Publications by authors named "Luc L Mertens"

Article Synopsis
  • - The right ventricle in hypoplastic left heart syndrome (HLHS) functions as the systemic ventricle, dealing with varying volume loads and pressures throughout a patient’s treatment, particularly before and after the Fontan procedure.
  • - Factors like the anatomy of HLHS, treatment choices, and heart valve issues affect the right ventricle's size and performance, which can lead to problems such as both systolic and diastolic dysfunction.
  • - This review gathers recent research findings to enhance understanding of right ventricle remodeling in HLHS, emphasizing the need for ongoing studies to maintain heart health during treatment.
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Rationale: Preterm neonates needing rescue treatments with inotropes and/or inhaled nitric oxide (iNO) (acute critical illnesses, ACIs) in neonatal intensive care units (NICUs) are at high risk of mortality. While targeted neonatal echocardiography consultations (TNE) are increasingly used to guide management, its clinical impact need evaluation.

Objectives: To investigate clinical outcomes in relation to TNE utilisation during episodes of ACIs among preterm neonates.

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Objectives: For neonates and infants with aortic valve pathology, the Ross procedure historically has been associated with high rates of morbidity and mortality. Data regarding long-term durability are lacking.

Methods: The international, multi-institutional Ross Collaborative included 6 tertiary care centers.

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Background: The relationship between genotype and phenotypical vascular and cardiac properties in paediatric Loeys-Dietz syndrome (LDS) patients are not well characterized. This study explores the phenotypical differences in aortic properties and cardiac structural and functional parameters between paediatric LDS patients with and mutations.

Methods: We included 32 LDS patients with either (n = 17) or (n = 15) mutations.

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The noninvasive assessment of ventricular function is an ongoing challenge, with new tools and measurements always being considered and tested. The noninvasive assessment of myocardial work via the pressure-strain relationship is one of the newer tools proposed to evaluate ventricular systolic function. However, prior to using any new tool, one should understand its properties, utility, and limitations.

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Article Synopsis
  • - Tetralogy of Fallot is a congenital heart defect that can lead to long-term complications like progressive right ventricular (RV) failure due to issues like pulmonic regurgitation, even after surgical correction.
  • - The cellular causes of RV failure involve microvascular and mitochondrial problems, which often result in exercise intolerance that can be measured through cardiopulmonary exercise testing to help predict outcomes.
  • - Management of RV failure includes using diuretics to balance fluid levels and, in cases of severe heart failure, employing inotropes or mechanical support while monitoring any remaining heart issues that could affect treatment effectiveness.
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Background: Pediatric hypertrophic cardiomyopathy (HCM) is associated with adverse events. The contribution of diastolic dysfunction to adverse events is poorly understood. The aim of this study was to explore the association between diastolic phenotype and outcomes in pediatric patients with HCM.

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Objectives: Atrioventricular valve (AVV) replacements in patients with single-ventricle circulations pose significant surgical risks and are associated with high morbidity and mortality.

Methods: From 1997 to 2021, 16 consecutive patients with functionally single-ventricle physiology underwent mechanical AVV replacement. Primary outcome was transplant-free survival.

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To evaluate clinical practice, neonatologists' attitudes, and the extent of training and accreditation regarding targeted neonatal echocardiography (TnEcho) among Chinese neonatologists. A web-based questionnaire was emailed to 331 neonatologists across China who completed training in subspecialty neonatology. The survey covered various aspects of TnEcho, including the characteristics of clinical practice, attitudes towards its usefulness, and perceived barriers to implementation and training methods.

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Hypoplastic left heart syndrome (HLHS) is the most common anatomic lesion in children born with single-ventricle physiology and is characterised by the presence of a dominant right ventricle and a hypoplastic left ventricle along with small left-sided heart structures. Diagnostic subgroups of HLHS reflect the extent of inflow and outflow obstruction at the aortic and mitral valves, specifically stenosis or atresia. If left unpalliated, HLHS is a uniformly fatal lesion in infancy.

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Background: Diagnosing left ventricular diastolic dysfunction (DD) noninvasively in children is difficult as no validated pediatric diagnostic algorithm is available. The aim of this study is to explore the use of machine learning to develop a model that uses echocardiographic measurements to explain patterns in invasively measured markers of DD in children.

Methods: Children at risk for developing DD were enrolled, including patients with Kawasaki disease, heart transplantation, aortic stenosis, and coarctation of the aorta when undergoing clinical left heart catheterization.

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Background: Del Nido cardioplegia (DNc) was designed for superior myocardial protection during cardiopulmonary bypass (CPB). We conducted a retrospective review to explore if DNc was associated with increase in systemic ventricle dysfunction (sVD) following pediatric CPB.

Methods And Results: This single-center, retrospective study included 1534 patients undergoing CPB between 2013 and 2016, 997 prior to center-wide conversion to DNc and 537 following.

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Article Synopsis
  • Coarctation of the aorta is a complex issue with ongoing debates about long-term health outcomes, particularly mortality risks that increase significantly after the age of 30.
  • New imaging techniques, like advanced echocardiography and MRI, are enhancing our ability to detect aortic coarctation in fetuses and understand how arch size affects blood flow and pressure, emphasizing the need for better neonatal intervention.
  • To improve long-term health for patients with aortic coarctation, it's crucial to focus on optimizing aortic arch size, managing hypertension, and monitoring neurodevelopmental risks following repair.
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Echocardiographic assessment of patients with transposition of the great arteries and congenitally corrected transposition requires awareness of the morphology and commonly associated lesions. The pre-operative echocardiography should include a full segmental and sequential analysis. Post-operative assessment is not possible without awareness of the type of surgical procedure performed and consists of assessing surgical connections and residual lesions.

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Aims: The objective of this study was to quantify imaging markers of myocardial fibrosis and assess myocardial function in long-term transposition of the great arteries survivors after the arterial switch operation (ASO).

Methods And Results: Paediatric ASO patients were prospectively studied by cardiac magnetic resonance imaging, including first-pass myocardial perfusion, late gadolinium enhancement, and T1 relaxometry, as well as echocardiography for left ventricular (LV) systolic and diastolic function including strain analysis, with comparison to healthy controls. Thirty ASO patients (mean age 15.

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Cardiac imaging is central to today's pediatric cardiology practice not only to diagnose structural congenital defects and delineate cardiac and extracardiac anatomy but also for determining the hemodynamic impact of the structural defects and acquired pediatric diseases. Not so long ago, clinicians had to heavily rely on angiography as the main cardiac imaging modality to visualize the heart. Particularly, the development of echocardiography in the 1970s and 1980s together with the development of magnetic resonance imaging (MRI) and computed tomography (CT) resulted in a non-invasive diagnostic revolution with diagnostic catheterization becoming obsolete apart for very specific indications.

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Article Synopsis
  • The study compared right ventricular (RV) function in patients with hypoplastic left heart syndrome who underwent either the Norwood procedure or a hybrid approach throughout different stages of treatment.
  • A total of 76 patients were analyzed retrospectively, with echocardiographic measurements taken at multiple stages, including before and after significant surgeries.
  • Results showed no significant differences in RV size and function between the two groups at various stages, suggesting that any small differences observed might be due to variations in patient physiology or the timing of surgeries rather than the procedures themselves.
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