4.2 Review

Comparison of Effectiveness and Safety between High-Power Short-Duration Ablation and Conventional Ablation for Atrial Fibrillation: A Systematic Review and Meta-Analysis

Journal

JOURNAL OF INTERVENTIONAL CARDIOLOGY
Volume 2022, Issue -, Pages -

Publisher

WILEY-HINDAWI
DOI: 10.1155/2022/6013474

Keywords

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Funding

  1. National Natural Science Foundation of China [81870254]
  2. Science and Technology Programs of Guangdong Province [2019B020230004]
  3. National Key Research and Development Project [2018YFC1312502]
  4. Guangdong Special Funds for Science and Technology Innovation Strategy, China

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This study evaluated the effectiveness and safety of high-power short-duration radiofrequency ablation (HPSD RFA) compared to conventional RFA in patients with atrial fibrillation. The results showed that HPSD RFA was associated with shorter procedure duration, lower risk of acute pulmonary vein reconnection, higher freedom from atrial arrhythmia at one year, and comparable safety. HPSD RFA may be more effective in certain conditions, but both methods showed similar effectiveness when the power setting was 50 W, and there was no significant difference in complications between the two groups.
Aim. We aimed to evaluate the effectiveness and safety between high-power short-duration (HPSD) radiofrequency ablation (RFA) and conventional RFA in patients with atrial fibrillation (AF). Methods. Studies comparing HPSD and traditional applications in patients undergoing initial catheter ablation for atrial fibrillation from inception through December 2021 were searched on Pubmed, Medline, Cochrane, and . Results. The meta-analysis included seventeen studies with a total of 4934 patients. HPSD group decreased procedure duration (mean difference (MD) -38.28 min, P < 0.001), RF duration (MD -20.51 min, P < 0.001), fluoroscopy duration (MD -5.19 min, P < 0.001), and acute pulmonary vein reconnection (Odds ratio (OR) 0.40, P < 0.001), while improving the freedom from atrial arrhythmia at one year (OR 1.48, 95% confidence interval (CI) 1.12-1.94, P=0.005) and rates of first-pass isolation (OR 8.92, P=0.001). Compared with the conventional group, freedom from atrial arrhythmia at one-year follow-up was higher in the HPSD group without the guidance of AI/LSI (OR 1.66, P=0.01) and studies with a power setting of 40-50 W (OR 1.93, P=0.002). Nevertheless, the two groups had similar effectiveness with a power setting of 50 W in the HPSD RFA (OR 1.10, P=0.52). There was no difference in complications between the two groups (P=0.71). Conclusion. HPSD RFA was associated with shorter procedure duration, higher freedom from atrial arrhythmia, and comparable safety compared to conventional RFA.

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