Edoxaban Treatment in routiNe clinical prActice in patients with non-valvular Atrial Fibrillation (ETNA-AF) in Iberia: Baseline data
Introduction and Objectives: Atrial fibrillation (AF) is the most common form of arrhythmia worldwide and a significant health burden. Edoxaban, a recent novel oral anticoagulant (NOAC), is being investigated in the European real-world ETNA-AF study of patients with non-valvular atrial fibrillation...
Ausführliche Beschreibung
Autor*in: |
Pedro Monteiro [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch ; Portugiesisch |
Erschienen: |
2020 |
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Schlagwörter: |
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Übergeordnetes Werk: |
In: Revista Portuguesa de Cardiologia - Elsevier, 2020, 39(2020), 11, Seite 651-662 |
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Übergeordnetes Werk: |
volume:39 ; year:2020 ; number:11 ; pages:651-662 |
Links: |
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DOI / URN: |
10.1016/j.repc.2020.09.003 |
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Katalog-ID: |
DOAJ044087381 |
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520 | |a Introduction and Objectives: Atrial fibrillation (AF) is the most common form of arrhythmia worldwide and a significant health burden. Edoxaban, a recent novel oral anticoagulant (NOAC), is being investigated in the European real-world ETNA-AF study of patients with non-valvular atrial fibrillation (NVAF). The aim of this study was to characterize the Iberian edoxaban-treated cohort of ETNA-AF at baseline and to compare it with previously retrieved Portuguese data. Methods: Patients with NVAF treated with edoxaban and followed in Portuguese and Spanish centers were consecutively enrolled between June 2017 and January 2018. Only patients with a previous clinical decision to receive edoxaban were included. Patients’ baseline demographic and clinical parameters, medical history, and AF-related characteristics were retrieved. Results: A total of 892 NVAF patients, with a mean age of 73.9 years, were included, 75.3% of whom received high-dose (60 mg) and 24.7% low-dose (30 mg) edoxaban. Most patients (55.9%) were male. Of the patients receiving 30 mg and 60 mg edoxaban, 55.9% and 37.9%, respectively, had an estimated CHA2DS2-VASc score ≥4. Previous bleeding event rates were low, with a predominance of clinically relevant non-major bleeding (1.9%). Most patients (47.5%) with NVAF had paroxysmal AF, followed by 26.4% with permanent AF. Median overall CHA2DS2-VASc score was 3.0 and median HAS-BLED score was 2.0. Previous treatments mostly included vitamin K antagonists (35.7%). A considerably higher proportion of patients on low-dose edoxaban required dose adjustments (71.4% vs. 8.6%). Overall adherence to label dosing recommendations was 86.5%. Conclusions: This study provides valuable data on disease and patient profiles and will provide valuable insights into disease management and progression, as well as the safety, effectiveness, and patterns of cardiovascular events associated with edoxaban. Resumo: Introdução e objetivos: A fibrilhação auricular (FA) é a arritmia mais comum globalmente e associa-se a um substancial ónus de saúde. O novo anticoagulante oral (NOAC) edoxabano está a ser investigado no estudo europeu de vida real ETNA-AF em doentes com fibrilhação auricular não valvular (FANV). O objetivo deste estudo é caracterizar a coorte ibérica do ETNA-AF na base de dados e compará-la com dados portugueses prévios. Métodos: Doentes com FANV tratados com edoxabano e seguidos em centros portugueses e espanhóis foram consecutivamente incluídos no estudo entre junho de 2017 e janeiro de 2018. Apenas doentes com indicação prévia para receber edoxabano foram incluídos e os seus dados clínicos e demográficos, história clínica e características relacionadas com a FA foram registados. Resultados: Fora, incluídos 892 doentes com FANV, com média de 73,9 anos, 75,3% dos quais receberam a dose elevada (60 mg) e 24,7% a dose reduzida (30 mg) de edoxabano. A maioria dos doentes (55,9%) era do sexo masculino. Dos doentes que receberam 30 mg e 60 mg de edoxabano, 55,9% e 37,9%, respetivamente, tinham CHA2DS2-VASc estimado ≥ 4. As taxas de eventos hemorrágicos prévios foram baixas, com predominância de hemorragia não major clinicamente relevante (1,9%). A maioria (47,5%) dos doentes com FANV tinha FA paroxística, seguidos de 26,4% com FA permanente. A mediana de CHA2DS2-VASc global foi 3,0 e a mediana de HAS-BLED, 2,0. Os tratamentos prévios incluíram sobretudo VKAs (35,7%). Uma proporção consideravelmente maior de doentes a receber dose reduzida de edoxabano necessitou de ajustes de dose (71,4% versus 8,6%). A adesão global às recomendações de dose foi de 86,5%. Conclusões: Este estudo fornece dados importantes sobre a doença e o perfil dos doentes e possibilitará considerações futuras acerca da gestão e progressão da doença, bem como de segurança, efetividade e padrões de eventos cardiovasculares associados a edoxabano. | ||
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10.1016/j.repc.2020.09.003 doi (DE-627)DOAJ044087381 (DE-599)DOAJ6a1eeab3a2fa490c9eaf0ab85f29cf75 DE-627 ger DE-627 rakwb eng por RC666-701 Pedro Monteiro verfasserin aut Edoxaban Treatment in routiNe clinical prActice in patients with non-valvular Atrial Fibrillation (ETNA-AF) in Iberia: Baseline data 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction and Objectives: Atrial fibrillation (AF) is the most common form of arrhythmia worldwide and a significant health burden. Edoxaban, a recent novel oral anticoagulant (NOAC), is being investigated in the European real-world ETNA-AF study of patients with non-valvular atrial fibrillation (NVAF). The aim of this study was to characterize the Iberian edoxaban-treated cohort of ETNA-AF at baseline and to compare it with previously retrieved Portuguese data. Methods: Patients with NVAF treated with edoxaban and followed in Portuguese and