Clinical evaluation of laboratory methods to monitor apixaban treatment in patients with atrial fibrillation
| Autor: | Maria Berndtsson, Faris Al-Khalili, Rickard E. Malmström, Lisbeth Söderblom, Mika Skeppholm, Yuko Rönquist-Nii, Anton Pohanka, Jovan P. Antovic, Fadiea Al-Aieshy, Annika Y. Östlund |
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| Rok vydání: | 2015 |
| Předmět: |
Male
medicine.medical_specialty Pyridones Renal function Tandem Mass Spectrometry Internal medicine Atrial Fibrillation medicine Humans In patient International Normalized Ratio Stroke Aged Aged 80 and over business.industry Atrial fibrillation Hematology Gold standard (test) medicine.disease Clinical trial Anesthesia Cohort Prothrombin Time Cardiology Pyrazoles Female Partial Thromboplastin Time Apixaban Drug Monitoring business Chromatography Liquid Factor Xa Inhibitors medicine.drug |
| Zdroj: | Thrombosis Research. 136:148-153 |
| ISSN: | 0049-3848 |
| Popis: | The direct factor-Xa inhibitor apixaban is approved e.g. for the prevention of stroke in patients with atrial fibrillation (AF). Although routine monitoring of apixaban therapy is currently not recommended, selective monitoring could be useful to optimize efficacy and safety in certain clinical situations. We studied the exposure and effect of apixaban using different laboratory methods in a clinical setting with a well-defined cohort of AF patients.Seventy AF patients (72±7.4years, 64 % men, mean CHADS2 score 1.7) treated with apixaban 2.5 (n=10) or 5mg BID (n=60). Trough plasma apixaban concentrations determined by liquid chromatography-tandem mass-spectrometry (LC-MS/MS) were compared to the coagulation assays Anti-factor Xa, PT-INR and aPTT.The apixaban plasma concentration determined by LC-MS/MS varied more than 10-fold overall. The range was between 15-83 and 29-186ng/mL for the 2.5mg BID and 5mg BID respectively, with patients receiving 5mg BID having significantly higher apixaban concentrations (p0.001). A strong correlation between LC-MS/MS and anti-FXa-assay was found (p0.001), while aPTT and PT-INR were not sensitive enough. There were no significant correlations between gender, creatinine clearance, body weight or age and apixaban exposure.Anti-FXa-assay performed well upon apixaban concentrations in a normal exposure range. Still LC-MS/MS remains the "gold standard" method, covering also low concentrations. Compared to clinical trials, we observed relatively lower apixaban exposure and a more pronounced difference between high and low dose. Additional information regarding apixaban exposure and benefit-risk profile is needed in order to individualize treatment. |
| Databáze: | OpenAIRE |
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