首都医科大学学报 ›› 2025, Vol. 46 ›› Issue (6): 1126-1132.doi: 10.3969/j.issn.1006-7795.2025.06.021

• 临床研究 • 上一篇    下一篇

帕金森病患者丙泊酚诱导意识消失的效应室浓度

王进飞熊蔚王云珍于芸韩如泉*   

  1. 首都医科大学附属北京天坛医院麻醉科, 北京 100070
  • 收稿日期:2025-02-21 修回日期:2025-09-28 出版日期:2025-12-21 发布日期:2025-12-19
  • 通讯作者: 韩如泉 E-mail:ruquan.han@ccmu.edu.cn
  • 基金资助:
    贝恩麻醉科学研究项目(bnmr-2023-009)。

Effect-site concentrations of propofol to induce loss of consciousness in patients with Parkinson's disease

Wang Jinfei, Xiong Wei, Wang Yunzhen, Yu Yun, Han Ruquan*   

  1. Department of Anesthesiology, Beijing Tiantan Hospital, Capital Medical University,Beijing 100070,China
  • Received:2025-02-21 Revised:2025-09-28 Online:2025-12-21 Published:2025-12-19
  • Supported by:
    This study was supported by Bethune Charitable Foundation (bnmr-2023-009).

摘要: 目的  观察帕金森病(Parkinsons disease, PD)患者与非PD患者丙泊酚诱导意识消失所需的效应室浓度(effect-site concentration, Ce)。方法  纳入2022年10月16日至2023年10月14日于首都医科大学附属北京天坛医院就诊的患者,筛选年龄50~80岁,美国麻醉医师协会(American Society of Anesthesiologists, ASA)分级Ⅱ- Ⅲ级,行双侧脑深部电刺激手术的PD患者(PD组),并按照年龄和性别匹配选取同期行非神经外科非心脏手术的非PD患者(Non-PD组)各37例为研究对象。采用Schnider模型靶控泵注丙泊酚,警觉/镇静观察(Observer’s Assessment of  Alertness/Sedation, OAA/S)评分达1分后20 s评估意识状态,采集5 min临床试验数据后停药,记录给药后OAA/S评分1分时、停药后OAA/S评分3分时丙泊酚的Ce、患者状态指数(patient state index, PSI)。结果  PD患者组诱导至无意识状态所需丙泊酚剂量明显少于Non-PD患者组[(2.2±0.4)mg/L vs (3.1±0.4)mg/L,P<0.05];与Non-PD患者比较,PD患者意识消失和意识恢复时的PSI值更高(P<0.05),意识恢复时间明显延长(P<0.05),意识恢复时丙泊酚Ce更低(P<0.05)。结论  PD患者诱导意识消失所需的丙泊酚剂量降低,且需要在更低的Ce下苏醒,苏醒时间明显长于非PD患者,在意识消失和苏醒时的PSI均高于非PD患者,麻醉管理中应予以重视。

关键词: 帕金森病, 丙泊酚, OAA/S, 效应室浓度, PSI, 意识消失, 意识恢复

Abstract: Objective  To observe the effect-site concentration (Ce) of propofol required for loss of consciousness during induction in patients with Parkinsons disease (PD) and non-PD patients. Methods  From October 16, 2022 to October 14, 2023, 37 PD patients (PD group) aged 50-80 years, with American Society of Anesthesiologists (ASA)  Ⅱ-Ⅲ, who underwent bilateral deep brain stimulation (DBS) surgery  at Beijing Tiantan Hospital, Capital Medical University, were enrolled. Another 37 non-PD patients (Non-PD group), who were age and gender matched with PD patients and underwent non-neurosurgical and non-cardiac surgeries during the same period, were selected as control group. Propofol was administered via target-controlled infusion (TCI) using the Schnider model. The level of consciousness was assessed 20 s after the Observer’s Assessment of Alertness/Sedation (OAA/S) score dropped to 1. The administration of propofol was stopped after 5 mins of clinical trial data collection. The Ce of propofol and patient state index (PSI) were recorded at loss of consciousness (OAA/S=1) and upon recovery of consciousness (OAA/S=3) . Results  The dose of propofol required to induce unconsciousness in the PD group was significantly lower than that in the Non-PD group [(2.2±0.4)mg/L vs (3.1±0.4)mg/L, P<0.05]. Compared with the Non-PD group, the PD group had higher PSI values both at the time of loss of consciousness and consciousness recovery (P<0.05), significantly longer consciousness recovery time (P<0.05), and lower propofol Ce at the time of consciousness recovery (P<0.05). Conclusion  PD patients require a lower dose of propofol to induce loss of consciousness and need to recover at a lower Ce. Their consciousness recovery time is significantly longer than that of Non-PD patients, and their PSI values are higher than those of Non-PD patients both at the time of loss of consciousness and recovery. These characteristics should be taken into account in anesthesia management for PD patients.

Key words: Parkinson's disease, propofol, OAA/S, effect-site concentration, PSI, loss of consciousness, recovery of consciousness

中图分类号: