Plasma levels of direct oral anticoagulants in real life patients with atrial fibrillation: Results observed in four anticoagulation clinics

Thromb Res. 2016 Jan:137:178-183. doi: 10.1016/j.thromres.2015.12.001. Epub 2015 Dec 2.

Abstract

Introduction: Direct oral anticoagulant (DOAC) intra- and inter-individual variability was previously reported, but its magnitude is still considered negligible for patient management.

Objective: To evaluate inter- and intra-individual variability in real-world atrial fibrillation patients on dabigatran, rivaroxaban or apixaban in four Italian anticoagulation clinics and to assess the correlation between DOAC plasma concentration and creatinine-clearance (CrCl).

Materials and methods: A total of 330 consecutive patients were enrolled, of which 160 were on dabigatran (70 and 90 taking 150 mg or 110 mg twice-daily, respectively), 71 on rivaroxaban (37 and 34 taking 20mg or 15 mg once-daily) and 99 on apixaban (73 and 26 taking 5mg or 2.5mg twice-daily). Blood was taken at trough and peak within the first month (15-25 days) of treatment. Diluted-thrombin-time (dTT) calibrated for dabigatran and anti-FXa calibrated for rivaroxaban or apixaban was performed.

Results: Mean inter-individual variability expressed as overall CV values for all drugs was lower at peak (CV=46%) than at trough (CV=63%). Mean CV% intra-individual variability was 36.6% at trough and 34.0% at peak. Correlation with CrCl was poor for all drugs and only dabigatran at trough showed a significant correlation.

Conclusion: This multicenter study confirms high DOAC inter-individual variability that cannot be explained by the rate of renal clearance to which the three DOAC were subjected since the correlation with CrCl was relatively poor. This poor correlation suggests caution in using CrCl as the sole laboratory parameter to indirectly evaluate residual circulating DOAC.

Keywords: Anti-FXa; Creatinine clearance; DOAC; Dilute thrombin time; Inter-individual variability; Intra-individual variability.

Publication types

  • Controlled Clinical Trial
  • Multicenter Study

MeSH terms

  • Administration, Oral
  • Aged
  • Anticoagulants / pharmacokinetics*
  • Anticoagulants / therapeutic use*
  • Atrial Fibrillation / blood*
  • Atrial Fibrillation / drug therapy
  • Atrial Fibrillation / epidemiology
  • Biological Availability
  • Comorbidity
  • Female
  • Glomerular Filtration Rate / drug effects*
  • Humans
  • Italy / epidemiology
  • Male
  • Prevalence
  • Reproducibility of Results
  • Risk Factors
  • Sensitivity and Specificity
  • Thromboembolism / blood*
  • Thromboembolism / epidemiology
  • Thromboembolism / prevention & control*
  • Treatment Outcome

Substances

  • Anticoagulants