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Congenital hydronephrosis: prenatal diagnosis and epidemiology in Europe

Congenital hydronephrosis: prenatal diagnosis and epidemiology in Europe
Congenital hydronephrosis: prenatal diagnosis and epidemiology in Europe
OBJECTIVE: To describe prevalence, prenatal diagnosis and epidemiology of congenital hydronephrosis (CH) in Europe. MATERIAL AND METHOD: Data from a large European database for surveillance of congenital malformations (EUROCAT). The 20 participating registries are all based on multiple sources of information and include information about livebirths, fetal deaths with gestational age >/=20 weeks and terminations of pregnancy after prenatal diagnosis of malformations. Included were all cases with CH and born 1995-2004. RESULTS: There were 3648 cases with CH giving an overall prevalence of 11.5 cases per 10,000 births. The large majority of cases were livebirths (3506, 96% of total) and only 17 cases were fetal deaths and 120 were terminations of pregnancy. Almost all livebirths were alive 1 week after birth. Boys accounted for 72% of all cases. A high proportion of the cases (86%) had an isolated renal malformation. There were large regional differences in prevalence of CH ranging from 2 to 29 per 10,000 births. There was little regional variation in the prevalence of postnatally diagnosed cases while there were large regional differences in prevalence of prenatally diagnosed cases. CONCLUSION: Cases with CH are mainly livebirths, boys and survive the first week after birth. The large difference in prevalence seems to be related to the availability of prenatal screening in the region. The impact of over-diagnosis and potential over-treatment in regions with high prevalence or under-diagnosis with implications for renal function later in life in regions with low prevalence needs further investigation
registries, prevalence, fetal, prenatal diagnosis, europe, fetal death, renal function, born, pregnancy, epidemiology, malformations, gestational age, birth, diagnosis, congenital
1477-5131
47-52
Garne, Ester
1e675ea0-ae2a-42a4-a851-894b4d1abd58
Loane, Maria
75179117-e1e8-4113-81d1-20458c7db2f2
Wellesley, Diana
17cbd6c1-0efb-4df1-ae05-64a44987c9c0
Barisic, Ingeborg
eecca9c6-6878-4b68-9b6c-ff0bbb3057ff
EUROCAT Working Group
Garne, Ester
1e675ea0-ae2a-42a4-a851-894b4d1abd58
Loane, Maria
75179117-e1e8-4113-81d1-20458c7db2f2
Wellesley, Diana
17cbd6c1-0efb-4df1-ae05-64a44987c9c0
Barisic, Ingeborg
eecca9c6-6878-4b68-9b6c-ff0bbb3057ff

Garne, Ester, Loane, Maria, Wellesley, Diana and Barisic, Ingeborg , EUROCAT Working Group (2009) Congenital hydronephrosis: prenatal diagnosis and epidemiology in Europe. Journal of Pediatric Urology, 5 (1), 47-52. (doi:10.1016/j.jpurol.2008.08.010).

Record type: Article

Abstract

OBJECTIVE: To describe prevalence, prenatal diagnosis and epidemiology of congenital hydronephrosis (CH) in Europe. MATERIAL AND METHOD: Data from a large European database for surveillance of congenital malformations (EUROCAT). The 20 participating registries are all based on multiple sources of information and include information about livebirths, fetal deaths with gestational age >/=20 weeks and terminations of pregnancy after prenatal diagnosis of malformations. Included were all cases with CH and born 1995-2004. RESULTS: There were 3648 cases with CH giving an overall prevalence of 11.5 cases per 10,000 births. The large majority of cases were livebirths (3506, 96% of total) and only 17 cases were fetal deaths and 120 were terminations of pregnancy. Almost all livebirths were alive 1 week after birth. Boys accounted for 72% of all cases. A high proportion of the cases (86%) had an isolated renal malformation. There were large regional differences in prevalence of CH ranging from 2 to 29 per 10,000 births. There was little regional variation in the prevalence of postnatally diagnosed cases while there were large regional differences in prevalence of prenatally diagnosed cases. CONCLUSION: Cases with CH are mainly livebirths, boys and survive the first week after birth. The large difference in prevalence seems to be related to the availability of prenatal screening in the region. The impact of over-diagnosis and potential over-treatment in regions with high prevalence or under-diagnosis with implications for renal function later in life in regions with low prevalence needs further investigation

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More information

Published date: February 2009
Keywords: registries, prevalence, fetal, prenatal diagnosis, europe, fetal death, renal function, born, pregnancy, epidemiology, malformations, gestational age, birth, diagnosis, congenital

Identifiers

Local EPrints ID: 70764
URI: http://eprints.soton.ac.uk/id/eprint/70764
ISSN: 1477-5131
PURE UUID: 09a2fafe-522b-4576-935e-198be5ff1780

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Date deposited: 06 Jan 2010
Last modified: 13 Mar 2024 20:07

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Contributors

Author: Ester Garne
Author: Maria Loane
Author: Diana Wellesley
Author: Ingeborg Barisic
Corporate Author: EUROCAT Working Group

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