Mode
Text Size
Log in / Sign up

Sacubitril/Valsartan plus RFCA improves rhythm control in hypertensive NPAF patients

Sacubitril/Valsartan plus RFCA improves rhythm control in hypertensive NPAF patients
Photo by Navy Medicine / Unsplash
Key Takeaway
Consider ARNI plus ablation for rhythm control in hypertensive NPAF patients, especially with reduced EF or low-voltage areas.

This randomized controlled trial enrolled 240 patients with nonparoxysmal atrial fibrillation and hypertension who underwent radiofrequency catheter ablation. Participants were assigned to receive sacubitril/valsartan (ARNI) plus ablation or ablation alone. The primary outcome was freedom from atrial fibrillation and atrial tachycardia/atrial flutter for at least 30 seconds without antiarrhythmic medications at 15 months after a 3-month blanking period.

At 15 months, maintenance of sinus rhythm was higher in the ARNI group (79.8%) versus the control group (69.4%), with a hazard ratio of 0.59 (95% CI 0.36 to 0.98; P=0.04). The ARNI group also had 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 recurred, AF incidence was lower in the ARNI group (50.0% vs 62.2%; P=0.01). Success rates were higher with ARNI in patients with EF <50% (93.6% vs 61.1%; P=0.01) and in those with low-voltage areas (80.0% vs 61.3%; P=0.02). Safety and tolerability data were not reported.

Key limitations include the specific population of hypertensive NPAF patients post-ablation and the 15-month follow-up duration. The practice relevance suggests ARNI may improve prognosis in this subgroup, particularly for those with reduced EF or low-voltage areas. Results should not be generalized to non-hypertensive patients.

Study Details

Study typeRct
EvidenceLevel 2
Follow-up3.0 mo
PublishedApr 2026
View Original Abstract ↓
PURPOSE: The efficacy of radiofrequency catheter ablation (RFCA) alone for nonparoxysmal atrial fibrillation (NPAF) is unsatisfactory. This study investigated the effect of sacubitril/valsartan, a type of angiotensin receptor neprilysin inhibitor (ARNI), on NPAF patients with hypertension who underwent RFCA and analysed the possible influencing factors. METHODS: In this prospective, randomized clinical trial, 240 NPAF patients were randomly divided into a control group (n = 121) and an ARNI group (n = 119). The primary outcome was freedom from atrial fibrillation (AF) and atrial tachycardia/atrial flutter (AT/AFL) for ≥ 30 s without antiarrhythmic medications at 15 months after the 3-month blanking period. The secondary outcomes included recurrence types, blood pressure, echocardiographic parameters and N-terminal pro-brain natriuretic peptide (NT-proBNP) levels. RESULTS: At 15 months, a higher maintenance rate of sinus rhythm was achieved in the ARNI group compared to the control group (79.8% vs. 69.4%, hazard ratio [HR] 0.59; 95% confidence interval [CI] 0.36-0.98; P = 0.04). Moreover, 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 level (adjusted median difference -34 pg/ml [95% CI -62 to -6], P = 0.03) were observed in the ARNI group than in the control group at 15 months. Among the patients who recurred, a lower incidence of AF (50.0% vs. 62.2%, P = 0.01) was found in the ARNI group, but presented a significantly higher incidence of AT/AFL. In the subgroup analysis, compared with those in the control group, more patients in the ARNI group achieved success in patients with EF < 50% (93.6% vs. 61.1%, P = 0.01) or low-voltage areas (LVAs) (80.0% vs. 61.3%, P = 0.02). Multivariate Cox regression analysis revealed that ARNI was an independent protective factor against AF or AT/AFL recurrence in patients with EF < 50% or LVAs at 15 months. CONCLUSION: ARNI is effective in NPAF patients with hypertension after RFCA, especially those with EF < 50% or LVAs, which can significantly improve their prognosis.
Free Newsletter

Clinical research that matters. Delivered to your inbox.

Join thousands of clinicians and researchers. No spam, unsubscribe anytime.