Risk, rate or rhythm control for new onset supraventricular arrhythmia during septic shock: protocol for the CAFS
Vincent Labbé1,2, Cyrielle Desnos3, Sebastien Preau4,5
1Department of Intensive Care, Université Libre de Bruxelles, Hôpital Universitaire de Bruxelles, Anderlecht, Brussels, Belgium vincent.labbe@hubruxelles.be.
BMJ Open
|April 1, 2025
Summary
New-onset supraventricular arrhythmia (NOSVA) in septic shock is common and deadly. The CAFS trial compares risk, rate, and rhythm control strategies to find the best treatment for these critically ill patients.
Area of Science:
- Critical Care Medicine
- Cardiology
- Clinical Trials
Background:
- New-onset supraventricular arrhythmia (NOSVA) is the most frequent arrhythmia in septic shock patients.
- NOSVA is linked to hemodynamic instability and increased mortality.
- Current management strategies for NOSVA in septic shock lack randomized trial data.
Purpose of the Study:
- To compare the efficacy and safety of three management strategies for NOSVA in septic shock.
- To evaluate risk control, rate control, and rhythm control in limiting shock duration and preventing organ dysfunction.
Main Methods:
- The Control Atrial Fibrillation in Septic shock (CAFS) study is a multicenter, randomized controlled superiority trial.
- 240 patients will be randomized 1:1:1 to risk control, rate control (low-dose amiodarone), or rhythm control (high-dose amiodarone and cardioversion).
- The primary endpoint is a hierarchical composite of all-cause mortality and septic shock duration at day 28.
Main Results:
- Primary results are pending as the trial is ongoing.
- Secondary outcomes include lactate clearance, cardiac rhythm control, organ dysfunction, adverse events, and length of stay.
Conclusions:
- The CAFS trial will provide crucial data on optimal NOSVA management in septic shock.
- Findings are expected to guide clinical practice and improve outcomes for septic shock patients with arrhythmias.
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