Left Atrial Appendage Closure or Medical Therapy in Atrial Fibrillation.
Summary
Left Atrial Appendage Closure or Medical Therapy in Atrial Fibrillation. Original Article Abstract Background Catheter-based closure of the left atrial appendage is an alternative to oral anticoagulation for stroke prevention in patients with atrial fibrillation. The effectiveness of this strategy, as compared with physician-directed best medical care, in patients at high risk for stroke and bleeding is unknown. Methods In this multicenter randomized trial conducted in Germany, we assig
Content
# Left Atrial Appendage Closure or Medical Therapy in Atrial Fibrillation.
*Original Article*
# Abstract
## Background
Catheter-based closure of the left atrial appendage is an
alternative to oral anticoagulation for stroke prevention in patients with
atrial fibrillation. The effectiveness of this strategy, as compared with
physician-directed best medical care, in patients at high risk for stroke and
bleeding is unknown.
## Methods
In this multicenter randomized trial conducted in Germany, we assigned
patients with atrial fibrillation and a high risk of stroke and bleeding to
undergo left atrial appendage closure or to receive physician-directed best
medical care (including direct oral anticoagulants, if eligible). The primary
end point, tested for noninferiority, was a composite of stroke (ischemic or
hemorrhagic), systemic embolism, major bleeding, or cardiovascular or
unexplained death, assessed in a time-to-event analysis. The noninferiority
margin was a hazard ratio of 1.3.
## Results
A total of 912 adult patients underwent randomization. The primary
end-point analysis included 446 patients who were assigned to undergo left
atrial appendage closure (device group) and 442 who were assigned to
physician-directed best medical care (medical-therapy group). The mean (±SD) age
was 77.9±7.1 years; 38.6% of the patients were women, the mean CHA2DS2-VASc
score was 5.2±1.5 (range, 0 to 9, with higher scores indicating a greater risk
of stroke), and the mean HAS-BLED score was 3.0±0.9 (range, 0 to 9, with higher
scores indicating higher risk of bleeding). After a median follow-up of 3 years
(interquartile range, 1.7 to 4.7), a first primary end-point event had occurred
in 155 patients (incidence per 100 patient-years, 16.8) in the device group and
in 127 patients (incidence per 100 patient-years, 13.3) in the medical-therapy
group (difference in restricted mean survival time, -0.36 years; 95% confidence
interval, -0.70 to -0.01; P = 0.44 for noninferiority). Serious adverse events
occurred in 368 patients (82.5%) in the device group and 342 (77.4%) in the
medical-therapy group.
## Conclusions
Among patients with atrial fibrillation at high risk for stroke and
bleeding, left atrial appendage closure was not noninferior to
physician-directed best medical care with regard to a composite end point of
stroke, systemic embolism, major bleeding, or cardiovascular or unexplained
death. (Funded by the German Center for Cardiovascular Research; CLOSURE-AF
ClinicalTrials.gov number, NCT03463317.).
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DOI: 10.1056/NEJMoa2513310