Department of Cardiology Alfred Hospital Melbourne Australia.
Heart Failure Research Group Baker Heart and Diabetes Institute Melbourne Australia.
J Am Heart Assoc. 2020 Jul 7;9(13):e015026. doi: 10.1161/JAHA.119.015026. Epub 2020 Jun 18.
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; =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]; =0.092). Heart rate (-1±5 versus -2±9 bpm; =0.9) and systolic blood pressure (-3±18 versus +1±12 mm Hg; =0.57) were unchanged. Early filling velocity/early mitral annular velocity (-0.3±3.0 versus -1.9±4.8; =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.
射血分数保留的心力衰竭(HFpEF)是一种日益流行的心力衰竭形式,占心力衰竭总负担的一半。我们假设使用新型米力农口服制剂调节磷酸二酯酶 3/环 AMP 可能通过肺和全身血管扩张以及增强心室舒张对 HFpEF 产生有利影响。我们评估了口服米力农对 HFpEF 患者生活质量和功能结局的安全性和疗效。
MilHFPEF(缓释口服米力农治疗射血分数保留的心力衰竭)研究是一项在 23 例有症状的 HFpEF 患者中进行的随机、双盲、安慰剂对照的初步研究。疗效终点包括基线时堪萨斯城心肌病问卷综合评分和 6 分钟步行距离的变化。主要安全性终点是临床显著心律失常的发生。与安慰剂相比,米力农治疗组的堪萨斯城心肌病问卷评分显著改善(+10±13 与-3±15;=0.046)。治疗组 6 分钟步行距离也较安慰剂组有改善趋势(+22[-8 至 49]与-47[-97 至 12];=0.092)。心率(-1±5 与-2±9bpm;=0.9)和收缩压(-3±18 与+1±12mmHg;=0.57)无变化。早期充盈速度/早期二尖瓣环速度(-0.3±3.0 与-1.9±4.8;=0.38)无变化。安慰剂组有 1 例患者因心力衰竭住院。动态心电图监测未显示米力农有致心律失常作用的证据。
在这项新的初步研究中,缓释口服米力农耐受性良好,可改善 HFpEF 患者的生活质量。需要进一步进行更长期的研究,以确定这种治疗方法在 HFpEF 中的作用。