# Efficacy and safety of midazolam versus dexmedetomidine in mechanically ventilated intensive care unit patients: a systematic review and meta-analysis

**Authors:** Wei Peng, Yuan-Yuan Lin, An-Ni Lin, Yong-Jia Zheng, Xu-Liang Cai, Yue-Fei Li, Qian-Yi Tang, Huan He

PMC · DOI: 10.3389/fphar.2026.1733161 · 2026-01-28

## TL;DR

This study compares midazolam and dexmedetomidine for ICU patients on ventilators, finding that dexmedetomidine reduces delirium and ventilation time but increases bradycardia risk.

## Contribution

A meta-analysis comparing midazolam and dexmedetomidine in ICU patients, revealing novel insights into efficacy and safety trade-offs.

## Key findings

- Dexmedetomidine reduced mechanical ventilation duration by nearly a day compared to midazolam.
- Dexmedetomidine lowered delirium risk but increased bradycardia incidence.
- No significant differences were found in ICU length of stay or mortality between the two drugs.

## Abstract

Midazolam and dexmedetomidine are widely used sedatives for mechanically ventilated patients in the intensive care unit (ICU). However, their comparative effectiveness and safety remain debated. This systematic review and meta-analysis aimed to evaluate randomized controlled trials (RCTs) directly comparing these agents.

The review followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. PubMed, The Cochrane Library, Web of Science, and Embase were searched through August 2025. Eligible studies were RCTs comparing midazolam with dexmedetomidine in adult ICU patients requiring invasive mechanical ventilation. Outcomes included mechanical ventilation duration, ICU length of stay, delirium, hemodynamic adverse events, and mortality. Pooled estimates were calculated using fixed- or random-effects models, with subgroup and sensitivity analyses performed to assess robustness.

Fifteen RCTs with diverse international populations were included. Dexmedetomidine significantly reduced mechanical ventilation duration (WMD = −0.96 days, 95% CI: −1.56 to −0.36) and lowered delirium risk (RR = 0.59, 95% CI: 0.52–0.68). It was, however, associated with a higher incidence of bradycardia (RR = 2.05, 95% CI: 1.61–2.62). No significant differences were observed in ICU length of stay (WMD = −0.89 days, 95% CI: −2.41 to 0.62) or all-cause mortality (RR = 0.96, 95% CI: 0.79–1.18). Sensitivity analyses confirmed the stability of pooled results. Subgroup analyses suggested stronger benefits of dexmedetomidine in Asian studies and in smaller trials, while the protective effect against delirium was more pronounced in older patient cohorts.

Dexmedetomidine demonstrated clinical advantages over midazolam by reducing delirium and ventilation duration but carried a greater risk of bradycardia. Sedative choice should balance efficacy with cardiovascular safety.

## Linked entities

- **Chemicals:** midazolam (PubChem CID 4192), dexmedetomidine (PubChem CID 5311068)

## Full-text entities

- **Diseases:** bradycardia (MESH:D001919), delirium (MESH:D003693)
- **Chemicals:** Midazolam (MESH:D008874), Dexmedetomidine (MESH:D020927)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12891203/full.md

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Source: https://tomesphere.com/paper/PMC12891203