The University of Southampton
University of Southampton Institutional Repository

Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions

Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions
Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions
Objective. To describe prevalence, prenatal diagnosis and epidemiological data on oesophageal atresia from 23 well-defined European regions and compare the prevalence between these regions.

Design. Population-based study using data from a large European database for surveillance of congenital anomalies (EUROCAT) for two decades (1987–2006).

Settings. Twenty-three participating registries based on multiple sources of information including information about live births, fetal deaths with gestational age ?20 weeks and terminations of pregnancy.

Patients. 1222 cases of oesophageal atresia in a population of 5019804 births.

Results. The overall prevalence was 2.43 cases per 10 000 births (95% CI 2.30 to 2.57). There were regional differences in prevalence ranging from 1.27 to 4.55. Prenatal detection rates varied by registry from >50% of cases to <10% of cases. A total of 546 cases (44.7%) had an isolated oesophageal anomaly, 386 (31.6%) were multiple malformed and 290 (23.7%) had an association or a syndrome. There were 1084 live born cases (88.7%), 43 cases were fetal deaths and 95 cases were terminations of pregnancy. One-week survival for live births was 86.9% and 99.2% if the gestational age was ?38 weeks and isolated oesophageal atresia was present. Males accounted for 57.3% of all cases and 38.5% of live born cases were born with gestational age <37 weeks.

Conclusion. There were regional differences in prevalence of oesophageal atresia in Europe. Half of all cases had associated anomalies. Prenatal detection rate increased from 26% to 36.5% over the two decades. Survival in infants with isolated oesophageal atresia born at term is high.
0003-9888
227-232
Pedersen, Rikke Neess
dc183a27-b254-4dcc-bba7-0d0719dd5800
Calzolari, Elisa
9daaa9c9-5719-464c-bc6e-8d24c44020ee
Husby, Steffan
83d4f6d9-c347-4f83-a3d1-a301f99fd32d
Garne, Ester
1e675ea0-ae2a-42a4-a851-894b4d1abd58
Wellesley, D.
17cbd6c1-0efb-4df1-ae05-64a44987c9c0
EUROCAT Working Group
Pedersen, Rikke Neess
dc183a27-b254-4dcc-bba7-0d0719dd5800
Calzolari, Elisa
9daaa9c9-5719-464c-bc6e-8d24c44020ee
Husby, Steffan
83d4f6d9-c347-4f83-a3d1-a301f99fd32d
Garne, Ester
1e675ea0-ae2a-42a4-a851-894b4d1abd58
Wellesley, D.
17cbd6c1-0efb-4df1-ae05-64a44987c9c0

Pedersen, Rikke Neess, Calzolari, Elisa, Husby, Steffan, Garne, Ester and Wellesley, D. , EUROCAT Working Group (2012) Oesophageal atresia: prevalence, prenatal diagnosis and associated anomalies in 23 European regions. Archives of Disease in Childhood, 97 (3), 227-232. (doi:10.1136/archdischild-2011-300597). (PMID:22247246)

Record type: Article

Abstract

Objective. To describe prevalence, prenatal diagnosis and epidemiological data on oesophageal atresia from 23 well-defined European regions and compare the prevalence between these regions.

Design. Population-based study using data from a large European database for surveillance of congenital anomalies (EUROCAT) for two decades (1987–2006).

Settings. Twenty-three participating registries based on multiple sources of information including information about live births, fetal deaths with gestational age ?20 weeks and terminations of pregnancy.

Patients. 1222 cases of oesophageal atresia in a population of 5019804 births.

Results. The overall prevalence was 2.43 cases per 10 000 births (95% CI 2.30 to 2.57). There were regional differences in prevalence ranging from 1.27 to 4.55. Prenatal detection rates varied by registry from >50% of cases to <10% of cases. A total of 546 cases (44.7%) had an isolated oesophageal anomaly, 386 (31.6%) were multiple malformed and 290 (23.7%) had an association or a syndrome. There were 1084 live born cases (88.7%), 43 cases were fetal deaths and 95 cases were terminations of pregnancy. One-week survival for live births was 86.9% and 99.2% if the gestational age was ?38 weeks and isolated oesophageal atresia was present. Males accounted for 57.3% of all cases and 38.5% of live born cases were born with gestational age <37 weeks.

Conclusion. There were regional differences in prevalence of oesophageal atresia in Europe. Half of all cases had associated anomalies. Prenatal detection rate increased from 26% to 36.5% over the two decades. Survival in infants with isolated oesophageal atresia born at term is high.

This record has no associated files available for download.

More information

Published date: March 2012
Organisations: Human Development & Health

Identifiers

Local EPrints ID: 337623
URI: http://eprints.soton.ac.uk/id/eprint/337623
ISSN: 0003-9888
PURE UUID: 3c1e45d3-dbac-4d67-a9d0-46b6f406100a

Catalogue record

Date deposited: 01 May 2012 12:59
Last modified: 14 Mar 2024 10:55

Export record

Altmetrics

Contributors

Author: Rikke Neess Pedersen
Author: Elisa Calzolari
Author: Steffan Husby
Author: Ester Garne
Author: D. Wellesley
Corporate Author: EUROCAT Working Group

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×