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May 14, 2026Cureus0 citationsOpen Access

When Rhythm Control Backfires: Flecainide-Precipitated Transient Cardiomyopathy in the Setting of Electrical Cardioversion

KMKeyshla Pagán MoralesDSDipak ShahDFDustin Feldman

Key Result

Flecainide precipitated severe, reversible transient cardiomyopathy with an ejection fraction of 15% to 20% in a 73-year-old male following electrical cardioversion for atrial fibrillation.

Key Points

  • This case describes a rare instance of transient cardiomyopathy precipitated by flecainide during electrical cardioversion in a patient with atrial fibrillation.
  • Described a 73-year-old male with persistent atrial fibrillation treated with flecainide and elective cardioversion.
  • Noted the patient's normal left ventricular function and absence of structural heart disease before treatment.
  • Emphasized prompt recognition and management of symptoms following the cardioversion.
  • Patient experienced profound conduction suppression and transient cardiomyopathy after flecainide administration and cardioversion.
  • Full recovery occurred post-management, underscoring the importance of careful patient selection for flecainide use.

Study Design

Type

Case Report (n=1)

Multicenter

No

Structured PICO

Does flecainide precipitate transient cardiomyopathy in the setting of electrical cardioversion in a patient with atrial fibrillation?

P
Population
73-year-old male with long-standing persistent atrial fibrillation, no structural heart disease, and normal left ventricular systolic function
I
Intervention
Flecainide started following successful AF ablation, followed by elective electrical cardioversion for recurrent AF
O
Outcome
Development of profound conduction suppression and transient cardiomyopathysafety

Flecainide may rarely precipitate transient cardiomyopathy and profound conduction suppression in the peri-cardioversion setting, even in patients without prior structural heart disease.

Limitations

  • Single case report
  • True incidence of flecainide-associated cardiomyopathy remains unknown

Abstract

Flecainide, a class Ic antiarrhythmic, is a potent sodium channel blocker that slows conduction through the atria, atrioventricular (AV) node, and His-Purkinje system. It is effective for rhythm control in atrial fibrillation (AF) in appropriately selected patients but carries a risk of significant bradyarrhythmia, conduction system suppression, and negative inotropy. Flecainide is generally considered safe in patients without structural heart disease, left ventricular dysfunction, or significant coronary artery disease; however, rare cases of reversible cardiomyopathy have been reported. Current guidelines continue to recommend flecainide for rhythm control in carefully selected patients with AF who do not have structural heart disease, including for cardioversion of recent-onset AF, pretreatment before direct current cardioversion, the “pill-in-the-pocket” approach, and ongoing maintenance of sinus rhythm. This case describes a 73-year-old male with long-standing persistent AF, no structural heart disease, and normal left ventricular systolic function who was started on flecainide following successful AF ablation. Subsequently, he developed recurrent AF and underwent elective cardioversion, which was complicated by profound conduction suppression and likely flecainide-precipitated transient cardiomyopathy in the setting of electrical cardioversion. Prompt recognition and management led to a full recovery, emphasizing the importance of careful patient selection and monitoring when using flecainide, as it may, in rare cases, be associated with or precipitate cardiomyopathy in the peri-cardioversion setting.

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Cite This Study

Morales et al. (2026) conducted a case report in Atrial fibrillation (n=1). Flecainide was evaluated on Transient cardiomyopathy. Flecainide precipitated severe, reversible transient cardiomyopathy with an ejection fraction of 15% to 20% in a 73-year-old male following electrical cardioversion for atrial fibrillation.

synapsesocial.com/papers/6a0566bda550a87e60a1ea34https://doi.org/10.7759/cureus.108713
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