Mental Health Conditions and Nonpersistence of Direct Oral Anticoagulant Use in Patients With Incident Atrial Fibrillation: A Nationwide Cohort Study

Background Mental health conditions (MHCs) are associated with poor outcomes in patients with atrial fibrillation. However, persistence of oral anticoagulation therapy in patients with atrial fibrillation and MHCs is unknown. We aimed to evaluate the effect of MHCs on the persistence of direct oral...

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Main Authors: Konsta Teppo, Jussi Jaakkola, K. E. Juhani Airaksinen, Fausto Biancari, Olli Halminen, Jukka Putaala, Pirjo Mustonen, Jari Haukka, Juha Hartikainen, Alex Luojus, Mikko Niemi, Miika Linna, Mika Lehto
Format: Article
Language:English
Published: Wiley 2022-03-01
Series:Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Subjects:
Online Access:https://www.ahajournals.org/doi/10.1161/JAHA.121.024119
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author Konsta Teppo
Jussi Jaakkola
K. E. Juhani Airaksinen
Fausto Biancari
Olli Halminen
Jukka Putaala
Pirjo Mustonen
Jari Haukka
Juha Hartikainen
Alex Luojus
Mikko Niemi
Miika Linna
Mika Lehto
author_facet Konsta Teppo
Jussi Jaakkola
K. E. Juhani Airaksinen
Fausto Biancari
Olli Halminen
Jukka Putaala
Pirjo Mustonen
Jari Haukka
Juha Hartikainen
Alex Luojus
Mikko Niemi
Miika Linna
Mika Lehto
author_sort Konsta Teppo
collection DOAJ
description Background Mental health conditions (MHCs) are associated with poor outcomes in patients with atrial fibrillation. However, persistence of oral anticoagulation therapy in patients with atrial fibrillation and MHCs is unknown. We aimed to evaluate the effect of MHCs on the persistence of direct oral anticoagulant (DOAC) use in patients with atrial fibrillation based on a nationwide cohort. Methods and Results The nationwide registry‐based FinACAF (Finnish Anticoagulation in Atrial Fibrillation) cohort included 67 503 patients with incident atrial fibrillation and indication for permanent oral anticoagulation (CHA2DS2‐VASc score >1 in men and >2 in women) starting DOAC therapy between 2011 and 2018. MHCs of interest were depression, bipolar disorder, anxiety disorder, schizophrenia, and composite of any MHC. The main outcome was nonpersistence of DOAC use, defined as the first 120‐day period without DOAC purchases after drug initiation. The mean age of the patients was 75.3±8.9 years, 53.6% were women, and the prevalence of any MHC was 17.8%. Persistence after 1 year from DOAC initiation was 79.3% in patients without MHCs and 77.2% in patients with any MHC, and after 2 years were 64.4% and 60.6%, respectively (P<0.001). Higher incidence of nonpersistence to DOACs was observed in all MHC categories: adjusted subdistribution hazard ratios, 1.16 (95% CI, 1.11–1.21) for any MHC, 1.32 (95% CI, 1.22–1.42) for depression, 1.44 (95% CI, 1.15–1.80) for bipolar disorder, 1.25 (95% CI, 1.11–1.41) for anxiety disorder, and 1.30 (95% CI, 1.02–1.64) for schizophrenia. However, patients with only anxiety disorder without other MHCs were not at higher risk of nonpersistence. Conclusions MHCs are associated with nonpersistence of DOAC use. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT04645537.
