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Adjunctive esketamine in propofol-based sedation for gastrointestinal endoscopy: a systematic review and meta-analysis of randomized trials.

Frontiers in pharmacology2025-12-11PubMed
Total: 74.0Innovation: 7Impact: 7Rigor: 8Citation: 7

Summary

Across 18 randomized trials, adjunctive esketamine with propofol significantly reduced hypotension (RR 0.32) and respiratory adverse events, without prolonging recovery or increasing cardiovascular complications.

Key Findings

  • Eighteen randomized trials were included with PROSPERO registration of the review.
  • Adjunctive esketamine reduced hypotension risk (RR 0.32; 95% CI 0.24–0.43).
  • Respiratory adverse events decreased with esketamine adjunct without prolonging recovery time.
  • No increase in cardiovascular complications was observed.

Clinical Implications

Consider low-dose esketamine adjunct during GI endoscopy sedation to reduce hypotension and hypoxemia, especially in high-risk patients; develop dosing algorithms integrated into ERAS and monitored anesthesia care.

Why It Matters

Provides higher-level evidence that a widely accessible adjunct can improve safety of propofol-based procedural sedation, with immediate practice implications.

Limitations

  • Heterogeneity in dosing regimens and sedation protocols not fully detailed in abstract
  • Patient-level moderators and long-term outcomes were not reported

Future Directions

Define optimal esketamine dosing strategies with patient-level meta-analyses; evaluate cognitive recovery and delirium risk; extend to non-GI procedural sedation.

Study Information

Study Type
Systematic Review/Meta-analysis
Research Domain
Treatment
Evidence Level
I - Systematic review and meta-analysis of randomized controlled trials
Study Design
OTHER