率为91%。结论:HLAC中VCAC的存在可以通过胎儿超声心动图诊断,主要发生在流出道梗阻和二尖瓣未闭的情况下。 EFE是经常并存的发现。在不同的解剖亚组和VCAC病例中,医院的生存率具有可比性。 HLH中VCAC的存在并不限制30天观察期内的手术缓解结果。

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