Ventricular arrhythmias in patients with functional mitral regurgitation and implantable cardiac devices: implications of mitral valve repair with Mitraclip®.

BACKGROUND: Limited information has been reported regarding the impact of percutaneous mitral valve repair (PMVR) on ventricular arrhythmic (VA) burden. The aim of this study was to address the incidence of VA and appropriate antitachycardia implantable cardiac defibrillator (ICD) therapies before and after PMVR.
METHODS: We retrospectively analyzed all consecutive patients with heart failure with reduce left ventricular ejection fraction (LVEF), functional mitral regurgitation (FMR) grade 3+ or 4+ and an active ICD or cardiac resynchronizer who underwent PMVR in any of the eleven recruiting centers. Only patients with complete available device VA monitoring from one-year before to one year after PMVR were included. Baseline clinical and echocardiographic characteristics were collected before PMVR and at 12-months follow-up.
RESULTS: Ninety-three patients (68.2±10.9 years old, male 88.2%) were enrolled. PMVR was successfully performed in all patients and device success at discharge was 91.4%. At 12-month follow-up, we observed a significant reduction in mitral regurgitation severity, NT-proBNP and prevalence of severe pulmonary hypertension and severe kidney disease. Patients also referred a significant improvement in NYHA functional class and showed a non-significant trend to reserve left ventricular remodeling. After PMVR a significant decrease in the incidence of non-sustained ventricular tachycardia (VT) (5.0±17.8 vs. 2.7±13.5, P=0.002), sustained VT or ventricular fibrillation (0.9±2.5 vs. 0.5±2.9, P=0.012) and ICD antitachycardia therapies (2.5±12.0 vs. 0.9±5.0, P=0.033) were observed.
CONCLUSIONS: PMVR was related to a reduction in arrhythmic burden and ICD therapies in our cohort. 2020 Annals of Translational Medicine. All rights reserved.

Introduction

Heart failure with reduced left ventricular ejection fraction (HFrEF) represents an increasingly prevalent condition associated with a high risk of adverse outcomes despite advances in HF therapies (1). Ventricular arrhythmias (VA) is a major cause of morbidity and mortality in this population, particularly in patients with advanced HFrEF (2). Functional mitral regurgitation (FMR) is a common finding among these patients, with a prevalence around 50% in either ischemic or non-ischemic dilated cardiomyopathy (DCM), and prognosis is poor if medically managed (3,4). From a theorical point of view, chronic MR induces volume overload of the left ventricle (LV) leading to LV adverse remodeling and fibrosis, enhanced myocardial stress and progression of HF (5). All these factors have been identified as potential triggers for VA in patients with HF and may explain that MR is associated to an increased incidence of VA in patients with DCM (6,7).

Percutaneous mitral valve repair (PMVR) with MitraClip® (Abbott Vascular, Santa Clara, USA) has proved to effectively reduce FMR in patients with HFrEF (8). Limited information has been reported regarding the impact of PMVR on VA burden (9,10). The aim of this study was to address the incidence of VA and appropriate antitachycardia pacing (ATP) and defibrillation shocks before and after PMVR in patients with HFrEF, FMR and implantable cardiac devices (ID).

Methods

We retrospectively included all consecutive patients with HF and FMR grade 3+ or 4+ who underwent MitraClip® implantation in any of the eleven participating European centers and fulfilled all the following inclusion criteria: (I) HF symptoms with New York Heart Association (NYHA) functional class ≥ II despite guideline-directed optimal medical therapy (GDOMT); (II) left ventricular ejection fraction (LVEF) ≤40%; (III) active implantable cardiac defibrillator (ICD) or cardiac resynchronization therapy (CRT) with or without ICD, implanted at least one year before PMVR; (IV) complete available device arrhythmic event monitoring from one-year before to one year after MitraClip®. Patients were excluded if they met any of the following exclusion criteria: (I) VT ablation or upgrade procedure for CRT therapy within the 2-year device observation period; (II) loss of follow-up, re-do MitraClip® or cardiac surgery during the first year follow-up after PMVR.

The study was carried out in eleven European high-volume centers. Indication for MitraClip® was discussed in an interdisciplinary heart team including interventional and clinical cardiologists, cardiac surgeons and specialists in cardiovascular imaging. All patients were deemed to be at GDOMT for HF at maximum tolerated doses at the time PMVR was performed according to the referring physician. Preprocedural 2D transthoracic and 3D transesophageal echocardiography were performed in all patients to address morphologic suitability for clip implantation, quantitative MR analysis and LVEF estimation by Simpson biplane method according to the European Association of Cardiovascular Imaging recommendations for heart valve disease and cardiac chambers assessments (11,12). The procedure was performed following standard practices under general anesthesia with fluoroscopic and transesophageal echocardiographic guidance.

