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Parenteral Manual |
Hyaluronidase (SPECIAL ACCESS PROGRAM)
Disclaimer: Official controlled document is the CHEO online copy. It is the responsibility of user to ensure that any paper copy version is the same as the online version before use.
Indications:
- Management of IV extravasation
Reconstitution and Stability:
- Available as a 150 units/mL 2mL vial
- Store unopened vials refrigerated (2-8°C)
Compatibility:
- Solutions Compatible: D5W, D10W, 0.45% NaCl, 0.9% NaCl, Ringer's solution, Ringer's lactate
Administration:
(For approved routes of administration by nursing personnel, refer to Policy for the Administration of Intravenous Medications.)
SC |
YES |
IM |
NO |
IV Push |
NO |
IV Intermittent
Infusion |
NO |
IV Continuous
Infusion |
NO |
Dosage:
(For neonatal dosages, refer to Neonatal IV Drug Manual.)
- Attach a 25 or 27 gauge needle to the syringe and administer 0.2 mL subcutaneously into the leading edge of the extravasation. Remove needle and apply new 25 or 27 gauge needle for each 0.2 mL injection around the site
- Administer a total of 150 units (5 x 0.2 mL injections) subcutaneously into the extravasation site at the leading edge
- A dose of 300 units (10 x 0.2 mL or 5 x 0.4 mL injections) can be used for large infiltrates of grade +2 or greater
- Use within 1 hour of extravasation for maximal effect
- Must be given within 4 hours of infiltration
Potential hazards of parenteral administration:
- Hyaluronidase is NOT for intravenous administration
- DO NOT inject into tumors, acute inflamed or infected areas
- Hyaluronidase has an immediate onset of action and a 24 - 48 hour duration of effect
- Corticosteroids may worsen toxicity
- Toxicity of hyaluronidase is NOT increased by the use of a cold pack
- Side effects: local swelling may occur. Urticaria and erythema possible
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