Next Article in Journal
Semaglutide in Cardiometabolic Diseases: SELECTing the Target Population
Previous Article in Journal
Association between Abdominal Aortic Calcification and Coronary Heart Disease in Essential Hypertension: A Cross-Sectional Study from the 2013–2014 National Health and Nutrition Examination Survey
Previous Article in Special Issue
Ultra-High-Frequency ECG in Cardiac Pacing and Cardiac Resynchronization Therapy: From Technical Concept to Clinical Application
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Is Conduction System Pacing a Valuable Alternative to Biventricular Pacing for Cardiac Resynchronization Therapy?

by
Davide Castagno
1,2,
Francesco Zanon
3,
Gianni Pastore
3,
Gaetano Maria De Ferrari
1,2 and
Lina Marcantoni
3,*
1
Division of Cardiology, Department of Medical Sciences, University of Turin, 10126 Turin, Italy
2
Division of Cardiology, Cardiovascular and Thoracic Department, “Citta della Salute e della Scienza” Hospital, 10126 Turin, Italy
3
Santa Maria della Misericordia Hospital, Arrhythmia and Electrophysiology Unit, 45100 Rovigo, Italy
*
Author to whom correspondence should be addressed.
J. Cardiovasc. Dev. Dis. 2024, 11(5), 144; https://doi.org/10.3390/jcdd11050144
Submission received: 29 March 2024 / Revised: 28 April 2024 / Accepted: 30 April 2024 / Published: 2 May 2024

Abstract

:
Cardiac resynchronization therapy (CRT) significantly improves clinical outcomes in patients with ventricular systolic dysfunction and dyssynchrony. Biventricular pacing (BVP) has a class IA recommendation for patients with symptomatic heart failure with reduced ejection fraction (HFrEF) and left bundle branch block (LBBB). However, approximately 30% of patients have a poor therapeutic response and do not achieve real clinical benefit. Pre-implant imaging, together with tailored programming and dedicated device algorithms, have been proposed as possible tools to improve success rate but have shown inconsistent results. Over the last few years, conduction system pacing (CSP) is becoming a real and attractive alternative to standard BVP as it can restore narrow QRS in patients with bundle branch block (BBB) by stimulating and recruiting the cardiac conduction system, thus ensuring true resynchronization. It includes His bundle pacing (HBP) and left bundle branch area pacing (LBBAP). Preliminary data coming from small single-center experiences are very promising and have laid the basis for currently ongoing randomized controlled trials comparing CSP with BVP. The purpose of this review is to delve into the emerging role of CSP as an alternative method of achieving CRT. After framing CSP in a historical perspective, the pathophysiological rationale and available clinical evidence will be examined, and crucial technical aspects will be discussed. Finally, evidence gaps and future perspectives on CSP as a technique of choice to deliver CRT will be summarized.

1. Introduction

Biventricular pacing (BVP) is the established strategy for delivering cardiac resynchronization therapy (CRT) and is currently recommended as a first-line approach by both European and American guidelines in patients with heart failure (HF), left ventricular ejection fraction (LVEF) ≤ 35%, and wide QRS (≥130 ms) and that are symptomatic despite optimal medical therapy (New York Heart Association [NYHA] functional class II/IV) [1,2]. By inducing left ventricular (LV) reverse remodeling, BVP can significantly improve survival, reduce HF hospitalizations, and ameliorate functional capacity and quality of life. The benefit of BVP derives from the correction of inhomogeneous and delayed left ventricular (LV) electrical activation through pacing delivered from a lead in the right ventricle (RV) and a lead positioned in a branch of the coronary sinus (CS), allowing for epicardial LV stimulation. However, epicardial LV stimulation is far from physiologic as electrical impulse propagates via slow cell-to-cell electrical activation with epicardial to endocardial direction; indeed, BVP can overcome LV dyssynchrony through fusion between RV paced or native endocardial activation and epicardial LV pacing. In addition, despite significant advances in delivery tools and leads, BVP is not always feasible. Difficulties in CS cannulation, lack of suitable CS tributaries, phrenic nerve capture, and high capture thresholds are some of the main pitfalls limiting successful implantation in up to 4% of cases. In some cases, a pro-arrhythmic effect of BVP has been demonstrated [3,4]. Multi-point (MPP), multi-lead (triventricular) pacing have been tested in the attempt to provide benefit when clinical improvement does not occur, but they failed to improve the clinical response as well as failed atrioventricular (AV) and interventricular (VV) intervals optimization. Even now, approximately one-third of patients fail to benefit from BVP with the rate of non-responders remaining constant over time [1,5]. Given such premises, it is not surprising that alternative pacing modalities to deliver CRT have been tested. Conduction system pacing (CSP) has generated great interest in this regard as it can correct conduction disturbances and possibly restore physiological ventricular activation by capturing distally to the site of the block (Figure 1). CSP can be achieved by His bundle pacing (HBP), which is the most physiological pacing modality, or by left bundle branch area pacing (LBBAP) by engaging the LV conduction system generating a minimal delay in RV activation. CSP has been increasingly used as an alternative to BVP to deliver CRT. Several observational studies have demonstrated the feasibility and efficacy of CSP in CRT-eligible patients in improving echocardiographic outcomes and functional capacity [6].

2. The Rationale for Using CSP as CRT Strategy: LBBB Correction

Landmark, large, randomized clinical trials have shown that QRS duration and left bundle branch block (LBBB) morphology are strongly associated with clinically meaningful response to CRT [7,8], and current guidelines include both parameters amongst the criteria for consideration when selecting patients for BVP [1,2]. A delayed LV activation pattern and the resulting inefficient myocardial mechanics make LBBB the ideal target for CRT. In this regard, the MADIT-CRT trial showed that patients with an LBBB pattern rather than non-LBBB (i.e., right bundle branch block [RBBB] or intraventricular conduction delay [IVCD]) derived significant benefit from BVP compared with an implantable cardioverter defibrillator (ICD) alone in terms of reduction of nonfatal HF events or deaths from any cause [9]. The rationale for using CSP as strategy for delivering CRT comes from the assumption that the fibers destined to become the LBB are distinct within the His bundle (HB) and can be recruited by pacing beyond the site of the block or in close proximity to it with high enough energy to overcome the conduction block. This mechanism, known as the longitudinal dissociation theory, has its anatomical basis on early histological studies by James and Sherf, who demonstrated that the HB comprised multiple bundles separated by thin collagen septa [10]. Subsequent observations in animal models [11] and preliminary clinical experiences [12] demonstrated the feasibility of QRS normalization by HB stimulation. However, restoration of normal conduction is not achievable in all LBBB patients, and the possibility to correct LBBB with HBP or LBBAP depends on the site of the conduction block. A preliminary study evaluated the LV activation pattern using electroanatomical mapping (EAM) in 10 patients with LBBB referred for BVP. The majority (71%) of patients with non-ischemic etiology showed a line of functional conduction block causing LBBB and responded to conventional BVP. In contrast, patients with a myocardial scar and homogenously slow conduction pattern from the LV septum to the lateral wall without a distinct line of conduction block often required endocardial or multisite pacing to achieve response [13]. Up to one third of patients showing an LBBB pattern have intact His-Purkinje activation, suggesting a more distal diffuse conduction disease [10]. Indeed, detection of an LBBB pattern on surface ECG could imply different disorders, such as a complete conduction block, either intra-Hisian or located at the proximal LBB; intact His-Purkinje activation; or coexistent proximal block and distal conduction delay [14], and it does not reliably predict if CSP can successfully correct the conduction disorder [15,16]. Upadhyay et al., using intracardiac linear multielectrode mapping catheters, assessed left-sided septal electrical activation among 72 patients with LBBBs [14]. They found that 36% of patients with LBBB patterns on surface ECG had preserved conduction through the His-Purkinje system, while the remaining 64% had complete conduction block at the level of the HB or LBB (44% and 18%, respectively). These findings highlight that patients with complete conduction block are potentially amenable to corrective HBP, either directly or indirectly via the “virtual cathode”. In contrast, those with intact Purkinje activation (and without complete conduction block) do not restore normal conduction during CSP, most likely because of more peripheral conduction slowing secondary to fibrosis, hypertrophy, or both [14]. Moreover, when the site of conduction block is nodal or high infranodal, HBP may represent the ideal solution, provided that good electrical parameters are achieved. When a conduction block occurs at the level of the proximal left bundle branch, LBBAP can more easily correct the underlying conduction disturbance. In the case of non-specific intraventricular conduction delay, CSP is unlikely to correct the conduction disturbance because the Purkinje system activation is intact and left ventricular activation time (LVAT) may be prolonged because of intramyocardial disease. In these circumstances, or in the case of multiple sites of blocks, hybrid approaches combining CSP and pacing through a lead placed into the CS (i.e., HOT-CRT [His-optimized CRT] and LOT-CRT [left bundle branch optimized CRT]) may be of help. When spontaneous conduction is maintained through the RBBB, fusion between the directly paced LBB and the intrinsic conduction through the right branch can generate the maximal electrical resynchronization and determine significant QRS narrowing.

