Elsevier

Heart Rhythm

Volume 19, Issue 1, January 2022, Pages 13-21
Heart Rhythm

Late Breaking Clinical Trials
Left bundle branch–optimized cardiac resynchronization therapy (LOT-CRT): Results from an international LBBAP collaborative study group

https://doi.org/10.1016/j.hrthm.2021.07.057Get rights and content

Background

Cardiac resynchronization therapy (CRT) based on the conventional biventricular pacing (BiV-CRT) technique sometimes results in broad QRS complex and suboptimal response.

Objective

We aimed to assess the feasibility and outcomes of CRT based on left bundle branch area pacing (LBBAP, in lieu of the right ventricular lead) combined with coronary venous left ventricular pacing in an international multicenter study.

Methods

LBBAP-optimized CRT (LOT-CRT) was attempted in nonconsecutive patients with CRT indications. Addition of the LBBA (or coronary venous) lead was at the discretion of the implanting physician, who was guided by suboptimal paced QRS complex, and/or on clinical grounds.

Results

LOT-CRT was successful in 91 of 112 patients (81%). The baseline characteristics were as follows: mean age 70 ± 11 years, female 22 (20%), left ventricular ejection fraction 28.7% ± 9.8%, left ventricular end-diastolic diameter 62 ± 9 mm, N-terminal pro–B-type natriuretic peptide level 5821 ± 8193 pg/mL, left bundle branch block 47 (42%), nonspecific intraventricular conduction delay 25 (22%), right ventricular pacing 26 (23%), and right bundle branch block 14 (12%). The procedure characteristics were as follows: mean fluoroscopy time 27.3 ± 22 minutes, LBBAP capture threshold 0.8 ± 0.5 V @ 0.5 ms, and R-wave amplitude 10 mV. LOT-CRT resulted in significantly greater narrowing of QRS complex from 182 ± 25 ms at baseline to 144 ± 22 ms (P < .0001) than did BiV-CRT (170 ± 30 ms; P < .0001) and LBBAP (162 ± 23 ms; P < .0001). At follow-up of ≥3 months, the ejection fraction improved to 37% ± 12%, left ventricular end-diastolic diameter decreased to 59 ± 9 mm, N-terminal pro–B-type natriuretic peptide level decreased to 2514 ± 3537 pg/mL, pacing parameters were stable, and clinical improvement was noted in 76% of patients (New York Heart Association class 2.9 vs 1.9).

Conclusion

LOT-CRT is feasible and safe and provides greater electrical resynchronization as compared with BiV-CRT and could be an alternative, especially when only suboptimal electrical resynchronization is obtained with BiV-CRT. Randomized controlled trials comparing LOT-CRT and BiV-CRT are needed.

Introduction

Left bundle branch area pacing (LBBAP) is a promising physiological pacing technique with potential for application in both patients with bradyarrhythmia and those with heart failure.1, 2, 3, 4 However, proximal left bundle branch (LBB) pacing is inherently limited in its ability to restore physiological activation of the lateral wall of the left ventricle (LV) in patients with distal conduction delay in the distal LBB, LV Purkinje network, or myocardium. Moreover, perhaps in a significant percentage of patients in whom LBBAP was attempted, only left ventricular septal (LVS) myocardial capture was obtained, resulting in a small but potentially important nonphysiological delay in LV lateral wall activation.4

Conventional cardiac resynchronization therapy (CRT) using biventricular (BiV) pacing based on right ventricular (RV) pacing and coronary venous (CV) pacing is also limited in its ability to fully restore physiological activation of the LV. Limitations of BiV-CRT are related, among others, to the potentially desynchronizing impact of myocardial pacing with the RV lead, single area nonphysiological epicardial LV pacing, latency, and suboptimal LV lead position (paraseptal/apical) due to the unfavorable anatomy of the cardiac veins and/or LV scars.5,6 Failure of BiV-CRT to restore physiological activation might express itself as QRS prolongation rather than narrowing. This is observed in one-third of patients who underwent BiV-CRT and related to poor prognosis.

Combining LBBAP and BiV pacing (Figures 1 and 2) might address some of the above-mentioned limitations of both techniques, providing narrower QRS complex and a more efficient form of CRT, especially in challenging cases and patients with more advanced heart failure.7

The aim of the study was to assess the feasibility and outcomes of CRT based on LBBAP (in lieu of the RV lead), combined with CV pacing, in an international multicenter study.

Section snippets

Methods

The data that support the findings of this study are available from the corresponding author on reasonable request. The study adhered to the Helsinki Declaration as revised in 2013; data collection was approved by respective institutional review boards.

Population

A total of 112 patients underwent LOT-CRT at 9 centers. Baseline group characteristics are summarized in Table 1. Briefly, the mean age of patients was 70.5 ± 11 years (20% female) and most patients had ischemic cardiomyopathy (61%) with a mean LVEF of 28.8% ± 9.8%. Seventy-two percent of patients were grouped under NYHA functional class III or IV. The mean follow-up duration in the study population was 7.8 ± 2.3 months. Because of the severe acute respiratory syndrome–related coronavirus

Discussion

This study presents multicenter experience with mid-term follow-up of the LOT-CRT technique in nonconsecutive patients with advanced heart failure and broad QRS complex. It addresses pertinent initial questions related to the rationale behind this new pacing method and provides data on its safety, feasibility, and outcomes.

Conclusion

LOT-CRT is feasible and safe and provides greater electrical resynchronization, compared with BiV-CRT, and could be an alternative to BiV-CRT, especially when only suboptimal electrical resynchronization is obtained with BiV-CRT. Randomized controlled trials comparing LOT-CRT and BiV-CRT are needed.

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  • Cited by (119)

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    Funding Sources: None.

    Disclosures: Drs Jastrzebski, Moskal, Huybrechts, and Curila have received consultant fees from Medtronic. Dr Herweg has received consultant fees from Abbott and Biotronik. Dr Sharma has received consultant fees from Abbott, Biotronik, Boston Scientific, and Medtronic. Dr Vijayaraman has received research and fellowship support as well as speaker and consultant fees from Medtronic. He has also received consultant fees from Abbott and Biotronik. The rest of the authors report no conflicts of interest.

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