Atrial fibrillation threshold predicted long-term efficacy of pharmacological treatment of patients without structural heart disease

Europace. 2002 Oct;4(4):383-9. doi: 10.1053/eupc.2002.0259.

Abstract

Aims: To ascertain if an electrophysiological study could predict long-term efficacy of anti-arrhythmic drugs in the treatment of lone atrial fibrillation.

Methods and results: Forty-four patients (36 males, 8 females, age 55.5 +/- 10.6) with paroxysmal atrial fibrillation were enrolled to undergo serial electrophysiological studies at the bedside. Two quadripolar catheters were inserted via the subclavian vein. Disopyramide (D: 2 mg/kg iv), cibenzoline (C: 1.4 mg/kg iv), aprindine (A: 2 mg/kg iv), pilsicainide (P: 2 mg/kg po) and flecainide (F: 3 mg/kg po) were tested. Atrial fibrillation threshold (AFT) was measured as the lowest current amplitude of rapid pacing (50 Hz for 1 s) to induce atrial fibrillation lasting more than 30 s. Before drug treatment, AFT was 3.9 +/- 0.3 mA. Pharmacological treatment raised AFT as follows: D 5.9 +/- 0.9 mA, C 7.6 +/- 1.2 mA, A 8.1 +/-1.1 mA, P 6.0 +/- 0.8 mA, F 7.3 +/- 1.1 mA. Recurrence of atrial fibrillation was observed during 1-year follow-up in 12% of cases when they were treated with a drug that raised AFT by 5 mA or more. On the other hand, the recurrence rate was 87% when patients were treated with a drug that raised AFT by less than 5 mA (P = 0.001).

Conclusion: AFT was a good predictor of long-term efficacy of pharmacological treatment against atrial fibrillation.

MeSH terms

  • Aged
  • Anti-Arrhythmia Agents / therapeutic use*
  • Aprindine / therapeutic use
  • Atrial Fibrillation / drug therapy*
  • Atrial Fibrillation / physiopathology
  • Disopyramide / therapeutic use
  • Electrophysiologic Techniques, Cardiac*
  • Female
  • Flecainide / therapeutic use
  • Humans
  • Imidazoles / therapeutic use
  • Lidocaine / analogs & derivatives*
  • Lidocaine / therapeutic use
  • Male
  • Middle Aged
  • Treatment Outcome

Substances

  • Anti-Arrhythmia Agents
  • Imidazoles
  • Aprindine
  • Lidocaine
  • pilsicainide
  • Disopyramide
  • Flecainide
  • cifenline