Study design is summarized in . Baseline characteristics and procedural outcomes were collected. Available NT-proBNP levels, glomerular filtration rate and echocardiographic data, as well as NYHA functional class and concomitant HF medical therapies were gathered before PMVR and at one-year follow-up. For statistical purposes, we followed the methodology reported in the COAPT trials (8) and considered as significant, changes in HF drugs consistent with a new drug class start or discontinuation, an increase by >100% or a decrease by <50% of preprocedural dose. VA recorded by ID were reviewed within 1-year before and 1-year after PMVR (8). Postprocedural results and clinical adverse events after MitraClip® were defined according to Mitral Valve Academic Research Consortium (MVARC) definitions (13).

Figure S1

Study design flow chart. NYHA, New York Heart Association; HFMT, Heart Failure Medical Therapy; TTE, transthoracic echocardiogram; PMVR, percutaneous mitral valve repair; VA, ventricular arrhythmias.

Frequency and characteristics of VA in all subjects and ICD antiarrhythmic therapies in case of patients with ICD or ICD-CRT were determined by assessment of clinical follow-up reports, device intracardiac recordings and remote monitoring electronic and local databases. Classification of VA events was performed by local experts according to the following prespecified criteria (14): (I) ventricular tachycardia (VT) was defined as a ventricular tachyarrhythmia with a cycle length between 300–400 ms and was classified as sustained (SVT) or non-sustained (NSVT) depending on duration ≥ or <30 seconds (but ≥4 beats), respectively; (II) VT with a cycle length between 400–600 ms were also included if considered clinically relevant (documented symptoms or prompting hospital admission or ICD antiarrhythmic therapy); (III) ventricular fibrillation and rapid VT (RVT) were defined as a sustained VT with a cycle length <300 ms, and analyzed together with SVT; (IV) ATP attempts and shocks in the subgroup of patients with ICD or ICD-CRT were collected only if appropriate (not triggered by any supraventricular arrhythmia or device malfunction).

Continuous variables were summarized as mean ± standard deviation (SD) or as medians and interquartile range (IQR), and were compared using paired or unpaired Student t tests, or the non-parametric Wilcoxon rank sum tests if the normal distribution the variables could not be demonstrated. Derangement from the normal distribution was assessed with the Shapiro-Wilk test. Categorical variables were described as percentages and compared using Chi-square or Fisher exact tests accordingly to expected frequency over or below 5, respectively. McNemar’s or exact binominal tests were used to compare before and after PMVR paired categorical variables depending sample size over or below 25. Survival curves for time-to-event were constructed on the basis of all available follow-up data using Kaplan-Meier estimates and comparisons between groups were performed using the log-rank test. A two-tailed P value <0.05 was regarded as statistically significant. Statistical analyses were performed using STATA software version 14.2.

Results

Study population

Ninety-three subjects (68.2±10.9 years old, male 88.2%) with HFrEF, an active ID and FMR grade 3+ or 4+ who underwent PMVR before December 2018 in one of the recruiting centers were enrolled in this study. Baseline characteristics of the population are summarized in . Included patients had a severely depressed LV function (LVEF 29.4±6.2) and were severely symptomatic at the time of the procedure so that 89.3% had been priorly admitted for HF and/or were in advanced functional class NYHA III–IV.

Table 1

Baseline characteristics of included cohort

Characteristics	Value
Age (years)	68.2±10.9
Men (%)	88.2
Diabetes mellitus (%)	28.0
Ischemic heart disease (%)	60.2
Prior myocardial infarction (%)	52.7
Atrial fibrillation (%)	52.7
Peripheral artery disease or Stroke (%)	19.4
Chronic obstructive pulmonary disease (%)	22.6
Chronic kidney disease with GFR ≤45 mL/min (%)	43.0
Prior heart failure admission (%)	74.2
Implantable cardiac device (%)
ICD	57.0
CRT ± ICD	43.0
Device stimulation (%)
One chamber	46.2
Two chambers	17.2
Three chambers	36.6
Time from device implantation (days)	1,932±1,407
Left ventricular ejection fraction (%)	29.4±6.2
EuroScore logistic (%)	13.1±13.4
EuroScore II (%)	6.2±5.1

GFR, glomerular filtration rate; ICD, implantable cardiac defibrillator; CRT, cardiac resynchronization therapy.

