Background: Adding clonidine to weak ropivacaine solutions (<0.2%) could po
tentially enhance analgesia as well as further reduce the risk for unwanted
motor blockade. The aim of the present study was to compare the postoperat
ive pain-relieving quality of a ropivacaine 0.1%-clonidine mixture to that
of plain ropivacaine 0.2% following caudal administration in children.
Methods: In a prospective, observer-blinded fashion, 40 ASA 1 paediatric pa
tients undergoing subumbilical surgery were randomly allocated to receive a
caudal injection of either plain ropivacaine 0.2% (1 ml/kg) (R0.2) or a mi
xture of ropivacaine 0.1% with clonidine 2 mu g/kg (1 ml/kg) (R0.1C). Objec
tive pain scale score and need for supplemental analgesia were used to eval
uate analgesia during the first 24 h postoperatively. Residual postoperativ
e sedation was also assessed.
Results: A significantly higher number of patients in the R0.1C group (18/2
0) could be managed without supplemental analgesia during the first 24 h po
stoperatively compared to the R0.2 group (11/20) (P=0.034). Both the degree
and the duration of postoperative sedation was similar in both groups. No
signs of postoperative motor blockade were observed.
Conclusions: The combination of clonidine (2 mu g/kg) and ropivacaine 0.1%
is associated with an improved quality of postoperative analgesia compared
to plain 0.2% ropivacaine. The improved analgesic duality of the clonidine-
ropivacaine mixture is achieved without causing any significant degree of p
ostoperative sedation.
(C) Acta Anaesthesiologica Scandinavica 44 (2000).