Summary & Overview
CPT 81406: Tier 2 Molecular Pathology Laboratory Procedure
CPT code 81406 is a Tier 2 Molecular Pathology Procedure used for specialized genetic and molecular testing in clinical laboratories. This code covers tests for specific analytes that are not individually listed in Tier 1, making it a critical tool for advanced diagnostics in areas such as genetic screening, chromosomal analysis, and metabolic disorder evaluation. Nationally, molecular pathology is a rapidly evolving field, and CPT code 81406 plays a significant role in expanding access to precision medicine.
Major payers including Aetna, Blue Cross Blue Shield, Cigna Health, and UnitedHealthcare provide coverage for these procedures, reflecting broad acceptance and integration into standard laboratory practice. Readers will gain insight into payer coverage, clinical indications, and related coding benchmarks, as well as policy updates relevant to laboratory medicine. The publication also highlights associated ICD-10 diagnoses, common modifiers, and related CPT codes, offering a comprehensive overview for stakeholders in clinical pathology and laboratory medicine.
This summary provides a clear understanding of the clinical context, payer landscape, and coding framework for CPT code 81406, supporting informed decision-making for laboratories, clinicians, and healthcare administrators.
CPT Code Overview
CPT code 81406 represents a Tier 2 Molecular Pathology Procedure, encompassing specialized laboratory tests for specific analytes not individually listed in Tier 1. These procedures are typically performed in an independent laboratory setting, designated as Place of Service 81. The service type is molecular pathology, which involves advanced genetic and molecular testing to aid in diagnosis, risk assessment, and treatment planning. These tests are essential for identifying genetic mutations, chromosomal anomalies, and other molecular markers relevant to patient care.
Clinical & Coding Specifications
Clinical Context
A patient is referred to an independent laboratory for molecular pathology testing to evaluate for potential genetic or chromosomal anomalies. The ordering provider may be a family medicine physician or a specialist in pathology. The laboratory performs a Tier 2 molecular pathology procedure, which involves testing for specific analytes not individually listed in Tier 1. The results may inform diagnosis, screening, or genetic counseling, and are typically used in cases where there is a family history of genetic disease, suspicion of metabolic disorders, or the need for chromosomal abnormality screening. The workflow includes specimen collection, laboratory analysis, and interpretation by a qualified pathologist.
Coding Specifications
-
Modifiers:
- Modifier
26: Used to indicate the professional component of the service, such as interpretation of laboratory results by a physician or pathologist. - Modifier
TC: Used to indicate the technical component, which covers the laboratory's performance of the test, including equipment and staff.
- Modifier
-
Provider Taxonomies:
Code Specialty