angiotensin II
General
Pronunciation:
an-jee-oh-ten-sin too
Trade Name(s)
- Giapreza
Ther. Class.
vasopressors
Pharm. Class.
vasopressors
Indications
Increases blood pressure in septic or other distributive shock.
Action
Causes vasoconstriction and release of aldosterone, which lead to an increase in blood pressure.
Therapeutic Effect(s):
Increase in mean arterial pressure.
Pharmacokinetics
Absorption: IV administration results in complete bioavailability.
Distribution: Unknown.
Metabolism and Excretion: Metabolized by aminopeptidase A and angiotensin converting enzyme 2 to angiotensin-(2-8) [angiotensin III] and angiotensin-(1-7), respectively in plasma, erythrocytes and many major organs.
Half-life: <1 min.
TIME/ACTION PROFILE (increase in mean arterial pressure)
ROUTE | ONSET | PEAK | DURATION |
---|---|---|---|
IV | minutes | 5 min | minutes |
Contraindication/Precautions
Contraindicated in:
- None.
Use Cautiously in:
- OB: Use only if potential maternal benefit outweighs potential fetal risk
- Lactation: Safety not established;
- Pedi: Safety and effectiveness in children not established.
Adverse Reactions/Side Effects
CNS: delirium
CV: THROMBOEMBOLIC EVENTS, peripheral ischemia, tachycardia
Endo: hyperglycemia
Hemat: thrombocytopenia
Misc: fungal infection
* CAPITALS indicate life-threatening.
Underline indicate most frequent.
Interactions
Drug-Drug
- Concurrent use with ACE inhibitors may ↑ vasopressor effects.
- Concurrent use with angiotensin receptor blockers may ↓ vasopressor effects.
Route/Dosage
IV (Adults) 20 ng/kg/min continuous infusion; may be titrated every 5 min of up to 15 ng/kg/min to achieve or maintain target mean arterial pressure. Do not exceed dose of 80 ng/kg/min during first 3 hr. During maintenance therapy, do not exceed dose of 40 ng/kg/min. Once shock has adequately improved, titrate down by 15 ng/kg/min every 5–15 min based on mean arterial pressure.
Availability
Solution for IV infusion (must be diluted): 2.5 mg/mL
Assessment
- Monitor blood pressure continuously or frequently during therapy.
- Monitor for deep venous thromboses. Use concurrent venous thromboembolism (VTE) prophylaxis (TED stockings, hydration) during therapy.
Potential Diagnoses
- Decreased cardiac output (Indications)
Implementation
- Rate:Administer based on rate in Route/Dosage. After sufficient improvement in underlying shock, down-titrate every 5–15 min by increments of up to 15 ng/kg/min based on blood pressure.
IV Administration
Continuous Infusion: Diluent: Dilute vial of angiotensin II in 250 ml for fluid restriction or 500 ml of 0.9% NaCl.Concentration: 5,000 ng/mL or 10,000 ng/mL.Store at room temperature or refrigerated for up to 24 hrs. Discard unused portion of vial or diluted solution after 24 hrs. Administer through central line.
Patient/Family Teaching
- Educate patient on purpose of angiotensin II.
- Advise female patient to notify health care profession if pregnant.
Evaluation/Desired Outcomes
Increase in mean arterial pressure.
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