右美托咪定增强胸壁筋膜平面阻滞在超快速通道微创心脏瓣膜手术中的应用:一项随机对照试验

IF 2 3区 医学 Q2 ANESTHESIOLOGY
Shen-Jie Jiang, Tian Jiang, Han-Wei Wei, Xiao-Kan Lou, Yu Wang, Mei-Juan Yan
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引用次数: 0

摘要

背景:微创心脏手术中胸骨肋关节损伤常导致剧烈疼痛,但围手术期镇痛尚无既定标准。这项随机对照试验评估了在0.375%罗哌卡因胸壁筋膜平面阻滞中添加1 μg/kg右美托咪定是否能增强超快速通道(UFT)微创心脏瓣膜手术中阿片类药物的节约。方法:76例择期患者采用双盲随机分组(1:1)。对照组给予0.375%罗哌卡因60 mL,右美托咪定组给予1 μg/kg右美托咪定+ 0.375%罗哌卡因60 mL。主要终点是术中瑞芬太尼的使用和术后24小时舒芬太尼的消耗,这是评估阿片类药物节约效果的共同主要终点。次要结局包括术后24小时舒芬太尼消耗、24小时羟考酮使用、患者自控镇痛(PCA)激活、48小时内视觉模拟评分(VAS)≥3次发作、意识恢复时间、拔管时间、重症监护病房(ICU)持续时间、住院时间和并发症。结果:DEX组术中瑞芬太尼用量明显减少(2.45±0.47 mg vs. 2.98±0.53 mg, p)。1 μg/kg右美托咪定联合罗哌卡因用于胸壁筋膜平面阻滞可减少阿片类药物的需求,缩短UFT心脏手术的ICU/住院时间,支持其安全性和有效性,但局限性包括单中心设计、固定右美托咪定剂量和不完整的并发症评估,需要多中心验证和标准化的安全监测。试验注册:ChiCTR2100051182。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dexmedetomidine-enhanced chest wall fascial plane blocks in ultra-fast-track minimally invasive heart valve surgery: a randomized controlled trial.

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.

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