TY - JOUR
T1 - Long-term effectiveness and safety of edoxaban in patients with atrial fibrillation
T2 - 4-year data from the ETNA-AF-Europe study
AU - ETNA-AF-Europe investigators
AU - Kirchhof, Paulus
AU - Bakhai, Ameet
AU - de Asmundis, Carlo
AU - de Groot, Joris R
AU - Deharo, Jean Claude
AU - Kelly, Peter
AU - Lopez-de-Sa, Esteban
AU - Monteiro, Pedro
AU - Fronk, Eva-Maria
AU - Lamparter, Mathias
AU - Laeis, Petra
AU - Smolnik, Rüdiger
AU - Steffel, Jan
AU - Waltenberger, Johannes
AU - Weiss, Thomas W
AU - De Caterina, Raffaele
N1 - Copyright © 2023. Published by Elsevier B.V.
PY - 2024/8/1
Y1 - 2024/8/1
N2 - Background: To assess long-term effectiveness and safety of edoxaban in Europe. Methods and results: ETNA-AF-Europe, a prospective, multinational, multi-centre, post-authorisation, observational study was conducted in agreement with the European Medicines Agency. The primary and secondary objectives assessed real-world safety (including bleeding and deaths) and effectiveness (including stroke, systemic embolic events and clinical edoxaban use), respectively. Median (interquartile range) age of the 13,164 patients was 75.0 (68.0–80.0) years; CHA
2DS
2-VASc and HAS-BLED scores were 3.0 (2.0–4.0) and 2.0 (1.0–2.0), respectively. Follow-up duration was 3.98 (3.21–4.05) years. Patients on edoxaban 30 mg (n = 3042) at baseline were older (80.0 vs 73.0 years), more likely assessed as frail by investigators (27.0% vs 6.6%) and had more comorbidities than those on edoxaban 60 mg (n = 9617; missing dosing information for n = 505). Annualised event rates of all-cause and cardiovascular death in the overall population, edoxaban 60 mg and edoxaban 30 mg groups were 4.1%, 2.8% and 8.4%, and 1.0%, 0.7% and 2.0%, respectively. Annualised rates of stroke were relatively constant throughout the follow-up, transient ischaemic attack and systemic embolism were < 1% in the overall population. Rates of any major and major gastrointestinal bleeding were low, with slightly higher rates for edoxaban 30 vs 60 mg group. Intracranial haemorrhage was uncommon (0.2%). Conclusions: In European patients with AF, long-term therapy with edoxaban is associated with low and relatively constant annualised rates of stroke and major bleeding. Differences in outcomes between the two approved doses are attributable to differences in clinical characteristics.
AB - Background: To assess long-term effectiveness and safety of edoxaban in Europe. Methods and results: ETNA-AF-Europe, a prospective, multinational, multi-centre, post-authorisation, observational study was conducted in agreement with the European Medicines Agency. The primary and secondary objectives assessed real-world safety (including bleeding and deaths) and effectiveness (including stroke, systemic embolic events and clinical edoxaban use), respectively. Median (interquartile range) age of the 13,164 patients was 75.0 (68.0–80.0) years; CHA
2DS
2-VASc and HAS-BLED scores were 3.0 (2.0–4.0) and 2.0 (1.0–2.0), respectively. Follow-up duration was 3.98 (3.21–4.05) years. Patients on edoxaban 30 mg (n = 3042) at baseline were older (80.0 vs 73.0 years), more likely assessed as frail by investigators (27.0% vs 6.6%) and had more comorbidities than those on edoxaban 60 mg (n = 9617; missing dosing information for n = 505). Annualised event rates of all-cause and cardiovascular death in the overall population, edoxaban 60 mg and edoxaban 30 mg groups were 4.1%, 2.8% and 8.4%, and 1.0%, 0.7% and 2.0%, respectively. Annualised rates of stroke were relatively constant throughout the follow-up, transient ischaemic attack and systemic embolism were < 1% in the overall population. Rates of any major and major gastrointestinal bleeding were low, with slightly higher rates for edoxaban 30 vs 60 mg group. Intracranial haemorrhage was uncommon (0.2%). Conclusions: In European patients with AF, long-term therapy with edoxaban is associated with low and relatively constant annualised rates of stroke and major bleeding. Differences in outcomes between the two approved doses are attributable to differences in clinical characteristics.
KW - Humans
KW - Thiazoles/adverse effects
KW - Pyridines/adverse effects
KW - Aged
KW - Atrial Fibrillation/drug therapy
KW - Male
KW - Female
KW - Europe/epidemiology
KW - Prospective Studies
KW - Factor Xa Inhibitors/adverse effects
KW - Aged, 80 and over
KW - Treatment Outcome
KW - Follow-Up Studies
KW - Time Factors
KW - Stroke/prevention & control
KW - Hemorrhage/chemically induced
UR - https://www.scopus.com/pages/publications/85193423006
U2 - 10.1016/j.ijcard.2024.132118
DO - 10.1016/j.ijcard.2024.132118
M3 - Article
C2 - 38697397
SN - 0167-5273
VL - 408
JO - International Journal of Cardiology
JF - International Journal of Cardiology
M1 - 132118
ER -