3. Dyssynchrony

LBBB results in the delayed and dyssynchronous activation of the LV, which is deleterious in patients with HF. BVP can improve this pathological activation pattern by shortening the LVAT and enhancing cardiac function. For a long time, BVP was the only feasible option to achieve CRT. However, despite the established benefits on morbidity and mortality, BVP relies on the fusion of two ventricular activation wavefronts (i.e., one epicardial and one endocardial), prompting a non-physiologic restoration of cardiac electrical and mechanical synchrony. By directly capturing the His-Purkinje system, CSP has the potential to restore ventricular physiological activation, resulting in a more efficient electrical resynchronization compared with BVP, as demonstrated by a greater reduction in LVAT and more pronounced hemodynamic improvements [17]. The depolarization front produced by His capture spreads across the ventricles via the His-Purkinje system, with a faster conduction speed than the cell-to-cell method through the myocardium (Figure 2). This true resynchronization can lead to the recovery of LV mechanical synchrony and reverse remodeling with consequent improvement in LVEF. Due to the inherent challenges and limitations of HBP, LBBAP has most recently been attracting increasing interest. Indeed, LBBAP offers several technical advantages compared with HBP (e.g., higher implant success rate, lower capture threshold, larger sensed R wave amplitude) (Figure 3). Furthermore, full LBBB correction is more often and more easily achieved with a subsequent higher rate of reverse remodeling and better clinical outcomes [18]. According to the recent prospective randomized study LBBP-RESYNC, LBBAP demonstrated greater LVEF improvement and greater left ventricular end-systolic volume reduction than BVP in 40 patients with non-ischemic cardiomyopathy, and LBBB followed over 6 months [19] A potential disadvantage is that the RV activation does not occur via the conduction system. In fact, during LBBAP, the ventricles are activated by two different wavefronts: from the conduction system and from the surrounding ventricular myocardium.

4. Hemodynamics

Hemodynamic studies have been used to compare CSP with BVP and to evaluate the acute impact of these pacing modalities on cardiac function. In 2016, Padeletti et al. [20], in a small prospective study (11 patients enrolled), showed enhanced systolic function and LV synchrony when LV epicardial pacing was combined with HBP, regardless of the atrioventricular delay settings. Based on these findings, the authors suggested that sequential HBP-LV activation can provide significant hemodynamic benefits by preserving intrinsic RV activation. More recently, a prospective study evaluated the acute electrophysiological and hemodynamic effects of BVP compared with temporary HBP and LV septal (LVS) pacing obtained by a quadripolar lead positioned at the level of the left ventricular endocardial side using a retrograde aortic approach. Both HBP and LVS pacing provided similar electrical resynchronization (i.e., QRS area and activation times reduction) and had superior results to BVP. The short-term hemodynamic effect measured by dP/dt max was similar for all three pacing configurations. Interestingly, the effects of LVS pacing were independent of the septal pacing location (i.e., basal, mid, apical septum) [21]. A within-patient comparison of the effects of HBP and BVP on ventricular activation time (measured using ECG imaging) and acute hemodynamic function was performed in patients with HF and LBBB. In 18 out of 23 patients, LVAT was significantly shortened by HBP, which produced more effective ventricular resynchronization than BVP (LVAT −26 ms; 95%CI: −41 to −21 ms; p 0.002). This translated into a greater improvement in hemodynamic response, with a 60% increase in acute systolic blood pressure compared with BVP (+4.6 mmHg; 95% CI: 0.2–9.1 mmHg; p 0.04). These findings suggest that, whenever HBP can successfully correct LBBB, it has the potential to deliver more effective ventricular resynchronization, ultimately improving cardiac function [17]. Whenever HBP fails to shorten QRS duration, HOT-CRT may offer a valuable alternative. In 19 candidates to CRT, because of LV impairment and concomitant conduction abnormalities, HOT-CRT produced a 24% greater reduction in LVAT compared with BVP (LVAT −22 ms; 95% CI: −33 to −10 ms; p 0.002) [22]. The acute hemodynamic effects of LBBAP versus BVP in patients with LBBB and concomitant LV impairment mainly of non-ischemic etiology were recently investigated. LBBAP produced a significantly greater reduction in QRS duration compared with BVP (−11 ms; 95% CI: −17 to −4 ms; p 0.003) and a greater reduction in QRS area (−85 μVs [95% CI, −113 to −56 μVs]; p < 0.001). These positive effects on ventricular resynchronization translated into a greater acute increase in LV dP/dt for LBBAP compared with BVP (6% [95% CI, 2%–9%]; p = 0.002) [23]. The LEVEL-AT (left ventricular activation time shortening with conduction system pacing vs. biventricular resynchronization therapy) study randomized 70 patients to CSP vs. BVP with the primary endpoint being the change in LVAT measured using electrocardiographic imaging (ECGi) 45 days post-implantation. In the intention-to-treat analysis, CSP resulted non-inferior to BVP in reducing LVAT (LVAT CSP: −28 ± 26 ms vs. BVP: −21 ± 20 ms; p < 0.001 for non-inferiority) [24]. In order to investigate whether RV delayed activation adversely impacted cardiac function, Ali et al. performed a within-patient acute hemodynamic study comparing HBP and LBBAP in 19 patients with LBBB and LV dysfunction. Noninvasive electrical mapping confirmed that the delayed RV activation with LBBAP did not adversely affect hemodynamic response (p 0.8); LBBAP was not inferior to HBP in reducing the LVAT (p 0.65). The HBP produced more rapid biventricular activation compared with LBBAP (P 0.03) [25].

5. CSP to Achieve CRT: Preliminary Experiences

HBP was the first pacing strategy tested to correct LBBB. The concept of functional longitudinal dissociation within the HB [10,11,12] provides the anatomical and pathophysiological foundation to the observation that, in some patients with LBBB, QRS narrowing and concomitant normalization of ventricular electromechanical synchrony can be achieved during HBP [11]. In the 1970s, Narula [12] firstly reported QRS normalization in 25 patients with LBBB advancing within the HB and pacing distally to the presumed site of block, thus suggesting that a block within the HB could be bypassed [12]. In patients with acute RBBB after myocardial infarction and patients with chronic LBBB, El-Sharif and colleagues [11] were able to normalize QRS with distal HBP. Furthermore, they demonstrated that in canine models where the septal artery was ligated, resulting in intra-hisian delay and BBB, distal pacing resulted in the normalization of the QRS in two-thirds of cases. In 2000, Deshmukh et al. [26] first described permanent HBP in twelve patients with chronic AF and LV systolic dysfunction undergoing AV node ablation. Clear beneficial effects, including reduction in LV end-diastolic and end-systolic diameters and increase in LVEF and fractional shortening were observed at follow-up. Since then, several studies have demonstrated the feasibility of permanent HBP and potential associated benefits compared with conventional RV pacing, including improvements in functional capacity, ventricular synchrony, and LVEF. In 2013, Barba-Pichardo et al. published the first experience of LBBB correction by permanent HBP [27]. Subsequently, Lustgarten presented the first crossover study on HBP compared with BVP in patients with HF and reduced LVEF. Both the HBP and CS lead were connected to the LV port by a Y-adapter to enable either pacing modality. Patients were randomized to HBP vs. BVP and, after 6 months, crossed over to the other pacing modality for another 6-month period. The feasibility of HBP, together with the possibility to re-engage preserved left fascicular tissue with QRS normalization in 72% of patients were demonstrated (mean QRS duration: baseline 171 + 13 ms; HBP 148 + 11 ms; BVP 158 + 21 ms, p < 0.0001). Clinical and echocardiographic responses were similar in HBP compared with BVP, with similar improvement in baseline LVEF from 26% to 32% (in HBP) and 31% (in BVP) at 6 months, suggesting that HBP was as efficient as BVP in this cohort [28]. Another study by a Spanish group published in 2011 showed how HBP used as bail out strategy whenever standard BVP via the CS was unsuccessful, in addition to electrical resynchronization and optimal clinical response, induced ventricular mechanical synchrony. Immediate abolition of septal-to-posterior wall delay and the disappearance of basal conduction disturbances due to LBBB were evident at the M-mode color tissue Doppler echocardiography during HBP; pulsed-wave tissue Doppler demonstrated the shortening of isovolumetric conduction time with higher peak systolic velocity whilst narrowing QRS by HBP; LVEF and LV diameters significantly improved [29]. Padeletti et al. tested simultaneous temporary HBP and LV epicardial pacing, showing an improvement in systolic function at hemodynamic evaluation beyond standard BVP regardless of the atrioventricular interval setting. The authors explained these findings, suggesting that HBP does not deliver an additional electric wave front to the right ventricle; instead, it takes advantage of the right bundle branch conduction (which is usually preserved in LBBB) and enables fusion between the LV pacing induced wavefront and intrinsic conduction [20]. More recently, Ajijola et al. tested the feasibility of HBP in lieu of an LV lead, obtaining a successful implant in 76% of cases (16 of the 21 patients enrolled). HBP induced a significant improvement in LVEF and functional class [30]. Starting from these preliminary experiences, several studies have been conducted to test CSP as an alternative to BVP in HFrEF patients, both in BVP non-responders and as a primary strategy. A recent comprehensive systematic review analyzed electrocardiographic, echocardiographic, and clinical outcomes after CSP compared with BVP in patients with CRT indications. Pooling the results from 6 randomized controlled studies and 12 observational nonrandomized studies, this meta-analysis showed the advantages of CSP in terms of QRS shortening, left ventricular remodeling, survival, and heart failure decompensation as compared with BVP [31].

