Evidence map›Paper›PMID 27125574›Full record

ArticleEpidemiology and infection2016

Patient-level analysis of incident vancomycin-resistant enterococci colonization and antibiotic days of therapy.

J A McKINNELL, D F Kunz, S A Moser, S Vangala, C-H Tseng, M Shapiro, L G Miller

Abstract read
In one paragraph

Article in Epidemiology and infection, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Prevalence and Antibiotic Susceptibility Trends of SelectedAntibiotics (Basel, Switzerland) · 2022
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Impact of antimicrobial therapy on the gut microbiome.The Journal of antimicrobial chemotherapy · 2019
    Review
  10. Article
  11. Review
  12. Article
  13. 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

7 authors.

J A McKINNELLInfectious Disease Clinical Outcomes Research Unit (ID-CORE),Division of Infectious Disease,Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center,Torrance,CA,USA.
D F KunzDivision of Infectious Disease,University of Alabama at Birmingham,Birmingham,AL,USA.
S A MoserDepartment of Pathology,University of Alabama at Birmingham,Birmingham,AL,USA.
S VangalaDepartment of Medicine Statistics Core,University of California,Los Angeles,Westwood,CA,USA.
C-H TsengDepartment of Medicine Statistics Core,University of California,Los Angeles,Westwood,CA,USA.
M ShapiroDivision of General Internal Medicine and Health Services Research,University of California,Los Angeles;Los Angeles,CA,USA.
L G MillerInfectious Disease Clinical Outcomes Research Unit (ID-CORE),Division of Infectious Disease,Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center,Torrance,CA,USA.

Funding

UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
The Center for Health Improvement of Minority ElderlyP30AG021684 · NIA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI RONALD Dale HAYS · 2002 to 2026
$19.7M
UCLA Clinical and Translational Science InstituteKL2TR000122 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$4.5M
NCATS NIH HHS KL2 TR000122NCATS NIH HHS UL1 TR000124
6 · The paper itself

Abstract

Vancomycin-resistant enterococci (VRE) infections are a public health threat associated with increased patient mortality and healthcare costs. Antibiotic usage, particularly cephalosporins, has been associated with VRE colonization and VRE bloodstream infections (VRE BSI). We examined the relationship between antimicrobial usage and incident VRE colonization at the individual patient level. Prospective, weekly surveillance was undertaken for incident VRE colonization defined by negative admission but positive surveillance swab in a medical intensive care unit over a 17-month period. Antimicrobial exposure was quantified as days of therapy (DOT)/1000 patient-days. Multiple logistic regression was used to analyse incident VRE colonization and antibiotic DOT, controlling for demographic and clinical covariates. Ninety-six percent (1398/1454) of admissions were swabbed within 24 h of intensive care unit (ICU) arrival and of the 380 patients in the ICU long enough for weekly surveillance, 83 (22%) developed incident VRE colonization. Incident colonization was associated in bivariate analysis with male gender, more previous hospital admissions, longer previous hospital stay, and use of cefepime/ceftazidime, fluconazole, azithromycin, and metronidazole (P < 0·05). After controlling for demographic and clinical covariates, metronidazole was the only antibiotic independently associated with incident VRE colonization (odds ratio 2·0, 95% confidence interval 1·2-3·3, P < 0·009). Our findings suggest that risk of incident VRE colonization differs between individual antibiotic agents and support the possibility that antimicrobial stewardship may impact VRE colonization and infection.

Indexed as

Drug UtilizationAdultAgedAnti-Bacterial AgentsCarrier StateEpidemiological MonitoringFemaleGram-Positive Bacterial InfectionsHumansIncidenceIntensive Care UnitsMaleMiddle AgedProspective StudiesRisk FactorsVancomycin-Resistant EnterococciAnti-Bacterial AgentsAntibioticsEnterococcusGram-positive bacteria

Identifiers

PMID27125574
PMCPMC5943038

What OpenQuestion holds

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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.