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Albumin
Pronunciation
U.S. Brand Names
Generic Available
Synonyms
Pharmacological Index
Use
Pregnancy Risk Factor
Contraindications
Warnings/Precautions
Adverse Reactions
Overdosage/Toxicology
Stability
Mechanism of Action
Usual Dosage
Test Interactions
Mental Health: Effects on Mental Status
Mental Health: Effects on Psychiatric Treatment
Patient Information
Nursing Implications
Dosage Forms

Pronunciation
(al BYOO min)

U.S. Brand Names
Albuminar®; Albumisol®; Albunex®; Albutein®; Buminate®; Plasbumin®

Generic Available

Yes


Synonyms
Albumin (Human); Normal Human Serum Albumin; Normal Serum Albumin (Human); Salt Poor Albumin; SPA

Pharmacological Index

Blood Product Derivative; Plasma Volume Expander, Colloid


Use

Plasma volume expansion and maintenance of cardiac output in the treatment of certain types of shock or impending shock; may be useful for burn patients, ARDS, and cardiopulmonary bypass; other uses considered by some investigators (but not proven) are retroperitoneal surgery, peritonitis, and ascites; unless the condition responsible for hypoproteinemia can be corrected, albumin can provide only symptomatic relief or supportive treatment; nutritional supplementation is not an appropriate indication for albumin


Pregnancy Risk Factor

C


Contraindications

Patients with severe anemia or cardiac failure, known hypersensitivity to albumin; avoid 25% concentration in preterm infants due to risk of idiopathic ventricular hypertrophy


Warnings/Precautions

Use with caution in patients with hepatic or renal failure because of added protein load; rapid infusion of albumin solutions may cause vascular overload. All patients should be observed for signs of hypervolemia such as pulmonary edema. Use with caution in those patients for whom sodium restriction is necessary. Rapid infusion may cause hypotension.


Adverse Reactions

1% to 10%:

Central nervous system: Fever, chills

Dermatologic: Rash

Gastrointestinal: Nausea, vomiting

Respiratory: Pulmonary edema


Overdosage/Toxicology

Symptoms of overdose include hypervolemia, congestive heart failure, pulmonary edema


Stability

Do not use solution if it is turbid or contains a deposit; use within 4 hours after opening vial


Mechanism of Action

Provides increase in intravascular oncotic pressure and causes mobilization of fluids from interstitial into intravascular space


Usual Dosage

I.V.:

25% should be used in patients in whom fluid and sodium intake must be minimized

Dose depends on condition of patient:

Children:

Emergency initial dose: 25 g

Nonemergencies: 25% to 50% of the adult dose

Adults: Usual dose: 25 g; no more than 250 g should be administered within 48 hours

Hypoproteinemia: 0.5-1 g/kg/dose; repeat every 1-2 days as calculated to replace ongoing losses

Hypovolemia: 0.5-1 g/kg/dose; repeat as needed; maximum dose: 6 g/kg/day


Test Interactions

alkaline phosphatase (S)


Mental Health: Effects on Mental Status

None reported


Mental Health: Effects on Psychiatric Treatment

None reported


Patient Information

Pregnancy precautions: Inform prescriber if you are pregnant.


Nursing Implications

Albumin administration must be completed within 4 hours after entering container, provided that administration is begun within 4 hours of entering the container; use 5 micron filter or larger, do not administer through 0.22 micron filter

Parenteral: I.V. after initial volume replacement:

5%: Do not exceed 2-4 mL/minute

25%: Do not exceed 1 mL/minute

Observe for signs of hypervolemia, pulmonary edema, and cardiac failure


Dosage Forms

Injection, as human: 5% [50 mg/mL] (50 mL, 250 mL, 500 mL, 1000 mL); 25% [250 mg/mL] (10 mL, 20 mL, 50 mL, 100 mL)


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