A method is proposed for counting the number of adhered platelets base
d on the determination of lactate dehydrogenase activity in bulk after
lysis of adhered platelets. This method was compared with the widely
used radioisotope labelling technique. It was concluded that the prese
nt lactate dehydrogenase method is effective in counting the adhered p
latelets, as no significant difference was found between the readings
of two methods when commercial polymers and glass were used as samples
.