Danaila Vlad, Archer Oliver, Stefani Luke, Ferkh Aaisha, Khanna Shaun, Pathan Faraz, Brown Paula, Thomas Liza
Department of Cardiology, Westmead Hospital, Western Sydney Local Health District, Parramatta, NSW, Australia.
Westmead Clinical School, University of Sydney, Sydney, NSW, Australia.
Int J Cardiovasc Imaging. 2025 Sep 3. doi: 10.1007/s10554-025-03499-3.
Left atrial strain (LAS) is a valuable echocardiographic marker of left atrial function with growing clinical utility. However, variability in LAS measurements across software vendors remains a barrier to its routine clinical use. This study aimed to compare LAS measurements obtained using a dedicated left atrial-specific measurement tool (AFI-LA (General Electric (GE)) with those derived from established LV-based strain platforms: GE EchoPAC (mid-myocardial and endocardial tracking) and TomTec-Arena (feature tracking), used for measurement of LAS. LAS was measured in 112 subjects (72 individuals in sinus rhythm and 40 paroxysmal atrial fibrillation (PAF) patients in sinus rhythm at the time of transthoracic echocardiography). Reservoir (ƐR), contractile (ƐCT), and conduit (ƐCD) phasic strain were measured using AFI-LA and compared with GE-mid, GE-endo, and TomTec strain measurements. Agreement was assessed using Bland-Altman analysis and Pearson correlation. Inter- and intra-observer reproducibility was evaluated. AFI-LA measurements showed good correlation with both platforms (r ≥ 0.7, p < 0.001). AFI-LA consistently underestimated strain values across all phases compared to GE-mid, GE-endo, and TomTec, with the smallest bias observed against GE-mid. Proportional bias was present, particularly at higher strain values. Inter- and intra-observer reproducibility of AFI-LA measurements was high (r > 0.85). AFI-LA provides LAS measurements that are most comparable to GE mid-myocardial strain but demonstrates systematic underestimation compared to GE endocardial and TomTec-derived values. These differences underscore the need for vendor-specific calibration before AFI-LA can be used for serial assessments or applied using existing clinical threshold values. Larger validation studies are needed to support standardization and broader clinical adoption.
左心房应变(LAS)是一种评估左心房功能的有价值的超声心动图指标,其临床应用价值日益凸显。然而,不同软件供应商对LAS的测量结果存在差异,这仍是其在临床常规应用中的障碍。本研究旨在比较使用专用的左心房特异性测量工具(AFI-LA,通用电气(GE)公司)与基于左心室的既定应变平台(GE EchoPAC(心肌中层和心内膜追踪)和TomTec-Arena(特征追踪))测量LAS的结果。在112名受试者(经胸超声心动图检查时,72名窦性心律个体和40名阵发性心房颤动(PAF)患者处于窦性心律)中测量LAS。使用AFI-LA测量储存期(ƐR)、收缩期(ƐCT)和管道期(ƐCD)的相位应变,并与GE心肌中层、GE心内膜和TomTec应变测量结果进行比较。采用Bland-Altman分析和Pearson相关性评估一致性。评估了观察者间和观察者内的可重复性。AFI-LA测量结果与两个平台均显示出良好的相关性(r≥0.7,p<0.001)。与GE心肌中层、GE心内膜和TomTec相比,AFI-LA在所有阶段均持续低估应变值,与GE心肌中层相比偏差最小。存在比例偏差,尤其是在较高应变值时。AFI-LA测量的观察者间和观察者内可重复性较高(r>0.85)。AFI-LA提供的LAS测量结果与GE心肌中层应变最具可比性,但与GE心内膜和TomTec得出的值相比存在系统性低估。这些差异强调了在AFI-LA可用于连续评估或应用现有临床阈值之前,需要进行特定供应商的校准。需要更大规模的验证研究来支持标准化和更广泛的临床应用。