Evidence map›Paper›PMID 30168006›Full record

ReviewHernia : the journal of hernias and abdominal wall surgery2018

A critical review of the in vitro and in vivo models for the evaluation of anti-infective meshes.

O Guillaume, B Pérez Kohler, R Fortelny, H Redl, F Moriarty, R G Richards, D Eglin, A Petter Puchner

Abstract readReview
PubMed Publisher
In one paragraph

Review in Hernia : the journal of hernias and abdominal wall surgery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Are late hernia mesh complications linked to Staphylococci biofilms?Hernia : the journal of hernias and abdominal wall surgery · 2022
    Observational
  3. Article
  4. Article
  5. Article
  6. Biofilms and effective porosity of hernia mesh: are they silent assassins?Hernia : the journal of hernias and abdominal wall surgery · 2020
    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

8 authors.

O GuillaumeAO Research Institute Davos, Clavadelerstrasse 8, 7270, Davos, Switzerland. olivier.guillaume@aofoundation.org.ORCID 0000-0003-0735-113X
B Pérez KohlerDepartment of Surgery, Medical and Social Sciences, Faculty of Medicine and Health Sciences, University of Alcalá, Madrid, Spain.
R FortelnyDepartment of General, Visceral and Oncologic Surgery, Wilhelminenspital, Montleartstrasse 37, 1160, Vienna, Austria.
H RedlLudwig Boltzmann Institute for Experimental and Clinical Traumatology, Donaueschingenstraße 13, 1200, Vienna, Austria.
F MoriartyAO Research Institute Davos, Clavadelerstrasse 8, 7270, Davos, Switzerland.
R G RichardsAO Research Institute Davos, Clavadelerstrasse 8, 7270, Davos, Switzerland.
D EglinAO Research Institute Davos, Clavadelerstrasse 8, 7270, Davos, Switzerland.
A Petter PuchnerDepartment of General, Visceral and Oncologic Surgery, Wilhelminenspital, Montleartstrasse 37, 1160, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfectious complications following mesh implantation for abdominal wall repair appear in 0.7 up to 26.6% of hernia repairs and can have a detrimental impact for the patient. To prevent or to treat mesh-related infection, the scientific community is currently developing a veritable arsenal of antibacterial meshes. The numerous and increasing reports published every year describing new technologies indicate a clear clinical need, and an academic interest in solving this problem. Nevertheless, to really appreciate, to challenge, to compare and to optimize the antibacterial properties of next generation meshes, it is important to know which models are available and to understand them. PURPOSE: We proposed for the first time, a complete overview focusing only on the in vitro and in vivo models which have been employed specifically in the field of antibacterial meshes for hernia repair. RESULTS AND

conclusionFrom this investigation, it is clear that there has been vast progress and breadth in new technologies and models to test them. However, it also shows that standardization or adoption of a more restricted number of models would improve comparability and be a benefit to the field of study.

Indexed as

HerniorrhaphyModels, AnimalModels, BiologicalSurgical MeshAnimalsAnti-Infective AgentsBacterial AdhesionBacteriolysisBiofilmsDisk Diffusion Antimicrobial TestsHumansMaterials TestingSurgical Wound InfectionAnti-Infective AgentsAbdominal herniaAnimal modelAntibacterial meshInfectionIn vitro

Identifiers

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.