Peer-reviewed article
Umbilical analgesic concentrations after labour analgesia with programmed intermittent epidural bolus: a prospective observational study.
Ijuin A, Sato M, Umehara N, Amari S, Saito J et al. ·
Summary
Written by AI, not yet AICS's view · claude-haiku-4-5-20251001This is a medical study measuring drug concentrations in umbilical cord blood following epidural pain relief during labour. It is not about child well-being, health outcomes, or interventions designed to improve children's lives, but rather a technical pharmacological measurement study for obstetric anaesthesia.
Key points
Limitations
Not applicable - this document is not relevant to child well-being research.
Abstract
Purpose The umbilical analgesic concentrations after using programmed intermittent epidural bolus (PIEB) and patient-controlled epidural analgesia (PCEA) without continuous infusion are unknown. We aimed to characterize umbilical ropivacaine and fentanyl concentrations and examine their influence on neonatal conditions at delivery. Methods We prospectively studied 50 parturients with singleton pregnancies who received combined spinal-epidural analgesia using PIEB (7 mL every 45 min) and PCEA (7 mL per bolus; lockout interval: 15 min) with 0.08% ropivacaine and 2 μg·mL-1 fentanyl, with clinician-administered boluses as necessary. We evaluated the umbilical venous analgesic concentrations and neonatal characteristics. Results The median [interquartile range (IQR)] hourly ropivacaine and fentanyl doses were 13 [11-15] mg·hr-1 and 39 [30-50] µg·hr-1, respectively. The ropivacaine and fentanyl concentrations were 77 [56-98] ng·mL-1 and 0.125 [0.125-0.20] ng·mL-1 at delivery, respectively. The umbilical analgesic concentrations were correlated with the labour duration and total dose. In parturients given clinician-administered boluses within 1 hr before delivery, the ropivacaine and fentanyl concentrations were similar to those without (81 [54-104] vs 77 [54-96] ng·mL-1 and 0.20 [0.125-0.20] vs 0.125 [0.05-0.20] ng·mL-1, respectively). The umbilical arterial pH was > 7.2 and the Apgar score at 5 min was ≥ 8 for all neonates. No neonates exhibited systemic local anesthetic toxicity. Respiratory support was required for 14 neonates. Conclusions Umbilical analgesic concentrations at delivery were low after labour analgesia using a regimen of PIEB with PCEA for up to 19 hr. An intermittent bolus dosing regimen may contribute to a decrease in umbilical analgesic concentrations.