Effect of Dexamethasone in Management of Postoperative Nausea, Vomiting and Pain After Tonsillectomy in Paediatric Patients

Md. Maminur Rahman, M. Islam, K. Kubra, N. Tania, A. Ferdous
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Abstract

Introduction: The effectiveness of dexamethasone (DEX) in reducing complication rates following paediatric tonsillectomy is still up for debate. The incidence of postoperative nausea and vomiting (PONV) and the severity of pain following paediatric tonsillectomy were examined by comparing concentrations of DEX 0.15 and DEX 0.5 mg/kg, respectively. Aim of the study: The aim of the study is to assess the effect of Dexamethasone in management of postoperative nausea, vomiting and pain after tonsillectomy where the targeted patients are of 3 to 10 years children. Methods: This prospective cross sectional study was conducted in the Department of Paediatric Anaesthesiology and Surgical ICU in Bangladesh Shishu Hospital and Institute, Dhaka, Bangladesh during July 2019 to June 2022. This study included 123 children undergoing elective tonsillectomy. The Institutional Ethics Committee approved this study and informed parental written consent was obtained from the parents before collecting the patients’ information. Results: The prevalence of early PONV was lower in both DEX groups (DEX 0.15: 22%; DEX 0.5: 26%; placebo: 48%; P=0.001). On the second day after surgery, the DEX groups had a lower rate of severe pain (DEX 0.15: 20%; DEX 0.5: 5%; placebo: 47%; P<0.001). The study was not conducted to assess a difference between the two dose groups of Dexamethasone. Conclusions: The frequency of early and late PONV and the level of pain on the second postoperative day were both reduced by an i.v injection of DEX during the induction of anesthesia. To reduce the incidence of PONV, it appeared that a dose of DEX 0.15 mg/kg was just as effective as a dose of DEX 0.5 mg/kg.
地塞米松治疗小儿扁桃体切除术后恶心、呕吐和疼痛的效果
前言:地塞米松(DEX)在降低儿童扁桃体切除术后并发症发生率方面的有效性仍存在争议。通过比较DEX 0.15和DEX 0.5 mg/kg的浓度,观察小儿扁桃体切除术后恶心呕吐(PONV)发生率和疼痛严重程度。研究目的:本研究的目的是评估地塞米松治疗扁桃体切除术后恶心、呕吐和疼痛的效果,目标患者为3 - 10岁儿童。方法:本前瞻性横断面研究于2019年7月至2022年6月在孟加拉国达卡Shishu医院和研究所儿科麻醉和外科ICU进行。本研究包括123名接受选择性扁桃体切除术的儿童。机构伦理委员会批准了本研究,并在收集患者信息前获得了知情父母的书面同意。结果:两组患者早期PONV患病率均较低(DEX 0.15: 22%;Dex 0.5: 26%;安慰剂:48%;P = 0.001)。术后第2天,DEX组剧烈疼痛发生率较低(DEX 0.15: 20%;Dex 0.5: 5%;安慰剂:47%;P < 0.001)。这项研究并不是为了评估地塞米松两个剂量组之间的差异。结论:麻醉诱导时静脉注射DEX可降低早期和晚期PONV的发生频率及术后第2天的疼痛程度。为了减少PONV的发生率,DEX 0.15 mg/kg的剂量似乎与DEX 0.5 mg/kg的剂量一样有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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