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在非电生理实验室中,使用新型改良三导联起搏系统分析仪心电图技术简化左束支区域起搏。

Simplification of left bundle branch area pacing using a novel modified 3-lead pacing system analyzer electrocardiogram technique in the non-electrophysiology laboratory.

作者信息

Canpolat Ugur, Dogan Mert, Aytemir Kudret

机构信息

Cardiac Pacing Unit, Department of Cardiology, Faculty of Medicine, Hacettepe University, Altindag, 06100, Ankara, Turkey.

出版信息

J Interv Card Electrophysiol. 2025 May 2. doi: 10.1007/s10840-025-02057-0.

Abstract

BACKGROUND

An electrophysiology (EP) recording system is recommended throughout the left bundle branch area pacing (LBBaP) procedure. However, the requirement of an EP recording system limits the wide adoption of LBBaP in non-EP laboratory settings. Thus, in this study, we proposed a novel set-up in non-EP laboratories using manufacturer pacing system analyzer (PSA)-derived electrogram guidance and fluoroscopy of the angiography system for LBBaP.

METHODS

Our study prospectively enrolled consecutive patients who underwent LBBaP for bradyarrhythmia indications. LBBaP was performed using a stylet-driven lead (SDL) delivered through a dedicated delivery sheath. Procedural characteristics were recorded at the implant. The agreement of measurements on the modified 3-lead ECG of PSA and standard 12-lead ECG was analyzed.

RESULTS

A total of 83 patients were enrolled (mean age 65.4 ± 11.8 years, 55.4% male). The LBBaP with an SDL was successful for all patients. The pacing response was observed as LBBP in 69.9% of cases, while 30.1% were classified as left ventricular septal pacing. The mean paced QRS duration (pQRSd) and the stimulus to left ventricular activation time (LVAT) were measured at 117.6 ± 11.4 ms and 68 ± 17 ms using a modified 3-lead ECG of PSA, compared to 118.5 ± 11.8 ms and 70 ± 13 ms using the standard 12-lead ECG, with agreements of 0.89 and 0.93, respectively. SDL-LBBaP resulted in low unipolar and bipolar pacing thresholds (0.7 ± 0.2 V at 0.4 ms and 0.8 ± 0.2 V at 0.4 ms), which remained stable at a median 12-month follow-up (p > 0.05). An atrial lead revision was needed for one (1.2%) patient during the first-month visit. Acute interventricular septal perforation occurred in two (2.4%) patients as a specific complication of LBBaP.

CONCLUSION

Our novel setting in non-EP laboratories, utilizing fluoroscopy from the angiography system and manufacturer-modified 3-lead ECG and EGM of PSA during LBBaP, is feasible, reliable, and widely available. LBB capture was confirmed by both the standard EP recording system and new modified PSA 3-lead ECG measurements, which showed good agreement. Further large-scale data is needed to validate our findings.

摘要

背景

在整个左束支区域起搏(LBBaP)过程中推荐使用电生理(EP)记录系统。然而,EP记录系统的需求限制了LBBaP在非EP实验室环境中的广泛应用。因此,在本研究中,我们提出了一种在非EP实验室中使用制造商起搏系统分析仪(PSA)衍生的电图引导和血管造影系统荧光透视进行LBBaP的新设置。

方法

我们的研究前瞻性纳入了因缓慢性心律失常适应症接受LBBaP的连续患者。使用通过专用输送鞘管递送的探针驱动导线(SDL)进行LBBaP。在植入时记录手术特征。分析了PSA改良3导联心电图和标准12导联心电图测量结果的一致性。

结果

共纳入83例患者(平均年龄65.4±11.8岁,男性占55.4%)。所有患者使用SDL进行LBBaP均成功。69.9%的病例起搏反应观察为左束支起搏,而30.1%被归类为左心室间隔起搏。使用PSA改良3导联心电图测量的平均起搏QRS波时限(pQRSd)和刺激至左心室激动时间(LVAT)分别为117.6±11.4毫秒和68±17毫秒,而使用标准12导联心电图测量的分别为118.5±11.8毫秒和70±13毫秒,一致性分别为0.89和0.93。SDL-LBBaP导致单极和双极起搏阈值较低(在0.4毫秒时分别为0.7±0.2伏和0.8±0.2伏),在中位12个月随访时保持稳定(p>0.05)。1例(1.2%)患者在首次随访时需要进行心房导线修正。2例(2.4%)患者发生急性室间隔穿孔,这是LBBaP的一种特殊并发症。

结论

我们在非EP实验室中的新设置,即在LBBaP期间利用血管造影系统的荧光透视以及制造商改良的3导联心电图和PSA的EGM,是可行、可靠且广泛可用的。标准EP记录系统和新的改良PSA 3导联心电图测量均证实了LBB捕获,两者显示出良好的一致性。需要进一步的大规模数据来验证我们的发现。

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