» Articles » PMID: 32427892

A Microbiological Survey of Handwashing Sinks in the Hospital Built Environment Reveals Differences in Patient Room and Healthcare Personnel Sinks

Overview
Journal Sci Rep
Specialty Science
Date 2020 May 20
PMID 32427892
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Handwashing sinks and their associated premise plumbing are an ideal environment for pathogen-harboring biofilms to grow and spread throughout facilities due to the connected system of wastewater plumbing. This study was designed to understand the distribution of pathogens and antibiotic resistant organisms (ARO) within and among handwashing sinks in healthcare settings, using culture-dependent methods to quantify Pseudomonas aeruginosa, opportunistic pathogens capable of growth on a cefotaxime-containing medium (OPP-C), and carbapenem-resistant Enterobacteriaceae (CRE). Isolates from each medium identified as P. aeruginosa or Enterobacteriaceae were tested for susceptibility to aztreonam, ceftazidime, and meropenem; Enterobacteriaceae were also tested against ertapenem and cefotaxime. Isolates exhibiting resistance or intermediate resistance were designated ARO. Pathogens were quantified at different locations within handwashing sinks and compared in quantity and distribution between healthcare personnel (HCP) and patient room (PR) sinks. ARO were compared between samples within a sink (biofilm vs planktonic samples) and between sink types (HCP vs. PR). The drain cover was identified as a reservoir within multiple sinks that was often colonized by pathogens despite daily sink cleaning. P. aeruginosa and OPP-C mean log CFU/cm counts were higher in p-trap and tail pipe biofilm samples from HCP compared to PR sinks (2.77  ± 2.39 vs. 1.23 ± 1.62 and 5.27 ± 1.10 vs. 4.74 ± 1.06) for P. aeruginosa and OPP-C, respectively. P. aeruginosa and OPP-C mean log CFU/ml counts were also higher (p < 0.05) in HCP compared to PR sinks p-trap water (2.21 ± 1.52 vs. 0.89 ± 1.44 and 3.87 ± 0.78 vs. 3.21 ± 1.11) for P. aeruginosa and OPP-C, respectively. However, a greater percentage of ARO were recovered from PR sinks compared to HCP sinks (p < 0.05) for Enterobacteriaceae (76.4 vs. 32.9%) and P. aeruginosa (25.6 vs. 0.3%). This study supports previous work citing that handwashing sinks are reservoirs for pathogens and ARO and identifies differences in pathogen and ARO quantities between HCP and PR sinks, despite the interconnected premise plumbing.

Citing Articles

Sodium dichloroisocyanurate: a promising candidate for the disinfection of resilient drain biofilm.

Martin A, Doyle N, OMahony T Infect Prev Pract. 2025; 7(1):100446.

PMID: 40008271 PMC: 11850130. DOI: 10.1016/j.infpip.2025.100446.


Biofilm Resilience: Molecular Mechanisms Driving Antibiotic Resistance in Clinical Contexts.

Almatroudi A Biology (Basel). 2025; 14(2).

PMID: 40001933 PMC: 11852148. DOI: 10.3390/biology14020165.


A call to action: the SHEA research agenda to combat healthcare-associated infections.

Kwon J, Advani S, Branch-Elliman W, Braun B, Cheng V, Chiotos K Infect Control Hosp Epidemiol. 2024; 1-18.

PMID: 39448369 PMC: 11518679. DOI: 10.1017/ice.2024.125.


Handwashing sinks as reservoirs of carbapenem-resistant in the intensive care unit: a prospective multicenter study.

Wei L, Feng Y, Lin J, Kang X, Zhuang H, Wen H Front Public Health. 2024; 12:1468521.

PMID: 39444981 PMC: 11496070. DOI: 10.3389/fpubh.2024.1468521.


Department-specific patterns of bacterial communities and antibiotic resistance in hospital indoor environments.

Yang Q, Zhang M, Tu Z, Sun Y, Zhao B, Cheng Z Appl Microbiol Biotechnol. 2024; 108(1):487.

PMID: 39412549 PMC: 11485044. DOI: 10.1007/s00253-024-13326-9.


References
1.
Perkins K, Reddy S, Fagan R, Arduino M, Perz J . Investigation of healthcare infection risks from water-related organisms: Summary of CDC consultations, 2014-2017. Infect Control Hosp Epidemiol. 2019; 40(6):621-626. PMC: 7883772. DOI: 10.1017/ice.2019.60. View

2.
Williams M, Armbruster C, Arduino M . Plumbing of hospital premises is a reservoir for opportunistically pathogenic microorganisms: a review. Biofouling. 2013; 29(2):147-62. PMC: 9326810. DOI: 10.1080/08927014.2012.757308. View

3.
Kanamori H, Rutala W, Gergen M, Weber D . Patient Room Decontamination against Carbapenem-Resistant Enterobacteriaceae and Methicillin-Resistant Staphylococcus aureus Using a Fixed Cycle-Time Ultraviolet-C Device and Two Different Radiation Designs. Infect Control Hosp Epidemiol. 2016; 37(8):994-996. DOI: 10.1017/ice.2016.80. View

4.
Tofteland S, Naseer U, Lislevand J, Sundsfjord A, Samuelsen O . A long-term low-frequency hospital outbreak of KPC-producing Klebsiella pneumoniae involving Intergenus plasmid diffusion and a persisting environmental reservoir. PLoS One. 2013; 8(3):e59015. PMC: 3594221. DOI: 10.1371/journal.pone.0059015. View

5.
Roux D, Aubier B, Cochard H, Quentin R, van der Mee-Marquet N . Contaminated sinks in intensive care units: an underestimated source of extended-spectrum beta-lactamase-producing Enterobacteriaceae in the patient environment. J Hosp Infect. 2013; 85(2):106-11. DOI: 10.1016/j.jhin.2013.07.006. View