Safety and efficacy of esketamine for postoperative analgesia in pediatric patients with hypospadias

ObjectiveTo explore the safety and efficacy of the combination of continuous intravenous infusion of esketamine with sacral block for postoperative analgesia in pediatric patients undergoing surgery for hypospadiasMethodsPediatric patients (n = 77) undergoing surgery for hypospadias were randomized...

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Main Authors: Yong Xu, Quan Chen, Ping Li, Xingrong Song
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-04-01
Series:Frontiers in Surgery
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fsurg.2023.1131137/full
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author Yong Xu
Yong Xu
Quan Chen
Ping Li
Xingrong Song
Xingrong Song
author_facet Yong Xu
Yong Xu
Quan Chen
Ping Li
Xingrong Song
Xingrong Song
author_sort Yong Xu
collection DOAJ
description ObjectiveTo explore the safety and efficacy of the combination of continuous intravenous infusion of esketamine with sacral block for postoperative analgesia in pediatric patients undergoing surgery for hypospadiasMethodsPediatric patients (n = 77) undergoing surgery for hypospadias were randomized into two groups: a hydromorphone group (H group, initial dose, 0.02 mg/kg; maintenance dose, 0.01 mg/kg/h) or an esketamine group (E group, initial dose, 0.3 mg/kg; maintenance dose 0.15 mg/kg/h). Caudal epidural block involved injection of 0.2% ropivacaine 1 ml/kg through the sacral hiatus. Age, weight, grade of hypospadias, intraoperative blood loss, operative time, and awaking time of patients were recorded. The Face, Legs, Activity, Cry and Consolability (FLACC) scale and Ramsay sedation scores were recorded when leaving the PACU (0 h) and at postoperative 2, 6, 12, 24, 36, and 48 h. The Pediatric Anesthesia Emergence Delirium Scale (PAED), incidence of hypotension, respiratory depression, nausea and vomiting and pruritus, and the time to first bowel movement after surgery were recorded.ResultsThere were no significant differences in demographic and clinical characteristics between the H group and the E group. There were no significant differences in FLACC scores at postoperative 0, 2, 6, 12, 24, 36, and 48 h in intra-group and inter-group comparisons. There were no significant differences in Ramsay sedation scores at postoperative 0, 2, 6, 12, 24, 36, and 48 h in the intra-group comparisons. Ramsay sedation scores were significantly lower at postoperative 2, 12, and 36 h in the H group compared to the E group. There were no significant differences in the PAED scale or incidence of nausea and vomiting or pruritus between the H group and the E group. The incidence of hypotension and respiratory depression was significantly lower, and the time to first bowel movement was significantly shorter in the E group compared to the H group. Urinary tryptophan, 5-hydroxytryptamine and substance P levels were significantly lower but arginine was significantly higher in the E group compared to the H group.ConclusionsThe combination of continuous intravenous infusion of esketamine with sacral block provided safe and effective postoperative analgesia for pediatric patients undergoing surgery for hypospadias.Trial registrationChinese Clinical Trial Register ChiCTR2200066967. Clinical trial registry URL: http://www.chictr.org.cn/edit.aspx?pid=185042&htm=4
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spelling doaj.art-b3491fcaea6d4c2e8b5529247f3f2e8c2023-04-04T05:11:46ZengFrontiers Media S.A.Frontiers in Surgery2296-875X2023-04-011010.3389/fsurg.2023.11311371131137Safety and efficacy of esketamine for postoperative analgesia in pediatric patients with hypospadiasYong Xu0Yong Xu1Quan Chen2Ping Li3Xingrong Song4Xingrong Song5Department of Anesthesiology, The First School of Clinical Medicine of Jinan University, Guangzhou, ChinaDepartment of Anesthesiology, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, ChinaDepartment of Anesthesiology, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, ChinaDepartment of Anesthesiology, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, ChinaDepartment of Anesthesiology, The First School of Clinical Medicine of Jinan University, Guangzhou, ChinaDepartment of Anesthesiology, Guangzhou Women and Children’s Medical Center, Guangzhou, ChinaObjectiveTo explore the safety and efficacy of the combination of continuous intravenous infusion of esketamine with sacral block for postoperative analgesia in pediatric patients undergoing surgery for hypospadiasMethodsPediatric patients (n = 77) undergoing surgery for hypospadias were randomized into two groups: a hydromorphone group (H group, initial dose, 0.02 mg/kg; maintenance dose, 0.01 mg/kg/h) or an esketamine group (E group, initial dose, 0.3 mg/kg; maintenance dose 0.15 mg/kg/h). Caudal epidural block involved injection of 0.2% ropivacaine 1 ml/kg through the sacral hiatus. Age, weight, grade of hypospadias, intraoperative blood loss, operative time, and awaking time of patients were recorded. The Face, Legs, Activity, Cry and Consolability (FLACC) scale and Ramsay sedation scores were recorded when leaving the PACU (0 h) and at postoperative 2, 6, 12, 24, 36, and 48 h. The Pediatric Anesthesia Emergence Delirium Scale (PAED), incidence of hypotension, respiratory depression, nausea and vomiting and pruritus, and the time to first bowel movement after surgery were recorded.ResultsThere were no significant differences in demographic and clinical characteristics between the H group and the E group. There were no significant differences in FLACC scores at postoperative 0, 2, 6, 12, 24, 36, and 48 h in intra-group and inter-group comparisons. There were no significant differences in Ramsay sedation scores at postoperative 0, 2, 6, 12, 24, 36, and 48 h in the intra-group comparisons. Ramsay sedation scores were significantly lower at postoperative 2, 12, and 36 h in the H group compared to the E group. There were no significant differences in the PAED scale or incidence of nausea and vomiting or pruritus between the H group and the E group. The incidence of hypotension and respiratory depression was significantly lower, and the time to first bowel movement was significantly shorter in the E group compared to the H group. Urinary tryptophan, 5-hydroxytryptamine and substance P levels were significantly lower but arginine was significantly higher in the E group compared to the H group.ConclusionsThe combination of continuous intravenous infusion of esketamine with sacral block provided safe and effective postoperative analgesia for pediatric patients undergoing surgery for hypospadias.Trial registrationChinese Clinical Trial Register ChiCTR2200066967. Clinical trial registry URL: http://www.chictr.org.cn/edit.aspx?pid=185042&htm=4https://www.frontiersin.org/articles/10.3389/fsurg.2023.1131137/fullesketaminepostoperative analgesiapediatrichypospadiasopioids
spellingShingle Yong Xu
Yong Xu
Quan Chen
Ping Li
Xingrong Song
Xingrong Song
Safety and efficacy of esketamine for postoperative analgesia in pediatric patients with hypospadias
Frontiers in Surgery
esketamine
postoperative analgesia
pediatric
hypospadias
opioids
title Safety and efficacy of esketamine for postoperative analgesia in pediatric patients with hypospadias
title_full Safety and efficacy of esketamine for postoperative analgesia in pediatric patients with hypospadias
title_fullStr Safety and efficacy of esketamine for postoperative analgesia in pediatric patients with hypospadias
title_full_unstemmed Safety and efficacy of esketamine for postoperative analgesia in pediatric patients with hypospadias
title_short Safety and efficacy of esketamine for postoperative analgesia in pediatric patients with hypospadias
title_sort safety and efficacy of esketamine for postoperative analgesia in pediatric patients with hypospadias
topic esketamine
postoperative analgesia
pediatric
hypospadias
opioids
url https://www.frontiersin.org/articles/10.3389/fsurg.2023.1131137/full
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