Advanced congestive heart failure (CHF) accounts for over 1 million hospital admissions
yearly in the U.S. and is also associated with a high rate of readmission to the hospital
within a short turn-around time period following discharge. CHF is associated with a
relatively high death rate, up to 40 or 50% in 2 years. The risk of sudden cardiac death in
patients with CHF is 6 to 9 times greater than that of the general population. Despite
medical advances, some patients are unresponsive to the oral medications used to treat CHF
and require added therapy. Such patients are typically New York Heart Association (NYHA)
Class III and IV, and require intravenous (IV) therapy with inotropic agents. Inotropic
agents are drugs that influence muscular contractility. IV administration with inotropic
drugs requires careful patient selection and close monitoring to ensure safe and effective
therapy.
There are many medical conditions that lead to worsening CHF and these underlying conditions
contribute to a significant and potentially life-threatening loss of cardiac function. Some
of these are conditions that lead to abnormal cardiac contraction and/or relaxation (e.g.,
coronary arterial disease, hypertension, diabetes, drug or alcohol toxicity); conditions that
lead to volume or pressure overload (mitral or tricuspid valve regurgitation,
hyperthyroidism); and conditions that limit ventricle filling (e.g., mitral or tricuspid
valve stenosis). However, many patients have a condition of dilated cardiomyopathy, an
abnormality of the heart muscle wall in which the walls of the heart become stretched and
weakened, with no easily identifiable cause. Any risk factor may cause CHF, but combinations
dramatically increase the risk of developing CHF.
Natriuretic peptides ANP and BNP are small molecules and are the group of naturally-occuring
substances that act in the body to oppose the activity of the renin-angiotensin-aldosterone
(RAA) system. They serve as counter-regulatory hormones and are secreted in response to the
increased atrial and ventricular stretching that occurs in secondary increased blood volume.
Natrecor (nesiritide) is the proprietary name for the IV formulation of human B-type
natriuretic peptide (hBNP).
In-patient treatment for acutely decompensated CHF with intravenous vasodilator therapy (such
as nitroglycerin or nitroprusside) is useful for a number of reasons. Vasodilators reduce
ventricular filling pressure and volume, decreasing pulmonary congestion and the resulting
symptoms of breathlessness. Intravenous vasodilators may also achieve afterload reduction
leading to decreased mitral regurgitation and increased forward stroke volume. IV
administration of externally produced hBNP leads to vasodilation, antagonism of the
renin-aldosterone system and an increase in diuresis. hBNP may be a potent agent for the
treatment of CHF, with a unique combination of desirable blood flow throughout the body,
hormones secreted by the sympathetic nervous system, and renal effects not possessed by
currently available therapies. In a 6-hour placebo-controlled comparison in patients with
acutely decompensated CHF, Natrecor® was associated with significant improvements in the
symptoms of CHF (including dyspnea and fatigue), a decrease in aldosterone, and an increase
in urine output. (According to LeJemtel et al 1998) The VMAC trial (Vasodilation in the
Management of Acute CHF) is a double-blinded, randomized, active-controlled and
placebo-controlled study in which the study drug would be added to standard care therapies
such as diuretics, dobutamine, or dopamine. This study compares the effects of the addition
of Natrecor®, nitroglycerin, or placebo to standard care (diuretics, dobutamine, dopamine, or
other long-term cardiac therapies) in patients requiring hospitalization for the treatment of
dyspnea at rest due to acutely decompensated CHF. Based on the cumulative experience with
Natrecor, the dose of Natrecor was modified for the VMAC trial to a 2-µg/kg bolus followed by
a 0.01-µg/kg/min infusion.
The primary objective of the VMAC study is to compare the blood flow and observe treatment
and safety effects of the new dose of Natrecor to placebo, when added to standard care, in
the treatment of acutely worsening CHF. The primary overall outcome that the study plan is
based upon are the changes from the beginning of a study to 3 hours after the start of study
drug, in pulmonary capillary wedge pressure (PCWP) (in subjects who have right heart
catheters only) and the subject's self-evaluation of their breathing difficulties. The
secondary objective is to compare the hemodynamic, (blood flow throughout the body) and
clinical effects of Natrecor® with IV nitroglycerin and placebo. Additional objectives
include a comparison of the use of other IV vasoactive agents and/or IV diuretics and the
effects on other hemodynamic variables. The hypothesis of this study is that using the
modified dose of Natrecor, (a 2-µg/kg bolus followed by a 0.01-µg/kg/min infusion) will
achieve peak effects sooner than with previously studied doses, to sustain effects for at
least 48 hours, and minimize excessive effects on blood pressure. Natrecor or placebo,
administered as an intravenous 2-µg/kg bolus, followed by a fixed-dose infusion of
0.01-µg/kg/min.