(nesiritide, Scios Inc.)
A recombinant form of human B-type natriuretic peptide (hBNP) for people with acutely decompensated congestive heart failure (CHF), with shortness of breath at rest or with minimal activity. This is the first new treatment approved for decompensated CHF in more than a decade.
Dosage: A loading IV bolus dose of 2 [micro]g/kg, followed by a continuous infusion at a dose of 0.01 [micro]g/kg.
Special Considerations: In the pivotal trial, the rate of symptomatic hypotension in the first 24 hours was similar with IV nitroglycerin (5% of patients) and Natrecor (4%). The episodes lasted significantly longer in those on Natrecor, which has a relatively long half-life and should be administered in a setting where blood pressure can be closely monitored.
Comment: This form of hBNP produced by the left ventricle in response to heart failure, increases cardiac output by relaxing arteries and veins. It does not increase the rate of arrhythmias, an issue with inotropic agents used in CHF, said Dr. Clyde W. Yancy, medical director of the CHE and transplant program at the University of Texas Southwestern Medical Center, Dallas.
In patients hospitalized with dyspnea at rest caused by acutely decompensated class IV CHF, those on Natrecor plus standard therapy had a quicker reduction in pulmonary capillary wedge pressure and improvements in dyspnea, without an increase in arrhythmias, compared with placebo plus standard care.
The approval "allows us to exploit a favorable component of the overall neurohormonal environment in which patients function," the natriuretic peptide system, said Dr. Yancy a member of the Scios Advisory Board.
COPYRIGHT 2001 International Medical News Group
COPYRIGHT 2001 Gale Group