Fetal i+D Fetal Medicine Research Center, BCNatal - Barcelona Center for Maternal-Fetal and Neonatal Medicine (Hospital Clínic and Hospital Sant Joan de Déu), Institut Clínic de Ginecologia Obstetricia i Neonatologia, Institut d'Investigacions Biomèdiques August Pi i Sunyer, Universitat de Barcelona and Centre for Biomedical Research on Rare Diseases (CIBER-ER), Barcelona, Spain.
Pediatric Cardiology, Hospital Sant Joan de Déu, Barcelona, Spain.
Ultrasound Obstet Gynecol. 2018 Mar;51(3):349-356. doi: 10.1002/uog.17456.
To define the pattern of fetal echocardiographic changes associated with isolated pulmonary valve stenosis (PS) and to correlate the echocardiographic findings with neonatal outcome and the need for postnatal pulmonary valvuloplasty within the first 12 months postpartum.
This was a prospective cohort study between January 2009 and October 2015 of 16 fetuses with isolated PS and 48 controls matched by gestational age at ultrasound examination (± 2 weeks) evaluated at the Fetal Cardiology Unit at BCNatal (Barcelona). Standard fetal ultrasound and comprehensive echocardiography, which included cardiovascular morphometric parameters, and systolic and diastolic functional and timing measurements, were performed in all cases. Baseline characteristics and perinatal outcome were retrieved from clinical records. Cases were followed up until 12 months of age, and admission to intensive care unit, days of hospitalization, need for prostaglandins and requirement for postnatal surgery were reviewed. Fetal PS cases were analyzed according to the need for postnatal pulmonary valvuloplasty.
The study groups were similar in terms of baseline, fetal ultrasound and perinatal characteristics. Median gestational age at diagnosis of PS was 33.4 (range, 20.0-36.5) weeks. Most cases corresponded to mild or moderate PS; only three fetuses had reversed flow in the ductus arteriosus before delivery. Six (37.5%) newborns, including all three with reversed flow in the ductus arteriosus prenatally, required postnatal pulmonary valvuloplasty. Fetuses with PS presented with larger and more globular hearts, with increased myocardial wall thickness in the third trimester. Despite preserved right ventricular (RV) ejection fraction and systolic longitudinal motion, PS cases showed increased right cardiac output and signs of diastolic dysfunction, with higher ductus venosus pulsatility index (0.72 ± 0.32 vs 0.53 ± 0.16, P = 0.004) and tricuspid E/E' ratio (7.52 ± 3.07 vs 5.76 ± 1.79, P = 0.022). In addition, fetuses with PS displayed a compensatory increase in left ventricular (LV) radial and longitudinal motion, as shown by a higher ejection fraction (79.3 ± 8.23% vs 67.6 ± 11.3%, P = 0.003) and mitral annular-plane systolic excursion (5.94 ± 1.38 vs 5.0 ± 1.22 mm, P = 0.035). Finally, fetuses requiring postnatal pulmonary valvuloplasty showed a different pattern of echocardiographic findings from those not requiring valvuloplasty, with a significantly smaller RV and pulmonary valve diameter, reduced tricuspid annular-plane systolic excursion (5.08 ± 1.59 vs 8.07 ± 1.93 mm, P = 0.028), increased LV cardiac output (340 ± 16 vs 176 ± 44 mL/min/kg, P = 0.003) and more pronounced signs of LV diastolic dysfunction (mitral E' velocity, 5.78 ± 0.90 vs 8.16 ± 1.58 cm/s, P = 0.008).
Fetuses with PS present with more hypertrophic, larger and more globular hearts in the third trimester of pregnancy, associated with a higher right cardiac output and impaired biventricular relaxation. In addition, signs of increased LV contraction were observed. Our data suggest that RV and LV functional parameters could be useful for predicting the need for postnatal pulmonary valvuloplasty. Copyright © 2017 ISUOG. Published by John Wiley & Sons Ltd.
确定单纯性肺动脉瓣狭窄(PS)胎儿心脏超声改变的模式,并将超声心动图结果与新生儿结局和出生后 12 个月内是否需要行肺动脉瓣成形术相关联。
这是一项前瞻性队列研究,纳入了 2009 年 1 月至 2015 年 10 月期间在巴塞罗那 BCNatal 胎儿心脏病学中心接受检查的 16 例单纯 PS 胎儿和 48 例匹配胎龄(超声检查±2 周)的对照组。所有病例均行标准胎儿超声心动图和全面的超声心动图检查,包括心血管形态学参数、收缩和舒张功能及时相测量。从临床记录中检索基线特征和围产期结局。随访病例直至 12 个月龄,观察入重症监护病房、住院天数、是否需要前列腺素和是否需要行出生后手术。根据是否需要行出生后肺动脉瓣成形术对 PS 胎儿进行分析。
两组在基线、胎儿超声和围产期特征方面相似。PS 的中位诊断孕周为 33.4 周(范围为 20.0-36.5 周)。大多数病例为轻度或中度 PS;仅 3 例胎儿在分娩前存在动脉导管内反流。6 例(37.5%)新生儿需要行出生后肺动脉瓣成形术,包括所有 3 例在产前存在动脉导管内反流的新生儿。PS 胎儿的心脏更大且呈球形,孕晚期心肌壁厚度增加。尽管右心室(RV)射血分数和收缩期纵向运动保留,但 PS 胎儿的右心输出量增加,舒张功能障碍的迹象更明显,表现为更高的静脉导管搏动指数(0.72±0.32 比 0.53±0.16,P=0.004)和三尖瓣 E/E'比值(7.52±3.07 比 5.76±1.79,P=0.022)。此外,PS 胎儿左心室(LV)径向和纵向运动代偿性增加,表现为射血分数更高(79.3±8.23%比 67.6±11.3%,P=0.003)和二尖瓣环平面收缩期位移更大(5.94±1.38 比 5.0±1.22 毫米,P=0.035)。最后,需要行出生后肺动脉瓣成形术的胎儿与不需要行瓣成形术的胎儿超声心动图表现不同,RV 和肺动脉瓣直径明显更小,三尖瓣环平面收缩期位移减少(5.08±1.59 比 8.07±1.93 毫米,P=0.028),LV 心输出量增加(340±16 比 176±44 毫升/分钟/千克,P=0.003),LV 舒张功能障碍的迹象更明显(二尖瓣 E'速度,5.78±0.90 比 8.16±1.58 厘米/秒,P=0.008)。
PS 胎儿在妊娠晚期心脏更大、更呈球形,与右心输出量增加和双心室舒张功能障碍有关。此外,还观察到 LV 收缩功能增强的迹象。我们的数据表明,RV 和 LV 功能参数可能有助于预测出生后是否需要行肺动脉瓣成形术。版权所有©2017 ISUOG。约翰威利父子公司出版。