Steiner C, Steurer M P, Mueller D, Zueger M, Dullenkopf A
Department of Anesthesia and Intensive Care, Kantonsspital Frauenfeld, Postfach Pfaffenholzstr. 4, 8501, Zurich, Switzerland.
Department of Anesthesia and Perioperative Care, University of California, San Francisco, USA.
BMC Anesthesiol. 2016 Oct 24;16(1):105. doi: 10.1186/s12871-016-0262-6.
Midazolam is commonly used as a pre-anesthesia anxiolytic. It`s elimination may not be fast enough for short procedures. In orally premedicated patients we obtained midazolam plasma concentrations at the end of surgical procedures and compared those to concentrations at anesthesia induction.
The study was conducted prospectively with consent of the local ethics committee (Ethikkomission Kanton Thurgau, Switzerland) and carried out with written informed consent of each patient. Female patients aged 20 to 60 years undergoing elective procedures with general anesthesia were included, and were divided in two groups according to the planned surgical time: group S (<30 min) and group L (90-120 min), respectively. All patients received 7.5 mg Midazolam po as premedication. Blood samples were drawn at anesthesia induction, and at the end of surgery. Data were compared with t-test (independent samples; significance level p <0.05).
Twenty-five patients per group were included. Four patients were excluded from analysis, since midazolam was not detectable in any samples. Time of premedication to the 1st blood sample was not statistically different between groups, neither were Midazolam plasma levels at this time point (p = 0.94). None of the patients from group L (n = 24), but five patients in group S (n = 22) did have a higher plasma level of Midazolam at the end of the case compared to the beginning.
The elimination half-life of oral Midazolam can lead to higher plasma levels at the end of a short procedure compared to those at induction of anesthesia.
German Clinical Trials Register (Deutsches Register Klinischer Studien), DRKS00005429 ; date of registration 3 January 2014.
咪达唑仑常用作麻醉前的抗焦虑药。对于短时间手术,其消除速度可能不够快。在口服术前用药的患者中,我们在手术结束时获取了咪达唑仑的血浆浓度,并将其与麻醉诱导时的浓度进行比较。
本研究经当地伦理委员会(瑞士图尔高州伦理委员会)批准后前瞻性开展,并获得每位患者的书面知情同意。纳入年龄在20至60岁之间接受全身麻醉择期手术的女性患者,根据计划的手术时间分为两组:S组(<30分钟)和L组(90 - 120分钟)。所有患者口服7.5毫克咪达唑仑作为术前用药。在麻醉诱导时和手术结束时采集血样。数据采用t检验进行比较(独立样本;显著性水平p <0.05)。
每组纳入25例患者。4例患者被排除在分析之外,因为在任何样本中均未检测到咪达唑仑。两组从术前用药到首次采血的时间无统计学差异,此时咪达唑仑的血浆水平也无差异(p = 0.94)。与开始时相比,L组(n = 24)的患者在手术结束时均未出现咪达唑仑血浆水平升高,但S组(n = 22)有五例患者出现这种情况。
与麻醉诱导时相比,口服咪达唑仑的消除半衰期可能导致短时间手术结束时血浆水平升高。
德国临床试验注册中心(Deutsches Register Klinischer Studien),DRKS00005429;注册日期2014年1月3日。