Evidence map›Paper›PMID 40385273›Full record

ReviewCardiovascular diagnosis and therapy2025

Diagnosis, management, and outcome of heart failure in congenitally corrected transposition of the great arteries (ccTGA)-a narrative review.

Motoki Komori, Maria Luisa Benesch Vidal, Kenta Imai, Yuji Tominaga, Keisuke Shibagaki, Rieko Kutsuzawa, Shota Kawai, Kentaro Hayashi, Kenichi Kurosaki, Hideo Ohuchi and 4 more

Abstract readReview
In one paragraph

Review in Cardiovascular diagnosis and therapy, 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

14 authors.

Motoki Komori *Department of Paediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Centre, Osaka, Japan.ORCID https://orcid.org/0000-0002-8321-7277
Maria Luisa Benesch Vidal *Department of Cardiology, University Heart and Vascular Centre Hamburg, Hamburg, Germany.
Kenta ImaiDepartment of Paediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Centre, Osaka, Japan.
Yuji TominagaDepartment of Paediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Centre, Osaka, Japan.
Keisuke ShibagakiDepartment of Paediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Centre, Osaka, Japan.
Rieko KutsuzawaDepartment of Paediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Centre, Osaka, Japan.
Shota KawaiDepartment of Paediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Centre, Osaka, Japan.
Kentaro HayashiDepartment of Paediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Centre, Osaka, Japan.
Kenichi KurosakiDepartments of Paediatric Cardiology, National Cerebral and Cardiovascular Centre, Osaka, Japan.
Hideo OhuchiDepartments of Paediatric Cardiology, National Cerebral and Cardiovascular Centre, Osaka, Japan.
Kouichi TodaDepartment of Cardiovascular Surgery, Dokkyo Medical University Saitama Medical Centre, Saitama, Japan.
Yoshikatsu SaikiDepartment of Cardiovascular Surgery, Tohoku University Graduate School of Medicine, Sendai, Japan.
Christoph Sinning *Department of Cardiology, University Heart and Vascular Centre Hamburg, Hamburg, Germany.
Shigemitsu Iwai *Department of Paediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Centre, Osaka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objective: Congenitally corrected transposition of the great arteries (ccTGA) remains a rare congenital disorder with a wide range of manifestations. The management of heart failure (HF) of the systemic right ventricle (RV), arrhythmias, heart block, and acquired cardiac conditions require a complex and multi-faceted approach. The objective of this manuscript is to present the current evidence regarding diagnostic, treatment, and management strategies for HF in ccTGA, including ventricular assist device (VAD) therapy and heart transplantation. Methods: A systematic review of the literature was conducted using PubMed, covering the period between 2010 and 2024. The search terms included "heart failure", "ccTGA", "VAD", "heart transplantation", and "systemic RV failure". Two clinical cases were included for illustrative purposes. Key Content and Findings: HF is a common occurrence in the context of ccTGA, primarily driven by progressive pressure and volume overload of the systemic RV, regurgitation of the systemic atrio-ventricular (AV) valve, and the development of arrhythmias, including complete heart block and (supra-)ventricular tachycardia. The use of HF medication is indicated for symptomatic patients, however, data on the efficacy of standardized HF medication remains limited. Timing of AV-valve replacement is essential to prevent further progression of HF. Conclusions: In ccTGA, the timing of surgery and interventional treatment approaches, the effect of pharmacological treatment in the context of HF, as well as the timing of initiation of a mechanical circulatory support, VAD and heart transplantation, are based on individualised consensus-level decisions. Optimal management remains a topic of debate due to the scarcity of outcome data. Future investigations should focus on identifying surrogate parameters for guiding treatment.

Indexed as

Adults with congenital heart disease (ACHD)congenitally corrected transposition of the great arteries (ccTGA)heart failure (HF)heart transplantationventricular assist device (VAD)

Identifiers

PMID40385273
PMCPMC12082246

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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.