35 results on '"Benbrik N"'
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2. Chapitre 56 - Persistance du canal artériel chez le prématuré
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Benbrik, N., Gournay, V., and Baruteau, A.
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- 2024
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3. Transcatheter closure of persistent ductus arteriosus in 2 to 6 kg infants: Preliminary results from an international, retrospective study
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Padovani, P., primary, Gewillig, M., additional, Butera, G., additional, Lucron, H., additional, Lefort, B., additional, Samion, H., additional, El Saiedi, S., additional, Ovaert, C., additional, Sirico, D., additional, Grunenwald Gronier, C., additional, Méot, M., additional, Benbrik, N., additional, Bonnet, D., additional, Malekzadeh-Milani, S., additional, and Baruteau, A.E., additional
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- 2022
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4. Perimembranous ventricular septal defect with left ventricular volume overload: Features of patients in the French Cohort Study (FRANCISCO)
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Sudaka, A., primary, Thambo, J.B., additional, Vaksmann, G., additional, Hadeed, K., additional, Houeijeh, A., additional, Khraiche, D., additional, Hery, E., additional, Vincenti, M., additional, Pangaud, N., additional, Benbrik, N., additional, Vastel, C., additional, Legendre, A., additional, Jalal, Z., additional, Guirgis, L., additional, and Hascoet, S., additional
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- 2022
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5. Évaluation de l’éducation au traitement anticoagulant et au système d’auto-mesure de l’INR CoaguChek XS® chez l’enfant
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Soulé, N., Benbrik, N., Gournay, V., and Chantepie, A.
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- 2013
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6. Unexplained near-drowning can reveal ALCAPA in children
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Bichali, S., Giroux, N., Benbrik, N., and Liet, J.-M.
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- 2021
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7. Transcatheter PDA closure in preterm: Where do we stand? A prospective multicenter French survey
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Malekzadeh-Milani, S., Lefort, B., Bakloul, M., Douchin, S., Dauphin, C., Akhavi, A., Benbrik, N., Meot, M., Bonnet, D., and Baruteau, A.
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- 2023
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8. Measurement, consequences and determinants of time to diagnosis in children with new-onset heart failure: A population-based retrospective study (DIACARD study)
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Bichali, S., primary, Malorey, D., additional, Benbrik, N., additional, Le Gloan, L., additional, Gras-Le Guen, C., additional, Baruteau, A.E., additional, and Launay, E., additional
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- 2021
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9. Cardiopathies et adolescence
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Le Gloan, L., Guérin, P., Romefort, B., Benbrik, N., Hauet, Q., Mugniot, A., Baron, O., and Gournay, V.
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- 2013
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10. Early management at less than three months and becoming symptomatic Fallot diseases
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Benbrik, N., primary, Romefort, B., additional, Prigent, S., additional, Baron, O., additional, Guerin, P., additional, legloan, L., additional, Warin, K., additional, and Gournay, V., additional
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- 2017
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11. État de choc sévère après injection de protamine chez un nouveau-né durant une chirurgie cardiaque sous circulation extracorporelle
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Joram, N., Benbrik, N., De Windt, A., Colas, H., and Liet, J.M.
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- 2013
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12. SFP PC-62 – Comparaison monocentrique de la chirurgie de Fallot tardive versus précoce
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Benbrik, N., primary, Gournay, V., additional, and Hauet, Q., additional
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- 2014
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13. Cardiac rhabdomyoma with hydrops fetalis: Prenatal management by abdominal drainage
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Lefizelier Emeline, Benbrik Nadir, Beneteau Claire, and Le Vaillant Claudine
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Cardiac rhabdomyoma ,Hydrops ,Fetal ,Peritoneal-amniotic shunting ,Gynecology and obstetrics ,RG1-991 - Abstract
Objective: We described a case of fetal cardiac rhabdomyoma complicated by hydrops. And we discussed our approach during pregnancy. Case Report: A 23-year-old woman primigravida was referred at 29 weeks of gestation (WG) to prenatal unit for a large hyperechogenic intracardiac mass associated with fetal hydrops. An intrauterine peritoneo-amniotic shunt was placed. Complete regression of ascites and pericardial effusions were observed after 34 WG with drain in good position. Conclusion: Cardiac rhabdomyoma is the most common prenatal cardiac tumor. These tumors are benign, asymptomatic and spontaneously regress after birth. However, in some cases, these tumors may cause severe obstructions on the fetal heart and need specific treatment.
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- 2021
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14. Évaluation de l'éducation au traitement anticoagulant et au système d'auto-mesure de l'INR CoaguChek XS® chez l'enfant.
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Soulé, N., Benbrik, N., Gournay, V., and Chantepie, A.
