TY - JOUR
T1 - Environmental shedding of toxigenic Clostridioides difficile by asymptomatic carriers
T2 - A prospective observational study
AU - Gilboa, M.
AU - Houri-Levi, E.
AU - Cohen, C.
AU - Tal, I.
AU - Rubin, C.
AU - Feld-Simon, O.
AU - Brom, A.
AU - Eden-Friedman, Y.
AU - Segal, S.
AU - Rahav, G.
AU - Regev-Yochay, G.
AU - Amital, Howard
AU - Beni, Sharon
AU - Ben-Zvi, Ilan
AU - Blausov, Natasha
AU - Brom, Adi
AU - Cohen, Carmit
AU - Feld-Simon, Olga
AU - Fluss, Ronen
AU - Gilboa, Mayan
AU - Eden-Friedman, Yehudit
AU - Halevy, Shiraz
AU - Houri-Levi, Esther
AU - Hupert, Amit
AU - Jbarien, Amnah
AU - Keller, Naty
AU - Leibowitz, Avshalom
AU - Mayan, Haim
AU - Maizels, Leonid
AU - Meltzer, Eyal
AU - Pinas-Zade, Nani
AU - Rahav, Galia
AU - Raibman-Spector, Shir
AU - Regev-Yochay (PI), Gili
AU - Romiantsev, Marina
AU - Shachar, Dalit
AU - Sharif, Kassem
AU - Segal, Gadi
AU - Segal, Shoshi
AU - Segev, Amitai
AU - Smollan, Gill
AU - Stienlauf, Shmuel
AU - Tal, Ilana
AU - Yonath, Hagit
AU - Zilberman-Daniels, Tal
AU - Zimlichman, Eyal
N1 - Publisher Copyright:
© 2019 European Society of Clinical Microbiology and Infectious Diseases
PY - 2020/8
Y1 - 2020/8
N2 - Objectives: The aim was to compare the burden of environmental shedding of toxigenic Clostridioides difficile among asymptomatic carriers, C. difficile-infected (CDI) patients and non-carriers in an inpatient non-epidemic setting. Methods: C. difficile carriage was determined by positive toxin-B PCR from rectal swabs of asymptomatic patients. Active CDI was defined as a positive two-step enzyme immunoassay/polymerase chain reaction (EIA/PCR) test in patients with more than three unformed stools/24 hr. C. difficile environmental contamination was assessed by obtaining specimens from ten sites in the patients' rooms. Toxigenic strains were identified by PCR. We created a contamination scale to define the overall level of room contamination that ranged from clean to heavy contamination. Results: One hundred and seventeen rooms were screened: 70 rooms inhabited by C. difficile carriers, 30 rooms by active CDI patients and 17 rooms by non C. difficile -carriers (control). In the carrier rooms 29 (41%) had more than residual contamination, from which 17 (24%) were heavily contaminated. In the CDI rooms 12 (40%) had more than residual contamination from which three (10%) were heavily contaminated, while in the control rooms, one room (6%) had more than residual contamination and none were heavily contaminated. In a multivariate analysis, the contamination score of rooms inhabited by carriers did not differ from rooms of CDI patients, yet both were significantly more contaminated than those of non-carriers odd ratio 12.23 and 11.16 (95% confidence interval 1.5–99.96 p 0.0195, and 1.19–104.49 p 0.035), respectively. Discussion: Here we show that the rooms of C. difficile carriers are as contaminated as those of patients with active CDI and significantly more than those of non-carriers.
AB - Objectives: The aim was to compare the burden of environmental shedding of toxigenic Clostridioides difficile among asymptomatic carriers, C. difficile-infected (CDI) patients and non-carriers in an inpatient non-epidemic setting. Methods: C. difficile carriage was determined by positive toxin-B PCR from rectal swabs of asymptomatic patients. Active CDI was defined as a positive two-step enzyme immunoassay/polymerase chain reaction (EIA/PCR) test in patients with more than three unformed stools/24 hr. C. difficile environmental contamination was assessed by obtaining specimens from ten sites in the patients' rooms. Toxigenic strains were identified by PCR. We created a contamination scale to define the overall level of room contamination that ranged from clean to heavy contamination. Results: One hundred and seventeen rooms were screened: 70 rooms inhabited by C. difficile carriers, 30 rooms by active CDI patients and 17 rooms by non C. difficile -carriers (control). In the carrier rooms 29 (41%) had more than residual contamination, from which 17 (24%) were heavily contaminated. In the CDI rooms 12 (40%) had more than residual contamination from which three (10%) were heavily contaminated, while in the control rooms, one room (6%) had more than residual contamination and none were heavily contaminated. In a multivariate analysis, the contamination score of rooms inhabited by carriers did not differ from rooms of CDI patients, yet both were significantly more contaminated than those of non-carriers odd ratio 12.23 and 11.16 (95% confidence interval 1.5–99.96 p 0.0195, and 1.19–104.49 p 0.035), respectively. Discussion: Here we show that the rooms of C. difficile carriers are as contaminated as those of patients with active CDI and significantly more than those of non-carriers.
KW - Asymptomatic carriers
KW - Clostridioides difficile
KW - Environmental contamination
KW - Infection control
KW - Isolation
UR - http://www.scopus.com/inward/record.url?scp=85079872297&partnerID=8YFLogxK
U2 - 10.1016/j.cmi.2019.12.011
DO - 10.1016/j.cmi.2019.12.011
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C2 - 31904567
AN - SCOPUS:85079872297
SN - 1198-743X
VL - 26
SP - 1052
EP - 1057
JO - Clinical Microbiology and Infection
JF - Clinical Microbiology and Infection
IS - 8
ER -