Spanish centers were consecutively enrolled between June 2017 and January 2018. Only patients with a previous clinical decision to receive edoxaban were included. Patients’ baseline demographic and clinical parameters, medical history, and AF-related characteristics were retrieved. Results: A total of 892 NVAF patients, with a mean age of 73.9 years, were included, 75.3% of whom received high-dose (60 mg) and 24.7% low-dose (30 mg) edoxaban. Most patients (55.9%) were male. Of the patients receiving 30 mg and 60 mg edoxaban, 55.9% and 37.9%, respectively, had an estimated CHA2DS2-VASc score ≥4. Previous bleeding event rates were low, with a predominance of clinically relevant non-major bleeding (1.9%). Most patients (47.5%) with NVAF had paroxysmal AF, followed by 26.4% with permanent AF. Median overall CHA2DS2-VASc score was 3.0 and median HAS-BLED score was 2.0. Previous treatments mostly included vitamin K antagonists (35.7%). A considerably higher proportion of patients on low-dose edoxaban required dose adjustments (71.4% vs. 8.6%). Overall adherence to label dosing recommendations was 86.5%. Conclusions: This study provides valuable data on disease and patient profiles and will provide valuable insights into disease management and progression, as well as the safety, effectiveness, and patterns of cardiovascular events associated with edoxaban. Resumo: Introdução e objetivos: A fibrilhação auricular (FA) é a arritmia mais comum globalmente e associa-se a um substancial ónus de saúde. O novo anticoagulante oral (NOAC) edoxabano está a ser investigado no estudo europeu de vida real ETNA-AF em doentes com fibrilhação auricular não valvular (FANV). O objetivo deste estudo é caracterizar a coorte ibérica do ETNA-AF na base de dados e compará-la com dados portugueses prévios. Métodos: Doentes com FANV tratados com edoxabano e seguidos em centros portugueses e espanhóis foram consecutivamente incluídos no estudo entre junho de 2017 e janeiro de 2018. Apenas doentes com indicação prévia para receber edoxabano foram incluídos e os seus dados clínicos e demográficos, história clínica e características relacionadas com a FA foram registados. Resultados: Fora, incluídos 892 doentes com FANV, com média de 73,9 anos, 75,3% dos quais receberam a dose elevada (60 mg) e 24,7% a dose reduzida (30 mg) de edoxabano. A maioria dos doentes (55,9%) era do sexo masculino. Dos doentes que receberam 30 mg e 60 mg de edoxabano, 55,9% e 37,9%, respetivamente, tinham CHA2DS2-VASc estimado ≥ 4. As taxas de eventos hemorrágicos prévios foram baixas, com predominância de hemorragia não major clinicamente relevante (1,9%). A maioria (47,5%) dos doentes com FANV tinha FA paroxística, seguidos de 26,4% com FA permanente. A mediana de CHA2DS2-VASc global foi 3,0 e a mediana de HAS-BLED, 2,0. Os tratamentos prévios incluíram sobretudo VKAs (35,7%). Uma proporção consideravelmente maior de doentes a receber dose reduzida de edoxabano necessitou de ajustes de dose (71,4% versus 8,6%). A adesão global às recomendações de dose foi de 86,5%. Conclusões: Este estudo fornece dados importantes sobre a doença e o perfil dos doentes e possibilitará considerações futuras acerca da gestão e progressão da doença, bem como de segurança, efetividade e padrões de eventos cardiovasculares associados a edoxabano. Fibrilhação auricular Edoxabano Baseline Vida real Diseases of the circulatory (Cardiovascular) system In Revista Portuguesa de Cardiologia Elsevier, 2020 39(2020), 11, Seite 651-662 (DE-627)642886164 (DE-600)2586869-X 21742030 nnns volume:39 year:2020 number:11 pages:651-662 https://doi.org/10.1016/j.repc.2020.09.003 kostenfrei https://doaj.org/article/6a1eeab3a2fa490c9eaf0ab85f29cf75 kostenfrei http://www.sciencedirect.com/science/article/pii/S0870255120304066 kostenfrei https://doaj.org/toc/0870-2551 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 39 2020 11 651-662 |
spelling |
10.1016/j.repc.2020.09.003 doi (DE-627)DOAJ044087381 (DE-599)DOAJ6a1eeab3a2fa490c9eaf0ab85f29cf75 DE-627 ger DE-627 rakwb eng por RC666-701 Pedro Monteiro verfasserin aut Edoxaban Treatment in routiNe clinical prActice in patients with non-valvular Atrial Fibrillation (ETNA-AF) in Iberia: Baseline data 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction and Objectives: Atrial fibrillation (AF) is the most common form of arrhythmia worldwide and a significant health burden. Edoxaban, a recent novel oral anticoagulant (NOAC), is being investigated in the European real-world ETNA-AF study of patients with non-valvular atrial fibrillation (NVAF). The aim of this study was to characterize the Iberian edoxaban-treated cohort of ETNA-AF at baseline and to compare it with previously retrieved Portuguese data. Methods: Patients with NVAF treated with edoxaban and followed in Portuguese and Spanish centers were consecutively enrolled between June 2017 and January 2018. Only patients with a previous clinical decision to receive edoxaban were included. Patients’ baseline demographic and clinical parameters, medical history, and AF-related characteristics were retrieved. Results: A total of 892 NVAF patients, with a mean age of 73.9 years, were included, 75.3% of whom received high-dose (60 mg) and 24.7% low-dose (30 mg) edoxaban. Most patients (55.9%) were male. Of the patients receiving 30 mg and 60 mg edoxaban, 55.9% and 37.9%, respectively, had an estimated CHA2DS2-VASc score ≥4. Previous bleeding event rates were low, with a predominance of clinically relevant non-major bleeding (1.9%). Most patients (47.5%) with NVAF had paroxysmal AF, followed by 26.4% with permanent AF. Median overall CHA2DS2-VASc score was 3.0 and median HAS-BLED score was 2.0. Previous treatments mostly included vitamin K antagonists (35.7%). A considerably higher proportion of patients on low-dose edoxaban required dose adjustments (71.4% vs. 8.6%). Overall adherence to label dosing recommendations was 86.5%. Conclusions: This study provides valuable data on disease and patient profiles and will provide