Evidence map›Paper›PMID 32026188›Full record

ArticleHernia : the journal of hernias and abdominal wall surgery2020

Anti-inflammatory coating of hernia repair meshes: a 5-rabbit study.

M Bredikhin, D Gil, J Rex, W Cobb, V Reukov, A Vertegel

Open access · bronzeAbstract read
In one paragraph

Article in Hernia : the journal of hernias and abdominal wall surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

2 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. 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

6 authors at 2 institutions in 1 country.

M BredikhinDepartment of Bioengineering, Clemson University, 301 Rhodes Hall, Clemson, SC, 29634, USA.
D GilDepartment of Bioengineering, Clemson University, 301 Rhodes Hall, Clemson, SC, 29634, USA.
J RexDepartment of Bioengineering, Clemson University, 301 Rhodes Hall, Clemson, SC, 29634, USA.
W CobbDepartment of Surgery, The Hernia Center, Prisma Health, 2104 Woodruff rd., Greenville, SC, 29607, USA.
V ReukovDepartment of Bioengineering, Clemson University, 301 Rhodes Hall, Clemson, SC, 29634, USA.
A VertegelDepartment of Bioengineering, Clemson University, 301 Rhodes Hall, Clemson, SC, 29634, USA. vertege@clemson.edu.ORCID 0000-0003-3342-5294
Clemson University · USPrisma Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePolymeric mesh implantation has become the golden standard in hernia repair, which nowadays is one of the most frequently performed surgeries in the world. However, many biocompatibility issues remain to be a concern for hernioplasty, with chronic pain being the most notable post-operative complication. Oxidative stress appears to be a major factor in the development of those complications. Lack of material inertness in vivo and oxidative environment formed by inflammatory cells result in both mesh deterioration and slowed healing process. In a pilot in vivo study, we prepared and characterized polypropylene hernia meshes with vitamin E (α-tocopherol)-a potent antioxidant. The results of that study supported the use of vitamin E as potential coating to alleviate post-surgical inflammation, but the pilot nature of the study yielded limited statistical data. The purpose of this study was to verify the observed trend of the pilot study statistically.

methodsIn this work, we conducted a 5-animal experiment where we have implanted vitamin E-coated and uncoated control meshes into the abdominal walls of rabbits. Histology of the mesh-adjacent tissues and electron microscopy of the explanted mesh surface were conducted to characterize host tissue response to the implanted meshes.

resultsAs expected, modified meshes exhibited reduced foreign body reaction, as evidenced by histological scores for fatty infiltrates, macrophages, neovascularization, and collagen organization, as well as by the surface deterioration of the meshes.

conclusionIn conclusion, results indicate that vitamin E coating reduces inflammatory response following hernioplasty and protects mesh material from oxidative deterioration.

Indexed as

Abdominal WallAnimalsAnti-Inflammatory AgentsDisease Models, AnimalHerniorrhaphyMalePilot ProjectsPolypropylenesRabbitsSurgical MeshAnti-Inflammatory AgentsPolypropylenesHerniaPolypropylene meshRabbit modelVitamin E

Identifiers

PMID32026188
PMCPMC7223801
OpenAlexW3005309738

What OpenQuestion holds

Textmetadata
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.