Search our extensive Laboratory Test Directory to find test codes, ordering recommendations, specimen stability information, Test Fact Sheets, and more.
Recommendations when to order or not order the test. May include related or preferred tests.
New York DOH Approval Status
Indicates whether a test has been approved by the New York State Department of Health.
This test is not New York state approved. ARUP cannot facilitate testing for New York state clients. Please work directly with a New York state-approved laboratory.
Specimen Required
Patient PreparationInstructions patient must follow before/during specimen collection.
CollectSpecimen type to collect. May include collection media, tubes, kits, etc.
Cervical specimen in a ThinPrep Pap Test Collection Vial, PK/25 (ARUP Supply #51325). Cytology collection devices available: Rover Combi Brush - PK/25 (ARUP Supply #64001) , Broom - PK/100 (ARUP Supply #22218) , Combi Brush/Spatula - PK/25 (ARUP Supply #51326) , Endocervical Brush - Each (ARUP Supply #11440). Available online through eSupply using ARUP Connect™ or contact ARUP Client Services at 800-522-2787. For specific instructions refer to Specimen Collection and Handling.
Specimen PreparationInstructions for specimen prep before/after collection and prior to transport.
Transport cervical specimen in the original collection kit.
Storage/Transport TemperaturePreferred temperatures for storage prior to and during shipping to ARUP. See Stability for additional info.
Ambient
Unacceptable ConditionsCommon conditions under which a specimen will be rejected.
Specimens not collected in a ThinPrep Pap Test collection vial. Specimens submitted in an expired collection vial.
RemarksAdditional specimen collection, transport, or test submission information.
StabilityAcceptable times/temperatures for specimens. Times include storage and transport time to ARUP.
Expected turnaround time for a result, beginning when ARUP has received the specimen.
3-7 days If reflexed, add 1-2 days.
Reference Interval
Normal range/expected value(s) for a specific disease state. May also include abnormal ranges.
Interpretive Data
May include disease information, patient result explanation, recommendations, or details of testing.
Refer to report.
Compliance Category
Note
Additional information related to the test.
If the ThinPrep Pap test is interpreted as atypical squamous of undetermined significance (ASCUS), then Human Papillomavirus (HPV), High Risk Screen by Transcription-Mediated Amplification (TMA), with Reflex to Genotypes 16 and 18/45 (ARUP test code 3016945) will be performed and reported under a separate accession. Additional charges apply.
The Pap test is a screening test for cervical cancer and its precursors with an inherent false-negative rate.
Store collection vials without cytologic samples at room temperature (15C to 30C). Do not use solution beyond expiration date marked on the vial.
Hotline History
N/A
CPT Codes
The American Medical Association Current Procedural Terminology (CPT) codes published in ARUP's Laboratory Test Directory are provided for informational purposes only. The codes reflect our interpretation of CPT coding requirements based upon AMA guidelines published annually. CPT codes are provided only as guidance to assist clients with billing. ARUP strongly recommends that clients confirm CPT codes with their Medicare administrative contractor, as requirements may differ. CPT coding is the sole responsibility of the billing party. ARUP Laboratories assumes no responsibility for billing errors due to reliance on the CPT codes published.
88175 (88142 if manual); If reviewed by pathologist add 88141; if reflexed, add 87624 HPV
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
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