Rate control drugs differ in the prevention of progression of atrial fibrillation

Author:

Koldenhof Tim12ORCID,Wijtvliet Petra E P J13ORCID,Pluymaekers Nikki A H A3ORCID,Rienstra Michiel2ORCID,Folkeringa Richard J4,Bronzwaer Patrick5,Elvan Arif6ORCID,Elders Jan7,Tukkie Raymond8,Luermans Justin G L M3ORCID,van Kuijk Sander M J3,Tijssen Jan G P9,van Gelder Isabelle C2ORCID,Crijns Harry J G M3,Tieleman Robert G12

Affiliation:

1. Department of Cardiology, Martini Hospital, Van Swietenplein 1, 9728 NT Groningen, The Netherlands

2. Department of Cardiology, University of Groningen, Hanzeplein 1, 9713 GZ Groningen, The Netherlands

3. Department of Cardiology, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Centre, P. Debyelaan 25, 6229 HX Maastricht, The Netherlands

4. Department of Cardiology, Medical Centre Leeuwarden, Henri Dunantweg 2, 8934 AD Leeuwarden, The Netherlands

5. Department of Cardiology, Zaans Medical Centre, Kon. Julianaplein 58, 1502 DV Zaandam, The Netherlands

6. Department of Cardiology, Isala Hospital, Dokter van Heesweg 2, 8025 AB Zwolle, The Netherlands

7. Department of Cardiology, Canisius Wilhelmina Hospital, Weg door Jonkerbos 100, 6532 SZ Nijmegen, The Netherlands

8. Department of Cardiology, Spaarne Hospital, Boerhaavelaan 22, 2035 RC Haarlem, The Netherlands

9. Amsterdam University Medical Centre (AMC), Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands

Abstract

Abstract Aims We hypothesize that in patients with paroxysmal atrial fibrillation (AF), verapamil is associated with lower AF progression compared to beta blockers or no rate control. Methods and results In this pre-specified post hoc analysis of the RACE 4 randomized trial, the effect of rate control medication on AF progression in paroxysmal AF was analysed. Patients using Vaughan-Williams Class I or III antiarrhythmic drugs were excluded. The primary outcome was a composite of first electrical cardioversion (ECV), chemical cardioversion (CCV), or atrial ablation. Event rates are displayed using Kaplan–Meier curves and multivariable Cox regression analyses are used to adjust for baseline differences. Out of 666 patients with paroxysmal AF, 47 used verapamil, 383 used beta blockers, and 236 did not use rate control drugs. The verapamil group was significantly younger than the beta blocker group and contained more men than the no rate control group. Over a mean follow-up of 37 months, the primary outcome occurred in 17% in the verapamil group, 33% in the beta blocker group, and 33% in the no rate control group (P = 0.038). After adjusting for baseline characteristics, patients using verapamil have a significantly lower chance of receiving ECV, CCV, or atrial ablation compared to patients using beta blockers [hazard ratio (HR) 0.40, 95% confidence interval (CI) 0.19–0.83] and no rate control (HR 0.64, 95% CI 0.44–0.93). Conclusion In patients with newly diagnosed paroxysmal AF, verapamil was associated with less AF progression, as compared to beta blockers and no rate control.

Funder

Netherlands healthcare insurance companies (DSW, ACHMEA, and CZ), Boehringer Ingelheim, Bayer, Pfizer, Bristol-Myers Squibb, and Daiichi Sankyo

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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