TY - JOUR
T1 - First-Line Catheter Ablation of Monomorphic Ventricular Tachycardia in Cardiomyopathy Concurrent With Defibrillator Implantation
T2 - The PAUSE-SCD Randomized Trial
AU - Tung, Roderick
AU - Xue, Yumei
AU - Chen, Minglong
AU - Jiang, Chenyang
AU - Shatz, Dalise Y.
AU - Besser, Stephanie A.
AU - Hu, Hongde
AU - Chung, Fa Po
AU - Nakahara, Shiro
AU - Kim, Young Hoon
AU - Satomi, Kazuhiro
AU - Shen, Lishui
AU - Liang, Er'peng
AU - Liao, Hongtao
AU - Gu, Kai
AU - Jiang, Ruhong
AU - Jiang, Jian
AU - Hori, Yuichi
AU - Choi, Jong Il
AU - Ueda, Akiko
AU - Komatsu, Yuki
AU - Kazawa, Shuichiro
AU - Soejima, Kyoko
AU - Chen, Shih Ann
AU - Nogami, Akihiko
AU - Yao, Yan
N1 - Funding Information:
The PAUSE-SCD trial was a prospective international, multicenter, randomized controlled trial conducted at 11 tertiary academic centers in China, Japan, South Korea, and Taiwan. All participating sites obtained approval by the local ethics board and institutional review board. The protocol and ablation strategy were developed at the University of Chicago, which served as the study coordinating site. Partial funding support was provided by Abbott to support database management, statistical analysis, and ICD devices in randomly assigned patients without insurance coverage (n=18). Additional funding support for the sites in China was obtained from the Ministry of Science and Technology of China for the National R&D Program (fund no. 2017YFC1307800), which is a peer-reviewed program to support the risk stratification and management of malignant ventricular arrhythmias. The funders did not have any role in the design, conduction, analysis, authorship, or submission of the article.
Publisher Copyright:
© 2022 American Heart Association, Inc.
PY - 2022/6/21
Y1 - 2022/6/21
N2 - Background: Catheter ablation as first-line therapy for ventricular tachycardia (VT) at the time of implantable cardioverter defibrillator (ICD) implantation has not been adopted into clinical guidelines. Also, there is an unmet clinical need to prospectively examine the role of VT ablation in patients with nonischemic cardiomyopathy, an increasingly prevalent population that is referred for advanced therapies globally. Methods: We conducted an international, multicenter, randomized controlled trial enrolling 180 patients with cardiomyopathy and monomorphic VT with an indication for ICD implantation to assess the role of early, first-line ablation therapy. A total of 121 patients were randomly assigned (1:1) to ablation plus an ICD versus conventional medical therapy plus an ICD. Patients who refused ICD (n=47) were followed in a prospective registry after stand-alone ablation treatment. The primary outcome was a composite end point of VT recurrence, cardiovascular hospitalization, or death. Results: Randomly assigned patients had a mean age of 55 years (interquartile range, 46-64) and left ventricular ejection fraction of 40% (interquartile range, 30%-49%); 81% were male. The underlying heart disease was ischemic cardiomyopathy in 35%, nonischemic cardiomyopathy in 30%, and arrhythmogenic cardiomyopathy in 35%. Ablation was performed a median of 2 days before ICD implantation (interquartile range, 5 days before to 14 days after). At 31 months, the primary outcome occurred in 49.3% of the ablation group and 65.5% in the control group (hazard ratio, 0.58 [95% CI, 0.35-0.96]; P=0.04). The observed difference was driven by a reduction in VT recurrence in the ablation arm (hazard ratio, 0.51 [95%CI, 0.29-0.90]; P=0.02). A statistically significant reduction in both ICD shocks (10.0% versus 24.6%; P=0.03) and antitachycardia pacing (16.2% versus 32.8%; P=0.04) was observed in patients who underwent ablation compared with control. No differences in cardiovascular hospitalization (32.0% versus. 33.7%; hazard ratio, 0.82 [95% CI, 0.43-1.56]; P=0.55) or mortality (8.9% versus 8.8%; hazard ratio, 1.40 [95% CI, 0.38-5.22]; P=0.62]) were observed. Ablation-related complications occurred in 8.3% of patients. Conclusions: Among patients with cardiomyopathy of varied causes, early catheter ablation performed at the time of ICD implantation significantly reduced the composite primary outcome of VT recurrence, cardiovascular hospitalization, or death. These findings were driven by a reduction in ICD therapies.
AB - Background: Catheter ablation as first-line therapy for ventricular tachycardia (VT) at the time of implantable cardioverter defibrillator (ICD) implantation has not been adopted into clinical guidelines. Also, there is an unmet clinical need to prospectively examine the role of VT ablation in patients with nonischemic cardiomyopathy, an increasingly prevalent population that is referred for advanced therapies globally. Methods: We conducted an international, multicenter, randomized controlled trial enrolling 180 patients with cardiomyopathy and monomorphic VT with an indication for ICD implantation to assess the role of early, first-line ablation therapy. A total of 121 patients were randomly assigned (1:1) to ablation plus an ICD versus conventional medical therapy plus an ICD. Patients who refused ICD (n=47) were followed in a prospective registry after stand-alone ablation treatment. The primary outcome was a composite end point of VT recurrence, cardiovascular hospitalization, or death. Results: Randomly assigned patients had a mean age of 55 years (interquartile range, 46-64) and left ventricular ejection fraction of 40% (interquartile range, 30%-49%); 81% were male. The underlying heart disease was ischemic cardiomyopathy in 35%, nonischemic cardiomyopathy in 30%, and arrhythmogenic cardiomyopathy in 35%. Ablation was performed a median of 2 days before ICD implantation (interquartile range, 5 days before to 14 days after). At 31 months, the primary outcome occurred in 49.3% of the ablation group and 65.5% in the control group (hazard ratio, 0.58 [95% CI, 0.35-0.96]; P=0.04). The observed difference was driven by a reduction in VT recurrence in the ablation arm (hazard ratio, 0.51 [95%CI, 0.29-0.90]; P=0.02). A statistically significant reduction in both ICD shocks (10.0% versus 24.6%; P=0.03) and antitachycardia pacing (16.2% versus 32.8%; P=0.04) was observed in patients who underwent ablation compared with control. No differences in cardiovascular hospitalization (32.0% versus. 33.7%; hazard ratio, 0.82 [95% CI, 0.43-1.56]; P=0.55) or mortality (8.9% versus 8.8%; hazard ratio, 1.40 [95% CI, 0.38-5.22]; P=0.62]) were observed. Ablation-related complications occurred in 8.3% of patients. Conclusions: Among patients with cardiomyopathy of varied causes, early catheter ablation performed at the time of ICD implantation significantly reduced the composite primary outcome of VT recurrence, cardiovascular hospitalization, or death. These findings were driven by a reduction in ICD therapies.
KW - catheter ablation
KW - defibrillators, implantable
KW - tachycardia, ventricular
UR - http://www.scopus.com/inward/record.url?scp=85132454471&partnerID=8YFLogxK
U2 - 10.1161/CIRCULATIONAHA.122.060039
DO - 10.1161/CIRCULATIONAHA.122.060039
M3 - Article
C2 - 35507499
AN - SCOPUS:85132454471
SN - 0009-7322
VL - 145
SP - 1839
EP - 1849
JO - Circulation
JF - Circulation
IS - 25
ER -