Literature DB >> 19117890

Has prenatal screening influenced the prevalence of comorbidities associated with Down syndrome and subsequent survival rates?

Jane Halliday1, Veronica Collins, Merilyn Riley, Danielle Youssef, Evelyne Muggli.   

Abstract

OBJECTIVES: With this study we aimed to compare survival rates for children with Down syndrome in 2 time periods, 1 before prenatal screening (1988-1990) and 1 contemporaneous with screening (1998-2000), and to examine the frequency of comorbidities and their influence on survival rates.
METHODS: Record-linkage was performed between the population-based Victorian Birth Defects Register and records of deaths in children up to 15 years of age collected under the auspice of the Consultative Council on Obstetric and Pediatric Mortality and Morbidity. Cases of Down syndrome were coded according to the presence or absence of comorbidities by using the International Classification of Diseases, Ninth Revision classification of birth defects. Kaplan-Meier survival functions and log rank tests for equality of survival distributions were performed.
RESULTS: Of infants liveborn with Down syndrome in 1998-2000, 90% survived to 5 years of age, compared with 86% in the earlier cohort. With fetal deaths excluded, the proportion of isolated Down syndrome cases in the earlier cohort was 48.7% compared with 46.1% in the most recent cohort. In 1988-1990 there was at least 1 cardiac defect in 41.1% of cases and in 45.4% in 1998-2000. There was significant variation in survival rates for the different comorbidity groupings in the 1988-1990 cohort, but this was not so evident in the 1998-2000 cohort.
CONCLUSIONS: Survival of children with Down syndrome continues to improve, and there is an overall survival figure of 90% to at least 5 years of age. It is clear from this study that prenatal screening technologies are not differentially ascertaining fetuses with Down syndrome and additional defects, because there has been no proportional increase in births of isolated cases with Down syndrome.

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Mesh:

Year:  2009        PMID: 19117890     DOI: 10.1542/peds.2007-2840

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  4 in total

1.  Major chromosomal anomalies among very low birth weight infants in the Vermont Oxford Network.

Authors:  Nansi S Boghossian; Jeffrey D Horbar; Joseph H Carpenter; Jeffrey C Murray; Edward F Bell
Journal:  J Pediatr       Date:  2011-12-16       Impact factor: 4.406

2.  Linking a European cohort of children born with congenital anomalies to vital statistics and mortality records: A EUROlinkCAT study.

Authors:  M Loane; J E Given; J Tan; A Reid; D Akhmedzhanova; G Astolfi; I Barišić; N Bertille; L B Bonet; C C Carbonell; O Mokoroa Carollo; A Coi; J Densem; E Draper; E Garne; M Gatt; S V Glinianaia; A Heino; E Den Hond; S Jordan; B Khoshnood; S Kiuru-Kuhlefelt; K Klungsøyr; N Lelong; L R Lutke; A J Neville; L Ostapchuk; A Puccini; A Rissmann; M Santoro; I Scanlon; G Thys; D Tucker; S K Urhoj; H E K de Walle; D Wellesley; O Zurriaga; J K Morris
Journal:  PLoS One       Date:  2021-08-27       Impact factor: 3.240

3.  Respiratory tract infection-related healthcare utilisation in children with Down's syndrome.

Authors:  Logan Manikam; Anne G M Schilder; Monica Lakhanpaul; Peter Littlejohns; Emma C Alexander; Andrew Hayward
Journal:  Infection       Date:  2020-03-14       Impact factor: 3.553

Review 4.  Neuro-Ophthalmological Manifestations in Children with Down Syndrome: Current Perspectives.

Authors:  Lavinia Postolache; Anne Monier; Sophie Lhoir
Journal:  Eye Brain       Date:  2021-07-21
  4 in total

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