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Vol. 33. Issue 11.
Pages 717-725 (November 2014)
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Vol. 33. Issue 11.
Pages 717-725 (November 2014)
Review article
Open Access
Cardiac resynchronization therapy in patients with atrial fibrillation: A meta-analysis
Terapêutica de ressincronização cardíaca em doentes com fibrilhação auricular: uma metanálise
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Cláudia Lopesa,
Corresponding author
claudia.o.lopes@hotmail.com

Corresponding author.
, Telmo Pereiraa, Sérgio Barrab
a Escola Superior de Tecnologia das Saúde de Coimbra, Departamento de Cardiopneumologia, Coimbra, Portugal
b Centro Hospitalar e Universitário de Coimbra, Departamento de Cardiologia, Coimbra, Portugal
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Table 1. Characteristics of the included studies.
Abstract
Background and Objective

To combine the results of the best scientific evidence in order to compare the effects of cardiac resynchronization therapy (CRT) in heart failure patients with atrial fibrillation (AF) and in sinus rhythm (SR) and to determine the effect of atrioventricular nodal ablation in AF patients.

Methods

The electronic databases PubMed, B-On and Cochrane CENTRAL were searched, and manual searches were performed, for randomized controlled trials and cohort studies up to November 2012. The endpoints analyzed were all-cause and cardiovascular mortality and response to CRT.

Results

We included 19 studies involving 5324 patients: 1399 in AF and 3925 in SR. All-cause mortality was more likely in patients with AF compared to patients in SR (OR=1.69; 95% CI: 1.20–2.37; p=0.002). There were no statistically significant differences in cardiovascular mortality (OR=1.36; 95% CI: 0.92–2.01; p=0.12). AF was associated with an increased likelihood of lack of response to CRT (OR=1.41; 95% CI: 1.15–1.73; p=0.001). Among subjects with AF, ablation of the atrioventricular node was associated with a reduction in all-cause mortality (OR=0.42; 95% CI: 0.22–0.80; p=0.008), cardiovascular death (OR=0.39; 95% CI: 0.20–0.75; p=0.005) and the number of non-responders to CRT (OR=0.30; 95% CI: 0.10–0.90; p=0.03).

Conclusions

The presence of AF is associated with increased likelihood of all-cause death and non-response to CRT, compared to patients in SR. However, many patients with AF benefit from CRT. Atrioventricular nodal ablation appears to increase the benefits of CRT in patients with AF.

Keywords:
Atrial fibrillation
Cardiac resynchronization therapy
Atrioventricular nodal ablation
Meta-analysis
Resumo
Introdução e objetivos

Combinar os resultados da melhor evidência científica de forma a comparar os efeitos da terapêutica de ressincronização cardíaca (TRC) em doentes com insuficiência cardíaca em fibrilhação auricular (FA) e em ritmo sinusal (RS) e determinar a influência da ablação auriculoventricular (AV) no grupo de doentes em FA.

Métodos

A pesquisa realizou-se nas bases de dados eletrónicas da PubMed, B-On e CENTRAL e de forma manual, incluindo ensaios clínicos controlados aleatorizados e estudos de coorte até novembro de 2012. Analisou-se a mortalidade total e cardiovascular e a resposta à TRC.

Resultados

Foram incluídos 19 estudos que envolveram 5324 pacientes: 1399 em FA e 3925 em RS. O grupo com doentes em FA apresenta maior risco de mortalidade total, comparativamente ao grupo de doentes em RS (OR=1,69; IC 1,20–2,37, p=0,002). Não foram verificadas diferenças estatisticamente significativas quanto à mortalidade cardiovascular (OR=1,36, IC 0,92–2,01, p=0,12). A não resposta à TRC foi maior no grupo em FA (OR=1,41; IC 1,15–1,73; p=0,001). Entre os indivíduos em FA, a ablação do nódulo auriculoventricular foi associada à redução da mortalidade total (OR=0,42; IC 0,22–0,80; p=0,008), mortalidade cardiovascular (OR=0,39; IC 0,20–0,75; p=0,005) e número de não respondedores à TRC (OR=0,30; IC 0,10–0,90; p=0,03).

Conclusões

A presença de FA está associada a maior probabilidade de morte por todas as causas e de não resposta à TRC, comparativamente aos doentes em RS. Contudo, um número significativo de doentes em FA beneficia da TRC. A ablação AV parece aumentar os benefícios da TRC nos doentes com FA.

Palavras-chave:
Fibrilhação auricular
Terapêutica de ressincronização cardíaca
Ablação auriculoventricular
Metanálise
Full Text
Introduction

Atrial fibrillation (AF) is the most common arrhythmia in patients with heart failure (HF) and is associated with increased mortality and morbidity.1 About 20% of patients treated with cardiac resynchronization therapy (CRT) are in AF.2,3 Despite the high prevalence of AF in patients with HF and the fact that many meet the criteria for CRT, randomized controlled trials have excluded these patients in most cases.4 Thus, the effect of this therapy in patients with AF is still controversial.

