Evidence map›Paper›PMID 39450245›Full record

ArticleJournal of medical imaging (Bellingham, Wash.)2024

Expanding generalized contrast-to-noise ratio into a clinically relevant measure of lesion detectability by considering size and spatial resolution.

Siegfried Schlunk, Brett Byram

Abstract read
In one paragraph

Article in Journal of medical imaging (Bellingham, Wash.), 2024. 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. Article
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

2 authors.

Siegfried SchlunkVanderbilt University, Nashville, Tennessee, United States.ORCID https://orcid.org/0000-0002-5170-8717
Brett ByramVanderbilt University, Nashville, Tennessee, United States.

Funding

Ultrasound clutter and noise improvements applied to echocardiographic left atrial appendage visualizationR01HL156034 · NHLBI · VANDERBILT UNIVERSITY · PI BYRAM, BRETT C, EAGLE, SUSAN · 2021 to 2024
$2.3M
Suppression and Analysis of Ultrasonic Clutter During Liver Focal Lesion BiopsyR01EB020040 · NIBIB · VANDERBILT UNIVERSITY · PI BYRAM, BRETT C · 2016 to 2019
$1.3M
High-Performance Computer Cluster for Biomedical ResearchS10OD023680 · OD · VANDERBILT UNIVERSITY · PI MEILER, JENS · 2017 to 2017
$587k
NHLBI NIH HHS R01 HL156034NIBIB NIH HHS R01 EB020040NIH HHS S10 OD023680
6 · The paper itself

Abstract

Purpose: Early image quality metrics were often designed with clinicians in mind, and ideal metrics would correlate with the subjective opinion of practitioners. Over time, adaptive beamformers and other post-processing methods have become more common, and these newer methods often violate assumptions of earlier image quality metrics, invalidating the meaning of those metrics. The result is that beamformers may "manipulate" metrics without producing more clinical information. Approach: In this work, Smith et al.'s signal-to-noise ratio (SNR) metric for lesion detectability is considered, and a more robust version, here called generalized SNR (gSNR), is proposed that uses generalized contrast-to-noise ratio (gCNR) as a core. It is analytically shown that for Rayleigh distributed data, gCNR is a function of Smith et al.'s Results: gSNR is shown to be equivalent to SNR for delay-and-sum (DAS) beamformed data, as intended. However, it is shown to be more robust against transformations and report lesion detectability more accurately for non-Rayleigh distributed data. In the simulation included, the SNR of DAS was Conclusions: Using gCNR as a component to estimate gSNR creates a robust measure of lesion detectability. Like SNR, gSNR can be compared with the Rose criterion and may better correlate with clinical assessments of image quality for modern beamformers.

Indexed as

generalized contrast-to-noise ratioimage qualitylesion detectabilitysignal-to-noise ratiospatial resolutionultrasound imaging

Identifiers

PMID39450245
PMCPMC11498315

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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.