Summary & Overview
HCPCS J7191: Factor VIII (porcine) per i.u.
HCPCS Level II code J7191 designates Factor VIII (antihemophilic factor (porcine)), billed per international unit, and captures porcine-derived factor replacement therapy used to treat hemophilia A. Nationally, accurate coding for high-cost biologics such as J7191 matters for clinical continuity, payer coverage determinations, and appropriate claims processing for complex coagulation care.
Key payers in the analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. The publication summarizes how these payers approach coverage, prior authorization, and coding expectations for porcine Factor VIII products and contrasts them with general biologics policies where relevant.
Readers will learn the clinical context for use of porcine Factor VIII, typical sites of service where dosing is administered, standard billing considerations tied to per i.u. reporting, and which payer categories are commonly involved in reimbursement decisions. The report provides benchmarking and policy-summary content to inform hospital revenue cycle teams, specialty pharmacy managers, and clinicians involved in hemophilia care. Data not available in the input where specific benchmarks, associated ICD-10 diagnoses, and related codes would normally appear.
Billing Code Overview
HCPCS Level II code J7191 represents Factor VIII (antihemophilic factor (porcine)), billable per international unit (i.u.). This code describes a derived hemostatic factor replacement therapy product used to treat or prevent bleeding in patients with hemophilia A, specifically formulations sourced from porcine (pig) plasma or recombinant porcine sequences.
Service type: Injectable biologic therapy (factor replacement)
Typical site of service: Hospital outpatient infusion centers, inpatient hospital settings, and specialty infusion clinics
Clinical & Coding Specifications
Clinical Context
A 42-year-old male with acquired hemophilia A secondary to autoimmune disease presents with acute spontaneous soft-tissue bleeding and a factor VIII inhibitor that renders human-derived factor VIII ineffective. The hematology team orders porcine-derived antihemophilic factor to achieve hemostasis. The patient is admitted to an inpatient hematology unit or observed in an infusion center with monitoring for response and adverse events. Pharmacy compounds the billed agent J7191 (Factor VIII, antihemophilic factor (porcine), per I.U.) and documents lot number, units dispensed, and administration details in the medication administration record. Nursing administers the IV infusion per weight-based dosing, monitors vital signs and infusion site, evaluates bleeding control, and records total IUs given. If dosing is adjusted for inadequate response, additional units are documented and billed. Billing captures the exact number of IUs administered using J7191, applies appropriate modifiers for circumstances (for example, QK/QX for physician assistant/assistant-at-surgery when applicable), and links the service to the admitting diagnosis such as hemophilia-related bleeding or inhibitor-associated hemorrhage. Typical sites of service include inpatient hospital units, hospital outpatient infusion centers, emergency departments, and specialty infusion clinics capable of handling high-acuity hemostatic agents.
Coding Specifications
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