Notwithstanding this controversy, according to the American Heart Association, American College of Cardiology and Heart Rhythm Society guidelines, CRT is a class IIa recommendation (level of evidence B) for patients with AF, left ventricular ejection fraction (LVEF) ≤35% and ventricular dyssynchrony, since a high percentage of biventricular capture can be ensured. Atrioventricular (AV) nodal ablation should be performed in cases of incomplete biventricular capture.5

AV nodal ablation offers the most effective method for rate control in AF patients, by creating a complete heart block and regularizing cardiac rhythm through permanent pacing. This approach enables complete biventricular pacing.6 Nevertheless, the importance of AV nodal ablation (compared to pharmacologic therapy) in achieving an optimized response to CRT in AF patients remains unclear.

The meta-analyses published by Upadhyay et al. in 20087 and by Wilton et al. in 20118 suggested significant differences in outcomes between patients in SR and those in AF, highlighting the need for further research.6

The aim of this meta-analysis was to investigate the effects of CRT in patients with AF compared with patients in SR, and to evaluate the effect of AV nodal ablation in the former group. To the best of our knowledge, this is the most recent and up-to-date meta-analysis on this subject.

MethodsSearch strategy

Searches were conducted in the electronic databases PubMed, B-On, and Cochrane Central Register of Controlled Trials, and included the following terms: “atrial fibrillation”, “heart failure”, “congestive heart failure”, “congestive cardiac failure”, “chronic heart failure”, “chronic cardiac failure”, “resynchronization therapy”, “cardiac resynchronization therapy”, “cardiac resynchronization”, “heart resynchronization”, “artificial biventricular pacemaker”, “biventricular pacemaker”, “biventricular pacing”, “biv”, “dual-chamber pacing”, “dual-chamber pacemaker”, “atrioventricular nodal ablation”, “atrioventricular junction ablation”, “ablation pacing”, “ablation techniques”, “ablation”, “AV nodal ablation”, “AVJ ablation”.

We considered studies in humans, published and unpublished, written in English or Portuguese, up to November 2012. In addition, we performed a manual search of abstracts in journals and conferences and in reference lists of selected articles.

Inclusion criteria

We included studies that met all of the following criteria: randomized controlled trials or cohort studies; individuals with a diagnosis of HF in NYHA class II–IV with LVEF ≤35%, in AF or SR; comparison between patients in AF and SR; implantation of cardiac resynchronization devices; study of all-cause mortality, cardiovascular mortality, non-responders to therapy and follow-up ≥6 months.

Data extraction

From each study, the following data were extracted and analyzed: characteristics of the study population, study design, methodological criteria, interventions, outcomes of interest and results. All text, tables and figures were reviewed for data extraction.

The primary endpoint was all-cause mortality. The secondary endpoints included cardiovascular mortality and non-response to CRT. If the investigators reported endpoints at two different follow-up times, endpoints for the longest available duration of follow-up were used.

Quality assessment

Assessment of studies’ quality and eligibility and their selection were performed independently by two investigators. Studies that did not meet the inclusion criteria were excluded from the meta-analysis. Disagreements were resolved by consensus. We included articles by the same author(s) if they had different samples or analyzed different outcomes.

The quality of included studies was assessed using a checklist developed by the reviewers. This instrument analyzed a series of items involving methodology, participants, interventions and outcomes, designed to minimize bias.

Statistical analysis

The statistical analysis was performed with Review Manager (RevMan) statistical software, version 5.1.

For dichotomous clinical outcomes, overall estimation of the treatment effect was performed with the Peto statistical method, through a random effects model. Odds ratios (OR) and corresponding 95% confidence intervals were calculated, and the Z-test was used to determine the statistical significance of the estimated overall effect. Statistical heterogeneity was quantified using Cochran's chi-square test. The I2 statistic was also calculated to assess the inter-study consistency of the results. An I2 of 25%, 50% and 75% indicates low, moderate or high heterogeneity, respectively. Sensitivity analysis was performed to identify reasons for heterogeneity. Different strategies included changing criteria for inclusion of studies according to their methodological characteristics; exclusion of studies that showed some ambiguity in their inclusion criteria; exclusion of unpublished studies; and re-evaluation of the data using different statistical methods, such as calculation of risk ratios (RR) instead of OR, calculated by both fixed and random effect models. These multivariate analyses were performed to determine whether modification of some criteria would be sufficient to change the combined result and thus assess the degree of confidence of the results of the meta-analysis.

A funnel plot was used to assess publication bias. This analysis identifies inter-study asymmetries that should be explored. In the absence of bias, dispersion of the points of the plot is similar to a symmetric pyramid. The presence of asymmetry in the graph suggests the existence of publication bias.

