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Peer-reviewedCC BY 4.0Pacing and Clinical Electrophysiology

Cryoballoon Versus Radiofrequency Ablation for Persistent Atrial Fibrillation: Meta‐Analysis of Randomized Trials

6 affiliations
  1. 1Faculty of Medicine Imperial College London, England London UK
  2. 2London Northwest Healthcare NHS Trust, England London UK
  3. 3Department of Internal Medicine University of Pennsylvania Philadelphia Pennsylvania USA
  4. 4Chelsea and Westminster Hospital NHS Foundation Trust, England London UK
  5. 5National Heart and Lung Institute Imperial College London, England London UK
  6. 6Department of Cardiology Imperial College Healthcare NHS Trust, England London UK

Abstract

Introduction: Pulmonary vein isolation (PVI) alone achieves modest arrhythmia freedom in persistent atrial fibrillation (PeAF). Cryoballoon ablation (CBA) offers a single‐shot alternative to radiofrequency ablation (RFA) that streamlines procedural workflow. We aimed to quantify the clinical efficacy, procedural efficiency, and safety of CBA versus RFA through a meta‐analysis of randomized controlled trials (RCTs).

Methods and Results: Systematic review of PubMed, Embase, and Scopus identified 5 RCTs enrolling 1,091 patients (515 CBA, 576 RFA). The primary endpoint was 12‐month freedom from any atrial arrhythmia, with isolated AF, and atrial tachycardia/flutter evaluated as secondary endpoints. Random‐effects models generated relative risks (RRs) and mean differences (MDs) with 95% confidence intervals (CI). Time‐to‐event data were pooled using a generic inverse‐variance approach to derive hazard ratios (HR). CBA and RFA demonstrated equivalent freedom from any arrhythmia (RR 0.97, 95% CI 0.81–1.15; p = 0.71). Time‐to‐event analysis corroborated a comparable recurrence hazard (HR 0.91, 95% CI 0.67–1.24; p = 0.56; I 2 = 0%). Repeat ablation rates were identical (RR 0.93; p = 0.50). CBA significantly reduced procedural time (MD −45.37 min; p < 0.0001), while major complications were comparable (1.5% vs. 2.7%; p = 0.18). Trial sequential analysis indicated that further randomization is unlikely to demonstrate superiority.

Conclusion: In PeAF, CBA and RFA achieve equivalent 12‐month arrhythmia‐free survival and comparable repeat‐ablation rates, while CBA confers a highly significant reduction in procedural time. However, reliance on 12‐month follow‐up and heterogeneous rhythm surveillance protocols may limit assessments of true long‐term durability.

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BibTeX
@article{bola2026cryoballoon,
  title = {{Cryoballoon Versus Radiofrequency Ablation for Persistent Atrial Fibrillation: Meta‐Analysis of Randomized Trials}},
  author = {Harroop Bola and Aksaan Arif and Joshua J. Hon and Gayathri Giritharan and Prachur Khandelwal and Rodrick Avakian and Amar Rai and Kiran Haresh Kumar Patel and Fu Siong Ng},
  journal = {Pacing and Clinical Electrophysiology},
  year = {2026},
  month = jul,
  doi = {10.1111/pace.70350},
  url = {https://doi.org/10.1111/pace.70350},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Cryoballoon Versus Radiofrequency Ablation for Persistent Atrial Fibrillation: Meta‐Analysis of Randomized Trials
AU  - Harroop Bola
AU  - Aksaan Arif
AU  - Joshua J. Hon
AU  - Gayathri Giritharan
AU  - Prachur Khandelwal
AU  - Rodrick Avakian
AU  - Amar Rai
AU  - Kiran Haresh Kumar Patel
AU  - Fu Siong Ng
PY  - 2026
DA  - 2026/07/03
JO  - Pacing and Clinical Electrophysiology
DO  - 10.1111/pace.70350
UR  - https://doi.org/10.1111/pace.70350
AB  - Introduction: Pulmonary vein isolation (PVI) alone achieves modest arrhythmia freedom in persistent atrial fibrillation (PeAF). Cryoballoon ablation (CBA) offers a single‐shot alternative to radiofrequency ablation (RFA) that streamlines procedural workflow. We aimed to quantify the clinical efficacy, procedural efficiency, and safety of CBA versus RFA through a meta‐analysis of randomized controlled trials (RCTs).  Methods and Results: Systematic review of PubMed, Embase, and Scopus identified 5 RCTs enrolling 1,091 patients (515 CBA, 576 RFA). The primary endpoint was 12‐month freedom from any atrial arrhythmia, with isolated AF, and atrial tachycardia/flutter evaluated as secondary endpoints. Random‐effects models generated relative risks (RRs) and mean differences (MDs) with 95% confidence intervals (CI). Time‐to‐event data were pooled using a generic inverse‐variance approach to derive hazard ratios (HR). CBA and RFA demonstrated equivalent freedom from any arrhythmia (RR 0.97, 95% CI 0.81–1.15; p = 0.71). Time‐to‐event analysis corroborated a comparable recurrence hazard (HR 0.91, 95% CI 0.67–1.24; p = 0.56; I 2 = 0%). Repeat ablation rates were identical (RR 0.93; p = 0.50). CBA significantly reduced procedural time (MD −45.37 min; p < 0.0001), while major complications were comparable (1.5% vs. 2.7%; p = 0.18). Trial sequential analysis indicated that further randomization is unlikely to demonstrate superiority.  Conclusion: In PeAF, CBA and RFA achieve equivalent 12‐month arrhythmia‐free survival and comparable repeat‐ablation rates, while CBA confers a highly significant reduction in procedural time. However, reliance on 12‐month follow‐up and heterogeneous rhythm surveillance protocols may limit assessments of true long‐term durability.
SN  - 0147-8389
SN  - 1540-8159
ER  -