Summary & Overview
HCPCS A9544: Iodine I-131 tositumomab, Diagnostic Study Dose
HCPCS Level II code A9544 denotes a diagnostic dose of Iodine I-131 tositumomab, a radiopharmaceutical used in nuclear medicine to assess biodistribution and disease characteristics prior to or alongside therapeutic planning. This code matters nationally because radiopharmaceutical diagnostic procedures inform cancer staging, treatment selection, and safe use of subsequent therapeutic radioimmunotherapy. Appropriate coding ensures accurate capture of specialized diagnostic services that have implications for care pathways and reimbursement of high-cost imaging agents.
Key payers examined include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of the clinical context for A9544, typical sites of service, and national implications for coverage and billing practice. The publication covers benchmarks for utilization and reimbursement where available, summaries of payer coverage patterns and prior authorization trends, and policy updates affecting radiopharmaceutical diagnostic services. Clinical considerations for safe administration and documentation elements needed for billing are summarized to support coding accuracy. Data not available in the input is noted where applicable.
Billing Code Overview
HCPCS Level II code A9544 represents Iodine I-131 tositumomab, diagnostic, billed per study dose. This code is used for diagnostic applications of the radiopharmaceutical Iodine I-131 tositumomab, typically administered as a single study dose to evaluate disease characteristics or biodistribution prior to or in conjunction with therapeutic planning.
Service type: Diagnostic radiopharmaceutical study dose
Typical site of service: Hospital outpatient department or nuclear medicine/diagnostic imaging center, where radioactive diagnostic agents are prepared and administered under specialized radiopharmacy and nuclear medicine protocols.
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Clinical & Coding Specifications
Clinical Context
A typical patient is a 65-year-old with relapsed or refractory non-Hodgkin B-cell lymphoma being evaluated for radioimmunodiagnostic staging using A9544 (Iodine I-131 tositumomab, diagnostic, per study dose). The multidisciplinary workflow begins in hematology/oncology: the oncologist orders the diagnostic radiolabeled antibody study to assess whole-body disease distribution and antigen expression prior to consideration of therapeutic radioimmunotherapy. On the day of service, the patient presents to an outpatient nuclear medicine or hospital-based radiology department. A nuclear medicine physician or authorized prescriber reviews prior imaging and labs (including thyroid function and pregnancy status), obtains informed consent, and documents indication and target sites. The radiopharmacy prepares and dispenses I-131 tositumomab per protocol; radiation safety and dose verification are completed. The radiopharmaceutical is administered intravenously under nuclear medicine supervision; post-injection imaging (planar and/or SPECT/CT) is performed at protocol-specified time points to document biodistribution and tumor targeting. Imaging and dose report are interpreted by the nuclear medicine physician, with results communicated to the referring oncologist to inform eligibility and planning for potential therapeutic I-131 tositumomab or other targeted treatments. Typical sites of service are outpatient nuclear medicine departments, hospital outpatient imaging centers, or specialized oncology infusion centers with nuclear medicine capability.
Coding Specifications
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