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利多卡因预防小儿扁桃体切除术后呕吐的随机临床试验。

Lidocaine and risk of postoperative vomiting in children undergoing tonsillectomy: a randomised clinical trial.

机构信息

Institute of Anesthesiology and Critical Care Medicine, China Three Gorges University and Yichang Central People's Hospital, Yichang, 443000, Hubei Province, China.

出版信息

Sci Rep. 2024 Aug 26;14(1):19752. doi: 10.1038/s41598-024-70804-w.

DOI:10.1038/s41598-024-70804-w
PMID:39187562
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11347638/
Abstract

The dose-response of intravenous lidocaine in preventing postoperative vomiting (POV) in children remains unclear. This study investigated whether intravenous lidocaine dose-dependently decreased POV risk within 24 h postoperatively in children undergoing tonsillectomy (with or without adenoidectomy) without severe complications. Patients aged 3-12 years (American Society of Anesthesiologists grade I-II) scheduled for elective tonsillectomy (with or without adenoidectomy) were enroled from December 2021 to March 2022. They were randomly grouped according to the lidocaine dose (A [0 mg kg], B [1 mg kg], C [1.5 mg kg], and D [2 mg kg]) and were administered the same induction protocol (sufentanil, propofol, and suxamethonium chloride). Anaesthesia was maintained with sevoflurane. The incidence of POV within 24 h postoperatively was 46, 40, 36, and 20% in groups A, B, C, and D, respectively, with significant differences between groups D and A. Postoperative analgesic rescues in groups A, B, C, and D were 62, 36, 34, and 16%, respectively, with significant differences between groups D and B, C and A, and D and A. No severe adverse events were reported. Intravenous lidocaine has a dose-dependent effect on reducing the risk of POV in children undergoing tonsillectomy (with or without adenoidectomy) without serious adverse events.Trial registration: Chinese Clinical Trial Registry, ChiCTR2100053006.

摘要

静脉利多卡因预防儿童术后呕吐(POV)的剂量反应仍不清楚。本研究旨在探讨静脉利多卡因是否在无严重并发症的情况下,剂量依赖性地降低行扁桃体切除术(伴或不伴腺样体切除术)的儿童术后 24 小时内 POV 风险。

2021 年 12 月至 2022 年 3 月,纳入年龄 3-12 岁(美国麻醉医师协会分级 I-II)、择期行扁桃体切除术(伴或不伴腺样体切除术)的患儿,根据利多卡因剂量(A[0mg/kg]、B[1mg/kg]、C[1.5mg/kg]和 D[2mg/kg])分为 4 组,并给予相同的诱导方案(舒芬太尼、丙泊酚和琥珀胆碱)。麻醉维持采用七氟醚。术后 24 小时内 POV 的发生率分别为 A、B、C 和 D 组的 46%、40%、36%和 20%,D 组与 A 组之间差异有统计学意义。A、B、C 和 D 组术后镇痛补救分别为 62%、36%、34%和 16%,D 组与 B、C 组与 A 组以及 D 组与 A 组之间差异有统计学意义。未报告严重不良事件。

静脉利多卡因可降低无严重不良事件的扁桃体切除术(伴或不伴腺样体切除术)患儿 POV 的风险,且呈剂量依赖性。

试验注册

中国临床试验注册中心,ChiCTR2100053006。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b347/11347638/d60fce752d99/41598_2024_70804_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b347/11347638/97935499339a/41598_2024_70804_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b347/11347638/d60fce752d99/41598_2024_70804_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b347/11347638/97935499339a/41598_2024_70804_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b347/11347638/d60fce752d99/41598_2024_70804_Fig2_HTML.jpg

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