Evidence map›Paper›PMID 42381936›Full record

ArticleJTCVS open2026

Changes in pulmonary artery size during and after staged extracardiac total cavopulmonary connection.

Teresa Lemmen, Thibault Schaeffer, Christina Ruda, Adrian Lehmann, Jonas Palm, Nicole Piber, Muneaki Matsubara, Paul Philipp Heinisch, Stanimir Georgiev, Alfred Hager and 3 more

Abstract read
In one paragraph

Article in JTCVS open, 2026. 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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0citing papers in PubMed
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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

13 authors.

Teresa LemmenDepartment of Congenital and Pediatric Heart Surgery, TUM University Hospital, German Heart Center, Munich, Germany.
Thibault SchaefferDepartment of Congenital and Pediatric Heart Surgery, TUM University Hospital, German Heart Center, Munich, Germany.
Christina RudaDepartment of Congenital and Pediatric Heart Surgery, TUM University Hospital, German Heart Center, Munich, Germany.
Adrian LehmannDepartment of Congenital and Pediatric Heart Surgery, TUM University Hospital, German Heart Center, Munich, Germany.
Jonas PalmDepartment of Congenital Heart Disease and Pediatric Cardiology, TUM University Hospital, German Heart Center, Munich, Germany.
Nicole PiberDepartment of Cardiovascular Surgery, TUM University Hospital, German Heart Center, Munich, Germany.
Muneaki MatsubaraDepartment of Congenital and Pediatric Heart Surgery, TUM University Hospital, German Heart Center, Munich, Germany.
Paul Philipp HeinischDepartment of Congenital and Pediatric Heart Surgery, TUM University Hospital, German Heart Center, Munich, Germany.
Stanimir GeorgievDepartment of Congenital Heart Disease and Pediatric Cardiology, TUM University Hospital, German Heart Center, Munich, Germany.
Alfred HagerDepartment of Congenital Heart Disease and Pediatric Cardiology, TUM University Hospital, German Heart Center, Munich, Germany.
Peter EwertDepartment of Congenital Heart Disease and Pediatric Cardiology, TUM University Hospital, German Heart Center, Munich, Germany.
Jürgen HörerDepartment of Congenital and Pediatric Heart Surgery, TUM University Hospital, German Heart Center, Munich, Germany.
Masamichi OnoDepartment of Congenital and Pediatric Heart Surgery, TUM University Hospital, German Heart Center, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Optimal development of the pulmonary arteries (PAs) is crucial for Fontan circulation. This study investigated longitudinal changes in PA size in patients who underwent staged Fontan palliation and analyzed their impact on outcomes. Methods: Serial PA angiograms at bidirectional cavopulmonary shunt (BCPS), extracardiac total cavopulmonary connection (TCPC), and after TCPC were reviewed. PA index (PAI), right and left PAI, and PA symmetry index were calculated, and serial changes were compared. Results: Among 391 patients, right BCPS was performed in 328 (83.9%). The median age at TCPC was 2.1 years (interquartile range: 1.7-2.6 years). The most frequent diagnosis was hypoplastic left heart syndrome, in 148 patients (37.9%). PAI did not change between BCPS and TCPC ( Conclusions: During the staged Fontan procedure, the left PAI decreased, whereas the PAI and right PAI remained stable or increased. A PA symmetry index <0.61 predicts mortality following TCPC. This progressive asymmetry in left-to-right PA size affects in-hospital morbidity and emphasizes the importance of achieving balanced PA growth prior to Fontan completion.

Indexed as

pulmonary artery sizesymmetry indextotal cavopulmonary connection

Identifiers

PMID42381936
PMCPMC13316346

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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.