6. Technical Considerations

Despite several investigations proving the feasibility and efficacy of HBP as CRT strategy, technical challenges associated with this pacing methodology had been an obstacle to its routine application. In more detail, the perceived lower implant success rate and higher pacing threshold associated with HBP are potential limitations to this approach. In contrast, LBBAP is associated with a low and stable capture threshold, optimal sensing, and higher procedural success rate thanks to the larger target area and smaller amount of surrounding fibrous tissue. This makes LBBAP suitable for sensing ventricular arrhythmias in addition to the aforementioned resynchronization capabilities. This possibility was tested in the CROSS-LEFT pilot study [32], which enrolled 10 patients with reduced ejection fraction and complete LBBB, who received a DF-1 dual chamber ICD with a single LBBAP lead connected to the IS-1 port; the defibrillator lead was positioned at the right ventricular apex to the DF-1 port of the device. At the time of implantation, ventricular fibrillation was induced, and both conventional (apical) and left bundle branch area sensing configurations were tested. No significant sensing differences were observed, but LBBAP was associated with electromechanical reverse remodeling and the improvement of LVEF at 6 months follow-up [32]. More recently, another study with a slightly bigger sample size (n = 30), assessed R-wave sensing and the long-term reliability of the LBBAP lead for the appropriate detection of ventricular arrhythmias in patients requiring CRT with defibrillator therapy [30]. During a mean follow-up of 23 months, ventricular arrhythmias detection from LLBAP lead was overall safe (i.e., 89% of episodes were appropriately detected), with 11% of episodes being inappropriately detected because of T wave oversensing in a single patient [30]. It should be noted that the adoption of LBBAP as a CRT strategy in ICD recipients requires the presence of multiple leads in the RV, possibly causing a lead-to-lead interaction, which can damage insulation and conductors and can increase the degree of tricuspid regurgitation. During implantation, great care should be taken to maintain adequate distance between the defibrillator coil and the ring of the LBBAP lead. Indeed, repetitive lead–lead interaction, especially when the defibrillator coil slides against the ring of the LBBAP lead, can determine insulation breach and damage the conductor, possibly causing lead fracture in the place where the lead is in contact with the coil [33]. This mechanism was clearly elucidated with bench tests reproducing fracture of the conduction cables within polyurethane-insulated leads [34]. Furthermore, noise-like signals on the LV channel caused by intermittent contact between the RV coil and the ring electrode of the LBBAP lead can lead to oversensing and inappropriate pacing inhibition from the LBBAP [35]. Whenever an LBBAP lead is added to a defibrillator lead, it is mandatory to check the leads’ position from multiple fluoroscopic views to avoid lead-to-lead interaction. This phenomenon may also be prevented by careful evaluation of both the bipolar (tip-to-ring) and the unipolar (ring-to-skin) signals during implantation. A first-in-human feasibility study with an ICD lead positioned at the level of the left bundle branch area was recently reported [36]. The implantation success rate was 60% (3 out of 5 patients), and the mean procedural and fluoroscopy duration were 170.0 ± 17.3 min and 28.8 ± 16.1 min, respectively [37]. In the near future, the availability of a dedicated LBBAP-defibrillator lead could make CSP and tachyarrhythmias detection/treatment with a single lead possible. CSP management during follow-up could be challenging. CSP leads generally pace multiple structures simultaneously (i.e., conduction system and surrounding myocardium) with or without the correction of the conduction block. Each tissue will show its own threshold, which should be identified to properly tailor output aiming to correct the bundle branch block. Furthermore, until now, available devices did not specifically address CSP programming requirements. Just recently, dedicated full systems (device and lead) for LBBAP have received CE approval.

7. Procedural Success Rate

Using CSP as strategy to achieve CRT does not guarantee a 100% implant success rate, as shown in both retrospective observational studies and in prospective randomized trials. His-SYNC and His-alternative randomized trials compared HBP with BVP. The HBP was equivalent or even superior to BVP in terms of QRS narrowing and echocardiographic response. However, crossover to BVP was required in a high proportion of patients randomized to HBP because of implantation failure. Moreover, in the His-SYNC pilot study, the high crossover rate was ascribed to the inclusion of patients with IVCD, not amenable to HBP-mediated QRS correction and reverse remodeling [36]. Unsurprisingly, in the His-alternative study, which excluded patients with IVCD, crossovers were less frequent, and the overall procedural success was higher [38]. Implantation success rates are usually satisfying with LBBAP, reaching >90% in the context of conventional bradyarrhythmic indications and >80% for HF indications, according to the MELOS study [39]. However, similarly to traditional BVP, the presence of a septal scar could be associated with implant failure. In a retrospective single-center study of 25 ischemic cardiomyopathy patients, LBBAP was unsuccessful in 36% of patients, showing a high scar burden on cardiac magnetic resonance and requiring BVP as alternative pacing modality to achieve CRT [40]. The presence of fibrotic tissue at the level of the mid-basal interventricular septum can hamper lead penetration and prevent the capture of the conduction system in the proximity of the LV subendocardium.

8. Complications

In a recent meta-analysis comparing CSP and BVP in CRT-eligible patients, the overall complications and lead revision rates were not significantly different between the two pacing modalities (6% in the CSP group vs. 8% in the BVP group, OR 0.80, 95% CI: 0.53–1.23). The rates of lead revision were also similar (OR 0.74, 95% CI:0.51–1.08). In addition, no significant differences were found for HBP versus LBBAP [41]. These results are concordant with the observations made in the MELOS study, where 27.5% of included patients had a primary pacing indication for HF. The overall complication rate with LBBAP was approximately 8%, including 4% of acute septal perforations, which usually do not have clinically relevant sequela following the intervention [39]. In another meta-analysis comparing LBBAP and BVP, the pacing threshold was lower in the former group, which was also associated with shorter QRS duration. Greater LVEF improvement, NYHA class, and lower risk of HF hospitalizations were also observed in patients receiving LBBAP compared with BVP [42]. Although HBP is highly effective at resynchronizing the heart, the unpredictable rise in capture threshold during follow-up is one of the greatest concerns with this pacing modality, which is especially relevant to premature battery depletion and the need for lead revision. Data on the long-term follow-up of HBP derive from the observational data of patients implanted for bradyarrthymias. Lead revision was required in up to 6% of cases, mainly due to technical pitfalls at the time of implant (i.e., abnormal slack shape, non-perpendicular angle of lead insertion) [43]. Recently, few cases of lead fracture of deep intraseptal leads have been reported. This problem seems to occur with both stylet-driven and lumenless leads, but with different underlying mechanisms. Although rare (i.e., 2/325, 0.6% of implants aiming at LBBAP), fractures of stylet-driven leads seem to occur relatively early during follow-up (median follow-up 18 months), with the conductor between the tip and ring of the electrode being involved [44]. A fractured lumenless lead proximally to the ring electrode was recently reported 2 years after a challenging implant (four tested positions), suggesting that the number of deployment attempts may be associated with a higher risk of fracture [45]. Altogether, the risk of lead fracture could be related to the repetitive mechanical stress imposed on deep intraseptal leads as well as to the possibility of lead damage resulting from multiple screwing attempts during implant. In addition, excessive lead angulation and preconditioning might contribute to early lead fracture. Because of the deep septal location achieved in LBBAP, extractability of malfunctioning or infected leads raises concerns, especially in the case of leads with long-dwelling times, for which clinical experience is still limited.

