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右美托咪定与芬太尼对丙泊酚诱发患者呼吸抑制EC50影响的比较 被引量:27

Comparison of effects of dexmedetomidine and fentanyl on median effective concentration of propofol required for inducing respiratory depression
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摘要 目的 比较右美托咪定与芬太尼对丙泊酚诱发患者呼吸抑制半数有效浓度(EC50)的影响.方法 择期妇科全麻手术患者,年龄30~50岁,体重50~75kg,BMI22~28kg/m2,ASA分级Ⅰ或Ⅱ级,采用随机数字表法,将其分为3组:对照组(C组)、右美托咪定组(D组)和芬太尼组(F组).D组和F组分别静脉输注右美托咪定0.5μg/kg和芬太尼1.5μg/kg,均以生理盐水稀释至10ml,10 min内输注完毕,C组以等容量生理盐水替代.随后静脉注射利多卡因后TCI丙泊酚,采用序贯法输注.C组、D组和F组初始血浆靶浓度分别为2.5、2.1、1.1μg/ml,相邻浓度梯度比为1.1,当患者出现呼吸抑制时为阳性反应.计算丙泊酚诱发呼吸抑制的EC50及其95%可信区间(CI).于入室(T0)、静脉输注右美托咪定、芬太尼或生理盐水后(T1)、丙泊酚TCI5 min (T2)、10 min (T3)及效应室浓度与血浆靶浓度平衡时(T4)记录BIS值及OAA/S评分.结果 C组、D组和F组丙泊酚诱发呼吸抑制的EC50及其95%CI分别为2.72(2.55~ 2.91)、2.15(2.05 ~ 2.27)、1.17(1.08~ 1.25) μg/ml.与C组比较,D组和F组EC50降低,F组BIS值和OAA/S评分明显升高(P<0.05),D组BIS值和OAA/S评分差异无统计学意义(P>0.05);与D组比较,F组EC50降低,BIS值和OAA/S评分升高(P<0.05).当BIS值降至65或OAA/S评分达3分时,D组和F组的效应室浓度较C组明显降低(P<0.05).在出现呼吸抑制的患者中,以舌后坠引起的上呼吸道梗阻为表现的患者在C组、D组和F组的比率分别为100%、60%和20%,以呼吸频率减慢或呼吸暂停为表现的患者在C组、D组和F组的比率分别为0、40%和80%.结论 右美托咪定虽然无明显呼吸抑制作用,但可增强丙泊酚呼吸抑制的效力,其效力低于小剂量芬太尼. Objective To compare the effects of dexmedetomidine and fentanyl on the median effective concentration (EC50) of propofol required for inducing respiratory depression.Methods ASA physical status Ⅰ or Ⅱ patients,aged 30-50 yr,weighing 50-75 kg,with body mass index of 22-28 kg/m2,scheduled for elective gynecological surgery under general anesthesia,were randomly divided into 3 groups:control group (group C),dexmedetomidine group (group D) and fentanyl group (group F).Dexmedetomidine 0.5 μg/kg and fentanyl 1.5 μg/kg in 10ml of normal saline were infused over 10 min in D and F groups,respectively,while the equal volume of normal saline was given in group C.Lidocaine was injected intravenously followed by target-controlled infusion of propofol.In C,D and F groups,the initial target concentration of propofol was 2.5,2.1 and 1.1 μg/ml,respectively,and the ratio between the two successive concentration gradients was 1.1.It was defined as positive when patients developed respiration depression.EC50 and 95% confidence interval of propofol inducing respiratory depression were calculated.BIS values and OAA/S scores were recorded after admission to operating room (T0),after infusion of dexmedetomidine,fentanyl or normal saline,at 5 and 10 min after the start of propofol target-controlled infusion and after the target effect-site and plasma concentrations were balanced.Results EC50 (95% confidence interval) of propofol required for inducing respiratory depression was 2.72 (2.55-2.91),2.15 (2.05-2.27)and 1.17(1.08-1.25) μg/ml in C,D and F groups,respectively.Compared with group C,the EC50 was significantly decreased in D and F groups and the BIS values and OAA/S scores were increased in group F (P < 0.05),and no significant changes were found in the BIS values and OAA/S scores in group D (P > 0.05).The EC50 was significantly decreased and the BIS values and OAA/S scores was increased in group F as compared with group D (P < 0.05).When the BIS values reached 65 or OAA/S scores was 3,the effect-site concentration was significantly lower in D and F groups than in group C (P < 0.05).In C,D and F groups,the percentage of patients who developed upper airway obstruction caused by glossocoma was 100%,60% and 20%,respectively,and who developed decreased respiratory rate or apnea (RR≤ 8 bpm or respiratory arrest time≥ 15 s) was 0,40% and 80%,respectively.Conclusion Although dexmedetomidine induces no respiratory depression,dexmedetomidine can enhance the potency of propofol required for inducing respiratory depression and the prtency is lower than that of small-dose fentanyl.
出处 《中华麻醉学杂志》 CAS CSCD 北大核心 2013年第8期940-943,共4页 Chinese Journal of Anesthesiology
关键词 右美托咪啶 芬太尼 二异丙酚 呼吸功能不全 剂量效应关系 药物 Dexmedetomidine Fentanyl Propofol Respiratory insufficiency Dose-response relationship, drug
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