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Titre du document / Document title

Second natural history study of congenital heart defects : results of treatment of patients with ventricular septal defects

Auteur(s) / Author(s)

KIDD L. ; DRISCOLL D. J. ; GERSONY W. M. ; HAYES C. J. ; KEANE J. F. ; O'FALLON W. M. ; PIERONI D. R. ; WOLFE R. R. ; WEIDMAN W. H. ;

Affiliation(s) du ou des auteurs / Author(s) Affiliation(s)

Johns Hopkins univ. school medicine, div. pediatric cardiology, Baltimore MD 21205, ETATS-UNIS

Résumé / Abstract

Background. From 1958 to 1969, 1,280 patients (mostly children) with ventricular septal defects (VSDs) were admitted to the First Natural History Study of Congenital Heart Defects (NHS-1) after cardiac catheterization. Most with small defects and Eisenmenger's syndrome were managed medically; most with large VSDs were managed surgically. Of those with moderate-size defects, some were managed medically, and some were managed surgically. Most had a second catheterization at the conclusion of NHS-1. More than 15 years have elapsed since NHS-1, and most of the cohort are adults

Revue / Journal Title

Monograph - American Heart Association   ISSN 0891-320X   CODEN AHMOAH 

Source / Source

1993, vol. 87 (1), no 2 (3 ref.), pp. I38-I51

Langue / Language

Anglais

Editeur / Publisher

American Heart Association, Dallas, TX, ETATS-UNIS  (1986) (Revue)

Mots-clés anglais / English Keywords

Ventricular septal defect ; Surgery ; Treatment ; Survival ; Cohort study ; Monograph ; Cardiovascular disease ; Heart disease ; Intracardiac defect ; Congenital disease ; Malformation ; Evolution ; Child ; Human ; Adult ; Statistical study ;

Mots-clés français / French Keywords

Communication interventriculaire ; Chirurgie ; Traitement ; Survie ; Etude cohorte ; Monographie ; Appareil circulatoire pathologie ; Cardiopathie ; Communication intracardiaque ; Maladie congénitale ; Malformation ; Evolution ; Enfant ; Homme ; Adulte ; Etude statistique ;

Mots-clés espagnols / Spanish Keywords

Comunicación interventricular ; Cirugía ; Tratamiento ; Sobrevivencia ; Estudio cohorte ; Monografía ; Aparato circulatorio patología ; Cardiopatía ; Comunicación intracardíaca ; Enfermedad congénita ; Malformación ; Evolución ; Niño ; Hombre ; Adulto ; Estudio estadístico ;

Localisation / Location

INIST-CNRS, Cote INIST : 5907 B, 35400003693703.0050

Nº notice refdoc (ud4) : 4680440

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