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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.

Publication ,  Journal Article
Patel, MA; Gadsden, JC; Nedeljkovic, SS; Bao, X; Zeballos, JL; Yu, V; Ayad, SS; Bendtsen, TF
Published in: Pain Med
February 1, 2020

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. 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. 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. CONCLUSIONS: Single-injection BPB with LB 133 mg provided analgesia through 48 hours postsurgery with reduced opioid use compared with placebo after shoulder surgery.

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Published In

Pain Med

DOI

EISSN

1526-4637

Publication Date

February 1, 2020

Volume

21

Issue

2

Start / End Page

387 / 400

Location

England

Related Subject Headings

  • Shoulder
  • Pain, Postoperative
  • Pain Management
  • Orthopedic Procedures
  • Middle Aged
  • Male
  • Humans
  • Female
  • Double-Blind Method
  • Bupivacaine
 

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Patel, M. A., Gadsden, J. C., Nedeljkovic, S. S., Bao, X., Zeballos, J. L., Yu, V., … Bendtsen, T. F. (2020). Brachial Plexus Block with Liposomal Bupivacaine for Shoulder Surgery Improves Analgesia and Reduces Opioid Consumption: Results from a Multicenter, Randomized, Double-Blind, Controlled Trial. Pain Med, 21(2), 387–400. https://doi.org/10.1093/pm/pnz103
Patel, Manish A., Jeffrey C. Gadsden, Srdjan S. Nedeljkovic, Xiaodong Bao, Jose L. Zeballos, Vincent Yu, Sabry S. Ayad, and Thomas F. Bendtsen. “Brachial Plexus Block with Liposomal Bupivacaine for Shoulder Surgery Improves Analgesia and Reduces Opioid Consumption: Results from a Multicenter, Randomized, Double-Blind, Controlled Trial.Pain Med 21, no. 2 (February 1, 2020): 387–400. https://doi.org/10.1093/pm/pnz103.
Journal cover image

Published In

Pain Med

DOI

EISSN

1526-4637

Publication Date

February 1, 2020

Volume

21

Issue

2

Start / End Page

387 / 400

Location

England

Related Subject Headings

  • Shoulder
  • Pain, Postoperative
  • Pain Management
  • Orthopedic Procedures
  • Middle Aged
  • Male
  • Humans
  • Female
  • Double-Blind Method
  • Bupivacaine