Literature DB >> 34183065

Controlling bacteriological contamination of environmental surfaces at the biological isolation and containment unit of a veterinary teaching hospital.

C Verdial1, C Carneiro1,2, I Machado2,3, L Tavares1,2, V Almeida1,2, M Oliveira1,2, S Gil4,5,6.   

Abstract

BACKGROUND: The Biological Isolation and Containment Unit (BICU) is a subunit of the Teaching Hospital of the Faculty of Veterinary Medicine of the University of Lisbon, Portugal, for the admission of animals with confirmed infectious diseases or under clinical suspicion and waiting for a diagnosis. As a high-risk environment for the transmission of infectious agents, it is extremely important to implement programs for the surveillance of nosocomial microorganisms in these facilities. The purpose of this study was to evaluate the level of bacterial contamination of the BICU environmental surfaces and to implement corrective actions on disinfection protocols. Swab samples were collected from selected environmental surfaces in 3 different areas of the BICU (isolation, work, and preparatory rooms) to evaluate the total aerobic bacterial load and investigate the presence of 4 nosocomial microorganisms: vancomycin-resistant Enterococcus spp., methicillin-resistant Staphylococcus aureus, 3rd-generation cephalosporin-resistant Escherichia coli, and carbapenem-resistant Pseudomonas aeruginosa. Bacterial quantification was performed by using non-selective media, while specific selective media were used for the isolation of the target microorganisms. Isolates were identified based on their macro and microscopic characteristics and their biochemical profile. Subsequently, new disinfection protocols were implemented, and their effectiveness evaluated.
RESULTS: The surfaces with the highest bacterial load in the isolation, preparatory, and worker's rooms were the cages, hand-held sponge, and telephone, respectively. Regarding the 4 pathogens investigated, Enterococcus spp. were the most frequently isolated (11.3%), followed by E. coli (1.5%) and P. aeruginosa (1.5%). One of the P. aeruginosa isolates obtained was resistant to imipenem. In the end, new disinfection protocols were implemented, which proved to be effective in reducing bacterial counts by 99.99% in cages and the sponge, and by 90 to 99% on the telephone.
CONCLUSIONS: This study allows to conclude that the cages and the human contact surfaces were the most contaminated in the isolation rooms. Nevertheless, the new disinfection strategies seemed to be effective in reducing environmental contamination, including by some potentially nosocomial agents, although more samples must be analyzed for definitive conclusions. These results may contribute to highlight the importance of infection prevention and control measures, as fundamental tools to reduce the spread of infectious agents in the hospital environment.

Entities:  

Keywords:  Bacteriological control; Hospital environment; Nosocomial infection; Surveillance

Year:  2021        PMID: 34183065     DOI: 10.1186/s13620-021-00197-z

Source DB:  PubMed          Journal:  Ir Vet J        ISSN: 0368-0762            Impact factor:   2.146


  41 in total

1.  Cluster of methicillin-resistant Staphylococcus aureus colonization in a small animal intensive care unit.

Authors:  J Scott Weese; Meredith Faires; Joyce Rousseau; Alexa M E Bersenas; Karol A Mathews
Journal:  J Am Vet Med Assoc       Date:  2007-11-01       Impact factor: 1.936

2.  Characteristics of biosecurity and infection control programs at veterinary teaching hospitals.

Authors:  Katharine M Benedict; Paul S Morley; David C Van Metre
Journal:  J Am Vet Med Assoc       Date:  2008-09-01       Impact factor: 1.936

Review 3.  The role played by contaminated surfaces in the transmission of nosocomial pathogens.

Authors:  Jonathan A Otter; Saber Yezli; Gary L French
Journal:  Infect Control Hosp Epidemiol       Date:  2011-07       Impact factor: 3.254

4.  2018 AAHA Infection Control, Prevention, and Biosecurity Guidelines.

Authors:  Jason W Stull; Erin Bjorvik; Joshua Bub; Glenda Dvorak; Christine Petersen; Heather L Troyer
Journal:  J Am Anim Hosp Assoc       Date:  2018 Nov/Dec       Impact factor: 1.023

5.  Transfer of multidrug-resistant bacteria to healthcare workers' gloves and gowns after patient contact increases with environmental contamination.

Authors:  Daniel J Morgan; Elizabeth Rogawski; Kerri A Thom; J Kristie Johnson; Eli N Perencevich; Michelle Shardell; Surbhi Leekha; Anthony D Harris
Journal:  Crit Care Med       Date:  2012-04       Impact factor: 7.598

6.  Relation of the inanimate hospital environment to endemic nosocomial infection.

Authors:  D G Maki; C J Alvarado; C A Hassemer; M A Zilz
Journal:  N Engl J Med       Date:  1982-12-16       Impact factor: 91.245

Review 7.  Escherichia coli and selected veterinary and zoonotic pathogens isolated from environmental sites in companion animal veterinary hospitals in southern Ontario.

Authors:  Colleen P Murphy; Richard J Reid-Smith; Patrick Boerlin; J Scott Weese; John F Prescott; Nicol Janecko; Lori Hassard; Scott A McEwen
Journal:  Can Vet J       Date:  2010-09       Impact factor: 1.008

8.  Evaluation of catheter-associated urinary tract infections and multi-drug-resistant Escherichia coli isolates from the urine of dogs with indwelling urinary catheters.

Authors:  Jennifer Ogeer-Gyles; Karol Mathews; J Scott Weese; John F Prescott; Patrick Boerlin
Journal:  J Am Vet Med Assoc       Date:  2006-11-15       Impact factor: 1.936

9.  Suspected transmission of methicillin-resistant Staphylococcus aureus between domestic pets and humans in veterinary clinics and in the household.

Authors:  J S Weese; H Dick; B M Willey; A McGeer; B N Kreiswirth; B Innis; D E Low
Journal:  Vet Microbiol       Date:  2006-02-07       Impact factor: 3.293

Review 10.  Hospital-associated infections in small animal practice.

Authors:  Jason W Stull; J Scott Weese
Journal:  Vet Clin North Am Small Anim Pract       Date:  2015-01-02       Impact factor: 2.093

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