9. Current Guidelines

The emerging role of CSP as an alternative pacing modality to achieve CRT lays its foundation for the high proportion of non-response following BVP. The recently published 2023 HRS/APHRS/LAHRS guidelines assign a class IIb recommendation for CSP (i.e., HBP or LBBAP) as an alternative to BVP in patients with EF < 35%, sinus rhythm, LBBB, QRS duration >150 ms, NYHA class II-IV on guideline-directed medical therapy [2]. A class IIa recommendation for CSP is considered in case an effective CRT cannot be achieved with BVP and in patients with EF 36–50% with anticipated substantial (i.e., ≥20–40%) ventricular pacing as an alternative to BVP. Similarly, the latest ESC guidelines on cardiac pacing proved a class IIa recommendation for HBP in CRT candidates in whom CS lead implantation is unsuccessful [1].

10. Relevant Studies and Ongoing Trial

Observational studies and a small number of randomized controlled trials have reported a greater improvement in soft endpoint such as LVEF improvement, QRS duration, and hemodynamic parameters and quality of life with CSP compared with BVP [46,47]. In the His optimized pacing evaluated for heart failure (HOPE-HF) randomized, double-blind, crossover trial enrolling patients with HFrEF and PR interval ≥200 ms and QRS ≤ 140 ms (or bundle branch block), HBP did not increase peak oxygen uptake but improved heart failure specific quality of life compared with a strategy of no pacing [48]. In the left bundle branch pacing versus biventricular pacing for cardiac resynchronization therapy (LBBP-RESYNC) trial, the efficacy of LBBAP was compared with BVP with respect to the improvement of LVEF and other measures of cardiac function among patients with nonischemic cardiomyopathy and complete LBBB. At 6 months follow-up, a greater improvement of LVEF was observed after LBBAP vs. BVP (mean difference 5.6%, 95% CI: 0.3–10.9; p-value = 0.039). LBBAP recipients also showed a greater reduction in end-systolic volume and in NT-proBNP levels compared with BVP, although QRS narrowing was comparable between the two groups [19]. More recently, the feasibility and efficacy of HOT-CRT was compared with BVP in patients with heart failure, reduced LVEF (<50%), and CRT indications. A higher procedural success was observed with HOT-CRT compared with BVP (96% vs. 82%, p-value 0.03). At 6 months follow-up, HOT-CRT resulted in greater LVEF improvement compared with BVP (12.4% ± 7.3% vs. 8.0% ± 10.1%, p-value = 0.02) [49]. A recent meta-analysis compared the hard clinical outcomes of CSP versus BVP. In total, 21 studies (4 observational and 17 randomized controlled trials) were analyzed, and 1960 patients assigned to CSP and 2367 patients assigned to BVP were included. After a median follow-up of 10.1 months, CSP was associated with a significant decrease in all-cause mortality (OR 0.68; 95% CI: 0.56–0.83, I2 0%) and in the risk of HF hospitalization (OR 0.52; 95% CI: 0.44–0.63, I2 0%). LVEF improvement and NYHA class reduction were also greater in the CSP group compared with the BVP group [41]. Of note, a number of randomized controlled studies are currently ongoing and will be terminated in the next few years, possibly providing results that will help change the current approach to CRT (Table 1).

11. Gaps and Unmet Needs

CSP could be reasonably considered a valid alternative to conventional BVP for CRT candidates, but the lack of large, randomized studies still precludes the dissemination of this approach in daily clinical practice. Indeed, according to current guidelines [1,2,50], CSP may be offered as a bail-out option in CRT patients when CS lead implantation fails; to maintain physiological ventricular activation when a high burden of ventricular pacing is anticipated in patients with mildly reduced LVEF; or in the context of a pace and ablation strategy in patients suffering from tachycardiomyopathy. A European Heart Rhythm Association (EHRA) consensus document was recently published in an attempt to standardize CSP implantation [51]. Further improvements in implantation techniques and the development of dedicated implant tools may lead to a further increase in the procedural success rate along with a decrease in complications. Based on the mechanism of re-establishing inter- and intraventricular synchrony, BVP gained the acronym of CRT, and over time, the terms BVP and CRT have been used interchangeably. Indeed, CRT is a more comprehensive term that comprises the whole setting of simultaneous and non-simultaneous BVP stimulation as well as LV-only pacing and CSP options. Experience with CSP has been increasing; however, CSP still lacks its own terminology, possibly generating some confusion, as now the acronym CRT is no longer synonymous with BVP only but could also refer to CSP. A terminology update is expected to include the resource of CSP [52].

12. Conclusions

Currently, BVP is the only pacing strategy in HFrEF that has been proven effective in improving cardiac function, functional capacity, and survival. However, response to BVP is variable, ranging from complete normalization of cardiac function to lack of benefit. CSP is increasingly used as an alternative to BVP to achieve CRT. Selected patients with HFrEF might experience a positive electro-mechanical resynchronization with CSP, which has shown promising preliminary results and is currently undergoing rigorous clinical investigations.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/jcdd11050144/s1, Video S1: RS prop 2; Video S2: His prop 3.

Author Contributions

Conceptualization, L.M. and D.C.; writing—original draft preparation, L.M. and D.C.; writing—review and editing, G.P.; visualization, F.Z. and G.M.D.F.; supervision, F.Z.; G.M.D.F. and G.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Conflicts of Interest

The authors declare no conflict of interest related to this project.

