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Effects of lidocaine, ketamine, and remifentanil on withdrawal response of rocuronium

BACKGROUND: Rocuronium has been well known to produce withdrawal response in 50-80% patients when administered intravenously. Several drugs are administered prior injection of rocuronium to prevent the withdrawal response. We compared the preventive effect of lidocaine, ketamine, and remifentanil on...

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Autores principales: Jung, Ki Tae, Kim, Hye Ji, Bae, Hyo Sung, Lee, Hyun Young, Kim, Sang Hun, So, Keum Young, Lim, Kyung Jun, Yu, Byung Sik, Jung, Jong Dal, An, Tae Hun, Park, Hong Chan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Anesthesiologists 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4188762/
https://www.ncbi.nlm.nih.gov/pubmed/25302093
http://dx.doi.org/10.4097/kjae.2014.67.3.175
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author Jung, Ki Tae
Kim, Hye Ji
Bae, Hyo Sung
Lee, Hyun Young
Kim, Sang Hun
So, Keum Young
Lim, Kyung Jun
Yu, Byung Sik
Jung, Jong Dal
An, Tae Hun
Park, Hong Chan
author_facet Jung, Ki Tae
Kim, Hye Ji
Bae, Hyo Sung
Lee, Hyun Young
Kim, Sang Hun
So, Keum Young
Lim, Kyung Jun
Yu, Byung Sik
Jung, Jong Dal
An, Tae Hun
Park, Hong Chan
author_sort Jung, Ki Tae
collection PubMed
description BACKGROUND: Rocuronium has been well known to produce withdrawal response in 50-80% patients when administered intravenously. Several drugs are administered prior injection of rocuronium to prevent the withdrawal response. We compared the preventive effect of lidocaine, ketamine, and remifentanil on the withdrawal response of rocuronium. METHODS: A total of 120 patients undergoing various elective surgeries were enrolled. Patients were allocated into 4 groups according to the pretreatment drugs (Group N, normal saline; Groups L, lidocaine 40 mg; Group K, ketamine 0.5 mg/kg; Group R, remifentanil 1 µg/kg). Patients received drugs prepared by dilution to 3 ml volume before injection of rocuronium. Withdrawal responses after injection of rocuronium were graded on a 4-point scale. Hemodynamic changes were observed before and after administration of pretreatment drugs and after endotracheal intubation. RESULTS: Incidence of withdrawal response was significantly lower in group L (20%), group K (30%), and group R (0%), than group N (87%). Severe withdrawal response was observed in 5 of the 30 patients (17%) in group L, and in 9 of the 30 patients (30%) in group K. There was no severe withdrawal response in group R. Mean blood pressure and heart rate were significantly decreased in group R compared to other groups. CONCLUSIONS: It seems that remifentanil (1 µg/kg intravenously) was the strongest and most effective in prevention of withdrawal response after rocuronium injection among the 3 drugs.
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spelling pubmed-41887622014-10-09 Effects of lidocaine, ketamine, and remifentanil on withdrawal response of rocuronium Jung, Ki Tae Kim, Hye Ji Bae, Hyo Sung Lee, Hyun Young Kim, Sang Hun So, Keum Young Lim, Kyung Jun Yu, Byung Sik Jung, Jong Dal An, Tae Hun Park, Hong Chan Korean J Anesthesiol Clinical Research Article BACKGROUND: Rocuronium has been well known to produce withdrawal response in 50-80% patients when administered intravenously. Several drugs are administered prior injection of rocuronium to prevent the withdrawal response. We compared the preventive effect of lidocaine, ketamine, and remifentanil on the withdrawal response of rocuronium. METHODS: A total of 120 patients undergoing various elective surgeries were enrolled. Patients were allocated into 4 groups according to the pretreatment drugs (Group N, normal saline; Groups L, lidocaine 40 mg; Group K, ketamine 0.5 mg/kg; Group R, remifentanil 1 µg/kg). Patients received drugs prepared by dilution to 3 ml volume before injection of rocuronium. Withdrawal responses after injection of rocuronium were graded on a 4-point scale. Hemodynamic changes were observed before and after administration of pretreatment drugs and after endotracheal intubation. RESULTS: Incidence of withdrawal response was significantly lower in group L (20%), group K (30%), and group R (0%), than group N (87%). Severe withdrawal response was observed in 5 of the 30 patients (17%) in group L, and in 9 of the 30 patients (30%) in group K. There was no severe withdrawal response in group R. Mean blood pressure and heart rate were significantly decreased in group R compared to other groups. CONCLUSIONS: It seems that remifentanil (1 µg/kg intravenously) was the strongest and most effective in prevention of withdrawal response after rocuronium injection among the 3 drugs. The Korean Society of Anesthesiologists 2014-09 2014-09-24 /pmc/articles/PMC4188762/ /pubmed/25302093 http://dx.doi.org/10.4097/kjae.2014.67.3.175 Text en Copyright © the Korean Society of Anesthesiologists, 2014 http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research Article
Jung, Ki Tae
Kim, Hye Ji
Bae, Hyo Sung
Lee, Hyun Young
Kim, Sang Hun
So, Keum Young
Lim, Kyung Jun
Yu, Byung Sik
Jung, Jong Dal
An, Tae Hun
Park, Hong Chan
Effects of lidocaine, ketamine, and remifentanil on withdrawal response of rocuronium
title Effects of lidocaine, ketamine, and remifentanil on withdrawal response of rocuronium
title_full Effects of lidocaine, ketamine, and remifentanil on withdrawal response of rocuronium
title_fullStr Effects of lidocaine, ketamine, and remifentanil on withdrawal response of rocuronium
title_full_unstemmed Effects of lidocaine, ketamine, and remifentanil on withdrawal response of rocuronium
title_short Effects of lidocaine, ketamine, and remifentanil on withdrawal response of rocuronium
title_sort effects of lidocaine, ketamine, and remifentanil on withdrawal response of rocuronium
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4188762/
https://www.ncbi.nlm.nih.gov/pubmed/25302093
http://dx.doi.org/10.4097/kjae.2014.67.3.175
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