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Preemptive caudal bupivacaine and morphine for postoperative analgesia in children
P Kundra1, K Deepalakshmi, M Ravishankar
1Department of Anesthesiology and Critical Care, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India.
Insights
Preemptive epidural bupivacaine and morphine before pediatric herniorraphy significantly improves postoperative pain relief. This approach offers longer-lasting analgesia and reduced morphine consumption compared to postincisional administration.
Area of Science:
- Anesthesiology
- Pediatric Surgery
- Pain Management
Background:
- Postoperative pain management in children undergoing herniorraphy is crucial for recovery.
- Epidural analgesia is a common technique for managing surgical pain.
Purpose of the Study:
- To evaluate the efficacy of preemptive epidural bupivacaine and morphine for postoperative pain relief in children after herniorraphy.
- To compare the effectiveness of administering the analgesic mixture before versus after surgery.
Main Methods:
- A double-blind study involving 60 children undergoing elective hernia repair.
- Random allocation into two groups: preemptive (Group I) and postincisional (Group II) epidural administration of bupivacaine and morphine.
- Pain assessment using an objective pain scale (OPS), time to first postoperative analgesic (TFA), and total morphine consumption over 24 hours.
Main Results:
- Group I showed significantly lower OPS scores at 0.5, 4, and 8 hours post-surgery compared to Group II.
- Median OPS score over 24 hours was significantly lower in Group I (0) than in Group II (2).
- Time to first postoperative analgesic was significantly prolonged in Group I (12.55 h vs. 10.62 h).
- Total postoperative morphine consumption was significantly less in Group I (2.24 mg vs. 3.34 mg).
- No significant difference in the incidence of nausea and vomiting between groups.
Conclusions:
- Preemptive epidural administration of bupivacaine and morphine before herniorraphy provides superior postoperative analgesia in children.
- This method leads to better pain control, prolonged analgesia, and reduced opioid requirements compared to postincisional administration.
Unlabelled:
We designed this double-blind study to evaluate the efficacy of preemptive epidural bupivacaine and small-dose morphine for postoperative analgesia in children after herniorraphy. Sixty children, ASA physical status I or II, who were undergoing elective hernia repair under general anesthesia were randomly allocated into two groups. Group I (preemptive group) received 0.66 mL/kg 0.25% bupivacaine with morphine 0.02 mg/kg caudally after the induction of anesthesia but 15 min before surgery. Group II (postincisional group) received the same drug mixture after surgery. Pain was assessed using an objective pain scale (OPS). Time to first postoperative analgesics (TFA), the number of supplementary analgesic used, and the amount of morphine consumed over the ensuing 24-h period were noted. The OPS score was significantly less in Group I at 0.5, 4, and 8 h (P < 0.05) than in Group II after surgery. The median OPS score recorded over 24 h was 0 for Group I and 2 for Group II, which was significantly different (P < 0.05). The TFA in Group I (12.55 +/- 3.06 h) was significantly (P < 0.05) prolonged compared with Group II (10.62 +/- 3.18 h). The total postoperative morphine consumption in Group I (2.24 +/- 1.4 mg) was significantly (P < 0.05) less than that in Group II (3.34 +/- 2.29 mg). Nevertheless, the incidence of nausea and vomiting was not significantly different between the groups. In this study, we demonstrated that preemptive epidural bupivacaine and small-dose morphine administration is superior to the same mixture given at the conclusion of surgery for pain relief.
Implications:
This study was performed on two groups of 30 children undergoing hernia repair. Group I received a bupivacaine-morphine mixture caudally before surgery, and Group II received the same drugs caudally at the completion of surgery. Postoperative assessment demonstrated longer and better pain relief in Group I.
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