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INTERNATIONAL normalized ratio , *PATIENT monitoring , *PATIENT education , *ANTICOAGULANTS , *EDUCATIONAL programs , *MEDICAL laboratories - Abstract
Résumé: Objectif: Évaluer le résultat de nos pratiques professionnelles relatives à l’éducation au traitement anticoagulant et à son monitorage par le système d’autocontrôle de l’international normalised ratio (INR) chez l’enfant. Patients et méthodes: Tous les enfants traités par anticoagulants avec monitorage de l’INR par auto-mesure, à Tours et Nantes, ont été inclus. Un questionnaire d’évaluation des connaissances relatives au traitement et à sa gestion a été adressé aux patients et à leur famille. Le taux d’INR dans la cible thérapeutique a été analysé. Résultats: Trente-trois enfants ont été inclus (âge moyen=10,9ans). Des connaissances insuffisantes concernant l’intérêt et les risques du traitement, l’INR cible, l’interprétation de l’INR, ont été observées. Dans 65,8 % des cas l’INR était dans la cible thérapeutique. Ce taux était plus élevé avec l’auto-mesure qu’avec les contrôles au laboratoire avant l’utilisation du système d’autocontrôle (69,7 % vs 49,1 %, p =0,003). Une corrélation modérée (K=0,57) a été observée entre les INR évalués par auto-mesure et ceux mesurés au laboratoire le même jour. Aucune complication majeure du traitement n’a été relevée. Conclusion: Le monitorage à domicile de l’INR permet un meilleur contrôle de l’équilibre du traitement anticoagulant. Des progrès doivent être réalisés dans le programme d’éducation afin d’améliorer les connaissances théoriques des familles et des enfants. [ABSTRACT FROM AUTHOR]
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- 2013
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15. PO9-42 - Early management at less than three months and becoming symptomatic Fallot diseases.
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Benbrik, N., Romefort, B., Prigent, S., Baron, O., Guerin, P., legloan, L., Warin, K., and Gournay, V.
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- 2017
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16. Device Closure of Hemodynamically Significant Patent Ductus Arteriosus in Premature Infants.
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Baruteau AE, Méot M, Benbrik N, Grunenwald C, Lwin N, Patkai J, Rozé JC, Bonnet D, and Malekzadeh-Milani S
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The patent ductus arteriosus is a very common condition in preterm infants, and a hemodynamically significant patent ductus arteriosus increases morbidity and mortality in these vulnerable patients. However, despite numerous randomized controlled trials, there is no consensus regarding management. Medical therapy is typically offered as first-line treatment, although it yields limited success and carries the potential for severe adverse events. In recent years, there has been rapid development in transcatheter patent ductus arteriosus closure primary with the use of the Amplatzer Piccolo Occluder, and this has gained widespread acceptance as a safe and effective alternative to surgical ligation in extremely low-birth-weight infants weighing over 700 g. This article aims to provide an appraisal of the patient selection process, a step-by-step procedural guide, and a comprehensive review of the outcomes associated with this approach., Competing Interests: Dr Alban-Elouen Baruteau is supported by the French Government as part of the “Investments of the Future” program managed by the National Research Agency (grant reference ANR-16-IDEX-0007); and is a consultant and proctor for Abbott. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose., (© 2024 The Authors.)
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- 2024
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17. Post-ligation cardiac syndrome after surgical versus transcatheter closure of patent ductus arteriosus in low body weight premature infants: a multicenter retrospective cohort study.
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Duboue PM, Padovani P, Bouteiller XP, Martin-Kabore F, Benbrik N, Gronier CG, Bouissou A, Garnier E, Mitanchez D, Flamant C, Rozé JC, Baruteau AE, and Lefort B
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- Humans, Retrospective Studies, Infant, Newborn, Female, Ligation methods, Ligation adverse effects, Male, Infant, Low Birth Weight, Incidence, Cardiac Surgical Procedures adverse effects, Cardiac Surgical Procedures methods, Syndrome, Propensity Score, Septal Occluder Device, Risk Factors, Infant, Premature, Diseases surgery, Infant, Premature, Diseases etiology, Infant, Premature, Diseases therapy, Infant, Premature, Diseases epidemiology, Ductus Arteriosus, Patent surgery, Cardiac Catheterization methods, Cardiac Catheterization adverse effects, Infant, Premature, Postoperative Complications epidemiology, Postoperative Complications etiology
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Transcatheter patent ductus arteriosus (PDA) closure is a safe and effective alternative to surgical ligation in low-body-weight infants. Post-ligation cardiac syndrome (PLCS) is defined as severe hemodynamic and respiratory collapse within 24 h of PDA closure, requiring initiation or an increase of an inotropic agent by > 20% of preligation dosing and an absolute increase of at least 20% in ventilation parameters compared with the preoperative value. Whilst PLCS is routinely observed after surgery, its incidence remains poorly described following transcatheter closure. This study aimed to compare the incidence of PLCS after surgical versus transcatheter closure of PDA in low-body-weight premature infants. Propensity scores were used to compare surgical (N = 78) and transcatheter (N = 76) groups of preterm infants who underwent PDA closure at a procedural weight less than 2000 g in two tertiary institutions between 2009 and 2021. The primary outcome was the incidence of PLCS. Secondary outcomes included overall mortality before discharge, risk factors for PLCS, and post-procedural complications. Procedural success was 100% in both groups. After matching, transcatheter group experienced no PLCS vs 15% in the surgical group (p = 0.012). Furthermore, overall mortality (2% vs 17%; p = 0.03) and major complications (2% vs 23%; p = 0.002) were higher in the surgical group. Surgery (100% vs 47%; p < 0.01), gestation age (25 ± 1 vs 26 ± 2 weeks, p < 0.05) and inotropic support before closure (90% vs 29%; p < 0.001) were associated with PLCS occurrence. Conclusion: Transcatheter PDA closure may be equally effective but safer than surgical PDA closure in low-body-weight premature infants. What is Known: • Post-ligation cardiac syndrome is a serious and common complication of surgical closure of the ductus arteriosus in preterm infants. • Transcatheter closure of preterm ductus arteriosus is a safe and effective technique that is becoming more and more common worldwide. What is New: • Device closure is safer than surgical ligation for patent ductus arteriosus closure in preterm infants and may be the first-line non-pharmacological therapeutic option in this indication in experienced teams. • Our findings should encourage neonatologists and pediatric cardiologists to start and/or strengthen a durable interventional program for transcatheter PDA closure in premature infants., (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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- 2024
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18. Risk of infective endocarditis after hybrid melody mitral valve replacement in infants: the French experience.
