Environmental Methicillin-resistant Staphylococcus aureus Contamination, Persistent Colonization, and Subsequent Skin and Soft Tissue Infection.


Journal

JAMA pediatrics
ISSN: 2168-6211
Titre abrégé: JAMA Pediatr
Pays: United States
ID NLM: 101589544

Informations de publication

Date de publication:
01 06 2020
Historique:
pubmed: 1 4 2020
medline: 23 3 2021
entrez: 1 4 2020
Statut: ppublish

Résumé

The longitudinal association among persistent Staphylococcus aureus colonization, household environmental contamination, and recurrent skin and soft tissue infection (SSTI) is largely unexplored to date. To identify factors associated with persistent S aureus colonization and recurrent SSTI in households with children with community-associated methicillin-resistant S aureus (MRSA) SSTI. This 12-month prospective cohort study included 150 children with community-associated MRSA SSTI, 542 household contacts, and 154 pets enrolled from January 3, 2012, through October 20, 2015. A total of 5 quarterly home visits were made to 150 households in the St Louis, Missouri, region. Statistical analysis was performed from September 18, 2018, to January 7, 2020. Covariates used in S aureus strain persistence and interval SSTI models included S aureus colonization and contamination measures, personal hygiene and sharing habits, health history, activities external to the home, and household characteristics (eg, cleanliness, crowding, home ownership, and pets). Serial samples to detect S aureus were collected from household members at 3 anatomic sites, from pets at 2 anatomic sites, and from environmental surfaces at 21 sites. Molecular epidemiologic findings of S aureus isolates were assessed via repetitive-sequence polymerase chain reaction. Individual persistent colonization was defined as colonization by an identical strain for 2 consecutive samplings. Longitudinal, multivariable generalized mixed-effects logistic regression models were used to assess factors associated with persistent S aureus personal colonization, environmental contamination, and interval SSTI. Among 692 household members in 150 households, 326 (47%) were male and 366 (53%) were female, with a median age of 14.82 years (range, 0.05-82.25 years). Of 540 participants completing all 5 samplings, 213 (39%) were persistently colonized with S aureus, most often in the nares and with the strain infecting the index patient at enrollment. Nine pets (8%) were persistently colonized with S aureus. Participants reporting interval intranasal mupirocin application were less likely to experience persistent colonization (odds ratio [OR], 0.44; 95% credible interval [CrI], 0.30-0.66), whereas increasing strain-specific environmental contamination pressure was associated with increased individual persistent colonization (OR, 1.17; 95% CrI, 1.06-1.30). Strains with higher colonization pressure (OR, 1.47; 95% CrI, 1.25-1.71) and MRSA strains (OR, 1.57; 95% CrI, 1.16-2.19) were more likely to persist. Seventy-six index patients (53%) and 101 household contacts (19%) reported interval SSTIs. Individuals persistently colonized with MRSA (OR, 1.56; 95% CrI, 1.17-2.11), those with a history of SSTI (OR, 2.55; 95% CrI, 1.88-3.47), and index patients (OR, 1.54; 95% CrI, 1.07-2.23) were more likely to report an interval SSTI. The study findings suggest that recurrent SSTI is associated with persistent MRSA colonization of household members and contamination of environmental surfaces. Future studies may elucidate the effectiveness of specific combinations of personal decolonization and environmental decontamination efforts in eradicating persistent strains and mitigating recurrent SSTIs.

Identifiants

pubmed: 32227144
pii: 2763351
doi: 10.1001/jamapediatrics.2020.0132
pmc: PMC7105954
doi:

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

552-562

Subventions

Organisme : NIAID NIH HHS
ID : K23 AI091690
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI097434
Pays : United States
Organisme : AHRQ HHS
ID : R01 HS024269
Pays : United States
Organisme : AHRQ HHS
ID : R01 HS021736
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002345
Pays : United States

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Auteurs

Patrick G Hogan (PG)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.

Ryan L Mork (RL)

Graduate Program in the Biophysical Sciences, University of Chicago, Chicago, Illinois.
Committee of Microbiology, University of Chicago, Chicago, Illinois.
Institute for Genomics and Systems Biology, University of Chicago, Chicago, Illinois.

Ryley M Thompson (RM)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.

Carol E Muenks (CE)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.

Mary G Boyle (MG)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.

Melanie L Sullivan (ML)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.

John J Morelli (JJ)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.

Caroline V Williams (CV)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.

Nataly Sanchez (N)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.

David A Hunstad (DA)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.
Department of Molecular Microbiology, Washington University School of Medicine in St Louis, St Louis, Missouri.

Juliane Bubeck Wardenburg (JB)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.

Sarah J Gehlert (SJ)

Department of Surgery, Washington University School of Medicine in St Louis, St Louis, Missouri.

Carey-Ann D Burnham (CD)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.
Department of Molecular Microbiology, Washington University School of Medicine in St Louis, St Louis, Missouri.
Department of Pathology and Immunology, Washington University School of Medicine in St Louis, St Louis, Missouri.
Department of Medicine, Washington University School of Medicine in St Louis, St Louis, Missouri.

Andrey Rzhetsky (A)

Department of Human Genetics, University of Chicago, Chicago, Illinois.

Stephanie A Fritz (SA)

Department of Pediatrics, Washington University School of Medicine in St Louis, St Louis, Missouri.

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Classifications MeSH