预防术后咽喉痛的静脉注射与袖套内碱化利多卡因:前瞻性随机对照试验。

IF 0.9 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Pan African Medical Journal Pub Date : 2024-05-24 eCollection Date: 2024-01-01 DOI:10.11604/pamj.2024.48.18.40317
Salma Ketata, Yassine Maktouf, Imen Zouche, Sarhane Feki, Mariem Keskes, Ayman Trigui, Amira Akrout, Rahma Daoud, Amine Chaabouni, Hichem Cheikhrouhou
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引用次数: 0

摘要

导言:术后咽喉痛(POST)是气管插管全身麻醉后因气管粘膜损伤引起的常见并发症。多种技术可预防术后咽喉痛(POST)。我们的研究旨在比较两种技术:静脉注射和袖带内利多卡因与安慰剂,以预防气管插管全身麻醉后的术后咽喉痛。方法:我们进行了一项前瞻性双盲随机对照临床试验,涉及拟在气管插管全身麻醉下进行预定手术时间少于 240 分钟的患者。患者被分为三组:L 组:注入生理盐水,袖带填充碱化利多卡因。S 组:注入 1.5 毫克/千克利多卡因,袖带注入生理盐水。T 组:安慰剂:注入生理盐水,袖带填充生理盐水。我们的主要结果是术后 24 小时内咽喉疼痛的发生率及其(视觉模拟量表)VAS 评分。我们的次要结果是咳嗽、发音障碍、吞咽困难以及术后恶心和呕吐的发生率。安慰剂组、"L "组和 "S "组在术后第 6 小时的 POST 发生率分别为 67%、30% 和 47%。而在术后第 24 小时,POST 发生率分别为 67%、13% 和 37%。静脉注射利多卡因可明显降低术后第24小时POST的VAS(S组:6.80 ± 20.70;T组:20.67 ± 18.182;P= 0.02)。碱化利多卡因在术后第 6 小时(L:8.17 ± 22.761;T:23 ± 21.838;p= 0.048)和第 24 小时(L:6.33 ± 20.592;T:20.67 ± 18.182;p= 0.019)明显降低了 POST 的 VAS,疼痛评分最低。术后 6 小时和 24 小时,L 组和 S 组之间的差异无统计学意义。两种利多卡因技术都能减少出院时的咳嗽,碱化利多卡因的效果更好(p=0.02)。结论:静脉注射和袖带内利多卡因能更好地控制术后咽喉痛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intravenous versus intracuff alkalinized lidocaine to prevent postoperative sore throat: a prospective randomized controlled trial.

Introduction: postoperative sore throat (POST) is a common complication after general anesthesia with endotracheal intubation caused by tracheal mucosal injury. Multiple techniques prevent postoperative sore throat (POST). Our study aimed to compare two techniques: intravenous and intracuff lidocaine versus placebo to prevent postoperative sore throat after general anesthesia with orotracheal intubation.

Methods: we conducted a prospective double-blind, randomized controlled clinical trial involving patients, proposed for a scheduled surgery less than 240 minutes under general anesthesia with orotracheal intubation. Patients were divided into three groups: L group: infused with saline, cuff filled with alkalinized lidocaine. S group: Infused with 1.5 mg/kg of lidocaine, cuff filled with saline. T group: placebo: infused with saline, cuff filled with saline. Our primary outcome was the incidence of sore throat and their (visual analog scale) VAS score in the first 24 postoperative hours. Our secondary outcomes were the incidence of cough, dysphonia, dysphagia, and postoperative nausea and vomiting.

Results: ninety patients were analyzed and divided into 3 groups of 30. The incidence of POST at the sixth postoperative hour, for placebo, the "L" group, and the "S" group, respectively, was 67%, 30%, and 47%. And at the 24th postoperative hours 67%, 13%, and 37%. Intravenous lidocaine reduced significantly the VAS of POST at the 24th hour (S: 6.80 ± 20.70; T: 20.67 ± 18.182; p= 0.02). Alkalinized lidocaine decreased significantly the VAS of POST in the sixth (L: 8.17 ± 22.761; T: 23 ± 21.838; p = 0.048) and the 24th postoperative hour (L: 6.33 ± 20.592; T: 20.67 ± 18.182; p= 0.019) with the lowest pain score. There was no statistically significant difference between the L and S groups at the 6 and 24 postoperative hours. Both lidocaine techniques reduced cough at emergence, with the superiority of alkalinized lidocaine (p=0.02). They decreased the incidence of cough, dysphonia, dysphagia, nausea, and vomiting compared to a placebo.

Conclusion: intravenous and intracuff lidocaine allowed better control of postoperative sore throat.

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Pan African Medical Journal
Pan African Medical Journal PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
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