Procedural outcomes

PMVR was successfully performed in all patients (technical success 100%) and more than one clip was implanted in 51 (53.8%) cases. All but 1 (98.9%) patient had a reduction in at least one degree in the severity of preprocedural MR and 90 (96.8%) subjects presented residual MR ≤2+. Postprocedural mean MV gradient was 2.8±1.4 mmHg and 3 (3.2%) patients had a mean gradient >5 mmHg. Major complications occurred in 4 (4.3%) cases: 2 patients had an in-hospital stroke, 1 patient had a cardiac tamponade and 1 patient presented a partial MitraClip® detachment. Overall, device success was 91.4%.

Arrhythmic outcomes

Overall, 55 (59.1%) patients presented at least one VA within the 2-year observation period before and after PMVR. In the year before PMVR, the following VA events were documented: 471 NSVTs in 31 (33.3%) patients, 85 SVT or VF in 28 (30.1%) patients, 151 ATPs in 18 (19.4%) patients and 77 appropriate ICD shocks in 19 (20.4%) patients. In the year after PMVR, we observed the following VA events: 251 NSVTs in 19 (20.4%) patients, 49 SVT or VF in 15 (16.1%) patients, 33 ATPs in 10 (10.8%) patients and 49 appropriate ICD shocks in 12 (12.9%) patients.

After PMVR a significant reduction in the prevalence and incidence of NSVT (32.3% vs. 20.4%, P=0.043; 5.0±17.8 vs. 2.7±13.5 per patient/year, P=0.002), SVT or VF (30.1% vs. 16.1%, P=0.012; 0.9±2.5 vs. 0.5±2.9 per patient/year, P=0.012) and any ICD antitachycardia therapy (31.2% vs. 18.3%, P=0.023; 2.5±12.0 vs. 0.9±5.0 per patient/year, P=0.033) were observed (, ). A non-significant decrease in the burden of appropriate ATP (19.4% vs. 10.8%, P=0.115; 1.6±9.0 vs. 0.4±2.2 per patient/year, P=0.021) or defibrillation shocks (20.4% vs. 12.9%, P=0.167; 0.8±3.5 vs. 0.5±2.9 per patient/year, P=0.235) were also noted.

Table 2

Ventricular arrhythmic burden before and after percutaneous mitral valve repair (events per patient per year) (n=93)

Ventricular arrhythmic events	Before PMVR	After PMVR	P value*
Non-sustained ventricular tachycardia	5.0±17.8	2.7±13.5	0.002
Sustained ventricular tachycardia or Ventricular fibrillation	0.9±2.5	0.5±2.9	0.012
Any ventricular tachycardia	5.9±17.9	3.2±15.4	<0.001
Anti-tachycardia pacing**	1.6±9.0	0.4±2.2	0.021
ICD shock**	0.8±3.5	0.5±2.9	0.235
Any ICD therapy**	2.5±12.0	0.9±5.0	0.033

*, Wilcoxon matched-pairs signed-ranks test; **, among patients with ICD or ICD-CRT.

Figure 1

Proportion of patients who presented ventricular arrhythmias and antitachycardia device therapies before and after MitraClip®. NSVT, non-sustained ventricular tachycardia; SVT, sustained ventricular tachycardia; VT, ventricular tachycardia; VF, ventricular fibrillation; ATP, antitachycardia pacing; ICD, implantable cardiac defibrillator.

Figure 2

Incidence of ventricular arrhythmias and antitachycardia device therapies before and after percutaneous mitral valve repair. NSVT, non-sustained ventricular tachycardia; SVT, sustained ventricular tachycardia; VT, ventricular tachycardia; VF, ventricular fibrillation; ATP, antitachycardia pacing; ICD, implantable cardiac defibrillator.

Echocardiographic outcomes

At one-year follow-up, PMVR was associated with a significant reduction in the degree of MR () so that 79.1% of patients remained with a residual MR ≤2+. Mean transmitral gradient at this point was 3.1±1.9 mmHg. PMVR was also related with a significant reduction in the prevalence of severe pulmonary hypertension (PH) (P=0.027) and to a non-significant reverse LV remodeling ().

Figure 3

Changes in the degree of functional mitral regurgitation (A) and NYHA functional class (B) at 12-month follow-up after percutaneous mitral valve repair.

