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    已发表论文

    艾司氯胺酮/丙泊酚与舒芬太尼/丙泊酚对支气管镜检查术中低氧血症影响的比较:一项随机试验

     

    Authors Huang X , Li X, Sun Y, Wu A , Ai P

    Received 7 August 2024

    Accepted for publication 13 May 2025

    Published 27 May 2025 Volume 2025:19 Pages 4429—4436

    DOI http://doi.org/10.2147/DDDT.S490423

    Checked for plagiarism Yes

    Review by Single anonymous peer review

    Peer reviewer comments 6

    Editor who approved publication: Prof. Dr. Georgios Panos


    Xiao Huang,1 Xueyang Li,1 Yuan Sun,2 Anshi Wu,1 Pan Ai1 

    1Department of Anesthesiology, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, People’s Republic of China; 2Department of Pharmacy, Peking University Third Hospital, Beijing, People’s Republic of China

    Correspondence: Yuan Sun, Department of Pharmacy, Peking University Third Hospital, No. 49 huayuan North Road, Haidian District, Beijing, 100191, People’s Republic of China, Email sunny5106@163.com Anshi Wu, Department of Anesthesiology, Beijing Chao-Yang Hospital, Capital Medical University, No. 8 Workers’ Stadium South Road, Chaoyang Distirct, Beijing, 100020, People’s Republic of China, Email wuanshi99@163.com

    Purpose: 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.
    Methods: 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.
    Main Results: 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.
    Conclusion: 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.
    Trial Registration: Chinese clinical trial registry: ChiCTR2200058990.

    Keywords: bronchoscopy, esketamine, hypoxemia, propofol, sufentanil

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