Evaluation of coagulation assays versus LC-MS/MS for determinations of dabigatran concentrations in plasma |
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Authors: | Jovan P. Antovic Mika Skeppholm Jaak Eintrei Elisabet Eriksson Boija Lisbeth Söderblom Eva-Marie Norberg Liselotte Onelöv Yuko Rönquist-Nii Anton Pohanka Olof Beck Paul Hjemdahl Rickard E. Malmström |
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Affiliation: | 1. Department of Coagulation Research, Institute for Molecular Medicine and Surgery, Karolinska Institutet, & Department of Clinical Chemistry, Karolinska University Hospital, Stockholm, Sweden 5. Department of Molecular Medicine & Surgery, Karolinska Institutet, Clinical Chemistry L700, Karolinska University Laboratory, Karolinska University Hospital, 171 76, Stockholm, Sweden 2. Department of Medicine, Clinical Pharmacology Unit, Division of Cardiovascular Medicine, Karolinska Institutet & Danderyd Hospital, Stockholm, Sweden 3. EQUALIS, External Quality Assessment, Uppsala, Sweden 4. Department of Medicine, Clinical Pharmacology Unit, Karolinska Institutet & Clinical Pharmacology, Karolinska University Hospital, Solna, Stockholm, Sweden
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Abstract: |
Background Dabigatran is an oral direct thrombin inhibitor for which routine laboratory monitoring is currently not recommended. However, there are situations in which measurements of the drug and its effect are desirable. We therefore compared and validated different coagulation methods for assessments of dabigatran in clinical samples in relation to measurements of plasma dabigatran, without the purpose of establishing effective and safe concentrations of dabigatran in plasma. Methods Samples were obtained from 70 atrial fibrillation patients treated with dabigatran etexilate. Plasma concentrations were measured using liquid chromatography-tandem mass spectrometry (LC-MS/MS) and were compared with coagulation methods Hemoclot thrombin inhibitors (HTI) and Ecarin clotting assay (ECA), as well as with prothrombin time-international normalized ratio (PT-INR) and activated partial thromboplastin time (aPTT). Results A wide range of dabigatran concentrations was determined by LC-MS/MS (<0.5–586 ng/mL). Correlations between LC-MS/MS results and estimated concentrations were excellent for both HTI and ECA overall (r2?=?0.97 and 0.96 respectively, p?0.0001), but the precision and variability of these assays were not fully satisfactory in the low range of dabigatran plasma concentrations, in which ECA performed better than HTI. aPTT performed poorly, and was normal (<40 s) even with dabigatran levels of 60 ng/mL. PT-INR was normal even at supratherapeutic dabigatran concentrations. Conclusion LC-MS/MS is the gold standard for measurements of dabigatran in plasma. Alternatively, either HTI or ECA assays may be used, but neither of these assays is dependable when monitoring low levels or to infer total absence of dabigatran. The aPTT assay is relatively insensitive to dabigatran, and normal aPTT results may be observed even with therapeutic dabigatran concentrations. |
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