Preparation of Bendamustine for Infusion
Proper preparation is a critical first step in bendamustine administration. Bendamustine is a hazardous drug, necessitating the use of appropriate personal protective equipment (PPE) and designated areas for preparation, following institutional guidelines.
Handling and Storage
- All formulations require refrigerated storage (2°C to 8°C or 36°F to 46°F).
- Allow vials to reach room temperature (15°C to 30°C or 59°F to 86°F) before use.
- Visually inspect the solution for particles or discoloration after reaching room temperature. Do not use if present.
Reconstitution and Dilution
- Lyophilized powder formulations require reconstitution with sterile water for injection, USP.
- All formulations are then diluted into an appropriate infusion bag and diluent.
- Prepared admixtures have limited stability and should be administered promptly.
Administering the Infusion
Bendamustine is administered intravenously by trained healthcare professionals. Dosage and schedule are determined by the physician based on the cancer type and the patient's body surface area (BSA).
Dosage and Schedule
- Dosage varies for Chronic Lymphocytic Leukemia (CLL) and non-Hodgkin's Lymphoma (NHL).
- Dosage adjustments or delays may be necessary due to adverse effects like myelosuppression.
Infusion Rate and Monitoring
- Infusion times vary by formulation. Bendeka can be infused over 10 minutes, while other formulations might require 30 or 60 minutes.
- Ensure secure venous access and closely monitor the infusion site throughout administration for any signs of extravasation. Extravasation can cause severe tissue damage.
- If extravasation occurs, stop the infusion immediately, leave the cannula in place for aspiration, and elevate the affected limb.
Comparison of Bendamustine Formulations
Feature | Bendeka (Ready-to-Dilute) | Treanda (Lyophilized Powder) |
---|---|---|
Formulation | Ready-to-dilute liquid | Lyophilized powder requiring reconstitution |
Vial Storage | Refrigerated (2-8°C), then room temp before use. | Room temp (≤25°C), protect from light. |
Infusion Volume | Typically 50 mL. | Typically 500 mL. |
Infusion Time | 10 minutes (CLL and NHL). | 30 minutes (CLL) or 60 minutes (NHL). |
Diluent Options | 0.9% NaCl, 2.5% Dextrose/0.45% NaCl, or 5% Dextrose. | Sterile Water for reconstitution, then 0.9% NaCl or 2.5% Dextrose/0.45% NaCl for dilution. |
Partial Vial Use | Multiple-dose; refrigerated storage up to 28 days. | Single-use; discard after use. |
Stability (Room Temp) | Up to 6 hours (in NaCl) or 3 hours (in Dextrose). | Up to 3 hours. |
Post-Administration Care and Conclusion
After infusion, patients are monitored for side effects such as myelosuppression, infections, fatigue, nausea, and rash. Healthcare providers should be aware of potential severe reactions.
Conclusion
Safe and effective bendamustine administration requires healthcare professionals to be proficient in the preparation and infusion procedures. Continuous monitoring for immediate and delayed toxicities is vital. Following strict guidelines and providing comprehensive patient information helps minimize risks and enhance therapeutic outcomes. For detailed professional prescribing information, refer to resources like {Link: Drugs.com https://www.drugs.com/pro/bendamustine-injection.html}.