A p-value of <0.05 was adopted as the criterion for statistical significance.

ResultsSearch results

The search retrieved 470 potentially relevant articles. The first stage of selection, based on titles, excluded 365 articles. Of the 105 studies considered, 75 were excluded after examination of the abstract. The full text of the remaining 30 publications was examined in more detail. Finally, 19 articles were included in our meta-analysis (Figure 1).

Figure 1.

Flow diagram of article selection. SR: sinus rhythm.

(0.23MB).
Description of included studies

Table 1 summarizes the characteristics of the included articles, which involved a total of 5325 patients (1399 with AF and 3925 in SR). Mean age was 67.7 years in the AF patients and 66.2 years in the SR patients. Comparing patients with and without AF, the proportion of males was 81.3% vs. 75.1%, ischemic cardiomyopathy was present in 40.6% vs. 45.5%, LVEF was 24.5% vs. 24.3%, and QRS duration was 171.8 ms vs. 167.9 ms, respectively. Most participants reported symptoms of advanced HF (NYHA functional class III and IV). Length of follow-up ranged from 6 to 34 months.

Table 1.

Characteristics of the included studies.

Study  Type  Patients (n)Age (years)Men (%)Follow-up (months)CRT-D (n)
    AF  SR  AF  SR  AF  SR  AF  SR  AF  SR 
Leclercq at al.35  Prosp  15  22  68±6  67±8  –  –  14  14  –  – 
Linde et al.37  RCT  64  67  65±9  63±10  81  75  12  12  –  – 
Molhoek et al.9  Prosp  30  30  63±10  68±8  90  80  19  25  13  15 
Gasparini et al.40  Prosp  162  511  66±8  63±10  86  77  25  26  79  299 
Delnoy et al.18  Prosp  96  167  73±8  72±9  75  68  23  23  –  – 
Buck et al.12  Prosp  56  58  63±11  62±12  70  79  18  18  –  – 
Ferreira et al.10  Retrosp  53  78  69±9  66±10  94  74  29  29  43  59 
Gasparini et al.4  Retrosp  243  42  66±9  63±10  82  75  34  34  –  – 
Khadjooi et al.43  Prosp  86  209  72±10  68±11  86  77  24  22  –  – 
Tolosana et al.15  Retrosp  126  34  69±7  67±9  81  76  12  12  65  215 
Schütte et al.44  Retrosp  36  64  –  –  –  –  11  11  –  – 
Kim et al.13  –  26  96  –  –  –  –  –  – 
Wo et al.11  Retrosp  16  40  68±13  66±14  69  67  –  – 
Luedorff et al.16  Retrosp  139  445  71±7  68±9  81  71  24  24  –  – 
Wilton et al.17  Retrosp  19  67  68±7  69±12  89  88  34  34  –  – 
Tolosana et al.14  Retrosp  46  156  68±9  66±9  71  77  12  12  33  136 
Himmel et al.45  Prosp  46  230  69±9  70±8  –  –  12  12  –  – 

Data expressed as mean ± SD. AF: atrial fibrillation; CRT-D: cardiac resynchronization therapy with defibrillator; Prosp: prospective; RCT: randomized controlled trial; Retrosp: retrospective; SR: sinus rhythm.

Diuretics were prescribed in 90% vs. 85% of patients, beta-blockers in 66% vs. 70%, angiotensin-converting enzyme inhibitors/angiotensin receptor blockers in 94% vs. 90%, amiodarone in 35% vs. 22% and digitalis in 56% vs. 39% in the AF and SR groups, respectively.

There were statistically significant differences in baseline characteristics between patients with AF and SR in most studies included.

All-cause mortality

When the results of the 11 randomized trials were pooled, the odds ratio for overall mortality was 1.69 (95% confidence interval [CI]: 1.20–2.37; p=0.002), meaning a 69% higher probability of death in patients with AF compared with patients in SR. We found statistical evidence of moderate heterogeneity (I2=54%; p=0.02) (Figure 2).

Figure 2.

Forest plot comparing all-cause mortality in patients with atrial fibrillation and sinus rhythm. AF: atrial fibrillation; M-H: Mantel-Haenszel; SR: sinus rhythm.

(0.31MB).

We explored potential causes of heterogeneity between studies through sensitivity analyses. After exclusion of an unpublished study (Nascimento C, Pereira T, Providência R, Rodrigues P), there was no change in the pooled estimate using a random effects model (OR: 1.74; 95% CI: 1.18–2.57; p=0.005; I2=59%). The inclusion of six studies in which no individuals underwent AV nodal ablation resulted in a total effect of 1.58 (95% CI: 0.97–2.56; p=0.06), with heterogeneity of 47%, compared to an OR of 1.87 (95% CI: 1.08–3.23; p=0.02) and heterogeneity of 68% in the other five studies.

