Evidence map›Paper›PMID 41022905›Full record

ArticleNPJ Regenerative medicine2025

Exosome injection as a prevention strategy for early postoperative mesh complications in a porcine model of sacrocolpopexy.

Cassandra K Kisby, Sam Faraguna, Abigail Hitt, Ilya Y Shadrin, Hunter Newman, Anna Gilpin, Cindy L Amundsen, Shyni Varghese

Abstract read
In one paragraph

Article in NPJ Regenerative medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Cassandra K KisbyDuke Health, Department of Obstetrics and Gynecology, Division of Urogynecology, Durham, NC, USA. Cassandra.kisby@duke.edu.ORCID http://orcid.org/0000-0002-0791-9103
Sam FaragunaDuke University, Durham, NC, USA.
Abigail HittDuke Health, Department of Pathology, Durham, NC, USA.
Ilya Y ShadrinDuke Health, Department of Medicine, Division of Cardiology, Durham, NC, USA.
Hunter NewmanDuke Health, Department of Orthopedics, Durham, NC, USA.
Anna GilpinDuke Health, Department of Orthopedics, Durham, NC, USA.
Cindy L AmundsenDuke Health, Department of Obstetrics and Gynecology, Division of Urogynecology, Durham, NC, USA.
Shyni VargheseDuke Health, Department of Orthopedics, Durham, NC, USA.ORCID http://orcid.org/0000-0002-0004-7947

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exosomes, an acellular regenerative biologic, have demonstrated success in resolving vaginal mesh exposures after pelvic reconstructive surgery; little data exists for their use for prevention of mesh-based complications. This study evaluated the early efficacy of purified exosome product (PEP) for preventing mesh exposures. Ten Yorkshire-crossed pigs underwent mesh sacrocolpopexy with two high-risk-for-exposure configurations: mesh fold ventrally, vaginotomy dorsally. PEP in hyaluronic acid (HA) or HA-only (control) was injected at baseline. Twelve weeks later, animals were euthanized and evaluated for mesh exposure and histologic changes. None of the PEP-treated tissues demonstrated mesh exposure (0/6); all control group animals experienced a mesh exposure (4/4 mesh fold configuration, 2/4 vaginotomy configuration). Control tissues exhibited higher fibrosis (vaginotomy fibrosis score: median(IQR); 3(3,3) control, 2(1,2) PEP; p = 0.03) and greater epithelial apoptosis (mesh fold TUNEL+area fraction: median 18.9 control vs 0.43 PEP; p = 0.02). Our study demonstrated that PEP treatment mitigated the risk of early mesh exposure.

Identifiers

PMID41022905
PMCPMC12480700

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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.