Does cytochrome 2D6 genotype affect the analgesic efficacy of codeine after ambulatory surgery? Prospective trial in 987 adults.

IF 1.9 4区 医学 Q2 ANESTHESIOLOGY Acta Anaesthesiologica Scandinavica Pub Date : 2025-01-01 DOI:10.1111/aas.14549
Satu Poikola, Hanna von Plato, Jukka Harju, Johanna I Kiiski, Kristiina Mattila, Klaus T Olkkola, Mikko Niemi, Eija Kalso, Vesa Kontinen
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Abstract

Background: Paracetamol-codeine combination tablet is widely used in pain management after day surgery. For safety reasons, its use has decreased in recent years. Codeine is a prodrug metabolised in the liver by the cytochrome P450 2D6 (CYP2D6) enzyme to morphine that produces the analgesic effect of codeine. CYP2D6 is highly polymorphic, and based on genotypes, individuals can be divided into four categories: poor-, intermediate-, normal- and ultrarapid metabolisers. Differences in morphine and its metabolite concentrations have been described between different CYP2D6 genotypes following codeine administration. The aim of the study was to investigate the possible effect of CYP2D6 genotype on codeine efficacy and adverse effects in a large cohort of adult patients undergoing ambulatory surgery.

Methods: A total of 987 patients scheduled for ambulatory surgery were included in the analyses. Operation types or anaesthesia methods were not limited in the study protocol. All study patients received a fixed dose of paracetamol (1000 mg) and codeine (60 mg) orally for premedication. A blood sample was drawn to identify the genotype of CYP2D6. At home, the first-line analgesic was paracetamol-codeine combination of 1-2 tablets at 1-3 times per day. Data on the efficacy and side effects of codeine were collected on the day of surgery and the following two postoperative days.

Results: Of the studied patients, 37 (3.7%) were poor CYP2D6 metabolisers, 264 (27%) were intermediate, 623 (63%) were normal and 63 (6.4%) were ultrarapid metabolisers. Activity scores ranged from 0 to 4. CYP2D6 genotype was not associated in a statistically significant manner with postoperative pain, opioid consumption or the adverse effects of codeine, except for constipation at home. Poor CYP2D6 metabolisers reported significantly less severe constipation compared with normal metabolisers (p = .009, OR 0.40, 95% Cl 0.20-0.80).

Conclusion: CYP2D6 genotype appears to be of minor importance for the analgesic efficacy of oral paracetamol-codeine combination therapy after ambulatory surgery in adult patients undergoing similar types of surgery as in the present study but it may affect the risk of constipation.

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细胞色素 2D6 基因型会影响可待因在非卧床手术后的镇痛效果吗?在 987 名成人中进行的前瞻性试验。
背景:扑热息痛-可待因复方片剂广泛用于日间手术后的疼痛治疗。出于安全考虑,近年来其使用量有所下降。可待因是一种原药,在肝脏中通过细胞色素 P450 2D6 (CYP2D6)酶代谢为吗啡,从而产生可待因的镇痛效果。CYP2D6 具有高度多态性,根据基因型可将个体分为四类:低代谢、中等代谢、正常代谢和超快速代谢。不同 CYP2D6 基因型的人在服用可待因后吗啡及其代谢物的浓度存在差异。本研究的目的是在一大批接受非卧床手术的成年患者中调查 CYP2D6 基因型对可待因疗效和不良反应的可能影响:共有 987 名计划接受门诊手术的患者参与了分析。研究方案不限制手术类型或麻醉方法。所有研究对象均口服固定剂量的扑热息痛(1000 毫克)和可待因(60 毫克)作为术前用药。抽取血液样本以确定 CYP2D6 基因型。在家中,一线镇痛药为扑热息痛-可待因复方制剂,每天 1-3 次,每次 1-2 片。收集了手术当天和术后两天可待因的疗效和副作用数据:在研究的患者中,37 人(3.7%)为 CYP2D6 代谢不良者,264 人(27%)为中等代谢者,623 人(63%)为正常代谢者,63 人(6.4%)为超快速代谢者。CYP2D6 基因型与术后疼痛、阿片类药物用量或可待因的不良反应(除在家便秘外)无统计学意义。与正常代谢者相比,CYP2D6代谢不良者报告的便秘严重程度明显较低(P = .009,OR 0.40,95% Cl 0.20-0.80):CYP2D6基因型对于接受与本研究类似类型手术的成人患者在门诊手术后口服扑热息痛-可待因联合疗法的镇痛效果似乎并不重要,但可能会影响便秘的风险。
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来源期刊
CiteScore
4.30
自引率
9.50%
发文量
157
审稿时长
3-8 weeks
期刊介绍: Acta Anaesthesiologica Scandinavica publishes papers on original work in the fields of anaesthesiology, intensive care, pain, emergency medicine, and subjects related to their basic sciences, on condition that they are contributed exclusively to this Journal. Case reports and short communications may be considered for publication if of particular interest; also letters to the Editor, especially if related to already published material. The editorial board is free to discuss the publication of reviews on current topics, the choice of which, however, is the prerogative of the board. Every effort will be made by the Editors and selected experts to expedite a critical review of manuscripts in order to ensure rapid publication of papers of a high scientific standard.
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