Key result
Repetitive, intermittent short-term intravenous milrinone significantly reduced median BNP levels from 882 to 631 pg/ml (p=0.017) and improved NYHA class without increasing ventricular tachycardia or hospitalizations.
Why the study?
Advanced HF patients poorly tolerate GDMT, while continuous outpatient inotrope use is hindered by excess morbidity, prompting evaluation of repetitive intermittent intravenous milrinone to stabilize patients and up-titrate GDMT.
Does repetitive, intermittent intravenous milrinone therapy safely improve symptoms and allow up-titration of GDMT in patients with ambulatory advanced heart failure?
Cohort (n=24)
Open-label
No
Does repetitive, intermittent intravenous milrinone therapy safely improve symptoms and allow up-titration of GDMT in patients with ambulatory advanced heart failure?
Repetitive, intermittent short-term milrinone infusions may safely stabilize ambulatory advanced HFrEF patients, improving surrogate markers and allowing further optimization of guideline-directed medical therapies.
May stabilize advanced HFrEF symptomatically; leaves open effects on GDMT up-titration and outcomes in randomized trials.
BACKGROUND: Advanced heart failure (HF) patients usually poorly tolerate guideline-directed HF medical therapy (GDMT) and suffer high rates of morbidity and mortality. The use of continuous inotropes in the outpatient settings is hampered by previous data showing excess morbidity. We aimed to assess the safety and efficacy of repetitive, intermittent, short-term intravenous milrinone therapy in advanced HF patients with an intention to introduce and up-titrate GDMT and improve functional class. HYPOTHESIS: Repetitive, intermittent milrinone therapy may assist with the stabilization of advanced HF patients. METHODS: Advanced HF patients treated with beta-blockers and implanted with defibrillators were initiated with repetitive, intermittent short-term intravenous milrinone therapy at our HF outpatient unit. Patients were prospectively followed with defibrillator interrogation, functional class assessment, B-natriuretic peptide (BNP) levels, and echocardiography parameters. RESULTS: The cohort included 24 patients with a mean 330 ± 240 days of milrinone therapy exposure. Mean age was 73 ± 6 years with male predominance (96%). Following milrinone therapy, median BNP levels decreased significantly (882 [286-3768] to 631 [278-1378] pg/ml, p = .017) with a significant reduction in the number of patients with New York Heart Association (NYHA) Class III and IV (p = .012, 0.013) and an increase in number of patients on GDMT. Importantly, the number of total sustained ventricular tachycardia events and HF hospitalizations did not change. CONCLUSIONS: In this small cohort of advanced HF, repetitive, intermittent, short-term milrinone therapy was found to be safe and potentially efficacious.
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Laufer‐Perl et al. (2022) conducted a cohort in Advanced heart failure (HFrEF) (n=24). Repetitive intermittent intravenous milrinone was evaluated on Change in median BNP levels (Decreased from 882 to 631 pg/ml, p=0.017). Repetitive, intermittent short-term intravenous milrinone significantly reduced median BNP levels from 882 to 631 pg/ml (p=0.017) and improved NYHA class without increasing ventricular tachycardia or hospitalizations.
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