A1 Refereed original research article in a scientific journal

Temporal trends in mortality and causes of death in patients with incident atrial fibrillation: a nationwide register study from 2010 to 2018




AuthorsKouki, Elis; Salmela, Birgitta; Aro, Aapo; Halminen, Olli; Teppo, Konsta; Haukka, Jari; Putaala, Jukka; Linna, Mika; Mustonen, Pirjo; Hartikainen, Juha; Airaksinen, Juhani K E; Lehto, Mika

PublisherBMJ Publishing Group

Publication year2024

Journal: BMJ Open

Journal name in sourceBMJ open

Article numbere080836

Volume14

Issue9

eISSN2044-6055

DOIhttps://doi.org/10.1136/bmjopen-2023-080836

Publication's open availability at the time of reportingOpen Access

Publication channel's open availability Open Access publication channel

Web address https://bmjopen.bmj.com/content/14/9/e080836

Self-archived copy’s web addresshttps://research.utu.fi/converis/portal/detail/Publication/458378893


Abstract

OBJECTIVES: Atrial fibrillation (AF) is associated with increased mortality. Previous studies have reported conflicting results in temporal trends of mortality after AF diagnosis. We aim to address this disparity by investigating the 1-year mortality and causes of death in Finnish patients diagnosed with AF between 2010 and 2017.

DESIGN: The Finnish AntiCoagulation in Atrial Fibrillation (FinACAF) study is a nationwide retrospective register-based cohort study.

SETTING: The FinACAF study has gathered information on all Finnish AF patients between 2004 and 2018, with information from all national healthcare registers and data from all levels of care (primary, secondary and tertiary care).

PARTICIPANTS: We included patients with an incident AF diagnosis (International Classification of Diseases, 10th Revision code I48) between 2010 and 2017. To ensure a cohort of only incident AF, we excluded patients who used any oral anticoagulant during the year before cohort entry as well as patients with a recorded use of warfarin between 2004 and 2006. Patients under 20 years of age were excluded, and patients with permanent migration abroad before 1 January 2019 were excluded, N=157 658.

PRIMARY OUTCOME MEASURES: 1-year all-cause, cardiovascular (CV) and cause-specific mortality following AF diagnosis.

RESULTS: The study cohort consisted of 157 658 incident AF cases (50.1% male, mean age 72.9 years). Both all-cause and CV mortality declined from cohort entry years 2010-2017 (from 12.9% to 10.6%, mortality rate ratio (MRR) 0.77; 95% CI 0.73 to 0.82 in cohort entry year 2017 with 2010 as reference; and from 7.4% to 5.2%, MRR 0.68; 95% CI 0.63 to 0.74, respectively). Overall mortality and CV mortality were lower in women than in men throughout the study period (MRR 0.66; 95% CI 0.63 to 0.69 and MRR 0.53; 95% CI 0.50 to 0.56, respectively). Deaths attributable to ischaemic heart disease decreased during the study period (from 30.7% to 21.6%, MRR 0.51; 95% CI 0.49 to 0.62 in 2017 vs 2010), whereas dementia and Alzheimer's disease increased as a cause of death over time (6.2% to 9.9%, MRR 1.19; 95% CI 0.96 to 1.48 in 2017 vs 2010). The CHA2DS2-VASc score associated strongly with 1-year survival (p<0.0001).

CONCLUSIONS: Our study reiterates that mortality after diagnosis of AF has decreased. The CHA2DS2-VASc score highlights the need to treat comorbidities as it strongly associates with patient 1-year survival after initial AF diagnosis.


Downloadable publication

This is an electronic reprint of the original article.
This reprint may differ from the original in pagination and typographic detail. Please cite the original version.




Funding information in the publication
Aarne Koskelo Foundation (Aarne Koskelon Säätiö, grant number NA), The Finnish Foundation for Cardiovascular Research (Sydäntutkimussäätiö, grant number NA), Yrjö Jahnsson Foundation (Yrjö Jahnssonin Säätiö, grant number NA), Sigrid Jusélius Foundation (Sigrid Juséliuksen Säätiö, grant number NA) and Helsinki and Uusimaa Hospital District research fund (Helsingin ja Uudenmaan Sairaanhoitopiiri, TYH2019309 and TYH2023319).


Last updated on 27/01/2025 07:56:25 PM