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Reference values for specific parameters of hemostasis determined with the automated analyzer

https://doi.org/10.33667/2078-5631-2026-7-37-43

Abstract

The article defines reference values for von Willebrand factor activity, von Willebrand factor ristocetin cofactor activity, von Willebrand factor antigen, Factor VIII Chromogenic assay activity, d‑dimer and Plasminogen activator inhibitor activity according to existing standards on the automatic coagulometer Sysmex CS‑2000i.

The aim of the study: to determine reference values for specific parameters of the hemostasis, which may vary depending on the type of analyzer and utilized reagents.

Materials and methods. After receiving informed voluntary consent from donors for medical survey and blood and (or) its components donation, blood samples were obtained from 100 donors of blood and (or) its components of both sexes: 51 males (51%) и 49 females (49%). We established reference values with the Sysmex CS‑2000i (Sysmex Corporation, Japan) hemostasis analyzer and reagents from Siemens (Healthcare GmbH, Germany).

Results. Reference values obtained for von Willebrand factor activity (46,65–181,45%), von Willebrand factor ristocetin cofactor activity (16,77– 164,37%), von Willebrand factor antigen (52,11% – 169,27%), Factor VIII chromogenic assay (45,08–158,35%), d‑dimer (17,69–368,13 mcg/l) and Plasminogen activator inhibitor activity (–2,54–4,48 E/ml), were compared with the literature data and the data presented in the instructions for the reagents used. The results obtained for von Willebrand factor antigen (52,11–169,27%) and d‑dimer (17,69–368,13 mcg/l) are comparable to the available data. There are no data on other studied parameters of hemostasis for the Sysmex CS‑2000i analyzer and the reagents used in the work. The obtained reference intervals are generally consistent with the manufacturer’s recommendations.

Conclusions. Reference values vary significantly depending on the analytical systems and reagent kits used, which confirms the need for local derivation or validation of reference intervals for each specific analytical system and in each laboratory.

About the Authors

L. A. Gorgidze
National Medical Research Center for Hematology
Russian Federation

Gorgidze Lana A., PhD Bio Sci, biologist at express laboratory of Intensive Care Dept with a Day Hospital and a Hemodialysis Group

Moscow



S. Yu. Mamleeva
National Medical Research Center for Hematology
Russian Federation

Mamleeva Svetlana Yu., clinical laboratory diagnostics specialist, head of Express Laboratory of Intensive Care Dept with a Day Hospital and a Hemodialysis Group

Moscow



D. V. Kamelskikh
National Medical Research Center for Hematology
Russian Federation

Kamelskikh Denis V., transfusion specialist, head of Transfusiology Organization and Safety Dept

Moscow



G. M. Galstyan
National Medical Research Center for Hematology
Russian Federation

Galstyan Gennady M., Dr Med Sci (habil.), head of Dept of Resuscitation and Intensive Care

Moscow



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64.


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Gorgidze L.A., Mamleeva S.Yu., Kamelskikh D.V., Galstyan G.M. Reference values for specific parameters of hemostasis determined with the automated analyzer. Medical alphabet. 2026;(7):37-43. (In Russ.) https://doi.org/10.33667/2078-5631-2026-7-37-43

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