Performance of the Sysmex XN‐V hematology analyzer in determining the immature platelet fraction in dogs: A preliminary study and reference values

Abstract

AbstractBackgroundImmature platelets (IPs) are newly formed platelets released into circulation that have been demonstrated as good markers of thrombopoiesis. Although many flow cytometric and fully automated‐based methods are available, the latest Sysmex XN‐V hematology analyzer for veterinary use is equipped with a specific fluorescent platelet channel (PLT‐F) that detects platelets using a platelet‐specific dye.ObjectivesThe aims of this study were to evaluate the performance of the Sysmex XSN‐1000 V in determining the IPF (immature platelet fraction) and other selected PLT‐F channel parameters and to propose IPF reference intervals (RIs) for canine blood samples.MethodsCanine EDTA blood samples were analyzed on the Sysmex XN‐1000 V to assess linearity, imprecision, carryover, stability, and the effect of platelet clumping on selected platelet parameters from the PLT‐F channel. We also reported the de novo generated RIs for the IPF in dogs.ResultsImprecision was acceptable (CV <10%) for all parameters except for the absolute IPF values (IPF#), in which the reproducibility was 12.15% for the normal‐low concentration samples. Linearity and carryover were excellent for all variables. Relative IPF values (IPF %) and IPF# remained stable for both storage conditions for up to 48 hours; however, a nonsignificant progressive increase in these parameters was observed from 12 hours at 4°C. We observed a statistical increase in IPF% and IPF# and a statistically significant decrease in PLT‐F counts after intentional in vitro platelet aggregation. RIs were generated for all reference samples (n = 69) and for samples with (n = 25) or without (n = 44) platelet clumps.ConclusionsThe performance of the new PLT‐F channel‐derived variables for dogs was excellent. Specific RIs for IPF should be used when platelet aggregates are present.