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可乐定作为静脉区域麻醉的辅助用药:一项随机、双盲、安慰剂对照的剂量范围研究。

Clonidine as an adjunct to intravenous regional anesthesia: A randomized, double-blind, placebo-controlled dose ranging study.

作者信息

Ivie Clarence S, Viscomi Christopher M, Adams David C, Friend Alexander F, Murphy Todd R, Parker Colleen

机构信息

Department of Anesthesiology, University of Vermont, Plattsburgh, NY, USA.

出版信息

J Anaesthesiol Clin Pharmacol. 2011 Jul;27(3):323-7. doi: 10.4103/0970-9185.83674.

Abstract

BACKGROUND

The addition of clonidine to lidocaine intravenous regional anesthesia (IVRA) has been previously reported to improve postoperative analgesia in patients undergoing upper extremity surgery. Our objective was to perform a dose ranging study in order to determine the optimal dose of clonidine used with lidocaine in IVRA. DESIGN #ENTITYSTARTX00026;

SETTING

We performed a double-blinded randomized placebo-controlled study with 60 patients scheduled for elective endoscopic carpal tunnel release under IVRA with 50 ml lidocaine 0.5%. University-affiliated outpatient surgery center. Data collected in operating rooms, recovery room, and by telephone after discharge from surgery center. MATERIALS #ENTITYSTARTX00026;

METHODS

Sixty adult ASA I or II patients undergoing outpatient endoscopic carpal tunnel release under intravenous regional anesthesia.Patients were randomized into five study groups receiving different doses of clonidine in addition to 50 ml 0.5% lidocaine in their IVRA. Group A received 0 mcg/kg, group B 0.25 mcg/kg, group C 0.5 mcg/kg, group D 1.0 mcg/kg and group E 1.5 mcg/kg of clonidine.Intraoperative fentanyl, recovery room pain scores, time to first postsurgical analgesic, total number of acetaminophen/codeine tablets consumed postsurgery, incidence of sedation, hypotension and bradycardia. RESULTS #ENTITYSTARTX00026;

CONCLUSIONS

There was no benefit from any dose of clonidine compared to placebo. There were no clonidine-related side effects seen within the dose range studied. In short duration minor hand surgery, the addition of clonidine to lidocaine-based intravenous regional anesthesia provides no measurable benefit.

摘要

背景

先前有报道称,在利多卡因静脉区域麻醉(IVRA)中添加可乐定可改善上肢手术患者的术后镇痛效果。我们的目的是进行一项剂量范围研究,以确定在IVRA中与利多卡因联合使用的可乐定的最佳剂量。

设计与设置

我们进行了一项双盲随机安慰剂对照研究,纳入60例计划在IVRA下接受择期内镜下腕管松解术的患者,使用50毫升0.5%的利多卡因。研究在大学附属医院的门诊手术中心进行。数据在手术室、恢复室收集,并在患者从手术中心出院后通过电话随访收集。

材料与方法

60例成年ASA I或II级患者在静脉区域麻醉下接受门诊内镜下腕管松解术。患者被随机分为五个研究组,除了在IVRA中使用50毫升0.5%的利多卡因外,还接受不同剂量的可乐定。A组接受0微克/千克可乐定,B组接受0.25微克/千克,C组接受0.5微克/千克,D组接受1.0微克/千克,E组接受1.5微克/千克可乐定。记录术中芬太尼用量、恢复室疼痛评分、首次术后镇痛时间、术后对乙酰氨基酚/可待因片的总消耗量、镇静、低血压和心动过缓的发生率。

结果与结论

与安慰剂相比,任何剂量的可乐定都没有益处。在所研究的剂量范围内未观察到与可乐定相关的副作用。在短时间的小型手部手术中,在基于利多卡因的静脉区域麻醉中添加可乐定没有可测量的益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8332/3161454/318abb7b3bdb/JOACP-27-323-g002.jpg

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