Casandra
Casandra Test Code QD61147Version 1 (DRAFT)
Performing Lab
SurePath™ Pap
Clinical Use
Order TestUse
This test is a liquid-based Pap test using the SurePath™ collection system for cervical cancer screening (cytology). It detects cellular abnormalities that may indicate cervical dysplasia or malignancy.
Special Instructions
Not provided.
Limitations
Not provided.
Test Details
Methodology
Not provided.
Biomarkers
Targets not provided.
Result Turnaround Time
Not provided.
Related Documents
For more information, please review the documents below
Specimen Requirements
Specimen
Other
Volume
Pap sample collected in 1 (1 minimum) SurePath™ pap vial
Minimum Volume
Not provided
Container
SurePath™ pap vial
Collection Instructions
Refer to Specimen Collection and Transport Guide
Causes for Rejection
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
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 28 days |
| Refrigerated | 6 months |
| Frozen | Unacceptable |
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