Anesthetic drugs & techniques

Remimazolam vs. propofol for induction and maintenance of general anesthesia: A systematic review and meta-analysis of emergence agitation risk in surgical populations

J Clin AnesthPublished Systematic review and meta-analysis of randomised trials

Pooled resultResult — go to the resultRelative risk 0.82 95 % CI 0.41–1.65

Authors' conclusion

The use of remimazolam for the induction and maintenance of general anesthesia does not lead to a higher occurrence of EA in adult patients undergoing surgery, relative to propofol. However, in patients with ASA III-IV, remimazolam may be linked to a greater risk of POD than propofol.

Study context

Population
Surgical patients undergoing GA
Participants
3,031 patients · 19 RCTs
Comparison
Remimazolam vs propofol for induction and maintenance of GA
Outcome
Incidence of emergence agitation (EA)
Methodological detailssubgroup analysis
  • Subgroup analysis

Pooled result

As reported in the abstract

Relative risk

0.82

95 % CI 0.41–1.65

P = 0.585

Remimazolam vs Propofol
RR 0.82 (95 % CI 0.41–1.65); P = 0.585

Further pooled results

Postoperative delirium (POD) incidence, extubation time, emergence time, post-anesthesia care unit (PACU) LOS

No significant intergroup differences

Extubation time and PACU LOS without routine postoperative antagonist (subgroup)

Prolonged with remimazolam vs propofol

Extubation, emergence times and PACU discharge time after flumazenil antagonism (subgroup)

Extubation and emergence times shorter with remimazolam; PACU discharge time comparable

Safety

Postinduction and intraoperative hypotension; Postoperative nausea and vomiting (PONV), intraoperative awareness, hypoxemia

Hypotension significantly reduced with remimazolam vs propofol
PONV, intraoperative awareness and hypoxemia comparable

Original publication

Remimazolam vs. propofol for induction and maintenance of general anesthesia: A systematic review and meta-analysis of emergence agitation risk in surgical populations. J Clin Anesth. Published 22 March 2025. doi:10.1016/j.jclinane.2025.111815

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