valuable insights into disease management and progression, as well as the safety, effectiveness, and patterns of cardiovascular events associated with edoxaban. Resumo: Introdução e objetivos: A fibrilhação auricular (FA) é a arritmia mais comum globalmente e associa-se a um substancial ónus de saúde. O novo anticoagulante oral (NOAC) edoxabano está a ser investigado no estudo europeu de vida real ETNA-AF em doentes com fibrilhação auricular não valvular (FANV). O objetivo deste estudo é caracterizar a coorte ibérica do ETNA-AF na base de dados e compará-la com dados portugueses prévios. Métodos: Doentes com FANV tratados com edoxabano e seguidos em centros portugueses e espanhóis foram consecutivamente incluídos no estudo entre junho de 2017 e janeiro de 2018. Apenas doentes com indicação prévia para receber edoxabano foram incluídos e os seus dados clínicos e demográficos, história clínica e características relacionadas com a FA foram registados. Resultados: Fora, incluídos 892 doentes com FANV, com média de 73,9 anos, 75,3% dos quais receberam a dose elevada (60 mg) e 24,7% a dose reduzida (30 mg) de edoxabano. A maioria dos doentes (55,9%) era do sexo masculino. Dos doentes que receberam 30 mg e 60 mg de edoxabano, 55,9% e 37,9%, respetivamente, tinham CHA2DS2-VASc estimado ≥ 4. As taxas de eventos hemorrágicos prévios foram baixas, com predominância de hemorragia não major clinicamente relevante (1,9%). A maioria (47,5%) dos doentes com FANV tinha FA paroxística, seguidos de 26,4% com FA permanente. A mediana de CHA2DS2-VASc global foi 3,0 e a mediana de HAS-BLED, 2,0. Os tratamentos prévios incluíram sobretudo VKAs (35,7%). Uma proporção consideravelmente maior de doentes a receber dose reduzida de edoxabano necessitou de ajustes de dose (71,4% versus 8,6%). A adesão global às recomendações de dose foi de 86,5%. Conclusões: Este estudo fornece dados importantes sobre a doença e o perfil dos doentes e possibilitará considerações futuras acerca da gestão e progressão da doença, bem como de segurança, efetividade e padrões de eventos cardiovasculares associados a edoxabano. Fibrilhação auricular Edoxabano Baseline Vida real Diseases of the circulatory (Cardiovascular) system In Revista Portuguesa de Cardiologia Elsevier, 2020 39(2020), 11, Seite 651-662 (DE-627)642886164 (DE-600)2586869-X 21742030 nnns volume:39 year:2020 number:11 pages:651-662 https://doi.org/10.1016/j.repc.2020.09.003 kostenfrei https://doaj.org/article/6a1eeab3a2fa490c9eaf0ab85f29cf75 kostenfrei http://www.sciencedirect.com/science/article/pii/S0870255120304066 kostenfrei https://doaj.org/toc/0870-2551 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 39 2020 11 651-662 |
allfields_unstemmed |
10.1016/j.repc.2020.09.003 doi (DE-627)DOAJ044087381 (DE-599)DOAJ6a1eeab3a2fa490c9eaf0ab85f29cf75 DE-627 ger DE-627 rakwb eng por RC666-701 Pedro Monteiro verfasserin aut Edoxaban Treatment in routiNe clinical prActice in patients with non-valvular Atrial Fibrillation (ETNA-AF) in Iberia: Baseline data 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction and Objectives: Atrial fibrillation (AF) is the most common form of arrhythmia worldwide and a significant health burden. Edoxaban, a recent novel oral anticoagulant (NOAC), is being investigated in the European real-world ETNA-AF study of patients with non-valvular atrial fibrillation (NVAF). The aim of this study was to characterize the Iberian edoxaban-treated cohort of ETNA-AF at baseline and to compare it with previously retrieved Portuguese data. Methods: Patients with NVAF treated with edoxaban and followed in Portuguese and Spanish centers were consecutively enrolled between June 2017 and January 2018. Only patients with a previous clinical decision to receive edoxaban were included. Patients’ baseline demographic and clinical parameters, medical history, and AF-related characteristics were retrieved. Results: A total of 892 NVAF patients, with a mean age of 73.9 years, were included, 75.3% of whom received high-dose (60 mg) and 24.7% low-dose (30 mg) edoxaban. Most patients (55.9%) were male. Of the patients receiving 30 mg and 60 mg edoxaban, 55.9% and 37.9%, respectively, had an estimated CHA2DS2-VASc score ≥4. Previous bleeding event rates were low, with a predominance of clinically relevant non-major bleeding (1.9%). Most patients (47.5%) with NVAF had paroxysmal AF, followed by 26.4% with permanent AF. Median overall CHA2DS2-VASc score was 3.0 and median HAS-BLED score was 2.0. Previous treatments mostly included vitamin K antagonists (35.7%). A considerably higher proportion of patients on low-dose edoxaban required dose adjustments (71.4% vs. 8.6%). Overall adherence to label dosing recommendations was 86.5%. Conclusions: This study provides valuable data on disease and patient profiles and will provide valuable insights into disease management and progression, as well as the safety, effectiveness, and patterns of cardiovascular events associated with edoxaban. Resumo: Introdução e objetivos: A fibrilhação auricular (FA) é a arritmia mais comum globalmente e associa-se a um substancial ónus de saúde. O novo anticoagulante oral (NOAC) edoxabano está a ser investigado no estudo europeu de vida real ETNA-AF em doentes com fibrilhação auricular não valvular (FANV). O objetivo deste estudo é caracterizar a coorte ibérica do ETNA-AF na base de dados e compará-la com dados portugueses prévios. Métodos: Doentes com FANV tratados com edoxabano e seguidos em centros portugueses e espanhóis foram consecutivamente incluídos no estudo entre junho de 2017 e janeiro de 2018. Apenas doentes com indicação prévia para receber edoxabano foram incluídos e os seus dados clínicos e demográficos, história clínica e características relacionadas com a FA foram registados. Resultados: Fora, incluídos 892 doentes com FANV, com média de 73,9 anos, 75,3% dos quais receberam a dose elevada (60 mg) e 24,7% a dose reduzida (30 mg) de edoxabano. A maioria dos doentes (55,9%) era do sexo masculino. Dos doentes