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Padovani P, Jalal Z, Fouilloux V, Benbrik N, Grunenwald C, Thambo JB, Aldebert P, Tagorti M, Roubertie F, Baron O, Ovaert C, Ly M, and Baruteau AE
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Objectives: Surgical management of mitral valve disease is challenging in infants <1 year old. We aimed at reviewing the French experience with Melody mitral valve replacement in critically ill infants., Methods: A retrospective cohort study reporting the French experience with Melody mitral valve replacement., Results: Seven symptomatic infants [complete atrioventricular septal defect (n = 4, Down syndrome: n = 3), hammock valve (n = 3)] underwent Melody mitral valve replacement [age: 3 months (28 days to 8 months), weight: 4.3 kg (3.2-6.4 kg)] because of severe mitral valve regurgitation (6) or mixed valve disease (1) and 14 mm (11-16 mm) mitral valve annulus. In 2 patients whose valve was felt irreparable, Melody mitral valve replacement was performed straightaway. The others underwent 2 (1-3) previous attempts of valve repair; 3 were on extracorporeal membrane oxygenation. Melody mitral valve replacement led to competent valve and low gradient [3 mmHg, (1-4 mmHg)]. One patient died 3 days post-implant from extracorporeal membrane oxygenation-related stroke. Of the 6 discharged home patients, 3 (50%) were readmitted for a definite diagnosis (1) or high suspicion (2) of infective endocarditis, of which 2 died. Over the follow-up, 1 underwent balloon expansions of the valve at 9- and 16-months post-implant, and mechanical mitral valve replacement at 2 years; another is currently planned for transcatheter Melody valve dilation., Conclusions: Melody mitral valve replacement may be considered in selected infants with small mitral valve annulus as an alternative to mechanical mitral valve replacement. Our experience highlights a high-risk of late infective endocarditis that deserves further consideration., (© The Author(s) 2024. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery.)
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- 2024
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19. Systemic primary carnitine deficiency induces severe arrhythmia due to shortening of QT interval.
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Lodewyckx P, Issa J, Gaschignard M, Lamireau D, De Lonlay P, Servais A, Barth M, Courapied S, Morin G, Benbrik N, Maillot F, Babuty D, Labarthe F, and Lefort B
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- Infant, Newborn, Child, Humans, Child, Preschool, Death, Sudden, Cardiac etiology, Death, Sudden, Cardiac prevention & control, Retrospective Studies, Arrhythmias, Cardiac complications, Carnitine metabolism, Electrocardiography adverse effects, Long QT Syndrome, Cardiomyopathies complications
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Background: Systemic primary carnitine deficiency (PCD) is characterized by cardiomyopathy and arrhythmia. Without carnitine supplementation, progression is usually towards fatal cardiac decompensation. While the cardiomyopathy is most likely secondary to energy deficiency, the mechanism of arrhythmia is unclear, and may be related to a short QT interval., Objective: We aim to describe rhythmic manifestations at diagnosis and with carnitine supplementation., Methods: French patients diagnosed for PCD were retrospectively included. Clinical and para clinical data at diagnosis and during follow-up were collected. Electrocardiograms with QT interval measurements were blinded reviewed by two paediatric cardiologists., Results: Nineteen patients (median age at diagnosis 2.3 years (extremes 0.3-28.9)) followed in 8 French centres were included. At diagnosis, 21% of patients (4/19) had arrhythmia (2 ventricular fibrillations, 1 ventricular tachycardia and 1 sudden death), and 84% (16/19) had cardiomyopathy. Six electrocardiograms before treatment out of 11 available displayed a short QT (QTc < 340 ms). Median corrected QTc after carnitine supplementation was 404 ms (extremes 341-447) versus 350 ms (extremes 282-421) before treatment (p < 0.001). The whole QTc was prolonged, and no patient reached the criterion of short QT syndrome with carnitine supplementation. Three patients died, probably from rhythmic cause without carnitine supplementation (two extra-hospital sudden deaths and one non-recoverable rhythmic storm before carnitine supplementation), whereas no rhythmic complication occurred in patients with carnitine supplementation., Conclusion: PCD is associated with shortening of the QT interval inducing severe arrhythmia. A potential explanation would be a toxic effect of accumulated fatty acid and metabolites on ionic channels embedded in the cell membrane. Carnitine supplementation normalizes the QTc and prevents arrhythmia. Newborn screening of primary carnitine deficiency would prevent avoidable deaths., Competing Interests: Declaration of Competing Interest None., (Copyright © 2023. Published by Elsevier Inc.)
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- 2023
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20. Fluoroscopy-free, echocardiography-guided hybrid stenting of native aortic coarctation in a 920-grams premature infant.
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Tagorti M, Benbrik N, and Baruteau AE
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- Infant, Newborn, Infant, Humans, Infant, Premature, Echocardiography, Infant, Extremely Low Birth Weight, Aortic Coarctation diagnostic imaging, Aortic Coarctation surgery
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Therapeutic options are limited for the management of extremely low-birth-weight infants with critical aortic coarctation despite high doses of prostaglandin infusion. We report successful hybrid, fluoroscopy-free, echocardiography-guided primary stenting of native aortic coarctation in a 920-grams premature infant.
