TY - JOUR
T1 - Meta-Analysis of Ablation of Atrial Flutter and Supraventricular Tachycardia
AU - Spector, Peter
AU - Reynolds, Matthew R.
AU - Calkins, Hugh
AU - Sondhi, Manu
AU - Xu, Yingxin
AU - Martin, Amber
AU - Williams, Catherine J.
AU - Sledge, Isabella
N1 - Funding Information:
This study was funded by Biosense Webster, Inc., Diamond Bar, California.
Funding Information:
Conflicts of interest: Dr. Spector is a consultant for Medtronic, Inc., Minneapolis, Minnesota; Biosense Webster, Inc.; and Boston Scientific Corporation, Natick, Massachusetts. Dr. Spector has received research grant support from Medtronic, Inc., and Biosense Webster, Inc. Dr. Reynolds is a consultant for Biosense Webster, Inc., and Sanofi-Aventis, Paris, France. Dr. Calkins is a consultant for Biosense Webster, Inc.; CryoCor, San Diego, California; Medtronic, Inc.; and ProRhythm, Inc., Ronkonkoma, New York. Drs. Sondhi, Xu, and Sledge and Ms. Martin and Ms. Williams were employees of United BioSource Corporation during the conduct of this study.
PY - 2009/9/1
Y1 - 2009/9/1
N2 - The purpose of this study was to perform a systematic review and meta-analysis to evaluate the safety and efficacy of radiofrequency ablation (RFA) of typical atrial flutter (AFL) and atrioventricular node-dependent supraventricular tachycardia (SVT) in adult patients. Medline and EMBASE were searched (1990 to 2007) for all study design trials of RFA. Data relating to single- and multiple-procedure success, arrhythmia recurrence, repeat ablation, adverse events, and death were extracted. For RFA in AFL, 18 primary studies with 22 treatment arms and 1,323 patients were identified. Single-procedure success for AFL was 91.7% (95% confidence interval [CI] 88.4% to 94.9%). Multiple-procedure success was 97.0% (95% CI 94.7% to 99.4%). Postablation arrhythmia was noted in 13.2% of patients (95% CI 7.5% to 18.9%), while repeat ablation was reported in 8% (95% CI 4.5% to 11.4%). For RFA of SVT, 39 primary studies with 49 treatment arms in 7,693 patients with accessory pathways and atrioventricular nodal reentrant tachycardia were identified. Single-procedure success for SVT was 93.2% (95% CI 90.8% to 95.5%). Multiple-procedure success was 94.6% (95% CI 92.4% to 96.9). Postablation arrhythmia was noted in 5.6% patients (95% CI 4.1% to 7.2%). Repeat ablation occurred in 6.5% (95% CI 4.7% to 8.3%). For AFL studies, all-cause mortality was 0.6%, and adverse events were reported in 0.5% of patients. For SVT studies, all-cause mortality was 0.1%, and adverse events were reported in 2.9% of patients. In conclusion, studies of RFA for the treatment of patients with AFL and SVT report high efficacy rates and low rates of complications.
AB - The purpose of this study was to perform a systematic review and meta-analysis to evaluate the safety and efficacy of radiofrequency ablation (RFA) of typical atrial flutter (AFL) and atrioventricular node-dependent supraventricular tachycardia (SVT) in adult patients. Medline and EMBASE were searched (1990 to 2007) for all study design trials of RFA. Data relating to single- and multiple-procedure success, arrhythmia recurrence, repeat ablation, adverse events, and death were extracted. For RFA in AFL, 18 primary studies with 22 treatment arms and 1,323 patients were identified. Single-procedure success for AFL was 91.7% (95% confidence interval [CI] 88.4% to 94.9%). Multiple-procedure success was 97.0% (95% CI 94.7% to 99.4%). Postablation arrhythmia was noted in 13.2% of patients (95% CI 7.5% to 18.9%), while repeat ablation was reported in 8% (95% CI 4.5% to 11.4%). For RFA of SVT, 39 primary studies with 49 treatment arms in 7,693 patients with accessory pathways and atrioventricular nodal reentrant tachycardia were identified. Single-procedure success for SVT was 93.2% (95% CI 90.8% to 95.5%). Multiple-procedure success was 94.6% (95% CI 92.4% to 96.9). Postablation arrhythmia was noted in 5.6% patients (95% CI 4.1% to 7.2%). Repeat ablation occurred in 6.5% (95% CI 4.7% to 8.3%). For AFL studies, all-cause mortality was 0.6%, and adverse events were reported in 0.5% of patients. For SVT studies, all-cause mortality was 0.1%, and adverse events were reported in 2.9% of patients. In conclusion, studies of RFA for the treatment of patients with AFL and SVT report high efficacy rates and low rates of complications.
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U2 - 10.1016/j.amjcard.2009.04.040
DO - 10.1016/j.amjcard.2009.04.040
M3 - Article
C2 - 19699343
AN - SCOPUS:68849131994
SN - 0002-9149
VL - 104
SP - 671
EP - 677
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 5
ER -