que receberam 30 mg e 60 mg de edoxabano, 55,9% e 37,9%, respetivamente, tinham CHA2DS2-VASc estimado ≥ 4. As taxas de eventos hemorrágicos prévios foram baixas, com predominância de hemorragia não major clinicamente relevante (1,9%). A maioria (47,5%) dos doentes com FANV tinha FA paroxística, seguidos de 26,4% com FA permanente. A mediana de CHA2DS2-VASc global foi 3,0 e a mediana de HAS-BLED, 2,0. Os tratamentos prévios incluíram sobretudo VKAs (35,7%). Uma proporção consideravelmente maior de doentes a receber dose reduzida de edoxabano necessitou de ajustes de dose (71,4% versus 8,6%). A adesão global às recomendações de dose foi de 86,5%. Conclusões: Este estudo fornece dados importantes sobre a doença e o perfil dos doentes e possibilitará considerações futuras acerca da gestão e progressão da doença, bem como de segurança, efetividade e padrões de eventos cardiovasculares associados a edoxabano. Fibrilhação auricular Edoxabano Baseline Vida real Diseases of the circulatory (Cardiovascular) system In Revista Portuguesa de Cardiologia Elsevier, 2020 39(2020), 11, Seite 651-662 (DE-627)642886164 (DE-600)2586869-X 21742030 nnns volume:39 year:2020 number:11 pages:651-662 https://doi.org/10.1016/j.repc.2020.09.003 kostenfrei https://doaj.org/article/6a1eeab3a2fa490c9eaf0ab85f29cf75 kostenfrei http://www.sciencedirect.com/science/article/pii/S0870255120304066 kostenfrei https://doaj.org/toc/0870-2551 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 39 2020 11 651-662 |
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10.1016/j.repc.2020.09.003 doi (DE-627)DOAJ044087381 (DE-599)DOAJ6a1eeab3a2fa490c9eaf0ab85f29cf75 DE-627 ger DE-627 rakwb eng por RC666-701 Pedro Monteiro verfasserin aut Edoxaban Treatment in routiNe clinical prActice in patients with non-valvular Atrial Fibrillation (ETNA-AF) in Iberia: Baseline data 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction and Objectives: Atrial fibrillation (AF) is the most common form of arrhythmia worldwide and a significant health burden. Edoxaban, a recent novel oral anticoagulant (NOAC), is being investigated in the European real-world ETNA-AF study of patients with non-valvular atrial fibrillation (NVAF). The aim of this study was to characterize the Iberian edoxaban-treated cohort of ETNA-AF at baseline and to compare it with previously retrieved Portuguese data. Methods: Patients with NVAF treated with edoxaban and followed in Portuguese and Spanish centers were consecutively enrolled between June 2017 and January 2018. Only patients with a previous clinical decision to receive edoxaban were included. Patients’ baseline demographic and clinical parameters, medical history, and AF-related characteristics were retrieved. Results: A total of 892 NVAF patients, with a mean age of 73.9 years, were included, 75.3% of whom received high-dose (60 mg) and 24.7% low-dose (30 mg) edoxaban. Most patients (55.9%) were male. Of the patients receiving 30 mg and 60 mg edoxaban, 55.9% and 37.9%, respectively, had an estimated CHA2DS2-VASc score ≥4. Previous bleeding event rates were low, with a predominance of clinically relevant non-major bleeding (1.9%). Most patients (47.5%) with NVAF had paroxysmal AF, followed by 26.4% with permanent AF. Median overall CHA2DS2-VASc score was 3.0 and median HAS-BLED score was 2.0. Previous treatments mostly included vitamin K antagonists (35.7%). A considerably higher proportion of patients on low-dose edoxaban required dose adjustments (71.4% vs. 8.6%). Overall adherence to label dosing recommendations was 86.5%. Conclusions: This study provides valuable data on disease and patient profiles and will provide valuable insights into disease management and progression, as well as the safety, effectiveness, and patterns of cardiovascular events associated with edoxaban. Resumo: Introdução e objetivos: A fibrilhação auricular (FA) é a arritmia mais comum globalmente e associa-se a um substancial ónus de saúde. O novo anticoagulante oral (NOAC) edoxabano está a ser investigado no estudo europeu de vida real ETNA-AF em doentes com fibrilhação auricular não valvular (FANV). O objetivo deste estudo é caracterizar a coorte ibérica do ETNA-AF na base de dados e compará-la com dados portugueses prévios. Métodos: Doentes com FANV tratados com edoxabano e seguidos em centros portugueses e espanhóis foram consecutivamente incluídos no estudo entre junho de 2017 e janeiro de 2018. Apenas doentes com indicação prévia para receber edoxabano foram incluídos e os seus dados clínicos e demográficos, história clínica e características relacionadas com a FA foram registados. Resultados: Fora, incluídos 892 doentes com FANV, com média de 73,9 anos, 75,3% dos quais receberam a dose elevada (60 mg) e 24,7% a dose reduzida (30 mg) de edoxabano. A maioria dos doentes (55,9%) era do sexo masculino. Dos doentes que receberam 30 mg e 60 mg de edoxabano, 55,9% e 37,9%, respetivamente, tinham CHA2DS2-VASc estimado ≥ 4. As taxas de eventos hemorrágicos prévios foram baixas, com predominância de hemorragia não major clinicamente relevante (1,9%). A maioria (47,5%) dos doentes com FANV tinha FA paroxística, seguidos de 26,4% com FA permanente. A mediana de CHA2DS2-VASc global foi 3,0 e a mediana de HAS-BLED, 2,0. Os tratamentos prévios incluíram sobretudo VKAs (35,7%). Uma proporção consideravelmente maior de doentes a receber dose reduzida de edoxabano necessitou de ajustes de dose (71,4% versus 8,6%). A adesão global às recomendações de dose foi de 86,5%. Conclusões: Este estudo fornece dados importantes sobre a doença e o perfil dos doentes e possibilitará considerações futuras acerca da gestão e progressão da doença, bem como de segurança, efetividade e padrões de eventos cardiovasculares associados a edoxabano. Fibrilhação auricular Edoxabano Baseline Vida real Diseases of the circulatory (Cardiovascular) system In Revista Portuguesa de Cardiologia Elsevier, 2020 39(2020), 11, Seite 651-662 (DE-627)642886164 (DE-600)2586869-X 21742030 nnns volume:39 year:2020 number:11 pages:651-662 https://doi.org/10.1016/j.repc.2020.09.003 kostenfrei https://doaj.org/article/6a1eeab3a2fa490c9eaf0ab85f29cf75 kostenfrei http://www.sciencedirect.com/science/article/pii/S0870255120304066 kostenfrei https://doaj.org/toc/0870-2551 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 39 2020 11 651-662 |
