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Hyaluronidase
Pronunciation
U.S. Brand Names
Generic Available
Pharmacological Index
Use
Pregnancy Risk Factor
Contraindications
Warnings/Precautions
Adverse Reactions
Overdosage/Toxicology
Drug Interactions
Stability
Mechanism of Action
Pharmacodynamics/Kinetics
Usual Dosage
Mental Health: Effects on Mental Status
Mental Health: Effects on Psychiatric Treatment
Dental Health: Local Anesthetic/Vasoconstrictor Precautions
Dental Health: Effects on Dental Treatment
Patient Information
Nursing Implications
Dosage Forms
References

Pronunciation
(hye al yoor ON i dase)

U.S. Brand Names
Wydase® Injection

Generic Available

No


Pharmacological Index

Antidote


Use

Increases the dispersion and absorption of other drugs; increases rate of absorption of parenteral fluids given by hypodermoclysis; enhances diffusion of locally irritating or toxic drugs in the management of I.V. extravasation


Pregnancy Risk Factor

C


Contraindications

Hypersensitivity to hyaluronidase or any component; do not inject in or around infected, inflamed, or cancerous areas


Warnings/Precautions

Drug infiltrates in which hyaluronidase is contraindicated: Dopamine, alpha-adrenergic agonists; an intradermal skin test for sensitivity should be performed before actual administration using 0.02 mL of a 150 units/mL of hyaluronidase solution


Adverse Reactions

<1%: Tachycardia, hypotension, dizziness, chills, urticaria, erythema, nausea, vomiting


Overdosage/Toxicology

Symptoms of overdose include local edema, urticaria, erythema, chills, nausea, vomiting, hypotension


Drug Interactions

Decreased effect: Salicylates, cortisone, ACTH, estrogens, antihistamines


Stability

Reconstituted hyaluronidase solution remains stable for only 24 hours when stored in the refrigerator; do not use discolored solutions


Mechanism of Action

Modifies the permeability of connective tissue through hydrolysis of hyaluronic acid, one of the chief ingredients of tissue cement which offers resistance to diffusion of liquids through tissues


Pharmacodynamics/Kinetics

Onset of action: Immediate by the subcutaneous or intradermal routes for the treatment of extravasation

Duration: 24-48 hours


Usual Dosage

Infants and Children:

Management of I.V. extravasation: Reconstitute the 150 unit vial of lyophilized powder with 1 mL normal saline; take 0.1 mL of this solution and dilute with 0.9 mL normal saline to yield 15 units/mL; using a 25- or 26-gauge needle, five 0.2 mL injections are made subcutaneously or intradermally into the extravasation site at the leading edge, changing the needle after each injection

Hypodermoclysis:

S.C.: 1 mL (150 units) is added to 1000 mL of infusion fluid and 0.5 mL (75 units) in injected into each clysis site at the initiation of the infusion

I.V.: 15 units is added to each 100 mL of I.V. fluid to be administered

Children <3 years: Limit volume of single clysis to 200 mL

Premature Infants: Do not exceed 25 mL/kg/day and not >2 mL/minute

Adults: Absorption and dispersion of drugs: 150 units are added to the vehicle containing the drug


Mental Health: Effects on Mental Status

May cause dizziness


Mental Health: Effects on Psychiatric Treatment

None reported


Dental Health: Local Anesthetic/Vasoconstrictor Precautions

No information available to require special precautions


Dental Health: Effects on Dental Treatment

No effects or complications reported


Patient Information

Report itching, pain, changes in respiration, or excessive dizziness. Pregnancy/breast-feeding precautions: Inform prescriber if you are or intend to be pregnant. Consult prescriber if breast-feeding.


Nursing Implications

Appropriate drugs for the management of an acute hypersensitivity (epinephrine, corticosteroids, and antihistamines) should be readily available


Dosage Forms

Injection, stabilized solution: 150 units/mL (1 mL, 10 mL)

Powder for injection, lyophilized: 150 units, 1500 units


References

Berger EY, "Nutrition by Hypodermoclysis," J Am Geriatr Soc, 1984, 32(3):199-203.

Bertelli G, "Prevention and Management of Extravasation of Cytotoxic Drugs," Drug Saf, 1995, 12(4):245-55.

Bertelli G, Dini D, Forno GB, et al, "Hyaluronidase as an Antidote to Extravasation of Vinca Alkaloids: Clinical Results," J Cancer Res Clin Oncol, 1994, 120(8):505-6.

Dorr RT, "Vinca Alkaloid Ulceration: Experimental Mouse Model and Effects of Local Antidotes," Proc Am Soc Clin Oncol, 1982, 1:428.

Elam EA, Dorr RT, Lagel KE, et al, "Cutaneous Ulceration Due to Contrast Extravasation. Experimental Assessment of Injury and Potential Antidotes," Invest Radiol, 1991, 26(1):13-6.

Lipschitz S, Campbell AJ, Roberts MS, et al, "Subcutaneous Fluid Administration in Elderly Subjects: Validation of an Underused Technique," J Am Geriatr Soc, 1991, 39(1):6-9.

Raszka WV Jr, Kueser TK, Smith FR, et al, "The Use of Hyaluronidase in the Treatment of Intravenous Extravasation Injuries," J Perinatol, 19909, 10(2):146-9.

Zenk KE, "Hyaluronidase: An Antidote for Intravenous Extravasations," CSHP Voice, 1981, 66-8.

Zenk KE, "Management of Intravenous Extravasations," Infusion, 1981, 5:77-9.

Zenk KE, "Treating I.V. Extravasations With Hyaluronidase," ASHP Signal, 1986, 10:25,29.

Zenk KE, Dungy CI, and Greene GR, "Nafcillin Extravasation Injury: Use of Hyaluronidase as an Antidote," Am J Dis Child, 1981, 135(12):1113-4.


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