The oral anticoagulant (OAC) apixaban’s absolute risks are lower than those of other OACs among patients with dementia compared to those without dementia, according to new findings, suggesting patients with dementia and atrial fibrillation (AF) may benefit from apixaban.1
Although randomized clinical trials (RCTs) have established both the effectiveness and safety of direct oral OACs in comparison to warfarin for patients with AF, older adults with frailty or dementia had not been adequately represented in these studies.
Summary
- This study found that apixaban has lower absolute risks compared to other oral anticoagulants (OACs) for patients with dementia and atrial fibrillation (AF).
- This study aimed to expand on the limited data on the efficacy and safety of OACs in the population of older adults with dementia and AF.
- There were 1,160,462 older adults with AF recruited for the study. The main exposures analyzed were apixaban, rivaroxaban, dabigatran, and warfarin.
- Participants with dementia had higher composite endpoint rates than apixaban users, although benefits associated with apixaban were similar in all comparisons, with a more distinct pattern for major bleeding than for ischemic stroke.
This research was conducted to expand upon what little RCT data there is on the role of dementia in the efficacy and safety of OACs. It was authored by Kueiyu Joshua Lin, MD, ScD, MPH, from the Department of Medicine at Brigham and Women’s Hospital and Harvard Medical School.
“We aimed to examine the comparative safety and effectiveness of specific OACs by assessing the risks of ischemic stroke and major bleeding events by dementia status among older patients with AF,” Lin and colleagues wrote.
Background and Findings
The investigators used a comparative effectiveness study, during which they analyzed data from 3 different sources: the Optum Clinformatics Data Mart, Medicare claims databases maintained by the Centers for Medicare & Medicaid Services (inpatient, outpatient, and pharmacy), and IBM MarketScan Research Database.
The team’s research focused on participants who were aged 65 years or older and had AF, with the researchers using 1:1 propensity score matching.
For inclusion in the study, participants had to meet certain criteria, including having 1 or more diagnoses of AF during the trial’s baseline assessment period and being enrolled in medical and pharmacy coverage for a minimum of 365 days.
The researchers excluded those who received hospice care, had major bleeding within the past 30 days, had other indications for OAC, or had valvular heart diseases or end-stage kidney or liver disease in the year prior to the baseline assessment period.
The main exposures analyzed by the investigators were apixaban, rivaroxaban, dabigatran, or warfarin, and the team used random-effects meta-analyses to pool data across their databases.
The composite endpoint evaluated was ischemic stroke or major bleeding events occurring during the 6-month period after OAC initiation.
The investigators enrolled 1,160,462 older adult patients with AF and a mean age of 77.4 years, among whom 80.5% were reported as White and 50.2% were reported as male. They established 3 comparative new-user study cohorts: warfarin versus apixaban, dabigatran versus apixaban, and rivaroxaban versus apixaban.