References

  1. Glikson, M.; Nielsen, J.C.; Kronborg, M.B.; Michowitz, Y.; Auricchio, A.; Barbash, I.M.; Barrabés, J.A.; Boriani, G.; Braunschweig, F.; Brignole, M.; et al. 2021 ESC Guidelines on cardiac pacing and cardiac resynchronization therapy. Eur. Heart J. 2021, 42, 3427–3520. [Google Scholar] [CrossRef] [PubMed]
  2. Chung, M.K.; Patton, K.K.; Lau, C.P.; Dal Forno, A.R.J.; Al-Khatib, S.M.; Arora, V.; Birgersdotter-Green, U.M.; Cha, Y.M.; Chung, E.H.; Cronin, E.M.; et al. 2023 HRS/APHRS/LAHRS guideline on cardiac physiologic pacing for the avoidance and mitigation of heart failure. Heart Rhythm. 2023, 20, e17–e91. [Google Scholar] [CrossRef] [PubMed]
  3. Keene, D.; Whinnett, Z. Advances in cardiac resynchronization therapy: Review of indications and delivery options. Heart 2022, 108, 889–897. [Google Scholar] [CrossRef] [PubMed]
  4. Deif, B.; Ballantyne, B.; Almehmadi, F.; Mikhail, M.; McIntyre, W.F.; Manlucu, J.; Yee, R.; Sapp, J.L.; Roberts, J.D.; Healey, J.S.; et al. Cardiac resynchronization is pro-arrhythmic in the absence of reverse ventricular remodelling: A systematic review and meta-analysis. Cardiovasc. Res. 2018, 114, 1435–1444. [Google Scholar] [CrossRef] [PubMed]
  5. Daubert, C.; Behar, N.; Martins, R.P.; Mabo, P.; Leclercq, C. Avoiding non-responders to cardiac resynchronization therapy: A practical guide. Eur. Heart J. 2017, 38, 1463–1472. [Google Scholar] [CrossRef] [PubMed]
  6. Kircanski, B.; Boveda, S.; Prinzen, F.; Sorgente, A.; Anic, A.; Conte, G.; Burri, H. Conduction system pacing in everyday clinical practice: EHRA physician survey. Europace. 2023, 25, 682–687. [Google Scholar] [CrossRef]
  7. Moss, A.J.; Hall, W.J.; Cannom, D.S.; Klein, H.; Brown, M.W.; Daubert, J.P.; Estes, N.A.M.; Foster, E.; Greenberg, E.; Higgins, S.L.; et al. Cardiac-resynchronization therapy for the prevention of heart-failure events. N. Engl. J. Med. 2009, 361, 1329–1338. [Google Scholar] [CrossRef] [PubMed]
  8. Tian, Y.; Zhang, P.; Li, X.; Gao, Y.; Zhu, T.; Wang, L.; Li, D.; Wang, J.; Yuan, C.; Guo, J. True complete left bundle branch block morphology strongly predicts good response to cardiac resynchronization therapy. Europace 2013, 15, 1499–1506. [Google Scholar] [CrossRef] [PubMed]
  9. Goldenberg, I.; Kutyifa, V.; Klein, H.U.; Cannom, D.S.; Brown, M.W.; Dan, A.; Daubert, J.P.; Mark Estes, N.A., 3rd; Foster, E.; Greenberg, H.; et al. Survival with cardiac-resynchronization therapy in mild heart failure. N. Engl. J. Med. 2014, 370, 1694–1701. [Google Scholar] [CrossRef]
  10. James, T.N.; Sherf, L. Fine structure of the His bundle. Circulation 1971, 44, 9–28. [Google Scholar] [CrossRef]
  11. El-Sherif, N.; Amay-Y-Leon, F.; Schonfield, C.; Scherlag, B.J.; Rosen, K.; Lazzara, R.; Wyndham, C. Normalization of bundle branch block patterns by distal His bundle pacing. Clinical and experimental evidence of longitudinal dissociation in the pathologic his bundle. Circulation 1978, 57, 473–483. [Google Scholar] [CrossRef] [PubMed]
  12. Narula, O.S. Longitudinal dissociation in the His bundle. Bundle branch block due to asynchronous conduction within the His bundle in man. Circulation 1977, 56, 996–1006. [Google Scholar] [CrossRef] [PubMed]
  13. Ginks, M.R.; Shetty, A.K.; Lambiase, P.D.; Duckett, S.G.; Bostock, J.; Peacock, J.L.; Rhode, K.S.; Bucknall, C.; Gill, J.; Taggart, P.; et al. Benefits of endocardial and multisite pacing are dependent on the type of left ventricular electric activation pattern and presence of ischemic heart disease: Insights from electroanatomic mapping. Circ. Arrhythm Electrophysiol. 2012, 5, 889–897. [Google Scholar] [CrossRef] [PubMed]
  14. Upadhyay, G.A.; Cherian, T.; Shatz, D.Y.; Beaser, A.D.; Aziz, Z.; Ozcan, C.; Broman, M.T.; Nayak, H.M.; Tung, R. Intracardiac Delineation of Septal Conduction in Left Bundle-Branch Block Patterns. Circulation 2019, 139, 1876–1888. [Google Scholar] [CrossRef] [PubMed]
  15. Jastrzębski, M.; Kukla, P.; Kisiel, R.; Fijorek, K.; Moskal, P.; Czarnecka, D. Comparison of four LBBB definitions for predicting mortality in patients receiving cardiac resynchronization therapy. Ann. Noninvasive Electrocardiol. 2018, 23, e12563. [Google Scholar] [CrossRef] [PubMed]
  16. Caputo, M.L.; van Stipdonk, A.; Illner, A.; D’Ambrosio, G.; Regoli, F.; Conte, G.; Moccetti, T.; Klersy, C.; Prinzen, F.W.; Vernooy, K.; et al. The definition of left bundle branch block influences the response to cardiac resynchronization therapy. Int. J. Cardiol. 2018, 269, 165–169. [Google Scholar] [CrossRef] [PubMed]
  17. Arnold, A.D.; Shun-Shin, M.J.; Keene, D.; Howard, J.P.; Sohaib, S.M.A.; Wright, I.J.; Cole, G.D.; Qureshi, N.A.; Lefroy, D.C.; Koa-Wing, M.; et al. His Resynchronization Versus Biventricular Pacing in Patients With Heart Failure and Left Bundle Branch Block. J. Am. Coll. Cardiol. 2018, 72, 3112–3122. [Google Scholar] [CrossRef] [PubMed]
  18. Baroni, M.; Preda, A.; Varrenti, M.; Vargiu, S.; Carbonaro, M.; Giordano, F.; Gigli, L.; Mazzone, P. Left Bundle Branch Area Pacing over His Bundle Pacing: How Far Have We Come? J. Clin. Med. 2023, 12, 3251. [Google Scholar] [CrossRef] [PubMed]
  19. Wang, Y.; Zhu, H.; Hou, X.; Wang, Z.; Zou, F.; Qian, Z.; Wei, Y.; Wang, X.; Zhang, L.; Li, X.; et al. Randomized Trial of Left Bundle Branch vs Biventricular Pacing for Cardiac Resynchronization Therapy. J. Am. Coll. Cardiol. 2022, 80, 1205–1216. [Google Scholar] [CrossRef]
  20. Padeletti, L.; Pieragnoli, P.; Ricciardi, G.; Innocenti, L.; Checchi, L.; Padeletti, M.; Michelucci, A.; Picariello, F.; Valsecchi, S. Simultaneous His Bundle and Left Ventricular Pacing for Optimal Cardiac Resynchronization Therapy Delivery: Acute Hemodynamic Assessment by Pressure-Volume Loops. Circ. Arrhythm Electrophysiol. 2016, 9, e003793. [Google Scholar] [CrossRef]
  21. Salden, F.C.W.M.; Luermans, J.G.L.M.; Westra, S.W.; Weijs, B.; Engels, E.B.; Heckman, L.I.B.; Lamerichs, L.J.M.; Janssen, M.H.G.; Clerx, K.J.H.; Cornelussen, R.; et al. Short-Term Hemodynamic and Electrophysiological Effects of Cardiac Resynchronization by Left Ventricular Septal Pacing. J. Am. Coll. Cardiol. 2020, 75, 347–359. [Google Scholar] [CrossRef]
  22. Zweerink, A.; Zubarev, S.; Bakelants, E.; Potyagaylo, D.; Stettler, C.; Chmelevsky, M.; Lozeron, E.D.; Hachulla, A.L.; Vallée, J.P.; Burri, H. His-Optimized Cardiac Resynchronization Therapy with Ventricular Fusion Pacing for Electrical Resynchronization in Heart Failure. JACC Clin. Electrophysiol. 2021, 7, 881–892. [Google Scholar] [CrossRef] [PubMed]
  23. Liang, Y.; Wang, J.; Gong, X.; Lu, H.; Yu, Z.; Zhang, L.; Li, M.; Pan, L.; Chen, X.; Cui, J.; et al. Left Bundle Branch Pacing Versus Biventricular Pacing for Acute Cardiac Resynchronization in Patients with Heart Failure. Circ. Arrhythm Electrophysiol. 2022, 15, e011181. [Google Scholar] [CrossRef]
  24. Pujol-Lopez, M.; Jiménez-Arjona, R.; Garre, P.; Guasch, E.; Borràs, R.; Doltra, A.; Ferró, E.; García-Ribas, C.; Niebla, M.; Carro, E.; et al. Conduction System Pacing vs Biventricular Pacing in Heart Failure and Wide QRS Patients: LEVEL-AT Trial. JACC Clin. Electrophysiol. 2022, 8, 1431–1445. [Google Scholar] [CrossRef] [PubMed]
  25. Ali, N.; Arnold, A.D.; Miyazawa, A.A.; Keene, D.; Chow, J.J.; Little, I.; Peters, N.S.; Kanagaratnam, P.; Qureshi, N.; Ng, F.S.; et al. Comparison of methods for delivering cardiac resynchronization therapy: An acute electrical and haemodynamic within-patient comparison of left bundle branch area, His bundle, and biventricular pacing. Europace 2023, 25, 1060–1067. [Google Scholar] [CrossRef] [PubMed]
  26. Deshmukh, P.; Casavant, D.A.; Romanyshyn, M.; Anderson, K. Permanent, direct His-bundle pacing: A novel approach to cardiac pacing in patients with normal His-Purkinje activation. Circulation 2000, 101, 869–877. [Google Scholar] [CrossRef]
  27. Barba-Pichardo, R.; Manovel Sanchez, A.; Fernandez-Gomez, J.M.; Morina-Vazquez, P.; Venegas-Gamero, J.; Herrera-Carranza, M. Ventricular resynchronization therapy by direct His-bundle pacing using an internal cardioverter defibrillator. Europace 2013, 15, 83–88. [Google Scholar] [CrossRef]
