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Effect of S-Ketamine on Postoperative Delirium in Elderly Patients Undergoing Arthroplasty: A Randomized Controlled Trial.

Anesthesiology2025-10-14PubMed
Total: 84.0Innovation: 8Impact: 0Rigor: 0Citation: 0

Summary

Among 372 elderly arthroplasty patients under neuraxial anesthesia, S-ketamine reduced postoperative delirium within 3 days (8.06% vs 20.43%; adjusted OR 0.29, 95% CI 0.14–0.63; P=0.002). Early postoperative pain during activity and rescue analgesia use were lower with S-ketamine, whereas hallucinations, dizziness, and nightmares were more frequent. Other complications were uncommon and similar between groups.

Key Findings

  • Postoperative delirium within 3 days: 8.06% (S-ketamine) vs 20.43% (placebo); adjusted OR 0.29 (95% CI 0.14–0.63; P=0.002).
  • Lower pain during exercise/physical therapy and reduced need for rescue analgesia on postoperative day 1 with S-ketamine.
  • Higher incidence of hallucinations, dizziness, and nightmares with S-ketamine; other complications were infrequent with no significant differences.

Clinical Implications

Perioperative teams may consider S-ketamine as part of multimodal analgesia under neuraxial anesthesia to prevent postoperative delirium in elderly arthroplasty patients, balancing benefits against increased psychotomimetic adverse effects and ensuring monitoring and counseling.

Why It Matters

This is a well-designed RCT demonstrating a substantial and clinically meaningful reduction in postoperative delirium with S-ketamine under neuraxial anesthesia, a high-risk scenario with limited proven preventive therapies.

Limitations

  • Single-center setting may limit generalizability; neuraxial anesthesia context may not extend to general anesthesia.
  • Short follow-up (3 days) for delirium assessment; increased psychotomimetic adverse events require mitigation strategies.

Future Directions

Multicenter trials to validate efficacy across settings, dose-finding to minimize psychotomimetic effects, evaluation under general anesthesia, and longer-term cognitive/functional outcomes.

Study Information

Study Type
RCT
Research Domain
Prevention
Evidence Level
I - Randomized controlled trial with statistically significant primary endpoint.
Study Design
OTHER