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- 2023
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21. Late aortic obstruction due to ductal vasoconstriction on pulmonic end after transcatheter patent ductus arteriosus closure in an extremely low-birth-weight infant.
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Padovani P, Benbrik N, and Baruteau AE
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- Infant, Newborn, Infant, Humans, Vasoconstriction, Infant, Premature, Infant, Extremely Low Birth Weight, Aorta, Ductus Arteriosus, Patent surgery
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Device-induced aortic obstruction is a known rare complication following transcatheter closure of patent ductus arteriosus in extremely low-birth-weight infants. Various mechanisms have been proposed. We report the first description of late aortic obstruction due to ductal vasoconstriction on pulmonic end causing device to be gradually pushed out of aortic end in a 980-gram premature infant.
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- 2023
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22. Long-term results of the Warden procedure for right partial anomalous pulmonary venous connection.
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Dubost C, Pavy C, Maminirina P, Benbrik N, and Baron O
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- Adolescent, Humans, Constriction, Pathologic, Follow-Up Studies, Treatment Outcome, Vena Cava, Superior abnormalities, Infant, Child, Preschool, Child, Young Adult, Adult, Middle Aged, Aged, Pulmonary Veins surgery, Pulmonary Veins abnormalities, Scimitar Syndrome surgery
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Introduction: Surgery is considered as the first-line therapeutic strategy of partial anomalous pulmonary venous connection. The Warden technique has very good short-term results. The aim of this study is to evaluate the stability of these good results over a long period of follow-up., Materials and Methods: We reviewed all patients who underwent a Warden procedure for partial anomalous pulmonary venous connection between 1997 and 2017 in our centre. A total of 73 patients were included. The median age was 14 years (5 months-72 years). Post-operative data were obtained through our hospital network. Late follow-up data were obtained through referrals, cardiologist letters and directly from the patient., Results: The mean length of follow-up was 8 years and the longest time was 22 years (range, 1-22). Twenty-five percent of our cohort had more than 10 years of follow-up. There were no cardio-vascular deaths. Eight (11.6%) patients suffered from post-operative rhythm disturbances, 5 (7.2%) of which were permanent. Two (2.9%) patients required a pacemaker implantation. At the end of the follow-up period, only one patient remained pacemaker dependent. There were no pulmonary vein obstructions. Two (2.9%) caval vein stenosis were detected, one at 7 months and the other at 7 years. These patients were treated by angioplasty alone. Five (6.8%) patients were lost to follow-up., Conclusions: The good short-term results of the Warden procedure for right partial anomalous pulmonary venous connection appear to persist in the long term, with excellent freedom from pulmonary and caval stenosis in adolescence through to adulthood.
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- 2023
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23. Medium-term follow-up of autologous pericardial patches for pediatric aortic arch reconstruction.
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Le Picault B, Pavy C, Maminirina P, Benbrik N, and Baron O
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- Aorta, Thoracic diagnostic imaging, Aorta, Thoracic surgery, Child, Follow-Up Studies, Glutaral, Humans, Infant, Retrospective Studies, Treatment Outcome, Aortic Coarctation diagnostic imaging, Aortic Coarctation surgery, Heart Valve Diseases
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Objectives: Direct anastomosis, like end-to-end anastomosis or end-to-side anastomosis, is commonly employed to repair aortic coarctation or interrupted aortic arch. Direct anastomosis of the aorta, however, may result in restenosis or bronchial compression. To circumvent these complications, we have applied a technique consisting of aortic reconstruction using glutaraldehyde-fixed autologous pericardial patches., Methods: Our database was queried for infants who underwent aortic arch reconstruction using autologous pericardial patches from 2007 to 2019. Medical records, including echography imaging, were reviewed, and Z-scores of aortic arch diameters were retrospectively assessed at baseline, immediately after surgery, and at follow-up end., Results: Overall, 58 patients met the inclusion criteria, with a median age of 9.8 days at surgery and median postoperative follow-up of 46 months. Re-coarctation requiring re-intervention by either surgery or percutaneous angioplasty was documented in 14.7% of patients. Overall, 9% of patients died of all-cause mortality. The Z-scores evolved favorably from baseline, which clearly indicated hypoplastic aortic arch, to early postoperative status, which clearly showed values close to those obtained in normal infants, with likewise normal values obtained at median 46-month follow-up., Conclusions: Glutaraldehyde-fixed autologous pericardial patches were shown to provide correct medium-term results for aortic arch reconstruction. The incidence of restenosis requiring re-intervention was shown to be low. Autologous pericardial patches can be considered as an acceptable and easily available solution for aortic arch repair surgery., (© 2022 Wiley Periodicals LLC.)
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- 2022
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24. Familial Recurrence Patterns in Congenitally Corrected Transposition of the Great Arteries: An International Study.
