Evidence map›Paper›PMID 41001516›Full record

ArticleInternational journal of cardiology. Congenital heart disease2025

Incidence and risk factors for the development of pulmonary arteriovenous malformations after stage 2 palliation.

Lea Behrend, Thibault Schaeffer, Muneaki Matsubara, Jonas Palm, Teresa Lemmen, Nicole Piber, Paul Philipp Heinisch, Stanimir Georgiev, Alfred Hager, Peter Ewert and 2 more

Abstract read
In one paragraph

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

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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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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

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5 · Who and what money

Authors and funding

12 authors.

Lea BehrendDepartment of Congenital and Pediatric Heart Surgery, German Heart Center Munich, University Hospital of Technische Universität München, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Europäisches Kinderherzzentrum München, Munich, Germany.
Thibault SchaefferDepartment of Congenital and Pediatric Heart Surgery, German Heart Center Munich, University Hospital of Technische Universität München, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Europäisches Kinderherzzentrum München, Munich, Germany.
Muneaki MatsubaraDepartment of Congenital and Pediatric Heart Surgery, German Heart Center Munich, University Hospital of Technische Universität München, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Europäisches Kinderherzzentrum München, Munich, Germany.
Jonas PalmDepartment of Congenital Heart Disease and Pediatric Cardiology, German Heart Center Munich, University Hospital of Technische Universität München, Munich, Germany.
Teresa LemmenDepartment of Congenital and Pediatric Heart Surgery, German Heart Center Munich, University Hospital of Technische Universität München, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Europäisches Kinderherzzentrum München, Munich, Germany.
Nicole PiberDepartment of Cardiovascular Surgery, German Heart Center Munich, University Hospital of Technische Universität München, Munich, Germany.
Paul Philipp HeinischDepartment of Congenital and Pediatric Heart Surgery, German Heart Center Munich, University Hospital of Technische Universität München, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Europäisches Kinderherzzentrum München, Munich, Germany.
Stanimir GeorgievDepartment of Congenital Heart Disease and Pediatric Cardiology, German Heart Center Munich, University Hospital of Technische Universität München, Munich, Germany.
Alfred HagerDepartment of Congenital Heart Disease and Pediatric Cardiology, German Heart Center Munich, University Hospital of Technische Universität München, Munich, Germany.
Peter EwertDepartment of Congenital Heart Disease and Pediatric Cardiology, German Heart Center Munich, University Hospital of Technische Universität München, Munich, Germany.
Jürgen HörerDepartment of Congenital and Pediatric Heart Surgery, German Heart Center Munich, University Hospital of Technische Universität München, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Europäisches Kinderherzzentrum München, Munich, Germany.
Masamichi OnoDepartment of Congenital and Pediatric Heart Surgery, German Heart Center Munich, University Hospital of Technische Universität München, Division of Congenital and Pediatric Heart Surgery, University Hospital of Munich, Ludwig-Maximilians-Universität, Europäisches Kinderherzzentrum München, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study evaluated the current incidence of pulmonary arteriovenous malformations (PAVMs) following stage 2 palliation (S2P). Methods: Patients who underwent S2P, either through a bidirectional cavopulmonary shunt (BCPS) or the Kawashima procedure (KP) between 1992 and 2022, were reviewed. The cumulative incidence of PAVMs was compared between BCPS and KP. Risk factors for the development of PAVMs were identified. Results: Among 682 patients who underwent S2P, 661 (96.9 %) underwent BCPS and 21 (3.1 %) KP. Median age at S2P was 5.1 (interquartile ranges (IQR): 3.6-9.6) months. During the median interstage follow-up of 1.6 (IQR: 1.6-2.2) years, PAVMs developed in 11 (1.6 %) patients (1.1 % (n = 7) after BCPS and 19.0 % (n = 4) after KP). Cumulative incidence of PAVMs was higher in patients after KP than those after BCPS (p < 0.001). PAVMs were observed in the right lung in 9 patients and both lungs in two. One patient with biliary atresia died of progressive PAVMs and liver cirrhosis after KP, and the remaining 10 patients underwent Fontan completion with a median interval of 1.9 (IQR: 1.5-2.4) years. PAVMs improved in all patients (9 resolutions and 1 improved). Independent risk factors for the development of PAVMs were KP (hazard ratio (HR): 16.364, p < 0.001) in all patients, anomalous pulmonary venous connection (HR: 6.772, p = 0.023) in BCPS patients, and hypoplastic left heart syndrome (HR: 18.819, p = 0.018) in KP patients. Conclusions: The incidence of PAVMs after S2P is very low after BCPS but still relevant after KP. Resolution or improvement of PAVMs is probable after Fontan completion.

Indexed as

Bidirectional cavopulmonary shuntKawashima procedurePulmonary arteriovenous malformationsTotal cavopulmonary connection

Identifiers

PMID41001516
PMCPMC12457743

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