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一种用于实时重建冠状动脉管腔轮廓的新型系统:临床前验证。

A novel system for the reconstruction of a coronary artery lumen profile in real time: a preclinical validation.

作者信息

Kassab Ghassan S, Choy Jenny S, Svendsen Mark, Sinha Anjan K, Alloosh Mouhamad, Sturek Mike, Huo Yunlong, Sandusky George E, Hermiller James

机构信息

Department of Biomedical Engineering, Indiana University-Purdue University Indianapolis (IUPUI), Indianapolis, IN 46202, USA.

出版信息

Am J Physiol Heart Circ Physiol. 2009 Jul;297(1):H485-92. doi: 10.1152/ajpheart.01224.2008. Epub 2009 May 22.

Abstract

Accurate sizing of vessel diameter is important for understanding the physiology of blood vessels as well as the treatment of coronary and peripheral artery disease. The objective of this study was to validate a novel catheter-based system [the LumenRECON (LR) system] for the real-time reconstruction of lumen cross-sectional area (CSA) along the length of a vessel segment. A total of 22 swine (20 Yorkshire and 2 atherosclerotic Ossabaw swine) were used to evaluate the accuracy, reproducibility, and safety of the system compared with intravascular ultrasound (IVUS). The CSA of the right coronary artery, left anterior descending coronary artery, and left circumflex artery were determined by IVUS and the LR system over a 3- to 4-cm segment in 12 Yorkshire and 2 atherosclerotic Ossabaw swine and 2 postmortem atherosclerotic human hearts. In eight chronic animals, the effect of the LR catheter on the vessel wall was evaluated at 1 day and 2 wk (4 animals each) after the intervention. A Bland-Altman plot of the LR and IVUS data showed a mean difference between the two measurements of 0.055 mm in diameter, which was not statistically significant from zero, indicating a lack of bias in the comparison of the LR system with IVUS. The root mean square error of the two measurements was 10.2% of the mean IVUS diameter. The repeatability of the LR system was assessed using duplicate measurements. The mean of the difference between the two measurements was nearly zero, and the repeatability coefficient was within 4.5% of the mean of the two measurements. No injury or intimal hyperplasia was found acutely or chronically after the use of the LR system. This study establishes the accuracy, reproducibility, and safety of a nonimaging 2.7-Fr catheter for lumen sizing of coronary arteries. The system provides a continuous quantitative axial profile of the mean vessel lumen in real time and may have significant utility in vascular research and clinically in the catheterization laboratory.

摘要

准确测量血管直径对于理解血管生理学以及治疗冠状动脉和外周动脉疾病至关重要。本研究的目的是验证一种基于导管的新型系统[LumenRECON(LR)系统],用于沿血管段长度实时重建管腔横截面积(CSA)。总共使用了22头猪(20头约克夏猪和2头动脉粥样硬化奥萨巴猪)来评估该系统与血管内超声(IVUS)相比的准确性、可重复性和安全性。在12头约克夏猪、2头动脉粥样硬化奥萨巴猪和2个死后动脉粥样硬化人类心脏中,通过IVUS和LR系统在3至4厘米的节段上测定右冠状动脉、左前降支冠状动脉和左旋支动脉的CSA。在八只慢性动物中,在干预后1天和2周(每组4只动物)评估LR导管对血管壁的影响。LR和IVUS数据的布兰德-奥特曼图显示,两次测量的平均直径差异为0.055毫米,与零无统计学显著差异,表明LR系统与IVUS比较时无偏差。两次测量的均方根误差为IVUS平均直径的10.2%。使用重复测量评估LR系统的可重复性。两次测量之间差异的平均值几乎为零,可重复性系数在两次测量平均值的4.5%以内。使用LR系统后,未发现急性或慢性损伤或内膜增生。本研究确定了一种用于冠状动脉管腔测量的非成像2.7F导管的准确性、可重复性和安全性。该系统实时提供平均血管腔的连续定量轴向轮廓,在血管研究和导管实验室临床中可能具有重要用途。

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