瞬时无波比联合配准与定量冠状动脉造影对弥漫性病变冠状动脉的评估

M. E. Hasan, M. El Emary,  A A Abd El Mageed,  H Fayed, M. Maher, A. Nammour, M. Ali
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引用次数: 0

摘要

目的:冠脉生理评估已成为导管实验室指导经皮冠状动脉介入治疗(PCI)的常规方法。目前,大多数生理评估都是以二元方式进行的,以确定血管是否需要干预。尽管研究报道了生理评估在减少需要治疗的血管数量方面具有很高的诊断效率,但人们普遍认为,在充血条件下存在串联病变或弥漫性疾病时对个别狭窄的检查使PCI计划变得复杂且不太实用。本研究的目的是通过连续瞬时无波比(iFR)共配准测量来评估压力导丝对冠状动脉病变的严重程度,并将冠状动脉造影和定量冠状动脉分析(QCA)进行比较,旨在减少手术次数,减少支架使用的数量和长度。方法:这项非随机对照试验于2020年2月至2022年9月在Benha大学国立心脏研究所(NHI)心内科进行。该研究包括一组30名患有弥漫性冠状动脉疾病并接受选择性PCI治疗的患者。研究发现:研究人群的危险因素分布为:HTN占54%,糖尿病占60%,血脂异常占64%,吸烟占57%。使用QCA评估的预期支架长度中位数为40.2 mm,标准差(SD) (8mm)高于iFR联合登记实际部署的检测结果。IFR共配使用的支架平均长度为20.2 mm (SD: 11.2 mm), p值为0.0000。此外,所有患者都需要通过QCA进行支架植入,而实际上只有86%的患者需要通过iFR联合注册评估进行支架植入,这导致每位患者放置的支架较少。差异有统计学意义p<0.0022。本研究表明,在静息条件下进行的iFR共配准可以高度准确地预测PCI的生理结果。与QCA相比,iFR共配准显著减少了血流动力学上重要的血流重建病变的数量和长度。建议:iFR联合登记应在静息条件下进行,以高度准确地预测PCI的生理结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of Diffusely Diseased Coronary Artery by Instantaneous Wave-Free Ratio Co-Registration versus Quantitative Coronary Angiography
Purpose: Coronary physiological assessment is now routinely applied in the catheter laboratory to guide percutaneous coronary intervention (PCI). Currently most physiological assessment is performed in a binary manner to determine whether a vessel requires intervention. Although studies have reported the high diagnostic efficiency of physiological assessment in minimizing the number of vessels requiring treatment, it is widely recognized that interrogation of individual stenosis in the presence of tandem lesions or diffuse disease under hyperemic conditions makes PCI planning complex and less practical. The aim of this study was to perform assessment of severity of coronary lesions of a pressure guide wire with continuous instantaneous wave-free ratio (iFR) co-registration measurement compared coronary angiography and quantitative coronary analysis (QCA) aiming to minimize the procedure, decrease number and length of stents used. Methodology: This non randomized controlled trial was conducted at Cardiology Department, Benha University, National Heart Institute (NHI) from February 2020 to September 2022. The study included a group of 30 patients presented with diffuse coronary artery disease and undergoing elective PCI. Findings: The study found out that the distribution of risk factors among studied groups was HTN representing 54%, regarding DM 60%, concerning dyslipidemia 64% and smokers represented 57%. The median of expected length of stent using QCA assessment was 40.2 mm with standard deviation (SD) (8mm) higher than detected actually deployed by iFR co-registration. The mean length of stents used by IFR co-registration was 20.2 mm stents (SD: 11.2 mm) and P-value was 0.0000.  Also, all patients needed stent via QCA while only 86% actually need stent application via iFR co-registration assessment, leading to a fewer stents placed per patient. The difference was statistically significant p<0.0022. This study demonstrates that iFR co-registration performed under resting conditions predicted the physiological outcome of PCI with a high degree of accuracy.  Compared with QCA, iFR co-registration significantly decreased the number and length of hemodynamically significant lesions identified for revascularization. iFR co-registration should be performed under resting Recommendation: iFR co-registration should be performed under resting conditions to predict the physiological outcome of PCI with a high degree of accuracy.
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