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