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Objective To investigate the sedative and hypnotic interaction between remifentanil and propofol by target-controlled infusion (TCI) during induction of anesthesia.Methods Third-two ASA Ⅰ or Ⅱpatients,aged 22-63 yr,body mass index 18-25 kg/m2,scheduled for elective surgery under general anesthesia,were randomly divided into 4 groups(n=8 each).Group Ⅰ only received TCI pmpofol.GroupⅡ,Ⅲ,and Ⅳreceived a target concentration of 2,4 or 6 ng/ml remifentanil respectively.While the blood-effect site concentrations of remifentanil were equilibrated,patients received TCI of propefol,with an initial target concentration of 0.5μg/ml.After the blood-effect site concentrations of propofol were equilibrated then with 0.5μg/ml increments until the loss consciousness was achieved.The eyelash reflex and state of consciousness were assessed and radial arterial blood sample 6 ml was taken every 3 min to determine the remifentanil and propofol concentrations in blood.Propofol and remifentanil concentrations in blood were measured by reversed-phase high-performance liquid chromatography and high-performance liquid chromatography with ultraviolet detection respectively.The sedative and hypnotic interaction between propofol and remifentanil was determined with a pharmacodynamie interaction model by regression analysis and determined using the isobolographic method.Results Propofol concentrations in blood were lower in group Ⅱ,Ⅲ and Ⅳ than group Ⅰ(P<0.05).The propofol concentratopms in blood were significantly decreased in trun with the increase in the remifentanil concentrations in blood in group Ⅱ-Ⅳ(P<0.05).At loss of eyelash reflex and loss of consciousness of patients,the pharmacodynamic interaction model by curve fitting was superior to linear regression (P<0.05).At loss of eyelash reflex of patients,the curve fitting result showed EC50,prop=2.77μg/ml and EC50,rem=26.67 ng/ml,and the isobolographic method equation is ECprop/2.77+ECrem/26.67=0.69.At loss of consciousness of patients,the curve fitting result showed EC50,prop==3.76μg/ml and EC50,rem=31.56ng/ml,and the isobolographic method equation is Ecprop/3.76+Ecrem/31.56=0.65.Conclusion Remifentanil (Cp 2-6 ng/ml) and propofol by TCI shows a synergistic type of pharmacodynamic interaction on the sedative and hypnotic during induction of anesthesia. 相似文献
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无痛人工流产受术者术前焦虑、抑郁状况的调查分析 总被引:1,自引:0,他引:1
目的:调查无痛人工流产受术者术前焦虑和抑郁状况.方法:选取2009年8~12月自愿接受无痛人工流产受术者150例,收集其年龄、文化程度、婚姻状况、生育史和人流史等一般资料,采用焦虑自评量表(SAS)和抑郁自评量表(SDS)进行测评.结果:无痛人工流产受术者SAS和SDS标准分均值分别为42.78和46.45,高于中国常模分值,术前SAS≥50分占52.7%,SDS≥53分占54.2%.不同文化程度之间的焦虑和抑郁程度比较无显著性差异,未婚和无生育史者的焦虑和抑郁程度明显高于已婚和有生育史者,接受过非无痛人流和初次无痛人流者焦虑和抑郁程度重于接受过无痛人流者.结论:不同人群对无痛人流术前的焦虑和抑郁程度不同,有必要对其进行心理干预. 相似文献
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目的:探讨2种方法使用利多卡因缓解异丙酚注射痛的效果及护理措施。方法:选择150例自愿接受无痛人工流产的患者,随机分3组,每组50例,Ⅰ组静注生理盐水2ml60s后静脉推注异丙酚;Ⅱ组静脉注射2%利多卡因2ml 60s后静脉推注异丙酚;Ⅲ组前臂扎止血带后静脉注射2%利多卡因2ml且维持止血带60s后静脉推注异丙酚。各组均进行心理护理、选择肘部静脉、选择留置针及局部按摩护理措施,采用4分评分法对异丙酚注射痛进行评价。结果:Ⅰ、Ⅱ、Ⅲ组异丙酚用药后注射部位无痛发生率分别为30%(15例)、66%(33例)、84%(42例),3组阍比较有统计学意义(P〈0.001)。绪论:扎止血带后静脉注射2%利多卡因2ml且维持止血带60s缓解异丙酚注射痛效果更好,同时配合有效的护理措施是减轻注射痛的保证。 相似文献
