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Published on: April 17, 2020
Oesophageal Atresia: Prevalence in the Valencian Region (Spain) and Associated Anomalies
Adriana Agurto-Ramírez1, Laura García-Villodre2, Ana Ruiz-Palacio2
1Service of Preventive Medicine, Valencia General University Hospital Consortium, 46014 Valencia, Spain.
Insights
Oesophageal atresia (OA) affects 2.4/10,000 births in the Valencian Region. Most cases occur in live births, often with other congenital anomalies, and mortality is linked to birth weight.
Area of Science:
- Pediatric Surgery
- Medical Genetics
- Public Health
Background:
- Oesophageal atresia (OA) is a congenital anomaly requiring early diagnosis and intervention.
- Understanding the prevalence and characteristics of OA is crucial for public health planning and resource allocation.
- Previous studies highlight variations in OA incidence and associated factors.
Purpose of the Study:
- To determine the prevalence of oesophageal atresia (OA) in the Valencian Region (VR) between 2007 and 2019.
- To describe the epidemiological and clinical characteristics of OA cases.
- To analyze mortality rates and associated factors in OA patients.
Main Methods:
- Population-based registry study using data from the Congenital Anomalies Registry of VR (RPAC-CV).
- Inclusion of live births (LB), stillbirths (SB), and terminations of pregnancy for fetal anomaly (TOPFA) diagnosed with OA.
- Calculation of prevalence rates (per 10,000 births) and analysis of socio-demographic and clinical variables.
Main Results:
- A total of 146 OA cases were identified, with an overall prevalence of 2.4/10,000 births.
- Prevalence was higher in live births (2.3/10,000) compared to stillbirths and TOPFA (0.03/10,000).
- Mortality rate was 0.03/1000 LB, with a significant association between mortality and birth weight. 71.2% of cases had associated anomalies, primarily heart defects.
Conclusions:
- The prevalence of OA in the VR is within the expected range, with lower rates in SB and TOPFA compared to EUROCAT data.
- An association between OA and birth weight, as well as other congenital anomalies, was confirmed.
- Significant variations in OA prevalence were observed during the study period, warranting further investigation.
Abstract:
The objective was to determine the prevalence of oesophageal atresia (OA) and describe the characteristics of OA cases diagnosed before the first year of life, born between 2007 and 2019, and residents in the Valencian Region (VR), Spain. Live births (LB), stillbirths (SB), and termination of pregnancy for fetal anomaly (TOPFA) diagnosed with OA were selected from the Congenital Anomalies population-based Registry of VR (RPAC-CV). The prevalence of OA per 10,000 births with 95% confidence interval was calculated, and socio-demographic and clinical variables were analyzed. A total of 146 OA cases were identified. The overall prevalence was 2.4/10,000 births, and prevalence by type of pregnancy ending was 2.3 in LB and 0.03 in both SB and TOPFA. A mortality rate of 0.03/1000 LB was observed. A relationship was found between case mortality and birth weight (p-value < 0.05). OA was primarily diagnosed at birth (58.2%) and 71.2% of the cases were associated with another congenital anomaly, mainly congenital heart defects. Significant variations in the prevalence of OA in the VR were detected throughout the study period. In conclusion, a lower prevalence in SB and TOPFA was identified compared to EUROCAT data. As several studies have identified, an association between OA cases and birth weight was found.
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