Patient-controlled epidural analgesia in labor: The addition of clonidine to bupivacaine-fentanyl

Background and Objectives: Epidural clonidine has not been evaluated as a component of patient-controlled epidural analgesia (PCEA) solutions during labor. A randomized, double-blind trial was conducted to investigate the efficacy and side effects of PCEA using bupivacaine and fentanyl, with or without clonidine. Methods: Seventy-five healthy parturients in active labor were assigned to a PCEA solution of 0.0625% bupivacaine and fentanyl 2 mu g/mL (4 mt demand bolus, 15 min lockout), with or without clonidine 4.5 mu g/mL. The primary outcome measure was parturient rating of analgesia; others assessments included pain scores, drug utilization, supplementation and side effects. Results: Thirty-one parturients received clonidine (group BFC) and 38 received control solution (group BF). Eight (6 group BE 2 group BFC, P = .28) failed to achieve satisfactory epidural. analgesia. There was a trend for parturient ratings of pain relief to be higher in group BFC, with significantly more reporting excellent first-stage analgesia (81% v 57%, P < .05). Pain scores were similar. Clonidine (median dose, 28 mu g/h) reduced total bupivacaine and fentanyl use (P < .01), and reduced supplementation (P < .01). Maternal blood pressure (BP) and recordings of systolic BP below 100 mm Hg did not differ. Group BFC had higher sedation scares (P < .01), but no one appeared oversedated. Shivering was reduced in group BFC (P < .01). Conclusions: The addition of clonidine to epidural bupivacaine and fentanyl for PCEA in labor improved analgesia, reduced the supplementation rate, and reduced shivering. Increased sedation and lower BP were not clinically important.