利用超快超声波对心肌灌注进行无创评估:先天性心脏病临床研究。

European heart journal. Imaging methods and practice Pub Date : 2025-01-16 eCollection Date: 2025-01-01 DOI:10.1093/ehjimp/qyaf007
Minh B Nguyen, Naiyuan Zhang, Luc L Mertens, David Barron, Osami Honjo, Maelys Venet, Jerome Baranger, Olivier Villemain
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引用次数: 0

摘要

目的:心肌灌注对危重型先天性心脏病(CCHD)手术修复后心功能的影响。心肌血容量在整个心动周期的时间变化评估可以作为灌注的替代指标。超快功率多普勒(UPD)是一种能够无创定量心肌血容量变化的超声成像技术。本研究的目的是证明围手术期经胸UPD评估的可行性,并确定UPD是否反映了心肌灌注的生理变化。方法和结果:前瞻性招募5例接受动脉转换手术(ASO)的新生儿大动脉转位(TGA), 5例接受1期姑息治疗(S1P)的左心发育不全综合征(HLHS),以及5例年龄/体重匹配的对照组。在手术前后进行经胸UPD采集。评估右/左心室节段性灌注(RV/LV)。对照组的心肌灌注模式在视觉上与已发表的人类两个心室的参考文献相似。ASO可改善左心室收缩/舒张心肌灌注差异(P = 0.03),但对左心室无影响(P = 0.99)。对于HLHS患者,S1P后左室(P = 0.16)和左室(P = 0.51)均无差异。结论:TGA患者心肌灌注谱似乎直接受到腔内压(直接驱动冠状动脉灌注压)的影响,即是全身心室还是肺下心室。我们的数据表明,UPD可以无创量化心肌灌注变化。冠心病患者血流动力学及手术状态对心肌灌注模式的影响。与临床结果的相关性有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Noninvasive assessment of myocardial perfusion using ultrafast ultrasound: clinical study for congenital heart disease.

Aims: Myocardial perfusion impacts cardiac function following surgical repair of critical congenital heart disease (CCHD). Temporal variation assessment of myocardial blood volume throughout the cardiac cycle can be a surrogate for perfusion. Ultrafast power Doppler (UPD) is an ultrasound imaging technique capable of noninvasively quantifying myocardial blood volume changes. The objective of this study is to demonstrate the feasibility of perioperative transthoracic UPD assessment and to determine if UPD reflects physiologic changes in myocardial perfusion.

Methods and results: Five neonatal transposition of the great arteries (TGA) undergoing arterial switch operation (ASO), five hypoplastic left heart syndrome (HLHS) undergoing Stage 1 palliation (S1P), and five age/weight-matched controls were prospectively recruited. Transthoracic UPD acquisitions were performed before/after operations. Segmental perfusion in right/left ventricles (RV/LV) was assessed. The controls' myocardial perfusion patterns are visually similar to published human references for both ventricles. Systolic/diastolic myocardial perfusion differences were modified by ASO in the RV (P = 0.03) but not for LV (P = 0.99). For HLHS patients, no difference after S1P was observed in either the RV (P = 0.16) nor the LV (P = 0.51).

Conclusion: For TGA patients, the perfusion profile of the myocardium seems to be directly influenced by the intracavitary pressure (directly driving coronary perfusion pressure), namely if it was the systemic or sub-pulmonary ventricle. Our data suggests that UPD could noninvasively quantify myocardial perfusion variation. Myocardial perfusion patterns change in CCHD according to their haemodynamic and surgical status. Correlation with clinical outcomes requires further study.

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