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

被引:5
作者
Glinianaia, Svetlana, V [1 ,2 ]
Rankin, Judith [2 ]
Tan, Joachim [3 ]
Loane, Maria [4 ]
Garne, Ester [5 ]
Cavero-Carbonell, Clara [6 ]
de Walle, Hermien E. K. [7 ]
Gatt, Miriam [8 ]
Gissler, Mika [9 ,10 ]
Klungsoyr, Kari [11 ,12 ]
Lelong, Natalie [13 ]
Neville, Amanda [14 ]
Pierini, Anna [15 ]
Tucker, David F. [16 ]
Urhoj, Stine Kjaer [5 ,17 ]
Wellesley, Diana Gay
Morris, Joan K. [3 ]
机构
[1] Newcastle Univ, Populat Hlth Sci Inst, Fac Med Sci, Newcastle Upon Tyne, Tyne & Wear, England
[2] Newcastle Univ, Populat Hlth Sci Inst, Newcastle Upon Tyne, Tyne & Wear, England
[3] St Georges Univ London, Populat Hlth Res Inst, London, England
[4] Ulster Univ, Fac Life & Hlth Sci, Ctr Maternal Fetal & Infant Res, Belfast, North Ireland
[5] Univ Hosp Southern Denmark, Lillebaelt Hosp, Dept Paediat & Adolescent Med, Kolding, Denmark
[6] FISABIO, Fdn Promot Hlth & Biomed Res Valencian Reg, Rare Dis Res Unit, Valencia, Spain
[7] Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands
[8] Directorate Hlth Informat & Res, Malta Congenital Anomalies Registry, Tal Pieta, Malta
[9] Finnish Inst Hlth & Welf, Dept Knowledge Brokers, Helsinki, Finland
[10] Princess Anne Hosp, Wessex Clin Genet Serv, Southampton, Region Stockhol, England
[11] Univ Bergen, Dept Global Publ Hlth & Primary Care, Bergen, Norway
[12] Norwegian Inst Publ Hlth, Div Mental & Phys Hlth, Bergen, Norway
[13] Univ Paris Cite, Obstet Perinatal & Paediat Epidemiol Res Team EPOP, CRESS, INSERM, Paris, France
[14] Univ Ferrara, Ctr Clin & Epidemiol Res, IMER Registry, Emilia Romagna Registry Birth Defects, Ferrara, Emilia Romagna, Italy
[15] CNR, Inst Clin Physiol, Unit Epidemiol Rare Dis & Congenital Anomalies, Pisa, Tuscany, Italy
[16] Publ Hlth Knowledge & Res, Publ Hlth Wales, Swansea, Wales
[17] Univ Copenhagen, Dept Publ Hlth, Sect Epidemiol, Copenhagen, Denmark
基金
欧盟地平线“2020”;
关键词
Child Health; Epidemiology; Genetics; Mortality; Syndrome; EXPERIENCE; ENGLAND;
D O I
10.1136/archdischild-2022-325068
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
ObjectiveTo investigate the survival to 10 years of age of children with trisomy 13 (T13) and children with trisomy 18 (T18), born 1995-2014. DesignPopulation-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. Setting13 regions in nine Western European countries. Patients252 live births with T13 and 602 with T18. Main outcome measuresSurvival 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. ResultsSurvival 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. ConclusionsThis 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.
引用
收藏
页码:461 / 467
页数:7
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