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Tortigue M, Nield LE, Karakachoff M, McLeod CJ, Belli E, Babu-Narayan SV, Prigent S, Boet A, Conway M, Elder RW, Ladouceur M, Khairy P, Kowalik E, Kalfa DM, Barron DJ, Mussa S, Hiippala A, Temple J, Abadir S, Le Gloan L, Lachaud M, Sanatani S, Thambo JB, Gronier CG, Amedro P, Vaksmann G, Charbonneau A, Koutbi L, Ovaert C, Houeijeh A, Combes N, Maury P, Duthoit G, Hiel B, Erickson CC, Bonnet C, Van Hare GF, Dina C, Karsenty C, Fournier E, Le Bloa M, Pass RH, Liberman L, Happonen JM, Perry JC, Romefort B, Benbrik N, Hauet Q, Fraisse A, Gatzoulis MA, Abrams DJ, Dubin AM, Ho SY, Redon R, Bacha EA, Schott JJ, and Baruteau AE
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- Arteries, Congenitally Corrected Transposition of the Great Arteries, Humans, Retrospective Studies, Ciliary Motility Disorders complications, Heart Defects, Congenital, Transposition of Great Vessels complications, Transposition of Great Vessels diagnosis, Transposition of Great Vessels genetics
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Background: Congenitally corrected transposition of the great arteries (ccTGA) is a rare disease of unknown cause. We aimed to better understand familial recurrence patterns., Methods: An international, multicentre, retrospective cohort study was conducted in 29 tertiary hospitals in 6 countries between 1990 and 2018, entailing investigation of 1043 unrelated ccTGA probands., Results: Laterality defects and atrioventricular block at diagnosis were observed in 29.9% and 9.3%, respectively. ccTGA was associated with primary ciliary dyskinesia in 11 patients. Parental consanguinity was noted in 3.4% cases. A congenital heart defect was diagnosed in 81 relatives from 69 families, 58% of them being first-degree relatives, including 28 siblings. The most prevalent defects in relatives were dextro-transposition of the great arteries (28.4%), laterality defects (13.6%), and ccTGA (11.1%); 36 new familial clusters were described, including 8 pedigrees with concordant familial aggregation of ccTGA, 19 pedigrees with familial co-segregation of ccTGA and dextro-transposition of the great arteries, and 9 familial co-segregation of ccTGA and laterality defects. In one family co-segregation of ccTGA, dextro-transposition of the great arteries and heterotaxy syndrome in 3 distinct relatives was found. In another family, twins both displayed ccTGA and primary ciliary dyskinesia., Conclusions: ccTGA is not always a sporadic congenital heart defect. Familial clusters as well as evidence of an association between ccTGA, dextro-transposition of the great arteries, laterality defects and in some cases primary ciliary dyskinesia, strongly suggest a common pathogenetic pathway involving laterality genes in the pathophysiology of ccTGA.
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- 2022
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25. Cardiovascular events in perimembranous ventricular septal defect with left ventricular volume overload: a French prospective cohort study (FRANCISCO).
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Guirgis L, Valdeolmillos E, Vaksmann G, Karsenty C, Houeijeh A, Hery E, Amedro P, Pangaud N, Benbrik N, Vastel C, Legendre A, Jalal Z, Hadeed K, Ladouceur M, Iserin L, Laux D, Iriart X, Warin Fresse K, Leobon B, Harchaoui S, Lambert V, Bonefoy R, Basquin A, Chalard A, Douchin S, Bouzguenda I, Denis C, Lucron H, Bosser G, Barre E, Urbina-Hiel B, Helms P, Ansquer H, Hauet Q, Leborgne AS, Cohen L, Lupoglazoff JM, Guirgis M, Gronier C, Maragnes P, Moceri P, Mauran P, Bertail C, Lefort B, Godart F, Baruteau AE, Ovaert C, Bonnet D, Combes N, Khraiche D, Houyel L, Thambo JB, Mostefa-Kara M, and Hascoet S
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- Cardiac Catheterization, Child, Child, Preschool, Heart Ventricles diagnostic imaging, Humans, Observational Studies as Topic, Prospective Studies, Treatment Outcome, Heart Failure, Heart Septal Defects, Ventricular epidemiology, Heart Septal Defects, Ventricular surgery, Septal Occluder Device
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The long-term prospective multi-centre nationwide (French) observational study FRANCISCO will provide new information on perimembranous ventricular septal defect with left ventricular overload but no pulmonary hypertension in children older than 1 year. Outcomes will be compared according to treatment strategy (watchful waiting, surgical closure, or percutaneous closure) and anatomic features of the defect. The results are expected to provide additional guidance about the optimal treatment of this specific population, which is unclear at present., Background: The management of paediatric isolated perimembranous ventricular septal defect (pmVSD) with left ventricle (LV) volume overload but no pulmonary arterial hypertension (PAH) remains controversial. Three therapeutic approaches are considered: watchful waiting, surgical closure, and percutaneous closure. We aim to investigate the long-term outcomes of these patients according to anatomic pmVSD characteristics and treatment strategy., Methods: The Filiale de Cardiologie Pediatrique et Congénitale (FCPC) designed the FRANCISCO registry, a long-term prospective nationwide multi-centre observational cohort study sponsored by the French Society of Cardiology, which enrolled, over 2 years (2018–2020), patients older than 1 year who had isolated pmVSD with LV volume overload. Prevalent complications related to pmVSD at baseline were exclusion criteria. Clinical, echocardiographic, and functional data will be collected at inclusion then after 1, 5, and 10 years. A core lab will analyse all baseline echocardiographic data to depict anatomical pmVSD features. The primary outcome is the 5-year incidence of cardiovascular events (infective endocarditis, sub-aortic stenosis, aortic regurgitation, right ventricular outflow tract stenosis, tricuspid regurgitation, PAH, arrhythmia, stroke, haemolysis, heart failure, or death from a cardiovascular event). We plan to enrol 200 patients, given the 10% estimated 5-year incidence of cardiovascular events with a 95% confidence interval of ±5%. Associations linking anatomical pmVSD features and treatment strategy to the incidence of complications will be assessed., Conclusions: The FRANSCICO study will provide the long-term incidence of complications in patients older than 1 year with pmVSD and LV volume overload. The results are expected to improve guidance for treatment decisions.
