ANESTHETIC POTENCY AND CARDIOPULMONARY EFFECTS OF SEVOFLURANE IN GOATS - COMPARISON WITH ISOFLURANE AND HALOTHANE
Citation
Y. Hikasa et al., ANESTHETIC POTENCY AND CARDIOPULMONARY EFFECTS OF SEVOFLURANE IN GOATS - COMPARISON WITH ISOFLURANE AND HALOTHANE, Canadian journal of veterinary research, 62(4), 1998, pp. 299-306
Categorie Soggetti
Veterinary Sciences
SICI code
0830-9000(1998)62:4<299:APACEO>2.0.ZU;2-4
Abstract
The anesthetic potency and cardiopulmonary effects of sevoflurane were
compared with those of isoflurane and halothane in goats. The (mean /- SD) minimal alveolar concentration (MAC) was 0.96 +/- 0.12% for hal
othane, 1.29 +/- 0.11% for isoflurane, and 2.33 +/- 0.15% for sevoflur
ane. Cardiopulmonary effects of sevoflurane, halothane and isoflurane
were examined at end-tidal concentrations equivalent to 1, 1.5 and 2 M
AC during either spontaneous or controlled ventilation (SV or CV). Dur
ing SV, there were no significant differences in respiration rate, tid
al volume and minute ventilation between anesthetics. Dose-dependent d
ecreases in both tidal volume and minute ventilation induced by haloth
ane were greater than those by either sevoflurane or isoflurane. Hyper
capnia and acidosis induced by sevoflurane were not significantly diff
erent from those by either isoflurane or halothane at 1 and 1.5 MAC, b
ut were less than those by halothane at 2 MAC. There was no significan
t difference in heart rate between anesthetics during SV and CV. Durin
g SV, all anesthetics induced dose-dependent decreases in arterial pre
ssure, rate pressure product, systemic vascular resistance, left ventr
icular minute work index and left ventricular stroke work index. Syste
mic vascular resistance with isoflurane at 2 MAC was lower than that w
ith sevoflurane. During CV, sevoflurane induced dose-dependent circula
tory depression (decreases in arterial pressure, cardiac index, rate p
ressure product, systemic vascular resistance, left ventricular minute
work index and right ventricular minute work index), similar to isofl
urane. Halothane did not significantly alter systemic vascular resista
nce from 1 to 2 MAC.