Effects of Perioperative Intranasal Dexmedetomidine Spray on Clinical Outcomes of Pulsed Radiofrequency in Patients with Zoster-Associated Pain: A Randomized Controlled Trial.

IF 3.1 3区 医学 Q2 CLINICAL NEUROLOGY
Journal of Pain Research Pub Date : 2026-09-28 eCollection Date: 2026-01-01 DOI:10.2147/JPR.S640449
Yi Wang, Mengjuan Dong, Miaomaio Xu, Huaichang Wen
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引用次数: 0

Abstract

Objective: To investigate the effects of perioperative intranasal dexmedetomidine spray on hemodynamic stability, postoperative analgesia and sleep quality in patients with zoster-associated pain (ZAP) undergoing pulsed radiofrequency (PRF), and assess its clinical efficacy and safety.

Methods: A single-center, randomized, double-blind, parallel-controlled trial was conducted. Sixty-eight ZAP patients receiving dorsal root ganglion PRF were randomly assigned (1:1) to the dexmedetomidine (Dex) group or control group. The Dex group received intranasal dexmedetomidine 40 μg 30 min preoperatively, followed by 40 μg twice daily for 3 postoperative days; the control group received equal-volume normal saline at matched time points. Perioperative mean arterial pressure (MAP) and heart rate (HR) were recorded. Pain intensity (VAS) and sleep quality (PSQI) were assessed at baseline and on postoperative days 1, 3, 7 and 14. The primary outcome was change in MAP from baseline to PRF treatment stage. Linear mixed-effects models were used for longitudinal analyses.

Results: Baseline characteristics were comparable between groups (all P>0.05). The Dex group showed significantly smaller MAP and HR fluctuations during puncture, nerve stimulation and PRF treatment (group × time interaction, all P<0.001). VAS and PSQI scores were markedly lower in the Dex group at all postoperative time points (all P<0.001 after Bonferroni correction). No severe adverse events occurred; mild-to-moderate transient bradycardia and hypotension in the Dex group required no specific intervention.

Conclusion: Perioperative intranasal dexmedetomidine spray effectively stabilizes perioperative hemodynamics, improves postoperative analgesia and sleep quality in ZAP patients undergoing PRF, with no serious safety signals observed in this study population. It provides evidence for optimized perioperative management strategies in this population.

Trial registration: Chinese Clinical Trial Registry, ChiCTR2500098608, first posted 11/03/2025.

围手术期鼻内右美托咪定喷雾剂对带状疱疹相关疼痛患者脉冲射频治疗临床结果的影响:一项随机对照试验。
目的:探讨右美托咪定鼻喷雾剂对带状带状相关疼痛(ZAP)患者行脉冲射频治疗(PRF)围手术期血流动力学稳定性、术后镇痛和睡眠质量的影响,并评价其临床疗效和安全性。方法:采用单中心、随机、双盲、平行对照试验。68例接受背根神经节PRF治疗的ZAP患者按1:1比例随机分为右美托咪定(Dex)组和对照组。右美托咪定组患者术前滴入右美托咪定40 μg 30 min,术后给予右美托咪定40 μg,每日2次,连用3 d;对照组在相应时间点给予等体积生理盐水。记录围手术期平均动脉压(MAP)和心率(HR)。在基线和术后第1、3、7、14天分别评估疼痛强度(VAS)和睡眠质量(PSQI)。主要终点是MAP从基线到PRF治疗阶段的变化。纵向分析采用线性混合效应模型。结果:两组间基线特征具有可比性(P < 0.05)。右美托咪定组在穿刺、神经刺激和PRF治疗过程中MAP和HR波动明显较小(组×时间相互作用,均为ppp)。结论:右美托咪定鼻内喷雾剂可有效稳定行PRF的ZAP患者围手术期血流动力学,改善术后镇痛和睡眠质量,本研究人群未观察到严重的安全信号。这为优化围手术期的管理策略提供了依据。试验注册:中国临床试验注册中心,ChiCTR2500098608,首次发布日期为2025年11月3日。
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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来源期刊
Journal of Pain Research
Journal of Pain Research CLINICAL NEUROLOGY-
CiteScore
4.50
自引率
3.70%
发文量
411
审稿时长
16 weeks
期刊介绍: Journal of Pain Research is an international, peer-reviewed, open access journal that welcomes laboratory and clinical findings in the fields of pain research and the prevention and management of pain. Original research, reviews, symposium reports, hypothesis formation and commentaries are all considered for publication. Additionally, the journal now welcomes the submission of pain-policy-related editorials and commentaries, particularly in regard to ethical, regulatory, forensic, and other legal issues in pain medicine, and to the education of pain practitioners and researchers.
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