Targeted Anticoagulation for Atrial Fibrillation Guided by Continuous Rhythm Assessment With an Insertable Cardiac Monitor: The Rhythm Evaluation for Anticoagulation With Continuous Monitoring (REACT.COM) Pilot Study

被引:90
作者
Passman, Rod [1 ]
Leong-Sit, Peter [2 ]
Andrei, Adin-Cristian [3 ]
Huskin, Anna [3 ]
Tomson, Todd T. [3 ]
Bernstein, Richard [1 ]
Ellis, Ethan [4 ]
Waks, Jonathan W. [4 ]
Zimetbaum, Peter [4 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, 676 N St Claire St,Suite 600, Chicago, IL 60611 USA
[2] Univ Western Ontario, London, ON, Canada
[3] NW Mem Hosp, Chicago, IL 60611 USA
[4] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
关键词
anticoagulation; atrial fibrillation; implantable cardiac monitor; REVEAL; stroke; TIA; TEMPORAL RELATIONSHIP; STROKE; RISK; WARFARIN; EVENTS; HEART; TACHYARRHYTHMIAS; CHA(2)DS(2)-VASC; ABLATION; THERAPY;
D O I
10.1111/jce.12864
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Rhythm Evaluation for Anticoagulation With Continuous Monitoring IntroductionChronic anticoagulation is recommended for patients with AF and additional stroke risk factors, even during long periods of sinus rhythm. Continuous rhythm assessment with an insertable cardiac monitor (ICM) and use of rapid onset novel oral anticoagulants (NOACs) allow for targeted anticoagulation only around an AF episode, potentially reducing bleeding complications without compromising stroke risk. MethodsThis multicenter, single-arm study enrolled patients on NOAC with nonpermanent AF and CHADS(2) score 1 or 2. After a 60-day run-in with no AF episodes 1 hour, NOACs were discontinued but reinitiated for 30 days following any AF episode 1 hour diagnosed through daily ICM transmissions. Major endpoints included time on NOAC, stroke, and bleeding. ResultsAmong 59 enrollees, 75% were male, age 67 8 years, 76% paroxysmal AF, 69% had prior AF ablation, and mean CHADS(2) score 1.3 +/- 0.5. Over 466 +/- 131 mean days of follow-up there were 24,004 ICM transmissions with a compliance rate of 98.7%. A total of 35 AF episodes 1 hour occurred in 18 (31%) patients, resulting in a total time on NOAC of 1,472 days. This represents a 94% reduction in the time on NOAC compared to chronic anticoagulation. There were three traumatic bleeds (all on aspirin), three potential transient ischemic attacks (all on aspirin with CHADS(2) score of 1), and no strokes or deaths. ConclusionsA targeted strategy of ICM-guided intermittent NOAC administration is feasible. A large-scale trial is necessary to evaluate the safety of this approach.
引用
收藏
页码:264 / 270
页数:7
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