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实时评估右美托咪定的独立镇痛疗效。

Real-time evaluation of the independent analgesic efficacy of dexmedetomidine.

机构信息

Department of Anesthesiology, Xuanwu Hospital, Capital Medical University, Beijing, 100053, China.

National Clinical Research Center for Geriatric Disorders, Beijing, China.

出版信息

BMC Anesthesiol. 2023 Mar 4;23(1):68. doi: 10.1186/s12871-023-02022-2.

Abstract

BACKGROUND

Dexmedetomidine has analgesic properties, but the intraoperative analgesic effect of dexmedetomidine is often masked by the effects of other general anaesthetics. Therefore, the degree to which it reduces intraoperative pain intensity remains unclear. The objective of this double-blind, randomised controlled trial was to evaluate the independent intraoperative analgesic efficacy of dexmedetomidine in real-time.

METHODS

This single-centre study enrolled 181 patients who were hospitalised for below-knee orthopaedic surgeries between 19 January 2021 to 3 August 2021 were eligible for this is single-centre study. Peripheral neural block was performed on patients scheduled for below-knee orthopaedic surgeries. Patients were randomly assigned to the dexmedetomidine or midazolam group and were intravenously administered with 1.5 µg kg h dexmedetomidine or 50 µg kg h midazolam, respectively. The analgesic efficacy was evaluated using the real-time non-invasive nociception monitoring. The primary endpoint was the attainment rate of the nociception index target. The secondary endpoints included the occurrence of intraoperative hypoxemia, haemodynamic parameters, the consciousness index, electromyography and patient outcomes.

RESULTS

On Kaplan-Meier survival analysis, the defined nociception index target was attained in 95.45% and 40.91% of patients receiving dexmedetomidine and midazolam, respectively. Log-rank analysis revealed that the dexmedetomidine group attained the nociception index target significantly faster and the median attainment time of the nociception index target in the dexmedetomidine group was 15 min. Dexmedetomidine group was associated with a significantly lower incidence of hypoxemia. There was no significant difference in blood pressure between the dexmedetomidine and midazolam groups. Further, the dexmedetomidine group had a lower maximum visual analogue scale score and lower analgesic consumption postoperatively.

CONCLUSIONS

Dexmedetomidine has independent analgesia and systemically administered as an adjuvant agent has better analgesic efficacy than midazolam without severe side effects.

TRIAL REGISTRATION

clinicaltrial.gov Registry Identifier: NCT-04675372.Registered on 19/12 /2020.

摘要

背景

右美托咪定具有镇痛作用,但在术中其镇痛效果常被其他全身麻醉药物的作用所掩盖。因此,其减轻术中疼痛强度的程度尚不清楚。本双盲、随机对照试验的目的是实时评估右美托咪定的独立术中镇痛效果。

方法

本单中心研究纳入了 2021 年 1 月 19 日至 2021 年 8 月 3 日期间因下肢矫形手术住院的 181 名患者,这些患者符合单中心研究条件。对计划进行下肢矫形手术的患者进行外周神经阻滞。患者被随机分配至右美托咪定或咪达唑仑组,并分别静脉给予 1.5μg·kg-1·h-1 的右美托咪定或 50μg·kg-1·h-1 的咪达唑仑。使用实时无创痛觉监测评估镇痛效果。主要终点是达到痛觉指数目标的比例。次要终点包括术中低氧血症的发生、血流动力学参数、意识指数、肌电图和患者结局。

结果

在 Kaplan-Meier 生存分析中,分别有 95.45%和 40.91%接受右美托咪定和咪达唑仑治疗的患者达到了定义的痛觉指数目标。对数秩检验显示,右美托咪定组达到痛觉指数目标的速度明显更快,右美托咪定组达到痛觉指数目标的中位时间为 15 分钟。右美托咪定组低氧血症的发生率显著降低。右美托咪定组和咪达唑仑组之间的血压无显著差异。此外,右美托咪定组术后最大视觉模拟评分和镇痛药物消耗量较低。

结论

右美托咪定具有独立的镇痛作用,作为辅助药物系统给药的镇痛效果优于咪达唑仑,且无严重副作用。

试验注册

clinicaltrial.gov 注册号:NCT-04675372.注册于 2020 年 12 月 19 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c730/9985296/f2dab97bb6b4/12871_2023_2022_Fig1_HTML.jpg

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