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dc.contributor.authorOben, Glenda
dc.contributor.authorCraig, Elizabeth
dc.contributor.authorGardner, R. Mac
dc.date.available2016-06-01T04:37:27Z
dc.date.copyright2014-11
dc.identifier.citationOben, G., Craig, E., & Gardner, R. (2014, November). Prevalence of congenital anomalies typically requiring surgery in New Zealand. Health of Children and Young People with Chronic Conditions and Disabilities presented at the Paediatric Society of New Zealand 66th Annual Scientific Meeting.en
dc.identifier.urihttp://hdl.handle.net/10523/6511
dc.description.abstractBackground: The indicator “congenital anomalies typically requiring surgery” (CARS) has not previously been documented for New Zealand, yet such anomalies place considerable burden on families and the health sector, for example, from lengthy stays in hospital or high fiscal costs. If treated with cost-effective surgical procedures, children with these anomalies have an improved long-term prognosis. This study describes the prevalence of CARS among total births (livebirths and fetal deaths) in New Zealand for the years 2000–2011. Methods: Information held in the National Minimum Dataset and the National Mortality Collection was used to identify cases of CARS. The selection comprised babies born live in hospital or fetal deaths with an ICD-10-AM diagnosis of: craniosynostosis, gastroschisis, omphalocele, severe congenital heart disease, digestive system malformations, or orofacial cleft. These anomalies were defined by EUROCAT (European network for the surveillance of congenital anomalies) for having a high pregnancy survival rate and a high requirement for surgery before the age of one year. Results: The birth prevalence of CARS was 4.11 per 1,000 births for 2000–2011. The most common CARS were orofacial clefts, severe congenital heart disease, and digestive malformations. The temporal trend was essentially stable for CARS, and only gastroschisis was significantly higher in 2011 than in 2000. Conclusion: The prevalence of CARS in New Zealand is comparable to rates observed for the English EUROCAT registers; however, the stable trend contrasts to the decreases seen for Europe. The requirement for paediatric surgical services is not presently monitored for New Zealand. This study highlights the continued need for these services; in particular, the increasing need for urgent post-delivery surgery for babies born with gastroschisis. This study reports CARS as diagnosed at birth, and consequently may underestimate prevalence. Extension of the indicator criteria from birth to diagnosis up to one year of age, and identification of terminations of pregnancy for fetal anomaly, warrant further investigation.en_NZ
dc.format.mimetypeapplication/pdf
dc.language.isoenen_NZ
dc.relation.ispartofseriesHealth of Children and Young People with Chronic Conditions and Disabilitiesen_NZ
dc.relation.urihttp://www.otago.ac.nz/nzcyesen_NZ
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCongenital anomaliesen_NZ
dc.subjectCongenital heart diseaseen_NZ
dc.subjectDigestive malformationsen_NZ
dc.subjectCongenital anomalies typically requiring surgeryen_NZ
dc.subjectGastroschisisen_NZ
dc.subjectSurgeryen_NZ
dc.subjectCraniosynostosisen_NZ
dc.subjectOmphaloceleen_NZ
dc.subjectOrofacial cleften_NZ
dc.titlePrevalence of congenital anomalies typically requiring surgery in New Zealanden_NZ
dc.typeConference or Workshop Item (Poster)en_NZ
dc.date.updated2016-05-31T02:10:39Z
otago.schoolWomen's and Children's Healthen_NZ
otago.openaccessOpenen_NZ
otago.event.placeNapier, New Zealanden_NZ
otago.event.titlePaediatric Society of New Zealand 66th Annual Scientific Meetingen_NZ
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Attribution-NonCommercial-NoDerivatives 4.0 International
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