@article{ff258d86f644405c84433c7a8ccb4c93,
title = "Contemporary management of patients with atrial fibrillation in the Netherlands and Belgium: a report from the EORP-AF long-term general registry",
abstract = "Background Contemporary data regarding the characteristics, treatment and outcomes of patients with atrial fibrillation (AF) are needed. We aimed to assess these data and guideline adherence in the EURObservational Research Programme on Atrial Fibrillation (EORP-AF) long-term general registry. Methods We analysed 967 patients from the EORP-AF long-term general registry included in the Netherlands and Belgium from 2013 to 2016. Baseline and 1-year follow-up data were gathered. Results At baseline, 887 patients (92%) received anticoagulant treatment. In 88 (10%) of these patients, no indication for chronic anticoagulant treatment was present. A rhythm intervention was performed or planned in 52 of these patients, meaning that the remaining 36 (41%) were anticoagulated without indication. Forty patients were not anticoagulated, even though they had an indication for chronic anticoagulation. Additionally, 63 of the 371 patients (17%) treated with a non-vitamin K antagonist oral anticoagulant (NOAC) were incorrectly dosed. In total, 50 patients (5%) were overtreated and 89 patients (9%) were undertreated. However, the occurrence of major adverse cardiac and cerebrovascular events (MACCE) was still low with 4.2% (37 patients). Conclusions Overtreatment and undertreatment with anticoagulants are still observable in 14% of this contemporary, West-European AF population. Still, MACCE occurred in only 4% of the patients after 1 year of follow-up.",
keywords = "Atrial fibrillation, Undertreatment, Overtreatment, Anticoagulant, EORP, Registry, EURO HEART SURVEY, MEMBER COUNTRIES, PROGRESSION",
author = "O. Erkuner and {Van Eck}, M. and O. Xhaet and H. Verheij and J. Neefs and A. Duygun and R. Nijmeijer and S.A.M. Said and H. Uiterwaal and V. Hagens and R. Bhagwandien and T. Szili-Torok and N. Bijsterveld and G. Tjeerdsma and J. Vijgen and A. Friart and E. Hoffer and P. Evrard and M. Srynger and J. Meeder and {De Groot}, J.R. and {Van Opstal}, J. and R. Gevers and G.Y.H. Lip and G. Boriani and H.J.G.M. Crijns and J.G.L.M. Luermans and G.H. Mairesse",
note = "Funding Information: The EURObservational Research Programme is supported by the following companies: Abbott Vascular Int. (2011–2014), Amgen Cardiovascular (2009–2018), AstraZeneca (2014–2017), Bayer AG (2009–2018), Boehringer Ingelheim (2009–2019), Boston Scientific (2009–2012), The Bristol Myers Squibb and Pfizer Alliance (2011–2016), The Alliance Daiichi Sankyo Europe GmbH and Eli Lilly and Company (2011–2017), Edwards (2016–2019), Gedeon Richter Plc. (2014–2017), Menarini Int. Op. (2009–2012), MSD-Merck & Co. (2011–2014), Novartis Pharma AG (2014–2017), ResMed (2014–2016), Sanofi (2009–2011), and SERVIER (2009–2018). Funding Information: We are very grateful to the alliance of Bristol-Myers Squibb and Pfizer for their financial support in performing the EORP-AF Long-Term General Registry in both the Netherlands and Belgium. The sponsor was not involved in the preparation or publication of this manuscript. Funding Information: We are grateful to all participating centres, investigators, and data collection officers for performing the registry. Data collection was conducted by the EURObservational Research Programme department from the European Cardiac Society by Patti-Ann McNeill as project officer and by Viviane Missiamenou as data manager. Overall activities were coordinated by Dr Aldo P. Maggioni (EORP Scientific Coordinator). We are very grateful to the alliance of Bristol-Myers Squibb and Pfizer for their financial support in performing the EORP-AF Long-Term General Registry in both the Netherlands and Belgium. The sponsor was not involved in the preparation or publication of this manuscript. The EURObservational Research Programme is supported by the following companies: Abbott Vascular Int. (2011–2014), Amgen Cardiovascular (2009–2018), AstraZeneca (2014–2017), Bayer AG (2009–2018), Boehringer Ingelheim (2009–2019), Boston Scientific (2009–2012), The Bristol Myers Squibb and Pfizer Alliance (2011–2016), The Alliance Daiichi Sankyo Europe GmbH and Eli Lilly and Company (2011–2017), Edwards (2016–2019), Gedeon Richter Plc. (2014–2017), Menarini Int. Op. (2009–2012), MSD-Merck & Co. (2011–2014), Novartis Pharma AG (2014–2017), ResMed (2014–2016), Sanofi (2009–2011), and SERVIER (2009–2018). This work was supported by the Netherlands Cardiovascular Research Initiative: an initiative with support of the Dutch Heart Foundation [CVON 2014‑9, RACE V: “Reappraisal of Atrial Fibrillation: interaction between hyperCoagulability, Electrical remodelling, and Vascular destabilisation in the progression of AF” to {\"O}.E., H.J.G.M.C., J.G.L.M.L]. Publisher Copyright: {\textcopyright} 2021, The Author(s).",
year = "2021",
month = nov,
doi = "10.1007/s12471-021-01634-y",
language = "English",
volume = "29",
pages = "584--594",
journal = "Netherlands Heart Journal",
issn = "1568-5888",
publisher = "Bohn Stafleu van Loghum",
number = "11",
}