医学
镇静
麻醉
异丙酚
内窥镜检查
随机对照试验
低氧血症
不利影响
优势比
入射(几何)
临床试验
生命体征
麻醉护士
美国麻醉师学会
术后恶心呕吐
外科
上消化道内窥镜检查
患者安全
前瞻性队列研究
脉搏血氧仪
食管胃十二指肠镜检查
围手术期
恶心
氧饱和度
吗啡
作者
Hailong Bing,Yan Wang,Shiying Li,Yuan-Wen Li,Qimin Wang,Liumei Li,Sheng-Qun Liu,Zhen-Hua Hu,Tianwei Wang,Qing-Wang Lu,Ran Ran,Y L Wu,Shu-Sheng Xu,Hui‐Jie Li,Jian Huo,C. Liu,HU An-Min,Zhongyuan Xia,Qin-Jun Chu
标识
DOI:10.1038/s41746-026-02657-8
摘要
The increasing demand for gastrointestinal endoscopic procedures, coupled with a global shortage of anesthesiologists, underscores the need for intelligent automation in anesthesia care. Reinforcement learning (RL) offers a promising strategy for autonomous anesthesia control, yet prospective clinical validation remains limited. We developed an RL-based automated anesthesia system for gastrointestinal endoscopy (AAS-GE) for automated ciprofol delivery and conducted a prospective, multicenter, randomized controlled trial across four centers in China between January 8 and August 27, 2025. Adults aged 18-65 years with American Society of Anesthesiologists physical status I-II undergoing gastrointestinal endoscopy were randomized 1:1 to receive either AAS-GE-controlled anesthesia or clinician-managed manual anesthesia. The primary outcome was the incidence of hypoxemia, defined as oxygen saturation below 92%, with secondary outcomes assessing hypoxemia severity, induction time, drug use, recovery, and adverse events. A total of 509 participants were included in algorithm development, and 418 were enrolled for clinical validation. The incidence of hypoxemia was comparable between groups (14.42 vs. 14.29%; odds ratio 1.01, 95% CI 0.59-1.75; P = 0.968), with no significant differences in secondary safety outcomes. AAS-GE achieved a shorter induction time (median 1.55 vs. 1.90 min; P < 0.001) without increasing total drug dose or recovery time. However, intraoperative body movement was more frequent in the AAS-GE group, consistent with lighter anesthesia depth. These results demonstrate the non-inferior safety and efficacy of AAS-GE compared with clinician management, supporting its potential to improve efficiency and standardize sedation care. Clinical registration: ClinicalTrials.gov on Feb. 26, 2025 (NCT06857344).
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