. | Limited ablation group . | Extended ablation group . | P . |
---|---|---|---|
n = 38 . | n = 36 . | ||
Primary endpoint | |||
– Documented arrhythmia recurrence >30 s without antiarrhythmic drugs after the 3-month blanking period | 17 (45%) | 15 (42%) | NS |
Secondary endpoints | |||
– Documented on-drug arrhythmia recurrence | 10 (26%) | 7 (19%) | NS |
– Symptoms of arrhythmia | 13 (34%) | 10 (28%) | NS |
– Patients with emergency visits/number of emergency visits per patient | 11 (29%)/2 (1; 3) | 9 (25%)/2 (1; 2) | NS/NS |
– Patients with hospitalization/number of hospitalizations per patient | 14 (37%)/1 (1; 2) | 13 (36%)/2 (1; 2) | NS/NS |
– Patients with cardiovascular emergency visits or hospitalization/number of events per patient | 13 (24%)/1 (1; 3) | 11 (31%)/1 (1; 2) | NS/NS |
– Mortality | 9 (24%) | 10 (28%) | NS |
– Antiarrhythmic drugs (post-blanking period) | 16 (42%) | 7 (19%) | 0.046 |
– Antiarrhythmic drugs (at the end of follow-up) | 11 (29%) | 7 (19%) | NS |
– Reablation rate | 5 (13%) | 3 (8%) | NS |
– Pacemaker implantation | 3 (8%) | 1 (3%) | NS |
– AV junction ablation | 0 | 1 (3%) | NS |
Other objectives (12-month visit—baseline difference) | |||
– 6-minute walking test (m) | −10 (−27; 55) | 9 (−28; 163) | NS |
– EQ-VAS | −4 (−12; 14) | 0 (−18; 22) | NS |
– NT-proBNP (pg/mL) | 239 (−312; 1120) | 98 (−512; 695) | NS |
Major procedural complications | 5 (13%) | 4 (11%) | NS |
. | Limited ablation group . | Extended ablation group . | P . |
---|---|---|---|
n = 38 . | n = 36 . | ||
Primary endpoint | |||
– Documented arrhythmia recurrence >30 s without antiarrhythmic drugs after the 3-month blanking period | 17 (45%) | 15 (42%) | NS |
Secondary endpoints | |||
– Documented on-drug arrhythmia recurrence | 10 (26%) | 7 (19%) | NS |
– Symptoms of arrhythmia | 13 (34%) | 10 (28%) | NS |
– Patients with emergency visits/number of emergency visits per patient | 11 (29%)/2 (1; 3) | 9 (25%)/2 (1; 2) | NS/NS |
– Patients with hospitalization/number of hospitalizations per patient | 14 (37%)/1 (1; 2) | 13 (36%)/2 (1; 2) | NS/NS |
– Patients with cardiovascular emergency visits or hospitalization/number of events per patient | 13 (24%)/1 (1; 3) | 11 (31%)/1 (1; 2) | NS/NS |
– Mortality | 9 (24%) | 10 (28%) | NS |
– Antiarrhythmic drugs (post-blanking period) | 16 (42%) | 7 (19%) | 0.046 |
– Antiarrhythmic drugs (at the end of follow-up) | 11 (29%) | 7 (19%) | NS |
– Reablation rate | 5 (13%) | 3 (8%) | NS |
– Pacemaker implantation | 3 (8%) | 1 (3%) | NS |
– AV junction ablation | 0 | 1 (3%) | NS |
Other objectives (12-month visit—baseline difference) | |||
– 6-minute walking test (m) | −10 (−27; 55) | 9 (−28; 163) | NS |
– EQ-VAS | −4 (−12; 14) | 0 (−18; 22) | NS |
– NT-proBNP (pg/mL) | 239 (−312; 1120) | 98 (−512; 695) | NS |
Major procedural complications | 5 (13%) | 4 (11%) | NS |
Data represent the number of cases (percentage) or median (interquartile range).
Details on major procedural complications are provided in Supplementary material online, Table S3.
EQ-VAS, European Quality of Life Group instrument self-report questionnaire visual analogue scale; NS, not significant.
