Rate Control Versus Electrical Cardioversion Trial 7–Acute Cardioversion Versus Wait and See - RACE 7 ACWAS
Contribution To Literature:
The RACE 7 ACWAS trial showed that delayed cardioversion was noninferior to early cardioversion at the presence of normal sinus rhythm at 4 weeks.
Description:
The goal of the trial was to evaluate delayed compared with early cardioversion among patients with recent-onset atrial fibrillation.
Study Design
- Randomized
- Parallel
Patients with new-onset atrial fibrillation were randomized to delayed cardioversion (n = 218) versus early cardioversion (n = 219). Patients randomized to delayed cardioversion received rate controlling agents and underwent cardioversion in 48 hours, if needed. Transesophageal echocardiography was not performed in any patient. Long-term anticoagulation was recommended according to the patient’s estimated stroke risk.
- Total number of enrollees: 437
- Duration of follow-up: 4 weeks
- Mean patient age: 65 years
- Percentage female: 40%
- Percentage with diabetes: 10%
Inclusion criteria:
- Onset of atrial fibrillation <36 hours
- Hemodynamically stable
Other salient features/characteristics:
- In the delayed cardioversion group, 69% spontaneously converted to normal sinus rhythm before 48 hours
Principal Findings:
The primary outcome, presence of normal sinus rhythm at 4 weeks, occurred in 91% of the delayed cardioversion group compared with 94% of the early cardioversion group (p = 0.005 for noninferiority).
Secondary outcomes:
- Ischemic stroke or transient ischemic attack: one patient in the delayed group vs. one patient in the early group
- Cardiovascular complications: 10 patients in the delayed group vs. eight patients in the early group
Interpretation:
Among patients with recent-onset atrial fibrillation, delayed cardioversion was noninferior to early cardioversion at maintaining atrial fibrillation at 4 weeks. Spontaneous cardioversion occurred in the majority of patients randomized to a delayed strategy before electrical or pharmacological cardioversion was required. This trial does not apply to patients in whom the duration of atrial fibrillation is unknown. Regardless of whether a rate or rhythm control strategy is selected, the patient’s risk for stroke needs to be estimated and anticoagulation initiated, if appropriate.
References:
Pluymaekers NA, Dudink EA, Luermans JG, et al., on behalf of the RACE 7 ACWAS Investigators. Early or Delayed Cardioversion in Recent-Onset Atrial Fibrillation. N Engl J Med 2019;380:1499-508.
Editorial: Healey JS, McIntyre WF. The RACE to Treat Atrial Fibrillation in the Emergency Department. N Engl J Med 2019;380:1578-9.
Clinical Topics: Anticoagulation Management, Arrhythmias and Clinical EP, Noninvasive Imaging, Prevention, Anticoagulation Management and Atrial Fibrillation, Implantable Devices, EP Basic Science, SCD/Ventricular Arrhythmias, Atrial Fibrillation/Supraventricular Arrhythmias, Echocardiography/Ultrasound
Keywords: Anti-Arrhythmia Agents, Anticoagulants, Arrhythmias, Cardiac, Atrial Fibrillation, Brain Ischemia, Echocardiography, Transesophageal, Electric Countershock, Ischemic Attack, Transient, Secondary Prevention, Risk, Secondary Prevention, Stroke, Thrombolytic Therapy, Vascular Diseases
< Back to Listings