A comparative study between hyperbaric prilocaine 2% versus hyperbaric bupivacaine 0.5% for intrathecal anesthesia in cesarean section
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Updated: Oct 31, 2026

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Published on: January 31, 2025
Elhadad Ali Mousa Hammam1, Mostafa Mohamed Abd El Jaber Ahmed2, Hala Mahmoud Hashim El Khaiat1
1Department of Anesthesia, Surgical ICU and Pain Management, Faculty of Medicine, Sohag University, Sohag, Egypt.
Background:
Bupivacaine has a variable block duration, while prilocaine provides a shorter, more predictable block but is less used in obstetrics. The goal is to compare the onset and duration of block induced by hyperbaric prilocaine 2% and hyperbaric bupivacaine 0.5% in intrathecal anesthesia for women undergoing elective cesarean sections (CS).
Methods:
A prospective randomized and double-blind clinical trial included 144 individuals with uncomplicated pregnancies belonging to the American Society of Anesthesiologists physical status I or II. Patients were divided into two equal groups randomly: prilocaine group (Group A): received 60 mg hyperbaric prilocaine 2% (3 ml) intrathecally, and bupivacaine group (Group B): received 12.5 mg hyperbaric bupivacaine 0.5% (2.5 ml) intrathecally and 0.5 ml of normal saline. As 60 mg hyperbaric prilocaine 2% is equipotent to 12.5 mg of hyperbaric bupivacaine 0.5%. Onset time and duration of sensory and motor block recorded.
Results:
Mean arterial blood pressure was higher in Group A than in Group B at 5, 10, 15, and 20 min (P < 0.001), with no differences at baseline or 25-45 min. Intraoperative heart rate was substantially higher in Group B at 5, 10, 15, and 20 min, with comparable values at other time points. Visual analog scale (VAS) scores were higher in Group A at 1 h (P < 0.001) but substantially lower at 2 and 3 h (P < 0.001); VAS scores at 4 h were similar between groups.
Conclusion:
Hyperbaric prilocaine 2% provides faster onset, shorter sensory and motor block duration, more stable hemodynamics and less maternal hypotension than hyperbaric bupivacaine 0.5% in CS, with similar neonatal outcomes and side effects.
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