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Updated: Sep 26, 2025

Catheter Ablation in Combination With Left Atrial Appendage Closure for Atrial Fibrillation
Published on: February 26, 2013
Sacubitril/valsartan attenuates atrial structural remodelling in atrial fibrillation patients
Liu Yang1, Min Zhang1,2, Zhiheng Hao1
1Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Insights
Sacubitril/valsartan (Sac/Val) significantly reduced atrial remodelling in patients after radiofrequency catheter ablation for atrial fibrillation (AF), outperforming valsartan. This suggests Sac/Val may improve outcomes for AF patients post-ablation.
Area of Science:
- Cardiology
- Electrophysiology
Background:
- Radiofrequency catheter ablation (RFCA) is a key treatment for atrial fibrillation (AF), but high recurrence rates persist.
- Sacubitril/valsartan (Sac/Val) has shown benefits in heart failure, yet its effect on atrial remodelling post-RFCA is unknown.
Purpose of the Study:
- To evaluate if Sac/Val offers superior atrial remodelling reversal compared to valsartan in AF patients undergoing RFCA.
- To assess the impact on AF recurrence and clinical outcomes.
Main Methods:
- A randomized trial of 64 AF patients post-RFCA, comparing Sac/Val (200 mg/day) to valsartan (160 mg/day) for 24 weeks.
- Primary endpoint: change in left atrial diameter. Secondary endpoints: AF recurrence, hospitalization, and death.
Main Results:
- Sac/Val significantly reduced left atrial diameter and volume index compared to baseline and valsartan group (P < 0.001).
- Right atrial diameter also decreased significantly with Sac/Val (P = 0.017).
- AF recurrence showed a numerical decrease with Sac/Val (9.4% vs. 15.6%), but not statistically significant (P = 0.708). No differences in hospitalization or death.
Conclusions:
- Sacubitril/valsartan is superior to valsartan in reducing atrial structural remodelling in AF patients treated with RFCA.
- These findings suggest a potential benefit of Sac/Val in managing AF post-ablation.
Aims:
Radiofrequency catheter ablation (RFCA) is now an established therapeutic option for patients with atrial fibrillation (AF), but the long-term recurrence rate of AF is still high. Sacubitril/valsartan (Sac/Val) is superior to valsartan in attenuating ventricular remodelling and improving clinical outcomes in heart failure patients, but whether this additional benefit exists in reversing atrial remodelling and reducing AF recurrence of RFCA-treated AF patients remains uncovered.
Methods And Results:
Patients that had undergone RFCA were enrolled and randomly assigned 1:1 to valsartan (160 mg/day) or Sac/Val (200 mg/day) treatment group, in addition to other standard treatment of AF. Patients were followed up for 24 weeks. Echocardiography and ambulatory Holter monitoring for 24 h was performed at 24 weeks after RFCA. The primary end point was the change of atrial diameter from baseline to 24 weeks after RFCA. Second end points included the recurrence rate of AF, all-cause hospitalization and all-cause death. A total of 64 AF patients were enrolled, 32 of which received Sac/Val and 32 received valsartan treatment. There was no difference in the age (64.8 ± 9.8 vs. 63.7 ± 9.0, P = 0.634), gender (per cent of male: 59.4% vs. 50.0%, P = 0.616), heart rate (84.7 ± 4.1 b.p.m. vs. 80.9 ± 2.6 b.p.m., P = 0.428), systolic (127.5 ± 15.4 mmHg vs. 130.0 ± 17.8 mmHg, P = 0.549) or diastolic (81.7 ± 9.8 mmHg vs. 79.9 ± 12.6, P = 0.537) blood pressure upon admission between valsartan and Sac/Val treatment groups. The percentage of persistent AF was also comparable (43.8% vs. 53.1%, P = 0.617) in both treatment groups. Patients receiving Sac/Val treatment displayed significant decrease in the left atrial diameter (4.3 ± 0.5 cm to 3.8 ± 0.5 cm, P < 0.001), volume index (48.0 ± 6.4 mL/m2 to 41.7 ± 7.0 mL/m2 , P < 0.001), and right atrial diameter (4.4 ± 0.8 cm to 3.9 ± 0.7 cm, P = 0.017) from baseline to 24 weeks after RFCA. This effect was not observed in valsartan treatment group. There was a numerical decrease in AF recurrence rate in the Sac/Val group compared with valsartan group (9.4% vs. 15.6%), although this difference did not reach a statistical significance (P = 0.708). No difference in all-cause hospitalization rate (6.3% in each group) or all-cause death rate (0% in each group) was observed.
Conclusions:
Our data indicate that Sac/Val is superior to valsartan in attenuating atrial structural remodelling in catheter ablation-treated AF patients.
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