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Potential Cytochrome P450 Drug-Drug Interaction Among Adult and Adolescent Patients Undergoing Tonsillectomy

机译:潜在的细胞色素P450成人和青少年患者中的药物 - 药物相互作用术治疗术

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Objective. To assess the frequency of potential drug-drug interactions affecting cytochrome P450 (CYP)–mediated metabolism of opioids among adult and adolescent patients who underwent adenotonsillectomy. Study Design. Retrospective chart review. Setting. Tertiary care university hospital. Patients and Methods. A retrospective review was conducted of 279 patients who underwent adenotonsillectomy at the University of Rochester. The discharge medication list was reviewed for all patients, and their postoperative medications were compared with a reference list published by the Food and Drug Administration and the University of Indiana’s Department of Clinical Pharmacology (Flockhart Table) to determine whether CYP-inducing or CYP-inhibiting medication was present. Results. Out of 279 patients, 197 different medications were taken postoperatively. Approximately 70% of patients were taking 2 medications in addition to the standard postoperative analgesics (acetaminophen, hydrocodone, oxycodone, morphine, and/or ibuprofen). The 5 most commonly prescribed medications excluding the posttonsillectomy medications were oral contraceptives, ondansetron, amoxicillin, albuterol, and methylprednisolone. Four percent of patients were taking a medication that inhibits CYP3A4; 1% were taking a medication that induces CYP3A4; and 15% were taking a medication that inhibits CYP2D6. Conclusions. Nearly 20% of the patients in this cohort were taking a medication that may alter opioid metabolism through induction or inhibition of CYP3A4 or CYP2D6. Some of these interactions have the potential to be more clinically relevant than others, particularly interactions that can lead to enhanced toxicity of opioids due to accumulation of active metabolites.
机译:客观的。评估影响细胞色素P450(CYP)的潜在药物 - 药物相互作用的频率,所述细胞色素P450(CYP)介绍的成人和青春期患者患者的阿片类药物的代谢。学习规划。回顾性图表评论。环境。第三大学医院。患者和方法。在罗切斯特大学进行了腺体肿瘤切除术的279名患者进行了回顾性评论。对所有患者进行审查的排放药物清单,并将其术后药物与食品药品和药物管理局和印第安纳州临床药理学大学(Flockhart Table)发表的参考名单进行比较,以确定类别诱导或CYP抑制吗?药物存在。结果。在279例患者中,术后197例不同的药物。除标准术后镇痛药(对乙酰氨基酚,氢酮,羟考酮,吗啡和/或布洛芬)之外,大约70%的患者服用了2种药物。除了PostoilleFoymy药物中的5种最常见的药物是口服避孕药,ondansetron,阿莫西林,氨基甲酸酚和甲基己酮醇。 4%的患者服用抑制CYP3A4的药物; 1%正在服用诱导CYP3A4的药物; 15%的药物服用抑制CYP2D6的药物。结论。该队列的近20%的患者正在服用可能通过诱导或抑制CYP3A4或CYP2D6来改变阿片类药物的药物。其中一些相互作用具有比其他相互作用更依然相关,特别是相互作用,这可能导致阿片类药物的毒性因活性代谢物的积累而导致阿片类药物的毒性。

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