Sugammadex reversal of rocuronium-induced neuromuscular blockade: a comparison with neostigmine-glycopyrrolate and edrophonium-atropine
- PMID: 17312210
- DOI: 10.1213/01.ane.0000248224.42707.48
Sugammadex reversal of rocuronium-induced neuromuscular blockade: a comparison with neostigmine-glycopyrrolate and edrophonium-atropine
Abstract
Background: Sugammadex is a modified [gamma] cyclodextrin compound, which encapsulates rocuronium to provide for a rapid reversal of residual neuromuscular blockade. We tested the hypothesis that sugammadex would provide for a more rapid reversal of a moderately profound residual rocuronium-induced blockade than the commonly used cholinesterase inhibitors, edrophonium and neostigmine.
Methods: Sixty patients undergoing elective surgery procedures with a standardized desflurane-remifentanil-rocuronium anesthetic technique received either sugammadex, 4 mg/kg IV (n = 20), edrophonium, 1 mg/kg IV and atropine, 10 microg/kg IV (n = 20), or neostigmine, 70 microg/kg IV and glycopyrrolate, 14 microg/kg IV (n = 20) for reversal of neuromuscular blockade at 15 min or longer after the last dose of rocuronium using acceleromyography to record the train-of-four (TOF) responses. Mean arterial blood pressure and heart rate values were recorded immediately before and for 30 min after reversal drug administration. Side effects were noted at discharge from the postanesthesia care unit.
Results: The three groups were similar with respect to their demographic characteristics and total dosages of rocuronium prior to administering the study medication. Although the initial twitch heights (T1) at the time of reversal were similar in all three groups, the time to achieve TOF ratios of 0.7 and 0.9 were significantly shorter with sugammadex (71 +/- 25 and 107 +/- 61 s) than edrophonium (202 +/- 171 and 331 +/- 27 s) or neostigmine (625 +/- 341 and 1044 +/- 590 s). All patients in the sugammadex group achieved a TOF ratio of 0.9 < or =5 min after reversal administration compared with none and 5% in the edrophonium and neostigmine groups, respectively. Heart rate values at 2 and 5 min after reversal were significantly higher in the neostigmine-glycopyrrolate group compared with that in sugammadex. Finally, the incidence of dry mouth was significantly reduced in the sugammadex group (5% vs 85% and 95% in the neostigmine and edrophonium groups, respectively).
Conclusion: Sugammadex, 4 mg/kg IV, more rapidly and effectively reversed residual neuromuscular blockade when compared with neostigmine (70 microg/kg IV) and edrophonium (1 mg/kg IV). Use of sugammadex was associated with less frequent dry mouth than that with the currently used reversal drug combinations.
Similar articles
-
The effect of residual neuromuscular blockade on the speed of reversal with sugammadex.Anesth Analg. 2009 Mar;108(3):846-51. doi: 10.1213/ane.0b013e31818a9932. Anesth Analg. 2009. PMID: 19224792 Clinical Trial.
-
Sugammadex provides faster reversal of vecuronium-induced neuromuscular blockade compared with neostigmine: a multicenter, randomized, controlled trial.Anesth Analg. 2010 Jan 1;110(1):64-73. doi: 10.1213/ane.0b013e3181ac53c3. Epub 2009 Aug 27. Anesth Analg. 2010. PMID: 19713265 Clinical Trial.
-
Reversal of rocuronium-induced (1.2 mg/kg) profound neuromuscular block by sugammadex: a multicenter, dose-finding and safety study.Anesthesiology. 2007 Aug;107(2):239-44. doi: 10.1097/01.anes.0000270722.95764.37. Anesthesiology. 2007. PMID: 17667567 Clinical Trial.
-
A novel approach to reversal of neuromuscular blockade.Minerva Anestesiol. 2009 May;75(5):349-51. Minerva Anestesiol. 2009. PMID: 19412157 Review.
-
Efficacy and safety of sugammadex compared to neostigmine for reversal of neuromuscular blockade: a meta-analysis of randomized controlled trials.J Clin Anesth. 2016 Dec;35:1-12. doi: 10.1016/j.jclinane.2016.06.018. Epub 2016 Aug 4. J Clin Anesth. 2016. PMID: 27871504 Review.
Cited by
-
Eliminating residual neuromuscular blockade: a literature review.Ann Transl Med. 2024 Aug 1;12(4):65. doi: 10.21037/atm-23-1743. Epub 2024 May 14. Ann Transl Med. 2024. PMID: 39118951 Free PMC article. Review.
-
Safety, tolerability and pharmacokinetics of sugammadex using single high doses (up to 96 mg/kg) in healthy adult subjects: a randomized, double-blind, crossover, placebo-controlled, single-centre study.Clin Drug Investig. 2010;30(12):867-74. doi: 10.1007/BF03256915. Clin Drug Investig. 2010. PMID: 20825252 Clinical Trial.
-
Comparison of reversal and adverse effects of sugammadex and combination of - Anticholinergic-Anticholinesterase agents in pediatric patients.J Res Med Sci. 2014 Aug;19(8):762-8. J Res Med Sci. 2014. PMID: 25422663 Free PMC article.
-
Important modifications by sugammadex, a modified γ-cyclodextrin, of ion currents in differentiated NSC-34 neuronal cells.BMC Neurosci. 2017 Jan 3;18(1):6. doi: 10.1186/s12868-016-0320-5. BMC Neurosci. 2017. PMID: 28049438 Free PMC article.
-
Perioperative Efficiency of Sugammadex Following Laparoscopic Cholecystectomy in Clinical Practice.Ochsner J. 2022 Winter;22(4):292-298. doi: 10.31486/toj.22.0064. Ochsner J. 2022. PMID: 36561110 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical