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Duodenal Atresia in Finland from 2004 to 2017: Prevalence, Mortality, and Associated Anomalies—A Population-Based Study
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Read the article on dx.doi.org ↗Article · Jun 2024 · 1 min read
In brief
In brief
This Finnish population-based study (2004-2017) reports a duodenal atresia prevalence of 3.08/10,000 births with 95% one-year survival. One-third of cases were syndromic, with trisomy 21 present in 25.3% and cardiac anomalies in 36.1%, the latter associated with increased mortality.
- DA prevalence in Finland: 2.75/10,000 live births, stable 2004-2017; 40% isolated cases, 33% syndromic, 27% multiple anomalies.
- Trisomy 21 present in 25% of DA cases; cardiac anomalies most common (36%), followed by GI tract anomalies (24%) and limb defects (7%).
- Excellent survival: 96.4% neonatal survival, 95% alive at 1 year; mortality strongly associated with cardiac anomalies.
- No terminations occurred in isolated DA cases; all 11 terminations involved syndromic or multiple anomaly presentations.
- 89% resulted in live births despite prenatal diagnosis capability; cardiac workup essential given 36% cardiac anomaly rate.
Written by the GCMD Library team from the article.
Introduction Duodenal atresia (DA) is the most common atresia of the small bowel. This study aims to assess the prevalence, mortality, and associated anomalies related to DA in Finland from 2004 to 2017. Material and Methods A nationwide study based on registers maintained by the Finnish Institute for Health and Welfare and Statistics Finland containing data on all live births and stillbirths and terminations of pregnancy. The cases were identified based on the ICD-9 and 10 (International Classification of Diseases revisions 9 and 10) codes. Associated anomalies were classified based on the EUROCAT criteria; minor anomalies were excluded. Results There were 249 DA cases including 222 (89.2%) live births, 16 (6.4%) stillbirths, and 11 (4.4%) terminations. There was no significant change in the prevalence rates between 2004 and 2017. Live birth prevalence was 2.75/10,000 and total prevalence was 3.08/10,000 births. A total of 100 (40.2%) cases were isolated, 67 (26.9%) had other multiple congenital anomalies, and 83 (33.3%) were syndromic. There were no terminations in isolated DA. Most associated anomalies were cardiac (36.1%), followed by other gastrointestinal tract anomalies (23.7%) and limb deformities/defects (7.2%). Trisomy 21 was observed in 63 cases (25.3%). Neonatal mortality was 3.6% (n = 8) and at 1 year 95.0% were alive. Both neonatal and infant mortalities were associated with cardiac anomalies (p
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