Effect of Prostaglandin E₁ Infusion in Severe Chronic Heart Failure

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• 作者：Richard Pacher ; Brigitte Stanek ; Martin Hc ; lsmann ; Helmut Sinzinger
• 关键词：PGE₁ infusion-catecholamines-chronic heart failure
• 刊名：Prostaglandins and Other Lipid Mediators
• 出版年：1997
• 出版时间：April 1997
• 年：1997
• 卷：53
• 期：4
• 页码：221-235
• 全文大小：1903 K

文摘

Prostaglandin E₁ (PGE₁, alprostadil) is a potent vasodilating agent that is frequently used to resolve cardiogenic pulmonary hypertension. To investigate the effect of PGE1 in refractory chronic heart failure in a double-blind trial, twenty patients (17 men, 3 women, 58 ± 2 years, cardiac index ≤ 2.51/min/m2, pulmonary capillary wedge pressure ≥ 20mmHg), who were in NYHA functional class IV on optimized treatment with ACE inhibitors and furosemide were infused with 30 ng/kg/min PGE₁ or placebo through 48 hours. All patients received a concomitant therapy with standardized catecholamine infusions which were given 24 hours in advance and were continued throughout the study. There was no difference in baseline values between the randomized groups before PGE₁ or placebo was added. PGE₁ resulted in decrements in pulmonary artery pressure (from 37 ± 4 to 30 ± 4 mmHg; p c; 0.01), pulmonary capillary wedge pressure (from 26 ± 4 to 19 ± 3 mmHg p c; 0.001) systemic vascular resistance index (from 2048 ± 213 to 1506 ± 13 dyn.sec/cm5.m2, p c; 0.05) and in increments in cardiac index and stroke volume index (from 2,2 ± 0,1 to 2.8 ± 0.2 1/min. m2; p c; 0.05 and from 23 ± 2 to 28 ± 2 1/m2; p c; 0.05, respectively). Moreover, creatinine clearance increased (p c; 0.05). Placebo infusions did not result in any hemodynamic or renal effect. Between groups percentage hemodynamic changes differed with respect to pulmonary artery pressure (p c; 0.01), cardiac index (p c; 0.05), stroke volume index (p c; 0.05) and pulmonary vascular resistance index (p c; 0.05). It is concluded that intravenous infusions with PGE₁ may add further substantial benefit to the hemodynamic state in refractory heart failure patients who are already stabilized on i.v. inotropic support with catecholamines. © 1997 by Elsevier Science Inc.