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Respiratory depression in women receiving propofol/esketamine versus propofol/fentanyl for abortion surgery or curettage: a randomized clinical trial.

Annals of medicine2025-04-02PubMed
Total: 74.0Innovation: 7Impact: 7Rigor: 8Citation: 7

Summary

In 176 women undergoing abortion or curettage with propofol-based non-intubated anesthesia, subanesthetic esketamine (0.15 mg/kg) reduced intra-anesthetic respiratory depression compared with fentanyl (1 µg/kg). Secondary outcomes included vital signs and propofol dosing, supporting esketamine as an opioid-sparing analgesic adjunct in this setting.

Key Findings

  • Randomized trial (n=176) showed significantly lower respiratory depression with subanesthetic esketamine (0.15 mg/kg) plus propofol versus fentanyl (1 µg/kg) plus propofol (11% vs 45%).
  • Secondary outcomes included respiratory rate, pulse oximetry, hemodynamics, propofol dose, and adverse events, supporting the feasibility of an opioid-sparing approach.

Clinical Implications

For brief gynecologic procedures under propofol without intubation, substituting low-dose esketamine for fentanyl can reduce respiratory compromise. Institutions should integrate monitoring and dosing protocols while considering hemodynamic and psychomimetic profiles of esketamine.

Why It Matters

This pragmatic RCT directly addresses a common ambulatory anesthesia scenario and demonstrates a clinically meaningful reduction in respiratory depression with an opioid-sparing strategy.

Limitations

  • Single-center peri-anesthetic study with limited generalizability beyond specific procedures and demographics
  • Blinding and allocation concealment details not provided; comprehensive safety endpoints (e.g., emergence phenomena) not fully reported in abstract

Future Directions

Multicenter, blinded RCTs comparing esketamine- versus opioid-based adjuncts across procedures, with standardized definitions of respiratory depression and comprehensive safety/experience outcomes.

Study Information

Study Type
RCT
Research Domain
Treatment
Evidence Level
II - Single randomized controlled trial in a specific surgical setting
Study Design
OTHER