ThinPrep Pap Test
Cytology · Women's Health
Liquid based Pap testing is intended for use in the screening and detection of cervical cancer, pre-cancerous lesions, atypical cells and all other cytologic categories as defined by the Bethesda system for reporting results of cervical cytology. Pap screening is not reliable for the detection of endometrial cancer.
Table Of Contents
Specimen Requirements
Acceptable specimen collection/transport containers are: •ThinPrep® Pap Vial
Storage and Transport
Specimens can be shipped and stored at 2 - 30°C. If shipping temperatures exceeding 30°C are anticipated, use cool plack. Viability after transfer to collection/transport tube is:
•ThinPrep® Pap Vial: 30 days
Specimen Rejection Criteria
All specimens must be submitted according to the test directory instructions. Before submitting specimen, please carefully review specimen requirements.
Listed below are possible causes for delays in specimen processing or possible specimen rejections or cancellations:
- No patient identification on requisition form
- No patient identification on specimen container or slides
- No referring provider
- No account information provided
- No test ordered on requisition
- No specimen source provided
- Inappropriate specimen type
- Insufficient volume for analysis
- Inappropriate specimen container
- Improper specimen transport
- Specimen leaked in transport
- Specimen submitted in incorrect or expired transport media
- Slides broken beyond repair on receipt
- Conflict between patient name on specimen and requisition form
- Specimen not properly preserved
- Sample containing a needle
Turn Around Time (TAT)
1-3 Days.
CPT Codes*
88175 which includes imaging, or 88142 if requires a manual screen with no imaging. Pap results requiring physician interpretation will be performed at an additional charge using CPT Code: 88141.