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Extended‐Release Oral Milrinone for the Treatment of Heart Failure With Preserved Ejection Fraction

BACKGROUND: Heart failure with preserved ejection fraction (HFpEF) is an increasingly prevalent form of heart failure, representing half of the total burden of heart failure. We hypothesised that modulation of the phosphodiesterase type 3/cyclic AMP using a novel oral formulation of milrinone might...

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Autores principales: Nanayakkara, Shane, Byrne, Melissa, Mak, Vivian, Carter, Kaye, Dean, Eliza, Kaye, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670502/
https://www.ncbi.nlm.nih.gov/pubmed/32552264
http://dx.doi.org/10.1161/JAHA.119.015026
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author Nanayakkara, Shane
Byrne, Melissa
Mak, Vivian
Carter, Kaye
Dean, Eliza
Kaye, David M.
author_facet Nanayakkara, Shane
Byrne, Melissa
Mak, Vivian
Carter, Kaye
Dean, Eliza
Kaye, David M.
author_sort Nanayakkara, Shane
collection PubMed
description BACKGROUND: Heart failure with preserved ejection fraction (HFpEF) is an increasingly prevalent form of heart failure, representing half of the total burden of heart failure. We hypothesised that modulation of the phosphodiesterase type 3/cyclic AMP using a novel oral formulation of milrinone might exert favorable effects HFpEF via pulmonary and systemic vasodilation and enhancement of ventricular relaxation. We assessed the safety and efficacy of oral milrinone on quality of life and functional outcomes in patients with HFpEF. METHODS AND RESULTS: The MilHFPEF (Extended Release Oral Milrinone for the Treatment of Heart Failure With Preserved Ejection Fraction) study was a randomized, double‐blind, placebo‐controlled pilot study in 23 patients with symptomatic HFpEF. Efficacy end points included changes from baseline in Kansas City Cardiomyopathy Questionnaire summary score and 6‐minute walk distance. The primary safety end point was the development of clinically significant arrhythmia. The Kansas City Cardiomyopathy Questionnaire score improved significantly in milrinone‐treated patients compared with placebo (+10±13 versus −3±15; P=0.046). Six‐minute walk distance also tended to improve in the treatment group compared with placebo (+22 [−8 to 49] versus −47 [−97 to 12]; P=0.092). Heart rate (−1±5 versus −2±9 bpm; P=0.9) and systolic blood pressure (−3±18 versus +1±12 mm Hg; P=0.57) were unchanged. Early filling velocity/early mitral annular velocity (−0.3±3.0 versus −1.9±4.8; P=0.38) was unchanged. One patient in the placebo arm was hospitalized for heart failure. Holter monitoring did not demonstrate evidence of a proarrhythmic effect of milrinone. CONCLUSIONS: In this novel pilot study, extended release oral milrinone was well tolerated and associated with improved quality of life in patients with HFpEF. Further longer‐term studies are warranted to establish the role of this therapeutic approach in HFpEF. REGISTRATION: URL: https://www.anzctr.org.au/; Unique identifier: ACTRN12616000619448.
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spelling pubmed-76705022020-11-23 Extended‐Release Oral Milrinone for the Treatment of Heart Failure With Preserved Ejection Fraction Nanayakkara, Shane Byrne, Melissa Mak, Vivian Carter, Kaye Dean, Eliza Kaye, David M. J Am Heart Assoc Original Research BACKGROUND: Heart failure with preserved ejection fraction (HFpEF) is an increasingly prevalent form of heart failure, representing half of the total burden of heart failure. We hypothesised that modulation of the phosphodiesterase type 3/cyclic AMP using a novel oral formulation of milrinone might exert favorable effects HFpEF via pulmonary and systemic vasodilation and enhancement of ventricular relaxation. We assessed the safety and efficacy of oral milrinone on quality of life and functional outcomes in patients with HFpEF. METHODS AND RESULTS: The MilHFPEF (Extended Release Oral Milrinone for the Treatment of Heart Failure With Preserved Ejection Fraction) study was a randomized, double‐blind, placebo‐controlled pilot study in 23 patients with symptomatic HFpEF. Efficacy end points included changes from baseline in Kansas City Cardiomyopathy Questionnaire summary score and 6‐minute walk distance. The primary safety end point was the development of clinically significant arrhythmia. The Kansas City Cardiomyopathy Questionnaire score improved significantly in milrinone‐treated patients compared with placebo (+10±13 versus −3±15; P=0.046). Six‐minute walk distance also tended to improve in the treatment group compared with placebo (+22 [−8 to 49] versus −47 [−97 to 12]; P=0.092). Heart rate (−1±5 versus −2±9 bpm; P=0.9) and systolic blood pressure (−3±18 versus +1±12 mm Hg; P=0.57) were unchanged. Early filling velocity/early mitral annular velocity (−0.3±3.0 versus −1.9±4.8; P=0.38) was unchanged. One patient in the placebo arm was hospitalized for heart failure. Holter monitoring did not demonstrate evidence of a proarrhythmic effect of milrinone. CONCLUSIONS: In this novel pilot study, extended release oral milrinone was well tolerated and associated with improved quality of life in patients with HFpEF. Further longer‐term studies are warranted to establish the role of this therapeutic approach in HFpEF. REGISTRATION: URL: https://www.anzctr.org.au/; Unique identifier: ACTRN12616000619448. John Wiley and Sons Inc. 2020-06-18 /pmc/articles/PMC7670502/ /pubmed/32552264 http://dx.doi.org/10.1161/JAHA.119.015026 Text en © 2020 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Nanayakkara, Shane
Byrne, Melissa
Mak, Vivian
Carter, Kaye
Dean, Eliza
Kaye, David M.
Extended‐Release Oral Milrinone for the Treatment of Heart Failure With Preserved Ejection Fraction
title Extended‐Release Oral Milrinone for the Treatment of Heart Failure With Preserved Ejection Fraction
title_full Extended‐Release Oral Milrinone for the Treatment of Heart Failure With Preserved Ejection Fraction
title_fullStr Extended‐Release Oral Milrinone for the Treatment of Heart Failure With Preserved Ejection Fraction
title_full_unstemmed Extended‐Release Oral Milrinone for the Treatment of Heart Failure With Preserved Ejection Fraction
title_short Extended‐Release Oral Milrinone for the Treatment of Heart Failure With Preserved Ejection Fraction
title_sort extended‐release oral milrinone for the treatment of heart failure with preserved ejection fraction
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670502/
https://www.ncbi.nlm.nih.gov/pubmed/32552264
http://dx.doi.org/10.1161/JAHA.119.015026
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