Excluding studies that included patients in NYHA class II, the increase in all-cause mortality in AF patients was even more pronounced (OR: 2.14; 95% CI: 1.47–3.09; p<0.0001; I2=32%). In the sensitivity analysis that included only cohort studies, a similar increase in all-cause mortality was observed (OR: 1.76; 95% CI: 1.22–2.54; p=0.003; I2=58%).

In order to explore statistical heterogeneity and investigate potential publication bias, a funnel plot was constructed, which revealed qualitative evidence of asymmetry in the distribution of the estimated effects in several studies. The analysis of all-cause mortality was redone excluding studies with greater dispersion. This produced an OR of 1.38 (95% CI: 1.07–1.78), a statistically significant difference (p=0.01), and a decrease in heterogeneity (I2=20%).

Cardiovascular mortality

Pooled analysis of six studies comparing cardiovascular mortality in patients with AF and SR after treatment with CRT showed no statistically significant differences between groups (OR: 1.36; 95% CI: 0.92–2.01; p=0.12), although there was a trend in favor of the SR group. There was mild heterogeneity (I2=33%; p=0.19) (Figure 3).

Figure 3.

Cardiovascular mortality for patients with atrial fibrillation versus sinus rhythm. AF: atrial fibrillation; M-H: Mantel-Haenszel; SR: sinus rhythm.

(0.21MB).
Non-response to cardiac resynchronization therapy

Response to CRT was defined as improvement of one NYHA functional class after six months,9,10 decrease in left ventricular end-systolic volume (LVESV) of 10% or 15% measured by cardiac ultrasound,2,11–13 or improvement in absolute LVEF of ≥5% after three months.13 In studies by Tolosana et al.,14,15 clinical responders were defined as those with an increase of ≥10% in the 6-minute walk test 12 months after implantation or improvement of at least one NYHA functional class. Echocardiographic responders were defined as patients who had a ≥10% reduction in LVESV.14 Other trials used a definition of CRT response that required both objective symptomatic improvement in quality of life and a ≥15% reduction in LVESV.8,13

The rate of non-response to CRT was significantly higher in individuals with AF (OR=1.41, 95% CI: 1.15–1.73, p=0.001). No statistical heterogeneity was found (I2=0%) (Figure 4). The overall mean proportion of responders was 65% in those with AF and 71% in those in SR. Excluding the three studies that included patients with paroxysmal AF gave similar results (OR=1.56, 95% CI: 1.23–1.99, p=0.0002, I2=0%).

Figure 4.

Meta-analysis of the odds ratios of non-response to cardiac resynchronization therapy in patients with atrial fibrillation and sinus rhythm. AF: atrial fibrillation; M-H: Mantel-Haenszel; SR: sinus rhythm.

(0.28MB).
The role of atrioventricular nodal ablation

We identified two studies that evaluated the impact of ablation on all-cause mortality in AF patients. In these studies, mortality was 58% (OR=0.42) lower in the group who underwent AV nodal ablation. Pooled analysis of three studies showed that cardiovascular mortality was 61% (OR=0.39) lower in this group than in those who did not undergo AV nodal ablation. In both analyses, the overall effect was statistically significant (p=0.008 and p=0.005, respectively), with no evidence of heterogeneity between studies (I2=0%) (Figure 5).

Figure 5.

Meta-analysis comparing all-cause mortality (A) and cardiovascular mortality (B) in patients with atrial fibrillation who did or did not undergo atrioventricular nodal ablation. ABL: atrioventricular nodal ablation; AF: atrial fibrillation; NABL: no atrioventricular nodal ablation (pharmacological therapy); SR: sinus rhythm.

(0.32MB).

In four studies analyzed, the likelihood of non-response to CRT was 69% lower in patients treated by ablation (OR: 0.31; 95% CI: 0.10–0.97; p=0.04; I2=72%). There was moderate inconsistency, which means the results should be treated with caution.

Discussion

This meta-analysis suggests that AF, compared to SR, is associated with increased all-cause mortality in patients undergoing CRT. This finding was particularly robust when re-evaluated in sensitivity analyses performed to explore heterogeneity. Furthermore, although cardiovascular mortality was not significantly different between groups, there was a trend in favor of SR, and the large standard deviation in some studies may have reduced the statistical significance of their results. Therefore, we cannot exclude small differences in cardiovascular mortality between patients with AF and SR. Finally, our meta-analysis suggests that AV nodal ablation decreases all-cause and cardiovascular mortality in AF patients. To the best of our knowledge, this is the most recent and up-to-date meta-analysis on this subject, which increases its clinical applicability.

