Zhou Shijie, AbdelWahab Amir, Wang Raymond, Dang Huan, Warren James W, Sapp John L
Department of Chemical, Paper, and Biomedical Engineering, College of Engineering and Computing, Miami University, Oxford, Ohio, USA; Department of Electrical and Computer Engineering, College of Engineering and Computing, Miami University, Oxford, Ohio, USA.
Cardiology Division, Department of Medicine, Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada.
Can J Cardiol. 2023 Oct;39(10):1410-1416. doi: 10.1016/j.cjca.2023.05.016. Epub 2023 Jun 1.
We previously developed an automated approach based on pace mapping to localise early left ventricular (LV) activation origin. To avoid a singular system, we require pacing from at least 2 more known sites than the number of electrocardiography (ECG) leads used. Fewer leads used means fewer pacing sites required. We sought to identify an optimal minimal ECG lead set for the automated approach.
We used 1715 LV endocardial pacing sites to create derivation and testing data sets. The derivation data set, consisting of 1012 known pacing sites pooled from 38 patients, was used to identify an optimal 3-lead set by means of random forest regression (RFR), and a second 3-lead set by means of exhaustive search. The performance of these sets and the calculated Frank leads was compared within the testing data set with 703 pacing sites pooled from 25 patients.
The RFR yielded III, V1, and V4, whereas the exhaustive search identified leads II, V2 and V6. Comparison of these sets and the calculated Frank leads demonstrated similar performance when using 5 or more known pacing sites. Accuracy improved with additional pacing sites, achieving mean accuracy of < 5 mm, after including up to 9 pacing sites when they were focused on a suspected area of ventricular activation origin (radius < 10 mm).
The RFR identified the quasi-orthogonal leads set to localise the source of LV activation, minimizing the training set of pacing sites. Localization accuracy was high with the use of these leads and was not significantly different from using leads identified by exhaustive search or empiric use of Frank leads.
我们先前开发了一种基于起搏标测的自动化方法来定位左心室(LV)早期激动起源。为避免单一系统,我们要求起搏的已知部位比所用电心电图(ECG)导联数至少多2个。使用的导联越少意味着所需的起搏部位越少。我们试图确定该自动化方法的最佳最小ECG导联组。
我们使用1715个LV心内膜起搏部位创建推导和测试数据集。推导数据集由从38例患者中汇总的1012个已知起搏部位组成,用于通过随机森林回归(RFR)识别最佳3导联组,并通过穷举搜索识别第二个3导联组。在测试数据集中,将这些导联组和计算出的Frank导联的性能与从25例患者中汇总的703个起搏部位进行比较。
RFR得出III、V1和V4导联,而穷举搜索识别出II、V2和V6导联。当使用5个或更多已知起搏部位时,对这些导联组和计算出的Frank导联进行比较,结果显示性能相似。随着起搏部位的增加,准确性提高,当聚焦于心室激动起源的可疑区域(半径<10 mm)并纳入多达9个起搏部位后,平均准确性达到<5 mm。
RFR识别出准正交导联组以定位LV激动源,使起搏部位的训练集最小化。使用这些导联时定位准确性很高,与使用通过穷举搜索识别的导联或凭经验使用Frank导联相比无显著差异。