Evidence map›Paper›PMID 39888889›Full record

ArticlePloS one2025

Ventricular function assessment using an ultrafast spoiled gradient echo sequence with an intravascular blood pool contrast agent in pediatric patients.

Tayaba Miah, Rithvik Gunda, Gerald Greil, Mohammad Hussain, Qing Zou

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Article in PloS one, 2025. 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

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Tayaba MiahDivision of Cardiology, Department of Pediatrics, UT Southwestern Medical Center, Dallas, Texas, United States of America.
Rithvik GundaDivision of Cardiology, Department of Pediatrics, UT Southwestern Medical Center, Dallas, Texas, United States of America.
Gerald GreilDivision of Cardiology, Department of Pediatrics, UT Southwestern Medical Center, Dallas, Texas, United States of America.
Mohammad HussainDivision of Cardiology, Department of Pediatrics, UT Southwestern Medical Center, Dallas, Texas, United States of America.
Qing ZouDivision of Cardiology, Department of Pediatrics, UT Southwestern Medical Center, Dallas, Texas, United States of America.ORCID 0000-0002-2729-2491

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBalanced steady-state free processing (bSSFP) MR sequence has long been considered the gold standard method for ventricular function assessment (VFA), and normal values are based on this acquisition. However, bSSFP sequence suffers from susceptibility artifacts due to scenarios such as cardiac implants. The T1-TFE sequence, also known as ultrafast spoiled gradient sequence, is less affected by such susceptibility artifacts. While it is unclear if T1-TFE sequence yields similar VFA results as the bSSFP sequence. PURPOSE: To validate if the T1-TFE sequence, with an intravascular blood pool contrast agent, yields similar results for VFA as the gold-standard non-contrast bSSFP approach, so that the T1-TFE sequence can be used for VFA when bSSFP approach fails.

methodsTwo sets of images from two different sequences were utilized in this study. T1-TFE (with contrast) scans were used as one while bSSFP-derived images were used as the other. 37 pediatric patients were recruited into this study. Semi-automated software (cvi42) was used to segment and derive ventricular volumes. Image quality was objectively assessed by comparing signal-to-noise (SNR) and contrast-to-noise ratio (CNR) scores. Last, two expert readers provided a subjective analysis of image quality. Paired t-tests were used to assess significant differences in volumetric values (end-diastolic and end-systolic) between T1-TFE and bSSFP sequences. A Bland-Altman analysis evaluated potential bias and agreement between these sequences.

resultsVentricular function assessment via volumetric data analysis resulted in no statistically significant differences (P > 0.05), and high R2 values. SNR and CNR scores also presented with no statistically significant differences (P > 0.05), and nearly identical scores (SNR T1-TFE mean: 29.5 ± 3.1, SNR bSSFP mean: 28.8 ± 3.7, CNR T1-TFE mean: 28.8 ± 3.3, CNR bSSFP mean: 28.1 ± 4.0). Image quality assessment via expert subjective image analysis scores is consistent with the data. All Bland-Altman plots show good agreement and reveal no systematic bias or random error.

conclusionT1-TFE sequences in combination with Ferumoxytol allow reliable ventricular function assessment and overcome the limitations of traditional bSSFP MR sequences in this context.

Indexed as

Contrast MediaHeart VentriclesMagnetic Resonance ImagingVentricular FunctionAdolescentChildChild, PreschoolFemaleHumansInfantMaleContrast Media

Identifiers

PMID39888889
PMCPMC11785336

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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.