NESIRITIDE (nes-ir'i-tide) Natrecor Classifications: cardiovascular agent; atrial natriuretic peptide hormone Pregnancy Category: C |
1.5 mg vial
Nesiritide is a human B-type natriuretic peptide (hBNP), produced by recombinant DNA, which mimics the actions of human atrial natriuretic hormone (ANH). ANH is secreted by the right atrium when atrial blood pressure increases. Nesiritide, like ANH, inhibits antidiuretic hormone (ADH) by increasing urine sodium loss by the kidney and triggering the formation of a large volume of dilute urine.
Nesiritide binds to a cyclic nucleic acid, which results in smooth muscle cell relaxation. The drug also causes dilation of veins and arteries. It is effective in managing dyspnea at rest in patients with acute congestive heart failure (CHF).
Acute treatment of decompensated CHF in patients who have dyspnea at rest or with minimal activity.
Hypersensitivity to nesiritide, patients with a systolic blood pressure <90 mm Hg, cardiogenic shock, patients with low cardiac filling pressures, patients who should not receive vasodilators, such as those with significant valvular stenosis, restrictive or obstructive cardiomyopathy, constrictive pericarditis, pericardial tamponade; pregnancy (category C).
Lactation, concurrent administration of ACE inhibitors or vasodilators. Safety and efficacy in pediatric patients have not been established.
Acute Decompensated CHF Adult: IV 2 mcg/kg bolus administered over 60 s, followed by a continuous infusion of 0.01 mcg/kg/min (0.1 mL/kg/h) (max: 0.03 mcg/kg/min). Monitor blood pressure closely. If hypotension occurs, the dose should be reduced or discontinued. The infusion can subsequently be restarted at a dose that is reduced by 30% (with no bolus administration) after stabilization of hemodynamics. |
Intravenous PREPARE: Direct: and IV Infusion: Reconstitute one 1.5 mg vial by adding 5 mL of IV solution removed from a 250 mL bag of selected diluent (i.e., D5W, NS, D5/0.45% NaCl, D5/0.2% NaCl). Rock the vial gently so that all surfaces, including the stopper, contact the diluent ensuring complete reconstitution. Do not shake the vial. Add the entire contents of the vial to the 250 mL IV bag to yield approximately 6 mcg/mL. Invert the bag several times to mix completely. Use within 24 h. Prime the IV tubing with 25 mL prior to connecting to the vascular access port. ADMINISTER: Direct: Withdraw the bolus dose from the prepared infusion bag. Determine dose as follows: bolus volume (mL) = (0.33) x (patient weight in kg). Give the bolus dose over 60 sec through an IV port in the tubing. IV Infusion: Infuse remainder of IV infusion immediately following the bolus dose. Determine the infusion rate as follows: flow rate (mL/h) = (0.1) x (patient weight in kg). INCOMPATIBILITIES Solution/additive and Y-site: Bumetanide, enalaprilate, ethacrynic acid, furosemide, heparin, hydralazine, insulin. |
Assessment & Drug Effects