Platelet estimation in whole blood

Abstract

An application of particle size analysis is described for the estimation of platelet counts in whole blood based on a variable size threshold and baseline. The simplicity of the sample preparation for this technique may enable its automation as a semiquantitative screening method. Platelets, defined as particles to the platelet side and above the minimum point between the platelet and red cell distributions were counted on specially designed electronics. The system divides the normal size distribution from the smallest platelet to the smallest red cell into four equal windows and performs three integrations to calculate the best result.