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Prevalence and One-Year Survival of Selected Major Congenital Anomalies in Germany: A Population-Based Cohort Study
Salmai Turial1, Friederike Stimming1, Anke Lux2
1Division of Pediatric Surgery, Pediatric Trauma Surgery and Pediatric Urology, University Medical Centre Magdeburg, Magdeburg, Germany.
Insights
Infant survival rates for congenital anomalies in Saxony-Anhalt are comparable internationally, with 88.3% of live births surviving the first year. Comprehensive data including all pregnancy outcomes is crucial for accurate survival analysis.
Area of Science:
- Pediatric Health
- Public Health Surveillance
- Medical Genetics
Background:
- Congenital anomalies significantly contribute to global infant mortality.
- Understanding prevalence and survival is key for public health interventions.
- Saxony-Anhalt, Germany, serves as the study region.
Purpose of the Study:
- To determine prevalence rates of major congenital anomalies.
- To analyze 1-year survival rates for these anomalies.
- To identify factors influencing infant survival.
Main Methods:
- Systematic data collection by the Malformation Monitoring Centre Saxony-Anhalt.
- Retrospective analysis of a cohort from 2000-2017.
- Survival analysis including all pregnancy outcomes and risk factors.
Main Results:
- 1,012 cases of congenital anomalies were registered.
- Prevalence rates ranged from 2.5 (CDH) to 5.8 (SB) per 10,000.
- Overall 1-year survival was 61.7% (including fetal losses), with 88.3% for live births.
- Survival rates varied by anomaly type (35.7% for genetic, 57.6% for multiple, 68.6% for isolated).
- Prenatally detected anomalies had lower survival (44.6%) than postnatally identified ones (85.2%).
- Preterm birth (<31 weeks) and low birth weight (<1000g) adversely impacted survival.
Conclusions:
- Survival rates in Saxony-Anhalt align with national and international findings.
- Inclusion of all pregnancy outcomes (live birth, stillbirth, fetal loss) is vital for accurate statistical analysis in malformation registers.
Introduction:
Congenital anomalies play an important role in infant mortality worldwide. The present study aims to present the current data on the prevalence rates and the 1-year survival rates for selected major congenital anomalies in Saxony-Anhalt, Germany.
Materials And Methods:
The data were collected systematically by the Malformation Monitoring Centre Saxony-Anhalt. Cohort from 2000 to 2017 was retrospectively analyzed to determine the prevalence rates and the survival rates of nine major congenital anomalies. The survival analysis was conducted, including all pregnancy outcomes and various risk factors.
Results:
In total, 1,012 cases of the selected congenital anomalies were registered. The total prevalence rates ranged from 2.5 (congenital diaphragmatic hernia [CDH]) to 5.8 (spina bifida [SB]) per 10,000. The live birth prevalence was lower. In total, 88.3% of live-born cases survived the first year. The 1-year survival rate of all cases, including fetal losses, was merely 61.7%. There was no continual improvement in survival during the study period noted. The 1-year survival rate was 35.7% for "genetic" malformations, 57.6% for "multiple congenital anomalies," and 68.6% for "isolated" cases, with 44.6% for prenatally detected anomalies and 85.2% for postnatally identified anomalies. Gestational age less than 31 weeks and birth weight below 1,000 g affected the survival rate adversely.
Conclusion:
The survival rate of infants suffering from congenital anomalies in Saxony-Anhalt is comparable to that reported by national and international studies. Registering all pregnancy outcomes irrespective of whether they result in a live birth, stillbirth, or fetal loss in a malformation register seems to be important as it affects the statistical survival analysis in general.
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