Predicting probability of perirectal colonization with carbapenem-resistant Enterobacteriaceae (CRE) and other carbapenem-resistant organisms (CROs) at hospital unit admission.


Journal

Infection control and hospital epidemiology
ISSN: 1559-6834
Titre abrégé: Infect Control Hosp Epidemiol
Pays: United States
ID NLM: 8804099

Informations de publication

Date de publication:
05 2019
Historique:
pubmed: 28 3 2019
medline: 24 3 2020
entrez: 28 3 2019
Statut: ppublish

Résumé

Targeted screening for carbapenem-resistant organisms (CROs), including carbapenem-resistant Enterobacteriaceae (CRE) and carbapenemase-producing organisms (CPOs), remains limited; recent data suggest that existing policies miss many carriers. Our objective was to measure the prevalence of CRO and CPO perirectal colonization at hospital unit admission and to use machine learning methods to predict probability of CRO and/or CPO carriage. We performed an observational cohort study of all patients admitted to the medical intensive care unit (MICU) or solid organ transplant (SOT) unit at The Johns Hopkins Hospital between July 1, 2016 and July 1, 2017. Admission perirectal swabs were screened for CROs and CPOs. More than 125 variables capturing preadmission clinical and demographic characteristics were collected from the electronic medical record (EMR) system. We developed models to predict colonization probabilities using decision tree learning. Evaluating 2,878 admission swabs from 2,165 patients, we found that 7.5% and 1.3% of swabs were CRO and CPO positive, respectively. Organism and carbapenemase diversity among CPO isolates was high. Despite including many characteristics commonly associated with CRO/CPO carriage or infection, overall, decision tree models poorly predicted CRO and CPO colonization (C statistics, 0.57 and 0.58, respectively). In subgroup analyses, however, models did accurately identify patients with recent CRO-positive cultures who use proton-pump inhibitors as having a high likelihood of CRO colonization. In this inpatient population, CRO carriage was infrequent but was higher than previously published estimates. Despite including many variables associated with CRO/CPO carriage, models poorly predicted colonization status, likely due to significant host and organism heterogeneity.

Sections du résumé

BACKGROUND
Targeted screening for carbapenem-resistant organisms (CROs), including carbapenem-resistant Enterobacteriaceae (CRE) and carbapenemase-producing organisms (CPOs), remains limited; recent data suggest that existing policies miss many carriers.
OBJECTIVE
Our objective was to measure the prevalence of CRO and CPO perirectal colonization at hospital unit admission and to use machine learning methods to predict probability of CRO and/or CPO carriage.
METHODS
We performed an observational cohort study of all patients admitted to the medical intensive care unit (MICU) or solid organ transplant (SOT) unit at The Johns Hopkins Hospital between July 1, 2016 and July 1, 2017. Admission perirectal swabs were screened for CROs and CPOs. More than 125 variables capturing preadmission clinical and demographic characteristics were collected from the electronic medical record (EMR) system. We developed models to predict colonization probabilities using decision tree learning.
RESULTS
Evaluating 2,878 admission swabs from 2,165 patients, we found that 7.5% and 1.3% of swabs were CRO and CPO positive, respectively. Organism and carbapenemase diversity among CPO isolates was high. Despite including many characteristics commonly associated with CRO/CPO carriage or infection, overall, decision tree models poorly predicted CRO and CPO colonization (C statistics, 0.57 and 0.58, respectively). In subgroup analyses, however, models did accurately identify patients with recent CRO-positive cultures who use proton-pump inhibitors as having a high likelihood of CRO colonization.
CONCLUSIONS
In this inpatient population, CRO carriage was infrequent but was higher than previously published estimates. Despite including many variables associated with CRO/CPO carriage, models poorly predicted colonization status, likely due to significant host and organism heterogeneity.

Identifiants

pubmed: 30915928
pii: S0899823X19000424
doi: 10.1017/ice.2019.42
pmc: PMC6613376
mid: NIHMS1034815
doi:

Substances chimiques

Carbapenems 0

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

541-550

Subventions

Organisme : NCEZID CDC HHS
ID : U01 CK000536
Pays : United States
Organisme : ACL HHS
ID : U54CK000447
Pays : United States
Organisme : ACL HHS
ID : U01CK000536
Pays : United States
Organisme : AHRQ HHS
ID : R36 HS025089
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI141580
Pays : United States
Organisme : NCEZID CDC HHS
ID : U54 CK000447
Pays : United States

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Auteurs

Katherine E Goodman (KE)

Department of Epidemiology,Johns Hopkins University Bloomberg School of Public Health,Baltimore, Maryland.

Patricia J Simner (PJ)

Division of Medical Microbiology, Department of Pathology,Johns Hopkins University School of Medicine,Baltimore, Maryland.

Eili Y Klein (EY)

Department of Epidemiology,Johns Hopkins University Bloomberg School of Public Health,Baltimore, Maryland.

Abida Q Kazmi (AQ)

Division of Medical Microbiology, Department of Pathology,Johns Hopkins University School of Medicine,Baltimore, Maryland.

Avinash Gadala (A)

Department of Hospital Epidemiology and Infection Control,The Johns Hopkins Health System,Baltimore, Maryland.

Matthew F Toerper (MF)

Department of Emergency Medicine,Johns Hopkins University School of Medicine,Baltimore, Maryland.

Scott Levin (S)

Department of Emergency Medicine,Johns Hopkins University School of Medicine,Baltimore, Maryland.

Pranita D Tamma (PD)

Department of Hospital Epidemiology and Infection Control,The Johns Hopkins Health System,Baltimore, Maryland.

Clare Rock (C)

Department of Hospital Epidemiology and Infection Control,The Johns Hopkins Health System,Baltimore, Maryland.

Sara E Cosgrove (SE)

Department of Hospital Epidemiology and Infection Control,The Johns Hopkins Health System,Baltimore, Maryland.

Lisa L Maragakis (LL)

Department of Epidemiology,Johns Hopkins University Bloomberg School of Public Health,Baltimore, Maryland.

Aaron M Milstone (AM)

Department of Epidemiology,Johns Hopkins University Bloomberg School of Public Health,Baltimore, Maryland.

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Classifications MeSH