The Journal of hospital infection · 2026
From imaging to infection: contrast dye contaminated with Klebsiella pneumoniae as a source of nosocomial infections.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Heireman L, Xavier B B, De Feyter S, De Grauwe T, De Munck J, De Smedt L, Dewaele A, De Wilde K, Dumez F, Monteyne T, Naesens R, Rossen J W A, Temmerman W, Van Laere J, Van Lint P, Van Puyvelde P, Verschraegen I, Verstrepen W, Vonck A, Swinnen W
Аннотация
INTRODUCTION: Klebsiella pneumoniae rapidly disseminates in clinical environments and is frequently responsible for hospital outbreaks. The present study highlights an under-recognized and concerning nosocomial transmission route involving intravenous contrast dye, after a cluster of seven patients became acutely ill after undergoing contrast-enhanced computed tomography (CT).
METHODS: All applied consumables, administration sets and the environment of the CT scanner were sampled and cultured. Whole-genome sequencing and phylogenetic analyses were performed on outbreak isolates, with a hypervirulent strain and a quality control strain serving as references.
RESULTS: A microbiological analysis of the residual contrast dye vials and associated administration set identified contamination with K. pneumoniae. Whole-genome sequencing confirmed a genetic link between these strains and the K. pneumoniae strain isolated from the patient's blood culture. Molecular characterization suggested that the detected strain represented a contaminant rather than a nosocomial outbreak clone belonging to ST45 with K62 serotype.
CONCLUSION: The exact source of contamination remains unknown as contamination in the pharmaceutical supply chain or hospital practices cannot be excluded. However, storing the opened contrast dye bottle at body temperature for 8 h before administration undoubtedly contributed to an increase in the bacterial load. This incident underscores the potential risk associated with storing an opened contrast dye bottle at body temperature-a common practice in the radiology department.
METHODS: All applied consumables, administration sets and the environment of the CT scanner were sampled and cultured. Whole-genome sequencing and phylogenetic analyses were performed on outbreak isolates, with a hypervirulent strain and a quality control strain serving as references.
RESULTS: A microbiological analysis of the residual contrast dye vials and associated administration set identified contamination with K. pneumoniae. Whole-genome sequencing confirmed a genetic link between these strains and the K. pneumoniae strain isolated from the patient's blood culture. Molecular characterization suggested that the detected strain represented a contaminant rather than a nosocomial outbreak clone belonging to ST45 with K62 serotype.
CONCLUSION: The exact source of contamination remains unknown as contamination in the pharmaceutical supply chain or hospital practices cannot be excluded. However, storing the opened contrast dye bottle at body temperature for 8 h before administration undoubtedly contributed to an increase in the bacterial load. This incident underscores the potential risk associated with storing an opened contrast dye bottle at body temperature-a common practice in the radiology department.