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

Arthur M. Feldman, Ron M. Oren, William T. Abraham, John P. Boehmer, Peter E. Carson, Eric Eichhorn, Edward M. Gilbert, Andrew Kao, Carl V. Leier, Brian D. Lowes, Michael A. Mathier, Frank A. McGrew, Marco Metra, Lawrence S. Zisman, Simon F. Shakar, Steven K. Krueger, Alastair D. Robertson, Bill G. White, Michael J. Gerber, Gwyn E. WoldMichael R. Bristow

Research output: Contribution to journalArticle

19 Scopus citations

Abstract

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.

Original languageEnglish (US)
Pages (from-to)861-869
Number of pages9
JournalAmerican Heart Journal
Volume154
Issue number5
DOIs
StatePublished - Nov 2007

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine

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    Feldman, A. M., Oren, R. M., Abraham, W. T., Boehmer, J. P., Carson, P. E., Eichhorn, E., Gilbert, E. M., Kao, A., Leier, C. V., Lowes, B. D., Mathier, M. A., McGrew, F. A., Metra, M., Zisman, L. S., Shakar, S. F., Krueger, S. K., Robertson, A. D., White, B. G., Gerber, M. J., ... Bristow, M. R. (2007). 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. American Heart Journal, 154(5), 861-869. https://doi.org/10.1016/j.ahj.2007.06.044