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- 2021
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26. Measurement, consequences and determinants of time to diagnosis in children with new-onset heart failure: A population-based retrospective study (DIACARD study).
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Bichali S, Malorey D, Benbrik N, Le Gloan L, Gras-Le Guen C, Baruteau AE, and Launay E
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- Adolescent, Child, Female, Humans, Male, Prognosis, Proportional Hazards Models, Retrospective Studies, Risk Factors, Cardiomyopathies, Heart Failure diagnosis, Heart Failure epidemiology
- Abstract
Background: Time from first symptoms to diagnosis, called time to diagnosis, is related to prognosis in several diseases. The aim of this study was to assess time to diagnosis in children with new-onset heart failure (HF) and assess its consequences and determinants., Methods: A retrospective population-based observational study was conducted between 2007 and 2016 in a French tertiary care center. We included all children under 16 years old with no known heart disease, and HF confirmed by echocardiography. With logistic regression used for outcomes and a Cox proportional-hazards model for determinants, analyses were stratified by HF etiology: congenital heart diseases (CHD) and cardiomyopathies/myocarditis (CM)., Results: A total of 117 children were included (median age [interquartile range (IQR)] 25 days (6-146), 50.4% were male, 60 had CHD and 57 had CM). Overall median (IQR) time to diagnosis was 3.3 days (1.0-21.2). The frequency of 1-year mortality was 17% and 1-year neuromotor sequel 18%. Death at 1 year was associated with low birth weight for all patients (adjusted odds ratio 0.24, 95% confidence interval [CI] 0.08-0.68) and time to diagnosis below the median with CM (0.09, 0.01-0.87) but not time to diagnosis above the median for all patients (0.59, 0.13-2.66). Short time to diagnosis was associated with clinical severity on the first day of symptoms for all patients (adjusted hazard ratio 3.39, 95% CI 2.01-5.72), and young age with CM (0.09, 0.02-0.41)., Conclusions: In children with new-onset HF presenting in our region, median time to diagnosis was short. Long time to diagnosis was not associated with poor outcome., (Copyright © 2020 Elsevier B.V. All rights reserved.)
- Published
- 2020
- Full Text
- View/download PDF
27. Improved ventilation in premature babies after transcatheter versus surgical closure of patent ductus arteriosus.
- Author
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Regan W, Benbrik N, Sharma SR, Auriau J, Bouvaist H, Bautista-Rodriguez C, Sirico D, Aw TC, di Salvo G, Foldvari S, Rozé JC, Baruteau AE, and Fraisse A
- Subjects
- Cardiac Catheterization, Humans, Infant, Infant, Low Birth Weight, Infant, Newborn, Infant, Premature, Retrospective Studies, Treatment Outcome, Ductus Arteriosus, Patent diagnostic imaging, Ductus Arteriosus, Patent surgery
- Abstract
Aims: Patent ductus arteriosus (PDA) is common in preterm infants and can contribute to morbidity and mortality. We aimed to compare results and outcome of transcatheter closure using the Amplatzer Piccolo Occluder versus surgical closure in 2 matched groups of preterm infants weighing <3000 g., Methods and Results: A total of 147 babies from three tertiary centres were retrospectively analysed. Sixty-four babies undergoing catheter closure were compared with 83 matched surgical cases. Patent ductus arteriosus closure was successful in all cases. During neonatal unit course, mortality was 6.3% (n = 4) after catheterization and 12% (n = 10) after surgery (p = 0.24). Median duration of mechanical ventilation was shorter after catheterisation than after surgery (3 vs 5 days, p = 0.035). Before 4 weeks of age the difference between transcatheter and surgical closure for mechanical ventilation was even more pronounced (3 vs 9 days, p = 0.022). Additionally, when catheterisation was performed before 4 weeks, babies were discharged home earlier as compared to those who underwent closure later in life (39
+1 vs. 42+1 weeks, p = 0.021). Such difference was not found in the surgical group., Conclusions: Transcatheter closure of patent ductus arteriosus is safe, effective and is associated with shorter mechanical ventilation than after surgery. Hospital stay might be shorter when performed earlier in life., Competing Interests: Declaration of competing interest Alain Fraisse is consultant and proctor for Abbott and for Occlutech. Alban-Elouen Baruteau is consultant and proctor for Abbott., (Copyright © 2020 Elsevier B.V. All rights reserved.)- Published
- 2020
- Full Text
- View/download PDF
28. Severe Late-Onset Kawasaki Disease Successfully Treated With Anakinra.
- Author
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Blonz G, Lacroix S, Benbrik N, Warin-Fresse K, Masseau A, Trewick D, Hamidou M, Stephan JL, and Néel A
- Subjects
- Adolescent, Age of Onset, Anticoagulants administration & dosage, Antirheumatic Agents administration & dosage, Humans, Male, Treatment Outcome, Aspirin administration & dosage, Computed Tomography Angiography methods, Coronary Aneurysm diagnostic imaging, Coronary Aneurysm etiology, Image Processing, Computer-Assisted methods, Immunoglobulins, Intravenous administration & dosage, Interleukin 1 Receptor Antagonist Protein administration & dosage, Mucocutaneous Lymph Node Syndrome blood, Mucocutaneous Lymph Node Syndrome epidemiology, Mucocutaneous Lymph Node Syndrome physiopathology, Mucocutaneous Lymph Node Syndrome therapy