Table 3

Echocardiographic and clinical changes at one-year follow-up (n=93)

Clinical or echocardiographic findings	Before PMVR	12-month follow-up	P value*
Mitral regurgitation (%)			<0.001
1+	–	38.4
2+	–	40.7
3+	15	11.6
4+	85	9.3
Severe pulmonary hypertension (%)	25.8	14.0	0.027
Left ventricular ejection fraction (mL)	29.2±6.1	30.4±10.3	0.312
Left ventricular end-diastolic volume (mL)	231.8±90.0	220.8±100.4	0.142
Left ventricular end-systolic volume (mL)	165.6±70.7	156.8±83.7	0.153
NYHA functional class (%)			<0.001
I	–	23.3
II	23.7	47.8
III	65.6	25.6
IV	10.8	3.3
NTproBNP (pg/mL)	2,991 [1,676–5,400]	2,460 [1,453–4,368]	0.010
Chronic kidney disease with GFR ≤45 mL/min (%)	43.0	26.9	0.004

NYHA, New Your Heart Association; GFR, glomerular filtration rate.

Clinical outcomes

At one-year follow-up, a significant improvement in NYHA functional class (P<0.001, ) and a significant reduction in NT-proBNP (P=0.010) and in the prevalence of advance chronic kidney disease (CKD) (P=0.004) were found.

Heart failure and antiarrhythmic medical therapy

Patients were deemed to be at optimal GDOMT at the time PMVR was performed: 89.3% were on beta-blockers, 86.2% were either on ACE inhibitors, angiotensin receptor blockers (ARB) or angiotensin receptor-neprilysin inhibitor (ARNI) and 74.2% were on mineralocorticoid receptor antagonist. Documented changes in HF drugs are displayed in . No significant differences were found in the proportion of patients who received each class of HF drug before and after PMVR. Up-titration, down-titration or changes in drug class occurred more frequently within blockers of the renin-angiotensin-aldosterone system. About a third of patients were on amiodarone at the time of MitraClip® procedure, with no significant changes during the entire follow-up.

Table 4

Pharmacological treatment for heart failure and antiarrhythmic drugs at the time percutaneous mitral valve repair was performed and at 12-month follow-up (n=93)

Medical therapy	Baseline	12-month Follow-up	P value
Beta-blockers (%)	89.3	89	1.0
Decrease dose by >50% or discontinue (%)	–	7.7
Increase dose by >100% or new drug class started (%)	–	7.7
ACEI/ARBII/ARNI (%)	86.2	84.2	1.0
Decrease dose by >50% or discontinue (%)	–	22
Increase dose by >100% or new drug class started (%)	–	20.4
Mineralocorticoid receptor antagonists (%)	74.2	67.0	0.263
Decrease dose by >50% or discontinue (%)	–	16.5
Increase dose by >100% or new drug class started (%)	–	7.9
Amiodarone (%)	30.1	29.9	0.804

ACEI, angiotensin converting enzyme inhibitor; ARB, angiotensin receptor blocker; ARNI, angiotensin receptor-neprilysin inhibitor.

Discussion

This study addressed the impact of MitraClip® on the incidence of VA among a multicenter cohort of patients with advanced HFrEF, moderate to severe FMR and ID who remained symptomatic despite GDOMT. The main finding of our report was that PMVR was associated with a significant decrease in overall VA and ICD therapies. Furthermore, a significant reduction in MR, NTproBNP and prevalence of severe PH and advanced CKD, as well as a significant improvement in NYHA functional class were noted at 12-month follow-up after MitraClip®. Some issues should be highlighted regarding these results.

From a pathological perspective, MR prompts a volume overload to left cardiac chambers leading to increased myocardial stress and progressive LV remodeling (5) and fibrosis (15), both associated with the development of VA (16,17). In fact, moderate to severe MR was independently associated with the incidence VA in patients with dilated cardiomyopathy (18). Theoretically, correcting MR may break the vicious circle of FMR, volume overload, LV remodeling and more FMR, preventing further disease progression and thus, reducing VA burden. In this regard, left ventricular unloading has been previously associated with a reduction in myocardial stress and arrhythmic burden in a preclinical model (19).

Previous studies, in accordance with our research, reported an effective reduction in MR severity after PMVR (8), which translated into a significant increase in cardiac output and a significant reduction in LV filling pressures and PH in invasive observational series of advanced HFrEF (20). In parallel, in our series a significant reduction in NTproBNP and in the prevalence of severe PH were documented at 12-month follow-up. NTproBNP is considered a major non-invasive marker of myocardial stress and has been independently related with the risk of VA (21). Similar reductions in brain natriuretic peptides in patients with HFrEF and FMR have been reported before in observational studies (18) and, more recently, in the COAPT randomized controlled trial after PMVR. In a subanalysis of this trial, MitraClip® was related to a significant reduction in BNP at 6 and 12 months, while no significant changes were observed in the conservative arm (22).

