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Analysis of Congenital Heart Defects in Mouse Embryos Using Qualitative and Quantitative Histological Methods
Published on: March 10, 2020
Spectrum of congenital heart defects in Croatia
1Department of Paediatric Cardiology, University Hospital Zagreb, Zagreb, Croatia. dilber_daniel@yahoo.com
Insights
This study found congenital heart disease (CHD) affects 0.72% of Croatian newborns, with ventricular septal defect being most common. While treatment outcomes are improving, further reducing the 3.85% mortality rate remains a goal.
Area of Science:
- Pediatric Cardiology
- Congenital Malformations
- Public Health Surveillance
Background:
- Congenital heart disease (CHD) represents a significant global health concern.
- Understanding the incidence and characteristics of CHD is crucial for effective public health strategies.
Purpose of the Study:
- To investigate the incidence of CHD in Croatian children over a 5-year period.
- To analyze associated extracardiac malformations, treatment, and outcomes.
- To establish baseline data for future public health interventions.
Main Methods:
- Retrospective analysis of medical data from 14 pediatric cardiology centers in Croatia.
- Data collection spanned October 1, 2002, to October 1, 2007.
- Diagnoses confirmed via clinical findings, ECG, chest X-ray, echocardiography, catheterization, or autopsy.
Main Results:
- A total of 205,051 live births yielded 1,480 cases of CHD (0.72% incidence).
- Ventricular septal defect was the most frequent (34.6%), followed by atrial septal defect (15.9%) and patent ductus arteriosus (9.8%).
- 14.5% of patients had associated chromosomal defects or major anomalies; the overall mortality rate was 3.85%.
Conclusions:
- The incidence of CHD in Croatia is comparable to international data.
- Early diagnosis of severe heart defects was achieved, with a low overall mortality rate.
- Continued efforts are needed to further improve survival rates for children with CHD.
Abstract:
The aim of our study was to investigate the incidence of congenital defects in children born in Croatia during a period of 5 years, its association with extracardiac malformations, its treatment, and outcome. Medical information about the patients was obtained from 14 paediatric cardiology centres that cover the whole country. Diagnosis was made by clinical findings, electrocardiography, chest X-ray, echocardiography, catheterisation, or autopsy. Between October 1, 2002 and October 1, 2007, there were 205,051 live births in Croatia, 1,480 of which were patients diagnosed with congenital heart disease, accounting for 0.72% of the live-born children. The distribution was made up of 34.6% children with ventricular septal defect, 15.9% with atrial septal defect, 9.8% with patency of arterial duct, 4.9% with pulmonary valvar stenosis, 3.3% with tetralogy of Fallot, 3.3% with transposed great arteries, 3.3% with aortic stenosis, 3.2% with aortic coarctation, 4.3% with atrioventricular septal defect and common atrioventricular orifice, 2.3% with hypoplastic left heart syndrome, and 8.3% other with severe defects. The average age in the time of diagnoses is 70.41 days (SD, 188.13), with low average time of diagnoses of severe heart defects, 9.6 days (SD, 32.52). Among patients, 14.5% had chromosomal defects, syndromes, and/or other congenital major anomalies. During the study, 57 patients died because of cardiac anomalies or other related problems, 24 who died were operated. The rates of specific cardiac defects and association with extracardiac malformations are generally comparable with those reported in similar studies. In spite of all problems, mortality rate of 3.85% is low but could be improved.
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