Temporal patterns and short-term progression of paroxysmal atrial fibrillation: data from RACE V

Author:

De With Ruben R1,Erküner Ömer23,Rienstra Michiel1ORCID,Nguyen Bao-Oanh1,Körver Frank W J23,Linz Dominik23,Cate Ten Hugo34,Spronk Henri34,Kroon Abraham A34ORCID,Maass Alexander H1,Blaauw Yuri1,Tieleman Robert G15,Hemels Martin E W67,de Groot Joris R8,Elvan Arif9ORCID,de Melis Mirko1011,Scheerder Coert O S1011,Al-Jazairi Meelad I H1,Schotten Ulrich312,Luermans Justin G L M23,Crijns Harry J G M23,Van Gelder Isabelle C1,

Affiliation:

1. Department of Cardiology, University Medical Centre Groningen, University of Groningen, P.O. Box 30.001, 9700 RB Groningen, The Netherlands

2. Department of Cardiology, Maastricht University Medical Centre +, Maastricht, The Netherlands

3. Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, The Netherlands

4. Department of Internal Medicine, Maastricht University Medical Centre, +, Maastricht, The Netherlands

5. Department of Cardiology, Martini Hospital Groningen, Groningen, The Netherlands

6. Department of Cardiology, Rijnstate Hospital, Arnhem, The Netherlands

7. Department of Cardiology, Radboud University Medical Centre, Nijmegen, The Netherlands

8. Department of Cardiology, Amsterdam University Medical Centre, University of Amsterdam, Amsterdam, The Netherlands

9. Department of Cardiology, Isala Hospital, Zwolle, The Netherlands

10. Medtronic Bakken Research Centre, Maastricht, The Netherlands

11. Medtronic Bakken Research Centre, Maastricht; currently employed at Medtronic Trading NL, Eindhoven, The Netherlands

12. Department of Physiology, University of Maastricht, Maastricht, The Netherlands Received 30 March 2020; editorial decision 25 April 2020; accepted after revision 9 May 2020; online publish-ahead-of-print 8 July 2020

Abstract

Abstract Aims Atrial fibrillation (AF) often starts as a paroxysmal self-terminating arrhythmia. Limited information is available on AF patterns and episode duration of paroxysmal AF. In paroxysmal AF patients, we longitudinally studied the temporal AF patterns, the association with clinical characteristics, and prevalence of AF progression. Methods and results In this interim analysis of the Reappraisal of AF: Interaction Between HyperCoagulability, Electrical Remodelling, and Vascular Destabilisation in the Progression of AF (RACE V) registry, 202 patients with paroxysmal AF were followed with continuous rhythm monitoring (implantable loop recorder or pacemaker) for 6 months. Mean age was 64 ± 9 years, 42% were women. Atrial fibrillation history was 2.1 (0.5–4.4) years, CHA2DS2-VASc 1.9 ± 1.3, 101 (50%) had hypertension, 69 (34%) heart failure. One-third had no AF during follow-up. Patients with long episodes (>12 hours) were often men with more comorbidities (heart failure, coronary artery disease, higher left ventricular mass). Patients with higher AF burden (>2.5%) were older with more comorbidities (worse renal function, higher calcium score, thicker intima media thickness). In 179 (89%) patients, 1-year rhythm follow-up was available. On a quarterly basis, average daily AF burden increased from 3.2% to 3.8%, 5.2%, and 6.1%. Compared to the first 6 months, 111 (62%) patients remained stable during the second 6 months, 39 (22%) showed progression to longer AF episodes, 8 (3%) developed persistent AF, and 29 (16%) patients showed AF regression. Conclusions In paroxysmal AF, temporal patterns differ suggesting that paroxysmal AF is not one entity. Atrial fibrillation burden is low and determined by number of comorbidities. Atrial fibrillation progression occurred in a substantial number. Trial registration number Clinicaltrials.gov identifier NCT02726698.

Funder

Netherlands Cardiovascular Research Initiative

Dutch Heart Foundation

Medtronic

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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