Test Directory
| Test Code | |
| 10465 | |
| Test Name | |
| Cytopathology,ThinPrep® plus Imager Pap Test | |
| Included Tests | |
| Cytologic examination of laboratory prepared ThinPrep® Pap Test. Testing options: *HPV Plus 16 & 18 Reflex HPV DNA High Risk on ASCUS only *HPV DNA High Risk primary screen in combination with ThinPrep Pap Test out of vial *HPV DNA High Risk only (For specimens sent without ThinPrep Pap Test.) *Chlamydia and/or Neisseria Gonorrhea by Amplified Probe (See Chlamydia by Amplified DNA Probe and Neisseria Gonorrhea by Amplified DNA Probe.) *Trichomonas out of vial | |
| Expected Turnaround Time | |
| 7 - 10 business days | |
| Clinical Utility | |
| To detect intraepithelial lesions, neoplastic lesions, and some infectious agents. | |
| Specimen and Container Info | |
|
Alternate Specimen: Min. Volume External: Exfoliated cells collected according to the ThinPrep® Liquid based specimen preparartion guidelines. Volume External: Alternate Container: |
|
| Collection Instructions | |
| Vials MUST be labeled with patient's FULL name (First initial and last name is unacceptable) and second patient identifier (i.e., DOB, MR#, SS#.) See Special instructions for "Cytobrush/Spatula Collection" listed under Specimen Collection, Preparation, and Handling Section" of the HNL LAB Medicine Test Directory. | |
| Processing and Submission Instructions | |
| Submit specimen with and EPIC order, Non-Gyn Cytology Requisition Form (HNL-32), or one of the laboratory's appropriate electronic forms. Ancillary Test Options (out of vial) are performed only from a ThinPrep® vial. Maturation Index, if desired, must be obtained from a lateral vaginal wall scrape. Patient should avoid douches for 48-72 hours prior to collection. Manual screening is performed on unsuccessful screen events. Cytology report reflects unsuccessful Imager screen. NOTE: The following additional criteria are required for Ancillary Test Options (out of vial) HPV DNA. * For HPV DNA testing, the specimen cannot be older than 30 days. *For Chlamydia and/or Neisseria Gonorrhea by Amplified Probe testing, the specimen cannot be older than 30 days. | |
| Causes for Rejection | |
| Expired collection fluid. Specimens collected past 6 weeks for Cytology and 30 days for ancillary testing. Incorrect fixative/container. | |
| Reference Intervals | |
| The Bethesda System 2014 | |
| Testing Schedule | |
| Routine, Monday - Friday no holidays |
The American Medical Association (AMA) Current Procedural Terminology (CPT) codes published by HNL Lab Medicine are guidelines and are intended for informational purposes only. CPT coding is the exclusive responsibility of the billing entity. View the Terms.
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