allfieldsSound |
10.1016/j.repc.2020.09.003 doi (DE-627)DOAJ044087381 (DE-599)DOAJ6a1eeab3a2fa490c9eaf0ab85f29cf75 DE-627 ger DE-627 rakwb eng por RC666-701 Pedro Monteiro verfasserin aut Edoxaban Treatment in routiNe clinical prActice in patients with non-valvular Atrial Fibrillation (ETNA-AF) in Iberia: Baseline data 2020 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction and Objectives: Atrial fibrillation (AF) is the most common form of arrhythmia worldwide and a significant health burden. Edoxaban, a recent novel oral anticoagulant (NOAC), is being investigated in the European real-world ETNA-AF study of patients with non-valvular atrial fibrillation (NVAF). The aim of this study was to characterize the Iberian edoxaban-treated cohort of ETNA-AF at baseline and to compare it with previously retrieved Portuguese data. Methods: Patients with NVAF treated with edoxaban and followed in Portuguese and Spanish centers were consecutively enrolled between June 2017 and January 2018. Only patients with a previous clinical decision to receive edoxaban were included. Patients’ baseline demographic and clinical parameters, medical history, and AF-related characteristics were retrieved. Results: A total of 892 NVAF patients, with a mean age of 73.9 years, were included, 75.3% of whom received high-dose (60 mg) and 24.7% low-dose (30 mg) edoxaban. Most patients (55.9%) were male. Of the patients receiving 30 mg and 60 mg edoxaban, 55.9% and 37.9%, respectively, had an estimated CHA2DS2-VASc score ≥4. Previous bleeding event rates were low, with a predominance of clinically relevant non-major bleeding (1.9%). Most patients (47.5%) with NVAF had paroxysmal AF, followed by 26.4% with permanent AF. Median overall CHA2DS2-VASc score was 3.0 and median HAS-BLED score was 2.0. Previous treatments mostly included vitamin K antagonists (35.7%). A considerably higher proportion of patients on low-dose edoxaban required dose adjustments (71.4% vs. 8.6%). Overall adherence to label dosing recommendations was 86.5%. Conclusions: This study provides valuable data on disease and patient profiles and will provide valuable insights into disease management and progression, as well as the safety, effectiveness, and patterns of cardiovascular events associated with edoxaban. Resumo: Introdução e objetivos: A fibrilhação auricular (FA) é a arritmia mais comum globalmente e associa-se a um substancial ónus de saúde. O novo anticoagulante oral (NOAC) edoxabano está a ser investigado no estudo europeu de vida real ETNA-AF em doentes com fibrilhação auricular não valvular (FANV). O objetivo deste estudo é caracterizar a coorte ibérica do ETNA-AF na base de dados e compará-la com dados portugueses prévios. Métodos: Doentes com FANV tratados com edoxabano e seguidos em centros portugueses e espanhóis foram consecutivamente incluídos no estudo entre junho de 2017 e janeiro de 2018. Apenas doentes com indicação prévia para receber edoxabano foram incluídos e os seus dados clínicos e demográficos, história clínica e características relacionadas com a FA foram registados. Resultados: Fora, incluídos 892 doentes com FANV, com média de 73,9 anos, 75,3% dos quais receberam a dose elevada (60 mg) e 24,7% a dose reduzida (30 mg) de edoxabano. A maioria dos doentes (55,9%) era do sexo masculino. Dos doentes que receberam 30 mg e 60 mg de edoxabano, 55,9% e 37,9%, respetivamente, tinham CHA2DS2-VASc estimado ≥ 4. As taxas de eventos hemorrágicos prévios foram baixas, com predominância de hemorragia não major clinicamente relevante (1,9%). A maioria (47,5%) dos doentes com FANV tinha FA paroxística, seguidos de 26,4% com FA permanente. A mediana de CHA2DS2-VASc global foi 3,0 e a mediana de HAS-BLED, 2,0. Os tratamentos prévios incluíram sobretudo VKAs (35,7%). Uma proporção consideravelmente maior de doentes a receber dose reduzida de edoxabano necessitou de ajustes de dose (71,4% versus 8,6%). A adesão global às recomendações de dose foi de 86,5%. Conclusões: Este estudo fornece dados importantes sobre a doença e o perfil dos doentes e possibilitará considerações futuras acerca da gestão e progressão da doença, bem como de segurança, efetividade e padrões de eventos cardiovasculares associados a edoxabano. Fibrilhação auricular Edoxabano Baseline Vida real Diseases of the circulatory (Cardiovascular) system In Revista Portuguesa de Cardiologia Elsevier, 2020 39(2020), 11, Seite 651-662 (DE-627)642886164 (DE-600)2586869-X 21742030 nnns volume:39 year:2020 number:11 pages:651-662 https://doi.org/10.1016/j.repc.2020.09.003 kostenfrei https://doaj.org/article/6a1eeab3a2fa490c9eaf0ab85f29cf75 kostenfrei http://www.sciencedirect.com/science/article/pii/S0870255120304066 kostenfrei https://doaj.org/toc/0870-2551 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 39 2020 11 651-662 |
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Of the patients receiving 30 mg and 60 mg edoxaban, 55.9% and 37.9%, respectively, had an estimated CHA2DS2-VASc score ≥4. Previous bleeding event rates were low, with a predominance of clinically relevant non-major bleeding (1.9%). Most patients (47.5%) with NVAF had paroxysmal AF, followed by 26.4% with permanent AF. Median overall CHA2DS2-VASc score was 3.0 and median HAS-BLED score was 2.0. Previous treatments mostly included vitamin K antagonists (35.7%). A considerably higher proportion of patients on low-dose edoxaban required dose adjustments (71.4% vs. 8.6%). Overall adherence to label dosing recommendations was 86.5%. Conclusions: This study provides valuable data on disease and patient profiles and will provide valuable insights into disease management and progression, as well as the safety, effectiveness, and patterns of cardiovascular events associated with edoxaban. 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RC666-701 Edoxaban Treatment in routiNe clinical prActice in patients with non-valvular Atrial Fibrillation (ETNA-AF) in Iberia: Baseline data Fibrilhação auricular Edoxabano Baseline Vida real |
