Effect of Intravenous Esketamine on Rebound Pain Following Single-Shot Brachial Plexus Block in Patients Undergoing Shoulder Arthroscopic Surgery: A Prospective, Randomized, Placebo-Controlled Study

Patients undergoing arthroscopic rotator cuff repair under combined single-shot interscalene brachial plexus block and general anesthesia exhibit a rebound pain incidence of approximately 25%. Intravenous administration of esketamine (0.5 mg/kg bolus followed by continuous infusion at 0.25 mg/kg/h) during the operation failed to significantly reduce the incidence of rebound pain post-block (<i>P</i>>0.05). However, it demonstrated significant reductions in pain scores at 8h, 12h, and 24h postoperatively (<i>P</i><0.05), with enhanced hemodynamic stability observed from anesthetic induction to pre-incision periods. No severe adverse events were reported.

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Publication Details

Journal
Journal of Pain Research
Published
2025-10-01
DOI
https://doi.org/10.2147/jpr.s533774
Primary Topic
Anesthesia and Pain Management
Type
article
Field-Weighted Citation Impact
0.00

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article

Effect of Intravenous Esketamine on Rebound Pain Following Single-Shot Brachial Plexus Block in Patients Undergoing Shoulder Arthroscopic Surgery: A Prospective, Randomized, Placebo-Controlled Study

Jun Chen, Jinwei Zheng, Zhihao Pan
Journal of Pain Research
Anesthesia and Pain Management
article

Effect of Intravenous Esketamine on Rebound Pain Following Single-Shot Brachial Plexus Block in Patients Undergoing Shoulder Arthroscopic Surgery: A Prospective, Randomized, Placebo-Controlled Study

Jun Chen, Jinwei Zheng, Zhihao Pan
article en

Abstract

Patients undergoing arthroscopic rotator cuff repair under combined single-shot interscalene brachial plexus block and general anesthesia exhibit a rebound pain incidence of approximately 25%. Intravenous administration of esketamine (0.5 mg/kg bolus followed by continuous infusion at 0.25 mg/kg/h) during the operation failed to significantly reduce the incidence of rebound pain post-block (<i>P</i>>0.05). However, it demonstrated significant reductions in pain scores at 8h, 12h, and 24h postoperatively (<i>P</i><0.05), with enhanced hemodynamic stability observed from anesthetic induction to pre-incision periods. No severe adverse events were reported.

Journal of Pain ResearchVol. Volume 18
Ningbo No. 2 Hospital (CN), Ningbo Medical Center Lihuili Hospital (CN), Ningbo No.6 Hospital (CN)
Medical Scientific Research Foundation of Zhejiang Province, China, Hwa Mei Hospital, University of Chinese Academy of Sciences
Openalex Percentile: Top 56%
Anesthesia and Pain Management
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