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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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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. |
format | Online Article Text |
id | pubmed-3371488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
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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