. | Limited ablation group . | Extended ablation group . | P . |
---|---|---|---|
n = 38 . | n = 36 . | ||
Primary endpoint | |||
– Documented arrhythmia recurrence >30 s without antiarrhythmic drugs after the 3-month blanking period | 17 (45%) | 15 (42%) | NS |
Secondary endpoints | |||
– Documented on-drug arrhythmia recurrence | 10 (26%) | 7 (19%) | NS |
– Symptoms of arrhythmia | 13 (34%) | 10 (28%) | NS |
– Patients with emergency visits/number of emergency visits per patient | 11 (29%)/2 (1; 3) | 9 (25%)/2 (1; 2) | NS/NS |
– Patients with hospitalization/number of hospitalizations per patient | 14 (37%)/1 (1; 2) | 13 (36%)/2 (1; 2) | NS/NS |
– Patients with cardiovascular emergency visits or hospitalization/number of events per patient | 13 (24%)/1 (1; 3) | 11 (31%)/1 (1; 2) | NS/NS |
– Mortality | 9 (24%) | 10 (28%) | NS |
– Antiarrhythmic drugs (post-blanking period) | 16 (42%) | 7 (19%) | 0.046 |
– Antiarrhythmic drugs (at the end of follow-up) | 11 (29%) | 7 (19%) | NS |
– Reablation rate | 5 (13%) | 3 (8%) | NS |
– Pacemaker implantation | 3 (8%) | 1 (3%) | NS |
– AV junction ablation | 0 | 1 (3%) | NS |
Other objectives (12-month visit—baseline difference) | |||
– 6-minute walking test (m) | −10 (−27; 55) | 9 (−28; 163) | NS |
– EQ-VAS | −4 (−12; 14) | 0 (−18; 22) | NS |
– NT-proBNP (pg/mL) | 239 (−312; 1120) | 98 (−512; 695) | NS |
Major procedural complications | 5 (13%) | 4 (11%) | NS |
. | Limited ablation group . | Extended ablation group . | P . |
---|---|---|---|
n = 38 . | n = 36 . | ||
Primary endpoint | |||
– Documented arrhythmia recurrence >30 s without antiarrhythmic drugs after the 3-month blanking period | 17 (45%) | 15 (42%) | NS |
Secondary endpoints | |||
– Documented on-drug arrhythmia recurrence | 10 (26%) | 7 (19%) | NS |
– Symptoms of arrhythmia | 13 (34%) | 10 (28%) | NS |
– Patients with emergency visits/number of emergency visits per patient | 11 (29%)/2 (1; 3) | 9 (25%)/2 (1; 2) | NS/NS |
– Patients with hospitalization/number of hospitalizations per patient | 14 (37%)/1 (1; 2) | 13 (36%)/2 (1; 2) | NS/NS |
– Patients with cardiovascular emergency visits or hospitalization/number of events per patient | 13 (24%)/1 (1; 3) | 11 (31%)/1 (1; 2) | NS/NS |
– Mortality | 9 (24%) | 10 (28%) | NS |
– Antiarrhythmic drugs (post-blanking period) | 16 (42%) | 7 (19%) | 0.046 |
– Antiarrhythmic drugs (at the end of follow-up) | 11 (29%) | 7 (19%) | NS |
– Reablation rate | 5 (13%) | 3 (8%) | NS |
– Pacemaker implantation | 3 (8%) | 1 (3%) | NS |
– AV junction ablation | 0 | 1 (3%) | NS |
Other objectives (12-month visit—baseline difference) | |||
– 6-minute walking test (m) | −10 (−27; 55) | 9 (−28; 163) | NS |
– EQ-VAS | −4 (−12; 14) | 0 (−18; 22) | NS |
– NT-proBNP (pg/mL) | 239 (−312; 1120) | 98 (−512; 695) | NS |
Major procedural complications | 5 (13%) | 4 (11%) | NS |
Data represent the number of cases (percentage) or median (interquartile range).
Details on major procedural complications are provided in Supplementary material online, Table S3.
EQ-VAS, European Quality of Life Group instrument self-report questionnaire visual analogue scale; NS, not significant.
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