Apixaban plasma concentrations before and after catheter ablation for atrial fibrillation.

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  • Additional Information
    • Source:
      Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
    • Publication Information:
      Original Publication: San Francisco, CA : Public Library of Science
    • Subject Terms:
    • Abstract:
      Background: Catheter ablation in patients with atrial fibrillation is associated with a transient increase in thromboembolic risk and adequate anticoagulation is highly important. When patients are anticoagulated with apixaban, monitoring of plasma concentrations of the drug is not routinely performed. This study aimed to assess the influence of clinical patient characteristics, concomitant drug treatment and self-reported adherence on apixaban concentrations, and to describe the intra- and inter-individual variability in apixaban concentrations in this group of patients. Method Apixaban concentrations from 141 patients were measured in plasma one week before ablation and two, six and ten weeks after ablation, employing ultra-high performance liquid chromatography coupled with tandem mass spectrometry. In samples not obtained at trough, apixaban concentrations were adjusted to trough levels. Self-reported adherence was registered by means of the 8-item Morisky Medication Adherence Scale before and after ablation.
      Results: There were statistically significant, positive correlations between apixaban concentrations and increased age, female sex, lower glomerular filtration rate, higher CHA2DS2-VASc score, use of cytochrome P450 3A4 and/or p-glycoprotein inhibitors, and use of amiodarone. Self-reported adherence was generally high. The mean intra-individual and inter-individual coefficients of variation were 29% and 49%, respectively.
      Conclusion: In patients undergoing catheter ablation for atrial fibrillation, age, sex, renal function, interacting drugs and cerebrovascular risk profile were all associated with altered plasma apixaban concentration. In this group of patients with a generally high self-reported adherence, intra-individual variability was modest, but the inter-individual variability was substantial, and similar to those previously reported in other patient apixaban-treated populations. If a therapeutic concentration range is established, there might be a need for a more flexible approach to apixaban dosing, guided by therapeutic drug monitoring.
      Competing Interests: The authors have declared that no competing interests exist.
      (Copyright: © 2024 Aakerøy et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
    • References:
      J Cardiovasc Electrophysiol. 2016 May;27(5):549-54. (PMID: 26766541)
      Front Pharmacol. 2017 Mar 01;8:100. (PMID: 28298894)
      Thromb Haemost. 2018 Mar;118(3):437-450. (PMID: 29433148)
      Thromb Res. 2016 Jan;137:178-183. (PMID: 26672898)
      Thromb Res. 2015 Jul;136(1):148-53. (PMID: 25981142)
      Circulation. 2019 Mar 5;139(10):e56-e528. (PMID: 30700139)
      Basic Clin Pharmacol Toxicol. 2024 Jan;134(1):175-185. (PMID: 37845026)
      Eur Heart J. 2021 Feb 1;42(5):373-498. (PMID: 32860505)
      N Engl J Med. 2017 Aug 24;377(8):745-755. (PMID: 28834469)
      Ann Pharmacother. 2018 Mar;52(3):251-256. (PMID: 29047306)
      Chest. 2018 Nov;154(5):1121-1201. (PMID: 30144419)
      J Am Heart Assoc. 2016 Feb 23;5(2):. (PMID: 26908412)
      Europace. 2016 Aug;18(8):1150-7. (PMID: 26830891)
      Clin Pharmacokinet. 2015 Jun;54(6):651-62. (PMID: 25573421)
      Br J Clin Pharmacol. 2013 Feb;75(2):476-87. (PMID: 22759198)
      Eur Heart J Cardiovasc Pharmacother. 2021 Apr 09;7(FI1):f72-f80. (PMID: 32324233)
      Blood Adv. 2020 Aug 11;4(15):3520-3527. (PMID: 32756938)
      Ther Drug Monit. 2018 Jun;40(3):369-376. (PMID: 29578938)
      J Clin Pharmacol. 2016 May;56(5):637-45. (PMID: 26358690)
      J Pharm Pharmacol. 2005 Jun;57(6):671-9. (PMID: 15969921)
      Europace. 2021 Oct 9;23(10):1612-1676. (PMID: 33895845)
      Heart Rhythm. 2017 Oct;14(10):e275-e444. (PMID: 28506916)
      Adv Ther. 2020 Feb;37(2):644-655. (PMID: 31873866)
      Ann Intern Med. 2009 May 5;150(9):604-12. (PMID: 19414839)
      Eur Heart J. 2018 Aug 21;39(32):2942-2955. (PMID: 29579168)
      J Thromb Haemost. 2022 Jan;20(1):92-103. (PMID: 34664401)
      Clin Pharmacokinet. 2019 Oct;58(10):1265-1279. (PMID: 31089975)
      J Clin Pharmacol. 2014 Nov;54(11):1280-9. (PMID: 24895078)
      Value Health. 2019 Feb;22(2):139-156. (PMID: 30711058)
      BMJ. 2018 Apr 26;361:k1453. (PMID: 29699974)
      Circulation. 2004 Aug 31;110(9):1042-6. (PMID: 15313941)
      N Engl J Med. 2017 Aug 24;377(8):733-744. (PMID: 28834483)
    • Accession Number:
      0 (Pyridones)
      3Z9Y7UWC1J (apixaban)
      0 (Pyrazoles)
      0 (Factor Xa Inhibitors)
    • Publication Date:
      Date Created: 20240731 Date Completed: 20240731 Latest Revision: 20240802
    • Publication Date:
      20240802
    • Accession Number:
      PMC11290617
    • Accession Number:
      10.1371/journal.pone.0308022
    • Accession Number:
      39083480