OBJECTIVE: To develop a cytopreparation protocol suitable for satisfactory
processing by the AutoCyte (R) PREP System with the gynecologic specimens c
ollected in PreservCyt (R) fluid for the ThinPrep (R) machine.
STUDY DESIGN. The residue of a number of gynecologic specimens collected in
PreservCyt (R) and processed by ThinPrep (R) were processed by AutoCyte (R
) PREP. Some modifications were made in the cytopreparatory protocol in ord
er to obtain satisfactory specimens.
RESULTS: The ThinPrep (R) and AutoCyte (R) PREP specimens were examined ind
ependently. The results were comparable, with a high degree of concordance
between the two techniques.
CONCLUSION: Gynecologic specimens collected in PreservCyt (R) and following
the ThinPrep (R) specimen collection protocol can be processed using the A
utoCyte (R) PREP System. Minor protocol modifications provided comparable d
iagnostic material. Additional studies are needed to explore the feasibilit
y of this approach and fulfill the various U.S. regulatory agency requireme
nts for the liquid-based Pap test.