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A metallo-beta-lactamase producing Enterobacteriaceae outbreak from a contaminated tea dispenser at a children’s hospital in Japan

Published online by Cambridge University Press:  27 December 2018

Kenta ItoOpen the ORCID record for Kenta Ito[Opens in a new window],
Hitoshi Honda,
Makiko Yoshida,
Kotaro Aoki,
Yoshikazu Ishii,
Shigeko Miyokawa and
Yuho Horikoshi
Kenta Ito*
Affiliation:
Division of Infectious Diseases, Department of Pediatrics, Tokyo Metropolitan Children’s Medical Center, Fuchu, Tokyo, Japan
Hitoshi Honda
Affiliation:
Division of Infectious Diseases, Department of Medicine, Tokyo Metropolitan Tama Medical Center, Fuchu, Tokyo, Japan
Makiko Yoshida
Affiliation:
Department of Infection Control and Laboratory Diagnostics, Tohoku University Graduate School of Medicine, Sendai, Japan
Kotaro Aoki
Affiliation:
Department of Microbiology and Infectious Diseases, Toho University School of Medicine, Tokyo, Japan
Yoshikazu Ishii
Affiliation:
Department of Microbiology and Infectious Diseases, Toho University School of Medicine, Tokyo, Japan
Shigeko Miyokawa
Affiliation:
Department of Nursing, Tokyo Metropolitan Children’s Medical Center, Fuchu, Tokyo, Japan. (Present affiliation: Department of General Pediatrics, Aichi Children’s Health and Medical Center, Ohbu, Aichi, Japan [K.I.].)
Yuho Horikoshi*
Affiliation:
Division of Infectious Diseases, Department of Pediatrics, Tokyo Metropolitan Children’s Medical Center, Fuchu, Tokyo, Japan
*
Author for correspondence: Kenta Ito MD, 2-8-29 Musashi-dai Fuchu-shi, Tokyo, Japan. E-mail: peaceplease1981@gmail.com Or Yuho Horikoshi MD, 2-8-29 Musashi-dai Fuchu-shi, Tokyo, Japan. E-mail: yuho_horikoshi@tmhp.jp
Author for correspondence: Kenta Ito MD, 2-8-29 Musashi-dai Fuchu-shi, Tokyo, Japan. E-mail: peaceplease1981@gmail.com Or Yuho Horikoshi MD, 2-8-29 Musashi-dai Fuchu-shi, Tokyo, Japan. E-mail: yuho_horikoshi@tmhp.jp
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Abstract

An outbreak of metallo-β-lactamase (MBL) producing Klebsiella pneumoniae occurred at a children’s hospital in Japan. MBL-producing K. pneumoniae was detected in tea dispenser in the hospital, the use of which was associated with the acquisition of the MBL-producing Enterobacteriaceae. The outbreak ceased after use of the tea dispenser was banned.

Information

Type
Concise Communication
Information
Infection Control & Hospital Epidemiology , Volume 40 , Issue 2 , February 2019, pp. 217 - 220
Copyright
© 2018 by The Society for Healthcare Epidemiology of America. All rights reserved. 

The emergence of carbapenemase-producing Enterobacteriaceae (CPE) is a public health threat requiring global action.Reference Magiorakos, Suetens, Monnet, Gagliotti and Heuer 1 Although CPE is still considered rare and constitutes <1% of the Enterobacteriaceae isolated in Japan,Reference Suzuki, Matsui, Suzuki, Tsutsui and Shibayama 2 the clinical impact of CPE infections on morbidity and mortality are substantial; the mortality rate due to CPE sepsis among adult patients in Japan was reportedly as high as 40%.Reference Hayakawa, Miyoshi-Akiyama and Kirikae 3

Healthcare-related outbreaks of metallo-β-lactamase (MBL)-producing Enterobacteriaceae have been reported in various settings including pediatric wards and pediatric intensive care units.Reference Stillwell, Green and Barbadora 4 We experienced an outbreak of MBL-producing Enterobacteriaceae lasting from May to December 2014 in a pediatric ward at Tokyo Metropolitan Children’s Medical Center. We report the subsequent outbreak investigation and the infection control measures implemented.

