Background/aim: Ralstonia species are opportunistic, waterborne microorganisms known for their ability to survive and proliferate in a wide range of water-based environments. They can contaminate solutions used for patient care and cause hospital outbreaks due to contaminated solutions. The aim of this study was to investigate the source and clonal relationship of Ralstonia insidiosa bacteremia detected in 28 patients between August and December 2021, as part of an unusual outbreak. Materials and methods: Active prospective surveillance studies were conducted, and environmental samples, including saline, antiseptic, and antibiotic solutions, injectors, arterial blood gas syringes, tap water, and hand soap, were collected from wards to determine the source of the outbreak. An arbitrary-primed polymerase chain reaction (AP-PCR) genotyping method was used to determine the clonal relationship between the isolates. Results: All the samples were cultured, and R. insidiosa was isolated from arterial blood gas syringes with the same location and time- based identifier (LOT number). All the arterial blood gas syringes were recalled from the hospital departments and sent back to the manufacturer. The outbreak was reported to the national health authorities. Clonal analysis between isolates from the patients and the blood gas syringes was performed using AP-PCR. It was observed that the R. insidiosa isolates were monoclonal and identical. Conclusion: It was concluded that these contaminated arterial blood gas syringes caused the R. insidiosa bacteremia, especially in immunocompromised patients.
机构:
QEII MC, Lab Med Western Australia PathW, Div Microbiol & Infect Dis, Nedlands, WA 6909, AustraliaUniv Bonn, Inst Med Mikrobiol & Immunol, D-53127 Bonn, Germany
机构:
Johannes Gutenberg Univ Mainz, Inst Organ Chem, D-55128 Mainz, GermanyUniv Bonn, Inst Med Mikrobiol & Immunol, D-53127 Bonn, Germany
Siering, C.
Inglis, T.
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QEII MC, Lab Med Western Australia PathW, Div Microbiol & Infect Dis, Nedlands, WA 6909, AustraliaUniv Bonn, Inst Med Mikrobiol & Immunol, D-53127 Bonn, Germany
Inglis, T.
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Schumann, P.
Yassin, A. F.
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Univ Bonn, Inst Med Mikrobiol & Immunol, D-53127 Bonn, GermanyUniv Bonn, Inst Med Mikrobiol & Immunol, D-53127 Bonn, Germany