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目的 研究艾司氯胺酮+丙泊酚静脉麻醉运用在小儿腹腔镜疝修补术中的价值。方法 简单随机选取2021年3月—2022年3月深圳市龙岗区人民医院收治的小儿腹腔镜疝修补术患儿80例,以随机数表法分为研究组和对照组,各40例。研究组采取艾司氯胺酮+丙泊酚静脉麻醉,对照组采用氯胺酮全麻。对比两组拔管、自主呼吸、指令性睁眼、PACU停留时间,测定两组麻醉前(T1)、麻醉后10 min(T2)、手术开始后5 min(T3)、手术开始后10 min(T4)、手术结束即刻(T5)、苏醒即刻(T6)的平均动脉压(MAP)、心率(HR),统计两组苏醒期躁动发生率与麻醉不良反应情况。结果 研究组拔管、自主呼吸、指令性睁眼、PACU停留时间均短于对照组,差异有统计学意义(t=4.023、3.678、6.556、3.657,P<0.05)。T1时,两组MAP、HR比较,差异无统计学意义(P>0.05);T2、T3、T4、T5、T6时,研究组MAP、HR均低于对照组,差异有统计学意义(t=9.769、11.841、10.213、9.201、9.298、9.436、14.664、15.686、14.892、... 相似文献
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Objective To investigate the sedative and hypnotic interaction between remifentanil and propofol by target-controlled infusion (TCI) during induction of anesthesia.Methods Third-two ASA Ⅰ or Ⅱpatients,aged 22-63 yr,body mass index 18-25 kg/m2,scheduled for elective surgery under general anesthesia,were randomly divided into 4 groups(n=8 each).Group Ⅰ only received TCI pmpofol.GroupⅡ,Ⅲ,and Ⅳreceived a target concentration of 2,4 or 6 ng/ml remifentanil respectively.While the blood-effect site concentrations of remifentanil were equilibrated,patients received TCI of propefol,with an initial target concentration of 0.5μg/ml.After the blood-effect site concentrations of propofol were equilibrated then with 0.5μg/ml increments until the loss consciousness was achieved.The eyelash reflex and state of consciousness were assessed and radial arterial blood sample 6 ml was taken every 3 min to determine the remifentanil and propofol concentrations in blood.Propofol and remifentanil concentrations in blood were measured by reversed-phase high-performance liquid chromatography and high-performance liquid chromatography with ultraviolet detection respectively.The sedative and hypnotic interaction between propofol and remifentanil was determined with a pharmacodynamie interaction model by regression analysis and determined using the isobolographic method.Results Propofol concentrations in blood were lower in group Ⅱ,Ⅲ and Ⅳ than group Ⅰ(P<0.05).The propofol concentratopms in blood were significantly decreased in trun with the increase in the remifentanil concentrations in blood in group Ⅱ-Ⅳ(P<0.05).At loss of eyelash reflex and loss of consciousness of patients,the pharmacodynamic interaction model by curve fitting was superior to linear regression (P<0.05).At loss of eyelash reflex of patients,the curve fitting result showed EC50,prop=2.77μg/ml and EC50,rem=26.67 ng/ml,and the isobolographic method equation is ECprop/2.77+ECrem/26.67=0.69.At loss of consciousness of patients,the curve fitting result showed EC50,prop==3.76μg/ml and EC50,rem=31.56ng/ml,and the isobolographic method equation is Ecprop/3.76+Ecrem/31.56=0.65.Conclusion Remifentanil (Cp 2-6 ng/ml) and propofol by TCI shows a synergistic type of pharmacodynamic interaction on the sedative and hypnotic during induction of anesthesia. 相似文献
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目的 探讨靶控输注(TCI)瑞芬太尼和异丙酚麻醉诱导时镇静催眠效应的相互作用.方法 择期全麻手术患者32例,ASAⅠ或Ⅱ级,年龄22~63岁,体重指数18~25 kg/m2.采用TCI异丙酚和瑞芬太尼诱导麻醉,随机分为4组(n=8):Ⅰ组单纯TCI异丙酚,Ⅱ组~Ⅳ组TCI瑞芬太尼,血浆靶浓度分别为2、4、6 ng/ml,当瑞芬太尼血浆靶浓度与效应室浓度达平衡时开始TCI异丙酚,异丙酚初始血浆靶浓度均为0.5μg/ml,当异丙酚血浆靶浓度与效应室浓度达平衡时以0.5μg/ml的浓度梯度递增诱导至患者意识消失.每隔3min观察睫毛反射和意识状态,同时抽取桡动脉血样6ml,分别采用反相高效液相色谱法和高效液相色谱-紫外法测定异丙酚和瑞芬太尼血药浓度.采用药效学相互作用模型公式和等辐射法分析两者镇静催眠效应的相互作用.结果 与Ⅰ组比较,Ⅱ组~Ⅳ组睫毛反射消失和意识消失时异丙酚血药浓度降低,而Ⅱ组~Ⅳ组随瑞芬太尼血药浓度升高,异丙酚血药浓度依次降低(P<0.05).睫毛反射消失和意识消失时,异丙酚和瑞芬太尼血药浓度用药效学相互作用模型曲线拟合均优于直线回归(P<0.05).拟合出睫毛反射消失时EC50,prop=2.77μg/ml、EC50,rem=26.67 ng/ml,其等辐射法公式EC prop/2.77+Ecrem/26.67=0.69;意识消失时EC50,prop=3.76μg/ml、EC50,rem=31.56 ng/ml,其等辐射法公式Ecprop/3.76+Ecrem/31.56=0.65.结论 麻醉诱导期间,TCI瑞芬太尼(血浆靶浓度2~6ng/ml)和异丙酚在镇静催眠效应上呈协同作用. 相似文献
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