Our findings are consistent with those of other studies.9,14,16,17 In a systematic review and meta-analysis of 23 studies, Wilton et al. suggested that AF was associated with a weaker clinical response to CRT and an increased risk of death from any cause.8 By contrast, Molhoek et al.9 and Delnoy et al.18 found no differences in survival between subjects with AF and SR. Some investigators have suggested that digoxin and amiodarone may increase morbidity and mortality in patients with HF.19–21 Some studies included in this meta-analysis showed significant differences in medication between the AF and SR groups, with more patients in the former treated with these drugs. This difference may have contributed to a worsening of all-cause mortality in these patients.

The Resynchronization for Ambulatory Heart Failure Trial (RAFT) randomized patients to an implantable cardioverter-defibrillator (ICD) and cardiac resynchronization therapy with defibrillator (CRT-D) in patients with permanent AF and found no differences in cardiovascular mortality, heart failure hospitalization, 6-minute walk test or rate of perioperative complications.22 Our meta-analysis contradicts these findings to some extent, as a clear benefit from CRT was shown in the AF group.

Patients with AF had a higher rate of lack of response to CRT. The rates of non-response in the two groups were similar to those of previous studies,9,11,23,24 despite the fact that the definition of response to CRT differs widely in the literature.25 In their 2011 meta-analysis of 23 studies, Wilton et al. reported higher rates of non-response to CRT in patients with AF and a clinical benefit from AV nodal ablation in this group,8 which is corroborated by our findings. In fact, our meta-analysis strongly suggests the ablation procedure may be associated with increased survival and response rate to CRT in subjects with AF.

Considering that AF in patients with HF is associated with worse prognosis and higher mortality,26 a higher adverse event rate and a lower probability of response to CRT would be expected in these patients. In this context, the benefits found in patients with this arrhythmia, although less than those reported in patients in SR, are clinically significant and may be proportional; in other words, CRT could have the same impact in patients in SR and AF when adjusted for the overall greater comorbidity and frailty of the latter group. On the other hand, the possibility that AF impacts directly on the outcome of CRT should be considered, as AF has already been unequivocally demonstrated to predict mortality in patients with structural cardiac abnormalities and HF.15,27–30 Our results suggest that CRT benefits patients with AF, even if less than those in SR.

AF can directly impair the function of CRT devices by reducing biventricular capture, due to loss of AV synchrony and rapid and irregular ventricular rate, which has been associated with adverse outcomes.31,32 Therefore, AV junction ablation may be of particular value, as it ensures adequate biventricular pacing in patients with AF. Nevertheless, potential benefits must be balanced against the risks associated with pacemaker dependency. Observational studies have investigated the effects of AV nodal ablation in patients with HF and AF treated with CRT and demonstrated benefits in left ventricular systolic function, NYHA class, mitral regurgitation and exercise capacity.9,10,33–38 A study by Brignole et al. included 186 patients randomized to CRT or conventional right ventricular (RV) pacing following AV junction ablation. These investigators proposed that CRT is superior to RV apical pacing in reducing the clinical manifestations of HF in patients with AF, providing further evidence that CRT is effective in patients with AF, especially if AV junction ablation is performed concurrently.39 Gasparini et al. found that patients with AF who underwent AV nodal ablation showed significant improvement in LVEF, NYHA class and exercise capacity, a better response to CRT and faster reverse remodeling. All-cause mortality was significantly lower in patients with AV nodal ablation compared with those treated pharmacologically. These data, together with the findings of our meta-analysis, suggest that patients with AF can benefit from ablation and pacing.4,40 AV nodal ablation ensures 100% capture and heart rate control, which are difficult to achieve with pharmacological treatment, overcoming the deleterious effects of rapid and irregular ventricular rate and competitive pacing.41 In fact, in the 2013 ACCF/HRS/AHA/ASE/HFSA/SCAI/SCCT/SCMR Appropriate Use Criteria, CRT was deemed appropriate to use in any situation where >40% RV pacing is anticipated, such as after AV junction ablation.42 Moreover, AV nodal ablation enables discontinuation of drugs such as digoxin and amiodarone, which can have a positive impact on mortality and morbidity in patients with HF, as mentioned above.

Notwithstanding such considerations, some authors have found that prognosis and symptomatic benefits are similar between patients with and without AV nodal ablation,15,19,43,44 adding to the controversy surrounding the subject. In a study by Himmel et al., no significant differences were found in functional status, LVEF or left ventricular end-diastolic dimensions between patients with and without AV nodal ablation. This suggests that AV nodal ablation might not be strictly required in all patients with permanent AF and biventricular pacemaker.45

A meta-analysis with similar objectives to ours was previously published,8 but ours also reported cardiovascular mortality in patients with AF and SR, as well as comparing mortality in AF patients who did or did not undergo AV nodal ablation.

In conclusion, the current meta-analysis confirms that CRT should not be ruled out in AF patients as it can have a positive impact on their clinical outcomes, especially when combined with AV nodal ablation.

