Effect of Concentration of Trisodium Citrate Anticoagulant on Calculation of the International Normalised Ratio and the International Sensitivity Index of Thromboplastin

E M Duncan; C R Casey; B M Duncan; J V Lloyd

doi:10.1055/s-0038-1648816

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 1994; 72(01): 084-088
DOI: 10.1055/s-0038-1648816

Original Article

Schattauer GmbH Stuttgart

Effect of Concentration of Trisodium Citrate Anticoagulant on Calculation of the International Normalised Ratio and the International Sensitivity Index of Thromboplastin

Authors

E M Duncan

The Haemostasis Section, Division of Haematology, Institute of Medical and Veterinary Science, Adelaide, Australia
C R Casey

The Haemostasis Section, Division of Haematology, Institute of Medical and Veterinary Science, Adelaide, Australia
B M Duncan

The Haemostasis Section, Division of Haematology, Institute of Medical and Veterinary Science, Adelaide, Australia
J V Lloyd

The Haemostasis Section, Division of Haematology, Institute of Medical and Veterinary Science, Adelaide, Australia

Abstract

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Summary

The aim of this study was to determine whether the concentration of trisodium citrate used to anticoagulate blood has an effect on the INR of the sample and the ISI of the thromboplastin. Five thromboplastins including and Australian reference material were used to measure the prothrombin time of normal and patient samples collected into two concentrations of trisodium citrate - 109 mM and 129 mM. There was no effect of citrate concentration on the INRs determined with the reference material. However for the other four thromboplastins there was a significant difference between INRs for the two citrate groups. The prothrombin times of the samples collected into 129 mM were longer than those collected into 109 mM. This difference was only slight in normal plasma but more marked in patients receiving oral anticoagulants, causing the INRs for patient plasmas collected into 129 mM citrate to be higher then the corresponding samples collected into 109 mM citrate.

From orthogonal regression of log prothrombin times by the reference method against each thromboplastin, we found that the ISI for each thromboplastin was approximately 10% lower when determined with samples collected into 129 mM citrate than with samples collected into 109 mM. These results suggest that the concentration of trisodium citrate used for collection of blood samples can affect the calculation of the INR and the calibration of the ISI of thromboplastin. This was found both for commercial thromboplastins prepared by tissue extraction and for a recombinant tissue factor.

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References

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