  28. Lustgarten, D.L.; Crespo, E.M.; Arkhipova-Jenkins, I.; Lobel, R.; Winget, J.; Koehler, J.; Liberman, E.; Sheldon, T. His-bundle pacing versus biventricular pacing in cardiac resynchronization therapy patients: A crossover design comparison. Heart Rhythm 2015, 12, 1548–1557. [Google Scholar] [CrossRef] [PubMed]
  29. Manovel, A.; Barba-Pichardo, R.; Tobaruela, A. Electrical and mechanical cardiac resynchronisation by novel direct his-bundle pacing in a heart failure patient. Heart Lung Circ. 2011, 20, 769–772. [Google Scholar] [CrossRef]
  30. Ponnusamy, S.S.; Ramalingam, V.; Mariappan, S.; Ganesan, V.; Anand, V.; Syed, T.; Murugan, S.; Kumar, M.; Vijayaraman, P. Left bundle branch pacing lead for sensing ventricular arrhythmias in implantable cardioverter-defibrillator: A pilot study (LBBP-ICD study). Heart Rhythm 2023, 21, 419–426. [Google Scholar] [CrossRef]
  31. Shresthaa, D.B.; Baniya, A.; Lamichhane, S.; Shahi, M.; Shtembari, J.; Deshmukhc, A.J.; Voruganti, D.; Patel, N.K.; Sangal, K.; Vallabhajosyulaf, S.; et al. Conduction system pacing vs. biventricular pacing for cardiac resynchronization therapy in heart failure with reduced ejection fraction: An updated systematic review and meta-analysis. Health Sci. Rev. 2023, 8, 100104. [Google Scholar] [CrossRef]
  32. Clementy, N.; Bodin, A.; Ah-Fat, V.; Babuty, D.; Bisson, A. Dual-chamber ICD for left bundle branch area pacing: The cardiac resynchronization and arrhythmia sensing via the left bundle (cross-left) pilot study. J. Interv. Card. Electrophysiol. 2023, 66, 905–912. [Google Scholar] [CrossRef] [PubMed]
  33. Mahajan, A.; Pokharel, P.; Vijayaraman, P. Lead-to-lead interaction leading to left bundle branch area pacing lead failure. Heart Rhythm Case Rep. 2022, 9, 72–75. [Google Scholar] [CrossRef]
  34. Pokharel, P.; Mahajan, A.; Himes, A.; Lowell, M.; Budde, R.; Vijayaraman, P. Mechanisms of damage related to ICD and pacemaker lead interaction. Heat Rhythm. O2 2023, 4, 820–822. [Google Scholar] [CrossRef] [PubMed]
  35. Francois, C.; De Becker, B.; De Smet, M.; Knecht, S.; Duytschaever, M.; Tavernier, R.; le Polain de, W. Interaction between left bundle branch area pacing and defibrillator lead: A case report. Heart Rhythm Case Rep. 2023, 10, 72–75. [Google Scholar] [CrossRef]
  36. Upadhyay, G.A.; Vijayaraman, P.; Nayak, H.M.; Verma, N.; Dandamudi, G.; Sharma, P.S.; Saleem, M.; Mandrola, J.; Genovese, D.; Tung, R.; et al. His Corrective Pacing or Biventricular Pacing for Cardiac Resynchronization in Heart Failure. J. Am. Coll. Cardiol. 2019, 74, 157–159. [Google Scholar] [CrossRef]
  37. Huybrechts, W.L.H.; Bergonti, M.; Saenen, J.B.; Miljoen, H.; Van Leuven, O.; Van Assche, L.; Van Herck, P.; Wittock, A.; De Cleen, D.; Sarkozy, A.; et al. Left Bundle Branch Area Defibrillator (LBBAD): A First-in-Human Feasibility Study. JACC Clin. Electrophysiol. 2023, 9, 620–627. [Google Scholar] [CrossRef] [PubMed]
  38. Vinther, M.; Risum, N.; Svendsen, J.H.; Møgelvang, R.; Philbert, B.T. A Randomized Trial of His Pacing Versus Biventricular Pacing in Symptomatic HF Patients With Left Bundle Branch Block (His-Alternative). JACC Clin. Electrophysiol. 2021, 7, 1422–1432. [Google Scholar] [CrossRef]
  39. Jastrzębski, M.; Kiełbasa, G.; Cano, O.; Curila, K.; Heckman, L.; De Pooter, J.; Chovanec, M.; Rademakers, L.; Huybrechts, W.; Grieco, D.; et al. Left bundle branch area pacing outcomes: The multicentre European MELOS study. Eur. Heart J. 2022, 43, 4161–4173. [Google Scholar] [CrossRef]
  40. Ponnusamy, S.S.; Murugan, M.; Ganesan, V.; Vijayaraman, P. Predictors of procedural failure of left bundle branch pacing in scarred left ventricle. J. Cardiovasc. Electrophysiol. 2023, 34, 760–764. [Google Scholar] [CrossRef]
  41. Kim, J.A.; Kim, S.E.; Ellenbogen, K.A.; Vijayaraman, P.; Chelu, M.G. Clinical outcomes of conduction system pacing versus biventricular pacing for cardiac resynchronization therapy: A systematic review and meta-analysis. J. Cardiovasc. Electrophysiol. 2023, 34, 1718–1729. [Google Scholar] [CrossRef] [PubMed]
  42. Parlavecchio, A.; Vetta, G.; Caminiti, R.; Coluccia, G.; Magnocavallo, M.; Ajello, M.; Pistelli, L.; Dattilo, G.; Foti, R.; Carerj, S.; et al. Left bundle branch pacing versus biventricular pacing for cardiac resynchronization therapy: A systematic review and meta-analysis. Pacing Clin. Electrophysiol. 2023, 46, 432–439. [Google Scholar] [CrossRef] [PubMed]
  43. Beer, D.; Subzposh, F.A.; Colburn, S.; Naperkowski, A.; Vijayaraman, P. His bundle pacing capture threshold stability during long-term follow-up and correlation with lead slack. Europace 2021, 23, 757–766. [Google Scholar] [CrossRef] [PubMed]
  44. Özpak, E.; Van Heuverswyn, F.; Timmermans, F.; De Pooter, J. Lead performance of stylet-driven leads in left bundle branch area pacing: Results from a large single-center cohort and insights from in vitro bench testing. Heart Rhythm. 2024. [Google Scholar] [CrossRef] [PubMed]
  45. Rangaswamy, V.V.; Ponnusamy, S.S. Late distal conductor fracture of the lumenless pacing lead after left bundle branch area pacing. Heart Rhythm. 2024, 21, 490–491. [Google Scholar] [CrossRef] [PubMed]
  46. Gui, Y.; Ye, L.; Wu, L.; Mai, H.; Yan, Q.; Wang, L. Clinical Outcomes Associated With His-Purkinje System Pacing vs. Biventricular Pacing, in Cardiac Resynchronization Therapy: A Meta-Analysis. Front. Cardiovasc. Med. 2022, 9, 707148. [Google Scholar] [CrossRef] [PubMed]
  47. Gin, J.; Chow, C.L.; Voskoboinik, A.; Nalliah, C.; Wong, C.; Van Gaal, W.; Farouque, O.; Mohamed, U.; Lim, H.S.; Kalman, J.M.; et al. Improved outcomes of conduction system pacing in heart failure with reduced ejection fraction: A systematic review and meta-analysis. Heart Rhythm. 2023, 20, 1178–1187. [Google Scholar] [CrossRef] [PubMed]
  48. Whinnett, Z.I.; Shun-Shin, M.J.; Tanner, M.; Foley, P.; Chandrasekaran, B.; Moore, P.; Adhya, S.; Qureshi, N.; Muthumala, A.; Lane, R.; et al. Effects of haemodynamically atrio-ventricular optimized His bundle pacing on heart failure symptoms and exercise capacity: The His Optimized Pacing Evaluated for Heart Failure (HOPE-HF) randomized, double-blind, cross-over trial. Eur. J. Heart Fail. 2023, 25, 274–283. [Google Scholar] [CrossRef] [PubMed]
  49. Vijayaraman, P.; Pokharel, P.; Subzposh, F.A.; Oren, J.W.; Storm, R.H.; Batul, S.A.; Beer, D.A.; Hughes, G.; Leri, G.; Manganiello, M.; et al. His-Purkinje Conduction System Pacing Optimized Trial of Cardiac Resynchronization Therapy vs Biventricular Pacing: HOT-CRT Clinical Trial. JACC-EP 2023, 9, 2628–2638. [Google Scholar]
  50. Brugada, J.; Katritsis, D.G.; Arbelo, E.; Arribas, F.; Bax, J.J.; Blomström-Lundqvist, C.; Calkins, H.; Corrado, D.; Deftereos, S.G.; Diller, G.P.; et al. 2019 ESC Guidelines for the management of patients with supraventricular tachycardiaThe Task Force for the management of patients with supraventricular tachycardia of the European Society of Cardiology (ESC). Eur. Heart J. 2020, 41, 655–720. [Google Scholar] [CrossRef]
  51. Burri, H.; Jastrzebski, M.; Cano, O.; Kurila, C.; de Pooter, J.; Huang, W.; Israel, C.; Joza, J.; Romer, J.; Vernooy, K.; et al. EHRA clinical consensus statement on conduction system pacing implantation: Endorsed by the Asia Pacific Heart Rhythm Society (APHRS), Canadian Heart Rhythm Society (CHRS), and Latin American Heart Rhythm Society (LAHRS). Europace 2023, 25, 1208–1236. [Google Scholar] [CrossRef] [PubMed]
  52. Marcantoni, L.; Pastore, G.; Biffi, M.; Zanon, F. The weakest point of cardiac resynchronization therapy: New technologies facing old terminology. Front. Cardiovasc. Med. 2023, 10, 1236369. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Conduction system pacing (CSP) can completely correct conduction disturbances and restore normal QRS by capturing distally to the site of the block. Panel (A) shows the 12-lead ECG of a man with a paroxysmal II degree AV block and left bundle branch block (LBBB) referred for PM implantation in 2006. The His bundle was targeted, and corrective His bundle pacing (HBP) was obtained. Panel (B) shows paced ECG and complete QRS normalization during HBP. Of note, negative T waves in the precordial leads were a sign of cardiac memory after LBBB normalization and disappeared at the 1-month follow-up.
