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胎儿左心室心肌致密化不全的超声心动图诊断及预后

Echocardiographic diagnosis and prognosis of fetal left ventricular noncompaction.

机构信息

Lucile Packard Children's Hospital, Stanford University Medical Center, Division of Pediatric Cardiology, Palo Alto, California 94304, USA.

出版信息

J Am Soc Echocardiogr. 2012 Jan;25(1):112-20. doi: 10.1016/j.echo.2011.09.019. Epub 2011 Oct 19.

Abstract

BACKGROUND

Left ventricular noncompaction (LVNC) has rarely been described in the fetus.

METHODS

The presence of associated congenital heart disease and rhythm disturbance was identified and the presence of heart failure was assessed using the cardiovascular profile score in all fetuses with LVNC presenting from January 1999 to July 2010. The left ventricle was divided into 12 segments-four segments each at the base, midpapillary, and apical regions-in the short-axis view to calculate the noncompaction/compaction ratio for each segment.

RESULTS

Of 24 fetuses with LVNC included in the study, 22 had significant congenital heart disease, and 15 had complete heart block. Of the 16 patients with adequate follow-up and not electively terminated, 12 (81%) died or progressed to heart transplantation. The average noncompaction/compaction ratios were 2.02 in patients who died or underwent heart transplantation and 1.67 in survivors (P = .2034). Fifty-seven of 93 measured segments (61%) of the left ventricle in the patients who died or underwent heart transplantation had noncompaction/compaction ratios ≥ 2 compared with five of 17 measured segments (29%) in survivors (P = .0837). The average cardiovascular profile score was 6. The apical region had greater involvement of noncompaction than the midpapillary and basal regions, with ratios of 2.27, 2.14, and 1.10, respectively (P = .00035).

CONCLUSIONS

Fetuses with LVNC have a poor prognosis that may be related to associated congenital heart disease, increased segmental involvement of noncompaction, and complete heart block and can be predicted by the cardiovascular profile score.

摘要

背景

左心室心肌致密化不全(LVNC)在胎儿中很少被描述。

方法

在 1999 年 1 月至 2010 年 7 月期间,对所有出现 LVNC 的胎儿,通过心血管特征评分来确定是否存在先天性心脏病和节律紊乱,并评估心力衰竭的存在。在短轴视图中,将左心室分为 12 个节段-基底、乳头肌中和心尖区各 4 个节段-以计算每个节段的非致密化/致密化比值。

结果

在纳入研究的 24 例 LVNC 胎儿中,22 例存在严重先天性心脏病,15 例存在完全性心脏阻滞。在 16 例有足够随访且未选择性终止妊娠的患者中,12 例(81%)死亡或进展为心脏移植。死亡或接受心脏移植的患者中非致密化/致密化比值的平均值为 2.02,而幸存者的平均值为 1.67(P=.2034)。在死亡或接受心脏移植的患者中,57 个(61%)测量的左心室节段中非致密化/致密化比值≥2,而幸存者中 17 个(29%)测量的节段中非致密化/致密化比值≥2(P=.0837)。平均心血管特征评分为 6 分。心尖区的非致密化比乳头肌和基底区更严重,比值分别为 2.27、2.14 和 1.10(P=.00035)。

结论

LVNC 胎儿的预后较差,可能与相关的先天性心脏病、非致密化节段受累增加和完全性心脏阻滞有关,可通过心血管特征评分预测。

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