BACKGROUND: Rapidly available and accurate platelet counts play an important role in the evaluation of haemorrhagic status and in assessing the need for platelet transfusions. We, therefore, evaluated platelet counting performance of haematology analysers using optical, impedance and immunological methods in thrombocytopenic patients. MATERIALS AND METHODS: We considered 99 patients with a platelet (plt) count under 50 x 10(9) plt/L. We compared the platelet counts obtained using ADVIA 2120 (optical method), Cell-Dyn Sapphire (optical, impedance and immunological methods with CD61) and a reference, double staining (CD41+CD61) immunological method. RESULTS: The platelet counts of all the considered methods showed good correlation with those of the reference method, despite an overestimation in platelet quantification. The degree of inaccuracy was greater for platelet counts under 20 x10(9) plt/L. CONCLUSIONS: Clinicians who use platelet thresholds below 20 x10(9) plt/L for making clinical decisions must be aware of the limitations in precision and accuracy of cell counters at this level of platelet count. Inaccurate counts of low platelet numbers could create problems if attempts are made to reduce the threshold below 20 x 10(9) plt/L.
BACKGROUND: Rapidly available and accurate platelet counts play an important role in the evaluation of haemorrhagic status and in assessing the need for platelet transfusions. We, therefore, evaluated platelet counting performance of haematology analysers using optical, impedance and immunological methods in thrombocytopenicpatients. MATERIALS AND METHODS: We considered 99 patients with a platelet (plt) count under 50 x 10(9) plt/L. We compared the platelet counts obtained using ADVIA 2120 (optical method), Cell-Dyn Sapphire (optical, impedance and immunological methods with CD61) and a reference, double staining (CD41+CD61) immunological method. RESULTS: The platelet counts of all the considered methods showed good correlation with those of the reference method, despite an overestimation in platelet quantification. The degree of inaccuracy was greater for platelet counts under 20 x10(9) plt/L. CONCLUSIONS: Clinicians who use platelet thresholds below 20 x10(9) plt/L for making clinical decisions must be aware of the limitations in precision and accuracy of cell counters at this level of platelet count. Inaccurate counts of low platelet numbers could create problems if attempts are made to reduce the threshold below 20 x 10(9) plt/L.
Authors: P Harrison; K A Ault; S Chapman; L Charie; B Davis; K Fujimoto; B Houwen; J Kunicka; F Lacombe; S Machin; R Raynor; L van Hove; O W van Assendelft Journal: Am J Clin Pathol Date: 2001-03 Impact factor: 2.493
Authors: C A Schiffer; K C Anderson; C L Bennett; S Bernstein; L S Elting; M Goldsmith; M Goldstein; H Hume; J J McCullough; R E McIntyre; B L Powell; J M Rainey; S D Rowley; P Rebulla; M B Troner; A H Wagnon Journal: J Clin Oncol Date: 2001-03-01 Impact factor: 44.544
Authors: Linda M Sandhaus; Ebenezer S Osei; Neeta N Agrawal; Chrisine A Dillman; Howard J Meyerson Journal: Am J Clin Pathol Date: 2002-08 Impact factor: 2.493
Authors: E Grimaldi; L Del Vecchio; F Scopacasa; C Lo Pardo; F Capone; S Pariante; G Scalia; M De Caterina Journal: Int J Lab Hematol Date: 2007-12-20 Impact factor: 2.877
Authors: D R Norfolk; P J Ancliffe; M Contreras; B J Hunt; S J Machin; W G Murphy; L M Williamson Journal: Br J Haematol Date: 1998-06 Impact factor: 6.998