Disease progression facilitates the development of arrhythmic triggers and substrate (23). Advanced NYHA functional class and impaired renal function, as markers of advanced HF, have been previously identified as independent predictors of sudden cardiac death and appropriate device therapies in patients with an ICD (24,25). Parallelly to hemodynamic enhancement, clinical improvement after MitraClip® has been consistently found in patients with FMR (26), although conflicting results were reported in recent randomized controlled trials (RCTs) regarding the superiority of this therapy over stand-alone medical treatment (8,27). Similarly, Wang et al. (28) published a statistically significant increase in GFR in patients with advanced CKD associated to the reduction in MR severity. As such, PMVR was related to a significant improvement in symptoms and to a reduction in the prevalence of advanced CKD at 12-month follow-up in our series.

On the contrary, although LV volumes tended to be lower at 12-month, no significant LV reverse remodeling was found in our cohort. In a recent meta-analysis including over 1,200 patients with FMR from 16 observational reports, a significant, albeit modest, favorable LA and LV remodeling was noted after PMVR (29). Nevertheless, these results were not reproduced in recent RCTs (8,27). In the COAPT study, despite reductions in brain natriuretic peptides and favorable clinical outcomes, LV dimension did increase and LVEF was reduced over time, with less negative remodeling in the interventional group at 12-month follow-up (30).

VA burden is related to pump failure progression (23) and increased rates of re-hospitalizations for HF and death (31). Furthermore, VA and sudden cardiac death are a frequent cause of mortality in patients with advanced HF (32) and ICD shocks also impair their prognosis (33). Little information is available regarding the impact of MitraClip® in the occurrence of VA and defibrillation shocks. A reduction in the incidence of VA and ICD therapies after successful PMVR were found in a small cohort of patients with HFrEF and FMR who had either a pacemaker, ICD or CRT implanted (9). Similarly, Ledwoch et al. (10) documented by 24-hour electrocardiographic monitoring a reduction in ectopic ventricular activity, NSVT and SVT at 6-month follow-up after PMVR. Whether these changes have any impact on mortality, has not been evaluated. To date, conflicting results of recently published RCTs regarding the survival impact of MitraClip® implantation over stand-alone medical treatment in patients with FMR makes this question yet unsolved (34).

Pharmacological HF therapies have shown to improve clinical outcomes in patients with HFrEF (35). Furthermore, a positive impact on VA burden and in the incidence of sudden cardiac death in this population has also been reported for most HF drugs (23). In our study, no major changes in the proportion of patients treated with either beta-blockers, renin-angiotensin system inhibitors or mineralocorticoid receptor antagonists were documented before and at 1-year after PMVR. Nevertheless, mild to moderate changes in dosing and type of drug administration occurred within follow-up that could influence the VA burden and even the clinical outcome of our patients. Unfortunately, this relation could not be evaluated from the data obtained in our study.

Limitations

To the best of our knowledge this is the largest multicenter registry to address VA and ICD therapies in patients with HFrEF, FMR and ID undergoing PMVR. Nevertheless, our study has some limitations. First, the retrospective design might have introduced selection bias, some confounding variables associated to the incidence of VA could be missed or inaccurate event adjudication. At this regard, invasive and non-invasive dedicated antiarrhythmic therapies were taken into consideration. Thus, patients who underwent VT ablation or upgrade to CRT during the observation period were excluded and concomitant administration of amiodarone was evaluated before PMVR and after the one year follow-up. On the contrary, differences in device programming, changes in the dose of antiarrhythmic drugs as a result of a documented VA, metabolic disturbances and incidence of new ischemic coronary events or revascularization procedures were not addressed. Regarding arrhythmic events adjudication, most patients were under device home monitoring which facilitates accurate recordkeeping. Second, a multilevel analysis was not performed to evaluated differences in baseline characteristics in-between patients from different participating centers. Third, patients who died before completing one year follow-up after PMVR were not included in the analysis, which may have underestimated the incidence of VA after MitraClip® since those might be the sickest subgroup of patients. Four, no control group was enrolled.

Conclusions

In conclusion, PMVR was related to a reduction in arrhythmic burden and ICD therapies in our cohort. Given the inherent limitations of this study, the results reported should be interpreted with caution as hypothesis generating. Further investigation should be performed to confirm these findings and address their potential impact on clinical outcomes.

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