Key result
Long-term IV milrinone is safe and linked to 60% cardiac recovery in pediatric decompensated DCM.
Why the study?
The study was conducted to assess the safety and efficacy of long-term milrinone therapy in children with acute decompensated heart failure due to dilated cardiomyopathy.
Does continuous long-term intravenous milrinone improve clinical outcomes and safety in children with acute decompensated heart failure due to dilated cardiomyopathy?
Cohort (n=47)
No
Does continuous long-term intravenous milrinone improve clinical outcomes and safety in children with acute decompensated heart failure due to dilated cardiomyopathy?
Long-term intravenous milrinone is safe and effective as a bridge to recovery in pediatric patients with acute decompensated dilated cardiomyopathy, potentially reducing the need for mechanical support or transplantation.
Supports milrinone as bridge in pediatric cardiomyopathy; hypothesis-generating, requiring randomized trials before practice change.
AIM: The aim of this study was to assess the safety and efficacy of long-term milrinone therapy in children with acute decompensated heart failure due to dilated cardiomyopathy (DCM). METHODS: A single-centre retrospective study of all children ≤18 years with acute decompensated heart failure and DCM who received continuous long-term (≥7 consecutive days) intravenous milrinone between January 2008 and January 2022. RESULTS: The 47 patients had a median age of 3.3 months [interquartile range (IQR) 1.0-18.1], weight of 5.7 kg [IQR 4.3-10.1] and fractional shortening of 11.9% [±4.7]. Idiopathic DCM (n = 19) and myocarditis (n = 18) were the most common diagnoses. The median milrinone infusion duration was 27 days [IQR 10-50, range 7-290]. No adverse events necessitated milrinone termination. Nine patients required mechanical circulatory support. Median follow-up was 4.2 years [IQR 2.7-8.6]. On initial admission, four patients died, six were transplanted and 79% [37/47] were discharged home. The 18 readmissions resulted in five more deaths and four transplantations. Cardiac function recovered in 60% [28/47], as measured by normalised fractional shortening. CONCLUSION: Long-term intravenous milrinone is safe and effective in paediatric acute decompensated DCM. Combined with conventional heart failure therapies, it can act as a bridge to recovery and thereby potentially reduce the need for mechanical support or heart transplantation.
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Brown et al. (2023) conducted a cohort in Acute decompensated heart failure due to dilated cardiomyopathy (n=47). Intravenous milrinone was evaluated on Cardiac function recovery. Long-term intravenous milrinone in children with acute decompensated dilated cardiomyopathy was safe, with no adverse events requiring termination, and resulted in cardiac function recovery in 60%.
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