SurePath™ Pap
Test Code
Clinical Significance
SurePath™ Pap - 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. Gynecologic cytology is a screening test which is subject to both false positive and false negative results. For that reason, the test is most reliable when a satisfactory sample is obtained on a regular repetitive basis. Hence, these results must be interpreted in the context of historic and current information.
Test Resources
Test Details
Methodology
Reference Range(s)
Preferred Specimen(s)
Pap sample collected in 1 SurePath™ pap vial
Minimum Volume
1 SurePath pap vial
Collection Instructions
For instructions refer to
//www.questdiagnostics.com/dms/Documents/Other/Specimen_Collection_and_Transport_Guide_2019.pdf
Transport Container
1 SurePath pap vial
Transport Temperature
Room temperature
Specimen Stability
- Room temperature: 28 days
Refrigerated: 90 days
Frozen: Unacceptable
Refer to local service area for specimen retention
Reject Criteria
SurePath vials without the head of the collection device(s) in the fluid • Swabs • SurePath vials received frozen • Cervical swabs in Digene® HC cervical sampler • Digene® vials
Setup Schedule
//www.questdiagnostics.com/dms/Documents/Other/Specimen_Collection_and_Transport_Guide_2019.pdf
Refrigerated: 90 days
Frozen: Unacceptable
Refer to local service area for specimen retention