Literature DB >> 27745705

Addressing the hidden mortality in CDH: A population-based study.

Carmen Mesas Burgos1, Björn Frenckner2.   

Abstract

BACKGROUND: Improvements in the clinical management of CDH have led to overall improved reported result from single institutions. However, population-based studies have highlighted a hidden mortality. AIM: To explore the incidence in Sweden and to address the hidden mortality for CDH during a 27-year period in a population-based setting.
MATERIALS AND METHODS: This is a population based cohort study that includes all patients diagnosed with CDH that were registered in the National Patient Register, the Medical Birth Register, the Register of Congenital Malformations and the Register for Causes of Death between 1987 and 2013. The mortality rates were calculated based on the number deaths divided by the number of live born cases. The hidden mortality was defined as the number of CDH cases that were not born (because of TOP or IUFD), cases of neonatal demise during birth or demise the same day of birth in patients who were in peripheral institutions and who never reached tertiary centers.
RESULTS: In total, 861 CDH patients were born in Sweden between 1987 and 2013, which corresponds to an incidence of 3.0 born CDH per 10,000 live births. When adding the cases of TOP and IUFD, the total incidence of CDH in Sweden was 3.5/10,000 live born. The mortality rate between 1987 and 2013 was 36%: 44% during the first time period 1987-1999 and 27% in the later period 2000-2013. The hidden mortality in the second period was 30%, resulting in a total mortality rate of 45%.
CONCLUSION: The incidence of CDH during a 27-year period remained unchanged in the population. However, we observed a decrease in the prevalence because of the increasing numbers of TOP. A significant hidden mortality exists, with overall mortality rate of 45% for CDH in this population. LEVEL OF EVIDENCE: II (cohort).
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Congenital diaphragmatic hernia (CDH); Hidden mortality; Incidence; Mortality; Population-based study

Mesh:

Year:  2016        PMID: 27745705     DOI: 10.1016/j.jpedsurg.2016.09.061

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  10 in total

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4.  Endoplasmic reticulum stress response is activated in pulmonary hypoplasia secondary to congenital diaphragmatic hernia, but is decreased by administration of amniotic fluid stem cells.

Authors:  Areti Tzanetakis; Lina Antounians; Alyssa Belfiore; Qi Ma; Mark Stasiewicz; Ornella Pellerito; Augusto Zani
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8.  Health-related quality of life in children born with congenital diaphragmatic hernia.

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Authors:  Laura C Guglielmetti; Arturo E Estrada; Ryan Phillips; Ralph F Staerkle; Jason Gien; John P Kinsella; Kenneth W Liechty; Ahmed I Marwan; Raphael N Vuille-Dit-Bille
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Review 10.  The Role of De Novo Variants in Patients with Congenital Diaphragmatic Hernia.

Authors:  Charlotte Bendixen; Heiko Reutter
Journal:  Genes (Basel)       Date:  2021-09-11       Impact factor: 4.096

  10 in total

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