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A Novel Quantitative Sampling Technique for Detection and Monitoring of Clostridium difficile Contamination in the Clinical Environment
Author(s) -
S. Ali,
M. Muzslay,
Peter Wilson
Publication year - 2015
Publication title -
journal of clinical microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.349
H-Index - 255
eISSN - 1070-633X
pISSN - 0095-1137
DOI - 10.1128/jcm.00376-15
Subject(s) - clostridium difficile , contamination , microbiology and biotechnology , spore , agar , medicine , biology , bacteria , antibiotics , genetics , ecology
The horizontal transmission ofClostridium difficile in the hospital environment is difficult to establish. Current methods to detectC. difficile spores on surfaces are not quantitative, lack sensitivity, and are protracted. We propose a novel rapid method to detect and quantifyC. difficile contamination on surfaces. Sponge swabbing was compared to contact plate sampling to assess thein vitro recovery ofC. difficile ribotype 027 contamination (∼100 , 101 , or 102 CFU of spores) from test surfaces (a bed rail, a stainless steel sheet, or a polypropylene work surface). Sponge swab contents were concentrated by vacuum filtration, and the filter membrane was plated onto selective agar. The efficacy of each technique for the recovery ofC. difficile from sites in the clinical environment that are touched at a high frequency was evaluated. Contact plates recovered 19 to 32% of the total contamination on test surfaces, whereas sponge swabs recovered 76 to 94% of the total contamination, and contact plates failed to detectC. difficile contamination below a detection limit of 10 CFU/25 cm2 (0.4 CFU/cm2 ). In use, contact plates failed to detectC. difficile contamination (0/96 contact plates; 4 case wards), while sponge swabs recoveredC. difficile from 29% (87/301) of the surfaces tested in the clinical environment. Approximately 74% (36/49) of the area in the vicinity of the patient was contaminated (∼1.34 ± 6.88 CFU/cm2 C. difficile spores). Reservoirs ofC. difficile extended to beyond the areas near the patient: a dirty utility room sink (2.26 ± 5.90 CFU/cm2 ), toilet floor (1.87 ± 2.40 CFU/cm2 ), and chair arm (1.33 ± 4.69 CFU/cm2 ).C. difficile was present on floors in ∼90% of case wards. This study highlights that sampling with a contact plate may fail to detectC. difficile contamination and result in false-negative reporting. Our sponge sampling technique permitted the rapid and quantitative measurement ofC. difficile contamination on surfaces with a sensitivity (limit, 0 CFU) greater than that which is otherwise possible. This technique could be implemented for routine surface hygiene monitoring for targeted cleaning interventions and as a tool to investigate routes of patient-patient transmission in the clinical environment.

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