Study limitations

Our study has several limitations. First, this meta-analysis included mainly observational studies, some with small sample sizes, rather than randomized controlled trials. Thus, we cannot exclude confounding factors as an alternative explanation for our results. Significant differences in baseline characteristics were noted between AF and SR patients in a number of studies. The conclusions of this analysis are limited by the available data. Another possible limitation of our study is the influence of publication bias. However, we included articles with several study designs, as well as abstracts and unpublished studies, so as to reduce the risk of publication bias and improve the sensitivity and power of the meta-analysis.

Significant heterogeneity was present in several analyses and was an important limitation. We applied sensitivity analysis to explore the reasons for heterogeneity.

Further limitations were: differences in total number of patients in each group, with fewer subjects in AF; small numbers of patients who underwent AV nodal ablation; differences in duration of follow-up; inclusion of individuals in paroxysmal, persistent and permanent AF; and the lack of a uniform definition of response to CRT. Finally, the lack of information regarding programming of resynchronization devices and left ventricular lead position may have impaired the homogeneity of the samples.

Conclusions

Patients with HF and AF benefit from CRT, although less than patients in SR. However, the former group is at increased risk of all-cause mortality and shows a higher non-response rate to CRT. AV nodal ablation is associated with a reduction in all-cause and cardiovascular mortality and non-response rate. Therefore, it seems reasonable to consider AV nodal ablation in patients with AF, although the exact extent of the benefits, and the long-term safety of this approach, still remain to be determined. Large randomized trials are needed to confirm our findings.

Ethical disclosuresProtection of human and animal subjects

The authors declare that no experiments were performed on humans or animals for this study.

Confidentiality of data

The authors declare that no patient data appear in this article.

Right to privacy and informed consent

The authors declare that no patient data appear in this article.

Conflicts of interest

The authors have no conflicts of interest to declare.