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edoxaban treatment in routine clinical practice in patients with non-valvular atrial fibrillation (etna-af) in iberia: baseline data |
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Edoxaban Treatment in routiNe clinical prActice in patients with non-valvular Atrial Fibrillation (ETNA-AF) in Iberia: Baseline data |
abstract |
Introduction and Objectives: Atrial fibrillation (AF) is the most common form of arrhythmia worldwide and a significant health burden. Edoxaban, a recent novel oral anticoagulant (NOAC), is being investigated in the European real-world ETNA-AF study of patients with non-valvular atrial fibrillation (NVAF). The aim of this study was to characterize the Iberian edoxaban-treated cohort of ETNA-AF at baseline and to compare it with previously retrieved Portuguese data. Methods: Patients with NVAF treated with edoxaban and followed in Portuguese and Spanish centers were consecutively enrolled between June 2017 and January 2018. Only patients with a previous clinical decision to receive edoxaban were included. Patients’ baseline demographic and clinical parameters, medical history, and AF-related characteristics were retrieved. Results: A total of 892 NVAF patients, with a mean age of 73.9 years, were included, 75.3% of whom received high-dose (60 mg) and 24.7% low-dose (30 mg) edoxaban. Most patients (55.9%) were male. Of the patients receiving 30 mg and 60 mg edoxaban, 55.9% and 37.9%, respectively, had an estimated CHA2DS2-VASc score ≥4. Previous bleeding event rates were low, with a predominance of clinically relevant non-major bleeding (1.9%). Most patients (47.5%) with NVAF had paroxysmal AF, followed by 26.4% with permanent AF. Median overall CHA2DS2-VASc score was 3.0 and median HAS-BLED score was 2.0. Previous treatments mostly included vitamin K antagonists (35.7%). A considerably higher proportion of patients on low-dose edoxaban required dose adjustments (71.4% vs. 8.6%). Overall adherence to label dosing recommendations was 86.5%. Conclusions: This study provides valuable data on disease and patient profiles and will provide valuable insights into disease management and progression, as well as the safety, effectiveness, and patterns of cardiovascular events associated with edoxaban. Resumo: Introdução e objetivos: A fibrilhação auricular (FA) é a arritmia mais comum globalmente e associa-se a um substancial ónus de saúde. O novo anticoagulante oral (NOAC) edoxabano está a ser investigado no estudo europeu de vida real ETNA-AF em doentes com fibrilhação auricular não valvular (FANV). O objetivo deste estudo é caracterizar a coorte ibérica do ETNA-AF na base de dados e compará-la com dados portugueses prévios. Métodos: Doentes com FANV tratados com edoxabano e seguidos em centros portugueses e espanhóis foram consecutivamente incluídos no estudo entre junho de 2017 e janeiro de 2018. Apenas doentes com indicação prévia para receber edoxabano foram incluídos e os seus dados clínicos e demográficos, história clínica e características relacionadas com a FA foram registados. Resultados: Fora, incluídos 892 doentes com FANV, com média de 73,9 anos, 75,3% dos quais receberam a dose elevada (60 mg) e 24,7% a dose reduzida (30 mg) de edoxabano. A maioria dos doentes (55,9%) era do sexo masculino. Dos doentes que receberam 30 mg e 60 mg de edoxabano, 55,9% e 37,9%, respetivamente, tinham CHA2DS2-VASc estimado ≥ 4. As taxas de eventos hemorrágicos prévios foram baixas, com predominância de hemorragia não major clinicamente relevante (1,9%). A maioria (47,5%) dos doentes com FANV tinha FA paroxística, seguidos de 26,4% com FA permanente. A mediana de CHA2DS2-VASc global foi 3,0 e a mediana de HAS-BLED, 2,0. Os tratamentos prévios incluíram sobretudo VKAs (35,7%). Uma proporção consideravelmente maior de doentes a receber dose reduzida de edoxabano necessitou de ajustes de dose (71,4% versus 8,6%). A adesão global às recomendações de dose foi de 86,5%. Conclusões: Este estudo fornece dados importantes sobre a doença e o perfil dos doentes e possibilitará considerações futuras acerca da gestão e progressão da doença, bem como de segurança, efetividade e padrões de eventos cardiovasculares associados a edoxabano. |
abstractGer |
Introduction and Objectives: Atrial fibrillation (AF) is the most common form of arrhythmia worldwide and a significant health burden. Edoxaban, a recent novel oral anticoagulant (NOAC), is being investigated in the European real-world ETNA-AF study of patients with non-valvular atrial fibrillation (NVAF). The aim of this study was to characterize the Iberian edoxaban-treated cohort of ETNA-AF at baseline and to compare it with previously retrieved Portuguese data. Methods: Patients with NVAF treated with edoxaban and followed in Portuguese and Spanish centers were consecutively enrolled between June 2017 and January 2018. Only patients with a previous clinical decision to receive edoxaban were included. Patients’ baseline demographic and clinical parameters, medical history, and AF-related characteristics were retrieved. Results: A total of 892 NVAF patients, with a mean age of 73.9 years, were included, 75.3% of whom received high-dose (60 mg) and 24.7% low-dose (30 mg) edoxaban. Most patients (55.9%) were male. Of the patients receiving 30 mg and 60 mg edoxaban, 55.9% and 37.9%, respectively, had an estimated CHA2DS2-VASc score ≥4. Previous bleeding event rates were low, with a predominance of clinically relevant non-major bleeding (1.9%). Most patients (47.5%) with NVAF had paroxysmal AF, followed by 26.4% with permanent AF. Median overall CHA2DS2-VASc score was 3.0 and median HAS-BLED score