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口服可乐定预处理可降低丙泊酚-氧化亚氮麻醉的诱导剂量并延长苏醒时间。

Oral clonidine premedication reduces induction dose and prolongs awakening time from propofol-nitrous oxide anesthesia.

作者信息

Goyagi T, Tanaka M, Nishikawa T

机构信息

Department of Anesthesia, Akita University School of Medicine, Akita-city, Japan.

出版信息

Can J Anaesth. 1999 Sep;46(9):894-6. doi: 10.1007/BF03012982.

Abstract

PURPOSE

To evaluate whether oral clonidine premedication affects the induction dose of propofol and awakening time from epidural and propofol anesthesia.

METHODS

Thirty-nine female patients (ASA I or II) were randomly allocated to receive 5 microg x kg(-1) clonidine p.o. or no clonidine 90 min before induction of anesthesia. After epidural anesthesia was achieved with lidocaine, general anesthesia was induced with continuous i.v. infusion of propofol at a rate of 50 mg x min(-1) until loss of eyelash reflex and responses to verbal commands, which were judged by a blinded observer. After a laryngeal mask airway was inserted, anesthesia was maintained with N2O 67%, O2 33% and propofol adjusted to maintain hemodynamic stability. After completion of surgery, a blinded observer recorded the time from discontinuance of propofol and N2O until the patient was awake and responsive (awakening time), and then, the laryngeal mask airway was removed.

RESULTS

The induction dose of propofol in the clonidine group (1.4 +/- 0.3 mg) was less than that in the control group (1.9 +/- 0.4 mg, P < 0.05), while the awakening time of the clonidine group (470 +/- 145 sec) was longer than that of the control group (329 +/- 123 sec, P < 0.05).

CONCLUSION

Premedication with 5 microg x kg(-1) clonidine p.o. reduced the induction dose of propofol, but delayed emergence from propofol anesthesia.

摘要

目的

评估口服可乐定预处理是否会影响丙泊酚的诱导剂量以及硬膜外麻醉联合丙泊酚麻醉后的苏醒时间。

方法

39例美国麻醉医师协会(ASA)分级为I或II级的女性患者被随机分为两组,一组在麻醉诱导前90分钟口服5μg·kg⁻¹可乐定,另一组不服用可乐定。在使用利多卡因完成硬膜外麻醉后,以50mg·min⁻¹的速率持续静脉输注丙泊酚诱导全身麻醉,直至睫毛反射消失且对言语指令无反应,由一位不知情的观察者进行判断。插入喉罩气道后,用67%的N₂O、33%的O₂及调整剂量的丙泊酚维持麻醉,以保持血流动力学稳定。手术结束后,由一位不知情的观察者记录从停止输注丙泊酚和N₂O至患者清醒且有反应的时间(苏醒时间),然后移除喉罩气道。

结果

可乐定组丙泊酚的诱导剂量(1.4±0.3mg)低于对照组(1.9±0.4mg,P<0.05),而可乐定组的苏醒时间(470±145秒)长于对照组(329±123秒,P<0.05)。

结论

口服5μg·kg⁻¹可乐定预处理可降低丙泊酚的诱导剂量,但会延迟丙泊酚麻醉后的苏醒。

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