Cryoballoon Ablation as Initial Therapy for Atrial Fibrillation

被引:404
作者
Wazni, Oussama M. [1 ]
Dandamudi, Gopi [3 ]
Sood, Nitesh [4 ]
Hoyt, Robert [5 ]
Tyler, Jaret [2 ]
Durrani, Sarfraz [6 ]
Niebauer, Mark [1 ]
Makati, Kevin [7 ]
Halperin, Blair [8 ]
Gauri, Andre [9 ]
Morales, Gustavo [10 ]
Shao, Mingyuan [1 ]
Cerkvenik, Jeffrey [11 ]
Kaplon, Rachelle E. [11 ]
Nissen, Steven E. [1 ]
机构
[1] Cleveland Clin, 9500 Euclid Ave, Cleveland, OH 44195 USA
[2] Ohio State Univ, Med Ctr, Columbus, OH 43210 USA
[3] CHI Franciscan, Tacoma, WA USA
[4] Southcoast Hlth Syst, Fall River, MA USA
[5] Iowa Heart Ctr, W Des Moines, IA USA
[6] MedStar Heart & Vas Inst, Washington, DC USA
[7] BayCare Med Grp, Tampa, FL USA
[8] Providence St Vincent, Portland, OR USA
[9] Spectrum Hlth Heart & Vasc, Grand Rapids, MI USA
[10] Grandview Med Ctr, Birmingham, AL USA
[11] Medtronic, Mounds View, MN USA
关键词
RADIOFREQUENCY ABLATION; CATHETER ABLATION; 1ST-LINE TREATMENT; ANTIARRHYTHMIC-DRUGS; RECURRENCE; 1ST;
D O I
10.1056/NEJMoa2029554
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND In patients with symptomatic paroxysmal atrial fibrillation that has not responded to medication, catheter ablation is more effective than antiarrhythmic drug therapy for maintaining sinus rhythm. However, the safety and efficacy of cryoballoon ablation as initial first-line therapy have not been established. METHODS We performed a multicenter trial in which patients 18 to 80 years of age who had paroxysmal atrial fibrillation for which they had not previously received rhythmcontrol therapy were randomly assigned (1:1) to receive treatment with anti-arrhythmic drugs (class I or III agents) or pulmonary vein isolation with a cryoballoon. Arrhythmia monitoring included 12-lead electrocardiography conducted at baseline and at 1, 3, 6, and 12 months; patient-activated telephone monitoring conducted weekly and when symptoms were present during months 3 through 12; and 24-hour ambulatory monitoring conducted at 6 and 12 months. The primary efficacy end point was treatment success (defined as freedom from initial failure of the procedure or atrial arrhythmia recurrence after a 90-day blanking period to allow recovery from the procedure or drug dose adjustment, evaluated in a Kaplan-Meier analysis). The primary safety end point was assessed in the ablation group only and was a composite of several procedure-related and cryoballoon system-related serious adverse events. RESULTS Of the 203 participants who underwent randomization and received treatment, 104 underwent ablation, and 99 initially received drug therapy. In the ablation group, initial success of the procedure was achieved in 97% of patients. The Kaplan-Meier estimate of the percentage of patients with treatment success at 12 months was 74.6% (95% confidence interval [CI), 65.0 to 82.0) in the ablation group and 45.0% (95% CI, 34.6 to 54.7) in the drug-therapy group (P<0.001 by log-rank test). Two primary safety end-point events occurred in the ablation group (Kaplan-Meier estimate of the percentage of patients with an event within 12 months, 1.9%; 95% CI, 0.5 to 7.5). CONCLUSIONS Cryoballoon ablation as initial therapy was superior to drug therapy for the prevention of atrial arrhythmia recurrence in patients with paroxysmal atrial fibrillation. Serious procedure-related adverse events were uncommon.
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收藏
页码:316 / 324
页数:9
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