Elsevier

Heart Rhythm

Volume 14, Issue 5, May 2017, Pages 661-667
Heart Rhythm

Revisiting pulmonary vein isolation alone for persistent atrial fibrillation: A systematic review and meta-analysis

https://doi.org/10.1016/j.hrthm.2017.01.003Get rights and content

Background

Early studies demonstrated relatively low success rates for pulmonary vein isolation (PVI) alone in patients with persistent atrial fibrillation (PeAF). However, the advent of new technologies and the observation that additional substrate ablation does not improve outcomes have created a new focus on PVI alone for treatment of PeAF.

Objective

The purpose of this study was to systematically review the recent medical literature to determine current medium-term outcomes when a PVI-only approach is used for PeAF.

Methods

An electronic database search (MEDLINE, Embase, Web of Science, PubMed, Cochrane) was performed in August 2016. Only studies of PeAF patients undergoing a ”PVI only” ablation strategy using contemporary radiofrequency (RF) technology or second-generation cryoballoon (CB2) were included. A random-effects model was used to assess the primary outcome of pooled single-procedure 12-month arrhythmia-free survival. Predictors of recurrence were also examined and a meta-analysis performed if ≥4 studies examined the parameter.

Results

Fourteen studies of 956 patients, of whom 45.2% underwent PVI only with RF and 54.8% with CB2, were included. Pooled single-procedure 12-month arrhythmia-free survival was 66.7% (95% confidence interval [CI] 60.8%–72.2%), with the majority of patients (80.5%) off antiarrhythmic drugs. Complication rates were very low, with cardiac tamponade occurring in 5 patients (0.6%) and persistent phrenic nerve palsy in 5 CB2 patients (0.9% of CB2). Blanking period recurrence (hazard ratio 4.68, 95% CI 1.70–12.9) was the only significant predictor of recurrence.

Conclusion

A PVI-only strategy in PeAF patients with a low prevalence of structural heart disease using contemporary technology yields excellent outcomes comparable to those for paroxysmal AF ablation.

Introduction

Although pulmonary vein isolation (PVI) is a well-established treatment of paroxysmal atrial fibrillation (AF), early studies of PVI only in patients with persistent AF (PeAF) reported suboptimal success rates. This led to the development of novel strategies to target atrial substrate, including linear lesion creation, ablation of complex fractionated atrial electrograms (CFAEs) and non-PV triggers, and more recently rotor ablation. However, data from STAR AF II indicated that addition of linear lesions or CFAE ablation did not improve outcomes over PVI alone.1 Similarly, evidence for rotor ablation efficacy is observational and has not been widely reproduced. In this context, and with the advent of more advanced technologies (including contact force-sensing catheters and the second-generation cryoballoon [CB2]), a number of recent studies have revisited the approach of PVI only for management of PeAF. The focus of this systematic review was to examine these recently reported success rates for “PVI only” in PeAF using the latest technology iterations and to identify predictors of success.

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Section snippets

Search strategy and data extraction

We performed a comprehensive literature search of MEDLINE, Embase, Web of Science, PubMed, and the Cochrane-controlled Trials Register in August 2016. The search was restricted to studies involving humans that were published in English. In addition, the reference lists of all relevant trials and reviews were hand searched. Key search terms were “persistent atrial fibrillation,” “catheter ablation,” “pulmonary vein isolation,” and “second generation cryoballoon.” With respect to trials involving

Results

From the 2218 citations first screened, 84 full-text articles were reviewed, and 14 met inclusion criteria for analysis of the primary outcome (Figure 1). Baseline patient characteristics and single-procedure 12-month arrhythmia-free survival rates of the included studies are given in Table 1, Table 2, respectively. Of the 956 patients with PeAF undergoing PVI only included in the analysis, 419 (45.2%) underwent PVI alone with RF, whereas 509 (54.8%) underwent cryoballoon PVI. Seven studies

Discussion

Based on results from recent studies using the latest technology, we observed a 66.7% single-procedure 12-month arrhythmia-free survival using PVI only in a PeAF population with a low prevalence of structural heart disease. This result is comparable to data reported in an earlier (2011) meta-analysis of PVI in paroxysmal AF, which observed a 12-month success rate of 66.6%.2 However, for PVI alone in PeAF, the same meta-analysis observed a 12-month success rate of just 51.9%. Improved success

Conclusion

In patients with PeAF and minimal structural heart disease, PVI alone yields a 1-year single-procedure arrhythmia-free survival of 66.7% and is a legitimate strategy. These medium-term outcomes in lower-risk patients are now comparable to results in the paroxysmal AF population, with very low complication rates. Ongoing technologic advances, earlier referral in the disease process, and addition of risk factor modification may further improve outcomes.

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  • Cited by (0)

    Dr. Voskoboinik is supported by a co-funded National Health and Medical Research Council of Australia (NHMRC)/National Heart Foundation of Australia (NHF) postgraduate scholarship and Baker IDI Bright Sparks scholarship. Profs. Kistler, Sanders, and Kalman are supported by practitioner fellowships from the NHMRC. Prof. Sanders is also supported by a practitioner fellowship from the NHF. This research is supported in part by the Victorian Government’s Operational Infrastructure Funding. Prof. Kalman sits on the advisory board of Biosense Webster and Boston Scientific; and receives research and fellowship support from Biosense Webster, Boston Scientific, St. Jude Medical, and Medtronic. Prof. Sanders has served on the advisory board of Biosense Webster, Medtronic, and St. Jude Medical; has received lecture fees from Biosense Webster, Medtronic, St. Jude Medical, Boston Scientific, and Merck; and has received research funding from Medtronic, St. Jude Medical, Boston Scientific, Biotronik, and Sorin.

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