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Prevention of anesthesia-induced injection pain of propofol in pediatric anesthesia

OBJECTIVE: Propofol is a new anesthetic agent in clinical practice, but randomized double-blinded prospective studies on its role in pediatric anesthesia remain limited. We aimed to compare the preventive effects of pre-injected lidocaine or ketamine and its pre-mixture on the anesthesia-induced inj...

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Autores principales: Cheng, Dabin, Liu, Lu, Hu, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Professional Medical Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5510140/
https://www.ncbi.nlm.nih.gov/pubmed/28811808
http://dx.doi.org/10.12669/pjms.333.12026
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author Cheng, Dabin
Liu, Lu
Hu, Zheng
author_facet Cheng, Dabin
Liu, Lu
Hu, Zheng
author_sort Cheng, Dabin
collection PubMed
description OBJECTIVE: Propofol is a new anesthetic agent in clinical practice, but randomized double-blinded prospective studies on its role in pediatric anesthesia remain limited. We aimed to compare the preventive effects of pre-injected lidocaine or ketamine and its pre-mixture on the anesthesia-induced injection pain of propofol using a randomized double-blinded prospective method, and to compare the outcomes with those of medium-/long-chain propofol (M/LCT). METHODS: A total of 360 pediatric patients (aged 5-12 years old) who received elective surgery were randomly divided into six groups (n= 60) as follows. S group: control group; L group: lidocaine group; L + P group: lidocaine + propofol group; K group: ketamine group; K + P group: ketamine + propofol group; M group: M/LCT group. After the drug fluid completely entered the cubital vein, the venous access was closed. During propofol injection, the injection pain was scored using the VRS 4-point scale. Meanwhile, the heart rates before and during injection were recorded, the adverse reactions during and after injection were observed, and the incidence rate and degree of pain were evaluated. RESULTS: The VRS 4-point scale showed that the incidence rates of injection pain of S group, L group, L + P group, K group, K + P group and M group were 78.3%, 66.67%, 51.66%, 43.33%, 48.33% and 45% respectively. The incidence rates of injection pain of all experimental groups were significantly lower than that of S group (P<0.01). The incidence rates of injection pain of L + P group, K group, K + P group and M group were significantly lower than that of L group (P<0.05). The differences among the other groups were not statistically significant. CONCLUSIONS: Intravenous pre-injection of lidocaine, ketamine or those mixed with propofol can all significantly reduce the incidence rate of injection pain of propofol.
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spelling pubmed-55101402017-08-15 Prevention of anesthesia-induced injection pain of propofol in pediatric anesthesia Cheng, Dabin Liu, Lu Hu, Zheng Pak J Med Sci Original Article OBJECTIVE: Propofol is a new anesthetic agent in clinical practice, but randomized double-blinded prospective studies on its role in pediatric anesthesia remain limited. We aimed to compare the preventive effects of pre-injected lidocaine or ketamine and its pre-mixture on the anesthesia-induced injection pain of propofol using a randomized double-blinded prospective method, and to compare the outcomes with those of medium-/long-chain propofol (M/LCT). METHODS: A total of 360 pediatric patients (aged 5-12 years old) who received elective surgery were randomly divided into six groups (n= 60) as follows. S group: control group; L group: lidocaine group; L + P group: lidocaine + propofol group; K group: ketamine group; K + P group: ketamine + propofol group; M group: M/LCT group. After the drug fluid completely entered the cubital vein, the venous access was closed. During propofol injection, the injection pain was scored using the VRS 4-point scale. Meanwhile, the heart rates before and during injection were recorded, the adverse reactions during and after injection were observed, and the incidence rate and degree of pain were evaluated. RESULTS: The VRS 4-point scale showed that the incidence rates of injection pain of S group, L group, L + P group, K group, K + P group and M group were 78.3%, 66.67%, 51.66%, 43.33%, 48.33% and 45% respectively. The incidence rates of injection pain of all experimental groups were significantly lower than that of S group (P<0.01). The incidence rates of injection pain of L + P group, K group, K + P group and M group were significantly lower than that of L group (P<0.05). The differences among the other groups were not statistically significant. CONCLUSIONS: Intravenous pre-injection of lidocaine, ketamine or those mixed with propofol can all significantly reduce the incidence rate of injection pain of propofol. Professional Medical Publications 2017 /pmc/articles/PMC5510140/ /pubmed/28811808 http://dx.doi.org/10.12669/pjms.333.12026 Text en Copyright: © Pakistan Journal of Medical Sciences http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Cheng, Dabin
Liu, Lu
Hu, Zheng
Prevention of anesthesia-induced injection pain of propofol in pediatric anesthesia
title Prevention of anesthesia-induced injection pain of propofol in pediatric anesthesia
title_full Prevention of anesthesia-induced injection pain of propofol in pediatric anesthesia
title_fullStr Prevention of anesthesia-induced injection pain of propofol in pediatric anesthesia
title_full_unstemmed Prevention of anesthesia-induced injection pain of propofol in pediatric anesthesia
title_short Prevention of anesthesia-induced injection pain of propofol in pediatric anesthesia
title_sort prevention of anesthesia-induced injection pain of propofol in pediatric anesthesia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5510140/
https://www.ncbi.nlm.nih.gov/pubmed/28811808
http://dx.doi.org/10.12669/pjms.333.12026
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