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Low-dose esketamine for the prevention of emergency agitation in children after tonsillectomy: A randomized controlled study

Background: Emergency agitation is a common postoperative complication in pediatric patients after general anesthesia. The aim of this study was to explore the effects of a low dose of esketamine on emergency agitation in children following tonsillectomy. Materials and Methods: Eighty children were...

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Autores principales: Li, Qi, Fan, Jiaming, Zhang, Wangping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807658/
https://www.ncbi.nlm.nih.gov/pubmed/36605396
http://dx.doi.org/10.3389/fphar.2022.991581
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author Li, Qi
Fan, Jiaming
Zhang, Wangping
author_facet Li, Qi
Fan, Jiaming
Zhang, Wangping
author_sort Li, Qi
collection PubMed
description Background: Emergency agitation is a common postoperative complication in pediatric patients after general anesthesia. The aim of this study was to explore the effects of a low dose of esketamine on emergency agitation in children following tonsillectomy. Materials and Methods: Eighty children were recruited prospectively to this study and divided into the esketamine group and the control group (40 cases in each group). The induction and maintenance of anesthesia were the same in both groups. At the end of surgery, the esketamine group received 0.25 μg/kg esketamine, while the control group received the same volume of normal saline. The extubation time, time to eye opening, Ramsay sedation scale and time to discharge from the post-anesthesia care unit (PACU) were recorded during post-anesthesia care unit. Postoperative complications, such as emergency agitation, respiratory depression, hypertension, tachycardia, nightmares, nausea, and vomiting, were also recorded. Results: The incidence of emergency agitation was lower in the esketamine group compared with that in the control group (5% vs. 27.5%, p = 0.006). The time to eye opening was longer in the esketamine group than in the control group (17.2 ± 2.7 vs. 15.5 ± 2.3 min, p = 0.005). However, the extubation time and time to discharge from PACU were similar between the two groups. Conclusion: Low-dose of esketamine decreases the incidence of emergency agitation in children after tonsillectomy without delaying extubation time and increasing the postoperative side effects. (www.chictr.org.cn, registration number: ChiCTR2100054178).
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spelling pubmed-98076582023-01-04 Low-dose esketamine for the prevention of emergency agitation in children after tonsillectomy: A randomized controlled study Li, Qi Fan, Jiaming Zhang, Wangping Front Pharmacol Pharmacology Background: Emergency agitation is a common postoperative complication in pediatric patients after general anesthesia. The aim of this study was to explore the effects of a low dose of esketamine on emergency agitation in children following tonsillectomy. Materials and Methods: Eighty children were recruited prospectively to this study and divided into the esketamine group and the control group (40 cases in each group). The induction and maintenance of anesthesia were the same in both groups. At the end of surgery, the esketamine group received 0.25 μg/kg esketamine, while the control group received the same volume of normal saline. The extubation time, time to eye opening, Ramsay sedation scale and time to discharge from the post-anesthesia care unit (PACU) were recorded during post-anesthesia care unit. Postoperative complications, such as emergency agitation, respiratory depression, hypertension, tachycardia, nightmares, nausea, and vomiting, were also recorded. Results: The incidence of emergency agitation was lower in the esketamine group compared with that in the control group (5% vs. 27.5%, p = 0.006). The time to eye opening was longer in the esketamine group than in the control group (17.2 ± 2.7 vs. 15.5 ± 2.3 min, p = 0.005). However, the extubation time and time to discharge from PACU were similar between the two groups. Conclusion: Low-dose of esketamine decreases the incidence of emergency agitation in children after tonsillectomy without delaying extubation time and increasing the postoperative side effects. (www.chictr.org.cn, registration number: ChiCTR2100054178). Frontiers Media S.A. 2022-12-20 /pmc/articles/PMC9807658/ /pubmed/36605396 http://dx.doi.org/10.3389/fphar.2022.991581 Text en Copyright © 2022 Li, Fan and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Li, Qi
Fan, Jiaming
Zhang, Wangping
Low-dose esketamine for the prevention of emergency agitation in children after tonsillectomy: A randomized controlled study
title Low-dose esketamine for the prevention of emergency agitation in children after tonsillectomy: A randomized controlled study
title_full Low-dose esketamine for the prevention of emergency agitation in children after tonsillectomy: A randomized controlled study
title_fullStr Low-dose esketamine for the prevention of emergency agitation in children after tonsillectomy: A randomized controlled study
title_full_unstemmed Low-dose esketamine for the prevention of emergency agitation in children after tonsillectomy: A randomized controlled study
title_short Low-dose esketamine for the prevention of emergency agitation in children after tonsillectomy: A randomized controlled study
title_sort low-dose esketamine for the prevention of emergency agitation in children after tonsillectomy: a randomized controlled study
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9807658/
https://www.ncbi.nlm.nih.gov/pubmed/36605396
http://dx.doi.org/10.3389/fphar.2022.991581
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