Low-dose oral enoximone enhances the ability to wean patients with ultra-advanced heart failure from intravenous inotropic support: Results of the oral enoximone in intravenous inotrope-dependent subjects trial

Background We determined whether low-dose oral enoximone could wean patients with ultra-advanced heart failure (UA-HF) from intravenous (IV) inotropic support. Chronic parenteral inotropic therapy in UA-HF is costly and requires an indwelling catheter. An effective and safe oral inotrope would have...

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Published in:	The American heart journal 2007-11, Vol.154 (5), p.861-869
Main Authors:	Feldman, Arthur M., MD, PhD, Oren, Ron M., MD, Abraham, William T., MD, Boehmer, John P., MD, Carson, Peter E., MD, Eichhorn, Eric, MD, Gilbert, Edward M., MD, Kao, Andrew, MD, Leier, Carl V., MD, Lowes, Brian D., MD, Mathier, Michael A., MD, McGrew, Frank A., MD, Metra, Marco, MD, Zisman, Lawrence S., MD, Shakar, Simon F., MD, Krueger, Steven K., MD, Robertson, Alastair D., PhD, White, Bill G., PhD, Gerber, Michael J., MD, Wold, Gwyn E., MSPH, Bristow, Michael R., MD, PhD
Format:	Article
Language:	eng
Subjects:	Administration, Oral Biological and medical sciences Cardiology. Vascular system Cardiomyopathy Cardiotonic Agents - administration & dosage Cardiovascular Dose-Response Relationship, Drug Drug Administration Schedule Drug dosages Drug therapy Enoximone - administration & dosage Female Follow-Up Studies Heart Heart failure Heart Failure - drug therapy Heart Failure - mortality Heart Failure - physiopathology Heart failure, cardiogenic pulmonary edema, cardiac enlargement Humans Infusions, Intravenous Male Medical sciences Middle Aged Mortality Myocardial Contraction - drug effects Myocardial Contraction - physiology Retrospective Studies Survival Rate Treatment Outcome United States - epidemiology Ventricular Function, Left - drug effects Ventricular Function, Left - physiology
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Summary:	Background We determined whether low-dose oral enoximone could wean patients with ultra-advanced heart failure (UA-HF) from intravenous (IV) inotropic support. Chronic parenteral inotropic therapy in UA-HF is costly and requires an indwelling catheter. An effective and safe oral inotrope would have value. Methods In this placebo-controlled study, 201 subjects with UA-HF requiring IV inotropic therapy were randomized to enoximone or placebo. Subjects receiving intermittent IV inotropes were administered study medication of 25 or 50 mg 3 times a day (tid). Subjects receiving continuous IV inotropes were administered 50 or 75 mg tid for 1 week, which was reduced to 25 or 50 mg tid. The ability of subjects to remain alive and free of inotropic therapy was assessed for up to 182 days. Results Thirty days after weaning, 51 (51%) subjects on placebo and 62 (61.4%) subjects in the enoximone group were alive and free of IV inotropic therapy (unadjusted primary end point P = 0.14, adjusted for etiology P = .17). At 60 days, the wean rate was 30% in the placebo group and 46.5% in the enoximone group (unadjusted P = .016) Kaplan-Meier curves demonstrated a trend toward a decrease in the time to death or reinitiation of IV inotropic therapy over the 182-day study period (hazard ratio 0.76 [95% CI 0.55-1.04]) and a reduction at 60 days (0.62 [95% CI 0.43-0.89], P = .009) and 90 days (0.69 [95% CI 0.49-0.97], P = .031) after weaning in the enoximone group. Conclusions Although there was no benefit over placebo in weaning patients from IV inotropes from 0 to 30 days, the EMOTE data suggest that low-dose oral enoximone can be used to wean a modest percentage of subjects from IV inotropic support for up to 90 days after initiation of therapy.
ISSN:	0002-8703 1097-6744