Summary & Overview
CPT 81560: Pediatric Liver and Small‑Bowel Allograft Rejection Risk Assay
CPT code 81560 represents a laboratory-developed molecular assay and algorithm (MAAA) that quantifies CD154+ T–cytotoxic memory cell responses to donor and third‑party leukocytes to generate a risk score for allograft rejection in pediatric liver and small‑bowel transplant patients. Nationally, this code is important for transplant centers, pediatric specialists, and clinical laboratories evaluating immune-mediated rejection risk where tailored monitoring can influence post‑transplant surveillance.
Key payers in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find an overview of the clinical context for use of the assay, how the service aligns with laboratory and outpatient hospital settings, and what payers typically consider when covering MAAA services. The publication outlines common billing considerations, expected sites of service, and the assay’s role in pediatric transplant care pathways.
This summary also prepares readers to interpret benchmarks and policy notes related to novel algorithm-linked laboratory tests: it identifies where coverage guidance and documentation expectations typically apply, highlights operational implications for laboratories and transplant programs, and summarizes the clinical rationale for measuring CD154+ T–cytotoxic memory cell responses in pediatric liver and small bowel rejection assessment.
Billing Code Overview
CPT code 81560 describes a laboratory-developed molecular assay and associated algorithmic analysis used to assess the risk of allograft rejection in pediatric liver or small–bowel transplant patients. The test measures levels of CD154+ T–cytotoxic memory cells after incubating the patient’s blood specimen with organ-donor and third-party leukocytes, and the MAAA produces a rejection risk score specific to pediatric liver or small bowel transplant recipients.
Service Type: Laboratory immunologic assay with algorithmic risk scoring (MAAA)
Typical Site of Service: Clinical laboratory or hospital outpatient laboratory
Clinical & Coding Specifications
Clinical Context
A pediatric liver or small–bowel transplant recipient (age 1–17 years) presents for routine post–transplant surveillance or for evaluation of suspected acute graft dysfunction (elevated liver enzymes, cholestasis, fever, or nonspecific GI symptoms). The transplant hepatology team orders a specialized immunologic blood assay to assess risk of allograft rejection. A phlebotomy specimen is collected in the outpatient infusion center, transplant clinic, or hospital inpatient unit and sent to a reference immunology laboratory. The laboratory performs an assay that incubates the patient’s peripheral blood with donor and third–party leukocytes, measures the proportion of CD154+ T–cytotoxic memory cells, and runs an algorithm that integrates the assay result (and optionally clinical variables) to produce a rejection risk score specific to pediatric liver or small–bowel transplants. Results are reported to the transplant physician or advanced practice provider, who incorporates the risk score into clinical decision-making (e.g., adjust immunosuppression, request biopsy, or increase monitoring). Typical sites of service include outpatient transplant clinic, hospital inpatient ward, and reference laboratory. Service type: laboratory diagnostic test with an associated multianalyte algorithmic analysis (MAAA).
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when billing only the professional interpretation component separate from the technical lab processing. |