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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Recurrent Stroke with Rivaroxaban Compared with Aspirin According to Predictors of Atrial Fibrillation: Secondary Analysis of the NAVIGATE ESUS Randomized Clinical Trial

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Συγγραφέας
Healey J.S., Gladstone D.J., Swaminathan B., Eckstein J., Mundl H., Epstein A.E., Haeusler K.G., Mikulik R., Kasner S.E., Toni D., Arauz A., Ntaios G., Hankey G.J., Perera K., Pagola J., Shuaib A., Lutsep H., Yang X., Uchiyama S., Endres M., Coutts S.B., Karliński M., Czlonkowska A., Molina C.A., Santo G., Berkowitz S.D., Hart R.G., Connolly S.J.
Ημερομηνία
2019
Γλώσσα
en
DOI
10.1001/jamaneurol.2019.0617
Λέξη-κλειδί
acetylsalicylic acid
rivaroxaban
acetylsalicylic acid
antithrombocytic agent
blood clotting factor 10a inhibitor
rivaroxaban
adult
aged
anticoagulation
Article
atrial fibrillation
brain ischemia
CHA2DS2-VASc score
computer assisted tomography
controlled study
disease association
disease severity
echocardiography
electrocardiography
female
follow up
HAVOC score
Health Stroke Scale score
Holter monitoring
human
major clinical study
male
nuclear magnetic resonance imaging
priority journal
randomized controlled trial
recurrent disease
scoring system
atrial fibrillation
brain embolism
cerebrovascular accident
comparative study
middle aged
recurrent disease
risk factor
secondary prevention
treatment outcome
very elderly
Aged
Aged, 80 and over
Aspirin
Atrial Fibrillation
Factor Xa Inhibitors
Female
Humans
Intracranial Embolism
Male
Middle Aged
Platelet Aggregation Inhibitors
Recurrence
Risk Factors
Rivaroxaban
Secondary Prevention
Stroke
Treatment Outcome
American Medical Association
Εμφάνιση Μεταδεδομένων
Επιτομή
Importance: The NAVIGATE ESUS randomized clinical trial found that 15 mg of rivaroxaban per day does not reduce stroke compared with aspirin in patients with embolic stroke of undetermined source (ESUS); however, it substantially reduces stroke risk in patients with atrial fibrillation (AF). Objective: To analyze whether rivaroxaban is associated with a reduction of recurrent stroke among patients with ESUS who have an increased risk of AF. Design, Setting, and Participants: Participants were stratified by predictors of AF, including left atrial diameter, frequency of premature atrial contractions, and HAVOC score, a validated scheme using clinical features. Treatment interactions with these predictors were assessed. Participants were enrolled between December 2014 and September 2017, and analysis began March 2018. Intervention: Rivaroxaban treatment vs aspirin. Main Outcomes and Measures: Risk of ischemic stroke. Results: Among 7112 patients with a mean (SD) age of 67 (9.8) years, the mean (SD) HAVOC score was 2.6 (1.8), the mean (SD) left atrial diameter was 3.8 (1.4) cm (n = 4022), and the median (interquartile range) daily frequency of premature atrial contractions was 48 (13-222). Detection of AF during follow-up increased for each tertile of HAVOC score: 2.3% (score, 0-2), 3.0% (score, 3), and 5.8% (score, >3); however, neither tertiles of the HAVOC score nor premature atrial contractions frequency impacted the association of rivaroxaban with recurrent ischemic stroke (P for interaction =.67 and.96, respectively). Atrial fibrillation annual incidence increased for each tertile of left atrial diameter (2.0%, 3.6%, and 5.2%) and for each tertile of premature atrial contractions frequency (1.3%, 2.9%, and 7.0%). Among the predefined subgroup of patients with a left atrial diameter of more than 4.6 cm (9% of overall population), the risk of ischemic stroke was lower among the rivaroxaban group (1.7% per year) compared with the aspirin group (6.5% per year) (hazard ratio, 0.26; 95% CI, 0.07-0.94; P for interaction =.02). Conclusions and Relevance: The HAVOC score, left atrial diameter, and premature atrial contraction frequency predicted subsequent clinical AF. Rivaroxaban was associated with a reduced risk of recurrent stroke among patients with ESUS and moderate or severe left atrial enlargement; however, this needs to be independently confirmed before influencing clinical practice.. © 2019 American Medical Association. All rights reserved.
URI
http://hdl.handle.net/11615/73940
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