References
[1]
K. Dickstein, P.E. Vardas, A. Auricchio, et al.
2010 Focused Update of ESC Guidelines on device therapy in heart failure: an update of the 2008 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure and the 2007 ESC guidelines for cardiac and resynchronization therapy. Developed with the special contribution of the Heart Failure Association and the European Heart Rhythm Association.
Eur Heart J, 31 (2010), pp. 2677-2687
[2]
M. Gasparini, M. Lunati, M. Santini, et al.
Long-term survival in patients treated with cardiac resynchronization therapy: a 3-year follow-up study from the InSync/InSync ICD Italian Registry.
Pacing Clin Electrophysiol, 29 (2006), pp. S2-S10
[3]
J. Geng, B. Wu, L. Zheng, et al.
Heart failure patients selection for cardiac resynchronization therapy.
Eur J Intern Med, 22 (2011), pp. 32-38
[4]
M. Gasparini, A. Auricchio, M. Metra, et al.
Long-term survival in patients undergoing cardiac resynchronization therapy: the importance of performing atrio-ventricular junction ablation in patients with permanent atrial fibrillation.
Eur Heart J, 29 (2008), pp. 1644-1652
[5]
A.E. Epstein, J.P. DiMarco, K.A. Ellenbogen, et al.
ACC/AHA/HRS 2008 guidelines for device-based therapy of cardiac rhythm abnormalities: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Revise the ACC/AHA/NASPE 2002 Guideline Update for Implantation of Cardiac Pacemakers and Antiarrhythmia Devices) developed in collaboration with the American Association for Thoracic Surgery and Society of Thoracic Surgeons.
J Am Coll Cardiol, 51 (2008), pp. e1-e62
[6]
G.S. Kamath, J.S. Steinberg.
Cardiac resynchronization therapy and atrial fibrillation.
Cardiol J, 16 (2009), pp. 4-10
[7]
G.A. Upadhyay, N.K. Choudhry, A. Auricchio, et al.
Cardiac resynchronization in patients with atrial fibrillation: a meta-analysis of prospective cohort studies.
J Am Coll Cardiol, 52 (2008), pp. 1239-1246
[8]
S.B. Wilton, A.A. Leung, W.A. Ghali, et al.
Outcomes of cardiac resynchronization therapy in patients with versus those without atrial fibrillation: a systematic review and meta-analysis.
Heart Rhythm, 8 (2011), pp. 1088-1094
[9]
S.G. Molhoek, J.J. Bax, G.B. Bleeker, et al.
Comparison of response to cardiac resynchronization therapy in patients with sinus rhythm versus chronic atrial fibrillation.
Am J Cardiol, 94 (2004), pp. 1506-1509
[10]
A.M. Ferreira, P. Adragão, D.M. Cavaco, et al.
Benefit of cardiac resynchronization therapy in atrial fibrillation patients vs. patients in sinus rhythm: the role of atrioventricular junction ablation.
Europace, 10 (2008), pp. 809-815
[11]
H.-T. Wo, P.-C. Chang, T.-H. Chen, et al.
Cardiac resynchronization therapy in patients with and without atrial fibrillation.
Acta Cardiol Sin, 27 (2011), pp. 46-51
[12]
S. Buck, M. Rienstra, A.H. Maass, et al.
Cardiac resynchronization therapy in patients with heart failure and atrial fibrillation: importance of new-onset atrial fibrillation and total atrial conduction time.
Europace, 10 (2008), pp. 558-565
[13]
K.H. Kim, C. Miyazaki, J.K. Oh, et al.
Differences of the response of cardiac resynchronization therapy according to the presence of atrial fibrillation.
Circulation, 120 (2009), pp. S788
[14]
J.M. Tolosana, A.M. Arnau, A.H. Madrid, et al.
Cardiac resynchronization therapy in patients with permanent atrial fibrillation. Is it mandatory to ablate the atrioventricular junction to obtain a good response.
Eur J Heart Fail, 14 (2012), pp. 635-641
[15]
J.M. Tolosana, A. Hernandez Madrid, J. Brugada, et al.
Comparison of benefits and mortality in cardiac resynchronization therapy in patients with atrial fibrillation versus patients in sinus rhythm (Results of the Spanish Atrial Fibrillation and Resynchronization [SPARE] Study).
Am J Cardiol, 102 (2008), pp. 444-449
[16]
G. Luedorff, R. Grove, M. Kowalski, et al.
Impact of chronic atrial fibrillation in patients with severe heart failure and indication for CRT: data of two registries with 711 patients (1999–2006 and 2007–6/2008).
Herzschrittmacherther Elektrophysiol, 22 (2011), pp. 226-232
[17]
S.B. Wilton, K.M. Kavanagh, S.G. Aggarwal, et al.
Association of rate-controlled persistent atrial fibrillation with clinical outcome and ventricular remodelling in recipients of cardiac resynchronization therapy.
Can J Cardiol, 27 (2011), pp. 787-793
[18]
P.P. Delnoy, J.P. Ottervanger, H.O. Luttikhuis, et al.
Comparison of usefulness of cardiac resynchronization therapy in patients with atrial fibrillation and heart failure versus patients with sinus rhythm and heart failure.
Am J Cardiol, 99 (2007), pp. 1252-1257
[19]
G.H. Bardy, K.L. Lee, D.B. Mark, et al.
Amiodarone or an implantable cardioverter-defibrillator for congestive heart failure.
N Engl J Med, 352 (2005), pp. 225-237
[20]
S.S. Rathore, J.P. Curtis, Y. Wang, et al.
Association of serum digoxin concentration and outcomes in patients with heart failure.
JAMA, 289 (2003), pp. 871-878
[21]
M.G. Whitbeck, R.J. Charnigo, P. Khairy, et al.
Increased mortality among patients taking digoxin – analysis from the AFFIRM study.
Eur Heart J, 34 (2013), pp. 1481-1488
[22]
J.S. Healey, S.H. Hohnloser, D.V. Exner, et al.
Cardiac resynchronization therapy in patients with permanent atrial fibrillation: results from the Resynchronization for Ambulatory Heart Failure Trial (RAFT).
Circ Heart Fail, 5 (2012), pp. 566-570
[23]
W.T. Abraham, W.G. Fisher, A.L. Smith, et al.
Cardiac resynchronization in chronic heart failure.
N Engl J Med, 346 (2002), pp. 1845-1853