Methods

The MBL-producing Enterobacteriaceae outbreak occurred at a single, pediatric, joint cardiology and ophthalmology ward with 27 beds. Apart from this outbreak, a patient colonized by MBL-producing Enterobacteriaceae had been hospitalized in isolation in the same ward for a prolonged period. In May 2014, MBL-producing Klebsiella pneumoniae was discovered incidentally while testing for Clostridium difficile in a stool culture of a patient with chronic diarrhea. The results of the test were negative for Clostridioides difficile. Shortly thereafter, MBL-producing Enterobacteriaceae were detected in 2 more patients in the same ward. Immediate active surveillance for the pathogen was implemented. Initial active surveillance by rectal swab identified 6 more patients colonized by the same pathogen. The unusually high occurrence of this strain confirmed an MBL-producing Enterobacteriaceae outbreak in the ward. The Ethics Committee of Tokyo Metropolitan Children’s Medical Center approved the study protocol (No. H26-108)

Weekly active surveillance to detect MBL-producing Enterobacteriaceae was conducted for all patients in the ward without a previous history of colonization or infection due to MBL-producing Enterobacteriaceae. 5 Rectal swab cultures were obtained from hospitalized patients once weekly.

Rectal swabs were inoculated onto a cefpodoxime-containing agar (ChromID ESBL SYSMEX, bioMerieux, Japan). The resulting blue or purple colonies were planted onto blood agar with a cefoxitin disc and boronic acid to inhibit the isolates from overproducing AmpC β-lactamase. The sodium mercaptoacetate (SMA) test (Eiken Chemical, Japan) was performed on these isolates to detect MBL-producing Enterobacteriaceae. Two discs containing ceftazidime with or without SMA were placed on Mueller-Hinton agar 4–5 cm apart. The bacterial strain was diluted by saline to the 0.5 McFarland standard and placed on Mueller-Hinton agar. A difference >5 mm in the growth inhibitory zone was considered evidence of the MBL-producing strain.Reference Arakawa, Shibata and Shibayama 6

We conducted the molecular biological analysis of the isolated MBL-producing Enterobacteriaceae (see Supplemental Materials online). To investigate possible contaminants in the immediate environment, environmental cultures were conducted eight times during the outbreak period from May to December 2014. In total, 195 samples were collected on eight different sampling days (see supplementary materials). A retrospective study was conducted to explore the risk factors of MBL-producing Enterobacteriaceae acquisition. We obtained demographic and clinical data of patients with an active surveillance culture (see Supplementary Materials online).

Statistical analysis

Univariate analysis was performed using the χ2 test and the Fisher exact test. The Mann-Whitney U test was used for continuous variables. Candidate variables with P <.10 in univariate analysis were included in the multivariate analysis. Sensitivity analysis controlling for other covariates was conducted. All statistical analyses were conducted with SPSS version 22 software (IBM, Armonk, NY).

Results

In total, 249 patients were admitted to the ward during the study period. Active surveillance was performed once weekly except at the time of admission; however, 104 patients did not undergo a rectal swab for the surveillance culture due to their shorter period of hospitalization. The 145 patients who had undergone a rectal swab were included for analysis. The characteristics of these patients are shown in Table 1.

Table 1

Characteristics of Patients who Received an Active Surveillance Culture

Note. MBL, metallo-β-lactamase; NS, not significant.

a Duration of exposure in all of the above categories was within 1 mo prior to obtaining a positive culture for positive patients and the last culture done for negative patients.

b No. (%) unless otherwise specified.

c By multivariate analysis. Multivariate analysis included use of the tea dispenser, bed bath, antacids, and antimicrobials, and duration of admission in days.

Overall, 36 patients (24.8 %) yielded a total of 39 strains of MBL-producing Enterobacteriaceae including 30 cases of K. pneumoniae, 5 cases of Escherichia coli, 2 cases of Citrobacter freundii, 1 case of Klebsiella oxytoca, and 1 case of Enterobacter aerogenes.

MBL-producing K. pneumoniae was isolated from 7 environmental samples (3.6 %). At the first sampling, a sink in the nurses’ station tested positive. At the third sampling, another sink in the nurse’s station and the milk bottle cabinet were positive. Finally, at the eighth sampling, 4 positive samples were obtained from the tea dispenser.

We sequenced the whole genome of 37 K. pneumoniae strains isolated from the clinical and environmental samples. All isolates harbored the bla IMP-1 gene. A core-genome single nucleotide polymorphism (SNP)–based phylogenetic analysis revealed that 33 of the bla IMP-1-positive K. pneumoniae strains had a common ancestor (see the Supplementary Materials online).

Risk factor analysis

The results of our univariate analysis exploring the risk factors of MBL-producing Enterobacteriaceae acquisition are shown in Table 1. Our multivariate analysis revealed that use of the tea dispenser (adjusted OR [aOR], 43.69; 95% CI, 7.33–260.49) and longer length of hospital stay (aOR, 1.03; 95% CI, 1.01–1.04) were associated with the acquisition of these pathogens. Sensitivity analysis controlling for other covariates did not affect the results of the multivariate analysis.

