Efficacy of Fentanyl versus Nalbuphine as Adjuvant agents in the induction phase of general anesthesia: A Comparative Study

Main Article Content

Voleti Sai Pratyusha, MD
Dr. D Haritha
K. Krishna chaithanya
Dr Venkateswara rao

Keywords

Propofol, Fentanyl, Nalbuphine, General anaesthesia, Haemodynamic stability

Abstract

Background: Propofol is the most commonly preferred intravenous induction agent but may cause dose-dependent cardiovascular depression. Opioid premedication reduces propofol requirements during induction. This study compared the propofol-sparing efficacy of fentanyl and nalbuphine during induction of general anaesthesia. Methods: In this prospective comparative study, 100 ASA physical status I–II adults undergoing elective surgery under general anaesthesia were randomized into two groups (n=50 each). Group F received intravenous fentanyl 3 μg/kg and Group N received intravenous nalbuphine 0.3 mg/kg six minutes before induction. Using propofol titrated to loss of the eyelash reflex. Primary outcomes were before propofol dose, Ramsay Sedation Scale score, and induction time. Secondary outcomes included haemodynamic changes and opioid-related adverse effects. Results: Fentanyl significantly reduced the propofol dose required for induction compared with nalbuphine 80.78 ± 14.30 mg vs 95.44 ± 15.69 mg (p < 0.001). Ramsay Sedation Scale scores were higher with nalbuphine 2.34 ± 0.35 vs 2.87 ± 0.56 (p < 0.001). Induction time was significantly shorter in the fentanyl group 43.52 ± 8.53 s vs 48.76 ± 10.24 s (p = 0.007). The incidences of hypotension, bradycardia, respiratory depression, postoperative nausea and vomiting, and pruritus were low and comparable between groups. Conclusion: Fentanyl demonstrated superior propofol-sparing efficacy compared with nalbuphine while maintaining comparable haemodynamic stability and safety. Nalbuphine produced greater pre-induction sedation and represents a suitable alternative opioid adjunct.

Abstract 0 | PDF Downloads 0

References

1.Langley MS, Heel RC. Propofol. A review of its pharmacodynamic and pharmacokinetic properties and use as an intravenous anaesthetic. Drugs 1988;35:334-72.
2.Goodchild CS. Propofol-induced cardiovascular depression: science and art. Br J Anaesth 2015;115:641-2.
3.Lundy JS. Balanced anesthesia. Minn Med 1926;9:399-404.
4.Ben-Shlomo I, Finger J, Bar-Av E, et al. Propofol and fentanyl act additively for induction of anaesthesia. Anaesthesia 1993;48:111-3.
5.Errick JK, Heel RC. Nalbuphine. A preliminary review of its pharmacological properties and therapeutic efficacy. Drugs 1983;26:191-211.
6.Duda D, Müller H, Brandt L. Comparative clinical study of nalbuphine and fentanyl. Effects and side effects with special reference to the induction phase. Anaesthesist 1987;36:407-11.
7.Marik PE. Propofol: therapeutic indications and side-effects. Curr Pharm Des 2004;10:3639-49.
8.Darlong V, Som A, Baidya DK, et al. Effect of varying time intervals between fentanyl and propofol administration on propofol requirement for induction of anaesthesia: a randomised controlled trial. Indian J Anaesth 2019;63:826-33.
9.Kaur J, Srilata M, Padmaja D, et al. Dose sparing of induction dose of propofol by fentanyl and butorphanol: a comparison based on entropy analysis. J Anaesthesiol Clin Pharmacol 2013;29:128-33.
10.Stoelting RK, Hillier SC. Pharmacology and Physiology in Anesthetic Practice. 5th ed. Philadelphia: Lippincott Williams & Wilkins; 2015.
11.Khan FA. Comparison of fentanyl and nalbuphine in total intravenous anaesthesia (TIVA). Journal of Pakistan Medical Association. 2002;52(10):459
12.Yaksh TL, Wallace MS. Opioids, analgesia and pain management. In: Brunton LL, Hilal-Dandan R, Knollmann BC, eds. Goodman & Gilman's The Pharmacological Basis of Therapeutics. 13th ed. New York: McGraw-Hill; 2018.