Evidence map›Paper›PMID 39442929›Full record

ArticleEuropean heart journal. Acute cardiovascular care2024

Right ventricular-pulmonary artery coupling for prognostication in acute pulmonary embolism.

Mads Dam Lyhne, Behnood Bikdeli, David Jiménez, Christopher Kabrhel, David M Dudzinski, Jorge Moisés, José Luis Lobo, Fernando Armestar, Leticia Guirado, Aitor Ballaz and 2 more

Abstract readMulticenter Study
In one paragraph

Article in European heart journal. Acute cardiovascular care, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Mads Dam LyhneDepartment of Anesthesiology and Intensive Care, Aarhus University Hospital, Aarhus, Denmark.ORCID 0000-0001-5279-260X
Behnood BikdeliCardiovascular Medicine Division, Brigham and Women's Hospital, Harvard Medical School, MA, USA.ORCID 0000-0003-1428-879X
David JiménezRespiratory Department, Hospital Ramón y Cajal, Madrid, Spain.ORCID 0000-0002-4571-7721
Christopher KabrhelDepartment of Emergency Medicine, Centre of Vascular Emergencies, Massachusetts General Hospital, Boston, MA, USA.ORCID 0000-0002-8699-7176
David M DudzinskiDepartment of Cardiology, Massachusetts General Hospital, Boston, MA, USA.
Jorge MoisésCIBER Enfermedades Respiratorias (CIBERES), Madrid, Spain.
José Luis LoboCIBER Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Fernando ArmestarDepartment of Intensive Care Medicine, Hospital German Trias i Pujol, Badalona, Barcelona, Spain.
Leticia GuiradoDepartment of Internal Medicine, Hospital Universitario Virgen de Arrixaca, Murcia, Spain.
Aitor BallazDepartment of Pneumonology, Hospital de Galdakao, Vizcaya, Spain.
Manuel MonrealCIBER Enfermedades Respiratorias (CIBERES), Madrid, Spain.
RIETE investigators

Funding

Supplemental Oxygen for Pulmonary Embolism (SO-PE) - A Mechanistic Clinical TrialR01HL168040 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI CHRISTOPHER KABRHEL · 2023 to 2026
$2.3M
NHLBI NIH HHS R01 HL168040NIH HHS R01-HL168040-01
6 · The paper itself

Abstract

aimsAcute pulmonary embolism (PE) increases pulmonary pressure and impair right ventricular (RV) function. Echocardiographic investigation can quantify this mismatch as the tricuspid annular plane systolic excursion (TAPSE) to pulmonary arterial systolic pressure (PASP) ratio. The aim of the study was to investigate the prognostic capabilities of TAPSE/PASP ratio in patients with acute PE. METHODS AND

resultsWe utilized the Registro Informatizado Enfermedad TromboEmbolica registry to analyse consecutive haemodynamically stable PE patients. We used multi-variable logistic regression analyses to assess the association between the TAPSE/PASP ratio and 30-day all-cause mortality across the strata of European Society of Cardiology (ESC) risk categories. We included 4478 patients, of whom 1326 (30%) had low-risk, 2425 (54%) intermediate-low risk and 727 (16%) intermediate-high risk PE. Thirty-day mortality rates were 0.7%, 2.3% and 3.4%, respectively. Mean TAPSE/PASP ratio was 0.65 ± 0.29 in low-risk patients, 0.46 ± 0.30 in intermediate-low risk and 0.33 ± 0.19 in intermediate-high risk patients. In multi-variable analyses, there was an inverse association between TAPSE/PASP ratio and 30-day mortality (adjusted OR 1.32 [95% CI 1.14-1.52] per 0.1 decrease in TAPSE/PASP). TAPSE/PASP ratio below optimal cut-points was associated with increased mortality in low- (<0.40, aOR: 5.88; 95% CI: 1.63-21.2), intermediate-low (<0.43, aOR: 2.96; 95% CI: 1.54-5.71) and intermediate-high risk patients (<0.34, aOR: 4.37; 95% CI: 1.27-15.0). TAPSE/PASP <0.44 showed net reclassification improvement of 18.2% (95% CI: 0.61-35.8) vs. RV/LV ratio >1, and 27.7% (95% CI: 10.2-45.1) vs. ESC risk strata.

conclusionDecreased TAPSE/PASP ratio was associated with increased mortality. The ratio may aid in clinical decision-making, particularly for intermediate-risk patients for whom the discriminatory capability of the current risk stratification tools is limited.

Indexed as

Pulmonary ArteryPulmonary EmbolismVentricular Function, RightAcute DiseaseAgedEchocardiographyFemaleHeart VentriclesHumansMaleMiddle AgedPrognosisRegistriesRisk AssessmentSurvival RateVentricular Dysfunction, RightEchocardiographyPulmonary pressureRight ventricular functionRisk stratificationTAPSE

Identifiers

PMID39442929
PMCPMC11666307

What OpenQuestion holds

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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.