Treatment of Esophageal Atresia in Germany: Analysis of National Hospital Discharge Data From 2016 to 2022.

Caseload Centralization Esophageal atresia Quality of care Volume-outcome relationship

Journal

Journal of pediatric surgery
ISSN: 1531-5037
Titre abrégé: J Pediatr Surg
Pays: United States
ID NLM: 0052631

Informations de publication

Date de publication:
31 Aug 2024
Historique:
received: 23 06 2024
revised: 27 08 2024
accepted: 28 08 2024
medline: 1 10 2024
pubmed: 1 10 2024
entrez: 30 9 2024
Statut: aheadofprint

Résumé

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. CATEGORY OF THE MANUSCRIPT AND TYPE OF STUDY: original article, observational cross-sectional study, secondary data analysis.

Sections du résumé

BACKGROUND BACKGROUND
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.
METHODS METHODS
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.
RESULTS RESULTS
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).
CONCLUSIONS CONCLUSIONS
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. CATEGORY OF THE MANUSCRIPT AND TYPE OF STUDY: original article, observational cross-sectional study, secondary data analysis.

Identifiants

pubmed: 39349343
pii: S0022-3468(24)00792-9
doi: 10.1016/j.jpedsurg.2024.161890
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

161890

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest Reinhard Busse is a member of the German government commission for modern and needs-based hospital care (Regierungskommission für eine moderne und bedarfsgerechte Krankenhausversorgung). The other authors have no conflict of interest.

Auteurs

Max Ungruh (M)

Marien Hospital Witten, Department of Pediatric Surgery, Ruhr-University Bochum, Bochum, Germany. Electronic address: max.ungruh@edu.ruhr-uni-bochum.de.

Jochen Hubertus (J)

Marien Hospital Witten, Department of Pediatric Surgery, Ruhr-University Bochum, Bochum, Germany.

Anke Widenmann (A)

Patient Organization for Esophageal Diseases (KEKS e.V.), Stuttgart, Germany.

Jost Kaufmann (J)

Children's Hospital Cologne, Department for Pediatric Anesthesia and Endoscopy, Cologne, Germany.

Heiko Reutter (H)

University Hospital Erlangen, Department of Pediatrics and Adolescent Medicine, Division of Neonatology and Pediatric Intensive Care, Erlangen, Germany.

Reinhard Busse (R)

Technische Universität Berlin, Department of Health Care Management, Berlin, Germany.

Miriam Wilms (M)

University Hospital Düsseldorf, Department of General-, Visceral-, Thorax and Pediatric Surgery, Düsseldorf, Germany; Patient Organization for People with Anorectal Malformations and Morbus Hirschsprung (SoMA e.V.), Munich, Germany.

Ulrike Nimptsch (U)

Technische Universität Berlin, Department of Health Care Management, Berlin, Germany.

Classifications MeSH