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Pain reduction on injection of microemulsion propofol via combination of remifentanil and lidocaine
BACKGROUND: Microemulsion propofol produces more frequent and severe pain upon injection than lipid emulsion propofol. This study examined the analgesic effect of lidocaine-premixed microemulsion propofol in patients pretreated with remifentanil. The induction of anesthesia with this combination was...
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Formato: | Texto |
Lenguaje: | English |
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The Korean Society of Anesthesiologists
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2881517/ https://www.ncbi.nlm.nih.gov/pubmed/20532050 http://dx.doi.org/10.4097/kjae.2010.58.5.435 |
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author | Han, Yong Ku Jeong, Cheol Won Lee, Hyung Gon |
author_facet | Han, Yong Ku Jeong, Cheol Won Lee, Hyung Gon |
author_sort | Han, Yong Ku |
collection | PubMed |
description | BACKGROUND: Microemulsion propofol produces more frequent and severe pain upon injection than lipid emulsion propofol. This study examined the analgesic effect of lidocaine-premixed microemulsion propofol in patients pretreated with remifentanil. The induction of anesthesia with this combination was compared with microemulsion propofol accompanied with either remifentanil or lidocaine. METHODS: One hundred twenty patients aged between 20-65 years old were allocated randomly into one of three groups (n = 40, in each). The patients in the remifentanil group received remifentanil 0.5 µg/kg IV for 30 seconds before a microemulsion propofol injection. The patients in the lidocaine group received propofol 2 mg/kg premixed with 40 mg lidocaine over a 60 second period. The patients in the combination group received both remifentanil and lidocaine. RESULTS: There was a significantly lower incidence of microemulsion propofol injection pain (severity 2 or more) in the combination group (12.5%) than in the remifentanil and lidocaine groups (90% and 65%, respectively, P < 0.05). The incidence of moderate pain disappeared completely in the combination group (0%) compared to that in the remifentanil and lidocaine group (32.5% and 20%, respectively, P < 0.05). Severe pain did not appear in any of the three groups. There were no complications on the injection site in the lidocaine alone and combination groups. CONCLUSIONS: The combination of microemulsion propofol premixed with lidocaine after a pretreatment with remifentanil was more effective in reducing the incidence of pain upon the injection of microemulsion propofol than either treatment alone. |
format | Text |
id | pubmed-2881517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Korean Society of Anesthesiologists |
record_format | MEDLINE/PubMed |
spelling | pubmed-28815172010-06-08 Pain reduction on injection of microemulsion propofol via combination of remifentanil and lidocaine Han, Yong Ku Jeong, Cheol Won Lee, Hyung Gon Korean J Anesthesiol Clinical Research Article BACKGROUND: Microemulsion propofol produces more frequent and severe pain upon injection than lipid emulsion propofol. This study examined the analgesic effect of lidocaine-premixed microemulsion propofol in patients pretreated with remifentanil. The induction of anesthesia with this combination was compared with microemulsion propofol accompanied with either remifentanil or lidocaine. METHODS: One hundred twenty patients aged between 20-65 years old were allocated randomly into one of three groups (n = 40, in each). The patients in the remifentanil group received remifentanil 0.5 µg/kg IV for 30 seconds before a microemulsion propofol injection. The patients in the lidocaine group received propofol 2 mg/kg premixed with 40 mg lidocaine over a 60 second period. The patients in the combination group received both remifentanil and lidocaine. RESULTS: There was a significantly lower incidence of microemulsion propofol injection pain (severity 2 or more) in the combination group (12.5%) than in the remifentanil and lidocaine groups (90% and 65%, respectively, P < 0.05). The incidence of moderate pain disappeared completely in the combination group (0%) compared to that in the remifentanil and lidocaine group (32.5% and 20%, respectively, P < 0.05). Severe pain did not appear in any of the three groups. There were no complications on the injection site in the lidocaine alone and combination groups. CONCLUSIONS: The combination of microemulsion propofol premixed with lidocaine after a pretreatment with remifentanil was more effective in reducing the incidence of pain upon the injection of microemulsion propofol than either treatment alone. The Korean Society of Anesthesiologists 2010-05 2010-05-29 /pmc/articles/PMC2881517/ /pubmed/20532050 http://dx.doi.org/10.4097/kjae.2010.58.5.435 Text en Copyright © The Korean Society of Anesthesiologists, 2010 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 Han, Yong Ku Jeong, Cheol Won Lee, Hyung Gon Pain reduction on injection of microemulsion propofol via combination of remifentanil and lidocaine |
title | Pain reduction on injection of microemulsion propofol via combination of remifentanil and lidocaine |
title_full | Pain reduction on injection of microemulsion propofol via combination of remifentanil and lidocaine |
title_fullStr | Pain reduction on injection of microemulsion propofol via combination of remifentanil and lidocaine |
title_full_unstemmed | Pain reduction on injection of microemulsion propofol via combination of remifentanil and lidocaine |
title_short | Pain reduction on injection of microemulsion propofol via combination of remifentanil and lidocaine |
title_sort | pain reduction on injection of microemulsion propofol via combination of remifentanil and lidocaine |
topic | Clinical Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2881517/ https://www.ncbi.nlm.nih.gov/pubmed/20532050 http://dx.doi.org/10.4097/kjae.2010.58.5.435 |
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