Feasibility of Continuous Ventricular Volumetric Quantification in Arrhythmias using Real-Time 3D CMR-MOTUS.

IF 5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Thomas Edi Olausson, Maarten Lennart Terpstra, Rizwan Ahmad, Edwin Versteeg, Casper Beijst, Yuchi Han, Marco Guglielmo, Birgitta Katinka Velthuis, Cornelis van den Berg, Alessandro Sbrizzi
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引用次数: 0

Abstract

Background: Conventional cardiovascular magnetic resonance (CMR) cine sequences rely on binning reconstructions that average multiple heartbeats, an assumption that breaks down in arrhythmic patients where beat-to-beat variations lead to motion artifacts and loss of clinically relevant functional information. While two-dimensional (2D) real-time imaging can capture individual heartbeats, a stack of 2D slices is sub-optimal to map the full complexity of incoherent cardiac dynamics during arrhythmia. We investigated the feasibility of three-dimensional (3D) real-time motion field reconstruction for continuous beat-to-beat volumetric quantification in patients with premature ventricular contractions (PVC) using a free-running CMR protocol.

Methods: We extended CMR-MOTUS to jointly reconstruct real-time 3D motion fields and a motion-corrected reference image from continuously acquired data without breath-holds or electrocardiogram (ECG) gating. A variable-density Cartesian sampling trajectory (OPRA) was used with a 3D spoiled gradient echo or balanced steady-state free precession sequence. The real-time volumetric beat-to-beat changes were quantified by propagating a single manual segmentation on the reference image, through all time frames using the reconstructed motion fields. The method was evaluated on a cardiac motion phantom with ground-truth static acquisitions and in 10 healthy volunteers and 10 patients with PVC. All in vivo datasets were acquired post contrast enhancement. The ejection fraction (EF) was compared to ground-truth values for the phantom and to standard 2D real-time cine EF measurement techniques for the in vivo subjects.

Results: Reconstructed mean EF values of the phantom experiment were close to the ground-truth (Mean EF = 17.86 ± 0.33% versus 17.27%). In healthy volunteers, narrow beat-to-beat EF distributions reflected normal physiological consistency. In PVC patients, the method revealed broader, sometimes bimodal EF distributions. Simultaneously acquired ECG signals supported the temporal correspondence between volume irregularities and PVC episodes.

Conclusions: 3D real-time joint motion field and image reconstruction from a free-running CMR protocol enables continuous beat-to-beat volumetric quantification in arrhythmic patients, revealing functional heterogeneity that conventional single-beat and averaging measurements (binning and gating) can obscure. Larger studies are needed before claims of clinical validation or replacement of standard 2D cine analysis.

实时三维CMR-MOTUS连续心室容量定量治疗心律失常的可行性。
背景:传统的心血管磁共振(CMR)电影序列依赖于平均多次心跳的分频重建,这种假设在心律失常患者中失效,因为心跳变化导致运动伪影和临床相关功能信息的丢失。虽然二维(2D)实时成像可以捕获单个心跳,但一叠二维切片对于绘制心律失常期间不连贯心脏动力学的全部复杂性是次优的。我们研究了三维(3D)实时运动场重建在室性早搏(PVC)患者中使用自由运行CMR方案进行连续搏动体积量化的可行性。方法:我们扩展了CMR-MOTUS,在没有屏气或心电图门控的情况下,从连续采集的数据中共同重建实时三维运动场和运动校正的参考图像。变密度笛卡尔采样轨迹(OPRA)采用三维渐变回波或平衡稳态自由进动序列。通过在参考图像上传播单个手动分割,利用重建的运动场在所有时间帧上量化实时体积拍对拍的变化。该方法在心脏运动假体、10名健康志愿者和10名PVC患者中进行了评估。所有体内数据集都是在对比度增强后获得的。将射血分数(EF)与假体的真值和体内受试者的标准2D实时电影射血分数测量技术进行比较。结果:幻像实验重建的平均EF值接近真实值(平均EF = 17.86±0.33% vs . 17.27%)。在健康志愿者中,较窄的搏动EF分布反映了正常的生理一致性。在PVC患者中,该方法显示更宽的EF分布,有时为双峰分布。同时获得的心电信号支持容量不规则和聚氯乙烯发作之间的时间对应。结论:自由运行CMR方案的三维实时关节运动场和图像重建可以对心律失常患者进行连续的搏动体积量化,揭示常规单拍和平均测量(分频和门控)可能掩盖的功能异质性。在要求临床验证或替代标准2D电影分析之前,需要进行更大规模的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.90
自引率
12.50%
发文量
61
审稿时长
6-12 weeks
期刊介绍: Journal of Cardiovascular Magnetic Resonance (JCMR) publishes high-quality articles on all aspects of basic, translational and clinical research on the design, development, manufacture, and evaluation of cardiovascular magnetic resonance (CMR) methods applied to the cardiovascular system. Topical areas include, but are not limited to: New applications of magnetic resonance to improve the diagnostic strategies, risk stratification, characterization and management of diseases affecting the cardiovascular system. New methods to enhance or accelerate image acquisition and data analysis. Results of multicenter, or larger single-center studies that provide insight into the utility of CMR. Basic biological perceptions derived by CMR methods.
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