- Published
- 2020
- Full Text
- View/download PDF
29. A step towards precision medicine in management of severe transient polyhydramnios: MAGED2 variant.
- Author
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Arthuis CJ, Nizon M, Kömhoff M, Beck BB, Riehmer V, Bihouée T, Bruel A, Benbrik N, Winer N, and Isidor B
- Subjects
- Adaptor Proteins, Signal Transducing blood, Antigens, Neoplasm blood, Bartter Syndrome therapy, Female, Humans, Infant, Newborn, Male, Mutation, Pedigree, Polyhydramnios therapy, Pregnancy, Young Adult, Bartter Syndrome genetics, Infant, Premature, Diseases genetics, Polyhydramnios genetics
- Published
- 2019
- Full Text
- View/download PDF
30. [Extracorporeal life support and heart-lung transplant in children].
- Author
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Hascoet S, Boet A, Nubret K, Lilot M, Feuillet S, Benbrik N, Guihaire J, Le Bret E, Fadel E, Fouilloux V, Amedro P, Houyel L, and Kreitmann B
- Subjects
- Child, Heart Failure complications, Humans, Respiratory Insufficiency complications, Extracorporeal Membrane Oxygenation ethics, Extracorporeal Membrane Oxygenation instrumentation, Heart Failure surgery, Heart-Lung Transplantation ethics, Respiratory Insufficiency surgery
- Abstract
Extracorporeal life support and heart and/or lung transplant are the last resort in children with end-stage cardiac and/or pulmonary failure and short-term life threaten. Currently, circulatory support is used as a bridge to recovery or as a bridge to transplant but not as a destination therapy. The Excor Berlin Heart is the long-lasting external pneumatic ventricular assist system that is currently available from infancy to adulthood. Long-term prognosis after pediatric cardiac and/or pulmonary transplant is conditioned by the occurrence of graft failure, coronary disease of the cardiac graft, viral infections and bronchiolitis obliterans of the pulmonary graft, the incidence of which increase with time. The scarcity of grafts and the risk of acute rejection due to lack of compliance with immunosuppressive treatment require the transplant specialized teams to choose the best candidates according to psychosocial and biological criteria. The next expected developments concern mainly long-term ventricular assistance with systems that allow for greater autonomy and a return to the child's home., (Copyright © 2018 Elsevier Masson SAS. All rights reserved.)
- Published
- 2018
- Full Text
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31. Three patients presenting with severe macrosomia and congenital hypertrophic cardiomyopathy: a case series.
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Vincent M, Benbrik N, Romefort B, Colombel A, Bézieau S, and Isidor B
- Subjects
- Adult, Birth Weight, Body Mass Index, Cardiomyopathy, Hypertrophic embryology, Cardiomyopathy, Hypertrophic physiopathology, DNA Copy Number Variations, Diabetes, Gestational blood, Female, Fetal Macrosomia physiopathology, Fetal Monitoring, Glucose Tolerance Test, Humans, Infant, Male, Pregnancy, Pregnancy Outcome, Pregnancy in Diabetics blood, Cardiomyopathy, Hypertrophic diagnosis, Diabetes, Gestational physiopathology, Fetal Macrosomia diagnosis, Hypoglycemia complications, Mothers, Pregnancy in Diabetics physiopathology
- Abstract
Background: Macrosomia and hypertrophic cardiomyopathy are two features often associated in neonates of diabetic mothers. We report the cases of three patients with severe macrosomia and critical hypertrophic cardiomyopathy without severely unbalanced maternal diabetes. Only three patients with those two features and no uncontrolled maternal diabetes have been previously reported., Case Presentation: The first patient was a 39-week-old girl, the second patient was a 39-week-old girl, and the third patient was a 41-week-old boy. The two French girls and the French boy had severe macrosomia and hypertrophic cardiomyopathy, leading to the death of the boy. The outcome of the two girls was favorable, with a standardization of growth curves and ventricular hypertrophy. Their mothers presented with high body mass index but no severe documented maternal diabetes; glycemic imbalance was only suspected on postnatal analyses. There was no hydramnios during pregnancy and no other environmental factor, especially toxic exposure. Their parents are from Mayotte, Guadeloupe, and Guinea-Conakry. The usual genetics causes, Beckwith-Wiedemann syndrome, and chromosomal copy number variation, were also excluded., Conclusions: This report suggests the implication of other factors in addition to glycemic disorders, including genetic factors, in the occurrence of macrosomia and severe hypertrophic cardiomyopathy in neonates. These three original observations indicate that gynecologists and neonatologists should pay attention to neonates from mothers with a high body mass index and when maternal diabetes is not documented.
- Published
- 2017
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32. Neonatal Marfan Syndrome: Report of a Case with an Inherited Splicing Mutation outside the Neonatal Domain.
