Buprenorphine, Clonidine, Dexamethasone, and Ropivacaine for Interscalene Nerve Blockade: A Prospective, Randomized, Blinded, Ropivacaine Dose-Response Study

被引:25
作者
YaDeau, Jacques T. [1 ]
Gordon, Michael A. [1 ]
Goytizolo, Enrique A. [1 ]
Lin, Yi [1 ]
Fields, Kara G. [1 ,3 ]
Goon, Amanda K. [1 ]
Holck, Guilherme [1 ,5 ]
Miu, Timothy W. [1 ,6 ]
Gulotta, Lawrence V. [2 ]
Dines, David M. [2 ]
Craig, Edward V. [2 ,4 ,7 ]
机构
[1] Weill Cornell Med Coll, Hosp Special Surg, Dept Anesthesiol, New York, NY USA
[2] Weill Cornell Med Coll, Hosp Special Surg, Dept Orthoped Surg, New York, NY USA
[3] Hosp Special Surg, Inst Healthcare Res, 535 E 70th St, New York, NY 10021 USA
[4] Univ Minnesota, Dept Orthoped Surg, Minneapolis, MN USA
[5] Hosp Ortopedia, Dept Anesthesiol, Rio De Janeiro, Brazil
[6] Kaiser Permanente Vacaville Med Ctr, Dept Anesthesiol, Vacaville, CA USA
[7] TRAI Orthoped Ctr, Bloomington, MN USA
基金
美国国家卫生研究院;
关键词
Buprenorphine; Clonidine; Dexamethasone; Interscalene Nerve Block; Ropivacaine; Total Shoulder Arthroplasty; BRACHIAL-PLEXUS BLOCK; PROVIDE POSTOPERATIVE ANALGESIA; MULTIMODAL PERINEURAL ANALGESIA; PERIPHERAL-NERVE; MEPIVACAINE PROLONGS; LOCAL-ANESTHETICS; LONGITUDINAL-DATA; SHOULDER SURGERY; DURATION; BUPIVACAINE;
D O I
10.1093/pm/pnv010
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Objective. This study investigated interscalene block for shoulder arthroplasty with various ropivacaine concentrations in the presence of clonidine, dexamethasone, and buprenorphine. The goal was prolonged analgesia with minimal motor blockade. Design. Prospective, double-blind, randomized controlled trial. Setting. University-affiliated orthopedic hospital. Methods. Patients (20/group) received acetaminophen, ketorolac, pregabalin, opioids, and "Control"; interscalene block, 0.375% ropivacaine, intravenous additives (buprenorphine, clonidine, dexamethasone); "High Dose"; 0.375% ropivacaine, perineural additives; "Medium Dose"; 0.2% ropivacaine, perineural additives; and "Low Dose"; 0.1% ropivacaine, perineural additives. Results. Pain with movement at 24 hours was 4.9 +/- 2.5 (mean +/- standard deviation [SD]) (Control), 4.5 +/- 3.0 (High Dose), 3.4 +/- 1.8 (Medium Dose), 4.2 +/- 2.4 (Low Dose). The difference between Medium Dose and Control was -1.5 (95% CI: -2.9, -0.1) (P = 0.040). Median time until need for opioids was 16.1 hours (Control) vs 23.7 hours (High Dose); hazard ratio 0.37 [95% CI: 0.17, 0.79]. High Dose had less pain with movement the morning after surgery, vs Control; 2.9 +/- 2.5 vs 4.9 +/- 2.7; P = 0.027. Pain with movement in the Post-Anesthesia Care Unit was higher in Low Dose, vs Control; 0.9 +/- 1.4 vs 0 +/- 0,P = 0.009. Low Dose had superior hand strength in the Post-Anesthesia Care Unit (mean +/- SD of pre-operative strength: 44.0 +/- 20.3%) compared to Control (27.5 +/- 24.5%) (P = 0.031). Conclusions. For maximum pain reduction, combining perineural additives with ropivacaine 0.375% or 0.2% is suggested. To minimize motor blockade, perineural additives can be combined with ropivacaine, 0.1%.
引用
收藏
页码:940 / 960
页数:21
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