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Comparison of intubating conditions between rocuronium with priming and without priming: Randomized and double-blind study

BACKGROUND: Rocuronium produces faster neuromuscular blockade compared with other neuromuscular blocking drugs. It produces comparable intubating conditions to that of succinylcholine, but does not have the short intubation time of the latter. Hence, it may not be preferable for rapid sequence intub...

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Autores principales: Rao, M Hanumantha, Venkatraman, Andal, Mallleswari, R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237150/
https://www.ncbi.nlm.nih.gov/pubmed/22174467
http://dx.doi.org/10.4103/0019-5049.89882
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author Rao, M Hanumantha
Venkatraman, Andal
Mallleswari, R
author_facet Rao, M Hanumantha
Venkatraman, Andal
Mallleswari, R
author_sort Rao, M Hanumantha
collection PubMed
description BACKGROUND: Rocuronium produces faster neuromuscular blockade compared with other neuromuscular blocking drugs. It produces comparable intubating conditions to that of succinylcholine, but does not have the short intubation time of the latter. Hence, it may not be preferable for rapid sequence intubation, but rocuronium with priming may produce comparable intubating time and conditions to that of succinylcholine. Rocuronium with priming may be an alternative to succinylcholine in rapid sequence intubation in conditions where succinylcholine is contraindicated. The present study was conducted to compare the intubating conditions and intubation time of rocuronium with and without priming. METHODS: Sixty patients of ASA physical status I and II, aged between 18 and 60 years, of both sexes, were divided into priming and control groups of 30 each. Patients in the priming group received 0.06 mg/kg of rocuronium and those in the control group received normal saline. All patients received fentanyl 1 μg/kg, followed by thiopentone 5 mg/kg for induction. Intubating dose of rocuronium 0.54 mg/kg in the priming group and 0.6 mg/kg in the control group were administered 3 min after priming. Onset time of intubation was assessed using a Train of Four stimuli, and the intubating conditions were compared by the Cooper scoring system. RESULTS: The onset time of intubation was 50.67±7.39 s in the priming group and 94.00±11.62 s in the control group, with excellent intubating conditions in both the groups and without any adverse effects. CONCLUSIONS: Priming with rocuronium provides excellent intubating conditions in less than 60 s with no adverse effects.
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spelling pubmed-32371502011-12-15 Comparison of intubating conditions between rocuronium with priming and without priming: Randomized and double-blind study Rao, M Hanumantha Venkatraman, Andal Mallleswari, R Indian J Anaesth Clinical Investigation BACKGROUND: Rocuronium produces faster neuromuscular blockade compared with other neuromuscular blocking drugs. It produces comparable intubating conditions to that of succinylcholine, but does not have the short intubation time of the latter. Hence, it may not be preferable for rapid sequence intubation, but rocuronium with priming may produce comparable intubating time and conditions to that of succinylcholine. Rocuronium with priming may be an alternative to succinylcholine in rapid sequence intubation in conditions where succinylcholine is contraindicated. The present study was conducted to compare the intubating conditions and intubation time of rocuronium with and without priming. METHODS: Sixty patients of ASA physical status I and II, aged between 18 and 60 years, of both sexes, were divided into priming and control groups of 30 each. Patients in the priming group received 0.06 mg/kg of rocuronium and those in the control group received normal saline. All patients received fentanyl 1 μg/kg, followed by thiopentone 5 mg/kg for induction. Intubating dose of rocuronium 0.54 mg/kg in the priming group and 0.6 mg/kg in the control group were administered 3 min after priming. Onset time of intubation was assessed using a Train of Four stimuli, and the intubating conditions were compared by the Cooper scoring system. RESULTS: The onset time of intubation was 50.67±7.39 s in the priming group and 94.00±11.62 s in the control group, with excellent intubating conditions in both the groups and without any adverse effects. CONCLUSIONS: Priming with rocuronium provides excellent intubating conditions in less than 60 s with no adverse effects. Medknow Publications & Media Pvt Ltd 2011 /pmc/articles/PMC3237150/ /pubmed/22174467 http://dx.doi.org/10.4103/0019-5049.89882 Text en Copyright: © Indian Journal of Anaesthesia http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigation
Rao, M Hanumantha
Venkatraman, Andal
Mallleswari, R
Comparison of intubating conditions between rocuronium with priming and without priming: Randomized and double-blind study
title Comparison of intubating conditions between rocuronium with priming and without priming: Randomized and double-blind study
title_full Comparison of intubating conditions between rocuronium with priming and without priming: Randomized and double-blind study
title_fullStr Comparison of intubating conditions between rocuronium with priming and without priming: Randomized and double-blind study
title_full_unstemmed Comparison of intubating conditions between rocuronium with priming and without priming: Randomized and double-blind study
title_short Comparison of intubating conditions between rocuronium with priming and without priming: Randomized and double-blind study
title_sort comparison of intubating conditions between rocuronium with priming and without priming: randomized and double-blind study
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3237150/
https://www.ncbi.nlm.nih.gov/pubmed/22174467
http://dx.doi.org/10.4103/0019-5049.89882
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