Evidence map›Paper›PMID 34215991›Full record

ArticleJournal of community genetics2021

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

Emer Gunne, Sally Ann Lynch, Cliona McGarvey, Karina Hamilton, Deborah M Lambert

Open access · greenAbstract read
In one paragraph

Article in Journal of community genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.0field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Emer GunneChildren's Health Ireland, Temple Street, Dublin, Republic of Ireland.ORCID http://orcid.org/0000-0002-6939-1586
Sally Ann LynchChildren's Health Ireland, Temple Street, Dublin, Republic of Ireland.ORCID http://orcid.org/0000-0003-3540-1333
Cliona McGarveyNational Paediatric Mortality Register, Dublin, Republic of Ireland.ORCID http://orcid.org/0000-0002-7266-9710
Karina HamiltonNational Paediatric Mortality Register, Dublin, Republic of Ireland.ORCID http://orcid.org/0000-0002-1900-4912
Deborah M LambertNational Rare Disease Office, Mater Misericordiae University Hospital, Dublin, Republic of Ireland. dlambert@mater.ie.ORCID http://orcid.org/0000-0003-0967-0476
Mater Misericordiae University Hospital · IEChildren's Health Ireland at Crumlin · IE

Funding

Temple Street Foundation RPAC 17-06
6 · The paper itself

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.

Indexed as

AnencephalyFatal fetal abnormalityLive-born survivalRenal agenesisThanatophoric dysplasiaTrisomy 13Trisomy 18

Identifiers

PMID34215991
PMCPMC8554881
OpenAlexW3174143719

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.