Key result
The availability of dabigatran and rivaroxaban did not significantly increase the rate of appropriate anticoagulant prescribing at hospital discharge in high-risk patients with non-valvular atrial fibrillation (77.1% vs 68.3%, RR 1.1, p=0.16).
Why the study?
Does the availability of novel oral anticoagulants (dabigatran and rivaroxaban) improve the rate of anticoagulant prescribing at hospital discharge in high-risk adult patients with non-valvular atrial fibrillation?
Cohort (n=200)
Yes
Does the availability of novel oral anticoagulants (dabigatran and rivaroxaban) improve the rate of anticoagulant prescribing at hospital discharge in high-risk adult patients with non-valvular atrial fibrillation?
Effect estimate: RR 1.1 (95% CI 0.9-1.3)
Absolute Event Rate: 77.1% vs 68.3%
p-value: p=.16
The introduction of novel oral anticoagulants did not significantly increase the overall rate of anticoagulant prescribing at hospital discharge for high-risk patients with non-valvular atrial fibrillation, which remains suboptimal.
NOAC availability was not associated with higher anticoagulation rates at discharge; leaves open whether targeted interventions beyond drug access are needed in high-risk AF.
BACKGROUND: Appropriate treatment reduces the risk of stroke in patients with atrial fibrillation (AF). Despite the known benefits of warfarin, anticoagulation prescribing rates remain inadequate in high-risk patients. Over the last 6 years, 4 novel oral anticoagulants have been approved for use for stroke prophylaxis in non-valvular AF (NVAF), which may allow prescribers to tailor therapy for each NVAF patient. OBJECTIVE: The goal of this investigation was to determine the effect of dabigatran and rivaroxaban availability on the rate of anticoagulant prescribing at hospital discharge in patients with a principal diagnosis of NVAF. METHODS: A retrospective chart review of adult patients presenting with NVAF (CHADS2 score ≥2) was conducted using a historical control group of patients from 2009 compared to patients admitted in 2012 following formulary availability of dabigatran and rivaroxaban. In addition to antithrombotic therapy prescribed, subsequent hospitalizations during a 1-year period were reviewed for major bleeding and stroke events. RESULTS: Two hundred patients were enrolled in the study. The rate of anticoagulant prescribing in the 2009 and 2012 groups was 68.3% and 77.1%, respectively (p = .16). Of the patients in the 2012 group prescribed an anticoagulant, 58 (64%) received warfarin, 26 (28%) received dabigatran, and 7 (8%) received rivaroxaban. One patient (1.2%) in the 2009 group and 4 patients (4.4%) in the 2012 group had a major bleed (p = .4). CONCLUSION: There was no statistical difference in the rate of anticoagulant prescribing between the 2 groups. Despite the availability of additional anticoagulant options, the rate of prescribing remains suboptimal in this high-risk population.
No takes yet. Share an insight, caveat, or question.
Marler et al. (2016) conducted a cohort in Non-valvular atrial fibrillation (n=200). Availability of dabigatran and rivaroxaban vs. Historical control (warfarin only) was evaluated on Appropriate antithrombotic therapy prescribing at hospital discharge (RR 1.1, 95% CI 0.9-1.3, p=.16). The availability of dabigatran and rivaroxaban did not significantly increase the rate of appropriate anticoagulant prescribing at hospital discharge in high-risk patients with non-valvular atrial fibrillation (77.1% vs 68.3%, RR 1.1, p=0.16).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: