Steady-State Serum Amiodarone Concentrations: Relationships with Antiarrhythmic Efficacy and Toxicity

  1. HESCHl H. ROTMENSCH, M.D.;
  2. BERNARD BELHASSEN, M.D.;
  3. BRIAN N. SWANSON, Ph.D.;
  4. DAVID SHOSHANI, M.D.;
  5. SCOTT R. SPIELMAN, M.D.;
  6. ARNOLD J. GREENSPON, M.D.;
  7. ALLAN M. GREENSPAN, M.D.;
  8. PETER H. VLASSES, Pharm.D.; and
  9. LEONARD N. HOROWITZ, M.D.
  1. Philadelphia, Pennsylvania; and Tel-Aviv
    , Israel

    Abstract

    The relationship of apparent steady-state serum concentrations of amiodarone and its metabolite, desethylamiodarone, to therapeutic and toxic effects was assessed in 127 patients who had treatment-resistant ventricular or supraventricular arrhythmias or were intolerant to other agents. After at least 2 months (mean, 9.8) of treatment with daily maintenance doses of 200 to 600 mg, arrhythmias were effectively suppressed in 78% of patients. Arrhythmias recurred in 47% of patients with serum amiodarone concentrations of less than 1.0 mg/L, whereas only 14% of patients with higher concentrations had recurrences (p < 0.005). Side effects, most of them mild, occurred in 57%; only 9 patients required discontinuation of drug therapy. The risk of developing adverse reactions was related to serum amiodarone concentrations (p < 0.0001). Adverse reactions were common in patients with serum values exceeding 2.5 mg/L, although pulmonary complications did occur at lower concentrations. Monitoring serum amiodarone concentrations may differentiate failure of drug therapy from suboptimal dosing and reduce the incidence of concentration-related side effects.

    Article and Author Information

    • ▸From the Divisions of Clinical Pharmacology and Cardiology, Departments of Medicine and Pharmacology, Jefferson Medical College, and Division of Clinical Cardiac Electrophysiology, Likoff Cardiovascular Institute, Hahnemann Medical College, Philadelphia, Pennsylvania; and Department of Cardiology, Tel-Aviv Medical Center, Sackler School of Medicine, Tel-Aviv, Israel.

    • ▸Requests for reprints should be addressed to Heschi H. Rotmensch, M.D.; Division of Clinical Pharmacology (M-502), Jefferson Medical College, 11th & Walnut Streets; Philadelphia, PA 19107.

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