On the monitoring of dabigatran treatment in "real life" patients with atrial fibrillation.

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On the monitoring of dabigatran treatment in "real life" patients with atrial fibrillation.

Thromb Res. 2014 Jul 6;

Authors: Skeppholm M, Hjemdahl P, Antovic JP, Muhrbeck J, Eintrei J, Rönquist-Nii Y, Pohanka A, Beck O, Malmström RE

Abstract
INTRODUCTION: The oral direct thrombin inhibitor dabigatran is increasingly used to prevent thromboembolic stroke in patients with atrial fibrillation (AF). Routine laboratory monitoring is currently not recommended, but measurements of dabigatran and/or its effect are desirable in certain situations. We studied dabigatran exposure and compared different tests for monitoring of dabigatran in a real-life cohort of AF patients.
MATERIAL AND METHODS: Ninety AF patients (68±9years, 67% men, mean CHADS2 score 1.5) were treated with dabigatran 150 (n=73) or 110mg BID (n=17). Trough plasma concentrations of total and free dabigatran by liquid chromatography-tandem mass-spectrometry (LC-MS/MS) were compared to indirect measurements by Hemoclot thrombin inhibitors (HTI) and Ecarin clotting assay (ECA), as well as PT-INR and aPTT.
RESULTS: Total plasma dabigatran varied 20-fold (12-237ng/mL with 150mg BID) and correlated well with free dabigatran (r(2)=0.93). There were strong correlations between LC-MS/MS and HTI or ECA (p<0.001) but these assays were less accurate with dabigatran below 50ng/mL. The aPTT assay was not dependable and PT-INR not useful at all. There were weak correlations between creatinine clearance (Cockcroft-Gault) and LC-MS/MS, HTI and ECA (p<0.001 for all). A high body weight with normal kidney function was associated with low dabigatran levels.
CONCLUSIONS: HTI and ECA reflect the intensity of dabigatran anticoagulation, but LC-MS/MS is required to quantify low levels or infer absence of dabigatran. Most real life patients with a normal creatinine clearance had low dabigatran levels suggesting a low risk of bleeding but possibly limited protection against stroke.

PMID: 25172669 [PubMed - as supplied by publisher]

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