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投稿时间:2025-07-07 网络发布日期:2025-11-26
投稿时间:2025-07-07 网络发布日期:2025-11-26
中文摘要: 目的 应用序贯法探讨复合瑞芬太尼时环泊酚抑制患者支气管镜置入反应的有效剂量,为临床合理用药提供参考依据。方法 选取2023年9月至2024年4月南方医科大学第八附属医院择期全身麻醉下行支气管镜检查术的患者作为研究对象,所有患者均先静脉注射瑞芬太尼1 μg/kg,随后采用改良Dixon序贯法进行试验:环泊酚起始剂量为0.4 mg/kg,剂量梯度为0.05 mg/kg。若支气管镜进入气管时出现呛咳、体动等影响检查操作的反应,则判定为“无效”,下一例患者环泊酚剂量增加一个梯度(即增加0.05 mg/kg);反之则判定为“有效”,下一例患者剂量降低一个梯度(即减少0.05 mg/kg)。重复此过程,直至出现7个剂量转折点。采用Probit法计算环泊酚抑制支气管镜置入反应的半数有效剂量(ED50)、95%有效剂量(ED95)及其95%CI。记录患者麻醉诱导开始前5 min(T0)、麻醉诱导后5 min(T1),置气管镜(T2)及手术结束时(T3)的平均动脉压(MAP)、心率(HR)、脉搏血氧饱和度(SpO2)。记录患者术中低血压、低氧血症、呛咳以及术后恶心呕吐等不良事件的发生情况。结果 共有26例患者进入试验,有效与无效各13例患者。复合瑞芬太尼时,环泊酚抑制患者支气管镜置入反应的ED50(95%CI)为0.471(0.433~0.509)mg/kg,ED95(95%CI)为0.546(0.509~0.770)mg/kg。环泊酚复合瑞芬太尼镇静期间,与T0相比,HR在T1和T3时显著降低(P<0.05),T2时较T1时回升(P<0.05);MAP在T1和T2时较T0显著下降(P<0.05),T3时部分恢复但仍低于T(0 P<0.05)。SpO2在各时点比较差异无统计学意义(P>0.05)。有效组与无效组不良反应发生率比较差异无统计学意义(P>0.05)。结论 复合瑞芬太尼时环泊酚抑制患者支气管镜置入反应的ED50和ED95分别为0.471 mg/kg和0.546 mg/kg。
Abstract:Objective To investigate the effective dose of ciprofol for suppressing insertion response during bronchoscopy when combined with remifentanil by using the sequential method ,and to provide a reference for rational clinical drug use. Methods Patients who underwent elective bronchoscopy under general anesthesia at the Eighth Affiliated Hospital of Southern Medical University from September 2023 to April 2024 were selected as research subjects. All patients were first administered an intravenous injection of remifentanil at a dose of 1 μg/kg. The modified Dixon’s up-and-down sequential method was used to determine the effective dose of ciprofol:the initial dose was set at 0.4 mg/kg,with a dose gradient of 0.05 mg/kg. If coughing,body movements,or other reactions that interfered with the examination occurred when the bronchoscope entered the trachea,this was termed“ineffective”,and the ciprofol dose for the next patient was increased by one dose gradient of 0.05 mg/kg. Conversely,if the reaction was“effective”,the ciprofol dose for the next patient was decreased by one dose gradient of 0.05 mg/kg. This process was repeated until seven turning points were observed.The Probit method was used to calculate the median effective dose(ED50),95% effective dose(ED95),and 95% confidence interval(CI)of ciprofol for inhibiting bronchoscope insertion response.Mean arterial pressure(MAP),heart rate(HR),and pulse oxygen saturation(SpO2)were recorded at 5 minutes before the start of anesthesia induction(T0),5 minutes after anesthesia induction(T1),at the time of bronchoscope insertion
(T2),and at the end of the operation(T3). The occurrence of adverse events such as intraoperative hypotension,hypoxemia,coughing,and postoperative nausea and vomiting(PONV)was also recorded. Results A total of 26 patients were enrolled in the trial,with 13 patients in the effective group and 13 in the ineffective group. The ED50(95%CI)of ciprofol for suppressing insertion response was 0.471(0.433-0.509)mg/kg and the ED95(95%CI)was 0.546(0.509-0.770)mg/kg. During sedation with ciprofol combined with remifentanil:compared with T0,HR significantly decreased at T1 and T3(P<0.05),and increased at T2 compared with T1(P<0.05);MAP significantly decreased at T1 and T2 compared with T0(P<0.05),and partially recovered at T3 but remained lower than that at T0(P<0.05);there was no statistically significant difference in SpO2 among all time points(P>0.05). Additionally,there was no statistically significant difference in the incidence of adverse events between the effective group and the ineffective group(P>0.05).Conclusion Ciprofol combined with remifentanil effectively suppresses insertion response during bronchoscopy,with ED50 and ED95 of 0.471 mg/kg and 0.546 mg/kg,respectively.
文章编号: 中图分类号:R614.2 文献标志码:A
基金项目:广东省基础与应用基础研究基金项目(2023A1515140142)
附件
引用文本:
付晖,张艳静,陈志强,等.复合瑞芬太尼时环泊酚抑制患者支气管镜置入反应的有效剂量[J].中国临床研究,2025,38(11):1705-1709.
付晖,张艳静,陈志强,等.复合瑞芬太尼时环泊酚抑制患者支气管镜置入反应的有效剂量[J].中国临床研究,2025,38(11):1705-1709.
