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主动脉缩窄修复术后新生儿心肌变形持续降低。

Persistent reduced myocardial deformation in neonates after CoA repair.

作者信息

Jashari Haki, Lannering Katarina, Ibrahimi Pranvera, Djekic Demir, Mellander Mats, Rydberg Annika, Henein Michael Y

机构信息

Department of Public Health and Clinical Medicine, Umeå University, Sweden.

Department of Pediatric Cardiology, Queen Silvia Children's Hospital at the Sahlgrenska University Hospital, Götenborg, Sweden.

出版信息

Int J Cardiol. 2016 Oct 15;221:886-91. doi: 10.1016/j.ijcard.2016.07.114. Epub 2016 Jul 9.

Abstract

INTRODUCTION

Surgical repair of coarctation of the aorta (CoA) is a safe procedure in children, however the condition is known for its potential recurrence and other related complications. The available evidence shows abnormal intrinsic properties of the aorta in CoA, thus suggesting additional effect, even after CoA repair, on left ventricular (LV) function. Accordingly, we sought to obtain a better understanding of LV myocardial mechanics in very early-corrected CoA using two-dimensional STE.

METHODS AND RESULTS

We retrospectively studied 21 patients with corrected CoA at a median age of 9 (2-53) days at three time points: 1) just before intervention, 2) at short-term follow-up and 3) at medium-term follow-up after intervention and compared them with normal values. Speckle tracking analysis was conducted via vendor independent software, Tomtec. After intervention, LV function significantly improved (from -12.8±3.9 to -16.7±1.7; p<0.001), however normal values were not reached even at medium term follow-up (-18.3±1.7 vs. -20±1.6; p=0.002). Medium term longitudinal strain correlated with pre intervention EF (r=0.58, p=0.006). Moreover, medium term subnormal values were more frequently associated with bicuspid aortic valve (33.3% vs. 66.6%; p<0.05).

CONCLUSION

LV myocardial function in neonates with CoA can be feasibly evaluated and followed up by speckle tracking echocardiography. LV subendocardial dysfunction however, remains in early infancy coarctation long after repair. Long-term follow-up through adulthood using myocardial deformation measurements should shed light on the natural history and consequences of this anomaly.

摘要

引言

主动脉缩窄(CoA)的外科修复在儿童中是一种安全的手术,但该病症因具有潜在复发及其他相关并发症而为人所知。现有证据表明CoA患者 aorta的内在特性异常,这表明即使在CoA修复后,对左心室(LV)功能仍有额外影响。因此,我们试图通过二维STE更好地了解早期矫正CoA患者的左室心肌力学。

方法与结果

我们回顾性研究了21例CoA矫正患者,这些患者的中位年龄为9(2 - 53)天,研究分三个时间点进行:1)干预前,2)短期随访时,3)干预后中期随访时,并将其与正常值进行比较。通过独立于供应商的软件Tomtec进行斑点追踪分析。干预后,左室功能显著改善(从 -12.8±3.9提升至 -16.7±1.7;p<0.001),但即使在中期随访时仍未达到正常值(-18.3±1.7 vs. -20±1.6;p = 0.002)。中期纵向应变与干预前的EF相关(r = 0.58,p = 0.006)。此外,中期低于正常的值更常与二叶式主动脉瓣相关(33.3% vs. 66.6%;p<0.05)。

结论

CoA新生儿的左室心肌功能可通过斑点追踪超声心动图进行可行的评估和随访。然而,左室心内膜下功能障碍在修复后很长时间内仍存在于婴儿早期CoA患者中。使用心肌变形测量对成年期进行长期随访应有助于阐明这种异常的自然病史和后果。

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