Evidence map›Paper›PMID 42100468›Full record

ArticleBiomedical sciences instrumentation2025

UTILITY OF CHEST ULTRASONOGRAPHY IN QUANTIFYING CLOT AND PLEURAL EFFUSION VOLUME IN PRECLINICAL MODELS OF PLEURAL DISEASE.

Christian J De Vera, Jincy Jacob, Sunil Christudas, Krishna Sarva, Elizabeth V Bailey, Andrey A Komissarov, Ali O Azghani, Steven Idell, Galina Florova

Abstract read
In one paragraph

Article in Biomedical sciences instrumentation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Christian J De VeraDepartment of Cellular and Molecular Biology, The UT Tyler School of Medicine, Tyler, TX.
Jincy JacobDepartment of Cellular and Molecular Biology, The UT Tyler School of Medicine, Tyler, TX.
Sunil ChristudasDepartment of Cellular and Molecular Biology, The UT Tyler School of Medicine, Tyler, TX.
Krishna SarvaDepartment of Cellular and Molecular Biology, The UT Tyler School of Medicine, Tyler, TX.
Elizabeth V BaileyDepartment of Cellular and Molecular Biology, The UT Tyler School of Medicine, Tyler, TX.
Andrey A KomissarovDepartment of Cellular and Molecular Biology, The UT Tyler School of Medicine, Tyler, TX.
Ali O AzghaniDepartment of Biology, The University of Texas at Tyler, TX.
Steven IdellDepartment of Cellular and Molecular Biology, The UT Tyler School of Medicine, Tyler, TX.
Galina FlorovaDepartment of Cellular and Molecular Biology, The UT Tyler School of Medicine, Tyler, TX.

Funding

Delivery of PAI-1-targeted intrapleural fibrinolytic therapy for empyemaR01HL130402 · NHLBI · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI FLOROVA, GALINA, IDELL, STEVEN · 2017 to 2024
$3.8M
Enhanced Delivery of Thrombolytic Carriers for EmpyemaR01HL152059 · NHLBI · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI KLEGERMAN, MELVIN E, KOMISSAROV, ANDREY · 2021 to 2024
$2.5M
Optimization of a Rabbit Retained Hemothorax Model for Evidence-Based Pharmacologic InterventionsR33HL154103 · NHLBI · UNIVERSITY OF TEXAS HLTH CTR AT TYLER · PI FLOROVA, GALINA, IDELL, STEVEN · 2020 to 2021
$881k
NHLBI NIH HHS R01 HL130402NHLBI NIH HHS R01 HL152059NHLBI NIH HHS R33 HL154103
6 · The paper itself

Abstract

Early detection and monitoring of pleural disease is critical in guiding appropriate treatment decisions. In the United States, chest radiography and computed tomography (CT) are the most employed imaging techniques to assess pleural disease for diagnosis and management. However, repeated imaging using these modalities exposes patients to cumulative ionizing radiation. In contrast, chest ultrasonography offers a safer, cost-effective, and portable alternative that could be of advantage to pediatric, rural, or resource-limited hospital settings. In addition, ultrasonography brings great utility to preclinical research where advanced imaging is limited. In this study, we developed and validated an ultrasound-based tool that enabled pleural effusion and clot volume quantification in our preclinical models of disease (early-stage empyema, advanced-stage empyema, and retained hemothorax). Four methods were tested for estimating pleural effusion and of the two of these most accurate methods were used to quantify clot volume. Across three animal models of pleural disease, both the Predicted Pleural Effusion and Clot Volume (mL) were closest to the actual volume (gold standard, mL) when area volumetry (pleural effusion or clot) was conducted in the coronal view of the pleural space of the subjects. Lastly, ultrasonographic imaging was able to distinguish the difference in clot dissolution (Predicted Clot Volume, mL) between subjects treated with vehicle control or fibrinolytic therapy, providing evidence of its utility in our preclinical model. These findings support the potential applications of these volumetric tools for preclinical and potential clinical use.

Indexed as

empyemapleural diseasepleural effusionrabbit modelretained hemothoraxultrasonography

Identifiers

PMID42100468
PMCPMC13148432

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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.