Reinforcement learning based automated anesthesia system for gastrointestinal endoscopy with a multicenter randomized trial

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
出处
期刊:npj digital medicine [Nature Portfolio]
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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