Circulation, Vol 56, 346-354, Copyright © 1977 by American Heart Association
NA Awan, RR Miller, AN DeMaria, KS Maxwell, A Neumann and DT Mason
The long-term efficacy of the new oral vasodilator, prazosin (PZ), was
evaluated in nine patients with refractory heart failure due to chronic
coronary heart disease. Ventricular function was assessed by cardiac
catheterization, echocardiography, and treadmill testing; symptomatic
evaluation was carried out for two to four months. One hour following 2- 7
mg PZ, control left ventricular filling pressure was reduced (32 to 18 mm
Hg, P less than 0.001) and cardiac index was elevated (1.95 to 2.89
L/min/m2, P less than 0.001) for a 6-hour period. After two weeks of PZ 2
to 7 mg four times daily, echographic end-diastolic dimension fell (5.7 to
5.4 cm, P less than 0.001) while shortening fraction increased (27.6 to
30.2%, P less than 0.005). Treadmill exercise duration increased from 209
to 317 seconds (P less than 0.001). Symptoms diminished throughout the
duration of follow-up (mean 94 days) with improvement in NYHA functional
class (3.7 to 2.2, P less than 0.001). Thus, prazosin possesses sustained
nitroprusside-like balanced dilator actions on the systemic arterial and
venous systems and is effective in the ambulatory management of chronic
severe heart failure.
ARTICLES
Efficacy of ambulatory systemic vasodilator therapy with oral prazosin in chronic refractory heart failure. Concomitant relief of pulmonary congestion and elevation of pump output demonstrated by improvements in symptomatology, exercise tolerance, hemodynamics and echocardiography
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