Department of Medicine, Imaging, and Biomedical Sciences, Cedars-Sinai Heart Institute, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
J Cardiovasc Comput Tomogr. 2011 Sep-Oct;5(5):301-9. doi: 10.1016/j.jcct.2011.08.003. Epub 2011 Aug 7.
Coronary computed tomographic angiography (CTA) allows for noninvasive identification of anatomic coronary artery disease (CAD) severity but does not discriminate whether a stenosis causes ischemia. Computational fluid dynamic techniques applied to CTA images now permit noninvasive computation of fractional flow reserve (FFR), a measure of lesion-specific ischemia, but the diagnostic performance of computed FFR (FFR(CT)) as compared with measured FFR at the time of invasive coronary angiography remains unexplored.
We determined the diagnostic accuracy of noninvasive FFR(CT) for the detection and exclusion of ischemia-causing stenoses.
DeFACTO (NCT01233518) is a prospective, international, multicenter study of 238 patients designed to evaluate the diagnostic performance of FFR(CT) for the detection of hemodynamically significant coronary artery stenoses identified by CTA, compared with invasive FFR as a reference standard. FFR values ≤ 0.80 will be considered hemodynamically significant. Patients enrolled in the DeFACTO study will undergo CTA, invasive coronary angiography, and 3-vessel FFR in the left anterior descending artery, left circumflex artery, and right coronary artery distributions. FFR(CT) will be computed with acquired CTA images, without modification to CTA image acquisition protocols and without additional image acquisition. Blinded core laboratory interpretation will be performed for CTA, invasive coronary angiography, FFR, and FFR(CT).
The primary endpoint of the DeFACTO study is the per-patient diagnostic accuracy of FFR(CT) for noninvasive assessment of the hemodynamic significance of CAD, compared with FFR during invasive coronary angiography as a reference standard. The secondary endpoints include additional per-patient as well as per-vessel diagnostic performance characteristics, including sensitivity, specificity, positive predictive value, and negative predictive value.
The DeFACTO study will determine whether the addition of FFR(CT) to conventional CTA improves the diagnosis of hemodynamically significant CAD.
冠状动脉计算机断层血管造影术(CTA)可用于无创性识别解剖学冠状动脉疾病(CAD)严重程度,但无法区分狭窄是否引起缺血。现在,应用于 CTA 图像的计算流体动力学技术可实现狭窄病变特异性缺血的无创性计算,即血流储备分数(FFR),但 CTA 计算的 FFR(FFR(CT))与在有创冠状动脉造影时测量的 FFR 的诊断性能仍有待探索。
我们旨在确定无创 FFR(CT)检测和排除引起缺血的狭窄的诊断准确性。
DeFACTO(NCT01233518)是一项前瞻性、国际、多中心研究,共纳入 238 例患者,旨在评估 CTA 识别的血流动力学显著冠状动脉狭窄的 FFR(CT)检测性能,将 FFR(CT)与有创 FFR 作为参考标准进行比较。FFR 值≤0.80 将被视为血流动力学显著狭窄。入组 DeFACTO 研究的患者将接受 CTA、有创冠状动脉造影和左前降支、左回旋支和右冠状动脉分布的 3 支血管 FFR 检查。FFR(CT)将通过采集的 CTA 图像计算得出,无需修改 CTA 图像采集方案,也无需额外采集图像。将对 CTA、有创冠状动脉造影、FFR 和 FFR(CT)进行盲法核心实验室解读。
DeFACTO 研究的主要终点是与有创冠状动脉造影作为参考标准相比,FFR(CT)在评估 CAD 血流动力学意义方面的每例患者诊断准确性。次要终点包括其他每例患者和每支血管的诊断性能特征,包括敏感性、特异性、阳性预测值和阴性预测值。
DeFACTO 研究将确定在常规 CTA 基础上增加 FFR(CT)是否可改善血流动力学显著 CAD 的诊断。