Evidence map›Paper›PMID 40740673›Full record

ArticleEuropean heart journal. Case reports2025

Wolff-Parkinson-White syndrome case due to a coronary sinus accessory pathway in a patient with unique congenital coronary venous anomaly: a case report.

Rita Conti, Nicola Forzati, Saverio Iacopino, Andrea Petretta, Angelo Squeri

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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. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

  1. Article
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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.

Rita ContiDepartment of Cardiology, Cardiovascular Imaging Unit, Maria Cecilia Hospital, GVM Care & Research, Via Corriera 1, 48010 Cotignola, Italy.
Nicola ForzatiDepartment of Cardiology, Cardiovascular Imaging Unit, Maria Cecilia Hospital, GVM Care & Research, Via Corriera 1, 48010 Cotignola, Italy.
Saverio IacopinoDepartment of Cardiology, Arrhythmology Unit, Maria Cecilia Hospital, GVM Care & Research, Via Corriera 1, 48010 Cotignola, Italy.
Andrea PetrettaDepartment of Cardiology, Arrhythmology Unit, Maria Cecilia Hospital, GVM Care & Research, Via Corriera 1, 48010 Cotignola, Italy.
Angelo SqueriDepartment of Cardiology, Cardiovascular Imaging Unit, Maria Cecilia Hospital, GVM Care & Research, Via Corriera 1, 48010 Cotignola, Italy.ORCID https://orcid.org/0000-0001-9115-5443

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Catheter ablation for Wolff-Parkinson-White syndrome (WPW) has a failure rate of 1-5%, particularly when accessory pathways (APs) are located in challenging regions like the posteroseptal or left posterior areas. These cases may involve coronary sinus (CS) APs and anomalies in the coronary venous system, especially in those with a previous failed ablation procedure. Imaging of the coronary venous system obtained by cardiac computed tomography (CT) can help the procedural planning in the presence of challenging anatomy. Case summary: We present the case of a 16-year-old male with WPW syndrome due to a posteroseptal AP, referred to our institution after two failed ablation procedures. Cardiac CT performed before the third attempt revealed CS drainage into the left atrium and a CS diverticulum near the basal segment of the left ventricle's inferior wall. During the electrophysiological study, the left atrium was accessed via transseptal catheterization. The target site was identified in the left posteroseptal region, where successful radiofrequency ablation was performed At a six-month follow-up, no supraventricular tachycardia recurrence was noted. Transthoracic echocardiography and cardiac magnetic resonance (CMR) further excluded communication between the diverticulum and the left ventricle, leading to a conservative follow-up strategy instead of surgical intervention. Discussion: A detailed understanding of coronary venous system anatomy, as provided by cardiac CT, could be useful for planning WPW ablation, particularly in complex cases. The combined use of CMR and echocardiography was pivotal in guiding management decisions for this unique congenital anomaly of the coronary venous system.

Indexed as

Accessory pathway ablationCase reportCongenital anomaliesCoronary sinus accessory pathwayMultimodality imagingWolff–Parkinson–White syndrome

Identifiers

PMID40740673
PMCPMC12308481

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