Key result
Disopyramide and erythromycin prolong RV action potential duration ~30% and induce proarrhythmias in dogs.
Why the study?
Does the sequential administration of disopyramide and erythromycin prolong ventricular repolarization and increase the incidence of arrhythmias in dogs with complete atrioventricular block?
Does the sequential administration of disopyramide and erythromycin prolong ventricular repolarization and increase the incidence of arrhythmias in dogs with complete atrioventricular block?
Absolute Event Rate: 321.8% vs 247%
p-value: p=<0.02
The sequential administration of disopyramide and erythromycin at clinically relevant doses causes a potentially fatal interaction by significantly prolonging ventricular repolarization and inducing torsades de pointes.
May caution against disopyramide-erythromycin co-use in AV block; leaves open human translation.
The combined effects of disopyramide (DP) and erythromycin (EM) on ventricular repolarization and the inciden-ces of ventricular premature contractions (VPCs) and torsades de pointes (TdP) were investigated in 12 anesthetized dogs with complete atrioventricular block. Monophasic action potentials (MAPs) were measured from the left and right ventricular (LV and RV) endocardium. The right or left ventricle was paced at a cycle length of 750-1000 msec. Dogs were divided into 2 groups and given either intravenous DP at 3 mg/kg and then intravenous EM at 50 mg/kg (group 1, n = 8), or intravenous EM at 50 mg/kg and then intravenous DP at 3 mg/kg (group 2, n = 4). MAP duration at 90% repolarization (MAPD(90)) was measured before drug administration (baseline) and again after administration of each drug. RV MAPD(90) and LV MAPD(90) increased significantly (P < 0.02) after administration of each drug in group 1 (RV MAPD(90): from 247.0 ± 36.3 [baseline] to 283.5 ± 38.3 to 321.8 ± 56.7; LV MAPD(90): from 262.6 ± 49.1 (baseline) to 296.1 ± 58.8 to 351.0 ± 80.6). Early afterdepolarizations developed in 2 group 1 dogs after administration of DP and in 4 additional dogs after administration of EM. Frequent VPCs occurred in 1 dog after administration of DP and in 2 additional dogs after administration of EM, and TdP and ventricular tachycardias developed in 2 of the 3 dogs after administration of EM. Similar trends occurred in group 2. These results indicate a potentially fatal interaction between DP and EM administered in clinically relevant doses.
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Watanabe et al. (2011) studied Complete atrioventricular block (n=12). Disopyramide and Erythromycin vs. Baseline was evaluated on Right ventricular monophasic action potential duration at 90% repolarization (RV MAPD90) (p=<0.02). Combined administration of disopyramide and erythromycin significantly prolonged right ventricular action potential duration from 247.0 ms to 321.8 ms and induced proarrhythmias in dogs.
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