Unit of Clinical Pharmacology, Department of Biomedical and Clinical Sciences L. Sacco, "Luigi Sacco" University Hospital, Università di Milano, Via GB Grassi 74, 20157, Milan, Italy.
Scientific Institute IRCCS Eugenio Medea, 23842 Bosisio Parini, Lecco, Italy.
Clin Pharmacokinet. 2019 Jul;58(7):875-886. doi: 10.1007/s40262-018-0720-z.
Qualitative studies on drug-drug interactions (DDIs) between anticonvulsants and antibiotics report pharmacokinetic changes that may increase the clinical risks in terms of adverse drug reactions (ADRs) and efficacy. However, no studies have provided a systematic and quantitative analysis of anticonvulsant-antibiotic pharmacokinetic DDIs. To provide such indications, we systematically and critically reviewed the literature on anticonvulsant-antibiotic DDIs in terms of quantitative pharmacokinetic changes and related ADRs. We also investigated less-known interactions for the possible occurrence of clinically relevant events.
We conducted a systematic review of all reports of DDIs between anticonvulsants and antibiotics assessing pharmacokinetic parameters published until 9 June 2017.
We were able to meta-analyse the effect of macrolides on carbamazepine area under the concentration-time curve from time zero to infinity [AUC] (+ 34.5 µg/mL*h, p = 0.005, n = 38), clearance (- 2.88 mL/min, p < 0.001, n = 46) and trough plasma concentration [Ct] (+ 8.0 µg/mL, p = 0.002, n = 23), and of carbapenems on valproic acid Ct (- 42.9 µg/mL, p < 0.001, n = 262). Pharmacokinetic parameters with other DDIs were insufficiently reported to allow a statistical analysis.
Therapeutic drug monitoring in patients receiving long-term antiepileptic therapies may help, in specific conditions, to improve safety while preserving efficacy. Such a procedure would also increase scientific information on how pharmacokinetic variations are associated with ADR occurrence, and possibly epileptological outcomes for those DDIs for which available information is suggestive of a relevant effect but is not yet sufficient to draw conclusions.
关于抗癫痫药物与抗生素之间药物-药物相互作用(DDI)的定性研究报告了药代动力学的变化,这些变化可能会增加不良反应(ADR)和疗效方面的临床风险。然而,尚无研究对抗癫痫药物-抗生素药代动力学 DDI 进行系统和定量分析。为了提供这些指示,我们系统地和批判性地审查了关于抗癫痫药物与抗生素之间 DDI 的文献,评估了药代动力学参数的定量变化和相关的 ADR。我们还研究了不太为人知的相互作用,以确定可能发生的临床相关事件。
我们对截至 2017 年 6 月 9 日发表的所有关于抗癫痫药物与抗生素之间 DDI 的报告进行了系统综述,评估了药代动力学参数。
我们能够对大环内酯类药物对卡马西平的药代动力学参数进行荟萃分析,包括 AUC(+ 34.5 µg/mL*h,p = 0.005,n = 38)、清除率(-2.88 mL/min,p < 0.001,n = 46)和谷浓度 [Ct](+ 8.0 µg/mL,p = 0.002,n = 23),以及碳青霉烯类药物对丙戊酸的 Ct(-42.9 µg/mL,p < 0.001,n = 262)。其他 DDI 的药代动力学参数报告不足,无法进行统计分析。
在接受长期抗癫痫治疗的患者中进行治疗药物监测可能有助于在特定情况下提高安全性,同时保持疗效。这种方法还将增加关于药代动力学变化与 ADR 发生之间关联的科学信息,对于那些可用信息提示存在相关影响但还不足以得出结论的 DDI 也是如此。