Research Articles
A prospective, randomised, controlled clinical trial to evaluate the effect of nitrous oxide on propofol requirement in elective craniotomy in which entropy was used to measure depth of anaesthesia
Southern African Journal of Anaesthesia and Analgesia | Vol 22, No 1 | a831 |
DOI: https://doi.org/10.1080/22201181.2015.1122708
| © 2016 Pragati Nanda, Paramanand Prakash, Kalyanpury Jawaharlal Choudhury, Verandera Pal Singh, Smita Prakash
| This work is licensed under Other
Submitted: 03 November 2025 | Published: 17 March 2016
Submitted: 03 November 2025 | Published: 17 March 2016
About the author(s)
Pragati Nanda, Department of Anaesthesia and Intensive Care, Indraprastha Apollo Hospitals, New Delhi, IndiaParamanand Prakash, Department of Neuroanaesthesia, Indraprastha Apollo Hospitals, New Delhi, India
Kalyanpury J. Choudhury, Department of Neuroanaesthesia, Indraprastha Apollo Hospitals, New Delhi, India
Verandera Pal Singh, Department of Neurosurgery, Indraprastha Apollo Hospitals, New Delhi, India
Smita Prakash, Department of Anaesthesia and Intensive Care, Indraprastha Apollo Hospitals, New Delhi, India
Full Text:
PDF (159KB)Abstract
Background: Propofol is known to have a favourable effect on cerebral haemodynamics. The role of nitrous oxide (N2O) in neurosurgical anaesthesia is still being debated. The primary aim of this study was to assess the dose-sparing effect of N2O on propofol infusion maintenance dosing.
Method: Fifty American Society of Anesthesiology (ASA) grade I and II adults scheduled for elective craniotomies for supratentorial tumours were enrolled in the study. The patients received a standard anaesthetic comprising a fentanyl 2 μg/kg bolus prior to propofol induction. Anaesthesia was maintained with an infusion of fentanyl (2 μg/kg/hour), atracurium and propofol. The patients were randomised into two groups. Group A received 67% N2O. Group B did not receive N2O concomitantly with the propofol infusion. Entropy was used to guide the titration of the propofol infusion in both groups.
Results: The propofol maintenance dose requirements were 47% lower in Group A (54.30 ± 11.47 μg/kg/minute) vs. Group B (102.30 ± 14.00 μg/kg/minute), (p < 0.001).
Conclusion: The use of supplemental N2O significantly decreased propofol infusion rate requirements, compared with the propofol infusion alone, in ASA I and II patients undergoing elective supratentorial tumour excision.
Method: Fifty American Society of Anesthesiology (ASA) grade I and II adults scheduled for elective craniotomies for supratentorial tumours were enrolled in the study. The patients received a standard anaesthetic comprising a fentanyl 2 μg/kg bolus prior to propofol induction. Anaesthesia was maintained with an infusion of fentanyl (2 μg/kg/hour), atracurium and propofol. The patients were randomised into two groups. Group A received 67% N2O. Group B did not receive N2O concomitantly with the propofol infusion. Entropy was used to guide the titration of the propofol infusion in both groups.
Results: The propofol maintenance dose requirements were 47% lower in Group A (54.30 ± 11.47 μg/kg/minute) vs. Group B (102.30 ± 14.00 μg/kg/minute), (p < 0.001).
Conclusion: The use of supplemental N2O significantly decreased propofol infusion rate requirements, compared with the propofol infusion alone, in ASA I and II patients undergoing elective supratentorial tumour excision.
Keywords
nitrous oxide; propofol; anaesthesia depth; entropy; intracranial surgery
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