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Survival of children born with congenital anomalies
S Dastgiri1, W H Gilmour, D H Stone
1University of Glasgow, UK.
Insights
Most children born with congenital anomalies survive to age 5. However, survival rates vary significantly by anomaly type, with chromosomal anomalies having the poorest outcomes. This data aids prognosis assessment and healthcare planning.
Area of Science:
- Pediatric Medicine
- Medical Genetics
- Public Health
Background:
- Congenital anomalies are a significant concern in pediatric health.
- Understanding long-term survival is crucial for affected families and healthcare providers.
Purpose of the Study:
- To determine the survival rates of children born with congenital anomalies up to age 5.
- To identify variations in survival based on specific types of anomalies.
Main Methods:
- Retrospective analysis of 6153 live-born cases registered with the Glasgow Register of Congenital Anomalies between 1980 and 1997.
- Follow-up assessment of survival status from birth to 5 years of age.
Main Results:
- Overall survival to 5 years was 88%.
- Survival rates varied significantly by anomaly type: chromosomal anomalies (48%) had the lowest survival, while Down's syndrome (84%) and nervous system anomalies (77%) had higher rates.
- Survival to the first week (94%) and first year (89%) were also reported.
Conclusions:
- While nearly 90% of infants with congenital anomalies survive to age 5, significant prognostic differences exist among anomaly types.
- These findings are vital for clinicians, geneticists, and families in assessing prognosis and planning healthcare.
- The data highlights the need for tailored health care strategies for high-risk populations.
Aim:
To describe the survival to age 5 years of children born with congenital anomalies.
Methods:
Between 1980 and 1997, 6153 live born cases of congenital anomaly were diagnosed and registered by the population based Glasgow Register of Congenital Anomalies. They were retrospectively followed to assess their survival status from birth up to the age of 5 years.
Results:
The proportions of all live born infants with congenital anomalies surviving to the end of the first week, and first and fifth year were 94%, 89%, and 88%, respectively. Survival to age 5, the end point of follow up, was significantly poorer for infants with chromosomal anomalies (48%) compared to neural tube defects (72%), respiratory system anomalies (74%), congenital heart disease (75%), nervous system anomalies (77%), and Down's syndrome (84%).
Conclusion:
Although almost 90% of all live born infants with congenital anomalies survive to 5 years, there are notable variations in survival between anomaly types. Our findings should be useful for both clinicians and geneticists to assess the prognosis of congenital anomalies. This information is also important for affected families and for the planning of health care needs for this high risk population.
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