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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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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. |
format | Online Article Text |
id | pubmed-7670502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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