Department of Pediatrics, Section of Pediatric Cardiology, Baylor College of Medicine/Texas Children's Hospital, 6651 Main St, FE1920, Houston, TX, 77030, USA.
Department of Pediatrics, Section of Pediatric Cardiology, Baylor College of Medicine/Texas Children's Hospital, 6651 Main St, E1920, Houston, TX, 77030, USA.
Pediatr Cardiol. 2022 Mar;43(3):655-664. doi: 10.1007/s00246-021-02770-3. Epub 2021 Nov 23.
The presence of a genetic condition is a risk factor for increased mortality in hypoplastic left heart syndrome (HLHS). Speckle tracking strain analysis in interstage echocardiograms have shown promise in identifying patients with HLHS at increased risk of mortality. We hypothesized that fetuses with a genetic condition and HLHS have impaired right ventricular global longitudinal strain compared with fetuses with HLHS and no evident genetic condition. We performed a retrospective analysis of 60 patients diagnosed in fetal life with HLHS from 11/2015 to 11/2019. We evaluated presenting echocardiograms and calculated right ventricular global longitudinal strain (RV GLS) and fractional area of change (FAC) using post-processing software. We first compared RV GLS and FAC between those with genetic conditions to those without. We examined the secondary outcome of mortality among those with and without genetic conditions and among HLHS subgroups. Of the 60 patients with available genetic testing, 11 (18%) had an identified genetic condition. Neither RV GLS nor FAC was significantly different between patients with and without genetic conditions. There was no difference in RV GLS or FAC among HLHS phenotype or those who died or survived as infants. However, patients with a genetic syndrome had increased neonatal and overall mortality. In this cohort, RV GLS did not differ between those with and without a genetic diagnosis, among HLHS phenotypes, or between those surviving and dying as infants. Further analysis of strain throughout gestation and after birth could provide insight into the developing heart in fetuses with HLHS.
存在遗传条件是左心发育不全综合征(HLHS)患者死亡率增加的一个风险因素。在中间期超声心动图中,斑点追踪应变分析显示出在识别 HLHS 患者中具有较高死亡率风险的患者方面具有前景。我们假设,与 HLHS 且无明显遗传条件的胎儿相比,具有遗传条件和 HLHS 的胎儿的右心室整体纵向应变受损。我们对 2015 年 11 月至 2019 年 11 月期间在胎儿期被诊断为 HLHS 的 60 例患者进行了回顾性分析。我们评估了现有的超声心动图,并使用后处理软件计算了右心室整体纵向应变(RV GLS)和分数面积变化(FAC)。我们首先比较了有遗传条件和无遗传条件的患者之间的 RV GLS 和 FAC。我们检查了有遗传条件和无遗传条件的患者之间以及 HLHS 亚组之间的死亡率的次要结局。在有可用基因检测的 60 例患者中,有 11 例(18%)存在明确的遗传条件。有遗传条件和无遗传条件的患者之间的 RV GLS 或 FAC 没有显著差异。HLHS 表型或死亡或存活为婴儿的患者之间的 RV GLS 或 FAC 没有差异。然而,具有遗传综合征的患者的新生儿和总体死亡率增加。在本队列中,有和无遗传诊断、HLHS 表型或存活和死亡为婴儿的患者之间的 RV GLS 没有差异。对整个妊娠期和出生后的应变进行进一步分析可以深入了解 HLHS 胎儿发育中的心脏。