Effect of Adding Esketamine to Patient-Controlled Intravenous Analgesia on Rebound Pain After Interscalene Brachial Plexus Block: A Randomized Controlled Trial.

Drug Des Devel TherOct 27, 2026 (epub)
Clinical ResearchAnesthesiologyOrthopedic SurgeryOpen access

Ruipeng Zhong, Lanhua Zhong, Hua Zhu et al.

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In 30 seconds

This randomized controlled trial evaluated whether adding esketamine to postoperative patient-controlled intravenous analgesia (PCIA) reduces rebound pain after interscalene brachial plexus block in patients undergoing shoulder arthroscopy. Among 132 randomized patients, rebound pain occurred in 25.8% with esketamine-containing PCIA and 39.4% with PCIA without esketamine; the difference was not statistically significant (OR, 0.53; 95% CI, 0.39 to 1.09; P =0.095). Esketamine was associated with better scores on several secondary pain, sleep, and recovery outcomes, but their clinical relevance was uncertain.

Key findings

  • Rebound pain incidence was 25.8% with esketamine versus 39.4% in controls (OR, 0.53; 95% CI, 0.39 to 1.09; P =0.095).
  • Among patients with rebound pain, the esketamine group had lower modified rebound pain scores and shorter pain duration.
  • Esketamine recipients had lower NRS scores at 12, 24, and 48 h, fewer PCIA demands, less rescue analgesic use, and higher QoR-15 and RCSQ scores (all P <0.05).
  • The incidence of assessed adverse events did not differ significantly between groups.

Why it matters

Rebound pain can undermine the analgesic benefit of a peripheral nerve block. In this trial, adding esketamine did not establish a reduction in its incidence, although several secondary outcomes favored esketamine. The findings distinguish a possible improvement in postoperative pain experience and recovery from evidence that the intervention prevents rebound pain.

What to keep in mind

The trial did not demonstrate a significant reduction in rebound pain incidence, and the clinical relevance of improvements in secondary outcomes was uncertain. The authors call for further multicenter studies.

Source

Published in Drug Des Devel Ther. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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