was 2.0. Previous treatments mostly included vitamin K antagonists (35.7%). A considerably higher proportion of patients on low-dose edoxaban required dose adjustments (71.4% vs. 8.6%). Overall adherence to label dosing recommendations was 86.5%. Conclusions: This study provides valuable data on disease and patient profiles and will provide valuable insights into disease management and progression, as well as the safety, effectiveness, and patterns of cardiovascular events associated with edoxaban. Resumo: Introdução e objetivos: A fibrilhação auricular (FA) é a arritmia mais comum globalmente e associa-se a um substancial ónus de saúde. O novo anticoagulante oral (NOAC) edoxabano está a ser investigado no estudo europeu de vida real ETNA-AF em doentes com fibrilhação auricular não valvular (FANV). O objetivo deste estudo é caracterizar a coorte ibérica do ETNA-AF na base de dados e compará-la com dados portugueses prévios. Métodos: Doentes com FANV tratados com edoxabano e seguidos em centros portugueses e espanhóis foram consecutivamente incluídos no estudo entre junho de 2017 e janeiro de 2018. Apenas doentes com indicação prévia para receber edoxabano foram incluídos e os seus dados clínicos e demográficos, história clínica e características relacionadas com a FA foram registados. Resultados: Fora, incluídos 892 doentes com FANV, com média de 73,9 anos, 75,3% dos quais receberam a dose elevada (60 mg) e 24,7% a dose reduzida (30 mg) de edoxabano. A maioria dos doentes (55,9%) era do sexo masculino. Dos doentes que receberam 30 mg e 60 mg de edoxabano, 55,9% e 37,9%, respetivamente, tinham CHA2DS2-VASc estimado ≥ 4. As taxas de eventos hemorrágicos prévios foram baixas, com predominância de hemorragia não major clinicamente relevante (1,9%). A maioria (47,5%) dos doentes com FANV tinha FA paroxística, seguidos de 26,4% com FA permanente. A mediana de CHA2DS2-VASc global foi 3,0 e a mediana de HAS-BLED, 2,0. Os tratamentos prévios incluíram sobretudo VKAs (35,7%). Uma proporção consideravelmente maior de doentes a receber dose reduzida de edoxabano necessitou de ajustes de dose (71,4% versus 8,6%). A adesão global às recomendações de dose foi de 86,5%. Conclusões: Este estudo fornece dados importantes sobre a doença e o perfil dos doentes e possibilitará considerações futuras acerca da gestão e progressão da doença, bem como de segurança, efetividade e padrões de eventos cardiovasculares associados a edoxabano. |
abstract_unstemmed |
Introduction and Objectives: Atrial fibrillation (AF) is the most common form of arrhythmia worldwide and a significant health burden. Edoxaban, a recent novel oral anticoagulant (NOAC), is being investigated in the European real-world ETNA-AF study of patients with non-valvular atrial fibrillation (NVAF). The aim of this study was to characterize the Iberian edoxaban-treated cohort of ETNA-AF at baseline and to compare it with previously retrieved Portuguese data. Methods: Patients with NVAF treated with edoxaban and followed in Portuguese and Spanish centers were consecutively enrolled between June 2017 and January 2018. Only patients with a previous clinical decision to receive edoxaban were included. Patients’ baseline demographic and clinical parameters, medical history, and AF-related characteristics were retrieved. Results: A total of 892 NVAF patients, with a mean age of 73.9 years, were included, 75.3% of whom received high-dose (60 mg) and 24.7% low-dose (30 mg) edoxaban. Most patients (55.9%) were male. Of the patients receiving 30 mg and 60 mg edoxaban, 55.9% and 37.9%, respectively, had an estimated CHA2DS2-VASc score ≥4. Previous bleeding event rates were low, with a predominance of clinically relevant non-major bleeding (1.9%). Most patients (47.5%) with NVAF had paroxysmal AF, followed by 26.4% with permanent AF. Median overall CHA2DS2-VASc score was 3.0 and median HAS-BLED score was 2.0. Previous treatments mostly included vitamin K antagonists (35.7%). A considerably higher proportion of patients on low-dose edoxaban required dose adjustments (71.4% vs. 8.6%). Overall adherence to label dosing recommendations was 86.5%. Conclusions: This study provides valuable data on disease and patient profiles and will provide valuable insights into disease management and progression, as well as the safety, effectiveness, and patterns of cardiovascular events associated with edoxaban. Resumo: Introdução e objetivos: A fibrilhação auricular (FA) é a arritmia mais comum globalmente e associa-se a um substancial ónus de saúde. O novo anticoagulante oral (NOAC) edoxabano está a ser investigado no estudo europeu de vida real ETNA-AF em doentes com fibrilhação auricular não valvular (FANV). O objetivo deste estudo é caracterizar a coorte ibérica do ETNA-AF na base de dados e compará-la com dados portugueses prévios. Métodos: Doentes com FANV tratados com edoxabano e seguidos em centros portugueses e espanhóis foram consecutivamente incluídos no estudo entre junho de 2017 e janeiro de 2018. Apenas doentes com indicação prévia para receber edoxabano foram incluídos e os seus dados clínicos e demográficos, história clínica e características relacionadas com a FA foram registados. Resultados: Fora, incluídos 892 doentes com FANV, com média de 73,9 anos, 75,3% dos quais receberam a dose elevada (60 mg) e 24,7% a dose reduzida (30 mg) de edoxabano. A maioria dos doentes (55,9%) era do sexo masculino. Dos doentes que receberam 30 mg e 60 mg de edoxabano, 55,9% e 37,9%, respetivamente, tinham CHA2DS2-VASc estimado ≥ 4. As taxas de eventos hemorrágicos prévios foram baixas, com predominância de hemorragia não major clinicamente relevante (1,9%). A maioria (47,5%) dos doentes com FANV tinha FA paroxística, seguidos de 26,4% com FA permanente. A mediana de CHA2DS2-VASc global foi 3,0 e a mediana de HAS-BLED, 2,0. Os tratamentos prévios incluíram sobretudo VKAs (35,7%). Uma proporção consideravelmente maior de doentes a receber dose reduzida de edoxabano necessitou de ajustes de dose (71,4% versus 8,6%). A adesão global às recomendações de dose foi de 86,5%. Conclusões: Este estudo fornece dados importantes sobre a doença e o perfil dos doentes e possibilitará considerações futuras acerca da gestão e progressão da doença, bem como de segurança, efetividade e padrões de eventos cardiovasculares associados a edoxabano. |
