Treatment of Esophageal Atresia in Germany: Analysis of National Hospital Discharge Data From 2016 to 2022
Esophageal atresia (EA) is a complex malformation. Multidisciplinary management is necessary, with the operative repair being the most challenging step in the treatment algorithm. The complete care structure for children with EA in Germany has not been analyzed yet. In the observed period 2016–2022,...
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Veröffentlicht in: | Journal of pediatric surgery 2025-01, Vol.60 (1), p.161890, Article 161890 |
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Zusammenfassung: | Esophageal atresia (EA) is a complex malformation. Multidisciplinary management is necessary, with the operative repair being the most challenging step in the treatment algorithm. The complete care structure for children with EA in Germany has not been analyzed yet.
In the observed period 2016–2022, inpatient EA cases were analyzed 1) during the hospital stay of birth, and 2) during the hospital stay of corrective surgery in patients aged up to 365 days, both based on national hospital discharge data. Patients’ comorbidities, hospital caseload, treatment characteristics (e.g. surgical approach) and outcome parameters were analyzed.
1) 1190 newborn EA cases were treated in 260 hospitals during the perinatal period. 54% had at least one additional malformation, and 16% had a birthweight below 1500 g. In-hospital mortality was 8.4%.
2) 1475 corrective operations for EA were performed in 111 hospitals with a consistent median annual caseload of 2 (P25–P95 1–8) per hospital. At least one indicator for a complicated perioperative course was documented in 63.7% of cases. The use of bronchoscopy was coded in 50% of cases. Median ventilation time during the entire hospital stay was 176 h (P25–P95: 95–1759 h).
Newborns with EA are complex and early postoperative complications are common. The care structure is decentralized, and there was no trend towards centralization in the observed period. The low documented use of bronchoscopy is noteworthy. Centralization of the highly complex and schedulable corrective surgery for EA is necessary to evaluate outcomes and might improve the quality of care and resource utilization.
original article, observational cross-sectional study, secondary data analysis.
•Esophageal atresia is a rare and complex malformation that is commonly associated with additional malformations.•The care structure is decentralized in Germany. Due to the overall low caseload per hospital, the establishment of a volume-outcome relationship seems not feasible. |
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ISSN: | 0022-3468 1531-5037 1531-5037 |
DOI: | 10.1016/j.jpedsurg.2024.161890 |