Suspected propofol infusion syndrome during normal targeted propofol concentration

被引:0
作者
Taku Ichikawa
Keiko Okuyama
Kotoe Kamata
Kenichi Masui
Makoto Ozaki
机构
[1] Tokyo Women’s Medical University,Department of Anesthesiology
[2] Tohoku University School of Medicine,Department of Anesthesiology and Perioperative Medicine
[3] Showa University School of Medicine,Department of Anesthesiology
来源
Journal of Anesthesia | 2020年 / 34卷
关键词
Propofol; Anesthesia; Plasma concentration; Propofol infusion syndrome;
D O I
暂无
中图分类号
学科分类号
摘要
To this day, the pathophysiology and risk factors of propofol infusion syndrome (PRIS) remain unknown. Moreover, there is no widely accepted definition of PRIS, even though it is a potentially fatal condition. While many suspected cases of PRIS have been reported in both pediatric and adult populations, the actual propofol plasma concentration (Cp) has never been clarified. In this clinical report, we described the first suspected PRIS case in which the propofol Cp was measured 25 min after 226 min of propofol infusion (7.2 µg/mL), which was 12 times higher than the predicted value (0.6 µg/mL). In the presented case, we observed gradually progressive uncontrollable hypercapnia and tachycardia, followed by severe lactic acidosis during surgical anesthesia based on the target-controlled infusion of propofol. Levels of liver enzymes were slightly elevated which suggests little or no liver damage though propofol is mainly metabolized by the liver. Meanwhile, renal impairment, a common secondary feature of PRIS, occurred concomitantly when hypercapnia and metabolic acidosis were manifested. In this case, low or delayed propofol clearance might have been a triggering factor causing severe lactic acidosis.
引用
收藏
页码:619 / 623
页数:4
相关论文
共 97 条
  • [1] Bray RJ(1998)Propofol infusion syndrome in children Paediatr Anaesth 8 491-499
  • [2] Sumi C(2018)Propofol induces a metabolic switch to glycolysis and cell death in a mitochondrial electron transport chain-dependent manner PLoS ONE 15 e0192796-e94
  • [3] Okamoto A(2018)Propofol related infusion syndrome: ultrastructural evidence for a mitochondrial disorder Crit Care Med 46 e91-607
  • [4] Tanaka H(2001)Impaired fatty acid oxidation in propofol infusion syndrome Lancet 357 606-459
  • [5] Nishi K(2019)Propofol infusion syndrome: a structured literature review and analysis of published case reports Br J Anaesth 122 448-817
  • [6] Kusunoki M(2009)Early phase pharmacokinetics but not pharmacodynamics are influenced by propofol infusion rate Anesthesiology 111 805-48
  • [7] Shoji T(1991)Pharmacokinetic model driven infusion of propofol in children Br J Anaesth 67 41-150
  • [8] Uba T(1988)Pharmacokinetics of Propofol (diprivan) in elderly patients Br J Anaesth 60 146-665
  • [9] Matsuo Y(1993)Propofol infusion for maintenance of anesthesia in morbidity obese patients receiving nitrous oxide Anesthesiology 78 657-379
  • [10] Adachi T(2010)The performance of compartmental and physiologically based recirculatory pharmacokinetic models for Propofol: a comparison using bolus, continuous, and target-controlled infusion data Anesth Analg 111 368-255