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右美托咪定增强在超快通道微创心脏瓣膜手术中的胸壁筋膜平面阻滞:一项随机对照试验

Dexmedetomidine-enhanced chest wall fascial plane blocks in ultra-fast-track minimally invasive heart valve surgery: a randomized controlled trial.

作者信息

Jiang Shen-Jie, Jiang Tian, Wei Han-Wei, Lou Xiao-Kan, Wang Yu, Yan Mei-Juan

机构信息

Department of Anesthesiology, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.

Center for Rehabilitation Medicine, Department of Anesthesiology, Zhejiang Provincial People's Hospital (Affiliated People's Hospital, Hangzhou Medical College), Research Institute of Anesthesiology and Perioperative Medicine, Hangzhou Medical College, Hangzhou, Zhejiang, China.

出版信息

Perioper Med (Lond). 2025 Jun 23;14(1):62. doi: 10.1186/s13741-025-00547-3.

Abstract

BACKGROUND

Injury to the sternocostal joint during minimally invasive cardiac surgery frequently results in severe pain, yet there is no established standard for perioperative analgesia. This randomized controlled trial evaluated whether adding 1 μg/kg dexmedetomidine to 0.375% ropivacaine for chest wall fascial plane blocks enhances opioid sparing in ultra-fast-track (UFT) minimally invasive heart valve surgery.

METHODS

Seventy-six elective patients were randomized (1:1) in a double-blind manner. The control group received 60 mL of 0.375% ropivacaine, while the DEX group was administered 60 mL of 1 μg/kg dexmedetomidine plus 0.375% ropivacaine. The primary outcomes were intraoperative remifentanil use and 24-h postoperative sufentanil consumption, which served as co-primary endpoints to evaluate opioid-sparing effects. Secondary outcomes included 24-h postoperative sufentanil consumption, 24-h oxycodone use, patient-controlled analgesia (PCA) activations, episodes of Visual Analog Scale (VAS) scores ≥ 3 within 48 h, time to recovery of consciousness, time to extubation, duration of intensive care unit (ICU), and hospital stays, and complications.

RESULTS

The DEX group exhibited significantly reduced intraoperative remifentanil consumption (2.45 ± 0.47 vs. 2.98 ± 0.53 mg, p < 0.001) and 24-h sufentanil use (median with interquartile range (IQR) 57 [54-60] vs. 63 [63-66] μg, p < 0.001). It also demonstrated lower 24-h oxycodone consumption (median [IQR] 5 [0-10] vs. 10 [10-20] mg, p < 0.001), fewer 24-h PCA activations (median [IQR] 3 [2-4] vs. 5 [5-6], p < 0.001), and less frequent VAS ≥ 3 episodes (median [IQR] 3 [2.5-4] vs. 6 [5-6], p < 0.001), alongside shorter lengths of ICU (21.34 ± 3.59 vs. 24.29 ± 4.07 h, p = 0.002) and hospital stays (6.51 ± 1.04 vs. 8.65 ± 1.80 days, p < 0.001). Postoperative complications did not differ significantly between groups, though dexmedetomidine-related hemodynamic effects were not systematically monitored.

CONCLUSION

The administration of 1 μg/kg dexmedetomidine in combination with ropivacaine for chest wall fascial plane blocks reduces opioid requirements and shortens ICU/hospital stays in UFT cardiac surgery, supporting its safety and efficacy, but limitations include the single-center design, fixed dexmedetomidine dosage, and incomplete complication assessment, warranting multicenter validation with standardized safety monitoring.

TRIAL REGISTRATION

ChiCTR2100051182.

摘要

背景

在微创心脏手术期间,胸肋关节损伤常导致严重疼痛,但围手术期镇痛尚无既定标准。本随机对照试验评估了在超快速通道(UFT)微创心脏瓣膜手术中,在0.375%罗哌卡因中添加1μg/kg右美托咪定进行胸壁筋膜平面阻滞是否能增强阿片类药物的节省效果。

方法

76例择期患者以1:1的比例进行双盲随机分组。对照组接受60mL 0.375%罗哌卡因,而DEX组给予60mL 1μg/kg右美托咪定加0.375%罗哌卡因。主要结局是术中瑞芬太尼的使用量和术后24小时舒芬太尼的消耗量,作为共同主要终点来评估阿片类药物节省效果。次要结局包括术后24小时舒芬太尼的消耗量、24小时羟考酮的使用量、患者自控镇痛(PCA)的启动次数、48小时内视觉模拟评分(VAS)≥3分的次数、意识恢复时间、拔管时间、重症监护病房(ICU)住院时间和住院时间以及并发症。

结果

DEX组术中瑞芬太尼消耗量显著降低(2.45±0.47 vs. 2.98±0.53mg,p<0.001),术后24小时舒芬太尼使用量降低(中位数及四分位数间距[IQR] 57 [54 - 60] vs. 63 [63 - 66]μg,p<0.001)。它还显示出24小时羟考酮使用量更低(中位数[IQR] 5 [0 - 10] vs. 10 [10 - 20]mg,p<0.001),24小时PCA启动次数更少(中位数[IQR] 3 [2 - 4] vs. 5 [5 - 6],p<0.001),VAS≥3分的发作频率更低(中位数[IQR] 3 [2.5 - 4] vs. 6 [5 - 6],p<0.001),同时ICU住院时间更短(21.34±3.59 vs. 24.29±4.07小时,p = 0.002)和住院时间更短(6.51±1.04 vs. 8.65±1.80天,p<0.001)。两组术后并发症无显著差异,不过未系统监测右美托咪定相关的血流动力学效应。

结论

在UFT心脏手术中,将1μg/kg右美托咪定与罗哌卡因联合用于胸壁筋膜平面阻滞可降低阿片类药物需求并缩短ICU/住院时间,证明了其安全性和有效性,但局限性包括单中心设计、右美托咪定固定剂量以及并发症评估不完整,需要多中心进行标准化安全监测的验证。

试验注册

ChiCTR2100051182。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15c8/12183839/2740c8a8fd2d/13741_2025_547_Fig1_HTML.jpg

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