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