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Le Gloan L, Hauet Q, David A, Hanna N, Arfeuille C, Arnaud P, Boileau C, Romefort B, Benbrik N, Gournay V, Joram N, Baron O, and Isidor B
- Abstract
We report a child and her mother affected by Marfan syndrome. The child presented with a phenotype of neonatal Marfan syndrome, revealed by acute and refractory heart failure, finally leading to death within the first 4 months of life. Her mother had a common clinical presentation. Genetic analysis revealed an inherited FBN1 mutation. This intronic mutation (c.6163+3_6163+6del), undescribed to date, leads to exon 49 skipping, corresponding to in-frame deletion of 42 amino acids (p.Ile2014_Asp2055del). FBN1 next-generation sequencing did not show any argument for mosaicism. Association in the same family of severe neonatal and classical Marfan syndrome illustrates the intrafamilial phenotype variability.
- Published
- 2016
- Full Text
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33. Late repair of tetralogy of Fallot during childhood in patients from developing countries.
- Author
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Benbrik N, Romefort B, Le Gloan L, Warin K, Hauet Q, Guerin P, Baron O, and Gournay V
- Subjects
- Developing Countries, Female, France, Humans, Male, Postoperative Complications, Retrospective Studies, Tetralogy of Fallot mortality, Tetralogy of Fallot surgery
- Abstract
Objectives: Although the current surgical approach of tetralogy of Fallot (TOF) is primary complete repair in infancy, late diagnosis and lack of surgical facilities in developing countries may delay surgical treatment. Some of these patients exposed to prolonged chronic hypoxaemia are transferred to more privileged countries to undergo surgical repair with the support of non-governmental organizations. The objective of this single-centre retrospective study was to compare the postoperative outcomes of these foreign patients undergoing delayed repair with those of patients born in France undergoing timely repair during the same time period., Methods: The computer database of our institution was searched for all cases of TOF in foreign patients younger than 15 years, supported by two non-profit organizations, who underwent complete repair between January 2007 and December 2013. The control population consisted of the patients with TOF born in France, who underwent timely complete repair during the same period., Results: The 47 foreign children were older (57.6 ± 38.4 vs 8.3 ± 9.1 months, P < 0.0001), more hypoxaemic (SaO2 79 ± 11 vs 91 ± 8%, P < 0.0001), more growth-retarded (body mass index Z-score -1.35 ± 1.5 vs -0.46 ± 1.3, P = 0.0034), and had higher haematocrit level (52.5 ± 11.7 vs 37.5 ± 6.1%, <0.0001) and worse left ventricular ejection fraction (LVEF 62 ± 8 vs 69 ± 3.8%, P < 0.0001) than the 90 French patients. Postoperative mortality and morbidity (sepsis, arrhythmia, bleeding and need for surgical revision) were similar in the two groups, except for a higher rate of pericardial and/or pleural effusion in foreign children (36 vs 17%, P = 0.02). Length of stay was shorter in foreign than in French patients (11 ± 6 vs 15 ± 15 days, P = 0.0012)., Conclusions: In our experience, despite the presence of several risk factors (growth retardation, chronic hypoxaemia, polycythaemia and left ventricular dysfunction), late repair of TOF was undertaken during childhood in patients from developing countries with no difference in postoperative morbidity and mortality compared with that of timely repair during infancy. These older patients can be discharged sooner. However, patients undergoing late surgery may be at higher risk of complications of right ventricular failure, such as pleural and/or pericardial effusion., (© The Author 2014. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.)
- Published
- 2015
- Full Text
- View/download PDF
34. [Severe shock after protamine infusion in a neonate undergoing cardio pulmonary bypass].
- Author
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Joram N, Benbrik N, De Windt A, Colas H, and Liet JM
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- Fatal Outcome, Heparin Antagonists administration & dosage, Histamine blood, Humans, Hypotension chemically induced, Hypotension physiopathology, Hypotension therapy, Infant, Newborn, Male, Prenatal Diagnosis, Protamines administration & dosage, Shock physiopathology, Transposition of Great Vessels surgery, Cardiopulmonary Bypass, Heparin Antagonists adverse effects, Protamines adverse effects, Shock chemically induced
- Abstract
Shock after protamine infusion are rare. We report here the case of a 6-day-old boy having presented severe and recurring hypotensions after protamine infusions during cardiac surgery under cardio pulmonary bypass. The physiopathology of these reactions is complex and, in the presented case, involved mechanism may not be anaphylactic., (Copyright © 2013 Société française d’anesthésie et de réanimation (Sfar). Published by Elsevier SAS. All rights reserved.)
- Published
- 2013
- Full Text
- View/download PDF
35. [Organization of patient management in level II centers in the Paris area: a prospective survey].
- Author
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Bolot P, Guérin F, Bolie S, Saillant A, Castel C, Denavit MF, Benbrik N, Alissa K, Séaume H, Ropert JC, de Gennes C, de Mongolfier I, Boissinot C, Guillot F, and Zupan-Simunek V
- Subjects
- Female, Hospitals, Maternity, Humans, Infant, Newborn, Paris, Pediatrics, Pregnancy, Prospective Studies, Asphyxia Neonatorum therapy, Intensive Care, Neonatal organization & administration
- Abstract
Perinatal asphyxia is a common emergency for both obstetricians and pediatricians. A prospective study was conducted in 14 maternity hospitals (type II centres) in the Paris suburbs in order to assess pediatric activity and neonatal morbidity associated with supposed perinatal asphyxia in term newborns. Pediatricians were called in at birth very frequently: 1/20 deliveries. Intubation and/or resuscitation procedures were needed in 20% of cases and 20% of infants were referred to a neonatal unit for birth asphyxia or associated pathology. Moderate encephalopathy was observed in 1.5% of all term newborns who needed medical intervention for supposed birth asphyxia.
- Published
- 2003
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