Key result
Pediatric mechanical circulatory support achieves ~82% 1-year survival, with worse outcomes in infants and smaller children.
Why the study?
The registry aimed to gather data on durable mechanical circulatory support to publish updated reports on therapy course, with expanded efforts to analyse younger and lower-weight patients.
What is the survival and adverse event rate in pediatric patients receiving mechanical circulatory support in a real-world European registry?
Observational (n=353)
Yes
What is the survival and adverse event rate in pediatric patients receiving mechanical circulatory support in a real-world European registry?
Mechanical circulatory support provides an 81.5% 1-year survival rate in pediatric patients with end-stage heart failure, serving as an effective bridge to transplant or recovery, though young age (<1 year) and low weight (<20 kg) remain significant risk factors.
Answers are grounded in this paper and cite their sources.
Supports MCS as bridge in pediatric HF with caution in infants <20 kg; extends EUROMACS data but leaves optimal strategies open.
OBJECTIVES A second paediatric report has been generated from the European Registry for Patients with Mechanical Circulatory Support (EUROMACS). The purpose of EUROMACS, which is operated by the European Association for Cardio-Thoracic Surgery, is to gather data related to durable mechanical circulatory support for scientific purposes and to publish reports with respect to the course of mechanical circulatory support therapy. Since the first report issued, efforts to increase compliance and participation have been extended. Additionally, the data provided the opportunity to analyse patients of younger age and lower weight. METHODS Participating hospitals contributed pre-, peri- and long-term postoperative data on mechanical circulatory support implants to the registry. Data for all implants in paediatric patients (≤19 years of age) performed from 1 January 2000 to 1 July 2019 were analysed. This report includes updates of patient characteristics, implant frequency, outcome (including mortality rates, transplants and recovery rates) as well as adverse events including neurological dysfunction, device malfunction, major infection and bleeding. RESULTS Twenty-nine hospitals contributed 398 registered implants in 353 patients (150 female, 203 male) to the registry. The most frequent aetiology of heart failure was any form of cardiomyopathy (61%), followed by congenital heart disease and myocarditis (16.4% and 16.1%, respectively). Competing outcomes analysis revealed that a total of 80% survived to transplant or recovery or are ongoing; at the 2-year follow-up examination, 20% died while on support. At 12 months, 46.7% received transplants, 8.7% were weaned from their device and 18.5% died. The 3-month adverse events rate was 1.69 per patient-year for device malfunction including pump exchange, 0.48 for major bleeding, 0.64 for major infection and 0.78 for neurological events. CONCLUSIONS The overall survival rate was 81.5% at 12 months following ventricular assist device implant. The comparison of survival rates of the early and later eras shows no significant difference. A focus on specific subgroups showed that survival was less in patients of younger age (<1 year of age) (P = 0.01) and lower weight (<20 kg) (P = 0.015). Transplant rates at 6 months continue to be low (33.2%) The fact that the EUROMACS registry is embedded within the European Association for Cardio-Thoracic Surgery Quality Improvement Programme offers opportunities to focus on improving outcomes.
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By et al. (2020) conducted an observational in Pediatric end-stage heart failure requiring mechanical circulatory support (n=353). Mechanical circulatory support (VAD) was evaluated on Overall survival at 12 months.
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