Catheter ablation | atrial fibrillation, in all type of patients | vs control | NS | by 52% | - | by 47% | by 17% | by 253% | - | - | - | - | - | - | by 76% | by 71% | by 299% | by 275% | by 155% | NS | Endpoint | TE [95% CI] | p val | I2 | n | k | trials |
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All cause death | 0.84 [0.60 1.18] | p=1.00 | 0 | 3781 | 8 | A4 (Jais), Wazni , APAF (Pappone), CAFCOAF (Stabile), Krittayaphong, ThermoCool AF, Forleo, CABANA, | Adverse events | 0.48 [0.25 0.92] | p=0.04 | 0 | 432 | 4 | Wazni , APAF (Pappone), CAFCOAF (Stabile), Krittayaphong, | hospitalisation for cardiovascular causes | no data | Atrial fibrillation recurrence | 0.53 [0.46 0.61] | p=0.04 | 0 | 2204 | 1 | CABANA, | death or hospitalization for cardiac causes | 0.83 [0.74 0.93] | p=0.04 | 0 | 2204 | 1 | CABANA, | atrial tachyarrhythmia recurrence free survival | 3.53 [2.37 5.25] | p=0.04 | 0 | 661 | 6 | Wazni , APAF (Pappone), CAFCOAF (Stabile), Krittayaphong, ThermoCool AF, Forleo, | Syncope | no data | ICD events | no data | Appropriate ICD shock | no data | Inappropriate ICD shock | no data | all ICD shock (appropriate and inappropriate) | no data | VT or VF | no data | Symptomatic Atrial Arrhythmia recurrence | 0.24 [0.15 0.39] | p=0.04 | 0 | 167 | 1 | ThermoCool AF, | Any Atrial Arrhythmia Recurrence | 0.29 [0.18 0.46] | p=0.04 | 0 | 167 | 1 | ThermoCool AF, | Freedom from arrhythmia at 12 months per protocol | 3.99 [2.66 6.00] | p=0.04 | 0 | 755 | 7 | A4 (Jais), Wazni , APAF (Pappone), CAFCOAF (Stabile), Krittayaphong, Oral, Forleo, | freedom from arrhythmia at 12 months - worst case | 3.75 [2.53 5.55] | p=0.04 | 0 | 763 | 7 | A4 (Jais), Wazni , APAF (Pappone), CAFCOAF (Stabile), Krittayaphong, Oral, Forleo, | Freedom from arrhythmia at 12 months - ITT | 2.55 [1.69 3.83] | p=0.04 | 0 | 763 | 7 | A4 (Jais), Wazni , APAF (Pappone), CAFCOAF (Stabile), Krittayaphong, Oral, Forleo, | death, stroke,stroke, serious bleeding, cardiac arrest | 0.86 [0.65 1.14] | p=1.00 | 0 | 2204 | 1 | CABANA, | TE: treatment effect; CI: confidence interval; k: nulmber of trials; n: total number of patients Trial | Studied treatment | Control | Patients |
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A4 (Jais), 2008 | catheter ablation | antiarrhythmic drugs | patients with paroxysmal AF resistant to at least 1 antiarrhythmic drug. | Wazni , 2005 | Pulmonary vein isolation | Flecainide, propafenone, or sotalol; amiodarone if needed | Drug-naive monthly symptomatic AF >=3mo | APAF (Pappone), 2006 | left atrial catheter ablation | Flecainide acetate, propafenone hydrochloride, or sotalol hydrochloride | Drug-refractory paroxysmal AF >=6mo | CAFCOAF (Stabile), 2006 | left atrial catheter ablation plus amiodarone or other drugs | Amiodarone or other drugs | Drug-refractory or drug-intolerant paroxysmal or persistent AF | Krittayaphong, 2003 | left atrial catheter ablation | amiodarone | drug-refractory amiodarone-naive paroxysmal or persistent AF >=6mo | ThermoCool AF, 2008 | catheter ablation | antiarrhythmic drug therapy with a class I or III drug | patients with AF who were nonresponsive to previous treatment with antiarrhythmic drugs | Oral, 2006 | circumferential pulmonary-vein ablation and amiodarione | amiodarone and two cardioversions during the first three months alone | patients with chronic atrial fibrillation | Forleo, 2009 | pulmonary vein isolation | antiarrhythmic drug treatment | patients with diabetes mellitus type 2 and paroxysmal or persistent AF | Lakkireddy, 2006 | | | | CABANA, 2018 | left atrial catheter ablation | current state-of-the-art therapy with either rate control or rhythm control drugs | patients with untreated or incompletely treated AF | STOP-AF, 2010 | cryo-balloon catheter for pulmonary vein isolation | nonfailed antiarrhythmic drugs | patients with paroxysmal atrial fibrillation |
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Catheter ablation | patients with implantable cardioverter defibrillators , in all type of patients | vs no ablation | NS | - | by 45% | - | - | - | NS | by 62% | by 49% | NS | NS | by 39% | - | - | - | - | - | - | Endpoint | TE [95% CI] | p val | I2 | n | k | trials |
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All cause death | 0.77 [0.34 1.77] | p=1.00 | 0 | 238 | 2 | VTACH, SMASH-VT, | Adverse events | no data | hospitalisation for cardiovascular causes | 0.55 [0.30 1.00] | p=0.04 | 0 | 110 | 1 | VTACH, | Atrial fibrillation recurrence | no data | death or hospitalization for cardiac causes | no data | atrial tachyarrhythmia recurrence free survival | no data | Syncope | 0.36 [0.07 1.83] | p=1.00 | 0 | 110 | 1 | VTACH, | ICD events | 0.38 [0.15 0.94] | p=0.04 | 0 | 128 | 1 | SMASH-VT, | Appropriate ICD shock | 0.51 [0.28 0.94] | p=0.04 | 0 | 238 | 2 | VTACH, SMASH-VT, | Inappropriate ICD shock | 0.69 [0.18 2.60] | p=1.00 | 0 | 110 | 1 | VTACH, | all ICD shock (appropriate and inappropriate) | 0.61 [0.28 1.32] | p=1.00 | 0 | 110 | 1 | VTACH, | VT or VF | 0.61 [0.37 1.00] | p=0.04 | 0 | 110 | 1 | VTACH, | Symptomatic Atrial Arrhythmia recurrence | no data | Any Atrial Arrhythmia Recurrence | no data | Freedom from arrhythmia at 12 months per protocol | no data | freedom from arrhythmia at 12 months - worst case | no data | Freedom from arrhythmia at 12 months - ITT | no data | death, stroke,stroke, serious bleeding, cardiac arrest | no data | TE: treatment effect; CI: confidence interval; k: nulmber of trials; n: total number of patients Trial | Studied treatment | Control | Patients |
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VTACH, 2009 | catheter ablation for ventricular tachycardia (VT) plus implantable cardioverter defibrillator | implantable cardioverter defibrillator alone | Patients undergoing implantation of an ICD Patients undergoing implantation of an ICD | SMASH-VT, 2007 | defibrillator implantation with adjunctive catheter ablation | defibrillator implantation alone | patients with a history of a myocardial infarction undergoing defibrillator implantation for spontaneous ventricular tachycardia or fibrillation |
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