Jm. Leung et Da. Pastor, DISSOCIATION BETWEEN HEMODYNAMICS AND SYMPATHETIC ACTIVATION DURING ANESTHETIC INDUCTION WITH DESFLURANES, Canadian journal of anaesthesia, 45(6), 1998, pp. 533-540
Purpose: To compare the simultaneous haemodynamic effects, sympathetic
activation and cardiac risks associated with desflurane used in a bal
anced technique, with those of isoflurane anaesthesia, Methods: A pros
pective, randomized, open label study was conducted at a University me
dical centre. Forty patients undergoing major non-cardiac surgery were
randomized to receive either desflurane or isoflurane as the primary
anaesthetic agent. After premedication, fentanyl and thiopentone were
administered iv, Anaesthesia was increased up to 1.0 MAC(ET) in O-2 vi
a controlled mask ventilation and maintained at 1.0 MAC before trachea
l intubation. Maintenance consisted of N2O, O-2 and desflurane or isof
lurane for 10 min. During the study, HR and arterial BP were continuou
sly measured, as were ECG ST-segments and ventricular dysrhythmias usi
ng a 3-channel Holler ECG recorder: Left ventricular global and region
al function were measured using precordial echocardiography, Serial pl
asma catecholamine concentrations were measured. Results: For both gro
ups, HR was maintained without increases over baseline values while sy
stolic BP showed a progressive decrease during induction. Use of beta
blockade during induction was higher in the desflurane (7/20 = 35%) th
an in the isoflurane group (1/20 = 5%), P = 0.04, The plasma norepinep
hrine concentrations progressively increased in the desflurane group b
ut not in the isoflurane group. Four patients in-the desflurane and th
ree in the isoflurane group developed transient worsening of regional
function but no change in mean left ventricular ejection fraction area
and no ECC; ischaemia occurred during anaesthetic induction. Conclusi
ons: Desflurane differs from isoflurane in thats:sympathetic stimulati
on persisted despite blunting of potential hyper dynamic haemodynamic
responses by narcotic and beta blockade. However; this sympathetic act
ivation did not appear to increase cardiac risks.