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Changes in Oral Anticoagulation Therapy over One Year in 51,000 Atrial Fibrillation Patients at Risk for Stroke: A
Stefan H Hohnloser1, Edin Basic2, Michael Nabauer3
1Division of Clinical Electrophysiology, Department of Cardiology, Johann Wolfgang Goethe University, Frankfurt, Germany.
Insights
Discontinuation rates for vitamin K antagonists (VKA) and non-vitamin K oral anticoagulants (NOACs) are similar in atrial fibrillation patients after one year. Switching from VKA to NOAC is more frequent than the reverse, often linked to clinical events.
Area of Science:
- Cardiology
- Pharmacology
- Health Services Research
Background:
- Atrial fibrillation (AF) management requires effective anticoagulation therapy.
- Non-vitamin K oral anticoagulants (NOACs) and vitamin K antagonists (VKAs) are primary treatment options.
- Understanding treatment changes is crucial for optimizing patient care.
Purpose of the Study:
- To assess temporal changes in anticoagulation therapy among patients with atrial fibrillation (AF).
- To evaluate discontinuation and switching patterns between NOACs and VKAs.
- To identify predictors of treatment modifications in AF patients.
Main Methods:
- Analysis of a large claims-based dataset (4 million individuals).
- Inclusion of AF patients initiating NOACs or VKAs between 2013-2016.
- Use of Cox proportional hazards regression to determine predictors of treatment changes.
Main Results:
- Comparable 1-year discontinuation rates for VKA (29.9%) and NOACs (29.5%).
- Higher switching from VKA to NOAC (10.7%) compared to NOAC to VKA (4.9%).
- Treatment changes, particularly among NOAC users, were associated with stroke, myocardial infarction, and gastrointestinal bleeding.
Conclusions:
- VKA and NOAC discontinuation rates are similar within the first year of AF treatment.
- Switching from VKA to NOAC is more prevalent than the reverse.
- Clinical events significantly influence anticoagulation treatment modifications in AF patients.
Background:
This study assessed changes in anticoagulation therapy over time in patients with atrial fibrillation (AF).
Methods:
Analyses were performed on a claims-based dataset of 4 million health-insured individuals. The study population consisted of patients newly initiating a non-vitamin-K oral anticoagulants (NOACs) or vitamin K antagonist (VKA) for AF between 2013 and 2016. The study outcomes consisted of the proportion of patients who had (1) discontinued OAC treatment, (2) switched from VKA to NOAC, (3) switched from NOAC to VKA or (4) switched from one NOAC to another. Predictors of discontinuation or switching of OAC treatment were determined by Cox proportional hazards regression models with time-independent and time-dependent covariates.
Results:
The study population comprised 51,606 AF patients initiating VKA (n = 21,468, 41.6%), apixaban (n = 8,832, 17.1%), dabigatran (n = 3,973, 7.7%) or rivaroxaban (n = 17,333, 33.6%). After 1 year, 29.9% of VKA and 29.5% of NOAC patients had discontinued OAC treatment without switching to another anticoagulant. A total of 10.7% of VKA patients switched to NOACs within 1 year, whereas 4.9% NOAC patients had switched to VKA. Of AF patients who were initiated on a NOAC, 5.2% switched to another NOAC. Treatment changes among NOAC starters were strongly associated with occurrence of stroke, myocardial infarction and gastrointestinal bleeding after treatment initiation. For VKA starters switching to a NOAC, stroke and bleeding events were associated with an increased likelihood of switching.
Conclusion:
Overall discontinuation rates of VKA and NOACs are comparable over the first year of therapy, while switching from VKA to NOAC was more common than from NOAC to VKA. The majority of treatment changes were associated with clinical events.
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