Summary & Overview
HCPCS Q5149: Aflibercept-abzv (Enzeevu) Injection, 1 mg
HCPCS Level II code Q5149 designates a 1 mg dose of aflibercept-abzv (Enzeevu), a biosimilar anti-VEGF agent administered by injection. This code is relevant for ophthalmology practices, ambulatory surgical centers, and payers managing specialty drug coverage for retinal disease therapies. Nationally, biosimilar entries like Q5149 influence formulary decisions, utilization patterns, and cost-management strategies for retinal vascular conditions treated with intravitreal anti-VEGF injections.
Key payers discussed include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise overview of what the code represents, the typical clinical setting, and which major payers are included in the analysis. The publication covers billing benchmarks, reimbursement considerations, and clinical context for intravitreal biosimilar aflibercept, plus practical notes on service delivery sites and coding nomenclature. Data not available in the input for specific modifiers, taxonomies, ICD-10 pairings, and payer-specific reimbursement rates are identified as unavailable.
This summary equips billing professionals, practice administrators, and policy analysts with a clear, national-level understanding of HCPCS Level II code Q5149 and its role in ophthalmic biosimilar therapy coding and coverage.
Billing Code Overview
HCPCS Level II code Q5149 denotes injection, aflibercept-abzv (Enzeevu), biosimilar, 1 mg. This code covers administration of a biosimilar formulation of aflibercept intended for intravitreal use in ophthalmology.
Service type: Intravitreal injection of a biosimilar anti-VEGF agent
Typical site of service: Outpatient ophthalmology clinic or ambulatory surgery center
Clinical & Coding Specifications
Clinical Context
A 72-year-old patient with neovascular (wet) age-related macular degeneration presents to an ophthalmology clinic for intravitreal pharmacologic therapy. The treating retinal specialist documents diminished central vision and active subretinal fluid on optical coherence tomography consistent with choroidal neovascularization. After informed consent, the patient is prepped in a procedure room or ambulatory surgical center; topical anesthetic and antiseptic are applied, and a single intravitreal injection of Q5149 (injection, aflibercept-abzv [enzeevu], biosimilar, 1 mg) is administered into the vitreous cavity under sterile technique. Post-injection, intraocular pressure is checked, and the patient receives post-procedure instructions and follow-up scheduling. Typical sites of service include an ophthalmology office procedure room, ambulatory surgical center, or hospital outpatient department. The typical patient scenario includes ongoing treatment of retinal vascular disorders such as neovascular age-related macular degeneration, diabetic macular edema, or retinal vein occlusion where anti-VEGF therapy with aflibercept biosimilar is clinically indicated.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
22 | Increased procedural services | Use when work required to provide the injection is substantially greater than typical (e.g., complex ocular anatomy, extensive additional procedures during same visit). |