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新生儿无右心室前向血流的 Ebstein 畸形的结局。

Outcomes of neonatal Ebstein's anomaly without right ventricular forward flow.

机构信息

Division of Pediatric Cardiology, Asan Medical Center, Seoul, South Korea.

Seoul Women's College of Nursing, Seoul, South Korea.

出版信息

J Thorac Cardiovasc Surg. 2016 Aug;152(2):516-21. doi: 10.1016/j.jtcvs.2016.03.084. Epub 2016 Apr 14.

Abstract

OBJECTIVE

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.

METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

目的

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。

方法

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。

结果

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)。

结论

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。

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