Prevalence, treatment, and outcome of heart disease in live-born children: a prospective analysis of 91,823 live-born children
Language English Country United States Media print
Document type Journal Article, Review
PubMed
2687820
DOI
10.1007/bf02083294
Knihovny.cz E-resources
- MeSH
- Aortic Valve Stenosis congenital epidemiology surgery MeSH
- Heart Septal Defects, Ventricular epidemiology mortality surgery MeSH
- Heart Septal Defects, Atrial epidemiology mortality surgery MeSH
- Aortic Coarctation epidemiology mortality surgery MeSH
- Infant MeSH
- Humans MeSH
- Heart Valve Diseases congenital epidemiology mortality surgery MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Prevalence MeSH
- Prospective Studies MeSH
- Pulmonary Valve Stenosis congenital epidemiology surgery MeSH
- Transposition of Great Vessels epidemiology mortality surgery MeSH
- Heart Defects, Congenital epidemiology mortality surgery MeSH
- Check Tag
- Infant MeSH
- Humans MeSH
- Male MeSH
- Infant, Newborn MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
- Geographicals
- Czechoslovakia MeSH
All 91,823 children born in 1980 in Bohemia (population 6.314 million; area 52,478 square kilometers) were examined at least four times during infancy and at the age of three and four years. All children who died were autopsied and those with heart disease were selected. A total of 779 children (8.223/1000 live births) were suspected by provincial pediatric cardiologists of having a heart disease. All of these were examined at the age of four years at our Center of Pediatric Cardiology. At this age heart disease was proved in 613 alive or deceased children (6.676/1000 live births), congenital cardiac malformations in 589 (6.415/1000 live births), and cardiomyopathies in 24. The most frequent congenital heart defects (CHD) were ventricular septal defect (VSD) (31.41%), atrial septal defect (ASD) (11.37%), aortic stenosis (AS) (7.64%), pulmonary stenosis (PS) (7.13%), coarctation of the aorta (CoA) (5.77%), and transposition of the great arteries (TGA) (5.43%), followed by persistent ductus arteriosus (PDA) (4.75%), atrioventricular septal defect (AVSD) and hypoplastic left heart syndrome (HLHS) (4.07% each), tetralogy of Fallot (TF) (3.56%), and pulmonary atresia (PA) (2.38%). A prevalence of less than 0.1/1000 live births was found for the remaining cardiovascular defects. One hundred fifty-nine (25.9%) patients were admitted to our highly specialized center, 116 (19.7%) catheterized and 85 (13.9%) treated surgically, during the first four years of life. A total of 440 (71.8%) patients survived the fourth year of life. The percentage of deaths was 25.6% among those with congenital heart diseases and 71% with cardiomyopathies. The overall mortality rate was 27% in surgically and 26% in medically treated patients.
See more in PubMed
Pediatrics. 1955 Jan;15(1):12-32 PubMed
Br Heart J. 1981 Jul;46(1):55-62 PubMed
Int J Cardiol. 1986 Apr;11(1):63-74 PubMed
Am J Obstet Gynecol. 1965 Jan 1;91:37-45 PubMed
Br Heart J. 1959 Jan;21(1):40-50 PubMed
Cor Vasa. 1981;23(1):1-3 PubMed
Br Med J. 1960 Jan 30;1(5169):309-15 PubMed
Can Med Assoc J. 1964 Jul 18;91:95-100 PubMed
Br Heart J. 1977 Apr;39(4):445-50 PubMed
Br Heart J. 1970 May;32(3):304-6 PubMed
Am J Hum Genet. 1958 Dec;10(4):398-445 PubMed
Can Med Assoc J. 1964 Aug 22;91:365-71 PubMed
Mayo Clin Proc. 1971 Dec;46(12):794-9 PubMed
Major heart defects: the diagnostic evaluations of first-year-olds
Children with congenital heart disease: probability of natural survival