Sacubitril/valsartan may improve sinus rhythm maintenance after ablation in NPAF patients with hypertension
This randomized controlled trial enrolled 240 patients with nonparoxysmal atrial fibrillation (NPAF) and hypertension who underwent radiofrequency catheter ablation (RFCA). Patients were assigned to receive sacubitril/valsartan (ARNI group, n=119) or standard care without ARNI (control group, n=121). The primary outcome was freedom from atrial fibrillation or atrial tachycardia/flutter for ≥30 seconds without antiarrhythmic drugs at 15 months after a 3-month blanking period.
At 15 months, 79.8% (95/119) of ARNI patients maintained sinus rhythm versus 69.4% (84/121) of controls (HR 0.59, 95% CI 0.36-0.98; P=0.04). The ARNI group showed a smaller left atrial diameter (adjusted mean difference -1.9 mm, 95% CI -3.2 to -0.5; P=0.02) and lower NT-proBNP levels (adjusted median difference -34 pg/ml, 95% CI -62 to -6; P=0.03). Among patients who experienced recurrence, the incidence of AF was lower in the ARNI group (50.0% vs 62.2%, P=0.01). Success rates appeared higher in ARNI-treated patients with reduced ejection fraction (93.6% vs 61.1%, P=0.01) and those with low-voltage areas (80.0% vs 61.3%, P=0.02).
Safety and tolerability data were not reported. Key limitations include the lack of reported adverse events, discontinuation rates, and specific antiarrhythmic drug regimens in the control group. The study setting and phase were also not reported. While the findings suggest a potential role for sacubitril/valsartan in improving post-ablation outcomes in this specific population, the absence of safety data and need for replication in broader populations warrant cautious interpretation.