دورية أكاديمية

The impact of pregnancy on the pharmacokinetics of antiseizure medications:A systematic review and meta-analysis of data from 674 pregnancies

التفاصيل البيبلوغرافية
العنوان: The impact of pregnancy on the pharmacokinetics of antiseizure medications:A systematic review and meta-analysis of data from 674 pregnancies
المؤلفون: Schoretsanitis, Georgios, Deligiannidis, Kristina M., Kasperk, Nicholas, Schmidt, Chiara Theresa, Kittel-Schneider, Sarah, Ter Horst, Peter, Berlin, Maya, Kohn, Elkana, Poels, Eline M.P., Zutshi, Deepti, Tomson, Torbjörn, Spigset, Olav, Paulzen, Michael
المصدر: Schoretsanitis , G , Deligiannidis , K M , Kasperk , N , Schmidt , C T , Kittel-Schneider , S , Ter Horst , P , Berlin , M , Kohn , E , Poels , E M P , Zutshi , D , Tomson , T , Spigset , O & Paulzen , M 2024 , ' The impact of pregnancy on the pharmacokinetics of antiseizure medications : A systematic review and meta-analysis of data from 674 pregnancies ' , Progress in Neuro-Psychopharmacology and Biological Psychiatry , vol. 133 , 111030 . https://doi.org/10.1016/j.pnpbp.2024.111030Test
سنة النشر: 2024
الوصف: Objective: Increasing evidence suggests that the physiological changes of pregnancy may impact pharmacokinetics of antiseizure medications (ASM), and this may affect treatment outcomes. The aim of this study was to quantify the pregnancy impact on the ASM pharmacokinetics. Methods: A systematic literature search was conducted in PubMed/EMBASE in November 2022 and updated in August 2023 for studies comparing levels of ASM in the same individuals during pregnancy and in the preconception/postpartum period. Alteration ratios between the 3rd trimester and baseline were estimated. We also performed a random-effects meta-analysis calculating between-timepoint differences in mean differences (MDs) and 95% confidence intervals (95%CIs) for dose-adjusted plasma concentrations (C/D ratios). Study quality was assessed using the ClinPK guidelines. Results: A total of 65 studies investigating 15 ASMs in 674 pregnancies were included. The largest differences were reported for lamotrigine, oxcarbazepine and levetiracetam (alteration ratio 0.42, range 0.07–2.45, 0.42, range 0.08–0.82 and 0.52, range 0.04–2.77 respectively): accordingly, C/D levels were lower in the 3rd trimester for lamotrigine, levetiracetam and the main oxcarbazepine metabolite monohydroxycarbazepine (MD = -12.33 × 10 −3 , 95%CI = -16.08 to −8.58 × 10 −3 (μg/mL)/(mg/day), p < 0.001, MD = -7.16 (μg/mL)/(mg/day), 95%CI = -9.96 to −4.36, p < 0.001, and MD = -4.87 (μg/mL)/(mg/day), 95%CI = -9.39 to −0.35, p = 0.035, respectively), but not for oxcarbazepine (MD = 1.16 × 10 −3 (μg/mL)/(mg/day), 95%CI = -2.55 to 0.24 × 10 −3 , p = 0.10). The quality of studies was acceptable with an average rating score of 11.5. Conclusions: Data for lamotrigine, oxcarbazepine (and monohydroxycarbazepine) and levetiracetam demonstrate major changes in pharmacokinetics during pregnancy, suggesting the importance of therapeutic drug monitoring to assist clinicians in optimizing treatment outcomes.
نوع الوثيقة: article in journal/newspaper
وصف الملف: application/pdf
اللغة: English
العلاقة: https://pure.eur.nl/en/publications/7612bee6-78f0-4fd1-89ec-79098d6a934aTest
DOI: 10.1016/j.pnpbp.2024.111030
الإتاحة: https://doi.org/10.1016/j.pnpbp.2024.111030Test
https://pure.eur.nl/en/publications/7612bee6-78f0-4fd1-89ec-79098d6a934aTest
https://pure.eur.nl/ws/files/149882724/1-s2.0-S0278584624000988-main.pdfTest
http://www.scopus.com/inward/record.url?scp=85193433591&partnerID=8YFLogxKTest
حقوق: info:eu-repo/semantics/openAccess
رقم الانضمام: edsbas.3EB71AD9
قاعدة البيانات: BASE