Abstract
Materials and Methods: Prospective randomized control trial, 100 patients aged 20-70 years, American Society of Anaesthesiologists physical class I and II posted for elective upper and lower abdominal laparoscopic surgeries. Patients were divided into two groups (n=50 in each group): opioid-free (Group A) and opioid (Group B). Group A received anesthetic doses of lidocaine, magnesium, and paracetamol in combination with Erector spinae plane block for post-operative pain relief, while group B received intermittent doses of fentanyl. Postoperatively, NRS was observed at 0, 2, 4, and 6 hours during rest and at 0, 2, 4, 6, and 24 hours during movement. Data were analyzed by independent t-test.
Results: Group A showed a significant decrease in NRS score at rest at 0, 2, 4, and 6 hours, whereas there was a significant decrease in NRS score at movement in group A at 0, 2, 6, and 24 hours compared to group B (P< 0.05). Total duration of analgesia (hour) was significantly more in group A (17.86 ± 7.85) as compared to group B (7.76 ± 3.98) (P<0.001). Intraoperative vitals were comparable. The total rescue analgesia (milligram) requirement was significantly low in group A (0.92 ± 0.8) as compared to group B (2.02 ± 0.38).
Conclusion: For patients undergoing elective upper and lower abdominal laparoscopic surgeries, multimodal analgesia was safe in unwanted opioid side-effects cases and unavailability of opioids.
Keywords
laparoscopic surgeries Block, magnesium opioid-free anaesthesia pain
References
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