Test Code CPAPS Conventional Smear-Screen, Varies
Ordering Guidance
Laboratory approval is required prior to ordering cytology testing.
Specimen submitted as endocervical curettage or endocervical brushing need to be ordered as CYTNG / Cytology Non-Gynecologic.
Necessary Information
1. An acceptable cytology request form must accompany specimen containers and include the following: Patient's name, medical record number, date of birth, sex, source (exact location and procedure used), date specimen was taken, name of ordering physician and pager number.
2. Submit any pertinent clinical information, including date of last menstrual period.
Specimen Required
Patient Preparation: For optimal interpretation, Papanicolaou smears should be collected near the middle of the menstrual cycle. No douching, lubricant use, or sexual intercourse for 24 hours prior to specimen collection.
Container/Tube: Slide
Specimen Volume: Circular scrape of cervical os
Collection Instructions:
1. Specimen containers must be labeled with a minimum of 2 unique identifiers (patient's name, and medical record number or date of birth). Containers should also be labeled with specimen source, and date collected.
2. Glass slides may be labeled with a single unique identifier, but 2 identifiers are preferred. If multiple slides are submitted, each slide must have proper identification. Glass slides should be identified with the patient's name and a second patient identifier that is also on the accompanying paperwork (ie, medical record number or date of birth)
3. Fix slides immediately in 95% alcohol or treat with commercially available spray fixative.
Forms
Useful For
Screening for cervical carcinoma and a number of infections of the female genital tract including human papillomavirus, herpes, Candida, and Trichomonas
Reflex Tests
Test ID | Reporting Name | Available Separately | Always Performed |
---|---|---|---|
CVSPC | Physician Interp Conventional | No | No |
Testing Algorithm
If Papanicolaou results are abnormal, a pathologist will review the case at an additional charge.
Special Instructions
Method Name
Light Microscopy
Reporting Name
Conventional Smear-ScreenSpecimen Type
VariesSpecimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Varies | Ambient (preferred) | SLIDE | |
Refrigerated | SLIDE |
Reject Due To
SurePath vial | Reject |
Reference Values
Satisfactory for evaluation
Negative for intraepithelial lesion or malignancy
Note: Abnormal results will be reviewed by a physician at an additional charge.
Interpretation
Standard reporting, as defined by the Bethesda System (TBS) is utilized.
Day(s) Performed
Monday through Friday
Report Available
2 to 5 daysPerforming Laboratory
Mayo Clinic Laboratories in RochesterTest Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
P3000
88164
88141-CVSPC (if appropriate)
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
CPAPS | Conventional Smear-Screen | In Process |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
71301 | Interpretation | 59465-5 |
71302 | Participated in the Interpretation | 19768-1 |
71303 | Report electronically signed by | 19139-5 |
71304 | Addendum | 35265-8 |
71305 | Gross Description | 22634-0 |
CY032 | Pap Test Source | 19763-2 |
CY033 | Clinical History | 22636-5 |
CY034 | Menstrual Status (LMP, PM, Pregnant) | 8678-5 |
CY035 | Hormone Therapy/Contraceptives | 8659-5 |
71572 | Disclaimer | 62364-5 |
71818 | Case Number | 80398-1 |