Evidence map›Paper›PMID 42455296›Full record

ArticlePediatric cardiology2026

Myocardial Deformation Analysis in Congenital Aortic Valve Stenosis: Comparison Across Clinical Phenotypes in Children.

Ali Abdulkarim, Matthew Beaver, Scott Anjewierden, Zhining Ou, John L Colquitt

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Article in Pediatric cardiology, 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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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

5 authors.

Ali AbdulkarimDivision of Pediatric Cardiology, Department of Pediatrics, University of Utah School of Medicine, Primary Children's Hospital, Salt Lake City, UT, USA. ali.abdulkarim@hsc.utah.edu.
Matthew BeaverDivision of Pediatric Cardiology, Department of Pediatrics, University of Utah School of Medicine, Primary Children's Hospital, Salt Lake City, UT, USA.
Scott AnjewierdenDivision of Pediatric Cardiology, Department of Pediatrics, University of Utah School of Medicine, Primary Children's Hospital, Salt Lake City, UT, USA.
Zhining OuDivision of Epidemiology, Department of Internal Medicine, School of Medicine, University of Utah, Salt Lake City, UT, USA.
John L ColquittDivision of Pediatric Cardiology, Department of Pediatrics, University of Utah School of Medicine, Primary Children's Hospital, Salt Lake City, UT, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Left ventricular (LV) longitudinal strain (LS) has prognostic value in adults with valvar aortic stenosis (AS), and impaired left atrial (LA) strain is associated with elevated filling pressures. The role of LA and LV strain in children with congenital AS is unclear. We hypothesized that LA and LV strain would be worse with higher gradients and/or greater ventricular mass. We performed a retrospective cross-sectional study (2015-2025) of children aged 1-18 years with isolated congenital AS and preserved systolic function, stratified by Doppler-derived mean gradient as mild (<20 mmHg), moderate (20-40 mmHg), or severe (>40 mmHg). Patients with critical neonatal AS, more than mild aortic regurgitation, prior intervention, genetic syndromes, or inadequate image quality were excluded. LA reservoir, conduit, and contraction strain and LV LS were measured by two-dimensional speckle-tracking echocardiography. Group comparisons and correlation analyses evaluated associations with aortic valve gradient, LV mass index, and mitral E/A ratio. Eighty-four children were identified (mean age 8.7 ± 4.6 years; 33% female). LA strain components (all p>0.2) and LV LS (p=0.8) did not differ across AS groups. Stratification by LV mass Z score (≤2 vs. >2) showed no differences in LA or LV strain. No strain parameter correlated with aortic valve gradient, LV mass index, or mitral E/A ratio (all p>0.05). In children with congenital AS, preserved systolic function, and no prior intervention, LA and LV strain are preserved across disease severity and ventricular hypertrophy categories, suggesting preserved myocardial function and absence of adverse ventricular remodeling.

Indexed as

Congenital aortic stenosisLeft atrial strainLeft ventricular longitudinal strainMyocardial deformationPediatric echocardiographySpeckle-tracking echocardiography

Identifiers

PMID42455296

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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.