Air sac lavage has become a routine diagnostic tool used in pet birds;
however, cytologic techniques for collection and handling of avian ce
lls have not been reported. In this study, directed endoscopy was used
to obtain the air sac washes. Different factors were compared that mi
ght affect final preservation of cell morphology, such as centrifugati
on speed, anticoagulant, storage temperature, time to processing, addi
tion of glutaraldehyde to the sample, and addition of protein. The goa
l was to find the processing technique best suited for the evaluation
of cells from air sac washes. The use of an anticoagulant did not infl
uence cell quality. Optimal cell morphology was achieved when the samp
le was centrifuged at a speed of 1000 rpm (89.4 X g) and when prepared
in less than an hour from the time of collection. Low temperature (5
C) tended to preserve cell quality better The addition of protein (fet
al bovine serum) helped to preserve cell quality and was of value if t
he sample storage time was greater than 30 min. The addition of glutar
aldehyde resulted in a significant reduction in cell quality.