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Test Code CPAPD Conventional Smear-Diagnostic


Advisory Information


Mayo Medical Laboratories' clients need prior laboratory approval to order 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 following: 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

Gyn-Cytology Patient Information (T601) in Special Instructions

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

Special Instructions

Method Name

Light Microscopy

Reporting Name

Conventional Smear-Diagnostic

Specimen Type

Varies

Specimen Stability Information

Specimen Type Temperature Time
Varies Ambient (preferred)
  Refrigerated 

Reject Due To

Hemolysis

NA

Lipemia

NA

Icterus

NA

Other

NA

Reference Values

Satisfactory for evaluation. Negative for intraepithelial lesion or malignancy.

Note: Abnormal results will be reviewed by a physician at an additional charge.

Day(s) and Time(s) Performed

Monday through Friday; Varies 8 a.m.-5 p.m.

Analytic Time

2 days

Performing Laboratory

Mayo Medical Laboratories in Rochester

Test Classification

This test has been cleared or approved by the U.S. 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
CPAPD Conventional Smear-Diagnostic In Process

 

Result ID Test Result Name Result LOINC Value
71306 Interpretation In Process
71307 Participated in the Interpretation No LOINC Needed
71308 Report electronically signed by In Process
71309 Addendum In Process
71310 Gross Description In Process
CY037 Pap Test Source 19763-2
CY038 Clinical History In Process
CY039 Menstrual Status (LMP, PM, Pregnant) In Process
CY040 Hormone Therapy/Contraceptives In Process
71573 Disclaimer 62364-5
71819 Case Number In Process