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Ten-year survival of children with trisomy 13 or trisomy 18: a multi-registry European cohort study

Glinianaia, SV; Rankin, J; Tan, JWL; Loane, M; Garne, E; Cavero-Carbonell, C; de Walle, HEK; Gatt, M; Gissler, M; Klungsøyr, K; et al. Glinianaia, SV; Rankin, J; Tan, JWL; Loane, M; Garne, E; Cavero-Carbonell, C; de Walle, HEK; Gatt, M; Gissler, M; Klungsøyr, K; Lelong, N; Neville, AJ; Pierini, A; Tucker, D; Urhoj, SK; Wellesley, DG; Morris, JK (2023) Ten-year survival of children with trisomy 13 or trisomy 18: a multi-registry European cohort study. Archives of Disease in Childhood, 108 (6). pp. 461-467. ISSN 0003-9888 https://doi.org/10.1136/archdischild-2022-325068
SGUL Authors: Tan, Joachim Wei Li

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Abstract

Objective To investigate the survival to 10 years of age of children with trisomy 13 (T13) and children with trisomy 18 (T18), born 1995–2014. Design Population-based cohort study that linked mortality data to data on children born with T13 or T18, including translocations and mosaicisms, from 13 member registries of EUROCAT, a European network for the surveillance of congenital anomalies. Setting 13 regions in nine Western European countries. Patients 252 live births with T13 and 602 with T18. Main outcome measures Survival at 1 week, 4 weeks and 1, 5 and 10 years of age estimated by random-effects meta-analyses of registry-specific Kaplan-Meier survival estimates. Results Survival estimates of children with T13 were 34% (95% CI 26% to 46%), 17% (95% CI 11% to 29%) and 11% (95% CI 6% to 18%) at 4 weeks, 1 and 10 years, respectively. The corresponding survival estimates were 38% (95% CI 31% to 45%), 13% (95% CI 10% to 17%) and 8% (95% CI 5% to 13%) for children with T18. The 10-year survival conditional on surviving to 4 weeks was 32% (95% CI 23% to 41%) and 21% (95% CI 15% to 28%) for children with T13 and T18, respectively. Conclusions This multi-registry European study found that despite extremely high neonatal mortality in children with T13 and T18, 32% and 21%, respectively, of those who survived to 4 weeks were likely to survive to age 10 years. These reliable survival estimates are useful to inform counselling of parents after prenatal diagnosis.

Item Type: Article
Additional Information: © Author(s) (or their employer(s)) 2023. Reuse of this manuscript version (excluding any databases, tables, diagrams, photographs and other images or illustrative material included where a another copyright owner is identified) is permitted strictly pursuant to the terms of the Creative Commons Attribution-Non Commercial 4.0 International (CC-BY-NC 4.0) http://creativecommons.org/licenses/by-nc/4.0/
Keywords: 1103 Clinical Sciences, 1114 Paediatrics and Reproductive Medicine, 1117 Public Health and Health Services, Pediatrics
SGUL Research Institute / Research Centre: Academic Structure > Population Health Research Institute (INPH)
Journal or Publication Title: Archives of Disease in Childhood
ISSN: 0003-9888
Dates:
DateEvent
18 May 2023Published
7 March 2023Published Online
3 February 2023Accepted
Publisher License: Creative Commons: Attribution-Noncommercial 4.0
Projects:
Project IDFunderFunder ID
733001European Commission Directorate-General for Research and InnovationUNSPECIFIED
URI: https://openaccess.sgul.ac.uk/id/eprint/115164
Publisher's version: https://doi.org/10.1136/archdischild-2022-325068

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