Rodieux Frédérique, Storelli Flavia, Curtin François, Manzano Sergio, Gervaix Alain, Posfay-Barbe Klara M, Desmeules Jules, Daali Youssef, Samer Caroline F
Division of Clinical Pharmacology and Toxicology, Department of Anesthesiology, Pharmacology, Intensive Care and Emergency Medicine, Geneva University Hospitals, University of Geneva, Rue Gabrielle-Perret-Gentil 4, 1205 Geneva, Switzerland.
Faculty of Medicine, University of Geneva, 1205 Geneva, Switzerland.
Pharmaceuticals (Basel). 2023 Aug 30;16(9):1227. doi: 10.3390/ph16091227.
Following the contraindication of codeine use in children, increasing use of tramadol has been observed in pain management protocols. However, tramadol's pharmacokinetics (PK) and pharmacodynamics are influenced by cytochrome P450 (CYP)2D6 activity, similarly to codeine. Previous studies in adults have demonstrated a correlation between pupillary response and tramadol PK. Our objective was to evaluate pupillometry as a phenotyping method to assess CYP2D6 activity in children treated with tramadol. We included 41 children (mean age 11 years) receiving a first dose of tramadol (2 mg/kg) in the emergency room (ER) as part of their routine care. CYP2D6 phenotyping and genotyping were performed. The concentrations of tramadol and its active metabolite, M1, were measured, and static and dynamic pupillometry was conducted using a handheld pupillometer at the time of tramadol administration and during the ER stay. Pupillometric measurements were obtained for 37 children. Tramadol affected pupillary parameters, with a decrease in pupil diameter in 83.8% of children ( = 0.002) (mean decrease 14.1 ± 16.7%) and a decrease in reflex amplitude constriction in 78.4% ( = 0.011) (mean decrease 17.7 ± 34.5%) at T150 compared to T0. We were unable to identify a correlation between pupillometry measurements and CYP2D6 activity. Likely confounding factors include light intensity, pain, and stress, making the procedure less feasible in paediatric emergency settings.
在儿童禁用可待因之后,疼痛管理方案中曲马多的使用量不断增加。然而,与可待因类似,曲马多的药代动力学(PK)和药效动力学受细胞色素P450(CYP)2D6活性的影响。此前针对成人的研究已证明瞳孔反应与曲马多PK之间存在关联。我们的目的是评估瞳孔测量法作为一种表型分析方法,以评估接受曲马多治疗的儿童的CYP2D6活性。我们纳入了41名儿童(平均年龄11岁),他们在急诊室(ER)接受首剂曲马多(2mg/kg)治疗,这是其常规治疗的一部分。进行了CYP2D6表型分析和基因分型。测量了曲马多及其活性代谢物M1的浓度,并在给予曲马多时以及在急诊室停留期间使用手持式瞳孔计进行了静态和动态瞳孔测量。对37名儿童进行了瞳孔测量。曲马多影响瞳孔参数,与T0相比,83.8%的儿童瞳孔直径减小(P = 0.002)(平均减小14.1±16.7%),78.4%的儿童反射性缩瞳幅度减小(P = 0.011)(平均减小17.7±34.5%),在T150时。我们未能确定瞳孔测量结果与CYP2D6活性之间的相关性。可能的混杂因素包括光照强度、疼痛和压力,这使得该方法在儿科急诊环境中不太可行。