A5017195194- Congenital Heart Disease Studies
- Coronary Artery Anomalies
- Cardiac Structural Anomalies and Repair
- Congenital heart defects research
- Cardiac Valve Diseases and Treatments
- Transplantation: Methods and Outcomes
- Cardiovascular Issues in Pregnancy
- Vascular anomalies and interventions
- Pulmonary Hypertension Research and Treatments
- Mechanical Circulatory Support Devices
- Congenital Diaphragmatic Hernia Studies
- Cardiac Arrhythmias and Treatments
- Tracheal and airway disorders
- Aortic Disease and Treatment Approaches
- Cardiovascular Function and Risk Factors
- Renal Transplantation Outcomes and Treatments
- Organ Transplantation Techniques and Outcomes
- Viral Infections and Immunology Research
- Prenatal Screening and Diagnostics
- Renal and Vascular Pathologies
- Kawasaki Disease and Coronary Complications
- Infective Endocarditis Diagnosis and Management
- Assisted Reproductive Technology and Twin Pregnancy
- Congenital Anomalies and Fetal Surgery
- Cardiovascular and Diving-Related Complications
Assistance Publique – Hôpitaux de Paris
2019-2025
Université Paris Cité
2018-2025
Hôpital Necker-Enfants Malades
2019-2025
Sorbonne Paris Cité
2019-2024
Inserm
2014-2024
Centre de Recherche Épidémiologie et Statistique
2024
Maternité Port Royal
2024
Institut Necker Enfants Malades
2020-2023
Délégation Paris 5
2018-2020
Hôpital Marie Lannelongue
2010-2019
The ESC Guidelines represent the views of and were produced after careful consideration scientific medical knowledge, evidence available at time their publication.The is not responsible in event any contradiction, discrepancy, and/or ambiguity between other official recommendations or guidelines issued by relevant public health authorities, particular relation to good use healthcare therapeutic strategies.Health professionals are encouraged take fully into account when exercising clinical...
Background: Cardiac injury and myocarditis have been described in adults with coronavirus disease 2019 (COVID-19). Severe acute respiratory syndrome 2 (SARS-CoV-2) infection children is typically minimally symptomatic. We report a series of febrile pediatric patients heart failure potentially associated SARS-CoV-2 the multisystem inflammatory as defined by US Centers for Disease Control Prevention. Methods: Over 2-month period, contemporary pandemic France Switzerland, we retrospectively...
<h3>Objective</h3> To assess the prevalence, timing of diagnosis and infant mortality congenital heart defects (CHD) with population-based data using a classification that allows regrouping International Paediatric Congenital Cardiac Code into manageable number categories based on anatomic clinical criteria (ACC-CHD). <h3>Design</h3> Population-based cohort study. <h3>Setting</h3> Greater Paris. <h3>Patients</h3> All cases (live births, terminations pregnancy for foetal anomaly (TOPFA),...
Abstract An internationally approved and globally used classification scheme for the diagnosis of CHD has long been sought. The International Paediatric Congenital Cardiac Code (IPCCC), which was produced maintained by Society Nomenclature Heart Disease (the Society), is widely, but spawned many “short list” versions that differ in content depending on user. Thus, efforts to have a uniform identification patients with using single up-to-date coordinated nomenclature system continue be...
Abstract Substantial progress has been made in the standardization of nomenclature for paediatric and congenital cardiac care. In 1936, Maude Abbott published her Atlas Congenital Cardiac Disease, which was first formal attempt to classify heart disease. The International Paediatric Code ( IPCCC ) is now utilized worldwide most recently become component Eleventh Revision Classification Diseases ICD-11 ). recent publication 2017. This manuscript provides an updated 2021 version . Society...
To estimate the risk of congenital heart defects (CHD) associated with assisted reproductive technologies (ART). We used data from Paris Registry Congenital Malformations on 5493 cases CHD and 3847 malformed controls for which no associations ART were reported in literature. Assisted included inductors ovulation only, vitro fertilization, intracytoplasmic sperm injection. Exposure to was higher than (4.7 vs. 3.6%, P= 0.008) a 40% increase maternal age, socioeconomic factors, year...