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Edoxaban Treatment in routiNe clinical prActice in patients with non-valvular Atrial Fibrillation (ETNA-AF) in Iberia: Baseline data |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">DOAJ044087381</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230501190657.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">230227s2020 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.repc.2020.09.003</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)DOAJ044087381</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)DOAJ6a1eeab3a2fa490c9eaf0ab85f29cf75</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield><subfield code="a">por</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">RC666-701</subfield></datafield><datafield tag="100" ind1="0" ind2=" "><subfield code="a">Pedro Monteiro</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Edoxaban Treatment in routiNe clinical prActice in patients with non-valvular Atrial Fibrillation (ETNA-AF) in Iberia: Baseline data</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2020</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Introduction and Objectives: Atrial fibrillation (AF) is the most common form of arrhythmia worldwide and a significant health burden. Edoxaban, a recent novel oral anticoagulant (NOAC), is being investigated in the European real-world ETNA-AF study of patients with non-valvular atrial fibrillation (NVAF). The aim of this study was to characterize the Iberian edoxaban-treated cohort of ETNA-AF at baseline and to compare it with previously retrieved Portuguese data. Methods: Patients with NVAF treated with edoxaban and followed in Portuguese and Spanish centers were consecutively enrolled between June 2017 and January 2018. Only patients with a previous clinical decision to receive edoxaban were included. Patients’ baseline demographic and clinical parameters, medical history, and AF-related characteristics were retrieved. Results: A total of 892 NVAF patients, with a mean age of 73.9 years, were included, 75.3% of whom received high-dose (60 mg) and 24.7% low-dose (30 mg) edoxaban. Most patients (55.9%) were male. Of the patients receiving 30 mg and 60 mg edoxaban, 55.9% and 37.9%, respectively, had an estimated CHA2DS2-VASc score ≥4. Previous bleeding event rates were low, with a predominance of clinically relevant non-major bleeding (1.9%). Most patients (47.5%) with NVAF had paroxysmal AF, followed by 26.4% with permanent AF. Median overall CHA2DS2-VASc score was 3.0 and median HAS-BLED score was 2.0. Previous treatments mostly included vitamin K antagonists (35.7%). A considerably higher proportion of patients on low-dose edoxaban required dose adjustments (71.4% vs. 8.6%). Overall adherence to label dosing recommendations was 86.5%. Conclusions: This study provides valuable data on disease and patient profiles and will provide valuable insights into disease management and progression, as well as the safety, effectiveness, and patterns of cardiovascular events associated with edoxaban. Resumo: Introdução e objetivos: A fibrilhação auricular (FA) é a arritmia mais comum globalmente e associa-se a um substancial ónus de saúde. O novo anticoagulante oral (NOAC) edoxabano está a ser investigado no estudo europeu de vida real ETNA-AF em doentes com fibrilhação auricular não valvular (FANV). O objetivo deste estudo é caracterizar a coorte ibérica do ETNA-AF na base de dados e compará-la com dados portugueses prévios. Métodos: Doentes com FANV tratados com edoxabano e seguidos em centros portugueses e espanhóis foram consecutivamente incluídos no estudo entre junho de 2017 e janeiro de 2018. Apenas doentes com indicação prévia para receber edoxabano foram incluídos e os seus dados clínicos e demográficos, história clínica e características relacionadas com a FA foram registados. Resultados: Fora, incluídos 892 doentes com FANV, com média de 73,9 anos, 75,3% dos quais receberam a dose elevada (60 mg) e 24,7% a dose reduzida (30 mg) de edoxabano. A maioria dos doentes (55,9%) era do sexo masculino. Dos doentes que receberam 30 mg e 60 mg de edoxabano, 55,9% e 37,9%, respetivamente, tinham CHA2DS2-VASc estimado ≥ 4. As taxas de eventos hemorrágicos prévios foram baixas, com predominância de hemorragia não major clinicamente relevante (1,9%). A maioria (47,5%) dos doentes com FANV tinha FA paroxística, seguidos de 26,4% com FA permanente. A mediana de CHA2DS2-VASc global foi 3,0 e a mediana de HAS-BLED, 2,0. Os tratamentos prévios incluíram sobretudo VKAs (35,7%). Uma proporção consideravelmente maior de doentes a receber dose reduzida de edoxabano necessitou de ajustes de dose (71,4% versus 8,6%). A adesão global às recomendações de dose foi de 86,5%. Conclusões: Este estudo fornece dados importantes sobre a doença e o perfil dos doentes e possibilitará considerações futuras acerca da gestão e progressão da doença, bem como de segurança, efetividade e padrões de eventos cardiovasculares associados a edoxabano.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Fibrilhação auricular</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Edoxabano</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Baseline</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Vida real</subfield></datafield><datafield tag="653" ind1=" " ind2="0"><subfield code="a">Diseases of the circulatory (Cardiovascular) system</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">In</subfield><subfield code="t">Revista Portuguesa de Cardiologia</subfield><subfield code="d">Elsevier, 2020</subfield><subfield code="g">39(2020), 11, 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