Summary & Overview
CPT 88167: Cervical/Vaginal Cytology Manual Review with Computer-Assisted Rescreen
CPT code 88167 covers a two-step cytopathology workflow in which a lab analyst performs a manual review of a cervical or vaginal cytology slide and then rescreens the same slide using computer-assisted cell selection and review, reporting results with the Bethesda System. This code reflects the integration of automated tools into conventional cytology practice, improving targeted review while maintaining supervised technical performance. Nationally, the code matters as laboratories adopt computer-assisted technologies that can affect workflow, documentation, and payer coverage policies.
Key payers discussed include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of clinical and billing context, common modifiers used with lab services, typical sites of service, and what to expect in payer coverage approaches. The publication also outlines benchmarks and policy considerations relevant to laboratories and billing professionals, and summarizes clinical reporting conventions tied to the Bethesda System.
The content is intended for laboratory managers, coding and billing staff, and policy analysts who need a clear national view of how 88167 fits into cytology service delivery, documentation, and payer interactions. Data not available in the input is noted where applicable.
Billing Code Overview
CPT code 88167 describes a laboratory procedure in which a qualified lab analyst performs a manual analysis of a cervical or vaginal cytopathology slide and then rescreens the identical slide using computer assistance that provides additional cell selection and review. The analyst conducts the technical component of the test under a physician’s supervision and reports results using the Bethesda System for cervical cytology interpretation.
-
Service type: Cytopathology slide analysis with manual review followed by computer-assisted rescreening and targeted cell selection.
-
Typical site of service: Clinical laboratory or pathology lab, often within hospitals, independent diagnostic laboratories, or specialized cytology laboratories.
Clinical & Coding Specifications
Clinical Context
A 32-year-old woman presents to a gynecology clinic for routine cervical cancer screening. A clinician collects a cervical cytology specimen (Pap smear) using a liquid-based cytology collection device and sends the slide to the laboratory. In the lab, a cytotechnologist or cytology laboratory analyst performs a manual microscopic review of the cervical or vaginal cytology slide to identify cellular abnormalities. After the manual screen, the analyst rescreens the same slide using computer-assisted cell selection software that highlights fields of interest based on programmed cell characteristics; the analyst performs additional targeted review of highlighted areas. The analyst completes the technical component under the supervision of a pathologist, and the final report is rendered using the Bethesda System terminology (e.g., negative for intraepithelial lesion or malignancy, ASC-US, LSIL, HSIL). Typical site of service is an outpatient clinical laboratory or hospital laboratory with cytopathology services. Typical patient scenario includes routine screening, follow-up of an abnormal prior Pap, or surveillance after treatment for cervical intraepithelial neoplasia where higher sensitivity from combined manual and computer-assisted review is desired. Billing is for the technical laboratory procedure performed by the analyst with computer-assisted rescreening documented and supervised by the reporting physician.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when reporting only the physician/pathologist interpretation separate from the laboratory technical work. |