Systemic toxicity and resuscitation in bupivacaine-, levobupivacaine-, or ropivacaine-infused rats

Citation
S. Ohmura et al., Systemic toxicity and resuscitation in bupivacaine-, levobupivacaine-, or ropivacaine-infused rats, ANESTH ANAL, 93(3), 2001, pp. 743-748
Citations number
31
Categorie Soggetti
Aneshtesia & Intensive Care","Medical Research Diagnosis & Treatment
Journal title
ANESTHESIA AND ANALGESIA
ISSN journal
00032999 → ACNP
Volume
93
Issue
3
Year of publication
2001
Pages
743 - 748
Database
ISI
SICI code
0003-2999(200109)93:3<743:STARIB>2.0.ZU;2-V
Abstract
We compared the systemic toxicity of bupivacaine, levobupivacaine, and ropi vacaine in anesthetized rats. We also compared the ability to resuscitate r ats after lethal doses of these local anesthetics. Bupivacaine, levobupivac aine, or ropivacaine was infused at a rate of 2 mg . kg(-1) . min(-1) while electrocardiogram, electroencephalogram, and arterial pressure were contin uously monitored. When asystole was recorded, drug infusion was stopped and a resuscitation sequence was begun. Epinephrine 0.01 mg/kg was administere d at 1-min intervals while external cardiac compressions were applied. Resu scitation was considered successful when a systolic arterial pressure great er than or equal to 100 mm Hg was achieved within 5 min. The cumulative dos es of levobupivacaine and ropivacaine that produced seizures were similar a nd were larger than those of bupivacaine. The cumulative doses of levobupiv acaine that produced dysrhythmias and asystole were smaller than the corres ponding doses of ropivacaine, but they were larger than those of bupivacain e. The number of successful resuscitations did not differ among groups. How ever, a smaller dose of epinephrine was required in the Ropivacaine group t han in the other groups. We conclude that the systemic toxicity of levobupi vacaine is intermediate between that of ropivacaine and bupivacaine when ad ministered at the same rate and that ropivacaine-induced cardiac arrest app ears to be more susceptible to treatment than that induced by bupivacaine o r levobupivacaine.