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Comparison of Esketamine/Propofol and Sufentanil/Propofol on Intraoperative Hypoxemia During Bronchoscopy: A Randomized Trial.

Xiao Huang, Xueyang Li, Yuan Sun, Anshi Wu, Pan Ai

Drug design, development and therapy January 1, 2025 DOI: 10.2147/DDDT.S490423 via PubMed

Summary

AI-generated from the abstract

In patients undergoing bronchoscopy, combining esketamine with propofol reduced the risk of dangerously low oxygen levels during the procedure compared with the standard combination of sufentanil and propofol. In a randomized trial, 27.2% of patients given esketamine experienced hypoxemia versus 66.7% given sufentanil. The esketamine group also had shorter episodes of low oxygen, higher minimum oxygen saturation, and faster recovery from anesthesia, though they required more propofol. Adverse reactions did not differ between groups. The authors suggest esketamine plus propofol may be a better option for preventing hypoxemia during bronchoscopy, but note that optimal dosing needs further study.

Study at a glance

Characteristics Randomized controlled trial Double-blind Peer reviewed
Sample size 66
Population Patients undergoing bronchoscopy
Interventions Esketamine Sufentanil
Dose 0.2 mg/kg esketamine, 0.2 μg/kg sufentanil
Topics Esketamine
Keywords Propofol Sufentanil Bronchoscopy/endoscopy/respiratory procedures Sedation/anesthesia/procedural sedation Hypoxemia/low oxygen/oxygen desaturation
Citations 5
Key finding Esketamine combined with propofol reduced the incidence of intraoperative hypoxemia compared with sufentanil combined with propofol in patients undergoing bronchoscopy.

Abstract

Propofol and sufentanil are the most commonly used anesthetics during bronchoscopy. Esketamine is an s-enantiomer of ketamine racemate and has both sedative and analgesic effects, it does not inhibit respiration and maintains hemodynamic stability. We aimed to compare the intraoperative hypoxemia risk of esketamine/propofol with sufentanil/propofol for patients in bronchoscopy. This study was an investigator-initiated, single-center, randomized, double-blind clinical trial. Patients undergoing bronchoscopy were randomly assigned to receive either sufentanil group (n = 33; sufentanil: 0.2 μg/kg) or esketamine group (n = 33; esketamine: 0.2 mg/kg) for sedation and analgesia. Clinical data, anesthetics usage, incidence of intraoperative hypoxemia, total time of hypoxemia, recovery time, and adverse events were recorded. The incidence of intraoperative hypoxemia was significantly lower in the esketamine group than in the sufentanil group (27.2% vs 66.7%, P=0.001, OR=5.333, 95% CI=1.859-15.301). Propofol usage was significantly higher in the esketamine group than in the sufentanil group (t=2.952, P=0.004). The duration of hypoxia was significantly lower in the esketamine group than in the sufentanil group (Z=-3.445, P<0.001), and the minimum oxygen saturation (SpO2) was significantly higher than in the sufentanil group (Z=-2.682, P=0.007). Recovery time from anesthesia was significantly lower in the esketamine group than in the sufentanil group (Z=-2.709, P=0.007). No difference was found in adverse reactions between the two groups. Esketamine combined with propofol reduced the incidence of intraoperative hypoxemia compared with sufentanil in bronchoscopy. Our results offer the possibility for a novel recommendation for the prevention of intraoperative hypoxemia during bronchoscopy. However, we mentioned the higher propofol use in the esketamine group. Additional clarification is necessary on the indications and the optimal dose of esketamine. Chinese clinical trial registry: ChiCTR2200058990.

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