Cohorting KPC+


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:
10 2020
Historique:
pubmed: 7 7 2020
medline: 1 9 2021
entrez: 7 7 2020
Statut: ppublish

Résumé

Cohorting patients who are colonized or infected with multidrug-resistant organisms (MDROs) protects uncolonized patients from acquiring MDROs in healthcare settings. The potential for cross transmission within the cohort and the possibility of colonized patients acquiring secondary isolates with additional antibiotic resistance traits is often neglected. We searched for evidence of cross transmission of KPC+ Klebsiella pneumoniae (KPC-Kp) colonization among cohorted patients in a long-term acute-care hospital (LTACH), and we evaluated the impact of secondary acquisitions on resistance potential. Genomic epidemiological investigation. A high-prevalence LTACH during a bundled intervention that included cohorting KPC-Kp-positive patients. Whole-genome sequencing (WGS) and location data were analyzed to identify potential cases of cross transmission between cohorted patients. Secondary KPC-Kp isolates from 19 of 28 admission-positive patients were more closely related to another patient's isolate than to their own admission isolate. Of these 19 cases, 14 showed strong genomic evidence for cross transmission (<10 single nucleotide variants or SNVs), and most of these patients occupied shared cohort floors (12 patients) or rooms (4 patients) at the same time. Of the 14 patients with strong genomic evidence of acquisition, 12 acquired antibiotic resistance genes not found in their primary isolates. Acquisition of secondary KPC-Kp isolates carrying distinct antibiotic resistance genes was detected in nearly half of cohorted patients. These results highlight the importance of healthcare provider adherence to infection prevention protocols within cohort locations, and they indicate the need for future studies to assess whether multiple-strain acquisition increases risk of adverse patient outcomes.

Identifiants

pubmed: 32624030
pii: S0899823X20002615
doi: 10.1017/ice.2020.261
doi:

Substances chimiques

Anti-Bacterial Agents 0
Bacterial Proteins 0
beta-Lactamases EC 3.5.2.6

Types de publication

Journal Article 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

1162-1168

Subventions

Organisme : NCEZID CDC HHS
ID : U54 CK000481
Pays : United States
Organisme : NCEZID CDC HHS
ID : U54 CK000607
Pays : United States

Auteurs

Shawn E Hawken (SE)

Department of Microbiology & Immunology, University of Michigan Medical School, Ann Arbor, Michigan.

Mary K Hayden (MK)

Division of Infectious Diseases, Rush University Medical Center, Chicago, Illinois.

Karen Lolans (K)

Division of Infectious Diseases, Rush University Medical Center, Chicago, Illinois.

Rachel D Yelin (RD)

Division of Infectious Diseases, Rush University Medical Center, Chicago, Illinois.

Robert A Weinstein (RA)

Division of Infectious Diseases, Rush University Medical Center, Chicago, Illinois.

Michael Y Lin (MY)

Division of Infectious Diseases, Rush University Medical Center, Chicago, Illinois.

Evan S Snitkin (ES)

Department of Microbiology & Immunology, University of Michigan Medical School, Ann Arbor, Michigan.
Division of Infectious Diseases, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan.

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Classifications MeSH