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Meta-analysis of remimazolam versus propofol in mechanically ventilated ICU patients

Meta-analysis of remimazolam versus propofol in mechanically ventilated ICU patients
Photo by Trust "Tru" Katsande / Unsplash
Key Takeaway
Consider remimazolam may reduce adverse events and delirium versus propofol in ventilated ICU patients, but mortality benefits are unproven.

This is a meta-analysis of randomized controlled trials evaluating remimazolam versus propofol in mechanically ventilated ICU patients. The analysis synthesized data from 220 patients with a 28-day follow-up. The authors found no statistically significant difference in mortality rates (OR 0.54; 95% CI: 0.26 to 1.12; p = 0.10) or 28-day survival rates (OR 1.59; 95% CI: 0.81 to 3.12; p = 0.18). There was no significant mean difference in ICU duration of stay (-1.50 days; 95% CI: -5.01 to 2.02; p = 0.40).

However, the meta-analysis reported a significant reduction in total adverse events with remimazolam (OR 0.38; 95% CI: 0.20 to 0.72; p = 0.00) and a significant reduction in the occurrence of delirium (OR 0.36; 95% CI: 0.16 to 0.83; p = 0.02). The authors did not report serious adverse events, discontinuations, or tolerability data.

Key limitations noted include the small total sample size of 220 patients and the absence of reported funding or conflicts of interest. The practice relevance was not reported. Clinicians should interpret these findings cautiously, as the evidence for safety benefits is derived from a limited dataset and requires confirmation in larger trials.

Study Details

Study typeMeta analysis
Sample sizen = 220
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
BACKGROUND AND AIM: The management of sedation in mechanically ventilated intensive care unit (ICU) patients is very challenging in critical care medicine. Remimazolam and propofol are used as sedative agents for ICU patients undergoing mechanical ventilation. This meta-analysis evaluates the efficacy and safety of remimazolam compared to propofol in mechanically ventilated ICU patients. METHODS: We conducted a comprehensive database search up to April 2025, included the studies that met our inclusion criteria. We evaluated mortality rates and other secondary outcomes to compare the efficacy of remimazolam and propofol. Odds ratios (OR) with 95% confidence intervals (95% CI) were calculated using RevMan software. RESULTS: Three RCTs were selected from a total of 745 retrieved articles, including 220 patients undergoing IMV in an ICU setting. The findings revealed no statistically significant difference in mortality rates (OR 0.54; 95% CI: 0.26 to 1.12; p = 0.10) or 28-day survival rates (OR 1.59; 95% CI: 0.81 to 3.12; p = 0.18), and the mean difference in ICU duration of stay was -1.50 days (95% CI: -5.01 to 2.02; p = 0.40) between the two sedatives. Remimazolam demonstrated a significant reduction in total adverse events (OR 0.38; 95% CI: 0.20 to 0.72; p = 0.00) and the occurrence of delirium (OR 0.36; 95% CI: 0.16 to 0.83; p = 0.02), with no observed heterogeneity (I = 0%). CONCLUSION: This meta-analysis shows that remimazolam provides comparable efficacy to propofol regarding mortality and survival, with significant advantages in reducing adverse events and delirium.
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