Classification of the overall spectrum congenital heart defects (CHD) has always been challenging, in part because diversity cardiac phenotypes, but also oft-complex associations. The purpose our study was to establish a comprehensive and easy-to-use classification CHD for clinical epidemiological studies based on long list International Paediatric Congenital Cardiac Code (IPCCC). We coded each individual malformation using six-digit codes from IPCCC. then regrouped all lesions into 10...
BACKGROUND AND OBJECTIVES: Preterm birth (PTB) and congenital heart defect (CHD) are 2 major causes of mortality disability perinatal origin. There limited data on the relation between CHD PTB. Our objective was to use population-based estimate risk PTB in newborns with study specific associations categories METHODS: We used from a cohort (EPIdémiologique sur le devenir des enfants porteurs de CARDiopathies congénitales study), including 2189 live births (excluding isolated atrial septal...
Are the risks of hypoplastic left heart syndrome, transposition great arteries, tetralogy Fallot (TOF) and coarctation aorta increased in infants conceived by different assisted reproductive techniques (ARTs)? ARTs, particularly intracytoplasmic sperm injection (ICSI), are specifically associated with a higher risk TOF. ARTs an increase overall birth defects. The for congenital defects (CHDs) has been evaluated as whole but there is limited information on specific CHDs. We conducted...
(1) Assess the population-level probability of prenatal diagnosis and termination pregnancy for fetal anomaly four major congenital heart defects; (2) Examine, using population-based data, relation between timing (prenatal vs postnatal) risk infant (ie, < 1 year) mortality defects (CHDs).Population-based cohort (the EPIdémiologie des CARDiopathies congénitales) study.Greater Paris area (Paris its surrounding suburbs).Three hundred fifty-four cases CHDs, including functionally univentricular...
Congenital heart disease is the most frequent birth defect and leading cause of death for fetus in first year life. The wide phenotypic diversity congenital defects requires expert diagnosis sophisticated repair surgery. Although these have been described since seventeenth century, it was only 2005 that a consensus international nomenclature adopted, followed by an classification 2017 to help provide better management patients. Advances genetic engineering, imaging, omics analyses uncovered...
Congenital heart defects (CHD) and preterm birth (PTB) are major causes of infant mortality. However, limited data exist on risk mortality associated with PTB for newborns CHD. Our objective was to assess impact CHD, while taking into account the role anomalies other potentially confounding factors. We used 2172 live births from a prospective population-based cohort study CHD (the EPICARD Study) compared neonatal, post-neonatal overall infants born at <32, 32–34 35–36 weeks vs. those term...
Substantial progress has been made in the standardization of nomenclature for paediatric and congenital cardiac care. In 1936, Maude Abbott published her Atlas Congenital Cardiac Disease, which was first formal attempt to classify heart disease. The International Paediatric Code (IPCCC) is now utilized worldwide most recently become component Eleventh Revision Classification Diseases (ICD-11). recent publication IPCCC 2017. This manuscript provides an updated 2021 version IPCCC.The Society...
To identify the surgical approaches and risk factors which influence longevity of right ventricle to pulmonary artery (RV-PA) conduits following first reoperation for obstruction.Between January 1993 August 2003, 114 patients underwent 141 reoperations RV-PA conduit obstruction. Diagnoses included 'Truncus Arteriosus' (n=52), 'Pulmonary atresia/Tetralogy fallot' (n=39), 'Double outlet ventricle' (n=10), 'Transposition great arteries, VSD, atresia' (n=9), 'Ross operation' (n=4). All had...
Biventricular repair of double outlet right ventricle non-committed ventricular septal defect (DORVncVSD) is usually achieved by a VSD rerouting to the aorta. This technique can be limited presence tricuspid chordae and pulmonary artery valve distance. Furthermore, there an important risk late subaortic obstruction related long patch required that creates potential akinetic area. Presented here another technique; infundibulum arterial switch.Ten patients, with DORVncVSD, underwent followed...