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Comparison of Esmolol Versus Landiolol on Mortality in Adult Patients With Sepsis: A Systematic Review and Network Meta-Analysis.

Critical care medicine2025-12-09PubMed
Total: 81.0Innovation: 7Impact: 8Rigor: 9Citation: 8

Summary

Across 10 RCTs (n=1,035), esmolol reduced 28-day mortality (RR 0.69, 95% CI 0.56–0.85) and heart rate versus standard care, while landiolol increased norepinephrine requirements versus SOC and was associated with higher 28-day mortality compared with esmolol (RR 1.57, 95% CI 1.08–2.30). Certainty was moderate for esmolol effects and low for landiolol comparisons.

Key Findings

  • Esmolol reduced 28-day mortality versus standard care (RR 0.69, 95% CI 0.56–0.85; moderate certainty).
  • Esmolol lowered 24-hour heart rate versus standard care (MD −16.92 bpm, 95% CI −23.49 to −10.36; moderate certainty).
  • Landiolol increased norepinephrine use compared with standard care (MD 0.09 μg/kg/min, 95% CI 0.01–0.18; moderate certainty).
  • Landiolol was associated with higher 28-day mortality versus esmolol (RR 1.57, 95% CI 1.08–2.30; low certainty).

Clinical Implications

Consider esmolol as the preferred short-acting β-blocker in septic patients requiring heart rate control, with close hemodynamic monitoring and awareness of catecholamine requirements; avoid extrapolating landiolol benefits until higher-certainty data are available.

Why It Matters

Provides comparative effectiveness evidence on short-acting β-blockers in sepsis, suggesting esmolol may confer survival benefit while landiolol may increase vasopressor needs.

Limitations

  • Low certainty for landiolol comparisons and potential heterogeneity in dosing strategies.
  • Limited head-to-head trials between esmolol and landiolol.

Future Directions

Conduct adequately powered head-to-head RCTs of esmolol versus landiolol with standardized titration protocols and patient-centered outcomes, and mechanistic studies to explain differential vasopressor effects.

Study Information

Study Type
Meta-analysis
Research Domain
Treatment
Evidence Level
I - Synthesis of randomized controlled trials via network meta-analysis
Study Design
OTHER