Stéphanie Douchin

ORCID: 0000-0002-6437-4648
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About
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Research Areas
  • Congenital Heart Disease Studies
  • Cardiac Arrhythmias and Treatments
  • Cardiovascular Conditions and Treatments
  • Radiation Dose and Imaging
  • Cardiovascular Issues in Pregnancy
  • Pericarditis and Cardiac Tamponade
  • Radiation Therapy and Dosimetry
  • Infective Endocarditis Diagnosis and Management
  • Vascular anomalies and interventions
  • Epilepsy research and treatment
  • Myasthenia Gravis and Thymoma
  • Cardiac Valve Diseases and Treatments
  • Cardiovascular and Diving-Related Complications
  • Aortic Disease and Treatment Approaches
  • Coronary Artery Anomalies
  • Mechanical Circulatory Support Devices
  • Cardiac electrophysiology and arrhythmias
  • Blood Coagulation and Thrombosis Mechanisms
  • Cardiovascular Syncope and Autonomic Disorders
  • Takotsubo Cardiomyopathy and Associated Phenomena
  • Cardiac pacing and defibrillation studies
  • Streptococcal Infections and Treatments
  • RNA modifications and cancer
  • Genetic Syndromes and Imprinting
  • Adrenal and Paraganglionic Tumors

Centre Hospitalier Universitaire de Grenoble
2006-2024

Hôpital Necker-Enfants Malades
2024

Université Grenoble Alpes
2000-2024

Hôpital Couple Enfant
2017-2023

Centre National de la Recherche Scientifique
2000

Cardiopulmonary fitness in congenital heart disease (CHD) decreases faster than the general population resulting impaired health-related quality of life (HRQoL). As standard care seems insufficient to encourage and maintain fitness, an early hybrid cardiac rehabilitation programme could improve HRQoL CHD. The QUALIREHAB multicentre, randomized, controlled trial evaluated implemented a 12-week centre- home-based programme, including multidisciplinary physical activity sessions. Adolescent...

10.1093/eurheartj/ehae085 article EN cc-by European Heart Journal 2024-03-02

Abstract Background Transcatheter closure of patent ductus arteriosus (PDA) in premature infants has been shown to be feasible small series. Outcomes larger series are currently lacking. Material All (< 36 weeks GA) who underwent transcatheter PDA were included a multicenter French national survey. Demographic data (gestational age [GA], birth weight [BW]) and procedural (weight [PW], at procedure [AP], success, fluoroscopy time, type device) collected. complications reviewed. Results...

10.1002/ccd.28502 article EN Catheterization and Cardiovascular Interventions 2019-10-14

Over the last few decades different strategies have been proposed to treat persistent ductal patency in premature infants. The advent of Amplatzer Duct Occluder II Additional Size (ADOIIAS) provided potential close patent ductus arteriosus (PDA). Opinions differ on significance and treatment PDA neonates. Because surgical ligation medical therapy both their drawbacks, interventional catheterisation can be considered as an alternative means closing arteriosus. Our aim was analyse feasibility,...

10.1136/archdischild-2016-312582 article EN Archives of Disease in Childhood Fetal & Neonatal 2017-10-24

The COCCINELLE study is a nationwide retrospective French cohort set up to evaluate the risk of cancer in patients who undergone cardiac catheterisation (CC) procedures for diagnosis or treatment congenital heart disease during childhood.Children CC from 1 January 2000 31 December 2013, before age 16 one 15 paediatric cardiology departments which perform mainland France were included. follow-up started at date first recorded procedure until exit date, that is, death, diagnosis, 18th birthday...

10.1136/bmjopen-2020-048576 article EN cc-by-nc BMJ Open 2021-08-01

The aim of this study was to assess the diagnostic performances 18F-fluorodeoxyglucose (18F-FDG) positron emission tomography (PET)/computed (CT) in congenital heart disease (CHD) patients with pulmonary prosthetic valve or conduit endocarditis (PPVE) suspicion.PPVE is a major issue growing CHD population. Diagnosis challenging, and usual imaging tools are not always efficient validated specific Particularly, yield 18F-FDG PET/CT remains poorly studied PPVE.A retrospective multicenter...

10.1016/j.jcmg.2021.07.015 article EN cc-by-nc-nd JACC. Cardiovascular imaging 2021-09-15

The role of blood pressure on carotid remodeling, using no indexed and parameters, was studied in essential hypertension. Carotid parameters were also compared to cardiac mass aortic stiffness. Forty untreated hypertensive men had echocardiography, ultrasonography carotidfemoral pulse wave velocity measurements. Cross-sectional area index associated essentially with the 24-hour systolic whereas intima-media thickness related especially pressure. cross-sectional indexes less variables than...

10.1081/ceh-100102003 article EN Clinical and Experimental Hypertension 2000-01-01

We report the case of a male aged 2 years 6 months with left temporal lobe epilepsy who presented ictal bradycardia syndrome leading to asystole. The clinical presentation was remarkable for occurrence clustering syncope. A seizure recorded on video electroencephalogram– electrocardiogram and analyzed. cardiac pacemaker implanted antiepileptic drug treatment initiated. suggest that syncope is an important feature in young child.

10.1017/s0012162206001447 article EN Developmental Medicine & Child Neurology 2006-07-12

This paper reports the case of a patient with Turner's syndrome, who developed myocardial infarction at age 36. associated gonadal insufficiency, increases atherosclerotic cardiovascular risks that must be assessed during patient's follow-up.

10.1002/clc.4960220320 article EN Clinical Cardiology 1999-03-01

10.1016/s1245-1789(17)86813-x article ES EMC - Pediatría 2017-12-01

A 9-year-old girl was admitted to the paediatric intensive care unit for acute heart failure associated with high blood pressure. She had a history of asthenia, abdominal pain and profuse sweating. The ECG showed elements compatible an anterolateral infarction elevated troponin I, but coronary angiogram normal (figure 1A). On echocardiogram left ventriculography, there severe ventricular systolic dysfunction (30%) …

10.1136/archdischild-2018-315083 article EN Archives of Disease in Childhood 2018-06-14
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