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Pronunciation |
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(al
BYOO
min) |
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U.S. Brand
Names |
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Albuminar®; Albumisol®;
Albunex®; Albutein®; Buminate®;
Plasbumin® |
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Generic
Available |
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Yes |
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Synonyms |
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Albumin (Human); Normal Human Serum Albumin; Normal Serum Albumin (Human); Salt
Poor Albumin; SPA |
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Pharmacological Index |
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Blood Product Derivative; Plasma Volume Expander, Colloid |
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Use |
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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 |
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|
Pregnancy Risk
Factor |
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C |
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Contraindications |
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Patients with severe anemia or cardiac failure, known hypersensitivity to
albumin; avoid 25% concentration in preterm infants due to risk of idiopathic
ventricular hypertrophy |
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Warnings/Precautions |
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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. |
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|
Adverse
Reactions |
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1% to 10%:
Central nervous system: Fever, chills
Dermatologic: Rash
Gastrointestinal: Nausea, vomiting
Respiratory: Pulmonary edema |
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Overdosage/Toxicology |
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Symptoms of overdose include hypervolemia, congestive heart failure,
pulmonary edema |
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Stability |
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Do not use solution if it is turbid or contains a deposit; use within 4 hours
after opening vial |
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Mechanism of
Action |
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Provides increase in intravascular oncotic pressure and causes mobilization
of fluids from interstitial into intravascular space |
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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
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Test
Interactions |
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alkaline phosphatase
(S) |
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|
Mental Health: Effects
on Mental Status |
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None reported |
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Mental Health:
Effects on Psychiatric
Treatment |
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None reported |
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Patient
Information |
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Pregnancy precautions: Inform prescriber if you are
pregnant. |
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Nursing
Implications |
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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
|
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Dosage Forms |
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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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