Gândara Maria Inês F, Efimov Igor R, Aras Kedar K
Department of Biomedical Engineering, NOVA University, 1099-085 Lisbon, Portugal.
Department of Biomedical Engineering, Northwestern University, Chicago, IL 60208, USA.
J Cardiovasc Dev Dis. 2024 Oct 12;11(10):322. doi: 10.3390/jcdd11100322.
The goal of this study was to identify the spatial resolution requirements for accurate rotor detection and localization in human right ventricular tachyarrhythmias. Poor spatial resolution is often cited as a reason for the inaccuracy of cardiac mapping catheters in detecting and localizing arrhythmia rotors. High-resolution (0.7 mm) arrhythmia data from optical recordings obtained from human donor hearts (n = 12) were uniformly downsampled to lower resolutions (1.4-7 mm) to approximate the spatial resolution (4 mm) of clinical mapping catheters. Rotors were tracked at various subresolutions and compared to the rotors in the original data by computing F1-scores to create accuracy profiles for both rotor detection and localization. Further comparisons were made according to arrhythmia type, donor sex, anatomical region, and mapped surface: endocardium or epicardium. For a spatial resolution of 4.2 mm, the accuracies of rotor detection and localization were 57% ± 4% and 61% ± 7%, respectively. Arrhythmia type affected the accuracy of rotor detection (monomorphic ventricular tachycardia, 58% ± 4%; ventricular fibrillation, 56% ± 8%) and localization (monomorphic ventricular tachycardia, 70% ± 4%; ventricular fibrillation, 54% ± 13%). However, donor sex, anatomical region (right ventricular outflow tract, mid, and apical), and mapped surface (epicardium and endocardium) did not significantly affect rotor detection or localization accuracy. To achieve rotor detection accuracy of 80%, a spatial resolution of 1.4 mm or better is needed. The accuracy profiles provided here serve as a guideline for future mapping device development.
本研究的目的是确定在人类右心室快速性心律失常中准确检测和定位转子所需的空间分辨率。空间分辨率差常被认为是心脏标测导管在检测和定位心律失常转子时不准确的原因。从人类供体心脏(n = 12)获得的光学记录中的高分辨率(0.7 mm)心律失常数据被均匀下采样到较低分辨率(1.4 - 7 mm),以近似临床标测导管的空间分辨率(4 mm)。在各种子分辨率下跟踪转子,并通过计算F1分数将其与原始数据中的转子进行比较,以创建转子检测和定位的准确性概况。根据心律失常类型、供体性别、解剖区域以及标测表面(心内膜或心外膜)进行了进一步比较。对于4.2 mm的空间分辨率,转子检测和定位的准确率分别为57% ± 4%和61% ± 7%。心律失常类型影响转子检测(单形性室性心动过速,58% ± 4%;心室颤动,56% ± 8%)和定位(单形性室性心动过速,70% ± 4%;心室颤动,54% ± 13%)的准确性。然而,供体性别、解剖区域(右心室流出道、中部和心尖部)以及标测表面(心外膜和心内膜)对转子检测或定位准确性没有显著影响。要实现80%的转子检测准确率,需要1.4 mm或更高的空间分辨率。此处提供的准确性概况可为未来标测设备的开发提供指导。