COMPARATIVE STUDY ON INTRATHECAL MAGNESIUM SULFATE AND FENTANYL AS A SPINAL ADJUVANT, COMBINED WITH 0.5% HYPERBARIC BUPIVACAINE FOR INFRAUMBILICAL SURGERIES

Main Article Content

Dr. Tilak Lokesh*

Keywords

spinal anaesthesia, hyperbaric bupivacaine, magnesium sulphate, fentanyl

Abstract


  1. Introduction
    Spinal anesthesia benefits from adjuvants that prolong block duration. Fentanyl is widely used, but magnesium sulfate, a non-opioid NMDA antagonist, is emerging as a promising alternative in regional anesthesia.

  2. Aims and Objectives


This study aims to evaluate and compare the onset, duration, and safety profile of intrathecal magnesium sulfate versus fentanyl, with a control group, to determine whether magnesium provides analgesic efficacy on par with the established opioid adjuvant.



  1. Materials and Methods


Seventy-five ASA I–II patients undergoing elective infraumbilical surgeries were randomized into three groups: Control (bupivacaine + saline), M100 (bupivacaine + 100 mg magnesium sulfate), and F (bupivacaine + 25 mcg fentanyl). Spinal anesthesia was administered under standard conditions. Parameters including onset and duration of sensory and motor block, and adverse effects like hypotension and bradycardia, were monitored. Data were analyzed using ANOVA, Chi-square, and posthoc LSD tests. A p-value < 0.05 was considered statistically significant.


4.Results
Group F demonstrated the longest sensory and motor block durations, while M100 showed a faster onset and moderately prolonged duration compared to Control. Control had the shortest block durations. Ephedrine usage, indicative of hypotension, was highest in M100 (32%), followed by F (24%), and none in Control, showing significant hemodynamic impact. Sensory and motor durations across all groups were statistically significant (p < 0.001), suggesting that both adjuvants enhanced block characteristics, with magnesium showing performance comparable to fentanyl.


5.Conclusions


Magnesium sulfate stands on par with fentanyl in prolonging spinal anesthesia, offering comparable block durations with a non-opioid profile. While onset is slower, its efficacy and safety render it a valuable alternative, particularly in patients where opioid use is limited or contraindicated. These findings support magnesium sulfate as a clinically relevant intrathecal adjuvant and justify its further use and study in spinal anesthesia protocols.

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