Elsevier

Heart Rhythm

Volume 18, Issue 3, March 2021, Pages 419-425
Heart Rhythm

Clinical
General
Intraprocedural dynamics of cardiac conduction during transcatheter aortic valve implantation: Assessment by simultaneous electrophysiological testing

https://doi.org/10.1016/j.hrthm.2020.10.018Get rights and content

Background

Transcatheter aortic valve implantation (TAVI) is an established treatment for patients with severe aortic stenosis and high to intermediate surgical risk. However, the proximity of the conduction system to the prosthesis landing zone bears the risk of atrioventricular conduction disorders. The underlying pathophysiology is not fully understood.

Objective

The purpose of this study was to characterize the impact of TAVI on the conduction system as assessed by simultaneous electrophysiological testing.

Methods

AH and HV intervals and QRS duration were measured using a quadripolar His catheter and surface electrocardiogram in 108 patients at baseline (BL), after balloon predilation (timepoint 1 [T1]), after implantation of the valve prosthesis (T2), and after postdilation, if deemed necessary (T3).

Results

Between BL and T2, significant increases of HV interval and QRS duration were observed, with a mean delta of +12.4 ms and +32.7 ms, respectively. Both balloon predilation and valve implantation had an impact on infranodal conduction. No significant increase of AH intervals was documented. The increase of QRS duration led to left bundle branch block (LBBB) in 57 patients (52.8%). Implantation depth positively correlated with QRS prolongation (ρ = 0.21, P = .042) but not with changes of AH or HV interval (ρ = –0.03, P = .762; and ρ = 0.15, P = .130, respectively).

Conclusion

Electrophysiological testing during TAVI shows impairment of infranodal atrioventricular conduction by balloon predilation and valve implantation. This impairment is positively correlated with valve implantation depth and results in an increase of QRS duration with mainly LBBB pattern on surface electrocardiogram.

Introduction

Transcatheter aortic valve implantation (TAVI) is an established treatment method for patients with severe aortic stenosis and high to intermediate surgical risk.1, 2, 3 However, the proximity of the cardiac conduction system to the prosthesis landing zone bears the risk of conduction abnormalities, such as atrioventricular (AV) block and/or left bundle branch block (LBBB).4,5 The pathophysiological mechanisms behind the impairment of the conduction system are not fully understood.

The rate of conduction disorders requiring pacemaker implantation is higher after TAVI compared to surgical aortic valve replacement (7%–43% vs 7%) and in self-expandable compared to balloon-expandable valve prostheses (median 28% vs 6%).6, 7, 8, 9

Total AV block is a class I indication for pacemaker implantation, whereas other conduction disturbances such as first-degree AV block or its combination with right bundle branch block (RBBB) or LBBB are not.10 However, these disorders have a certain risk of progression to total AV block, especially when they occur after structural cardiac interventions such as TAVI. Recommendations for the duration of rhythm monitoring or uniform indications for prophylactic pacemaker implantation after TAVI are not available. Although different predictors of the development of total AV block have been described, including peri-interventional increase of PR interval >40 ms,11 pre-existing or new-onset RBBB or LBBB,9,11,12 aortic annular or left ventricular outflow tract (LVOT) calcification,13 type of valve prosthesis, depth of implantation, and oversizing,12, 13, 14 data are too scarce to draw clinically relevant conclusions.

Three clinical trials that included electrophysiological (EP) testing before and after TAVI showed distinct prolongations of AV conduction.15, 16, 17 However, to our knowledge, a simultaneous intraprocedural evaluation has never been performed before.

The aim of our study was to characterize the impact of each key procedural step (predilation, valve implantation, postdilation) of TAVI on AH and HV intervals as well as QRS duration by simultaneous EP testing and 12-lead electrocardiographic tracings.

Section snippets

Methods

The study was designed as a prospective, nonrandomized, single-center, single-cohort pilot trial and was conducted in accordance with the Declaration of Helsinki. The study protocol was approved by the Ethics Committee of the Federal State of Upper Austria. Before enrollment in the study, all subjects provided written informed consent.

Baseline characteristics

Baseline characteristics of 108 consecutive study patients are listed in Table 1, and the rates of conduction disorders at baseline are listed in Table 2. According to the inclusion criteria, all patients were in sinus rhythm at baseline.

EP testing was successfully conducted in all 108 individuals. The AH interval could be measured in all but 1 patient, in whom sudden onset of persistent atrial fibrillation occurred before EP testing. Ten patients developed total AV block (1 after balloon

Discussion

The present study aimed to evaluate the impact of major interventional steps of TAVI on AH and HV intervals and QRS duration as assessed by intraprocedural EP testing. Three main findings emerged from this study. First, simultaneous measurement of AH and HV intervals via a quadripolar His catheter during TAVI is a feasible, safe, and effective option for assessment of its impact on the cardiac conduction system. Second, both balloon dilation of the native calcified aortic valve as well as

Conclusion

As assessed by simultaneous EP testing, TAVI procedures with self-expandable valve prostheses significantly affect the infranodal conduction system but not the AV node itself. Implantation depth correlates with new-onset LBBB but not total AV block during TAVI. The significant increases in HV intervals and QRS duration place patients at risk for delayed occurrence of total AV block and/or bundle branch block–related deterioration of ventricular function, which both result in worse long-term

Acknowledgments

The authors thank EP technicians Martin Patrasso and Roman Kneidinger for their support in performing EP testing during TAVI.

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    Funding sources: The authors have no funding sources to disclose. Disclosures: The authors have no conflicts of interest or relationships relevant to the contents of this paper to disclose.

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