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Brachial Plexus Block with Liposomal Bupivacaine for Shoulder Surgery Improves Analgesia and Reduces Opioid Consumption: Results from a Multicenter, Randomized, Double-Blind, Controlled Trial.
- Source :
-
Pain medicine (Malden, Mass.) [Pain Med] 2020 Feb 01; Vol. 21 (2), pp. 387-400. - Publication Year :
- 2020
-
Abstract
- Objective: The utility of single-injection and continuous peripheral nerve blocks is limited by short duration of analgesia and catheter-related complications, respectively. This double-blind, multicenter trial evaluated the efficacy, safety, and pharmacokinetics of single-injection, ultrasound-guided brachial plexus block (BPB) with liposomal bupivacaine (LB) added to a standardized pain management protocol for shoulder surgery.<br />Methods: Adults undergoing total shoulder arthroplasty or rotator cuff repair were randomized to receive LB 133 mg, LB 266 mg (pharmacokinetic and safety analyses only), or placebo, added to a standardized analgesia protocol. The primary end point was area under the curve (AUC) of visual analog scale pain intensity scores through 48 hours postsurgery. Secondary end points were total opioid consumption, percentage of opioid-free patients, and time to first opioid rescue through 48 hours. Pharmacokinetic samples were collected through 120 hours and on days 7 and 10. Adverse events were documented.<br />Results: One hundred fifty-five patients received treatment (LB 133 mg, N = 69; LB 266 mg, N = 15; placebo, N = 71). BPB with LB 133 mg was associated with significantly improved AUC of pain scores (least squares mean [SE] = 136.4 [12.09] vs 254.1 [11.77], P < 0.0001), opioid consumption (least squares mean [SE] = 12.0 [2.27] vs 54.3 [10.05] mg, P < 0.0001), median time to opioid rescue (4.2 vs 0.6 h, P < 0.0001), and percentage of opioid-free patients (treatment difference = 0.166, 95% confidence interval = 0.032-0.200, P = 0.008) through 48 hours vs placebo. Adverse event incidence was comparable between groups.<br />Conclusions: Single-injection BPB with LB 133 mg provided analgesia through 48 hours postsurgery with reduced opioid use compared with placebo after shoulder surgery.<br /> (© 2019 American Academy of Pain Medicine.)
- Subjects :
- Aged
Analgesia methods
Analgesics, Opioid therapeutic use
Double-Blind Method
Female
Humans
Male
Middle Aged
Orthopedic Procedures adverse effects
Pain, Postoperative etiology
Anesthetics, Local administration & dosage
Brachial Plexus Block methods
Bupivacaine administration & dosage
Pain Management methods
Pain, Postoperative prevention & control
Shoulder surgery
Subjects
Details
- Language :
- English
- ISSN :
- 1526-4637
- Volume :
- 21
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Pain medicine (Malden, Mass.)
- Publication Type :
- Academic Journal
- Accession number :
- 31150095
- Full Text :
- https://doi.org/10.1093/pm/pnz103