Key result
IV magnesium sulfate followed by nifekalant is linked to ~49% AFL termination within 60 minutes.
Why the study?
Pharmacologic cardioversion of atrial flutter remains challenging, and while nifekalant is effective, it is limited by QT prolongation and risk of torsades de pointes, which magnesium sulfate may mitigate.
Does intravenous magnesium sulfate followed by nifekalant improve atrial flutter termination in patients with symptomatic persistent atrial flutter?
Observational (n=86)
Yes
Does intravenous magnesium sulfate followed by nifekalant improve atrial flutter termination in patients with symptomatic persistent atrial flutter?
An intravenous nifekalant-magnesium cocktail successfully terminated symptomatic persistent atrial flutter in 48.8% of patients without inducing torsades de pointes, suggesting a feasible chemical cardioversion strategy.
May support nifekalant-magnesium for chemical cardioversion in persistent AFL; leaves open confirmation in randomized trials.
BACKGROUND: Pharmacologic cardioversion of atrial flutter (AFL) remains challenging, particularly in older or frail patients who are not candidates for catheter ablation. Nifekalant is effective for AFL but is limited by QT prolongation and the risk of torsades de pointes (TdP). Magnesium sulfate may mitigate this risk. METHODS: In this multicenter, investigator-initiated pilot study, 86 patients with symptomatic persistent AFL received intravenous magnesium sulfate followed by nifekalant. The primary outcome was AFL termination within 60 min. Time to termination and safety outcomes, including TdP, were assessed. Multivariable logistic regression analyses were performed to identify factors associated with AFL termination. RESULTS: AFL terminated in 42 patients (48.8%). Among patients with successful cardioversion, 80% achieved termination within 20 min. Larger left atrial diameter was associated with a lower likelihood of AFL termination. Adverse events occurred in 2 patients (2.3%), including sinus pauses requiring pacemaker implantation and transient hypotension requiring vasopressor support. No cases of TdP were observed. CONCLUSIONS: These findings suggest that the nifekalant-magnesium cocktail may be a feasible and potentially safe option for chemical cardioversion of AFL, warranting further investigation in larger studies.
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Sairaku et al. (2026) conducted an observational in symptomatic persistent atrial flutter (n=86). intravenous magnesium sulfate followed by nifekalant was evaluated on AFL termination within 60 min. Intravenous magnesium sulfate followed by nifekalant achieved atrial flutter termination within 60 minutes in 48.8% of patients, with no cases of torsades de pointes observed.
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