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细胞色素P450 2D6(CYP2D6)介导的药物相互作用(DDI)的负担与管理:老年人中美托洛尔与帕罗西汀或氟西汀的联合用药

The burden and management of cytochrome P450 2D6 (CYP2D6)-mediated drug-drug interaction (DDI): co-medication of metoprolol and paroxetine or fluoxetine in the elderly.

作者信息

Bahar Muh Akbar, Hak Eelko, Bos Jens H J, Borgsteede Sander D, Wilffert Bob

机构信息

University of Groningen, Groningen Research Institute of Pharmacy, Department of PharmacoTherapy, -Epidemiology & -Economics, Groningen, The Netherlands.

Hasanuddin University, Faculty of Pharmacy, Makassar, Indonesia.

出版信息

Pharmacoepidemiol Drug Saf. 2017 Jul;26(7):752-765. doi: 10.1002/pds.4200. Epub 2017 Mar 26.

Abstract

PURPOSE

Metoprolol and paroxetine/fluoxetine are inevitably co-prescribed because cardiovascular disorders and depression often coexist in the elderly. This leads to CYP2D6-mediated drug-drug interactions (DDI). Because systematic evaluations are lacking, we assessed the burden of metoprolol-paroxetine/fluoxetine interaction in the elderly and how these interactions are managed in Dutch community pharmacies.

METHOD

Dispensing data were collected from the University of Groningen pharmacy database (IADB.nl, 1999-2014) for elderly patients (≥60 years) starting beta-blockers and/or antidepressants. Based on the two main DDI alert systems (G-Standard and Pharmabase), incidences were divided between signalled (metoprolol-fluoxetine/paroxetine) and not-signalled (metoprolol-alternative antidepressants and alternative beta-blockers-paroxetine/fluoxetine) combinations. Incident users were defined as patients starting at least one signalled or a non-signalled combination. G-Standard signalled throughout the study period, whereas Pharmabase stopped after 2005.

RESULTS

A total of 1763 patients had 2039 metoprolol-paroxetine/fluoxetine co-prescriptions, despite DDI alert systems, and about 57.3% were signalled. The number of metoprolol-alternative antidepressant combinations (incidences = 3150) was higher than alternative beta-blocker-paroxetine/fluoxetine combinations (incidences = 1872). Metoprolol users are more likely to be co-medicated with an alternative antidepressant (incidences = 2320) than paroxetine/fluoxetine users (incidences = 1232) are. The number of paroxetine/fluoxetine users co-prescribed with alternative beta-blockers was comparable to those co-medicated with metoprolol (about 50%). Less than 5% of patients received a substitute therapy after using metoprolol-paroxetine/fluoxetine. Most of the metoprolol users (90%) received a low dose (mean DDD = 0.47) regardless whether they were prescribed paroxetine/fluoxetine.

CONCLUSION

Despite the signalling software, metoprolol-paroxetine/fluoxetine combinations are still observed in the elderly population. The clinical impact of these interactions needs further investigation. Copyright © 2017 John Wiley & Sons, Ltd.

摘要

目的

美托洛尔与帕罗西汀/氟西汀不可避免地会联合处方,因为心血管疾病和抑郁症在老年人中常常并存。这会导致细胞色素P450 2D6(CYP2D6)介导的药物相互作用(DDI)。由于缺乏系统性评估,我们评估了老年人中美托洛尔 - 帕罗西汀/氟西汀相互作用的负担,以及荷兰社区药房如何处理这些相互作用。

方法

从格罗宁根大学药房数据库(IADB.nl,1999 - 2014年)收集≥60岁开始使用β受体阻滞剂和/或抗抑郁药的老年患者的配药数据。基于两个主要的药物相互作用警示系统(G - 标准和Pharmabase),将发生率分为有警示(美托洛尔 - 氟西汀/帕罗西汀)和无警示(美托洛尔 - 其他抗抑郁药以及其他β受体阻滞剂 - 帕罗西汀/氟西汀)组合。发生用药情况的患者定义为开始使用至少一种有警示或无警示组合的患者。G - 标准在整个研究期间都有警示,而Pharmabase在2005年后停止。

结果

尽管有药物相互作用警示系统,仍有1763名患者存在2039次美托洛尔 - 帕罗西汀/氟西汀联合处方,其中约57.3%有警示。美托洛尔与其他抗抑郁药的组合数量(发生率 = 3150)高于其他β受体阻滞剂与帕罗西汀/氟西汀的组合数量(发生率 = 1872)。美托洛尔使用者比帕罗西汀/氟西汀使用者更有可能同时使用其他抗抑郁药(发生率 = 2320)。与其他β受体阻滞剂联合处方帕罗西汀/氟西汀的使用者数量与与美托洛尔联合用药的使用者数量相当(约50%)。使用美托洛尔 - 帕罗西汀/氟西汀后,不到5%的患者接受了替代疗法。大多数美托洛尔使用者(90%)接受低剂量治疗(平均限定日剂量 = 0.47),无论他们是否同时使用帕罗西汀/氟西汀。

结论

尽管有警示软件,老年人中仍可观察到美托洛尔 - 帕罗西汀/氟西汀组合。这些相互作用的临床影响需要进一步研究。版权所有© 2017约翰威立父子有限公司。

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