FREE BREATHING 3D CARDIAC MRI
FREE BREATHING 3D CARDIAC MRI
批准号:
7360391
负责人:
Bruno Madore
金额:
$1.34万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-08-01 至 2007-07-31
中文摘要
这个子项目是利用由NIH/NCRR资助的中心拨款提供的资源的许多研究子项目之一。子项目和调查员(PI)可能从另一个NIH来源获得了主要资金,因此可能会出现在其他CRISE条目中。列出的机构是针对中心的,而不一定是针对调查员的机构。在心脏MRI的应用中,冻结或解决心脏和呼吸运动的需要是一个困难的挑战。我们提出了一种新的方法来检测和纠正复杂的呼吸诱导的心脏运动,同时捕获其跳动的运动。将开发一种呼吸补偿的3D心脏成像方法,并与我们目前的临床室壁运动方案进行比较,测试其评估心肌运动的能力。具体目标是:1.开发和实施一种非常快速的3D成像策略。并行成像、展开方法和部分傅立叶成像的算法将被融合,由此产生的混合方法将在3D稳态自由进动(SSFP)成像序列上实现。2.开发、实施和评估针对特定目标开发的快速成像方法的进一步补充1.将研究抑制脂肪信号、进一步抑制潜在伪影和提高空间/时间分辨率的新策略。由此产生的快速成像方法将用于生成时间序列的3D心脏图像,其时间分辨率足以解析呼吸周期(S每1到1.5帧)。3.开发一种在第一步中检测/校正呼吸运动,并在第二步中产生心相图像的方法。心脏呼吸运动的检测将以两种互补的方式进行:传统的呼吸监测可伸展带将提供非常高时间分辨率的(非定量)信息,而在特定目标1和2中开发的3D成像方案将提供丰富的空间/几何定量运动相关信息。将这两个来源的知识结合起来,可以检测到心脏在空间/时间上复杂的呼吸运动,并对其进行校正。在第二步中,经过呼吸校正的数据将从时间序列转换为高质量3D图像的心脏时相序列。4.与我们机构目前使用的方案相比,评估该方法在捕获心肌运动任务中的性能,这是当前最先进的代表性实例。目的是验证我们的方法提供的信噪比、空间分辨率(包括空间模糊)和诊断价值优于当前协议的假设。将对志愿者和患者进行体模实验、模拟和成像。对这些结果的评估将包括客观标准(定量测量)和主观标准(临床医生对图像质量的印象)。
英文摘要
This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. In cardiac MRI applications, the need to freeze or resolve both cardiac and respiratory motion poses a difficult challenge. We propose a novel approach to detect and correct for the complex respiration-induced motion of the heart, while capturing its beating motion. A respiration compensated, 3D cardiac imaging method will be developed and tested in its ability to evaluate myocardium motion, as compared to our current clinical wall-motion protocol. The specific aims are: 1. To develop and implement a very fast 3D imaging strategy. The algorithms for parallel imaging, for our UNFOLD method and for partial-Fourier imaging will be fused, and the resulting hybrid method will be implemented on a 3D steady-state free-precession (SSFP) imaging sequence. 2. To develop, implement and evaluate further additions to the fast imaging approach developed in Specific Aim 1. Novel strategies will be investigated to suppress fat signal, further suppress potential artifacts and improve spatial/temporal resolution. The resulting fast imaging method will be used to generate time series of 3D cardiac images with temporal resolution sufficient to resolve the respiratory cycle (one frame every 1 to 1.5 s). 3. To develop a method for detecting/correcting respiratory motion in a first step, and generating cardiac-phase images in a second step. The heart respiratory motion will be detected in two complementary ways: A conventional respiration monitoring stretchable belt will provide (non-quantitative) information with very high temporal resolution, while the 3D imaging scheme developed in Specific Aims 1 and 2 will provide a wealth of spatial/geometrical quantitative motionrelated information. Combining the knowledge from these two sources will allow the spatially/temporally complex respiratory-motion of the heart to be detected and correct for. In a second step, the respiration-corrected data will be converted from a time series to a cardiac-phase series of high quality 3D images. 4. To evaluate the method's performance in the task of capturing myocardium motion as compared to the protocol currently in use at our institution, a representative example of the current state-of-the-art. The goal is to verify the hypothesis that our method provides SNR, spatial resolution (which includes spatial blurring) and diagnostic value superior to those of the current protocol. Phantom experiments, simulations and imaging of volunteers and patients will be performed. The evaluation of these results will involve both objective criteria (quantitative measurements) as well as subjective criteria (clinicians' impressions on image quality).
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