Single-centred experience with levosimendan in paediatric decompensated dilated cardiomyopathy
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Pierre-Emmanuel Séguéla1, Philippe Mauriat2, Jean-Baptiste Mouton1
1Paediatric Cardiology Unit, Bordeaux University Hospital, Bordeaux, France.
Insights
Levosimendan improved hemodynamics in children with advanced heart failure, potentially delaying mechanical support needs while awaiting heart transplants. This inotropic agent is a valuable consideration for pediatric heart failure management.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Pharmacology
- Heart Failure Management
Background:
- Children with dilated cardiomyopathy often face prolonged waits for heart transplantation, necessitating mechanical circulatory support.
- Levosimendan, a positive inotropic agent, shows promise in treating pediatric heart failure.
Purpose of the Study:
- To evaluate the clinical experience of using levosimendan in pediatric patients with decompensated dilated cardiomyopathy.
Main Methods:
- Retrospective analysis of pediatric patients with dilated cardiomyopathy awaiting transplantation.
- Levosimendan infusions administered prior to mechanical circulatory support consideration.
- Analysis of biological markers (B-type natriuretic peptide) and echocardiographic parameters (ejection fraction, velocity time integral).
Main Results:
- Significant reduction in B-type natriuretic peptide levels post-infusion (P=0.003).
- Trend towards improved left ventricular ejection fraction (P=0.054-0.068).
- Significant increase in subaortic velocity time integral, indicating improved cardiac output (P=0.041).
Conclusions:
- Levosimendan demonstrates hemodynamic benefits in pediatric decompensated dilated cardiomyopathy.
- Repeated levosimendan infusions may postpone the need for mechanical circulatory support.
- Levosimendan should be considered as an adjunct to standard inotropic therapies in this patient population.
Background:
Children with dilated cardiomyopathy in advanced heart failure may spend a long time awaiting heart transplantation. Consequently, mechanical circulatory support is sometimes required as a bridge to transplantation. Levosimendan, a positive inotropic agent, has been reported to be safe and efficient for the treatment of paediatric heart failure.
Aims:
To report our experience with levosimendan in children with decompensated dilated cardiomyopathy.
Methods:
Paediatric patients with dilated cardiomyopathy on the transplant waiting list and with criteria for mechanical support were included in this single-centred retrospective study. Each patient received at least one 24-hour infusion of levosimendan before mechanical circulatory support was considered. Biological and echocardiographic data were analysed.
Results:
Six patients were included over a 24-month period. The median age was 25.5months (7.7-34.2months); 82 infusions were performed. Median B-type natriuretic peptide concentration decreased significantly between days 0 and 2 (2443ng/L [1458-3819ng/L] vs 1358ng/L [1025-2534ng/L]; P=0.003). While only a trend was noted in left ventricular ejection fraction improvement (P=0.054 by Simpson's method and P=0.068 by the Teicholz method), the subaortic velocity time integral rose significantly between days 0 and 8 (12.8cm/s [10-14.5cm/s] vs 15.3cm/s [14.3-16.9cm/s]; P=0.041).
Conclusions:
Levosimendan seems to improve haemodynamics in children with decompensated dilated cardiomyopathy; repeated infusions may delay the need for mechanical circulatory support while awaiting heart transplantation. This therapeutic agent should be systematically considered in this setting, in addition to conventional inotropic drugs.
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