Cardiovascular events in perimembranous ventricular septal defect with left ventricular volume overload: a French prospective cohort study (FRANCISCO).


Journal

Cardiology in the young
ISSN: 1467-1107
Titre abrégé: Cardiol Young
Pays: England
ID NLM: 9200019

Informations de publication

Date de publication:
Oct 2021
Historique:
pubmed: 24 9 2021
medline: 5 11 2021
entrez: 23 9 2021
Statut: ppublish

Résumé

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. 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. 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. 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.

Sections du résumé

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 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 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 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.

Identifiants

pubmed: 34551835
pii: S1047951121002717
doi: 10.1017/S1047951121002717
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1557-1562

Auteurs

Lisa Guirgis (L)

Department of Pediatric and Adult Congenital Heart Diseases, Marie Lannelongue Hospital, Groupe Hospitalier Paris Saint-Joseph, centre de reference cardiopathies congénitales complexes M3C, université Paris-Sud, Le Plessis-Robinson, France.

Estibaliz Valdeolmillos (E)

Department of Pediatric Cardiology, Centre Hospitalier Universitaire Haut Leveque, centre de reference cardiopathies congénitales complexes M3C, IHU Lyric, Bordeaux, France.

Guy Vaksmann (G)

Department of Pediatric Cardiology, Private hospital La Louvière, Lille, France.

Clément Karsenty (C)

Department of Pediatric Cardiology, centre de compétence M3C, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.

Ali Houeijeh (A)

Department of Pediatric Cardiology, centre de compétence M3C, Centre Hospitalier Universitaire de Lille, Lille, France.

Eric Hery (E)

Department of Cardiology, Centre Hospitalier Privé Sainte Marie, Osny, France.

Pascal Amedro (P)

Department of Paediatric and Congenital Cardiology, M3C Regional Reference Centre, Montpellier University Hospital, PhyMedExp, INSERM, CNRS, Montpellier, France.

Nicolas Pangaud (N)

Department of Pediatric Cardiology, Clinique du Val d'Ouest, Lyon, France.

Nadir Benbrik (N)

Department of Pediatric Cardiology and Pediatric Cardiac Surgery, centre de compétence M3C, Centre Hospitalier Universitaire de Nantes, institut du thorax, INSERM, CNRS, UNIV Nantes, CHU Nantes, Nantes, France.

Carine Vastel (C)

Department of Pediatric Cardiology, Centre de spécialités pédiatriques de l'est parisien, Créteil, France.

Antoine Legendre (A)

Department of Adult Congenital Heart Disease, centre de reference M3C, Hospital Europen Georges Pompidou, Paris, France.

Zakaria Jalal (Z)

Department of Pediatric Cardiology, Centre Hospitalier Universitaire Haut Leveque, centre de reference cardiopathies congénitales complexes M3C, IHU Lyric, Bordeaux, France.

Khaled Hadeed (K)

Department of Pediatric Cardiology, centre de compétence M3C, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.

Magalie Ladouceur (M)

Department of Adult Congenital Heart Disease, centre de reference M3C, Hospital Europen Georges Pompidou, Paris, France.

Laurence Iserin (L)

Department of Adult Congenital Heart Disease, centre de reference M3C, Hospital Europen Georges Pompidou, Paris, France.

Daniela Laux (D)

Department of Pediatric and Adult Congenital Cardiology, UE3C Lowendal, Paris, France.

Xavier Iriart (X)

Department of Pediatric Cardiology, Centre Hospitalier Universitaire Haut Leveque, centre de reference cardiopathies congénitales complexes M3C, IHU Lyric, Bordeaux, France.

Karine Warin Fresse (K)

Department of Pediatric Cardiology and Pediatric Cardiac Surgery, centre de compétence M3C, Centre Hospitalier Universitaire de Nantes, institut du thorax, INSERM, CNRS, UNIV Nantes, CHU Nantes, Nantes, France.

Bertrand Leobon (B)

Department of Pediatric Cardiology, centre de compétence M3C, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.

Samir Harchaoui (S)

Department of Pediatric and Adult Congenital Cardiology, Lisieux, France.

Virginie Lambert (V)

Department of Pediatric and Adult Congenital Cardiology, Institut Mutualiste Montsouris, Paris, France.

Ronan Bonefoy (R)

Department of Pediatric Cardiology, Hopital Robert Debré, Paris, France.

Adeline Basquin (A)

Department of Pediatric Cardiology, Rennes, France.

Aurélie Chalard (A)

Department of Pediatric Cardiology, centre de competence M3C, Centre Hospitalier Universitaire Gabriel Montpied, Clermont Ferrand, France.

Stéphanie Douchin (S)

Department of Pediatric Cardiology, centre de competence M3C, Centre Hospitalier Universitaire Grenoble Alpes, Grenoble, France.

Ivan Bouzguenda (I)

Department of Pediatric Cardiology, Private hospital La Louvière, Lille, France.

Charlotte Denis (C)

Department of Pediatric Cardiology, centre de competence M3C, Centre Hospitalier Universitaire Dijon, Dijon, France.

