Division of Pediatric Cardiology, Asan Medical Center, Seoul, South Korea.
Seoul Women's College of Nursing, Seoul, South Korea.
J Thorac Cardiovasc Surg. 2016 Aug;152(2):516-21. doi: 10.1016/j.jtcvs.2016.03.084. Epub 2016 Apr 14.
In neonates with Ebstein's anomaly and absent right ventricular forward flow, pulmonary valve morphology is normal or abnormal. Although initial postnatal presentations of these 2 conditions are similar, clinical courses and therapeutic strategies for each category differ greatly.
Among 29 neonates with Ebstein's anomaly without right ventricular forward flow on initial postnatal echocardiography, 16 had a normal pulmonary valve and 13 had an abnormal pulmonary valve.
During the postnatal follow-up of the normal pulmonary valve group, right ventricular forward flow commenced approximately 10 days after birth (1-15 days). The ductus arteriosus was surgically ligated in 3 neonates to facilitate right ventricular forward flow. Biventricular or 1 1/2 ventricular physiology was eventually achieved in 14 patients in the normal pulmonary valve group (14/16, 88%) and 2 patients in the abnormal pulmonary valve group (2/13, 15.3%). With respect to the preoperative echocardiographic findings, the normal pulmonary valve group had a significantly larger pulmonary valve annulus (8.2 ± 1.4 mm in the normal pulmonary valve group and 6.4 ± 1.8 mm in the abnormal pulmonary valve group, P = .002) and smaller cardiothoracic ratio (0.79 ± 0.05 in the normal pulmonary valve group and 0.85 ± 0.07 in the abnormal pulmonary valve group, P = .03). Mild to moderate pulmonary regurgitation was present in all patients (16/16, 100%) in the normal pulmonary valve group, but 3 patients (3/13, 23%) in the abnormal pulmonary valve group also had pulmonary regurgitation. On logistic regression analysis, only pulmonary valve annulus size remained as an indicator of a normal pulmonary valve (P = .03).
In patients with Ebstein's anomaly and absent right ventricular forward flow, large pulmonary valve annulus size indicated a normal pulmonary valve. Patients with a normal pulmonary valve showed better survival and had a higher probability of achieving biventricular hemodynamics.
在患有埃布斯坦畸形且右心室无前向血流的新生儿中,肺动脉瓣形态正常或异常。尽管这两种情况的初始出生后表现相似,但每种类别的临床过程和治疗策略差异很大。
在 29 名最初超声心动图检查无右心室前向血流的埃布斯坦畸形新生儿中,16 名患儿肺动脉瓣正常,13 名患儿肺动脉瓣异常。
在正常肺动脉瓣组的出生后随访期间,右心室前向血流约在出生后 10 天开始(1-15 天)。3 名新生儿行动脉导管结扎术以促进右心室前向血流。在正常肺动脉瓣组中,14 名患者(14/16,88%)最终实现了双心室或 1 1/2 心室生理功能,2 名患者(2/13,15.3%)在异常肺动脉瓣组中实现了双心室或 1 1/2 心室生理功能。就术前超声心动图发现而言,正常肺动脉瓣组的肺动脉瓣环明显较大(正常肺动脉瓣组为 8.2±1.4mm,异常肺动脉瓣组为 6.4±1.8mm,P=0.002),心胸比更小(正常肺动脉瓣组为 0.79±0.05,异常肺动脉瓣组为 0.85±0.07,P=0.03)。正常肺动脉瓣组所有患者(16/16,100%)均有轻度至中度肺动脉瓣反流,但异常肺动脉瓣组 3 名患者(3/13,23%)也有肺动脉瓣反流。在逻辑回归分析中,只有肺动脉瓣环大小仍然是正常肺动脉瓣的指标(P=0.03)。
在患有埃布斯坦畸形且无右心室前向血流的患者中,较大的肺动脉瓣环大小提示肺动脉瓣正常。肺动脉瓣正常的患者存活率更高,更有可能实现双心室血流动力学。