Abstract P1019: Patient Values and Anticoagulant Decisions in Atrial Fibrillation: a Secondary Analysis of the RED-AF Shared Decision-Making Trial

A Alexander Kolomaya (University of Utah, Salt Lake City, Utah, United States) J Joshua Christensen (University of Utah, Salt Lake City, Utah, United States) M Michael Throolin (University of Utah, Salt Lake City, Utah, United States) D Daniel Witt (University of Utah College of Pharm, Salt Lake City, Utah, United States) G Geoffrey Barnes (University of Michigan, Ann Arbor, Michigan, United States) K Kenzie Cameron R Rod Passman (Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States) P Peter Noseworthy (MAYO CLINIC, Rochester, Minnesota, United States) K Kerri Cavanaugh (Vanderbilt University Medical Cente, Nashville, Tennessee, United States) A Angie Fagerlin (University of Utah, Salt Lake City, Utah, United States) B Benjamin Steinberg (University of Utah, Salt Lake City, Utah, United States) E Elissa Ozanne (University of Utah, Salt Lake Cty, Utah, United States)

Abstract

Background: Deciding to use oral anticoagulation (OAC) for stroke prevention in patients with atrial fibrillation (AF) is complex. For many, the decision between treatment and non-treatment requires a primary tradeoff between the risks of potential stroke and increased bleeding. Hypothesis: We hypothesized that patient values and empiric stroke risk measured by CHA 2 DS 2 -VASc score would influence OAC decisions. Methods: We conducted a secondary analysis of a randomized clinical trial where eligible clinicians and patients were independently randomized to one of two decision aids (DAs) – a patient decision aid and/or an encounter decision aid. Eligible patients were adults with AF with CHA 2 DS 2 -VASc≥1 for men or ≥2 for women. Patients newly prescribed (OAC-naive subgroup) or already taking OAC (OAC-experienced subgroup) were included. We assessed patient values using a 5-point Likert scale between stroke prevention and bleeding risk after SDM during a clinical encounter. We report preliminary results using descriptive statistics and adjusted analysis to investigate the effects of CHA 2 DS 2 -VASc and expressed values on OAC use. Results: 1005 patients were included in the analysis. 828 (82%) patients valued stroke prevention over bleeding risk. Among the OAC-naive group, 175 (63%) valued stroke prevention more than bleed avoidance, 58 (20%) valued bleed avoidance more than stroke prevention, and 47 (17%) were neutral. In the unadjusted analysis, patients were more likely to value stroke prevention if they were OAC-experienced (p<0.001), older (p<0.001), female (p< 0.001), had patient-reported bleeding (p=0.003), or if CHA 2 DS 2 -VASc ≥ 2 if male, ≥3 if female (p<0.001) Table 1 . After adjustments, there were significant associations for OAC use among patients who valued stroke prevention (OR 5.35, 95%CI 3.13-9.13, p<0.001) or had higher CHA 2 DS 2 -VASc (OR 2.03, 95%CI 1.26-3.27, p=0.004). Patients who valued bleed avoidance had an opposing association not to use OAC (OR 0.23, 95%CI 0.11-0.48, p<0.001). Conclusions: Patients with elevated risk (CHA 2 DS 2 -VASc score, age, and female), and those who reported a prior bleeding event valued stroke prevention more than bleeding avoidance. Both empiric stroke risk and patient values were associated with the decision to use OAC. While the tradeoff between stroke prevention and bleeding risk is only one aspect of the decision-making process, these results indicate variability in patient values may influence OAC use.

Article Details

Journal Circulation
Volume / Issue Vol. 151, Issue Suppl_1
Published March 11, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (12)

A

Alexander Kolomaya

University of Utah, Salt Lake City, Utah, United States

J

Joshua Christensen

University of Utah, Salt Lake City, Utah, United States

M

Michael Throolin

University of Utah, Salt Lake City, Utah, United States

D

Daniel Witt

University of Utah College of Pharm, Salt Lake City, Utah, United States

G

Geoffrey Barnes

University of Michigan, Ann Arbor, Michigan, United States

K

Kenzie Cameron

R

Rod Passman

Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States

P

Peter Noseworthy

MAYO CLINIC, Rochester, Minnesota, United States

K

Kerri Cavanaugh

Vanderbilt University Medical Cente, Nashville, Tennessee, United States

A

Angie Fagerlin

University of Utah, Salt Lake City, Utah, United States

B

Benjamin Steinberg

University of Utah, Salt Lake City, Utah, United States

E

Elissa Ozanne

University of Utah, Salt Lake Cty, Utah, United States