RESUSCITATION FROM BUPIVACAINE-INDUCED ASYSTOLE IN RATS - COMPARISON OF DIFFERENT CARDIOACTIVE DRUGS

The objective of this study was to compare the success of resuscitatio n attempts with different cardioactive drugs after bupivacaine-induced asystole. Saline, amrinone (1 mg/kg), dopamine (5 (mu g/kg), norepine phrine (2 mu g/kg), epinephrine (10 mu g/kg), or isoproterenol (1 mu g /kg) were tested. Sixty rats assigned to six treatment groups (n = 10/ group) were Lightly anesthetized (0.5% halothane, 70% N2O), paralyzed (doxacurium), and given bupivacaine intravenously at 4 mg . kg(-1). mi n(-1) until asystole. Five seconds later up to three treatment drug do ses were given at 30-s intervals. Then external cardiac massage was in stituted as needed. Spontaneous heartbeat was restored in all animals given norepinephrine or epinephrine. It was not restored in one saline -one dopamine-treated, one isoproterenol-treated and three amrinone-tr eated animals. The highest (best) arbitrary scores for overall resusci tation success were achieved with norepinephrine and the lowest with a mrinone (P < 0.05). The incidence of ventricular arrhythmias after res uscitation was significantly higher (P < 0.05) in epinephrine- and iso proterenol-treated animals versus other animals. Cardiac rhythm distur bance disappeared within 20 min after successful resuscitation with no repinephrine. Amrinone was no more effective than saline in treating b upivacaine-induced asystole. A drug such as norepinephrine, which has both cardiostimulator (beta(1)-receptor agonist) and peripheral vasoco nstrictor (alpha(1)-receptor agonist) activity, may be the drug of cho ice for treating asystole induced by bupivacaine.