Hugues Lucron (H)

Department of Pediatric Cardiology, centre de competence M3C, Hopital Pierre Zobda Quitman Fort de France, Martinique, France.

Gilles Bosser (G)

Department of Pediatric Cardiology, centre de competence M3C, Hopital Brabois, Vandoeuvre Les Nancy, France.

Elise Barre (E)

Department of Pediatric Cardiology, centre de competence M3C, Centre Hospitalier Universitaire Charles Nicolle, Rouen, France.

Bérangère Urbina-Hiel (B)

Department of Pediatric Cardiology, centre de competence M3C, Centre Hospitalier Universitaire Amiens, Amiens, France.

Pauline Helms (P)

Department of Pediatric Cardiology, centre de competence M3C, Centre Hospitalier Universitaire de Hautepierre, Strasbourg, France.

Hélène Ansquer (H)

Department of Pediatric Cardiology, centre de competence M3C, Centre Hospitalier Régional Universitaire Morvan de Brest, Brest, France.

Quentin Hauet (Q)

Department of Pediatric Cardiology and Pediatric Cardiac Surgery, centre de compétence M3C, Centre Hospitalier Universitaire de Nantes, institut du thorax, INSERM, CNRS, UNIV Nantes, CHU Nantes, Nantes, France.

Anne-Sophie Leborgne (AS)

Department of Pediatric Cardiology, Centre Hospitalier Yves le Foll, St Brieuc, France.

Laurence Cohen (L)

Pediatric Cardiology, Massy, France.

Jean Marc Lupoglazoff (JM)

Centre Cardiologique du Nord, St Denis, France.

Maurice Guirgis (M)

Department of Pediatric Cardiology, Polyclinique la Roseraie, Aubervilliers, France.

Céline Gronier (C)

Department of Pediatric Cardiology and Pediatric Cardiac Surgery, centre de compétence M3C, Centre Hospitalier Universitaire de Nantes, institut du thorax, INSERM, CNRS, UNIV Nantes, CHU Nantes, Nantes, France.

Pascale Maragnes (P)

Department of Pediatric Cardiology, centre de competence M3C, Centre Hospitalier Universitaire Cote de Nacre, Caen, France.

Pamela Moceri (P)

Department of Pediatric and Adult Cardiology, Centre Hospitalier Universitaire Lenval, centre de competence M3C UR2CA, Université Côte d'Azur, CHU de Nice, Nice, France.

Pierre Mauran (P)

Department of Pediatric Cardiology, centre de competence M3C, American Memorial Hospital, Reims, France.

Claire Bertail (C)

Department of Pediatric Cardiology, entre de competence M3C, hospices civils de Lyon, Centre Hospitalier Universitaire Louis Pradel de Bron, Lyon, France.

Bruno Lefort (B)

Department of Pediatric Cardiology, centre de competence M3C, Centre Hospitalier Universitaire, Tours, France.

François Godart (F)

Department of Pediatric Cardiology, centre de compétence M3C, Centre Hospitalier Universitaire de Lille, Lille, France.

Alban-Elouen Baruteau (AE)

Department of Pediatric Cardiology and Pediatric Cardiac Surgery, centre de compétence M3C, Centre Hospitalier Universitaire de Nantes, institut du thorax, INSERM, CNRS, UNIV Nantes, CHU Nantes, Nantes, France.

Caroline Ovaert (C)

Department of Pediatric Cardiology, centre de competence M3C, Assistance Publique des Hopitaux de Marseille, Centre Hospitalier Universitaire La Timone, Marseille, France.

Damien Bonnet (D)

Department of Pediatric Cardiology, centre coordinateur reseau M3C, Assistance Publique des Hopitaux de Paris, Necker Enfants Malades Hospital, Paris, France.

Nicolas Combes (N)

Department of Pediatric Cardiology, Clinique Pasteur, Toulouse, France.

Diala Khraiche (D)

Department of Pediatric Cardiology, centre coordinateur reseau M3C, Assistance Publique des Hopitaux de Paris, Necker Enfants Malades Hospital, Paris, France.

Lucile Houyel (L)

Department of Pediatric Cardiology, centre coordinateur reseau M3C, Assistance Publique des Hopitaux de Paris, Necker Enfants Malades Hospital, Paris, France.

Jean Benoit Thambo (JB)

Department of Pediatric Cardiology, Centre Hospitalier Universitaire Haut Leveque, centre de reference cardiopathies congénitales complexes M3C, IHU Lyric, Bordeaux, France.

Meriem Mostefa-Kara (M)

Department of Pediatric and Adult Congenital Heart Diseases, Marie Lannelongue Hospital, Groupe Hospitalier Paris Saint-Joseph, centre de reference cardiopathies congénitales complexes M3C, université Paris-Sud, Le Plessis-Robinson, France.

Sébastien Hascoet (S)

Department of Pediatric and Adult Congenital Heart Diseases, Marie Lannelongue Hospital, Groupe Hospitalier Paris Saint-Joseph, centre de reference cardiopathies congénitales complexes M3C, université Paris-Sud, Le Plessis-Robinson, France.

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