TY - JOUR
T1 - Evaluation of the sporicidal activity of different chemical disinfectants used in hospitals against Clostridium difficile
AU - Speight, S.
AU - Moy, A.
AU - Macken, S.
AU - Chitnis, R.
AU - Hoffman, Peter
AU - Davies, A.
AU - Bennett, Allan
AU - Walker, J. T.
PY - 2011/9
Y1 - 2011/9
N2 - Decontamination of surfaces and medical equipment is integral to the control of Clostridium difficile transmission, and many products claim to inactivate this bacterium effectively. Thirty-two disinfectants were tested against spores of C. difficile in a suspension test based on European Standard BS EN 13704:2002, with contact times of 1 and 60min in simulations of clean (0.3% albumin) and dirty (3% albumin) conditions. The addition of a 1-min contact time was chosen as a more realistic simulation of probable real-life exposures in the situation being modelled than the 60min specified by the Standard. The manufacturer's lowest recommended concentrations for use were tested. Sixteen products achieved >10 3 reduction in viability after 60 min (the pass criterion for the Standard) under both clean and dirty conditions. However, only eight products achieved >10 3 reduction in viability within 1min under dirty conditions. Three products failed to reduce the viability of the C. difficile spores by a factor of 10 3 in any of the test conditions. This study highlights that the application of disinfectants claiming to be sporicidal is not, in itself, a panacea in the environmental control of C. difficile, but that carefully chosen environmental disinfectants could form part of a wider raft of control measures that include a range of selected cleaning strategies.
AB - Decontamination of surfaces and medical equipment is integral to the control of Clostridium difficile transmission, and many products claim to inactivate this bacterium effectively. Thirty-two disinfectants were tested against spores of C. difficile in a suspension test based on European Standard BS EN 13704:2002, with contact times of 1 and 60min in simulations of clean (0.3% albumin) and dirty (3% albumin) conditions. The addition of a 1-min contact time was chosen as a more realistic simulation of probable real-life exposures in the situation being modelled than the 60min specified by the Standard. The manufacturer's lowest recommended concentrations for use were tested. Sixteen products achieved >10 3 reduction in viability after 60 min (the pass criterion for the Standard) under both clean and dirty conditions. However, only eight products achieved >10 3 reduction in viability within 1min under dirty conditions. Three products failed to reduce the viability of the C. difficile spores by a factor of 10 3 in any of the test conditions. This study highlights that the application of disinfectants claiming to be sporicidal is not, in itself, a panacea in the environmental control of C. difficile, but that carefully chosen environmental disinfectants could form part of a wider raft of control measures that include a range of selected cleaning strategies.
KW - Clostridium difficile
KW - Disinfection testing
KW - Hospital acquired infections
KW - Nosocomial infections
KW - Sporicides
UR - http://www.scopus.com/inward/record.url?scp=80051469719&partnerID=8YFLogxK
U2 - 10.1016/j.jhin.2011.05.016
DO - 10.1016/j.jhin.2011.05.016
M3 - Article
C2 - 21802172
AN - SCOPUS:80051469719
SN - 0195-6701
VL - 79
SP - 18
EP - 22
JO - Journal of Hospital Infection
JF - Journal of Hospital Infection
IS - 1
ER -