Discontinuation and dose adjustment of metoprolol after metoprolol-paroxetine/fluoxetine co-prescription in Dutch elderly

被引:11
作者
Bahar, Muh. Akbar [1 ,2 ]
Wang, Yuanyuan [1 ]
Bos, Jens H. J. [1 ]
Wilffert, Bob [1 ,3 ]
Hak, Eelko [1 ]
机构
[1] Univ Groningen, Groningen Res Inst Pharm, Dept PharmacoTherapy Epidemiol & Econ, Groningen, Netherlands
[2] Hasanuddin Univ, Fac Pharm, Makassar, Indonesia
[3] Univ Med Ctr Groningen, Dept Clin Pharm & Pharmacol, Groningen, Netherlands
关键词
citalopram; CYP2D6; drug-drug interactions (DDI); metoprolol; mirtazapine; paroxetine; fluoxetine; pharmacoepidemiology; DRUG-DRUG INTERACTIONS; SEROTONIN REUPTAKE INHIBITORS; HUMAN-LIVER; INTRAINDIVIDUAL VARIABILITY; CLINICAL-PHARMACOLOGY; TREATED PATIENTS; CYP2D6; GENOTYPE; PAROXETINE; FLUOXETINE; PHARMACOKINETICS;
D O I
10.1002/pds.4422
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
PurposeCo-prescription of paroxetine/fluoxetine (a strong CYP2D6 inhibitor) in metoprolol (a CYP2D6 substrate) users is common, but data on the clinical consequences of this drug-drug interaction are limited and inconclusive. Therefore, we assessed the effect of paroxetine/fluoxetine initiation on the existing treatment with metoprolol on the discontinuation and dose adjustment of metoprolol among elderly. MethodsWe performed a cohort study using the University of Groningen IADB.nl prescription database (www.IADB.nl). We selected all elderly (60years) who had ever been prescribed metoprolol and had a first co-prescription of paroxetine/fluoxetine, citalopram (weak CYP2D6 inhibitor), or mirtazapine (negative control) from 1994 to 2015. The exposure group was metoprolol and paroxetine/fluoxetine co-prescription, and the other groups acted as controls. The outcomes were early discontinuation and dose adjustment of metoprolol. Logistic regression was applied to estimate adjusted odds ratios (OR) and 95% confidence intervals (CI). ResultsCombinations of metoprolol-paroxetine/fluoxetine, metoprolol-citalopram, and metoprolol-mirtazapine were started in 528, 673, and 625 patients, respectively. Compared with metoprolol-citalopram, metoprolol-paroxetine/fluoxetine was not significantly associated with the early discontinuation and dose adjustment of metoprolol (OR=1.07, 95% CI:0.77-1.48; OR=0.87, 95% CI:0.57-1.33, respectively). In comparison with metoprolol-mirtazapine, metoprolol-paroxetine/fluoxetine was associated with a significant 43% relative increase in early discontinuation of metoprolol (OR=1.43, 95% CI:1.01-2.02) but no difference in the risk of dose adjustment. Stratified analysis by gender showed that women have a significantly high risk of metoprolol early discontinuation (OR=1.62, 95% CI:1.03-2.53). ConclusionParoxetine/fluoxetine initiation in metoprolol prescriptions, especially for female older patients, is associated with the risk of early discontinuation of metoprolol.
引用
收藏
页码:621 / 629
页数:9
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