Evidence map›Paper›PMID 28959736›Full record

ArticlemSphere

Comparative Analysis of Bacterial Community Composition and Structure in Clinically Symptomatic and Asymptomatic Central Venous Catheters.

Franziska A Stressmann, Elodie Couve-Deacon, Delphine Chainier, Ashwini Chauhan, Aimee Wessel, Sylvaine Durand-Fontanier, Marie-Christine Escande, Irène Kriegel, Bruno Francois, Marie-Cécile Ploy and 2 more

Open access · goldAbstract read
In one paragraph

Article in mSphere. 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
1.6field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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

12 authors at 4 institutions in 1 country.

Franziska A StressmannUnité de Génétique des Biofilms, Département de Microbiologie, Institut Pasteur, Paris, France.
Elodie Couve-DeaconUniversité Limoges, INSERM, CHU Limoges, UMR 1092, Limoges, France.
Delphine ChainierUniversité Limoges, INSERM, CHU Limoges, UMR 1092, Limoges, France.
Ashwini ChauhanUnité de Génétique des Biofilms, Département de Microbiologie, Institut Pasteur, Paris, France.
Aimee WesselUnité de Génétique des Biofilms, Département de Microbiologie, Institut Pasteur, Paris, France.
Sylvaine Durand-FontanierCHU de Limoges, Service de chirurgie digestive générale et endocrinienne, Limoges, France.
Marie-Christine EscandeInstitut Curie, Hôpital, Laboratoire de Microbiologie Médicale, Paris, France.
Irène KriegelInstitut Curie, Hôpital, Service Anesthésie-Réanimation-Douleur, Paris, France.
Bruno FrancoisUniversité Limoges, INSERM, CHU Limoges, UMR 1092, Limoges, France.
Marie-Cécile PloyUniversité Limoges, INSERM, CHU Limoges, UMR 1092, Limoges, France.
Christophe BeloinUnité de Génétique des Biofilms, Département de Microbiologie, Institut Pasteur, Paris, France.
Jean-Marc GhigoUnité de Génétique des Biofilms, Département de Microbiologie, Institut Pasteur, Paris, France.
Institut Pasteur · FRUniversité de Limoges · FRInstitut Curie · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Totally implanted venous access ports (TIVAPs) are commonly used catheters for the management of acute or chronic pathologies. Although these devices improve health care, repeated use of this type of device for venous access over long periods of time is also associated with risk of colonization and infection by pathogenic bacteria, often originating from skin. However, although the skin microbiota is composed of both pathogenic and nonpathogenic bacteria, the extent and the consequences of TIVAP colonization by nonpathogenic bacteria have rarely been studied. Here, we used culture-dependent and 16S rRNA gene-based culture-independent approaches to identify differences in bacterial colonization of TIVAPs obtained from two French hospitals. To explore the relationships between nonpathogenic organisms colonizing TIVAPs and the potential risk of infection, we analyzed the bacterial community parameters between TIVAPs suspected (symptomatic) or not (asymptomatic) of infection. Although we did not find a particular species assemblage or community marker to distinguish infection risk on an individual sample level, we identified differences in bacterial community composition, diversity, and structure between clinically symptomatic and asymptomatic TIVAPs that could be explored further. This study therefore provides a new view of bacterial communities and colonization patterns in intravascular TIVAPs and suggests that microbial ecology approaches could improve our understanding of device-associated infections and could be a prognostic tool to monitor the evolution of bacterial communities in implants and their potential susceptibility to infections.

Indexed as

bacterial communitybiofilmcatheter colonizationecology

Identifiers

PMID28959736
PMCPMC5615130
OpenAlexW2756941193

What OpenQuestion holds

Textmetadata
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.