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Effect of remimazolam versus propofol anaesthesia on postoperative delirium in neurovascular surgery: a randomised noninferiority trial.

British journal of anaesthesia2026-10-29PubMed 42957499
Design
Design 9 of 10
Novelty
Novelty 8 of 10
Journal
Journal 8 of 10
Clinical
Clinical 8 of 10

Summary

In 686 patients undergoing elective neurovascular surgery, postoperative delirium occurred in 12.8% of patients receiving remimazolam and 10.8% receiving propofol. Remimazolam met the prespecified noninferiority criterion for delirium and produced a lower hypotensive burden and higher operating-room extubation rate.

Key Findings

  • Postoperative delirium occurred in 12.8% of the remimazolam group and 10.8% of the propofol group.
  • Remimazolam was noninferior to propofol for postoperative delirium using a 10-percentage-point noninferiority margin.
  • Hypotensive burden below a mean arterial pressure of 65 mm Hg was lower with remimazolam, and operating-room extubation was more frequent.

Clinical Implications

Remimazolam-based total intravenous anesthesia may be considered when rapid emergence, reduced hypotension, or operating-room extubation is desirable, provided that delirium risk is monitored and local experience with flumazenil reversal is adequate.

Why It Matters

This rigorous randomized trial directly addresses whether a reversible benzodiazepine can replace propofol in a high-risk neurosurgical setting without worsening delirium. It also links anesthetic choice to clinically relevant hemodynamic and recovery outcomes.

Limitations

  • The study was conducted at a single centre, which may limit generalizability to other neuroanesthetic practices.
  • The observed delirium incidence was lower than anticipated when the noninferiority margin was defined.

Future Directions

Multicenter pragmatic trials should assess remimazolam across broader neurosurgical populations, evaluate longer-term cognitive outcomes, and examine cost-effectiveness and optimal flumazenil strategies.

Study Information

Study Type
RCT
Research Domain
Treatment
Evidence Level
I - Double-blind randomized noninferiority trial with prospective clinical trial registration.
Study Design