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Birth prevalence and survival of exomphalos in England and Wales: 2005 to 2011

Birth prevalence and survival of exomphalos in England and Wales: 2005 to 2011
Birth prevalence and survival of exomphalos in England and Wales: 2005 to 2011
Background
Exomphalos occurs in 2.2 per 10,000 births with 76% of these babies surviving to discharge. The aim of this study was to determine the birth prevalence and survival of babies with this anomaly in England and Wales.
Methods
Six BINOCAR regional congenital anomaly registers in England and Wales (covering 36% of births) between 2005 and 2011 provided cases for this study. Cases included live births, stillbirths (24+ weeks' gestation), late miscarriages (20–23 weeks' gestation), and terminations of pregnancy with fetal anomaly.
Results
The overall birth prevalence was 3.8 (95% confidence interval [CI]: 3.6–4.0) per 10,000 births; 1.4 (1.2–1.6) for isolated cases, 1.2 (1.1–1.4) for cases with multiple anomalies, and 1.2 (1.1–1.4) for cases with chromosomal anomalies. The live birth prevalence was 0.8 (0.7–0.9), 0.5 (0.4–0.6), and 0.1 (0.0–0.1) per 10,000 live births, respectively. Edwards syndrome, congenital heart defects, and nervous system anomalies were the most common anomalies associated with exomphalos. A prenatal diagnosis was made in 83% of isolated, 95% of multiple, and 99% of chromosomal cases. Fifty-five percent of isolated and multiple cases were live born, whereas 85% of cases with chromosomal anomalies resulted in a termination of pregnancy with fetal anomaly. The 1-year survival of live born babies with an isolated exomphalos was 92% compared with 81% in cases with multiple anomalies and 27% in cases with chromosomal anomalies (p?<?0.001).
Conclusion
We report a higher birth prevalence than has previously been reported. The proportion of infants surviving with exomphalos remained unchanged over the time period
prevalence, survival, exomphalos, omphalocele, prenatal diagnosis
1542-0752
721-725
Springett, Anna
a5e82b0e-ac85-421a-a0c0-f7354f422c6a
Draper, Elizabeth S.
9c1d3580-fa21-4268-a182-6ffc62d0520a
Rankin, Judith
ddb311fa-7fd1-4d3a-a10a-727fc52320a9
Rounding, Catherine
21b05f79-8ab1-4dd7-bcd3-8363041c849d
Tucker, David
e3a643e6-8dfb-402c-9e20-4e79bf604d39
Stoianova, Sylvia
18428e52-6362-486e-98da-e00f12116e56
Wellesley, Diana
17cbd6c1-0efb-4df1-ae05-64a44987c9c0
Morris, Joan K.
166e8a8b-5205-4819-b52b-96edfda3e68b
Springett, Anna
a5e82b0e-ac85-421a-a0c0-f7354f422c6a
Draper, Elizabeth S.
9c1d3580-fa21-4268-a182-6ffc62d0520a
Rankin, Judith
ddb311fa-7fd1-4d3a-a10a-727fc52320a9
Rounding, Catherine
21b05f79-8ab1-4dd7-bcd3-8363041c849d
Tucker, David
e3a643e6-8dfb-402c-9e20-4e79bf604d39
Stoianova, Sylvia
18428e52-6362-486e-98da-e00f12116e56
Wellesley, Diana
17cbd6c1-0efb-4df1-ae05-64a44987c9c0
Morris, Joan K.
166e8a8b-5205-4819-b52b-96edfda3e68b

Springett, Anna, Draper, Elizabeth S., Rankin, Judith, Rounding, Catherine, Tucker, David, Stoianova, Sylvia, Wellesley, Diana and Morris, Joan K. (2014) Birth prevalence and survival of exomphalos in England and Wales: 2005 to 2011. Birth Defects Research Part A: Clinical and Molecular Teratology, 100 (9), 721-725. (doi:10.1002/bdra.23301).

Record type: Article

Abstract

Background
Exomphalos occurs in 2.2 per 10,000 births with 76% of these babies surviving to discharge. The aim of this study was to determine the birth prevalence and survival of babies with this anomaly in England and Wales.
Methods
Six BINOCAR regional congenital anomaly registers in England and Wales (covering 36% of births) between 2005 and 2011 provided cases for this study. Cases included live births, stillbirths (24+ weeks' gestation), late miscarriages (20–23 weeks' gestation), and terminations of pregnancy with fetal anomaly.
Results
The overall birth prevalence was 3.8 (95% confidence interval [CI]: 3.6–4.0) per 10,000 births; 1.4 (1.2–1.6) for isolated cases, 1.2 (1.1–1.4) for cases with multiple anomalies, and 1.2 (1.1–1.4) for cases with chromosomal anomalies. The live birth prevalence was 0.8 (0.7–0.9), 0.5 (0.4–0.6), and 0.1 (0.0–0.1) per 10,000 live births, respectively. Edwards syndrome, congenital heart defects, and nervous system anomalies were the most common anomalies associated with exomphalos. A prenatal diagnosis was made in 83% of isolated, 95% of multiple, and 99% of chromosomal cases. Fifty-five percent of isolated and multiple cases were live born, whereas 85% of cases with chromosomal anomalies resulted in a termination of pregnancy with fetal anomaly. The 1-year survival of live born babies with an isolated exomphalos was 92% compared with 81% in cases with multiple anomalies and 27% in cases with chromosomal anomalies (p?<?0.001).
Conclusion
We report a higher birth prevalence than has previously been reported. The proportion of infants surviving with exomphalos remained unchanged over the time period

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More information

Accepted/In Press date: 1 September 2014
Published date: September 2014
Keywords: prevalence, survival, exomphalos, omphalocele, prenatal diagnosis
Organisations: Human Development & Health

Identifiers

Local EPrints ID: 368715
URI: http://eprints.soton.ac.uk/id/eprint/368715
ISSN: 1542-0752
PURE UUID: a13dfb11-d7ea-43d1-9ef5-1d68cf7d530e

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Date deposited: 09 Sep 2014 13:52
Last modified: 14 Mar 2024 17:52

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Contributors

Author: Anna Springett
Author: Elizabeth S. Draper
Author: Judith Rankin
Author: Catherine Rounding
Author: David Tucker
Author: Sylvia Stoianova
Author: Diana Wellesley
Author: Joan K. Morris

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