Evidence map›Paper›PMID 40336938›Full record

ArticleEuropean heart journal. Case reports2025

Congenitally corrected transposition of the great arteries: one disease, diverse manifestations-a case series.

Maria Luisa Benesch Vidal, Han Ki Park, Kouichi Toda, Geetha Kandavello, Lucy Youngmin Eun, Dominica Zentner, Motoki Komori, Christoph Sinning

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in European heart journal. Case reports, 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.

Maria Luisa Benesch VidalDepartment of Cardiology, University Heart and Vascular Centre Hamburg, Martinistr. 52, 20251 Hamburg, Germany.ORCID https://orcid.org/0009-0002-2303-7976
Han Ki ParkDivision of Cardiovascular Surgery, Department of Thoracic and Cardiovascular Surgery, Severance Cardiovascular Hospital, Yonsei University College of Medicine, 50-1, Yonsei-Ro, Seodaemun-gu, Seoul 03722, Korea.
Kouichi TodaDepartment of Cardiovascular Surgery, Dokkyo Medical University Saitama Medical Centre, 2 Chome-1-50 Minamikoshigaya, Koshigaya, Saitama 343-8555, Japan.
Geetha KandavelloPaediatric and Congenital Heart Centre, Institute Jantung Negara (National Heart Institute), 145, Jln Tun Razak, 50400 Kuala Lumpur, Wilayah Persekutuan Kuala Lumpur, Malaysia.
Lucy Youngmin EunDivision of Paediatric Cardiology, Department of Paediatrics, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul, Korea.
Dominica ZentnerDepartment of Cardiology, The Royal Melbourne Hospital, Walter and Eliza Hall Institute/1G Royal Parade, Parkville, Melbourne, VIC 3050, Australia.ORCID https://orcid.org/0000-0003-0437-1581
Motoki KomoriDepartment of Paediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Centre, 6-1 Kishibeshinmachi, Suita, Osaka 564-8565, Japan.ORCID https://orcid.org/0000-0002-8321-7277
Christoph SinningDepartment of Cardiology, University Heart and Vascular Centre Hamburg, Martinistr. 52, 20251 Hamburg, Germany.ORCID https://orcid.org/0000-0002-7331-8840

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Congenitally corrected transposition of the great arteries (ccTGA) is a rare congenital heart defect with heterogenous clinical manifestations that can pose both diagnostic and management challenges throughout life. Case summary: We describe four patients with ccTGA and different presentations including sudden cardiac arrest, progressive heart failure, post-partum heart failure, and NSTEMI. Aims and Discussion: This case series aims to illustrate the importance of multimodality imaging to assist the diagnosis and support treatment strategies in patients with ccTGA. Direct long-term sequalae, such as arrythmias and heart failure, and the associated management challenges are highlighted. Additionally, the challenges of managing pregnancy with a sRV and the development of acquired heart disease demonstrate the clinical care challenges in caring for this population across the life span.

Indexed as

Cardio-obstetric managementCase seriesCongenitally corrected transposition of the great arteriesCoronary artery diseaseHeart failureVentricular assist device

Identifiers

PMID40336938
PMCPMC12056722

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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.