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Intubating conditions following rapid sequence induction with three doses of succinylcholine

BACKGROUND: The aim of this prospective, randomized, double-blind study was to compare tracheal intubating conditions and the duration of apnoea following administration of 0.4, 0.6 and 1.0 mg/kg of succinylcholine during simulated rapid sequence induction of anaesthesia. METHODS: Anaesthesia was in...

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Autores principales: Prakash, Smita, Barde, Sushma, Thakur, Preeti, Gogia, Anoop Raj, Singh, Rajvir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371488/
https://www.ncbi.nlm.nih.gov/pubmed/22701204
http://dx.doi.org/10.4103/0019-5049.96309
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author Prakash, Smita
Barde, Sushma
Thakur, Preeti
Gogia, Anoop Raj
Singh, Rajvir
author_facet Prakash, Smita
Barde, Sushma
Thakur, Preeti
Gogia, Anoop Raj
Singh, Rajvir
author_sort Prakash, Smita
collection PubMed
description BACKGROUND: The aim of this prospective, randomized, double-blind study was to compare tracheal intubating conditions and the duration of apnoea following administration of 0.4, 0.6 and 1.0 mg/kg of succinylcholine during simulated rapid sequence induction of anaesthesia. METHODS: Anaesthesia was induced with fentanyl 2 μg/kg and propofol 2 mg/kg followed by application of cricoid pressure. Patients were randomly allocated to three groups according to the dose of succinylcholine administered (0.4, 0.6 or 1.0 mg/kg). Intubating conditions were assessed at 60 s after succinylcholine administration. Time to first diaphragmatic contraction (apnoea time) and time to resumption of regular spontaneous breathing were noted. RESULTS: Excellent intubating conditions were obtained in 52.4%, 95.7% and 100% of the patients after 0.4, 0.6 and 1.0 mg/kg succinylcholine, respectively; P<0.001. Acceptable intubating conditions (excellent and good grade combined) were obtained in 66.7%, 100% and 100% of the patients after 0.4, 0.6 and 1.0 mg/ kg succinylcholine, respectively; P<0.001. Apnoea time and resumption of regular spontaneous breathing were dose-dependent. Apnoea time was 3.8±1.1 min, 4.3±0.9 min and 8.2±3.4 min in groups 0.4, 0.6 and 1.0 mg/kg, respectively; P<0.001. Time to regular spontaneous breathing was 5.3±1.2 min, 5.5±1.1 min and 8.9±3.5 min in groups 0.4, 0.6 and 1.0 mg/kg, respectively; P<0.001. CONCLUSION: A dose of 0.6 mg/kg succinylcholine can be used for rapid sequence induction of anaesthesia as it provides acceptable intubating conditions with a shorter apnoea time compared with a dose of 1 mg/kg.
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spelling pubmed-33714882012-06-14 Intubating conditions following rapid sequence induction with three doses of succinylcholine Prakash, Smita Barde, Sushma Thakur, Preeti Gogia, Anoop Raj Singh, Rajvir Indian J Anaesth Clinical Investigation BACKGROUND: The aim of this prospective, randomized, double-blind study was to compare tracheal intubating conditions and the duration of apnoea following administration of 0.4, 0.6 and 1.0 mg/kg of succinylcholine during simulated rapid sequence induction of anaesthesia. METHODS: Anaesthesia was induced with fentanyl 2 μg/kg and propofol 2 mg/kg followed by application of cricoid pressure. Patients were randomly allocated to three groups according to the dose of succinylcholine administered (0.4, 0.6 or 1.0 mg/kg). Intubating conditions were assessed at 60 s after succinylcholine administration. Time to first diaphragmatic contraction (apnoea time) and time to resumption of regular spontaneous breathing were noted. RESULTS: Excellent intubating conditions were obtained in 52.4%, 95.7% and 100% of the patients after 0.4, 0.6 and 1.0 mg/kg succinylcholine, respectively; P<0.001. Acceptable intubating conditions (excellent and good grade combined) were obtained in 66.7%, 100% and 100% of the patients after 0.4, 0.6 and 1.0 mg/ kg succinylcholine, respectively; P<0.001. Apnoea time and resumption of regular spontaneous breathing were dose-dependent. Apnoea time was 3.8±1.1 min, 4.3±0.9 min and 8.2±3.4 min in groups 0.4, 0.6 and 1.0 mg/kg, respectively; P<0.001. Time to regular spontaneous breathing was 5.3±1.2 min, 5.5±1.1 min and 8.9±3.5 min in groups 0.4, 0.6 and 1.0 mg/kg, respectively; P<0.001. CONCLUSION: A dose of 0.6 mg/kg succinylcholine can be used for rapid sequence induction of anaesthesia as it provides acceptable intubating conditions with a shorter apnoea time compared with a dose of 1 mg/kg. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3371488/ /pubmed/22701204 http://dx.doi.org/10.4103/0019-5049.96309 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
Prakash, Smita
Barde, Sushma
Thakur, Preeti
Gogia, Anoop Raj
Singh, Rajvir
Intubating conditions following rapid sequence induction with three doses of succinylcholine
title Intubating conditions following rapid sequence induction with three doses of succinylcholine
title_full Intubating conditions following rapid sequence induction with three doses of succinylcholine
title_fullStr Intubating conditions following rapid sequence induction with three doses of succinylcholine
title_full_unstemmed Intubating conditions following rapid sequence induction with three doses of succinylcholine
title_short Intubating conditions following rapid sequence induction with three doses of succinylcholine
title_sort intubating conditions following rapid sequence induction with three doses of succinylcholine
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371488/
https://www.ncbi.nlm.nih.gov/pubmed/22701204
http://dx.doi.org/10.4103/0019-5049.96309
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