Figure 1. Conduction system pacing (CSP) can completely correct conduction disturbances and restore normal QRS by capturing distally to the site of the block. Panel (A) shows the 12-lead ECG of a man with a paroxysmal II degree AV block and left bundle branch block (LBBB) referred for PM implantation in 2006. The His bundle was targeted, and corrective His bundle pacing (HBP) was obtained. Panel (B) shows paced ECG and complete QRS normalization during HBP. Of note, negative T waves in the precordial leads were a sign of cardiac memory after LBBB normalization and disappeared at the 1-month follow-up.
Jcdd 11 00144 g001
Figure 2. HBP that captures the His-Purkinje system has the potential to restore normal physiological activation. The depolarization front produced by His capture spreads to the ventricles by the His-Purkinje system with a faster conduction speed than through the myocardium. The figure shows the case of a man with LBBB and severe left ventricular disfunction with CRT indication. The HBP was targeted, and complete QRS normalization was obtained. Panel (A) shows the spontaneous ECG (first three beats); complete LBBB and QRS duration 176 ms, followed by selective HBP-paced QRS (last five beats), with normalization of the QRS morphology and duration (88 ms). Panel (B,C) show the 3D electroanatomical reconstruction of the His cloud and the left ventricular activation mapped through a BMW guidewire inserted in all CS branches. The color code is clarified in the left margin: purple identifies late activation, while red identifies early activation. During spontaneous LBBB, the LV activation is completely delayed, with additional intraventricular delay showed by the green point at the sparkle map appearing at different times between different CS branches. During selective HBP with QRS normalization, LV activation is equally distributed in green-yellow colors, with the green dot points contemporarily appearing in all CS branches. Panel (D) shows the 12-lead ECG at baseline (LBBB) and the unipolar signal recorded from the His lead (“HIS”), confirming a distal position, where a small atrial signal “A”, sharp His potential “H” and big ventricular signal “V” are recorded. Panel (E) shows the His cloud (yellow, white, and red tags highlight, respectively, the proximal, median, and distal portion of the His Bundle). The green dot shows the exact final position of the HBP lead (Tendril lead in this case). See Supplementary Materials for the sparkle maps video.
Figure 2. HBP that captures the His-Purkinje system has the potential to restore normal physiological activation. The depolarization front produced by His capture spreads to the ventricles by the His-Purkinje system with a faster conduction speed than through the myocardium. The figure shows the case of a man with LBBB and severe left ventricular disfunction with CRT indication. The HBP was targeted, and complete QRS normalization was obtained. Panel (A) shows the spontaneous ECG (first three beats); complete LBBB and QRS duration 176 ms, followed by selective HBP-paced QRS (last five beats), with normalization of the QRS morphology and duration (88 ms). Panel (B,C) show the 3D electroanatomical reconstruction of the His cloud and the left ventricular activation mapped through a BMW guidewire inserted in all CS branches. The color code is clarified in the left margin: purple identifies late activation, while red identifies early activation. During spontaneous LBBB, the LV activation is completely delayed, with additional intraventricular delay showed by the green point at the sparkle map appearing at different times between different CS branches. During selective HBP with QRS normalization, LV activation is equally distributed in green-yellow colors, with the green dot points contemporarily appearing in all CS branches. Panel (D) shows the 12-lead ECG at baseline (LBBB) and the unipolar signal recorded from the His lead (“HIS”), confirming a distal position, where a small atrial signal “A”, sharp His potential “H” and big ventricular signal “V” are recorded. Panel (E) shows the His cloud (yellow, white, and red tags highlight, respectively, the proximal, median, and distal portion of the His Bundle). The green dot shows the exact final position of the HBP lead (Tendril lead in this case). See Supplementary Materials for the sparkle maps video.
Jcdd 11 00144 g002
Figure 3. Conduction system pacing applied in a patient with LBBB and LV ejection fraction 34% as a CRT strategy. Panel (A): baseline spontaneous ECG (recorded at 50 mm/s speed) shows an LBBB pattern and QRSd of 176 ms. Panel (B): “ENDO” (red trace) represents the EGM recorded in unipolar fashion from the tip of the lead on the His Bundle (lead “His” in panel (F)). A: Atrial signal; H: His signal; V: ventricular signal. Panel (C): pacing from the His bundle produced a non-selective capture with LBBB correction at high output (threshold for LBBB correction 3 V@1 ms). A decreasing output (panel (D)) selective capture without LBBB correction was obtained. Considering the high output needed to correct LBBB, an additional lead was inserted to test the intraseptal left bundle branch capture and paced QRS duration, aiming to leave in place the lead with better electrical parameters and which was associated with shorter paced QRS duration. Panel (E) shows the paced QRS determined by the intraseptal LBB lead: the capture threshold was optimal (0.7 V@0.4 ms), left ventricular activation time (LVAT) was 72 ms, and final paced QRS duration was 132 ms. Panel (F) is the left anterior oblique view of the three leads: the RV coil (apical septum); “His”, the first lead implanted to test His position, thereafter moved to the atrium; and “LB”, the second lead, implanted while being aimed at intraseptal LBBB pacing. Panel (G) shows the right anterior oblique view and the final position of the three leads: the RV coil in the apical septum, LB in LBBB, and atrial lead after moving the lead from His to the atrium.
Figure 3. Conduction system pacing applied in a patient with LBBB and LV ejection fraction 34% as a CRT strategy. Panel (A): baseline spontaneous ECG (recorded at 50 mm/s speed) shows an LBBB pattern and QRSd of 176 ms. Panel (B): “ENDO” (red trace) represents the EGM recorded in unipolar fashion from the tip of the lead on the His Bundle (lead “His” in panel (F)). A: Atrial signal; H: His signal; V: ventricular signal. Panel (C): pacing from the His bundle produced a non-selective capture with LBBB correction at high output (threshold for LBBB correction 3 V@1 ms). A decreasing output (panel (D)) selective capture without LBBB correction was obtained. Considering the high output needed to correct LBBB, an additional lead was inserted to test the intraseptal left bundle branch capture and paced QRS duration, aiming to leave in place the lead with better electrical parameters and which was associated with shorter paced QRS duration. Panel (E) shows the paced QRS determined by the intraseptal LBB lead: the capture threshold was optimal (0.7 V@0.4 ms), left ventricular activation time (LVAT) was 72 ms, and final paced QRS duration was 132 ms. Panel (F) is the left anterior oblique view of the three leads: the RV coil (apical septum); “His”, the first lead implanted to test His position, thereafter moved to the atrium; and “LB”, the second lead, implanted while being aimed at intraseptal LBBB pacing. Panel (G) shows the right anterior oblique view and the final position of the three leads: the RV coil in the apical septum, LB in LBBB, and atrial lead after moving the lead from His to the atrium.
Jcdd 11 00144 g003
Table 1. Principal ongoing RCTs comparing CSP vs. BVP to achieve CRT.
Table 1. Principal ongoing RCTs comparing CSP vs. BVP to achieve CRT.
Nct NumberStudy TitleLocationStatusStudy DesignPrimary
Outcomes
Number of PatientsFollow-up
NCT06278844Exercise Capacity Improvement by Conduction System Pacing in heArt Failure patieNts Without Compelling CRT inDication (ESCPAND)BelgiumRecruitingInterventional
Randomized
Parallel assignment
Open label
