Evidence map›Paper›PMID 40132157›Full record

ReviewBlood2025

Structure-based design of therapeutics to control hemostasis.

Luke J Tucker, Krista Hilmas, Ashley C Brown

Abstract readReview
In one paragraph

Review in Blood, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Platelet Products and Artificial Platelets for Regenerative Medicine.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2026
    Review
  4. Article
  5. Review
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

3 authors.

Luke J TuckerJoint Department of Biomedical Engineering, The University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC.ORCID 0000-0001-9226-385X
Krista HilmasJoint Department of Biomedical Engineering, The University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC.ORCID 0000-0001-5316-7611
Ashley C BrownJoint Department of Biomedical Engineering, The University of North Carolina at Chapel Hill and North Carolina State University, Raleigh, NC.ORCID 0000-0001-6995-1785

Funding

Anti-microbial platelet-like-particles to treat internal bleeding and augment subsequent healingR01HL162809 · NHLBI · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Ashley Carson Brown · 2023 to 2026
$2.3M
Training Grant in Comparative Molecular MedicineT32GM133393 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI Matthew B Fisher, Caroline Laplante · 2021 to 2026
$1.7M
NC State Chemistry of Life Training Program (CLTP)T32GM141887 · NIGMS · NORTH CAROLINA STATE UNIVERSITY RALEIGH · PI PIERCE, JOSHUA G. · 2021 to 2025
$1.3M
American Heart Association-American Stroke Association 969368NHLBI NIH HHS R01 HL162809NIGMS NIH HHS T32 GM133393NIGMS NIH HHS T32 GM141887
6 · The paper itself

Abstract

abstractHemorrhage causes millions of deaths and hundreds of billions of dollars in medical costs every year, and a large percentage of trauma bleeding-associated deaths occur in the prehospital setting. Bleeding is typically treated with transfused blood products, but this is difficult in the prehospital setting due to limitations in transportation and storage, especially in rural and remote military settings. Advancements in cold-stored platelets and lyophilized blood products have the potential to address some of these limitations. However, devising novel products that continue to improve shelf life, portability, scalability, cost, and safety for patients experiencing bleeding in prehospital settings could greatly improve treatment options and patient outcomes. This review primarily focuses on rational design of material-based approaches to develop novel hemostatic agents that strive to meet limitations of current blood products, especially for use in the prehospital setting. Key topics of consideration include how material design can lead to identification of effective therapies that stop bleeding as well as strategies to iterate on existing designs to enhance healing after cessation of bleeding. Improving performance and functionality of existing and emerging materials could be achieved through the incorporation of transglutaminases, growth factors, cellular components, or inorganic molecules. Finally, consideration of patient-specific factors that influence bleeding, such as patient sex and age, through evaluation of therapies in specific populations and/or design of materials targeted for specific patient populations, is a key area for development of next-generation hemostatic materials.

Indexed as

Drug DesignHemorrhageHemostasisHemostaticsAnimalsHumansHemostatics

Identifiers

PMID40132157
PMCPMC12883855

What OpenQuestion holds

Textmetadata
LicenceTDM
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.