摘要
目的评价氯胺酮对七氟醚抑制50%腹部手术患者切皮时应激反应的最低肺泡有效浓度(MACBAR)的影响。方法择期腹部手术患者44例,ASAⅠ或Ⅱ级,年龄30-60岁,随机分为2组(n=22):对照组(K0组)和氯胺酮组(K1组)。麻醉诱导:静脉注射异丙酚2mg/kg、芬太尼3μg/kg和顺阿曲库铵0.15mg/kg,气管插管后行机械通气。K组吸入七氟醚,K1组吸入七氟醚的同时静脉输注氯胺酮14μg·kg^-1·min^-1。初始七氟醚呼气末浓度为3.0%。采用改良的序贯法进行试验,切皮时患者的心率或平均动脉压升高幅度≥基础值的15%定义为阳性反应,记录平衡点后各个由阳性反应到阴性反应的中点的浓度,取其平均值,即为MACBAR并计算其95%可信区间。结果K0组七氟醚MACBAR为3.25%(95%可信区间为3.05%~3.45%);K1组七氟醚MACBAR为2.20%(95%可信区间为1.96%~2.44%),K1组七氟醚MAC。低于K0组(P〈0.05)。结论静脉输注氯胺酮14μg·kg^-1·min^-1可降低腹部手术患者七氟醚MACBAR,增强七氟醚抑制应激反应的效应。
Objective To evaluate the effects of ketamine on the minimum alveolar concentration of sevoflurane for blunting adrenergic responses to skin incision (MACBAR) in patients undergoing abdominal surgery. Methods Forty-four ASA Ⅰ or Ⅱ patients aged 30-60 yr undergoing elective abdominal surgery were randomly divided into 2 groups ( n = 22 each) : control group (group K0 ) and ketamine group (group K1 ). Anesthesia was induced with propofol 2 mg/kg and fentanyl 3 μg/kg. Tracheal intubation was facilitated with cisatracurium 0.15 mg/kg. The patients were mechanically ventilated. Anesthesia was maintained with sevoflurane inhalation (the initial end-tidal concentration 3 % ). Ketamine at 14 μg· kg^-1· min^-1 was infused at the same time in group K1 . The patients' response to skin incision was described as positive if MAP or HR increased by ≥15% . If the response was positive, the end-tidal concentration of sevoflurane for the next patient was increased by 0.5%, while if negative, decreased by 0.5 % . Results The MACBAR of sevoflurane was 3.25 % (95 % confidence interval 3.05%-3.45%) in group Ko, and 2.20% (95% confidence interval 1.96%-2.44%) in group Ki. The MACBAR. of sevofiurane was significantly lower in group K, than in group K0 ( P 〈 0. 05). Conclusion Ketamine infusion at 14μg· kg^-1· min^-1 can reduce MACBAR of sevoflurane and enhance the inhibitory effect of sevoflurane on the stress response.
出处
《中华麻醉学杂志》
CAS
CSCD
北大核心
2009年第12期1073-1075,共3页
Chinese Journal of Anesthesiology
关键词
氯胺酮
麻醉药
吸入
剂量效应关系
药物
Ketamine
Anesthetics, inhalation
Dose-response relationship, drug