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文拉法辛的药代动力学相关性:相关不良反应。

Pharmacokinetic correlates of venlafaxine: associated adverse reactions.

机构信息

Department of Psychiatry, The Zucker Hillside Hospital, Northwell Health, Glen Oaks, NY, USA.

Clinical Pharmacology, Department of Psychiatry and Psychotherapy, University of Regensburg, Regensburg, Germany.

出版信息

Eur Arch Psychiatry Clin Neurosci. 2019 Oct;269(7):851-857. doi: 10.1007/s00406-019-01005-0. Epub 2019 Mar 28.

Abstract

To address the potential correlation between plasma concentrations of venlafaxine (VEN), its active metabolite O-desmethylvenlafaxine (ODVEN) and the active moiety, AM, (ODVEN + VEN) and adverse drug reactions (ADR) in a large naturalistic sample of in- and outpatients. We compared plasma concentrations of VEN, ODVEN and AM and dose-adjusted (C/D) levels as well the ODVEN/VEN ratios between patients complaining ADRs, following the Udvalg for Kliniske Undersogelser side effect rating scales (UKU) (n = 114) and patients without ADRs (control group, n = 688) out of a naturalistic database. We also investigated potential pharmacokinetic correlates of the four UKU categories by comparing patients complaining ADRs with those who did not. Based on previous literature we applied different ODVEN/VEN ratio values as cut-offs to split our sample into two groups at a time and compare frequencies of ADRs between the groups. No differences for demographic and pharmacokinetic variables including plasma and C/D concentrations as well as ODVEN/VEN ratios were observed between study groups. Neither the comparisons between females and males nor between elderly and non-elderly patients revealed significant differences (p > 0.05 in all cases). No differences were also reported exploring the patients complaining ADRs from the 4 UKU categories separately. After applying various ODVEN/VEN cut-offs, groups did not display differences in frequencies of ADRs (p > 0.05 in all cases). Our findings do not demonstrate a direct link between venlafaxine metabolism measures and ADRs. Therefore, additional dimensions are needed to be considered in future trials aiming to disentangle the involved aspects of ADRs in patients receiving venlafaxine.

摘要

为了在一个大型自然样本的门诊和住院患者中,确定文拉法辛(VEN)的血浆浓度、其活性代谢物 O-去甲文拉法辛(ODVEN)和活性部分(ODVEN+VEN)与不良药物反应(ADR)之间的潜在相关性。我们比较了抱怨 ADR 的患者(n=114)和无 ADR 的患者(对照组,n=688)的血浆 VEN、ODVEN 和 AM 浓度以及剂量调整(C/D)水平以及 ODVEN/VEN 比值,根据 Udvalg for Kliniske Undersogelser 副作用评定量表(UKU)。我们还通过比较抱怨 ADR 的患者和未抱怨 ADR 的患者,调查了四个 UKU 类别的潜在药代动力学相关性。基于之前的文献,我们应用不同的 ODVEN/VEN 比值作为界值,将样本分为两组,并比较两组之间 ADR 的发生率。研究组之间在人口统计学和药代动力学变量方面,包括血浆浓度和 C/D 浓度以及 ODVEN/VEN 比值均无差异。在所有情况下,比较女性和男性以及比较老年和非老年患者也未发现显著差异(p>0.05)。分别比较 4 个 UKU 类别中抱怨 ADR 的患者也未报告差异。应用不同的 ODVEN/VEN 界值后,各组 ADR 的发生率也无差异(在所有情况下,p>0.05)。我们的研究结果并未表明文拉法辛代谢测量值与 ADR 之间存在直接联系。因此,需要在未来的试验中考虑其他维度,以厘清接受文拉法辛治疗的患者中 ADR 涉及的方面。

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