Literature DB >> 21381187

Paper 4: EUROCAT statistical monitoring: identification and investigation of ten year trends of congenital anomalies in Europe.

Maria Loane1, Helen Dolk, Alan Kelly, Conor Teljeur, Ruth Greenlees, James Densem.   

Abstract

BACKGROUND: As part of EUROCAT's surveillance of congenital anomalies in Europe, a statistical monitoring system has been developed to detect recent clusters or long-term (10 year) time trends. The purpose of this article is to describe the system for the identification and investigation of 10-year time trends, conceived as a "screening" tool ultimately leading to the identification of trends which may be due to changing teratogenic factors.
METHODS: The EUROCAT database consists of all cases of congenital anomalies including livebirths, fetal deaths from 20 weeks gestational age, and terminations of pregnancy for fetal anomaly. Monitoring of 10-year trends is performed for each registry for each of 96 non-independent EUROCAT congenital anomaly subgroups, while Pan-Europe analysis combines data from all registries. The monitoring results are reviewed, prioritized according to a prioritization strategy, and communicated to registries for investigation. Twenty-one registries covering over 4 million births, from 1999 to 2008, were included in monitoring in 2010.
CONCLUSIONS: Significant increasing trends were detected for abdominal wall anomalies, gastroschisis, hypospadias, Trisomy 18 and renal dysplasia in the Pan-Europe analysis while 68 increasing trends were identified in individual registries. A decreasing trend was detected in over one-third of anomaly subgroups in the Pan-Europe analysis, and 16.9% of individual registry tests. Registry preliminary investigations indicated that many trends are due to changes in data quality, ascertainment, screening, or diagnostic methods. Some trends are inevitably chance phenomena related to multiple testing, while others seem to represent real and continuing change needing further investigation and response by regional/national public health authorities.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21381187     DOI: 10.1002/bdra.20778

Source DB:  PubMed          Journal:  Birth Defects Res A Clin Mol Teratol        ISSN: 1542-0752


  49 in total

1.  Disruption of copper-dependent signaling pathway in the nitrofen-induced congenital diaphragmatic hernia.

Authors:  Toshiaki Takahashi; Florian Friedmacher; Hiromizu Takahashi; Alejandro Daniel Hofmann; Prem Puri
Journal:  Pediatr Surg Int       Date:  2014-10-16       Impact factor: 1.827

2.  MMP-1 and -3 haplotype is associated with congenital anomalies of the kidney and urinary tract.

Authors:  Tamara Djuric; Maja Zivkovic; Biljana Milosevic; Magdalena Andjelevski; Mirjana Cvetkovic; Mirjana Kostic; Aleksandra Stankovic
Journal:  Pediatr Nephrol       Date:  2014-01-12       Impact factor: 3.714

3.  Decreased pulmonary c-Cbl expression and tyrosine phosphorylation in the nitrofen-induced rat model of congenital diaphragmatic hernia.

Authors:  Florian Friedmacher; Jan-Hendrik Gosemann; Hiromizu Takahashi; Nicolae Corcionivoschi; Prem Puri
Journal:  Pediatr Surg Int       Date:  2013-01       Impact factor: 1.827

4.  Prenatal administration of all-trans retinoic acid upregulates leptin signaling in hypoplastic rat lungs with experimental congenital diaphragmatic hernia.

Authors:  Florian Friedmacher; Alejandro Daniel Hofmann; Toshiaki Takahashi; Hiromizu Takahashi; Balazs Kutasy; Prem Puri
Journal:  Pediatr Surg Int       Date:  2014-10-21       Impact factor: 1.827

5.  Rare cases of ectopic ureter: Analysis from a single centre with review of the literature.

Authors:  Pritesh Jain; Debansu Sarkar; Krishnendu Maiti; Sandeep Gupta; Dilip Kumar Pal
Journal:  Turk J Urol       Date:  2018-11-21

6.  A clinical predictive model of renal injury in children with congenital solitary functioning kidney.

Authors:  Isabel V Poggiali; Ana Cristina Simões E Silva; Mariana A Vasconcelos; Cristiane S Dias; Izabella R Gomes; Rafaela A Carvalho; Maria Christina L Oliveira; Sergio V Pinheiro; Robert H Mak; Eduardo A Oliveira
Journal:  Pediatr Nephrol       Date:  2018-10-15       Impact factor: 3.714

7.  Using scan statistics for congenital anomalies surveillance: the EUROCAT methodology.

Authors:  Conor Teljeur; Alan Kelly; Maria Loane; James Densem; Helen Dolk
Journal:  Eur J Epidemiol       Date:  2015-05-31       Impact factor: 8.082

8.  Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract.

Authors:  Laurence Heidet; Vincent Morinière; Charline Henry; Lara De Tomasi; Madeline Louise Reilly; Camille Humbert; Olivier Alibeu; Cécile Fourrage; Christine Bole-Feysot; Patrick Nitschké; Frédéric Tores; Marc Bras; Marc Jeanpierre; Christine Pietrement; Dominique Gaillard; Marie Gonzales; Robert Novo; Elise Schaefer; Joëlle Roume; Jelena Martinovic; Valérie Malan; Rémi Salomon; Sophie Saunier; Corinne Antignac; Cécile Jeanpierre
Journal:  J Am Soc Nephrol       Date:  2017-05-31       Impact factor: 10.121

Review 9.  Embryology of the urogenital tract; a practical overview for urogynecologic surgeons.

Authors:  Tiffanie Tam; Rachel N Pauls
Journal:  Int Urogynecol J       Date:  2020-10-29       Impact factor: 2.894

10.  Risk factors for congenital diaphragmatic hernia in the Bogota birth defects surveillance and follow-up program, Colombia.

Authors:  Ana M García; S Machicado; G Gracia; I M Zarante
Journal:  Pediatr Surg Int       Date:  2015-11-16       Impact factor: 1.827

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