Literature DB >> 34215991

Fatal fetal abnormality Irish live-born survival-an observational study.

Emer Gunne1, Sally Ann Lynch1,2, Cliona McGarvey3, Karina Hamilton3, Deborah M Lambert4.   

Abstract

The aim of the study was to provide accurate information regarding live-born infant survival after diagnosis of fatal fetal anomaly (FFA) to aid decision-making in respect of pregnancy management, and to ascertain the natural history of live-born infants with FFAs via a retrospective analysis of death records (2006-2018), from the National Paediatric Mortality Registry (source Central Statistics Office 2019). Diagnoses and survival times were ascertained from narrative records with further ascertainment and reconciliation of trisomies 13 and 18 cases by review of cytogenetic test records, the National Death Events Register and National Perinatal Epidemiology Centre data. During the study period, termination of pregnancy was not permitted under the Irish Constitution. Patients are live-born babies with fatal fetal anomalies whose deaths were registered in the Republic of Ireland. The main outcome measure was construction of anomaly-specific survival curves, or survival time range and median for those anomalies with rare occurrence. Survival curves for anencephaly, bilateral renal agenesis, thanatophoric dysplasia, trisomy 13, and trisomy 18 show that 90% (n = 95), 93% (n = 60), 100% (n = 14), 37% (n = 92) and 33% (n = 162), respectively, were deceased by 24 h and 98%, 100%, 100%, 73%, and 53%, respectively, by 1 week post-delivery. Survival time range and median were calculated for triploidy (3.5 h-20 days; 10.5 days), whose occurrence was rare. Anhydramnios, craniorachischisis, hydranencephaly and severe hydrocephalus were extremely rare and all deaths were neonatal deaths. Our results provide 13 years of national natural history data of live birth FFA survival. This provides objective information to aid obstetric counselling of couples upon diagnosis of an FFA.

Entities:  

Keywords:  Anencephaly; Fatal fetal abnormality; Live-born survival; Renal agenesis; Thanatophoric dysplasia; Trisomy 13; Trisomy 18

Year:  2021        PMID: 34215991     DOI: 10.1007/s12687-021-00534-3

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  6 in total

1.  Conjoined twins: experience in an Irish tertiary centre.

Authors:  C M McCarthy; K O'Donoghue
Journal:  J Obstet Gynaecol       Date:  2014-01-31       Impact factor: 1.246

2.  The natural history of anencephaly.

Authors:  Nidaa Obeidi; Noirin Russell; John R Higgins; Keelin O'Donoghue
Journal:  Prenat Diagn       Date:  2010-04       Impact factor: 3.050

3.  Survival of children with trisomy 13 and trisomy 18: A multi-state population-based study.

Authors:  Robert E Meyer; Gang Liu; Suzanne M Gilboa; Mary K Ethen; Arthur S Aylsworth; Cynthia M Powell; Timothy J Flood; Cara T Mai; Ying Wang; Mark A Canfield
Journal:  Am J Med Genet A       Date:  2015-12-10       Impact factor: 2.802

4.  Prenatally Diagnosed Fetal Aneuploidy: Natural History and Subsequent Management.

Authors:  N C Murphy; H Dunne; K Flood
Journal:  Ir Med J       Date:  2020-03-13

5.  Fetal medicine specialist experiences of providing a new service of termination of pregnancy for fatal fetal anomaly: a qualitative study.

Authors:  S Power; S Meaney; K O'Donoghue
Journal:  BJOG       Date:  2020-10-13       Impact factor: 6.531

6.  The natural history of pregnancies with a diagnosis of trisomy 18 or trisomy 13; a retrospective case series.

Authors:  Orla A Houlihan; Keelin O'Donoghue
Journal:  BMC Pregnancy Childbirth       Date:  2013-11-18       Impact factor: 3.007

  6 in total

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