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Evaluation of intubating conditions after rocuronium bromide in adults induced with propofol or thiopentone sodium

AIM: The aims of present study were to compare the propofol and rocuronium with thiopentone and rocuronium in terms of clinically satisfactory intubating conditions and to co-relate intubating conditions with degree of paralysis in adductor pollicis muscle using train of four ratio (TOFR). The intub...

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Autores principales: Md Shahnawaz, Moazzam, Shahjahan, Bano, Sarwar, Siddiqui Suhail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications Pvt Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127302/
https://www.ncbi.nlm.nih.gov/pubmed/21772683
http://dx.doi.org/10.4103/0970-9185.81829
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author Md Shahnawaz, Moazzam
Shahjahan, Bano
Sarwar, Siddiqui Suhail
author_facet Md Shahnawaz, Moazzam
Shahjahan, Bano
Sarwar, Siddiqui Suhail
author_sort Md Shahnawaz, Moazzam
collection PubMed
description AIM: The aims of present study were to compare the propofol and rocuronium with thiopentone and rocuronium in terms of clinically satisfactory intubating conditions and to co-relate intubating conditions with degree of paralysis in adductor pollicis muscle using train of four ratio (TOFR). The intubating conditions were evaluated after rocuronium bromide 0.6 mg kg(-1) at 60 s. MATERIALS AND METHODS: 60 patients of ASA grades I-II of either sex, age 18-50 years, undergoing various elective surgical procedures were randomly divided into two groups, propofol rocuronium (PR group) and thiopentone rocuronium (TR group) of 30 patients in each. In the PR group, patients received propofol 2.5 mg kg(-1) and rocuronium 0.6 mg kg(-1); in TR group, patients received thiopentone 5 mg kg(-1) and rocuronium 0.6 mg kg(-1). In all patients the intubating conditions were evaluated by the observer at 60 s. TOFR was measured at the time of intubation by an assistant. RESULTS: In the PR group the number of the patients placed in intubating conditions grades I, II, III and IV were 40%, 36.67%, 13.33% and 10% and their mean TOFR were 31.8±17.9%, 61.8±;14.6%, 61.7±27.9%, and 78.3±5.7% respectively. While in theTR group the number of patients placed in intubating condition grade I, II, and III were 60%, 26.67%, and 13.33% and their mean TOFR , 41.2±28.3%, 68.0±10.9% and 78.7±6.8%, respectively. There was no patient in grade lV in theTR group. CONCLUSION: The clinical intubating conditions and degree of paralysis of adductor pollicis muscle after rocuronium 0.6 mg kg(-1) at 60 s in adults induced with propofol or thiopentone sodium are comparable.
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spelling pubmed-31273022011-07-19 Evaluation of intubating conditions after rocuronium bromide in adults induced with propofol or thiopentone sodium Md Shahnawaz, Moazzam Shahjahan, Bano Sarwar, Siddiqui Suhail J Anaesthesiol Clin Pharmacol Original Article AIM: The aims of present study were to compare the propofol and rocuronium with thiopentone and rocuronium in terms of clinically satisfactory intubating conditions and to co-relate intubating conditions with degree of paralysis in adductor pollicis muscle using train of four ratio (TOFR). The intubating conditions were evaluated after rocuronium bromide 0.6 mg kg(-1) at 60 s. MATERIALS AND METHODS: 60 patients of ASA grades I-II of either sex, age 18-50 years, undergoing various elective surgical procedures were randomly divided into two groups, propofol rocuronium (PR group) and thiopentone rocuronium (TR group) of 30 patients in each. In the PR group, patients received propofol 2.5 mg kg(-1) and rocuronium 0.6 mg kg(-1); in TR group, patients received thiopentone 5 mg kg(-1) and rocuronium 0.6 mg kg(-1). In all patients the intubating conditions were evaluated by the observer at 60 s. TOFR was measured at the time of intubation by an assistant. RESULTS: In the PR group the number of the patients placed in intubating conditions grades I, II, III and IV were 40%, 36.67%, 13.33% and 10% and their mean TOFR were 31.8±17.9%, 61.8±;14.6%, 61.7±27.9%, and 78.3±5.7% respectively. While in theTR group the number of patients placed in intubating condition grade I, II, and III were 60%, 26.67%, and 13.33% and their mean TOFR , 41.2±28.3%, 68.0±10.9% and 78.7±6.8%, respectively. There was no patient in grade lV in theTR group. CONCLUSION: The clinical intubating conditions and degree of paralysis of adductor pollicis muscle after rocuronium 0.6 mg kg(-1) at 60 s in adults induced with propofol or thiopentone sodium are comparable. Medknow Publications Pvt Ltd 2011 /pmc/articles/PMC3127302/ /pubmed/21772683 http://dx.doi.org/10.4103/0970-9185.81829 Text en © Journal of Anaesthesiology Clinical Pharmacology 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 Original Article
Md Shahnawaz, Moazzam
Shahjahan, Bano
Sarwar, Siddiqui Suhail
Evaluation of intubating conditions after rocuronium bromide in adults induced with propofol or thiopentone sodium
title Evaluation of intubating conditions after rocuronium bromide in adults induced with propofol or thiopentone sodium
title_full Evaluation of intubating conditions after rocuronium bromide in adults induced with propofol or thiopentone sodium
title_fullStr Evaluation of intubating conditions after rocuronium bromide in adults induced with propofol or thiopentone sodium
title_full_unstemmed Evaluation of intubating conditions after rocuronium bromide in adults induced with propofol or thiopentone sodium
title_short Evaluation of intubating conditions after rocuronium bromide in adults induced with propofol or thiopentone sodium
title_sort evaluation of intubating conditions after rocuronium bromide in adults induced with propofol or thiopentone sodium
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3127302/
https://www.ncbi.nlm.nih.gov/pubmed/21772683
http://dx.doi.org/10.4103/0970-9185.81829
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