Summary & Overview
HCPCS Level II C9167: Injection, recombinant ADAMTS13, 10 IU
HCPCS Level II code C9167 denotes an injection of recombinant ADAMTS13 (recombinant-krhn), packaged per 10 international units. This biologic therapy is used to replace or supplement ADAMTS13 activity and has significance for rare hematologic conditions where enzyme replacement is clinically indicated. National attention centers on access to high-cost biologics, appropriate site-of-care utilization, and payer coverage policies for novel recombinant therapies.
Key payers addressed in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. The publication summarizes payer coverage patterns, expected service settings, clinical context, and considerations for billing and claims adjudication related to a stabilized biotherapeutic injection.
Readers will find benchmarks on where this service is typically administered (hospital inpatient, outpatient infusion centers, emergency departments, and clinic-based injection suites), an overview of billing considerations tied to HCPCS Level II coding, and a concise clinical context explaining the therapeutic role of ADAMTS13 replacement. Where specific payer policy details, taxonomies, or ICD-10 linkage data are not provided in the input, the publication notes that such data are not available and focuses on the code definition, service type, and national policy relevance instead.
Billing Code Overview
HCPCS Level II code C9167 represents an injection of recombinant ADAMTS13 (recombinant-krhn), dosed per 10 international units. The code describes a biologic replacement therapy administered via parenteral injection intended to provide ADAMTS13 activity.
Service Type: Therapeutic injection (biologic replacement therapy)
Typical Site of Service: Hospital inpatient or outpatient infusion/administration setting, emergency department, or clinic-based injection suite, depending on clinical need and local practice patterns.
Data not available in the input.
Clinical & Coding Specifications
Clinical Context
A typical patient is an adult or adolescent diagnosed with immune-mediated thrombotic thrombocytopenic purpura (iTTP) presenting with acute thrombocytopenia, microangiopathic hemolytic anemia, and organ ischemia (neurologic symptoms, renal dysfunction, or cardiac ischemia). The treating clinician assesses ADAMTS13 deficiency and inhibitory antibodies; while plasma exchange and immunosuppression are standard, administration of recombinant ADAMTS13 (C9167 — Injection, adamts13, recombinant-krhn, 10 IU) may be ordered in a hospital inpatient or outpatient infusion center as part of replacement therapy.
Typical workflow: initial hematology consult, laboratory confirmation of severe ADAMTS13 deficiency, placement of intravenous access, review of concurrent therapies (plasma exchange, corticosteroids, rituximab), preparation and verification of the recombinant ADAMTS13 dose by pharmacy, administration via IV infusion in the inpatient bed or outpatient infusion suite, monitoring for infusion reactions and clinical response, documentation of dose, lot number, and patient tolerance, and follow-up hematology assessments to guide further dosing and adjunctive therapy.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
22 | Increased procedural services | Use when administration requires substantially greater resources than typical (e.g., complicated access, prolonged monitoring). |