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Pain alleviation in patients undergoing cardiac surgery;
presternal local anesthetic and magnesium infiltration
versus conventional intravenous analgesia:
a randomized double-blind study

Research Authors
Emad Zarief Kamel1, Sayed Kaoud Abd-Elshafy1, Jehan Ahmed Sayed1,
Mohammed Mahmoud Mostafa2, and Mohamed Ismail Seddi
Research Journal
Korean J Pain
Research Publisher
NULL
Research Rank
1
Research Vol
Vol. 31, No. 2:
Research Website
https://www.ncbi.nlm.nih.gov/pubmed/29686807
Research Year
2018
Research_Pages
93-101
Research Abstract

Background: Magnesium is one of the effective, safe local anesthetic adjuvants that can exert an analgesic
effect in conditions presenting acute and chronic post-sternotomy pain. We studied the efficacy of continuous
infusion of presternal magnesium sulfate with bupivacaine for pain relief following cardiac surgery.
Methods: Ninety adult patients undergoing valve replacement cardiac surgery randomly allocated into three
groups. In all patients; a presternal catheter was placed for continuous infusion of either 0.125% bupivacaine
and 5% magnesium sulfate (3 ml/h for 48 hours) in group 1, or 0.125% bupivacaine only in the same rate
in group 2, versus conventional intravenous paracetamol and ketorolac in group 3. Rescue analgesia was iv
25 g fentanyl. Postoperative Visual Analog Scale (VAS) and fentanyl consumption during the early two
postoperative days were assessed. All patients were followed up over two months for occurrence of chronic
post-sternotomy pain.
Results: VAS values showed high significant differences during the first 48 hours with the least pain scale
in group 1 and significantly least fentanyl consumption (30.8 ± 7 g in group 1 vs. 69 ± 18 g in group
2, and 162 ± 3 in group 3 respectively). The incidence of chronic pain has not differed between the three
groups although it was more pronounced in group 3.
Conclusions: Continuous presternal bupivacaine and magnesium infusion resulted in better postoperative
analgesia than both presternal bupivacaine alone or conventional analgesic groups.