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spelling doaj.art-6fd6fc6955444b2188dba6148a8ca6a22023-03-28T04:20:50ZengWileyJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease2047-99802022-03-0111610.1161/JAHA.121.024119Mental Health Conditions and Nonpersistence of Direct Oral Anticoagulant Use in Patients With Incident Atrial Fibrillation: A Nationwide Cohort StudyKonsta Teppo0Jussi Jaakkola1K. E. Juhani Airaksinen2Fausto Biancari3Olli Halminen4Jukka Putaala5Pirjo Mustonen6Jari Haukka7Juha Hartikainen8Alex Luojus9Mikko Niemi10Miika Linna11Mika Lehto12Faculty of Medicine University of Turku Turku FinlandFaculty of Medicine University of Turku Turku FinlandFaculty of Medicine University of Turku Turku FinlandClinica Montevergine Gruppo Villa Maria Care &amp; Research Mercogliano ItalyDepartment of Industrial Engineering and Management Aalto University Espoo FinlandDepartment of Neurology Helsinki University Hospital Helsinki FinlandFaculty of Medicine University of Turku Turku FinlandFaculty of Medicine University of Helsinki FinlandFaculty of Medicine University of Eastern Finland Kuopio FinlandHeart and Lung Center Helsinki University Hospital Helsinki FinlandDepartment of Clinical Pharmacology University of Helsinki FinlandDepartment of Industrial Engineering and Management Aalto University Espoo FinlandHeart and Lung Center Helsinki University Hospital Helsinki FinlandBackground Mental health conditions (MHCs) are associated with poor outcomes in patients with atrial fibrillation. However, persistence of oral anticoagulation therapy in patients with atrial fibrillation and MHCs is unknown. We aimed to evaluate the effect of MHCs on the persistence of direct oral anticoagulant (DOAC) use in patients with atrial fibrillation based on a nationwide cohort. Methods and Results The nationwide registry‐based FinACAF (Finnish Anticoagulation in Atrial Fibrillation) cohort included 67 503 patients with incident atrial fibrillation and indication for permanent oral anticoagulation (CHA2DS2‐VASc score >1 in men and >2 in women) starting DOAC therapy between 2011 and 2018. MHCs of interest were depression, bipolar disorder, anxiety disorder, schizophrenia, and composite of any MHC. The main outcome was nonpersistence of DOAC use, defined as the first 120‐day period without DOAC purchases after drug initiation. The mean age of the patients was 75.3±8.9 years, 53.6% were women, and the prevalence of any MHC was 17.8%. Persistence after 1 year from DOAC initiation was 79.3% in patients without MHCs and 77.2% in patients with any MHC, and after 2 years were 64.4% and 60.6%, respectively (P<0.001). Higher incidence of nonpersistence to DOACs was observed in all MHC categories: adjusted subdistribution hazard ratios, 1.16 (95% CI, 1.11–1.21) for any MHC, 1.32 (95% CI, 1.22–1.42) for depression, 1.44 (95% CI, 1.15–1.80) for bipolar disorder, 1.25 (95% CI, 1.11–1.41) for anxiety disorder, and 1.30 (95% CI, 1.02–1.64) for schizophrenia. However, patients with only anxiety disorder without other MHCs were not at higher risk of nonpersistence. Conclusions MHCs are associated with nonpersistence of DOAC use. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT04645537.https://www.ahajournals.org/doi/10.1161/JAHA.121.024119atrial fibrillationdepressiondirect oral anticoagulantsmental health conditionspersistence
spellingShingle Konsta Teppo
Jussi Jaakkola
K. E. Juhani Airaksinen
Fausto Biancari
Olli Halminen
Jukka Putaala
Pirjo Mustonen
Jari Haukka
Juha Hartikainen
Alex Luojus
Mikko Niemi
Miika Linna
Mika Lehto
Mental Health Conditions and Nonpersistence of Direct Oral Anticoagulant Use in Patients With Incident Atrial Fibrillation: A Nationwide Cohort Study
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
atrial fibrillation
depression
direct oral anticoagulants
mental health conditions
persistence
title Mental Health Conditions and Nonpersistence of Direct Oral Anticoagulant Use in Patients With Incident Atrial Fibrillation: A Nationwide Cohort Study
title_full Mental Health Conditions and Nonpersistence of Direct Oral Anticoagulant Use in Patients With Incident Atrial Fibrillation: A Nationwide Cohort Study
title_fullStr Mental Health Conditions and Nonpersistence of Direct Oral Anticoagulant Use in Patients With Incident Atrial Fibrillation: A Nationwide Cohort Study
title_full_unstemmed Mental Health Conditions and Nonpersistence of Direct Oral Anticoagulant Use in Patients With Incident Atrial Fibrillation: A Nationwide Cohort Study
title_short Mental Health Conditions and Nonpersistence of Direct Oral Anticoagulant Use in Patients With Incident Atrial Fibrillation: A Nationwide Cohort Study
title_sort mental health conditions and nonpersistence of direct oral anticoagulant use in patients with incident atrial fibrillation a nationwide cohort study
topic atrial fibrillation
depression
direct oral anticoagulants
mental health conditions
persistence
url https://www.ahajournals.org/doi/10.1161/JAHA.121.024119
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