Infliximab (Remicade)
Gastrointestinal Agent | Immunological Agent
Black Boxed Warning: Remicade carries a black boxed warning for:
- Serious infections leading to hospitalization or death, including tuberculosis (TB) and bacterial sepsis. Testing for latent TB should be performed before starting Remicade.
- Increased risk of lymphoma and other malignancies due to immunosuppression.
Clinical Pearls for Remicade (Infliximab):
- Indications: Remicade is approved for treating several inflammatory conditions including Crohn's disease, ulcerative colitis, rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, and plaque psoriasis.
- Mechanism of Action: Infliximab works by neutralizing tumor necrosis factor-alpha (TNF-α), a cytokine involved in systemic inflammation, thereby reducing the inflammatory response which is a hallmark of autoimmune disorders.
- Pre-Treatment Screening: Prior to initiating therapy, screen for latent tuberculosis and perform tests for hepatitis B virus due to potential reactivation. Continue to monitor patients throughout treatment for signs of active TB and other infections.
- Dosing and Administration: Infliximab is administered by intravenous infusion, typically at 0, 2, and 6 weeks as an induction phase, followed by a maintenance phase every 8 weeks. Dosing adjustments or interval changes may be necessary based on patient response and tolerability.
- Risk of Infusion Reactions: Administer pre-medication (antihistamines, corticosteroids, or acetaminophen) to reduce the risk of acute infusion reactions. Monitor patients during and after infusion for any signs of hypersensitivity.
- Handling and Preparation: Remicade must be reconstituted and diluted before use, adhering strictly to aseptic techniques as it does not contain any preservatives. Infusions should be prepared and used within 3 hours of reconstitution.
- Monitoring for Immunosuppressive Effects: Regularly assess patients for signs of immunosuppression, including opportunistic infections. Educational emphasis on reporting any symptoms suggestive of infection is key.
- Management of Side Effects: Closely monitor for symptoms of heart failure, as infliximab can exacerbate HF symptoms. Patients with pre-existing HF should be treated with caution, and infliximab should be discontinued if new onset or worsening symptoms occur.
- Patient Education and Compliance: Inform patients about the importance of completing the full infusion schedule and not missing doses to prevent loss of response due to antibody formation against infliximab.
- Cancer Surveillance: Due to the increased risk of lymphoma and other cancers, maintain vigilant long-term surveillance for the development of malignancies in patients treated with infliximab.
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