The drug treatment of heart failure, once simple, has become complex. Apart
from a loop diuretic and digoxin, most patients should now be receiving an
angiotensin-converting enzyme inhibitor (or angiotensin II receptor blocke
r), a beta-blocker and spironolactone. Newer drugs, such as endothelin-rece
ptor antagonists and combined blockers of converting-enzyme and neutral end
opeptidase, might soon become available. When to introduce these drugs and
what dose is optimal for any individual, are questions that currently vex c
linicians. We proposed that plasma levels of the cardiac hormone brain natr
iuretic peptide (BNP, or better, its 1-76 amino-acid N-terminal fragment, N
-BNP), would provide an objective index for guiding drug treatment in patie
nts with established, stable cardiac failure. In a pilot study, 69 patients
were randomized to drug treatment based on clinical criteria, or based on
plasma levels of N-BNP. After a median followup of 9.6 months, those in the
N-BNP group had fewer clinical end-points than those in the group managed
by clinical criteria alone (19 vs 54; P = 0.02). These preliminary data enc
ourage the concept that the increasingly complex pharmacotherapy for heart
failure, both chronic (as in this trial) and acute, might best be guided by
an objective measure such as plasma levels of BNP or N-BNP.