Evidence map›Paper›PMID 41420650›Full record

ArticleEuropean journal of pediatrics2025

Clinical course and perinatal management of fetuses and newborns affected by trisomy 13 and 18: a retrospective single-centre cohort study.

Theresa Reischer, Tim Dorittke, Katrin Klebermaß-Schrehof, Angelika Berger, Paul Dremsek, Julia Ragossnig, Paula Höfinger, Gülen Yerlikaya-Schatten

Abstract read
In one paragraph

Article in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Theresa ReischerDepartment of Obstetrics and Gynaecology, Division of Obstetrics and Feto-Maternal Medicine, Medical University of Vienna, Vienna, Austria.
Tim DorittkeDepartment of Obstetrics and Gynaecology, Division of Obstetrics and Feto-Maternal Medicine, Medical University of Vienna, Vienna, Austria.
Katrin Klebermaß-SchrehofDepartment of Pediatrics and Adolescent Medicine, Division of Neonatology, Intensive Care and Neuropediatrics, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
Angelika BergerDepartment of Pediatrics and Adolescent Medicine, Division of Neonatology, Intensive Care and Neuropediatrics, Comprehensive Center for Pediatrics, Medical University of Vienna, Vienna, Austria.
Paul DremsekCenter for Pathobiochemistry and Genetics, Medical University of Vienna, Vienna, Austria.
Julia RagossnigDepartment of Obstetrics and Gynaecology, Division of Obstetrics and Feto-Maternal Medicine, Medical University of Vienna, Vienna, Austria.
Paula HöfingerDepartment of Obstetrics and Gynaecology, Division of Obstetrics and Feto-Maternal Medicine, Medical University of Vienna, Vienna, Austria.
Gülen Yerlikaya-SchattenDepartment of Obstetrics and Gynaecology, Division of Obstetrics and Feto-Maternal Medicine, Medical University of Vienna, Vienna, Austria. guelen.yerlikaya-schatten@meduniwien.ac.at.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives Trisomy 13 (T13) and 18 (T18) are lethal chromosomal abnormalities. While the prognosis is generally poor, recent evidence suggests that some infants with T13 and T18 are able to survive longer than previously supposed. These findings underline the importance of an individualised approach to perinatal/neonatal care. Methods This retrospective study included 193 pregnancies with T13 and T18 in a single tertiary center between 2005 and 2023. Fetal and maternal characteristics, overall survival, and perinatal and postnatal management were analysed. Results Of 193 affected fetuses, 142 (73.6%) were diagnosed with T18 and 51 (26.4%) with T13. Associated malformations were present in 90.7% (175 cases), with congenital heart defects being the most common (42%). A total of 161 (83,4%) women opted for termination of pregnancy (TOP). Gestational age at diagnosis was significantly higher among women opting to continue pregnancy compared to those opting for TOP. Among women continuing pregnancy, 65.6% (21/32) experienced intrauterine fetal death. Eleven pregnancies resulted in live births. Survival times for infants born alive ranged from 6 min to 60 days, with a median survival time of 18 h. Newborns affected by T18 lived significantly longer than those with T13 (median 33 h vs 6.5 h).Conclusion: The duration of survival in infants with T13 and T18 remains highly variable and difficult to predict. Management strategies must therefore be clarified within an interdisciplinary framework, supporting families through informed, individualised decision-making while balancing the poor prognosis with a focus on comfort, dignity, and quality of life.

Indexed as

Perinatal CareTrisomy 13 SyndromeTrisomy 18 SyndromeAdultFemaleGestational AgeHumansInfant, NewbornMalePregnancyPrognosisRetrospective StudiesPalliative carePerinatal managementSurvival timeTermination of pregnancyTrisomy 13 and 18

Identifiers

PMID41420650
PMCPMC12718251

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.