81228 Cytog alys chrml abnr cgh
Also known as: Cytogenetic microarray, aCGH array for cancer
Cytogenetic analysis using array Comparative Genomic Hybridization (aCGH) to detect chromosomal abnormalities in solid tumors.
In Plain Language
cancer chromosome test; genetic abnormality detection
Clinical Context
Used in solid tumor analysis to identify chromosomal deletions, amplifications, and translocations for prognostic stratification and treatment planning.
RVU Information
CPT 81228 does not have a physician work RVU assigned by CMS. Reimbursement for this code is determined by payer-specific fee schedules.
Billing & Documentation
Lab and pathology codes require an order from the treating provider with clinical indication. For molecular pathology and genetic testing, document the specific analytes tested and clinical rationale.
How This Code Compares
This code has a work RVU of 0.00, meaning it does not have a physician work component assigned by CMS. In the Pathology & Lab category, 94% of codes share this characteristic.
Specialties
Frequently Asked Questions
What is CPT code 81228?
CPT 81228 (Cytog alys chrml abnr cgh) is a Pathology & Lab code. Cytogenetic analysis using array Comparative Genomic Hybridization (aCGH) to detect chromosomal abnormalities in solid tumors.
Who uses CPT code 81228?
CPT 81228 is used by Oncology, Pathology, Molecular Medicine. Used in solid tumor analysis to identify chromosomal deletions, amplifications, and translocations for prognostic stratification and treatment planning.
When is CPT 81228 used?
Used in solid tumor analysis to identify chromosomal deletions, amplifications, and translocations for prognostic stratification and treatment planning.
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CPT® is a registered trademark of the American Medical Association. Data sourced from CMS Physician Fee Schedule RVU26A. Descriptions, synonyms, and clinical context are original content by RVU Edge.