Measurement of dabigatran plasma concentrations by calibrated thrombin clotting time in comparison to LC-MS/MS in human volunteers on dialysis

- Comparison of dabigatran concentrations determined by HEMOCLOT® dTT and LC-MS/MS.
- Samples were obtained from end-stage renal disease patients on haemodialysis.
- HEMOCLOT®-dTT derived dabigatran concentrations paralleled those from LC-MS/MS.
- The dTT assay is suitable for measuring plasma dabigatran in this population.

IntroductionDabigatran etexilate is an oral direct thrombin inhibitor. Although routine anticoagulation monitoring with dabigatran is not usually required, a simple and precise laboratory test to measure dabigatran concentrations in patient plasma may be useful in certain clinical circumstances, such as emergency situations. The HEMOCLOT® Thrombin Inhibitors assay has demonstrated accurate and precise determination of dabigatran concentrations within a range of 50-500 ng/ml. The objective of this study was to assess comparability of dabigatran concentrations determined by HEMOCLOT® and by liquid chromatography/tandem mass spectrometry (LC-MS/MS) in plasma samples from human volunteers with end-stage renal disease (ESRD) undergoing regular haemodialysis (HD) during a Phase I study.Materials and MethodsOverall, 304 plasma samples were obtained from seven ESRD patients in dabigatran steady-state for measurement by HEMOCLOT® (calibrated diluted thrombin time [dTT]) and by LC-MS/MS. Agreement of dabigatran concentrations was assessed by regression analysis and difference plots.ResultsThe measurements of calibration standards of the HEMOCLOT® assay showed excellent precision with coefficients of variation < 5%. Accuracy determined by analysis of two quality control samples was 90% and 111%. HEMOCLOT®-derived dabigatran plasma concentrations paralleled those obtained by LC-MS/MS. The mean ratio of the LC-MS/MS and dTT-derived concentrations was 0.955 (67% limits of agreement: 0.771-1.18).ConclusionsThe HEMOCLOT® Thrombin Inhibitors assay is suitable for measuring dabigatran plasma concentrations in volunteers with ESRD undergoing haemodialysis. The agreement between dabigatran concentrations determined by the HEMOCLOT® assay and the LC-MS/MS reference method met bioanalytical acceptance criteria.