Rwh. Skilton et al., Dose response study of subarachnoid diamorphine for analgesia after elective caesarean section, INT J OB AN, 8(4), 1999, pp. 231-235
Subarachnoid diamorphine provides excellent analgesia after elective caesar
ean section but the optimum dose is still uncertain. We therefore investiga
ted the effects of three regimens of subarachnoid diamorphine. Forty partur
ients were assigned to one of four groups. A control group received no diam
orphine in their subarachnoid bupivacaine and three study groups received 0
.1 mg, 0.2 mg or 0.3 mg diamorphine added to 12.5 mg hyperbaric bupivacaine
0.5% in a semi-blind randomised design study. All women received a 100 mg
diclofenac suppository at the end of the caesarean section and were provide
d with morphine patient controlled analgesia (PCA) postoperatively. The pat
ients were assessed for pain, morphine usage and side-effects at 2, 4, 8 an
d 24 h after the subarachnoid injection. Postoperative visual analogue scor
es for pain and PCA morphine consumption were significantly lower, and mean
time to first use of morphine was significantly longer in the 0.3 mg diamo
rphine group. The mean (SD) dose of PCA morphine used over 24 h was 39.4 (1
4.7), 25.6 (16.5), 21.6 (15.9) and 3.1 (3.6) mg, and mean time to first use
of morphine was 1.6 (0.5), 3.0 (1.4), 3.4 (2.4) and 14.1 (9.4) h, in the 0
, 0.1 mg, 0.2 mg and 0.3 mg groups respectively. Side-effects of pruritus,
nausea and vomiting were dependent on the dose of spinal diamorphine but di
d not require treatment in any patients. We conclude that 0.3 mg subarachno
id diamorphine provides significantly better postoperative pain relief than
the smaller doses with an acceptable increase in side-effects. (C) 1999 Ha
rcourt Publishers Ltd.