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. 2023 Jun 20;3(4):oead065.
doi: 10.1093/ehjopen/oead065. eCollection 2023 Jul.

Comparison of phenprocoumon with direct oral anticoagulants in catheter ablation of atrial fibrillation

Affiliations

Comparison of phenprocoumon with direct oral anticoagulants in catheter ablation of atrial fibrillation

Diona Gjermeni et al. Eur Heart J Open. .

Abstract

Aims: In patients undergoing catheter ablation for atrial fibrillation (AF), direct oral anticoagulants (DOACs) are as effective and safe as the vitamin K antagonist (VKA) warfarin. Phenprocoumon has a different pharmacokinetic profile compared with warfarin and is the most used VKA in Germany. The aim of the study was to compare DOAC with phenprocoumon.

Methods and results: In this retrospective single-centre cohort study, 1735 patients who underwent 2219 consecutive catheter ablations for AF between January 2011 and May 2017 were included. All patients were in-hospital for at least 48 h after catheter ablation. The primary outcome was defined as peri-procedural thrombo-embolic events. The secondary outcome was any bleeding according to the International Society on Thrombosis and Haemostasis (ISTH). The mean age of the patients was 63.3 years. Phenprocoumon was prescribed in 929 (42%) of the cases, and in 697 (31%) dabigatran, 399 (18%) rivaroxaban, and 194 (9%) apixaban. During hospitalization, 37 (1.6%) thrombo-embolic events occurred, including 23 transient ischaemic attacks (TIAs). Compared with the use of phenoprocoumon, the use of DOAC was significantly associated with a lower thrombo-embolic risk [16 (1.2%) vs. 21 (2.2%), odds ratio (OR)], 0.5 [95% confidence interval (CI) 0.2-0.9], P = 0.04. No statistically significant association with bleeding risk was observed [phenprocomoun: 122 (13%); DOAC: 163 (12.6%); OR 0.9 (95% CI 0.7-1.2); P = 0.70]. Interruption of oral anticoagulation (OAC) was associated with an increased risk for thrombo-embolic complications [OR 2.2 (1.1-4.3); P = 0.031], and bleeding [OR 2.5 (95% CI 1.8-3.2), P = 0.001].

Conclusion: In patients undergoing catheter ablation for AF, the use of DOAC was associated with a reduced risk of thrombo-embolic events compared with phenprocoumon. Non-interrupted oral anticoagulation (OAC) therapy was associated with a reduced risk of peri-procedural thrombo-embolic and any bleeding complications.

Keywords: Atrial fibrillation; Catheter ablation; Oral anticoagulation; Phenprocoumon.

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Figures

Graphical Abstract
Graphical Abstract
Figure 1
Figure 1
Rates of non-major but clinically relevant and major bleedings (%) for phenprocoumon (vitamin K antagonist), rivaroxaban, dabigatran, and apixaban. Figure 1 was made with Prism 9.2.0 (GraphPad software, La Jolla, CA, USA).

References

    1. Valderrama AL, Dunbar SB, Mensah GA. Atrial fibrillation. Am J Prev Med 2005;29:75–80. - PubMed
    1. Andersson T, Magnuson A, Bryngelsson I-L, Frøbert O, Henriksson KM, Edvardsson N, Poçi D. All-cause mortality in 272,186 patients hospitalized with incident atrial fibrillation 1995-2008: a Swedish nationwide long-term case-control study. Eur Heart J 2013;34:1061–1067. - PMC - PubMed
    1. Calkins H, Kuck KH, Cappato R, Brugada J, Camm AJ, Chen S-A, Crijns HJG, Damiano RJ, Davies DW, DiMarco J, Edgerton J, Ellenbogen K, Ezekowitz MD, Haines DE, Haissaguerre M, Hindricks G, Iesaka Y, Jackman W, Jalife J, Jais P, Kalman J, Keane D, Kim Y-H, Kirchhof P, Klein G, Kottkamp H, Kumagai K, Lindsay BD, Mansour M, Marchlinski FE, McCarthy PM, Mont JL, Morady F, Nademanee K, Nakagawa H, Natale A, Nattel S, Packer DL, Pappone C, Prystowsky E, Raviele A, Reddy V, Ruskin JN, Shemin RJ, Tsao H-M, Wilber D, Calkins H, Kuck KH, Cappato R, Chen S-A, Prystowsky EN, Kuck KH, Natale A, Haines DE, Marchlinski FE, Calkins H, Davies DW, Lindsay BD, Damiano R, Packer DL, Brugada J, Camm AJ, Crijns HJG, DiMarco J, Edgerton J, Ellenbogen K, Ezekowitz MD, Haissaguerre M, Hindricks G, Iesaka Y, Jackman WM, Jais P, Jalife J, Kalman J, Keane D, Kim Y-H, Kirchhof P, Klein G, Kottkamp H, Kumagai K, Mansour M, Marchlinski F, McCarthy P, Mont JL, Morady F, Nademanee K, Nakagawa H, Nattel S, Pappone C, Raviele A, Reddy V, Ruskin JN, Shemin RJ, Tsao H-M, Wilber D. 2012 HRS/EHRA/ECAS expert consensus statement on catheter and surgical ablation of atrial fibrillation: recommendations for patient selection, procedural techniques, patient management and follow-up, definitions, endpoints, and research trial design. Europace 2012;14:528–606. - PubMed
    1. Petersen P, Boysen G, Godtfredsen J, Andersen ED, Andersen B. Placebo-controlled, randomised trial of warfarin and aspirin for prevention of thromboembolic complications in chronic atrial fibrillation. The Copenhagen AFASAK study. Lancet 1989;1:175–179. - PubMed
    1. Ufer M. Comparative pharmacokinetics of vitamin K antagonists: warfarin, phenprocoumon and acenocoumarol. Clin Pharmacokinet 2005;44:1227–1246. - PubMed