Summary & Overview
HCPCS J7193: Factor IX (non-recombinant) per IU
HCPCS Level II code J7193 denotes purified, non-recombinant Factor IX (antihemophilic factor) billed per international unit. This code captures administration and supply of a critical clotting product used for treatment and prophylaxis in patients with hemophilia B and acquired Factor IX deficiency. Nationally, access and cost for clotting factors are high-priority issues because they affect long-term outcomes, supply logistics, and specialty pharmacy management.
Key payers in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of billing context, typical sites of service, and the clinical role of Factor IX products. The publication summarizes common billing modifiers and coding considerations, payer coverage patterns, and benchmarking context where available. It also outlines clinical context relevant to utilization: replacement therapy, perioperative management, and prophylaxis for bleeding prevention.
This summary provides a national-level briefing for revenue cycle managers, specialty pharmacy administrators, and policy analysts on how HCPCS Level II code J7193 is used in practice, what to expect in payer interactions, and where to look for policy or reimbursement updates. Data not available in the input is noted where applicable.
Billing Code Overview
HCPCS Level II code J7193 represents Factor IX (antihemophilic factor, purified, non-recombinant) billed per international unit (i.u.). This code is used for the billing of purified, non-recombinant Factor IX concentrate used to treat and prevent bleeding in patients with hemophilia B and other Factor IX deficiency states.
Service Type: Replacement therapy / clotting factor administration
Typical Site of Service: Hospital outpatient infusion center, ambulatory infusion center, physician office, or home infusion
Clinical & Coding Specifications
Clinical Context
A typical patient is an adult or pediatric male with Hemophilia B (congenital factor IX deficiency) presenting for factor replacement therapy. Indications include routine prophylaxis to prevent spontaneous bleeding, on-demand treatment for an acute joint or soft-tissue bleed, perioperative management for a scheduled procedure, or treatment of traumatic bleeding. The clinical workflow begins with hematology assessment documenting weight, target factor IX activity, bleeding history, inhibitor status, and the planned indication (prophylaxis, on-demand, or surgical). Pharmacy calculates the required international units (IU) of J7193 based on the patient’s weight and desired rise in factor IX activity. A nurse or infusion specialist prepares and administers the product via intravenous infusion in an outpatient infusion center, hospital infusion unit, emergency department, or ambulatory surgical center. Vital signs and infusion tolerance are monitored during and after administration. Documentation includes indication, total IU dispensed and administered, lot number, reconstitution details, site of service, any applicable modifier(s), and payer information for claims processing. Typical sites of service are outpatient infusion centers, hospital inpatient wards for severe bleeds or perioperative care, emergency departments for acute bleeding, and ambulatory surgical centers for procedures requiring factor coverage.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
JW |