围手术期应用右美托咪定对腹腔镜子宫肌瘤手术患者术后疼痛和应激的影响:随机对照研究

Xiaxia Cao, Xu Ding, Huihui Sun, Lihong Zhang, Xiang Li
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引用次数: 0

摘要

背景:本研究旨在评估右美托咪定(DEX)能否缓解腹腔镜子宫肌瘤(UF)手术后的疼痛并减轻应激反应。方法:这项随机对照研究纳入了 100 名年龄在 40-60 岁之间、美国麻醉医师协会(ASA)1-2 级、在 2020 年 1 月至 2023 年 10 月期间接受腹腔镜子宫肌瘤手术的患者。患者被随机分配到 DEX 组(50 人)和非 DEX 组(50 人)。记录视觉模拟量表(VAS)、里士满躁动镇静量表(RASS)评分、麻醉时间、自主呼吸恢复时间、意识恢复时间、拔管时间和恢复室时间。结果:半小时后,地塞米松组的 VAS 小于非地塞米松组,但 1 小时、12 小时和 24 小时后的 VAS 无显著差异。两组在自主呼吸恢复时间、意识恢复时间、拔管时间、恢复室时间、寒战和恶心方面存在差异。结论:在围手术期应用 DEX 可减轻腹腔镜 UF 手术后的疼痛和应激反应。临床试验注册:该研究已在 https://classic.clinicaltrials.gov/ 上注册(注册号:NCT03524950)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Application of Dexmedetomidine in Perioperative Period on Postoperative Pain, Stress in Patients Undergoing Laparoscopic Uterine Fibroids Surgery: A Randomized Controlled Study
Background : This study aimed to evaluate whether dexmedetomidine (DEX) can relieve postoperative pain and reduce stress reaction after laparoscopic uterine fibroids (UF) surgery. Methods : This randomized controlled study included 100 patients age range of 40–60 years, American Society of Anesthesiologists (ASA) 1–2 grade, admitted for laparoscopic UF surgery from January 2020 to October 2023. The patients were randomly allocated to the DEX group (n = 50) and non-DEX group (n = 50). The visual analogue scale (VAS), Richmond Agitation-Sedation Scale (RASS) score, anesthesia time, spontaneous breathing recovery time, consciousness recovery time, extubation time, and recovery room time were recorded. Results : The VAS of the DEX group was smaller than that of the non-DEX group at half an hour, but there was no significant difference in VAS at 1 h, 12 h and 24 h. Dex group has a RASS value closer to zero than non-DEX group at half an hour. There was no significant difference in RASS at 1 h, 12 h, or 24 h. There were differences in spontaneous breathing recovery time, consciousness recovery time, extubation time, recovery room time, chills and nausea between the two groups. Conclusion : Application of DEX in perioperative period can relieve postoperative pain, reduce stress reaction after laparoscopic UF surgery. Clinical Trial Registration : The study has been registered on https://classic.clinicaltrials.gov/ (registration number: NCT03524950).
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