[24]
J.J. Bax, T. Abraham, S.S. Barold, et al.
Cardiac resynchronization therapy: Part 2 – issues during and after device implantation and unresolved questions.
J Am Coll Cardiol, 46 (2005), pp. 2168-2182
[25]
A. Auricchio, F.W. Prinzen.
Non-responders to cardiac resynchronization therapy: the magnitude of the problem and the issues.
Circ J, 75 (2011), pp. 521-527
[26]
T.J. Wang, M.G. Larson, D. Levy, et al.
Temporal relations of atrial fibrillation and congestive heart failure and their joint influence on mortality: the Framingham Heart Study.
Circulation, 107 (2003), pp. 2920-2925
[27]
A. Ahmed, P. Thornton, G.J. Perry, et al.
Impact of atrial fibrillation on mortality and readmission in older adults hospitalized with heart failure.
Eur J Heart Fail, 6 (2004), pp. 421-426
[28]
W.S. Aronow, C. Ahn, I. Kronzon.
Prognosis of congestive heart failure after prior myocardial infarction in older persons with atrial fibrillation versus sinus rhythm.
Am J Cardiol, 87 (2001), pp. 224-225
[29]
M.D. Smit, A.H. Maass, H.L. Hillege, et al.
Prognostic importance of natriuretic peptides and atrial fibrillation in patients receiving cardiac resynchronization therapy.
Eur J Heart Fail, 13 (2011), pp. 543-550
[30]
R.J. van Bommel, C.J. Borleffs, C. Ypenburg, et al.
Morbidity and mortality in heart failure patients treated with cardiac resynchronization therapy: influence of pre-implantation characteristics on long-term outcome.
Eur Heart J, 31 (2010), pp. 2783-2790
[31]
B.A. Koplan, A.J. Kaplan, S. Weiner, et al.
Heart failure decompensation and all-cause mortality in relation to percent biventricular pacing in patients with heart failure: is a goal of 100% biventricular pacing necessary?.
J Am Coll Cardiol, 53 (2009), pp. 355-360
[32]
G.S. Kamath, D. Cotiga, J.N. Koneru, et al.
The utility of 12-lead Holter monitoring in patients with permanent atrial fibrillation for the identification of nonresponders after cardiac resynchronization therapy.
J Am Coll Cardiol, 53 (2009), pp. 1050-1055
[33]
I. Hay, V. Melenovsky, B.J. Fetics, et al.
Short-term effects of right-left heart sequential cardiac resynchronization in patients with heart failure, chronic atrial fibrillation, and atrioventricular nodal block.
Circulation, 110 (2004), pp. 3404-3410
[34]
E. Puggioni, M. Brignole, M. Gammage, et al.
Acute comparative effect of right and left ventricular pacing in patients with permanent atrial fibrillation.
J Am Coll Cardiol, 43 (2004), pp. 234-238
[35]
C. Leclercq, S. Walker, C. Linde, et al.
Comparative effects of permanent biventricular and right-univentricular pacing in heart failure patients with chronic atrial fibrillation.
Eur Heart J, 23 (2002), pp. 1780-1787
[36]
A.R. Leon, J.M. Greenberg, N. Kanuru, et al.
Cardiac resynchronization in patients with congestive heart failure and chronic atrial fibrillation: effect of upgrading to biventricular pacing after chronic right ventricular pacing.
J Am Coll Cardiol, 39 (2002), pp. 1258-1263
[37]
C. Linde, C. Leclercq, S. Rex, et al.
Long-term benefits of biventricular pacing in congestive heart failure: results from the MUltisite STimulation in cardiomyopathy (MUSTIC) study.
J Am Coll Cardiol, 40 (2002), pp. 111-118
[38]
K. Dong, W.K. Shen, B.D. Powell, et al.
Atrioventricular nodal ablation predicts survival benefit in patients with atrial fibrillation receiving cardiac resynchronization therapy.
Heart Rhythm, 7 (2010), pp. 1240-1245
[39]
M. Brignole, G. Botto, L. Mont, et al.
Cardiac resynchronization therapy in patients undergoing atrioventricular junction ablation for permanent atrial fibrillation: a randomized trial.
Eur Heart J, 32 (2011), pp. 2420-2429
[40]
M. Gasparini, A. Auricchio, F. Regoli, et al.
Four-year efficacy of cardiac resynchronization therapy on exercise tolerance and disease progression: the importance of performing atrioventricular junction ablation in patients with atrial fibrillation.
J Am Coll Cardiol, 48 (2006), pp. 734-743
[41]
T. Szili-Torok, A. Mihalcz, L. Jordaens.
The ‘Happy Ending Problem’ of cardiac pacing? Cardiac resynchronization therapy for patients with atrial fibrillation and heart failure after atrioventricular junction ablation.
Europace, 10 (2008), pp. 779-781
[42]
A.M. Russo, R.F. Stainback, S.R. Bailey, et al.
ACCF/HRS/AHA/ASE/HFSA/SCAI/SCCT/SCMR 2013 appropriate use criteria for implantable cardioverter-defibrillators and cardiac resynchronization therapy: a report of the American College of Cardiology Foundation Appropriate Use Criteria Task Force, Heart Rhythm Society, American Heart Association, American Society of Echocardiography, Heart Failure Society of America, Society for Cardiovascular Angiography and Interventions, Society of Cardiovascular Computed Tomography, and Society for Cardiovascular Magnetic Resonance.
Heart Rhythm, 10 (2013), pp. e11-e58
[43]
K. Khadjooi, P.W. Foley, S. Chalil, et al.
Long-term effects of cardiac resynchronisation therapy in patients with atrial fibrillation.
Heart, 94 (2008), pp. 879-883
[44]
F. Schütte, G. Lüdorff, R. Grove, et al.
Atrioventricular node ablation is not a prerequisite for cardiac resynchronization therapy in patients with chronic atrial fibrillation.
Cardiol J, 16 (2009), pp. 246-249
[45]
F. Himmel, M. Reppel, K. Mortensen, et al.
A strategy to achieve CRT response in permanent atrial fibrillation without obligatory atrioventricular node ablation.
Pacing Clin Electrophysiol, 35 (2012), pp. 943-947
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