Infection control measures

We applied strict cohorting of patients with MBL-producing Enterobacteriaceae. Use of public areas such as the playroom and dining hall in the ward was banned due to the potential sources of transmission. Staff education in appropriate standard and contact precautions was reinforced. Routine environmental cleaning, including cleaning of the sinks and frequently touched areas using 0.1 % hypochlorite was increased from 1 to 3 times daily. Admission to the ward was restricted twice during the outbreak to prevent spreading the pathogens. No MBL-producing Enterobacteriaceae were isolated from patients admitted to the ward or occupying the ward environment after banning the use of the tea dispenser.

Discussion

We have described the largest documented pediatric outbreak of bla IMP-1-positive K. pneumoniae in Japan. Environmental sampling and epidemiological investigation identified a tea dispenser in the ward as the contaminant source.

The tea dispenser, placed in a public area in the ward for the use of patients and visitors, automatically mixes barley tea powder with hot water in a shaker before diluting with cold water and dispensing the liquid as iced tea. The maintenance and cleaning of the tea dispenser were done by the cleaning staff using detergents once daily according to the manufacturer’s instructions. The cleaning staff were also responsible for the disposal of the children’s diapers in the ward. MBL-producing Enterobacteriaceae were detected in the shaker, which was handled only by the cleaning staff, suggesting that it had become contaminated by their handling. An interview of the cleaning staff later revealed that their knowledge and practice of hand hygiene were inadequate. Self-service tea and water dispensers, commonly available to patients in medical facilities throughout Japan, may readily act as a medium for infection among a patient population if contaminated.

However, reports of CPE outbreaks among the pediatric population are rare, and the mode of transmission has never been clarified.Reference Liu, Li, Wan, Jiang, Li and Yang 7 , Reference Benenson, Warburg and Hidalgo-Grass 8 Moreover, existing reports have focused on the molecular characteristics of CPE or were unable to determine the route of transmission due to inadequate outbreak investigation. In contrast, in our study, rigorous outbreak investigation and comprehensive molecular typing demonstrated that a tea dispenser was the likely source of transmission. The surveillance cultures of the environmental samples in the present study revealed that 2 cultures from the sinks in the nurses’ station were positive for MBL-producing K. pneumoniae. It is likely that these positive results are due to environmental contamination because the outbreak continued despite rigorous cleaning of these areas. Another hypothesis proposes that water supplied in the hospital was contaminated by MBL-producing K. pneumoniae, but this is unlikely because none of the clinical samples from other wards yielded the pathogens, and cultures of the water samples from the tea dispenser were also negative.

The phylogenetic analysis based on core-genome SNPs revealed that the bla IMP-1-positive ST34 K. pneumoniae isolated in the outbreak had a common ancestor (see Supplementary Materials online). Therefore, the analysis suggested that the tea dispenser was the source.

Also, a longer stay in the ward was significantly related to CPE colonization. Usually, a long hospital stay is a risk factor for acquiring CPE,Reference Montagnani, Prato and Scolfaro 9 but its relationship to CPE acquisition is weaker than in the present case of the use of the tea dispenser. We assume that the longer hospital stay created more opportunities for using the contaminated tea dispenser.

In summary, we experienced an outbreak of IMP-1 MBL-producing Enterobacteriaceae among pediatric patients in a tertiary-care children’s hospital. After rigorous investigation, a cold tea dispenser was identified as the source of contamination. Despite the rarity of this mode of transmission, infection control personnel should be aware of its possibility whenever a MBL-producing Enterobacteriaceae outbreak occurs.

Supplementary materials

To view supplementary material for this article, please visit https://doi.org/10.1017/ice.2018.331

Acknowledgments

We thank Dr Isao Miyairi, Mie Sugawara, Dr Ken Hori, Dr Naoya Fukushima, and Dr Masaru Miura for their cooperation and advice in our outbreak investigation and James R. Valera for his assistance in editing the manuscript.

Financial support

No financial support was provided relevant to this article.

Conflicts of interest

All authors report no conflicts of interest relevant to this article.

Footnotes

PREVIOUS PRESENTATION: These data were presented at IDWeek 2015, October 8, 2015, in San Diego, California, as the winning entry in the International Investigator Awards.

Cite this article: Ito K, et al. (2019) A metallo-beta-lactamase producing Enterobacteriaceae outbreak from a contaminated tea dispenser at a children’s hospital in Japan. Infection Control & Hospital Epidemiology 2019, 40, 217–220. doi: 10.1017/ice.2018.331

References

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Table 1Characteristics of Patients who Received an Active Surveillance Culture

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