Van Daele Ruth, Wauters Joost, De Cock Pieter, Buyle Franky, Leys John, Van Brantegem Pieter, Gijsen Matthias, Annaert Pieter, Debaveye Yves, Lagrou Katrien, Peetermans Willy E, Brüggemann Roger J, Spriet Isabel
Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, 3000 Leuven, Belgium.
Pharmacy Department, University Hospitals Leuven, 3000 Leuven, Belgium.
Antibiotics (Basel). 2021 Sep 15;10(9):1112. doi: 10.3390/antibiotics10091112.
Voriconazole is an antifungal drug used as one of the first-line treatments for invasive aspergillosis. This drug is extensively metabolized, predominantly via cytochrome P450 enzymes. An interaction between flucloxacillin and voriconazole, leading to subtherapeutic voriconazole concentrations, has previously been reported. We aimed to demonstrate that flucloxacillin independently influences voriconazole exposure.
Patients from three Belgian hospitals, treated with a combination of voriconazole and flucloxacillin, were included in this retrospective study. Voriconazole concentrations were collected both in a timeframe with and without flucloxacillin co-treatment. Multivariate analyses were performed to study the independent effect of flucloxacillin treatment on voriconazole exposure and the possible influence of the flucloxacillin dose.
Thirty-three patients were included in this study and 145 trough concentrations (51 with, and 94 without concomitant flucloxacillin treatment) were analyzed. The median (IQR) voriconazole trough concentration sampled during flucloxacillin co-treatment was 0.5 (0-1.8) mg/L, whereas samples without flucloxacillin co-treatment had a median (IQR) voriconazole trough concentration of 3.5 (1.7-5.1) mg/L ( = 0.002), while receiving similar voriconazole doses. Subtherapeutic concentrations (<1 mg/L) were observed in 69% and 7% of the samples with flucloxacillin co-treatment versus samples without flucloxacillin co-treatment, respectively.
This study shows that flucloxacillin co-treatment independently decreases voriconazole exposure. Caution is needed when these two drugs are administered simultaneously.
伏立康唑是一种抗真菌药物,用作侵袭性曲霉病的一线治疗药物之一。该药物主要通过细胞色素P450酶进行广泛代谢。此前曾报道氟氯西林与伏立康唑之间存在相互作用,导致伏立康唑浓度低于治疗水平。我们旨在证明氟氯西林会独立影响伏立康唑的暴露量。
本回顾性研究纳入了比利时三家医院中接受伏立康唑和氟氯西林联合治疗的患者。收集了同时使用和未使用氟氯西林联合治疗期间的伏立康唑浓度。进行多变量分析以研究氟氯西林治疗对伏立康唑暴露量的独立影响以及氟氯西林剂量的可能影响。
本研究纳入了33例患者,分析了145个谷浓度(51个为同时使用氟氯西林治疗时的,94个为未同时使用氟氯西林治疗时的)。在同时使用氟氯西林治疗期间采集的伏立康唑谷浓度中位数(IQR)为0.5(0 - 1.8)mg/L,而未同时使用氟氯西林治疗时的样本中伏立康唑谷浓度中位数(IQR)为3.5(1.7 - 5.1)mg/L(P = 0.002),且伏立康唑剂量相似。与未同时使用氟氯西林治疗的样本相比,同时使用氟氯西林治疗的样本中分别有69%和7%观察到低于治疗水平的浓度(<1 mg/L)。
本研究表明,联合使用氟氯西林会独立降低伏立康唑的暴露量。同时使用这两种药物时需要谨慎。