Abstract

BackgroundFeline platelets are prone to clumping after blood collection, rendering the determination of accurate platelet counts difficult for clinical laboratories and resulting in a high incidence of pseudothrombocytopenia in feline haematology reports. No information is available about the kinetics of platelet aggregate formation in feline ethylenediaminetetraacetic acid blood and the course of platelet counts over a clinically relevant time period. The aim of the present study was to determine platelet counts in healthy cats over a time period of 24 h after blood collection at 9 time points; to assess potential effects of platelet aggregates, anaesthesia and bleeding conditions on feline platelets and white blood cell counts; and finally, to investigate if glucose concentration is associated with the presence of aggregates. From 30 clinically healthy cats, blood samples were analysed at 9 different time points using two different haematology instruments (using fluorescence and impedance-based flow cytometry) in the counting chamber and by blood smear evaluation.ResultsFourteen of the 30 samples were thrombocytopenic at one to 8 time points after collection as analysed on a fluorescence flow cytometry haematology analyser. At the 24-h timepoint, all thrombocytopenic samples had returned to normal platelet counts. Seventeen of the 30 samples showed platelet aggregates in the counting chamber. Significant differences in platelet counts were associated with the presence and size of aggregates and time since bleeding. No statistically significant differences in counts were found with regard to the quality of blood collection or the use of anaesthesia. Platelet aggregation and, therefore, pseudothrombocytopenia occurred in 57 % of the investigated samples at different time points.ConclusionFor the first time, deaggregation of feline platelet aggregates could be demonstrated as a reversible effect of platelet aggregation. For clinical laboratories or veterinarians, it may be helpful to rerun feline samples with pseudothrombocytopenia to obtain a more reliable platelet count. The quality of blood collection seems not to be causative for platelet aggregation. Blood smear evaluation is absolutely indicated in cases when haematology instruments give PLT counts below the reference interval.Electronic supplementary materialThe online version of this article (doi:10.1186/s12917-015-0590-7) contains supplementary material, which is available to authorized users.

Highlights

  • Feline platelets are prone to clumping after blood collection, rendering the determination of accurate platelet counts difficult for clinical laboratories and resulting in a high incidence of pseudothrombocytopenia in feline haematology reports

  • To the authors’ knowledge no information is available about the kinetics of PLT aggregate formation in feline ethylenediaminetetraacetic acid (EDTA) blood samples, and the course of PLT counts over a clinical relevant time period of 24 h (h)

  • The aim of the present study was to determine PLT counts in healthy cats over a time period of 24 h at 9 time points, and to: (1) assess potential effects of PLT aggregates, anaesthesia and bleeding conditions on feline platelet counts measured on a fluorescence flow cytometry-based instrument (Sysmex XT-2000iV) and an impedance-based haematology instrument (Mythic 18); (2) to describe potential effects of aggregates, anaesthesia and bleeding conditions on white blood cell (WBC) counts measured by both technologies; and (3) to assess if glucose concentration is associated with the presence of aggregates

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Summary

Introduction

Feline platelets are prone to clumping after blood collection, rendering the determination of accurate platelet counts difficult for clinical laboratories and resulting in a high incidence of pseudothrombocytopenia in feline haematology reports. To the authors’ knowledge no information is available about the kinetics of PLT aggregate formation in feline ethylenediaminetetraacetic acid (EDTA) blood samples, and the course of PLT counts over a clinical relevant time period of 24 h (h). The aim of the present study was to determine PLT counts in healthy cats over a time period of 24 h at 9 time points, and to: (1) assess potential effects of PLT aggregates, anaesthesia (yes vs no) and bleeding conditions (without any problem vs difficulties) on feline platelet counts measured on a fluorescence flow cytometry-based instrument (Sysmex XT-2000iV) and an impedance-based haematology instrument (Mythic 18); (2) to describe potential effects of aggregates, anaesthesia and bleeding conditions on WBC counts measured by both technologies; and (3) to assess if glucose concentration is associated with the presence of aggregates. The results of the present study provide insights into the kinetics of feline PLT counts and influencing factors, which affect the results of laboratory diagnostic testing

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