唑类抗真菌药物在他克莫司移植患者中的安全性

D. Canales, J. Teller, F. Torre, I. G. Barrios, Jandira Ramos, Maeva Montero, Jm Ferrari Piquero
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引用次数: 0

摘要

背景与重要性他克莫司与唑类抗真菌药物的潜在相互作用常在真菌定植或感染的移植患者中检测到。目的与目的比较伏立康唑与依舒康唑对他克莫司维持血浆水平的影响并分析其安全性。材料与方法对某五级医院所有接受他克莫司免疫抑制并同时接受伏立康唑或异唑康唑治疗的2年以上患者按聚类分类进行回顾性观察研究。收集的变量包括年龄、开始联合用药后10天他克莫司的血浆水平以及整个治疗过程中与唑相关的毒性。计算他克莫司水平的标准偏差,以确定哪种抗真菌药物在血浆水平中产生更多的振荡。对于定性变量,使用绝对频率和相对频率,对于定量变量,使用中位数(IQR)。对于假设对比,根据变量的类型进行Fisher精确检验或Mann-Whitney U检验。结果纳入45例患者,其中伏立康唑23例,异舒康唑22例。伏立康唑组的中位年龄为62岁(56-67岁),而异戊康唑组的中位年龄为63岁(54-68岁)(p=0.91)。34.8% (n=8)的voriconazole患者在联合用药后10天内他克莫司浓度>20 ng/mL(毒性浓度),而isavuconazole患者的这一比例为14.3% (n=3) (p=0.1685)。伏立康唑组血药浓度的中位标准差为3.76 ng/mL(2.89 ~ 4.5),异戊康唑组为3.17 ng/mL (1.4 ~ 5) (p=0.272)。因药物浓度高及相关毒性而暂时停止他克莫司治疗的患者比例,依唑康唑组为18.2% (n=4),伏立康唑组为34.8% (n=8) (p=0.318)。在治疗耐受性方面,28.57%的患者使用异戊康唑治疗后出现与唑相关的不良反应,而伏立康唑治疗后出现与唑相关的不良反应的比例为82.6% (p)。结论及相关性异戊康唑治疗后他克莫司中毒发生率较低,但差异无统计学意义。此外,用异戊康唑治疗更安全,副作用更少,不需要停药。参考文献和/或致谢利益冲突无利益冲突
本文章由计算机程序翻译,如有差异,请以英文原文为准。
5PSQ-142 Safety of azole antifungals in transplanted patients receiving tacrolimus
Background and importance Potential interaction between tacrolimus and azole antifungals is often detected in transplanted patients with fungal colonisation or infection. Aim and objectives To compare the influence of voriconazole and isavuconazole on maintenance of plasma levels of tacrolimus and to analyse their safety. Material and methods A retrospective observational study was conducted according to cluster classification in all patients immunosuppressed with tacrolimus and receiving concomitant treatment with voriconazole or isavuconazole over a 2 year period in a class 5 hospital. The variables collected included age, plasma levels of tacrolimus for 10 days after the start of the combination, and toxicity associated with azole throughout treatment with it. The standard deviation of tacrolimus levels was calculated to determine which of the antifungals had generated more oscillation in plasma levels. For qualitative variables, absolute and relative frequencies were obtained, and for quantitative variables, the median (IQR) were used. For hypothesis contrast, Fisher’s exact test or the Mann–Whitney U test was performed according to the type of variable. Results 45 patients were included, 23 received voriconazole and 22 isavuconazole. Median age was 62 years (56–67) for those receiving voriconazole versus 63 years (54–68) for those receiving isavuconazole (p=0.91). 34.8% (n=8) of patients treated with voriconazole achieved concentrations of tacrolimus >20 ng/mL (toxic concentration) within 10 days from the start of the combination compared with 14.3% (n=3) of patients treated with isavuconazole (p=0.1685). The median standard deviation of plasma concentrations was 3.76 ng/mL (2.89–4.5) with voriconazole versus 3.17 ng/mL (1.4–5) with isavuconazole (p=0.272). The proportion of patients who temporarily discontinued tacrolimus treatment due to high level concentrations and associated toxicity was 18.2% (n=4) with isavuconazole versus 34.8% (n=8) with voriconazole (p=0.318). Regarding tolerance to treatment, 28.57% of patients treated with isavuconazole had side effects associated with azole, compared with 82.6% of those treated with voriconazole (p Conclusion and relevance Treatment with isavuconazole resulted in fewer tacrolimus poisonings, although the difference was not statistically significant. In addition, treatment with isavuconazole was found to be safer, had fewer side effects and did not require antifungal discontinuation. References and/or acknowledgements Conflict of interest No conflict of interest
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