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Epidemiology and One-Year Follow-Up of Neonates with CDH-Data from Health Insurance Claims in Germany
Congenital diaphragmatic hernia (CDH) is a major congenital malformation with high mortality. Outcome data on larger unselected patient groups in Germany are unavailable as there is no registry for CDH. Therefore, routine data from the largest German health insurance fund were analyzed for the years...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924040/ https://www.ncbi.nlm.nih.gov/pubmed/33672568 http://dx.doi.org/10.3390/children8020160 |
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author | Wittekindt, Boris Doberschuetz, Nora Schmedding, Andrea Theilen, Till-Martin Schloesser, Rolf Gfroerer, Stefan Rolle, Udo |
author_facet | Wittekindt, Boris Doberschuetz, Nora Schmedding, Andrea Theilen, Till-Martin Schloesser, Rolf Gfroerer, Stefan Rolle, Udo |
author_sort | Wittekindt, Boris |
collection | PubMed |
description | Congenital diaphragmatic hernia (CDH) is a major congenital malformation with high mortality. Outcome data on larger unselected patient groups in Germany are unavailable as there is no registry for CDH. Therefore, routine data from the largest German health insurance fund were analyzed for the years 2009–2013. Main outcome measures were incidence, survival and length of hospital stay. Follow-up was 12 months. 285 patients were included. The incidence of CDH was 2.73 per 10,000 live births. Overall mortality was 30.2%. A total of 72.1% of the fatalities occurred before surgery. Highest mortality (64%) was noted in patients who were admitted to specialized care later as the first day of life. Patients receiving surgical repair had a better prognosis (mortality: 10.8%). A total of 67 patients (23.5%) were treated with ECMO with a mortality of 41.8%. The median cumulative hospital stay among one-year survivors was 40 days and differed between ECMO- and non-ECMO-treated patients (91 vs. 32.5 days, p < 0.001). This is the largest German cohort study of CDH patients with a one-year follow-up. The ECMO subgroup showed a higher mortality. Another important finding is that delayed treatment in specialized care increases mortality. Prospective clinical registries are needed to elucidate the treatment outcomes in detail. |
format | Online Article Text |
id | pubmed-7924040 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79240402021-03-03 Epidemiology and One-Year Follow-Up of Neonates with CDH-Data from Health Insurance Claims in Germany Wittekindt, Boris Doberschuetz, Nora Schmedding, Andrea Theilen, Till-Martin Schloesser, Rolf Gfroerer, Stefan Rolle, Udo Children (Basel) Article Congenital diaphragmatic hernia (CDH) is a major congenital malformation with high mortality. Outcome data on larger unselected patient groups in Germany are unavailable as there is no registry for CDH. Therefore, routine data from the largest German health insurance fund were analyzed for the years 2009–2013. Main outcome measures were incidence, survival and length of hospital stay. Follow-up was 12 months. 285 patients were included. The incidence of CDH was 2.73 per 10,000 live births. Overall mortality was 30.2%. A total of 72.1% of the fatalities occurred before surgery. Highest mortality (64%) was noted in patients who were admitted to specialized care later as the first day of life. Patients receiving surgical repair had a better prognosis (mortality: 10.8%). A total of 67 patients (23.5%) were treated with ECMO with a mortality of 41.8%. The median cumulative hospital stay among one-year survivors was 40 days and differed between ECMO- and non-ECMO-treated patients (91 vs. 32.5 days, p < 0.001). This is the largest German cohort study of CDH patients with a one-year follow-up. The ECMO subgroup showed a higher mortality. Another important finding is that delayed treatment in specialized care increases mortality. Prospective clinical registries are needed to elucidate the treatment outcomes in detail. MDPI 2021-02-20 /pmc/articles/PMC7924040/ /pubmed/33672568 http://dx.doi.org/10.3390/children8020160 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wittekindt, Boris Doberschuetz, Nora Schmedding, Andrea Theilen, Till-Martin Schloesser, Rolf Gfroerer, Stefan Rolle, Udo Epidemiology and One-Year Follow-Up of Neonates with CDH-Data from Health Insurance Claims in Germany |
title | Epidemiology and One-Year Follow-Up of Neonates with CDH-Data from Health Insurance Claims in Germany |
title_full | Epidemiology and One-Year Follow-Up of Neonates with CDH-Data from Health Insurance Claims in Germany |
title_fullStr | Epidemiology and One-Year Follow-Up of Neonates with CDH-Data from Health Insurance Claims in Germany |
title_full_unstemmed | Epidemiology and One-Year Follow-Up of Neonates with CDH-Data from Health Insurance Claims in Germany |
title_short | Epidemiology and One-Year Follow-Up of Neonates with CDH-Data from Health Insurance Claims in Germany |
title_sort | epidemiology and one-year follow-up of neonates with cdh-data from health insurance claims in germany |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7924040/ https://www.ncbi.nlm.nih.gov/pubmed/33672568 http://dx.doi.org/10.3390/children8020160 |
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