Objective: To identify whether programmed intermittent epidural bolus analgesia is effective and safe to the parturients and neonates.Methods: Sixty healthy ASA class I or II, term (≥37weeks' gestation), nulliparous women were recruited in our study. Epidural analgesia was initiated with a solution of 0.15% ropivacaine 10 mL and maintained with 0.12% ropivacaine combined with fentanyl 2ug/mL by continuous epidural infusion at a rate of 5mL/h and combined with a patient-controlled epidural analgesia bolus of 5 mL and intermittent bolus of 5mL and combined with a patient-controlled epidural analgesia bolus of 5 mL, lockout interval was 20 minutes. After 20 minutes of the first dosage the VAS score was obtained in every 60 minutes. The maternal and fetal outcome, total consumption of analgesic solution and were oxytocin compared among the groups.Result: There was no difference of the maternal and fetal outcomes among the groups. The dosage consumption of oxytocin in non-labor analgesia group was significant lower than analgesia groups, the first and second stage of labor in non-labor analgesia group was significant longer than two analgesia groups. There was a significant difference in the epidural ropivacaine total consumption between the two analgesia groups. (51.27±9.61mg vs 70.44±12.78 mg, P=0.00 )
Conclusion:The use of programmed intermittent bolus combined with PECA was more effective than continuous infusion combined with PECA, it could be useful as the mode of maintenance for epidural labor analgesia.