Abstract

Henry O. Ogedegbe, PhD, BB(ASCP)SC Department of Environmental Health, Molecular and Clinical Sciences, Florida Gulf Coast University, Fort Myers, FL anti-factor Xa of 0.20 U/mL with a range of 0.01 to 1.00 U/mL. The average bias for these 54 paired samples was 0.01 U/mL, indicating no meaningful effect of the pneumatic tube delivery on anti-factor Xa measurements. As shown in T2, the 37 rapid, higher speed centrifugation comparison samples had a median anti-factor Xa of 0.17 U/mL with a range of 0.01 to 0.89 U/mL. The average bias for these 37 paired samples was 0.00 U/mL, indicating no meaningful effect of rapid, higher speed centrifugation on anti-factor Xa measurements. Discussion The anti-factor Xa assay is sensitive to the release of the heparin neutralizing substance platelet factor 4 from normal blood platelets.2 Although several previous studies of pneumatic tube delivery and rapid, higher-speed centrifugation did not detect effects on platelet counts, coagulation factor levels, prothrombin times, activated partial thromboplastin times, or fibrinogen concentrations,6,7 we found no reports studying the anti-factor Xa assay. Neither pneumatic tube delivery nor rapid, higher-speed centrifugation caused a detectable effect on the antifactor Xa assay in this study. These technologies speed coagulation laboratory work and appear to be acceptable for chromogenic anti-factor Xa assay monitoring of heparin therapy.

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