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The Hemodynamic Effects of Long‐Term ACE Inhibition with Fosinopril in Patients with Heart Failure

 

作者: Satish,   Sharma David,   Deitchman Judianne,   Eni Kate,   Gelperin John,   Ilgenfritz Mel,  

 

期刊: American Journal of Therapeutics  (OVID Available online 1999)
卷期: Volume 6, issue 4  

页码: 181-190

 

ISSN:1075-2765

 

年代: 1999

 

出版商: OVID

 

关键词: angiotensin-converting enzyme inhibitor;fosinopril;heart failure.

 

数据来源: OVID

 

摘要:

The objective of this study was to evaluate the hemodynamic and clinical effects of fosinopril in patients with heart failure. This was a prospective, multicenter, double-blind, randomized, parallel-group study. Patients 18 to 80 years of age who were receiving diuretics with a systolic blood pressure (SBP) > 90 mm Hg, New York Heart Association (NYHA) functional class II-IV, left ventricular ejection fraction < 40%, pulmonary capillary wedge pressure (PCWP) > 18 mm Hg, and a cardiac index (CI) < 2.6 L/min/m2were eligible. A total of 179 patients were randomized to a single, double-blind oral dose of placebo or fosinopril at 1, 20, or 40 mg, and hemodynamic monitoring was performed for 24 hours postdose; 155 patients with SBP > 90 mm Hg were re-randomized to 10 weeks of double-blind fosinopril at 1, 20, or 40 mg once daily. Hemodynamic monitoring was repeated at the last visit, beginning at 24 hours postdose (trough) and continuing for 12 hours thereafter. Significant decreases in preload (PCWP) and afterload (mean arterial blood pressure [MABP] and systemic vascular resistance [SVR]) were evident 3 to 4 hours after a single dose of fosinopril at 20 and 40 mg and continuing for up to 8 to 12 hours postdose for PCWP and SVR and for up to 24 hours postdose for MABP (P< .05vplacebo and baseline). Sustained decreases in PCWP, MABP, SVR, and heart rate and increases in CI and stroke volume index were observed after 10 weeks of treatment with fosinopril at 20 and 40 mg once daily (P< .05v1 mg group for PCWP and MABP at most time points andP< .05vbaseline for other parameters at most time points). Dose-related trends toward reduced supplemental diuretic use (P= .027) and reduced symptoms of dyspnea (P= .008) were observed with the 20-mg and 40-mg fosinopril dose groups. Once daily administration of fosinopril at 20 and 40 mg was safe and well tolerated, provided a sustained beneficial hemodynamic effect, improved left ventricular performance, and reduced symptoms of dyspnea, resulting in a reduced need for supplemental diuretic therapy.

 

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