SummaryIn this randomised, controlled study, we compared the hourly dose requirement of ropivacaine 0.125% (group R, n 16) with bupivacaine 0.125% (group B, n 16) provided by demand-only (bolus 5 ml, lockout 10 min) parturient-controlled epidural analgesia during labour. The hourly dose requirement was comparable although group R had a lower successful to total demands ratio (p , 0.05). We also found that both groups were clinically indistinguishable in terms of pain relief and side-effects. No difference in maternal or fetal outcome was detected. We conclude that, at a concentration of 0.125%, ropivacaine and bupivacaine were equally effective when self-administered using this patient-controlled regimen.Keywords Anaesthetics, local: ropivacaine; bupivacaine. Anaesthetic techniques: regional; patient-controlled epidural. Ropivacaine, an amide local anaesthetic, has gained much popularity as an agent for obstetric epidural analgesia because of a reduced propensity for causing cardiotoxicty and a purportedly greater selectivity for sensory fibres compared with bupivacaine [1±3]. However, the expected advantage of reduced motor block was not evident in earlier studies comparing ropivacaine with bupivacaine for labour epidural analgesia administered by intermittent top-ups, continuous infusion or continuous infusion with patient-controlled top-ups [4±6]. Furthermore, recent studies have suggested that epidurally administered ropivacaine is 40% less potent than bupivacaine based on the index of the`50% effective dose' (ED 50 ) [7,8]. However, their potency ratio at a more clinically relevant dose, such as the ED 95 , remains to be determined.In an earlier study, we found that demand-only patientcontrolled epidural analgesia (PCEA) was dose sparing. PCEA also produced a reduced incidence of lower limb motor block and greater patient satisfaction than a continuous infusion [9]. We also found that, with PCEA, 0.125% ropivacaine was associated with a lower incidence of motor block despite producing as effective analgesia as 0.2% ropivacaine [10].In this study, we compared PCEA ropivacaine with bupivacaine in identical concentrations (0.125%). As a demand-only PCEA regimen allows the flexibility of parturient`self-titration' to reach satisfactory pain relief, we hypothesised that the consumption of bupivacaine would be lower than ropivacaine if the potency ratio based on ED 50 values was clinically applicable under the current circumstances.
MethodsWith the approval of the hospital ethics committee, this prospective, randomised, double-blinded controlled trial was conducted on 32 primigravid parturients in spontaneously established labour (at least one painful contraction every 5 min). All parturients were of ASA physical status I and had given written, informed consent for participation in the study. Women were not studied if: cervical dilatation . 5 cm, body weight . 100 kg, age . 40 -years, they had obstetric complications (e.g. nonsingleton pregnancy, previous Caesarean delivery and prematurity).A total of 0.5 l of Ri...