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Retrospective Analysis of Methotrexate Elimination When Coadministered With Levetiracetam

机译:与左乙拉西坦联合应用甲氨蝶呤消除的回顾性分析

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摘要

Background: Delayed elimination of methotrexate was previously reported in 2 patients receiving concomitant levetiracetam. Objective: To explore the potential interaction between methotrexate and levetiracetam in patients receiving high-dose methotrexate. Methods: This retrospective study reviewed the records of 81 adults receiving 280 cycles of methotrexate to determine the effects of levetiracetam on methotrexate elimination. Institutional review board approval was obtained. Results: Levetiracetam was administered in 33 (12%) cycles of methotrexate. Patients receiving levetiracetam had significantly lower 24-hour methotrexate concentrations compared with those not receiving levetiracetam (2.91 vs 7.37 µmol/L, P = 0.005). Despite this difference, concentrations at 48 and 72 hours were similar between groups. Times to nontoxic methotrexate concentration (u3c0.1 µmol/L) were the same regardless of the presence of levetiracetam. The frequency of delayed elimination at 24, 48, and 72 hours was similar in both groups as was the frequency of delayed elimination at any time point. Cox regression demonstrated that levetiracetam was not a significant predictor of time to nontoxic methotrexate concentration (P = 0.796; HR = 1.058; 95% CI = 0.692-1.617), and logistic regression demonstrated that levetiracetam was not a significant predictor of delayed elimination at any time point. Levetiracetam use was similar between groups when comparing patients experiencing delayed elimination at any time point with those without delayed elimination (13% vs 10%, respectively, P = 0.527). Conclusion: This study does not support the previous reports of a significant interaction between levetiracetam and methotrexate. A clinically significant interaction is unlikely in those without additional risk factors for delayed elimination.
机译:背景:先前有2例同时使用左乙拉西坦的患者报道了氨甲蝶呤的延迟消除。目的:探讨甲氨蝶呤与左乙拉西坦在接受大剂量甲氨蝶呤治疗中的潜在相互作用。方法:这项回顾性研究回顾了接受280次甲氨蝶呤治疗的81名成年人的记录,以确定左乙拉西坦对消除甲氨蝶呤的影响。已获得机构审查委员会的批准。结果:左乙拉西坦以甲氨蝶呤的33(12%)周期给药。与未接受左乙拉西坦的患者相比,接受左乙拉西坦的患者的24小时甲氨蝶呤浓度显着降低(2.91对7.37 µmol / L,P = 0.005)。尽管存在这种差异,但两组之间在48小时和72小时的浓度相似。无论是否存在左乙拉西坦,达到无毒甲氨蝶呤浓度( u3c0.1 µmol / L)的时间都相同。两组在24、48和72小时的延迟消除频率与在任何时间点的延迟消除频率相似。 Cox回归表明左乙拉西坦不是无毒甲氨蝶呤浓度时间的重要预测因子(P = 0.796; HR = 1.058; 95%CI = 0.692-1.617),逻辑回归表明,左乙拉西坦在任何情况下都不是延迟消除的重要预测因子时间点。在比较在任何时间点经历延迟消除的患者与未延迟消除的患者之间,两组之间的左乙拉西坦使用相似(分别为13%和10%,P = 0.527)。结论:本研究不支持先前关于左乙拉西坦与甲氨蝶呤之间显着相互作用的报道。在没有其他风险因素延迟消除的人群中,临床上重要的相互作用是不可能的。

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