NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Effects of pre-analytical variables on the anti-activated factor X chromogenic assay when monitoring unfractionated heparin and low molecular weight heparin anticoagulation.

Author(s): McGlasson DL, Kaczor DA, Krasuski RA, Campbell CL, Kostur MR, Adinaro JT

Publication: Blood Coagul Fibrinolysis, 2005, Vol. 16, Page 173-6

PubMed ID: 15795534 PubMed Review Paper? No

Purpose of Paper

The purpose of this paper was to determine the effects of different specimen collection methods on anti-activated factor X (anti-FXa) assay and activated partial thromboplastin time (aPTT) results for patients receiving unfractionated heparin (UFH) and low molecular weight heparin (LMWH) therapy.

Conclusion of Paper

Specimens from UFH patients collected into 3.8% sodium citrate with ratio of 6:1 (blood: anticoagulant) showed a statistically significant increase in aPTT. No other combinations of anticoagulant and blood/anticoagulant ratio resulted in statistically significant differences in aPTT for patients receiving UFH or LMWH therapy. Importantly, neither blood to anticoagulant ratio nor type of anticoagulant affected anti-FXa assay results for either heparin therapy suggesting this assay is better suited for monitoring heparin patients.

Studies

  1. Study Purpose

    The purpose of this study was to determine if the use of different anticoagulants or the ratio of blood to anticoagulant during specimen collection affects anti-FXa assay results or aPTT for patients receiving UFH and LMWH therapy. Plasma specimens were stored at -70 degrees C prior to analysis.

    Summary of Findings:

    Specimens from UFH patients collected into 3.8% sodium citrate with ratio of 6:1 (blood: anticoagulant) showed a statistically significant increase in aPTT (p=0.06) with an average time of 127.2 s versus 105.4 s when specimens were collected using standard methods (3.2% sodium citrate and a 9:1 blood to anticoagulant ratio). However, some UFH specimens had aPTT times over 300 s which could have skewed the mean. No other combinations of anticoagulant and blood/anticoagulant ratio resulted in statistically significant differences in aPTT for patients receiving UFH or LMWH therapy. There were several aPTT times which did not correlate with the amount of heparin, indicating an effect of other variables besides heparin on aPTT. Importantly, neither blood to anticoagulant ratio nor type of anticoagulant affected anti-FXa assay results for either heparin therapy suggesting this assay is better suited for monitoring heparin patients.

    Biospecimens
    Preservative Types
    • Frozen
    Diagnoses:
    • Coronary Artery Disease
    • Other diagnoses
    Platform:
    AnalyteTechnology Platform
    Protein Hematology/ auto analyzer
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Preaquisition Diagnosis/ patient condition Deep vein thrombosis
    Antiphospholipid antibody syndrome
    Recurrent spontaneous abortion
    Other diagnoses
    Preaquisition Other drugs Low molecular weight heparin
    Unfractionated heparin
    Biospecimen Acquisition Anticoagulant Sodium citrate
    Citrate-theophylline-adenosine-dipyridamole
    Biospecimen Aliquots and Components Aliquot size/volume 9:1 blood to anticoagulant ratio
    6:1 blood to anticoagulant ratio

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