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Department of Anesthesiology and Surgical Intensive Care, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland
Address correspondence to Stuart G. Morrison, FFARCSI, Department of Anesthesiology, University Hospital of Maastricht, P Debyelaan 25, 6202 AZ Maastricht, The Netherlands. Address e-mail to katrin.mignolet{at}planetinternet.be
We sought, in this observer-blinded study, to determine the lethal dose for each of the local anesthetics levobupivacaine (L), racemic bupivacaine (B), and ropivacaine (R), and to compare their respective effects on the QRS interval of the precordial electrocardiograph after intracoronary injection. Anesthetized swine were instrumented with a left anterior descending artery coronary angiography catheter and injected with increasing doses of L, B, or R according to a randomized protocol. The doses administered were 0.375, 0.75, 1.5, 3.0, and 4.0 mg, with further doses increasing in 1-mg increments until death occurred. Plotting the mean maximum QRS interval as a function of the log10 mmol dose allowed the following cardiotoxicity potency ratios to be determined for a doubling of QRS durationB:L:R = 2.1:1.4:1. The lethal doses in millimoles (median/range) for L and R were (0.028/0.0240.031) and (0.032/0.0130.032), respectively, and were significantly higher than for B (0.015/0.0120.019) - (P < 0.05, n = 7 for all groups). The lethal dose did not differ between R and L. Thus, the cardiotoxicity potency ratios for the three anesthetics based on lethal dose were: 2.1:1.2:1. If the anesthetic potencies for B and L are similar, the latter should have less potential for cardiotoxicity in the clinical situation.
Implications: Animal experiments have shown levobupivacaine and ropivacaine to be less cardiotoxic than racemic bupivacaine. This in vivo study, using a validated swine model, compared the relative direct cardiotoxicities of these three local anesthetics. The lethal dose did not differ between levobupivacaine and ropivacaine, but was lowest for racemic bupivacaine.
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