Evidence map›Paper›PMID 30356250›Full record

ArticlePloS one2018

RV adaptation to increased afterload in congenital heart disease and pulmonary hypertension.

Mieke M P Driessen, Tim Leiner, Gertjan Tj Sieswerda, Arie P J van Dijk, Marco C Post, Mark K Friedberg, Luc Mertens, Pieter A Doevendans, Repke J Snijder, Erik H Hulzebos and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
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

15 citing papers in PubMed, 20 citations in OpenAlex.

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  8. 3D regional evaluation of right ventricular myocardial work from cineCT.medRxiv : the preprint server for health sciences · 2024
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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

11 authors at 5 institutions in 2 countries.

Mieke M P DriessenDepartment of Cardiology, University Medical Centre Utrecht, Utrecht, the Netherlands.ORCID 0000-0001-9713-378X
Tim LeinerDepartment of Radiology, University Medical Centre Utrecht, Utrecht, the Netherlands.
Gertjan Tj SieswerdaDepartment of Cardiology, University Medical Centre Utrecht, Utrecht, the Netherlands.
Arie P J van DijkDepartment of Cardiology, Radboud University Medical Centre Nijmegen, Nijmegen, the Netherlands.
Marco C PostDepartment of Cardiology, Antonius Hospital, Nieuwegein, the Netherlands.
Mark K FriedbergDepartment of Paediatric Cardiology, Labatt Family Heart Center, Toronto, Canada.
Luc MertensDepartment of Paediatric Cardiology, Labatt Family Heart Center, Toronto, Canada.
Pieter A DoevendansDepartment of Cardiology, University Medical Centre Utrecht, Utrecht, the Netherlands.
Repke J SnijderDepartment of Pulmonology, Antonius Hospital, Nieuwegein, the Netherlands.
Erik H HulzebosDepartment of Paediatric Physical Therapy and Exercise Physiology, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
Folkert J MeijboomDepartment of Cardiology, University Medical Centre Utrecht, Utrecht, the Netherlands.
University Medical Center Utrecht · NLCanadian Heart Research Centre · CASt. Antonius Ziekenhuis · NLRadboud University Nijmegen · NLWilhelmina Children's Hospital · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe various conditions causing a chronic increase of RV pressure greatly differ in the occurrence of RV failure, and in clinical outcome. To get a better understanding of the differences in outcome, RV remodeling, longitudinal function, and transverse function are compared between patients with pulmonary stenosis (PS), those with a systemic RV and those with pulmonary hypertension (PH). MATERIALS AND

methodsThis cross-sectional study prospectively enrolled subjects for cardiac magnetic resonance imaging (CMR), functional echocardiography and cardiopulmonary exercise testing. The study included: controls (n = 37), patients with PS (n = 15), systemic RV (n = 19) and PH (n = 20). Statistical analysis was performed using Analysis of Variance (ANOVA) with posthoc Bonferroni.

resultsPS patients had smaller RV volumes with higher RV ejection fraction (61.1±9.6%; p<0.05) compared to controls (53.8±4.8%). PH and systemic RV patients exhibited dilated RVs with lower RV ejection fraction (36.9±9.6% and 46.3±10.1%; p<0.01 versus controls). PH patients had lower RV stroke volume (p = 0.02), RV ejection fractions (p<0.01) and VO2 peak/kg% (p<0.001) compared to systemic RV patients. Mean apical transverse RV free wall motion was lower and RV free wall shortening (p<0.001) was prolonged in PH patients-resulting in post-systolic shortening and intra-ventricular dyssynchrony. Apical transverse shortening and global longitudinal RV deformation showed the best correlation to RV ejection fraction (respectively r = 0.853, p<0.001 and r = 0.812, p<0.001).

conclusionsRV remodeling and function differed depending on the etiology of RV pressure overload. In contrast to the RV of patients with PS or a systemic RV, in whom sufficient stroke volumes are maintained, the RV of patients with PH seems unable to compensate for its increase in afterload completely. Key mediators of RV dysfunction observed in PH patients, were: prolonged RV free wall shortening, resulting in post-systolic shortening and intra-ventricular dyssynchrony, and decreased transverse function.

Indexed as

Ventricular RemodelingAdultAgedCardiac OutputEchocardiographyExercise TestFemaleHeart Defects, CongenitalHeart VentriclesHumansHypertension, PulmonaryLinear ModelsMagnetic Resonance ImagingMaleMiddle AgedPulmonary Valve Stenosis

Identifiers

PMID30356250
PMCPMC6200212
OpenAlexW2898453594

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.