We describe a method for measuring platelet aggregation in whole blood by single platelet
counting. The importance of a low stirring speed (100 rpm) to obtain agonist-specific
aggregation is stressed. Despite this low stirring speed, the sensitivity to agonists
equals that of the turbidometric technique in platelet-rich plasma. The optimal concentration
of formaldehyde for fixing the aggregates, the effects of storage times and anticoagulant
are studied. Applicability to the study of platelet function inhibitors or of inherited
platelet function disorders is illustrated. It is concluded that this technique, used
under the appropriate conditions, combines the advantage of measuring platelet aggregation
in a more physiologtc environment with the advantages of the turbidometric technique
such as high sensitivity.
Keywords
Platelet aggregation, whole blood - Platelet aggregation, platelet counting