A phase III, open label, randomized study was conducted in 50 patients
comparing halothane and sevoflurane for paediatric day case surgery A
graded inhalational induction resulted in only slightly more rapid in
duction with sevoflurane (3.34+/-0.92 versus 3.85+/-1.02 minutes; P>0.
05). In children receiving sevoflurane, systolic blood pressure decrea
sed to a lesser extent during induction (14.3+/-19.2 versus 26.9+/-10.
9 per cent decrease from resting values; P<0.01) and heart rate was ma
intained. Respiratory events (coughing, breath-holding, bronchospasm,
laryngospasm) were more common during induction with halothane, rind e
xcitement more common in children receiving sevoflurane. Emergence tim
es were significantly more rapid in children who had received sevoflur
ane (21.4+/-10.9 versus 33.1+/-13.7 minutes; P<0.01). Objective pain/d
iscomfort scores were higher in patients receiving sevoflurane at 10,
20, 30 and 40 minutes after arrival in the recovery room, and the inci
dence of excitement during emergence was higher in this group. It is c
oncluded that sevoflurane is well tolerated for inhalational induction
and has an improved cardiovascular profile compared to halothane. Eme
rgence was significantly more rapid following sevoflurane.