Evidence map›Paper›PMID 37206230›Full record

ArticleBioengineering & translational medicine2023

A polymer-based systemic hemostat for managing uncontrolled bleeding.

Yongsheng Gao, Mayumi Ikeda-Imafuku, Zongmin Zhao, Maithili Joshi, Samir Mitragotri

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Transfusion biomaterials for hemostasis.Journal of thrombosis and haemostasis : JTH · 2025
    Review
  4. Article
  5. Article
  6. Review
  7. A polymer-based systemic hemostat for managing uncontrolled bleeding.Bioengineering & translational medicine · 2023
    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

5 authors at 1 institution in 1 country.

Yongsheng GaoJohn A. Paulson School of Engineering and Applied Sciences, Harvard University Allston Massachusetts 02134 USA.ORCID https://orcid.org/0000-0002-2347-1855
Mayumi Ikeda-ImafukuJohn A. Paulson School of Engineering and Applied Sciences, Harvard University Allston Massachusetts 02134 USA.ORCID https://orcid.org/0000-0002-7254-3050
Zongmin ZhaoJohn A. Paulson School of Engineering and Applied Sciences, Harvard University Allston Massachusetts 02134 USA.ORCID https://orcid.org/0000-0001-8979-844X
Maithili JoshiJohn A. Paulson School of Engineering and Applied Sciences, Harvard University Allston Massachusetts 02134 USA.ORCID https://orcid.org/0000-0002-1871-4234
Samir MitragotriJohn A. Paulson School of Engineering and Applied Sciences, Harvard University Allston Massachusetts 02134 USA.ORCID https://orcid.org/0000-0002-2459-8305
Harvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Uncontrolled bleeding is a life-threatening emergency that requires immediate intervention. Currently available on-site bleeding interventions largely rely on the use of tourniquets, pressure dressing, and other topical hemostatic agents, which can only treat bleeding injuries that are known, accessible, and potentially compressible. Synthetic hemostats that are stable at room temperature, easy to carry, field-usable, and able to stop internal bleeding at multiple or unknown sources, are still lacking. We recently developed a hemostatic agent via polymer peptide interfusion (HAPPI), which can selectively bind to activated platelets and injury sites after intravascular administration. Here we report that HAPPI is highly effective in treating multiple lethal traumatic bleeding conditions in normal as well as hemophilia models via either systemic administration or topical application. In a rat liver traumatic model, intravenous injection of HAPPI resulted in a significant decrease in blood loss and a four-fold reduction in mortality rate within 2 h after injury. When applied topically on liver punch biopsy wounds in heparinized rats, HAPPI achieved a 73% of reduction in blood loss and a five-fold increase in survival rate. HAPPI also exhibited hemostatic efficacy in hemophilia A mice by reducing blood loss. Further, HAPPI worked synergistically with rFVIIa to induce immediate hemostasis and 95% reduction in total blood loss compared to the saline-treated group in hemophelia mice models. These results demonstrate that HAPPI is a promising field-usable hemostatic agent for a broad range of different hemorrhagic conditions.

Indexed as

hemophiliahemostasishyaluronic acidsystemic hemostattraumatic bleeding

Identifiers

PMID37206230
PMCPMC10189483
OpenAlexW4365515719

What OpenQuestion holds

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LicenceCC BY
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.