停用伏立康唑后伏立康唑对肾移植受者他克莫司血药浓度的影响

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Lijuan Feng, Guiyi Liao, Hui Liu, Yihou Luo, Chunlan Yang, Yan Du, Dujuan Xu, Su Yong
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引用次数: 0

摘要

已知信息和目标。伏立康唑(VRC)会增加他克莫司(TAC)的血药浓度。然而,VRC 停药后 TAC 谷浓度(TAC C0)的变化规律和剂量调整方案尚未见报道。我们旨在探讨停用 VRC 后 TAC C0 的变化规律,并为肾移植受者的 TAC 剂量调整和血药浓度监测提供策略。方法回顾性记录了46例肾移植患者服用VRC前、服用VRC期间以及停用VRC期间的临床数据,包括TAC和VRC的剂量和血药浓度0、肝肾功能等生化指标以及CYP3A5、CYP3A4和CYP2C19基因类型。结果与讨论。停用 VRC 2-4 天后,虽然 TAC C0 和 TAC 剂量调整后谷浓度(C/D)分别比停用 VRC 前高 2.43 倍和 3.35 倍,但 81% 的患者恢复了最初的 TAC 剂量。5-7 天后,TAC C0 和 C/D 逐渐恢复。当 VRC 谷浓度(VRC C0)大于 2.43 mg/L 时,停用 VRC 后 TAC C/D 明显升高;CYP3A5、CYP3A4 和 CYP2C19 基因型以及服用红霉素不会影响 TAC C/D 的变化。新内容和结论。与服用 VRC 前相比,停用 VRC 2-4 天后 TAC C/D 仍会升高,停用 VRC 5-7 天后可观察到 TAC C/D 逐渐恢复。为避免血液中 TAC C0 过高,停用 VRC 2-4 天后不应立即恢复初始 TAC 剂量。VRC C0 是影响停用 VRC 后 TAC C/D 比率变化的关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Voriconazole on Tacrolimus Blood Concentration in Renal Transplant Recipients after Voriconazole Discontinuation

What is Known and Objective. Voriconazole (VRC) increases the blood concentration of Tacrolimus (TAC). However, the patterns of changes in TAC trough concentration (TAC C0) and dose-adjustment regimens after VRC discontinuation have not been reported. We aimed to explore the changing pattern of TAC C0 after VRC discontinuation and provide strategies for TAC dose adjustment and blood concentration monitoring in renal transplant recipients. Methods. The clinical data of 46 renal transplant patients pre- and during VRC medication and VRC discontinuation were retrospectively recorded, including doses and concentrations 0 of TAC and VRC; biochemical indicators such as liver and kidney function; and CYP3A5, CYP3A4, and CYP2C19 gene types. Results and Discussion. After discontinuing VRC for 2–4 days, 81% of the patients returned to their initial TAC dose, although TAC C0 and TAC dose-adjusted trough concentration (C/D) were 2.43-fold and 3.35-fold higher, respectively, than pre-VRC administration. After 5–7 days, TAC C0 and C/D gradually recovered. TAC C/D was significantly higher after VRC discontinuation when the VRC trough concentration (VRC C0) was greater than 2.43 mg/L; CYP3A5, CYP3A4, and CYP2C19 genotypes and the administration of erythromycin did not affect the change in TAC C/D. What is New and Conclusion. TAC C/D remains elevated 2–4 days after discontinuing VRC compared to pre-VRC administration, with gradual recovery observed 5–7 days after VRC discontinuation. To avoid excessive blood TAC C0 , the initial TAC dose should not be immediately reinstated upon VRC discontinuation for 2–4 days. VRC C0 are a critical factor influencing the change in TAC C/D ratio after VRC discontinuation.

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来源期刊
CiteScore
4.10
自引率
5.00%
发文量
226
审稿时长
6 months
期刊介绍: The Journal of Clinical Pharmacy and Therapeutics provides a forum for clinicians, pharmacists and pharmacologists to explore and report on issues of common interest. Reports and commentaries on current issues in medical and pharmaceutical practice are encouraged. Papers on evidence-based clinical practice and multidisciplinary collaborative work are particularly welcome. Regular sections in the journal include: editorials, commentaries, reviews (including systematic overviews and meta-analyses), original research and reports, and book reviews. Its scope embraces all aspects of clinical drug development and therapeutics, including: Rational therapeutics Evidence-based practice Safety, cost-effectiveness and clinical efficacy of drugs Drug interactions Clinical impact of drug formulations Pharmacogenetics Personalised, stratified and translational medicine Clinical pharmacokinetics.
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