How low can we go? The effect of acquisition duration on cardiac volume and function measurements in free-running cardiac and respiratory motion-resolved 5D whole-heart cine MRI at 1.5T.

IF 4.2 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Robert J Holtackers, Augustin C Ogier, Ludovica Romanin, Estelle Tenisch, Isabel Montón Quesada, Ruud B van Heeswijk, Christopher W Roy, Jérôme Yerly, Milan Prsa, Matthias Stuber
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引用次数: 0

Abstract

Introduction: Cardiovascular magnetic resonance (CMR) is the gold standard for assessing cardiac volumes and function using 2D breath-held cine imaging. This technique, however, requires a reliable ECG signal, repetitive breath-holds, and the time-consuming and proficiency-demanding planning of cardiac views. Recently, a free-running framework has been developed for cardiac and respiratory motion-resolved 5D whole-heart imaging without the need for an ECG signal, repetitive breath-holds, and meticulous plan scanning. In this study, we investigate the impact of acquisition time on cardiac volumetric and functional measurements, when using free-running imaging, compared to reference standard 2D cine imaging.

Methods: Sixteen healthy adult volunteers underwent CMR at 1.5T, including standard 2D breath-held cine imaging and free-running imaging using acquisition durations ranging from 1 to 6min in randomized order. All datasets were anonymized and analysed for left-ventricular end-systolic and end-diastolic volumes, as well as ejection fraction. In a subset of data, intra- and inter-observer agreement was assessed. In addition, image quality and observer confidence were scored using a 4-point Likert scale. Finally, acquisition efficiency was reported for both imaging techniques, which was defined as the time required for data sampling divided by the total scan time.

Results: No significant differences in left-ventricular EDV and ESV were found between free-running imaging for 1, 2, 3, 5, and 6minutes and standard 2D breath-held cine imaging. Biases in EDV ranged from -2.4 to -7.4mL, while biases in ESV ranged from -3.8 to 2.1mL. No significant differences in ejection fraction were found between free-running imaging of any acquisition duration and standard 2D breath-held cine imaging. Biases in ejection fraction ranged from -2.8% to 0.94%. Both image quality and observer confidence in free-running imaging improved when the acquisition duration increased. However, they were always lower than standard 2D breath-held cine imaging. Acquisition efficiency improved from 13% for standard 2D cine imaging to 50% or higher for free-running imaging.

Discussion: Free-running CMR with an acquisition duration as short as one minute can provide left-ventricular cardiac volumes and ejection fraction comparable to standard 2D breath-held cine imaging, albeit at the expense of both image quality and observer confidence.

我们能降到多低?获取持续时间对1.5T自由运行心脏和呼吸运动分辨率5D全心MRI心脏容量和功能测量的影响。
简介:心血管磁共振(CMR)是使用2D屏气电影成像评估心脏容量和功能的金标准。然而,这项技术需要可靠的心电图信号,反复屏气,以及耗时且要求熟练的心脏视图规划。最近,一种自由运行的框架被开发出来,用于心脏和呼吸运动分辨率的5D全心成像,而不需要ECG信号、重复屏气和细致的计划扫描。在这项研究中,我们研究了在使用自由运行成像时,与参考标准2D电影成像相比,采集时间对心脏容量和功能测量的影响。方法:16名健康成年志愿者在1.5T时进行CMR,包括标准的2D屏气电影成像和自由运行成像,采集时间随机顺序为1 ~ 6min。所有数据集匿名化并分析左心室收缩末期和舒张末期容积以及射血分数。在数据子集中,评估了观察员内部和观察员之间的一致性。此外,使用4点李克特量表对图像质量和观察者信心进行评分。最后,报告了两种成像技术的采集效率,其定义为数据采样所需的时间除以总扫描时间。结果:自由奔跑1、2、3、5、6分钟左室EDV和ESV与标准2D屏气电影成像无显著差异。EDV的偏倚范围为-2.4至-7.4mL,而ESV的偏倚范围为-3.8至2.1mL。在任意采集时间的自由奔跑成像和标准的2D屏气电影成像之间,射血分数没有显著差异。射血分数偏差范围为-2.8% ~ 0.94%。随采集时间的增加,图像质量和观察者对自由运行成像的信心都有所提高。然而,它们总是低于标准的2D屏气电影成像。采集效率从标准2D电影成像的13%提高到自由运行成像的50%或更高。讨论:自由运行的CMR采集时间短至1分钟,可以提供与标准2D屏气电影成像相当的左心室心脏容量和射血分数,尽管以牺牲图像质量和观察者信心为代价。
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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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