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Injection, factor viii, (antihemophilic factor, recombinant), (afstyla), 1 i.u.

HCPCS code

Name of the Procedure:

  • Common Name: Injection of Recombinant Factor VIII (Afstyla)
  • Technical/Medical Term: Injection, Factor VIII, (Antihemophilic Factor, Recombinant), (Afstyla), 1 I.U. (J7210)

Summary

This procedure involves the injection of a recombinant form of Factor VIII called Afstyla, which is essential for blood clotting. It is used to prevent or treat bleeding episodes in patients with Hemophilia A, a genetic disorder characterized by deficient or defective Factor VIII.

Purpose

  • Medical Conditions Addressed: Hemophilia A
  • Goals: To reduce bleeding episodes, prevent bleeding complications, and improve the overall quality of life for individuals with Hemophilia A.

Indications

  • Symptoms such as spontaneous bleeding, joint bleeds, or bleeding after injury or surgery.
  • Patients diagnosed with Hemophilia A who require regular Factor VIII replacement therapy.

Preparation

  • Pre-procedure instructions: No special preparation is usually required.
  • Assessments: A blood test to determine the Factor VIII levels and confirm the diagnosis of Hemophilia A may be needed.

Procedure Description

  1. The healthcare provider will clean the injection site with an antiseptic.
  2. Afstyla is prepared and drawn into a syringe under sterile conditions.
  3. The injection is administered intravenously, usually in the arm.
  4. Post-injection, the site may be monitored for any immediate reactions.
  • Tools/Equipment: Syringe, antiseptic solution, Afstyla medication.
  • Anesthesia/Sedation: Not required.

Duration

The injection process itself typically takes less than 10 minutes.

Setting

The procedure is usually performed in a hospital, outpatient clinic, or at home after proper training.

Personnel

Typically administered by:

  • Healthcare professionals such as nurses, or by trained patients/caregivers.

Risks and Complications

  • Common Risks: Mild pain, swelling, or redness at the injection site.
  • Rare Risks: Allergic reactions, inhibitor development (where the body starts neutralizing Factor VIII), blood clots.

Benefits

  • Reduces the frequency of bleeding episodes.
  • Provides better control of bleeds when they occur.
  • Improves quality of life by allowing participation in normal activities.

Recovery

  • Post-procedure care: Monitor the injection site for any signs of infection or adverse reactions.
  • Recovery Time: Immediate return to normal activity is usually possible.
  • Follow-Up: Regular follow-up appointments may be needed to adjust dosage and monitor Factor VIII levels.

Alternatives

  • Other Options: Plasma-derived Factor VIII, other recombinant Factor VIII products, gene therapy (in select cases), desmopressin (for mild cases).
  • Pros and Cons: Plasma-derived products may carry a slightly higher risk of virus transmission, while gene therapy is still in experimental stages and not widely available.

Patient Experience

  • During the Procedure: A mild prick of the needle, generally minimal discomfort.
  • After the Procedure: Patients can resume normal activities swiftly; any mild pain at the injection site can be managed with over-the-counter pain relief if necessary. Regular monitoring and follow-up ensure the treatment is working effectively.

Medical Policies and Guidelines for Injection, factor viii, (antihemophilic factor, recombinant), (afstyla), 1 i.u.

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