Evidence map›Paper›PMID 39713576›Full record

ArticleInternational journal of cardiology. Congenital heart disease2023

Partial anomalous pulmonary venous return in adults: Insight into pulmonary hypertension.

Nour Rahnama, Linda Kubangumusu, Agnes Pasquet, Annie Robert, Anne-Catherine Pouleur, Karlien Carbonez, Joelle Kefer, Stéphane Moniotte, Alain Poncelet, Geoffroy de Becco and 2 more

Abstract read
In one paragraph

Article in International journal of cardiology. Congenital heart disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. The latest definition and classification of pulmonary hypertension.International journal of cardiology. Congenital heart disease · 2024
    Review
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

12 authors.

Nour RahnamaDivision of Cardiology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Linda KubangumusuDivision of Cardiology, Clinique Sainte-Elisabeth, Brussels, Belgium.
Agnes PasquetDivision of Cardiology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Annie RobertEpidemiology and Biostatistics Division, Institut de Recherche Expérimentale et Clinique (IREC), Faculté de Santé Publique, Université Catholique de Louvain, Brussels, Belgium.
Anne-Catherine PouleurDivision of Cardiology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Karlien CarbonezDivision of Pediatric Cardiology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Joelle KeferDivision of Cardiology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Stéphane MoniotteDivision of Pediatric Cardiology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Alain PonceletDivision of Cardiovascular Surgery, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Geoffroy de BeccoDivision of Cardiovascular Surgery, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Benoit GhayeDivision of Radiology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Sophie PierardDivision of Cardiology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Partial anomalous pulmonary venous return (PAPVR) is a rare condition that may lead to pulmonary arterial hypertension (PAH). We sought to determine the prevalence of PAPVR, the follow-up rate of incidentally discovered PAPVR, the repercussions of volume and pressure overload on the right ventricle (RV), and the prevalence and predictors of PAH. Methods and results: Fifty PAPVR patients aged ≥18 years were included. All underwent transthoracic echocardiography and multislice imaging. PAPVR prevalence was 0.2% (23/13,606 chest computed tomography reports). Of the 26 incidentally diagnosed patients, 14 (54%) did not have a cardiac follow-up. Seven (14%) patients had PAH, of whom one third (28%) had Eisenmenger syndrome. The left-to-right shunt ratio (Qp/Qs) was the only predictor of PAH. PAPVR-induced volume overload led to increased right chamber volumes (RV basal diameter 45±8 mm, RV mid-diameter 38±9 mm, RV/left ventricle ratio 1.2 ± 0.2, indexed RV end-diastolic area 14±4 cm Conclusions: PAPVR prevalence was 0.2%. When incidentally diagnosed, its management was often neglected despite potentially serious consequences (14% PAH). Only the Qp/Qs ratio was predictive of PAH. PAPVR-induced volume overload was shown to increase right heart volumes, while PAH-induced pressure overload caused alterations of RV functional parameters.

Indexed as

Congenital cardiopathyPartial anomalous pulmonary venous returnPulmonary hypertension

Identifiers

PMID39713576
PMCPMC11657667

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Registered trials

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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.