TY - JOUR
T1 - Buprenorphine, clonidine, dexamethasone, and ropivacaine for interscalene nerve blockade
T2 - A prospective, randomized, blinded, ropivacaine dose-response study
AU - Yadeau, Jacques T.
AU - Gordon, Michael A.
AU - Goytizolo, Enrique A.
AU - Lin, Yi
AU - Fields, Kara G.
AU - Goon, Amanda K.
AU - Holck, Guilherme
AU - Miu, Timothy W.
AU - Gulotta, Lawrence V.
AU - Dines, David M.
AU - Craig, Edward V
N1 - Publisher Copyright:
© 2015 American Academy of Pain Medicine. All rights reserved.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - 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 (mean6standard 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) (P50.040). 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%.
AB - 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 (mean6standard 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) (P50.040). 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%.
KW - Buprenorphine
KW - Clonidine
KW - Dexmethasone
KW - Interscalene nerve block
KW - Ropivacaine
KW - Total shoulder arthroplasty
UR - https://www.scopus.com/pages/publications/84982196295
UR - https://www.scopus.com/inward/citedby.url?scp=84982196295&partnerID=8YFLogxK
U2 - 10.1093/pm/pnv010
DO - 10.1093/pm/pnv010
M3 - Article
C2 - 26814246
AN - SCOPUS:84982196295
SN - 1526-2375
VL - 17
SP - 940
EP - 960
JO - Pain Medicine (United States)
JF - Pain Medicine (United States)
IS - 5
ER -