Exercise capacity (change in VO2 peak from baseline to 24 weeks)7524 weeks
NCT04409119Direct HIS/LBB Pacing as an Alternative to Biventricular Pacing in Patients with HFrEF and a Typical LBBB (HIS-alt_2)DenmarkRecruitingRandomized
Parallel assignment
Double masking (participant, outcome assessor)
Change in Left ventricular end-systolic volume (decrease in left ventricular systolic volume of ≥15% of baseline)
Success rate of implanting a HIS-bundle lead with capture of the left bundle branch or a LBB-lead with narrowing of QRS
1256 months
NCT05650658Left vs. Left Randomized Clinical TrialUSARecruitingRandomized
Parallel assignment
Triple masking (participant, care provider, outcome assessor)
Combined clinical endpoint of all-cause mortality and hospitalization for heart failure21365.5 years
NCT06105580Conduction System Pacing vs. Biventricular Pacing in Systolic Dysfunction and Wide QRS: Mortality, Heart Failure Hospitalization or Cardiac Transplant (CONSYST-CRT II)SpainRecruitingInterventional
Randomized
Parallel assignment
Single masking (participant)
All-cause mortality, cardiac transplant, or heart failure hospitalization 320 12 months
NCT06241651CSP Versus BiVP for Heart Failure Patients With RVP Upgraded to Cardiac Resynchronization Therapy: a Prospective Multicenter Non-inferiority Randomized Controlled Study (CSP-UPGRADE)ChinaRecruitingInterventional
Randomized
Parallel assignment
Open label
ΔLVEF (change in LVEF from baseline)666 months
NCT05467163Conduction System Pacing Versus Biventricular Pacing After Atrioventricular Node Ablation (CONDUCT-AF trial)Austria, Bulgaria, Belgium, CroatiaRecruitingInterventional
Randomized
Parallel assignment
Open label
Change in left ventricular ejection fraction 826 months
NCT05428787Resynchronization in Patients With HF in AF Trial Undergoing Pace & AVNA Strategy With LBBAP Compared With BiV Pacing (RAFT-P&A)CanadaRecruitingRandomized
Parallel assignment
Masking double (participant, outcome assessor)
Change in NT-proBNP from baseline 2846 months
NCT05434962The Left Bundle Cardiac Resynchronization Therapy Trial (LEFT-BUNDLE-CRT)Spain RecruitingRandomized
Parallel assignment
Open label
Non-inferiority.
CRT response (improvement of a clinical composite score or ≥15% reduction in left ventricular end-systolic volume)1766 months
NCT06052475Physiological Versus Right Ventricular Outcome Trial Evaluated for Bradycardia Treatment Upgrades (PROTECT-UP)UKRecruitingRandomized
Crossover assignment
Masking quadruple (participant, care provider, investigator, outcome assessor)
SF-36 physical component summary 15514 months
NCT05265520His-Bundle Corrective Pacing in Heart Failure (HIS-CRT)USARecruitingRandomized
Parallel assignment
Single masking (outcome assessor)
Change in left ventricular ejection fraction in heart failure patients with Right bundle branch block (RBBB)1206 months
NCT05572957LBBP as Initial Therapy in Patients With Non-ischemic Heart Failure and LBBB (LIT-HF)ChinaRecruitingRandomized
Parallel assignment
Open label
Proportion of patients requiring ICD implantation for prevention of sudden cardiac death after treatment with two strategies (GDMT, LBBP + GDMT), the percentages of LVEF still ≤35% and/or ventricular arrhythmia events was assessed in both groups.506 months
NCT05814263HIS Alternative II—UK SiteUKRecruitingRandomized
Parallel assignment
Double masking (participant, outcome assessor)
Change in left ventricular end-systolic volume (decrease in left ventricular systolic volume of ≥ 15% of baseline)
Success rate of implanting a HIS-bundle lead with capture of the left bundle branch or a LBB-lead with narrowing of QRS
The success rate of implanting a pacing lead to the HIS-bundle, with capture of the left bundle at a threshold < 2.5 V at 1 ms or implantation of a LBB lead with narrowing of the QRS duration and maintaining this effect at 6 month follow-up
406 months
NCT03803995Mapping and Pacing of the His Bundle for Heart Failure Patients With Left Bundle Branch Block (MAP HIS HF)USARecruiting Single group assignment
Open label
Successful HB pacing sites
Collect 3D Locations and electrogram characteristics (morphology and activation time) at the sites where His bundle (HB) pacing is associated with left bundle recruitment and corrects electrical dyssynchrony at HB pacing implant procedure.
30N/A
NCT05769036Conventional Biventricular Versus Left Bundle Branch Pacing on Outcomes in Heart Failure Patients (RECOVER-HF)RussiaRecruitingRandomized
Parallel assignment
Open label
All-cause mortality or worsening of heart failure requiring unplanned hospitalization (%)6024 months
NCT05187611Conduction System Pacing vs. Biventricular Resynchronization Therapy in Systolic Dysfunction and Wide QRS: CONSYST-CRT.SpainActive, not recruitingnon-inferiority trial
Randomized
Parallel assignment
Single masking (participant)
Composite endpoint consisting of all-cause mortality, cardiac transplant, heart failure hospitalizations, and left ventricular ejection fraction (LVEF) improvement <5 points
1301 year
NCT05572736Conduction System Pacing Versus Biventricular Resynchronization in Patients With Chronic Heart Failure (PhysioSync-HF)BrazilActive, not recruitingInterventional
Randomized
Parallel assignment
Masking Double (participant, outcomes assessor)
Non-inferiority of clinical benefit, a hierarchical composite of all-cause death, any hospitalization for heart failure, any urgent heart failure visit, and left ventricular ejection fraction change at 12 months.17912 months
NCT05155865Conduction System Pacing Versus Biventricular Pacing for Cardiac resynchronization (CSP-SYNC)SloveniaActive, not recruitingInterventional
Randomized
Parallel assignment
Open label
Change in left ventricular volume, left ventricular ejection fraction, difference in heart failure class, proBNP value, 6-min walk test distance, EQ-5D index score6212 months
NCT05760924Left Bundle Branch Pacing on Outcomes and Ventricular Remodeling in Biventricular CRT Nonresponders (RESCUE)RussiaNot yet recruiting Randomized
Parallel assignment
Open label
All-cause mortality or worsening of heart failure requiring unplanned hospitalization (%) 3024 months
NCT06207383Atrial Fibrillation Ablation Versus Atrioventricular Nodal Ablation With Conduction System Pacing in Heart Failure (ABACUS trial)GeneveNot yet recruitingInterventional
Randomized
Parallel assignment
Masking single (outcome assessor)
Superiority endpoint: incidence of mortality and cardiovascular hospitalization in each arm
Non-inferiority endpoint: incidence of mortality and heart failure hospitalization in each arm
2201–4 years
NCT06342492Conduction System Vs Surgical Left Ventricular Epicardial Pacing For Coronary Sinus Lead Failure (KCHRRF_CS Lead Failure_0025)USANot yet recruitingObservational
Cohort
Retrospective
Need for lead revision between conduction system pacing (CSP) and transthoracic left ventricular (LV) epicardial pacing approach100N/A
NCT05793502Left Bundle Branch Pacing (LBBP) for the Treatment of Cardiac Dysfunction With Safety and Efficacy Study in Patients With Atrioventricular BlockChina Not yet recruitingProspective
Case-control
Change in LVEF16012 months
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Castagno, D.; Zanon, F.; Pastore, G.; De Ferrari, G.M.; Marcantoni, L. Is Conduction System Pacing a Valuable Alternative to Biventricular Pacing for Cardiac Resynchronization Therapy? J. Cardiovasc. Dev. Dis. 2024, 11, 144. https://doi.org/10.3390/jcdd11050144

AMA Style

Castagno D, Zanon F, Pastore G, De Ferrari GM, Marcantoni L. Is Conduction System Pacing a Valuable Alternative to Biventricular Pacing for Cardiac Resynchronization Therapy? Journal of Cardiovascular Development and Disease. 2024; 11(5):144. https://doi.org/10.3390/jcdd11050144

Chicago/Turabian Style

Castagno, Davide, Francesco Zanon, Gianni Pastore, Gaetano Maria De Ferrari, and Lina Marcantoni. 2024. "Is Conduction System Pacing a Valuable Alternative to Biventricular Pacing for Cardiac Resynchronization Therapy?" Journal of Cardiovascular Development and Disease 11, no. 5: 144. https://doi.org/10.3390/jcdd11050144

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop