Outbreaks of Fungal Infections in Hospitals: Epidemiology, Detection, and Management
Abby P. Douglas,
Adam G. Stewart,
Catriona L. Halliday
et al.
Abstract:Nosocomial clusters of fungal infections, whilst uncommon, cannot be predicted and are associated with significant morbidity and mortality. Here, we review reports of nosocomial outbreaks of invasive fungal disease to glean insight into their epidemiology, risks for infection, methods employed in outbreak detection including genomic testing to confirm the outbreak, and approaches to clinical and infection control management. Both yeasts and filamentous fungi cause outbreaks, with each having general and specif… Show more
“…Based on current recommendations [ 17 ], this high rate of mold IFI in patients in the HR-IFI-AL group, along with high mortality in those who developed mold IFI, justifies anti-mold prophylaxis usage in such patients. Since almost all mold IFI in our center occurred during 2018/2019, when there was construction in the department, with virtually no instances in the study years before and after, a prophylactic approach is warranted during periods of construction in proximity to departments hospitalizing patients at risk [ 25 ]. In contrast, the rate of proven/probable mold IFI in patients in the non-HR-IFI-AL group was 1/41 (2.4%).…”
Invasive fungal infections (IFI) cause morbidity and mortality in children with acute leukemia (AL). We retrospectively collected data on febrile neutropenic episodes (FNE) in AL children (2016–2021) and assessed factors associated with proven/probable IFI. Ninety-three children developed 339 FNE. Seventeen (18.3%) children developed 19 proven/probable IFI (11 yeast; eight molds). The proven/probable yeast IFI rate was 6/52 (11.5%) in children who belong to the high risk for IFI category (HR-IFI-AL: high-risk acute lymphocytic leukemia (ALL), acute myeloid leukemia, relapse); and 5/41 (12.2%) in the non-HR-IFI-AL category (standard/intermediate risk ALL). The proven/probable mold IFI rate was 7/52 (13.5%) in HR-IFI-AL children and 1/41 (2.4%) in the non-HR-IFI-AL category. In the multivariable analysis, underlying genetic syndrome, oral mucositis, and older age were significantly associated with proven/probable IFI, while a longer time since AL diagnosis was protective. Two of 13 (15.4%) HR-IFI-AL children died because of IFI. The elevated risks of proven/probable mold IFI and the associated mortality in HR-IFI-AL children, and high risk of invasive candidiasis in the non-HR-IFI-AL group, emphasize the need for the close monitoring of local epidemiology and the adjustment of practices accordingly.
“…Based on current recommendations [ 17 ], this high rate of mold IFI in patients in the HR-IFI-AL group, along with high mortality in those who developed mold IFI, justifies anti-mold prophylaxis usage in such patients. Since almost all mold IFI in our center occurred during 2018/2019, when there was construction in the department, with virtually no instances in the study years before and after, a prophylactic approach is warranted during periods of construction in proximity to departments hospitalizing patients at risk [ 25 ]. In contrast, the rate of proven/probable mold IFI in patients in the non-HR-IFI-AL group was 1/41 (2.4%).…”
Invasive fungal infections (IFI) cause morbidity and mortality in children with acute leukemia (AL). We retrospectively collected data on febrile neutropenic episodes (FNE) in AL children (2016–2021) and assessed factors associated with proven/probable IFI. Ninety-three children developed 339 FNE. Seventeen (18.3%) children developed 19 proven/probable IFI (11 yeast; eight molds). The proven/probable yeast IFI rate was 6/52 (11.5%) in children who belong to the high risk for IFI category (HR-IFI-AL: high-risk acute lymphocytic leukemia (ALL), acute myeloid leukemia, relapse); and 5/41 (12.2%) in the non-HR-IFI-AL category (standard/intermediate risk ALL). The proven/probable mold IFI rate was 7/52 (13.5%) in HR-IFI-AL children and 1/41 (2.4%) in the non-HR-IFI-AL category. In the multivariable analysis, underlying genetic syndrome, oral mucositis, and older age were significantly associated with proven/probable IFI, while a longer time since AL diagnosis was protective. Two of 13 (15.4%) HR-IFI-AL children died because of IFI. The elevated risks of proven/probable mold IFI and the associated mortality in HR-IFI-AL children, and high risk of invasive candidiasis in the non-HR-IFI-AL group, emphasize the need for the close monitoring of local epidemiology and the adjustment of practices accordingly.
“…NGS also has important roles in epidemiological contexts including studies of fungal evolution, the mycobiome and host genomic susceptibility to IFDs, all of which are beyond the scope of this review. With respect to IFD outbreak investigations, we highlight some key developments, but also direct readers to recent comprehensive reviews [158,159].…”
Section: Whole Genome Sequencingmentioning
confidence: 99%
“…The clinical utility of NGS within fungal outbreak situations is well established and comprehensively reviewed by Douglas et al [158]. Its application in the case clusters of yeasts, Pneumocystis, mould and endemic mycoses have met with varying degrees of success, depending on the pathogen.…”
Section: Whole Genome Sequencingmentioning
confidence: 99%
“…Likewise, bioinformatic analyses are often laborious and require significant experience. For instance, further experience is required for cluster definitions by SNP distance; while this is well defined for yeast outbreaks, delineating mould outbreaks is more difficult [158]. Finally, limiting factors associated computing power, storage space, expertise and cost are especially applicable for medical mycology applications [194].…”
Invasive fungal diseases (IFDs) comprise a growing healthcare burden, especially given the expanding population of immunocompromised hosts. Early diagnosis of IFDs is required to optimise therapy with antifungals, especially in the setting of rising rates of antifungal resistance. Molecular techniques including nucleic acid amplification tests and whole genome sequencing have potential to offer utility in overcoming limitations with traditional phenotypic testing. However, standardisation of methodology and interpretations of these assays is an ongoing undertaking. The utility of targeted Aspergillus detection has been well-defined, with progress in investigations into the role of targeted assays for Candida, Pneumocystis, Cryptococcus, the Mucorales and endemic mycoses. Likewise, whilst broad-range polymerase chain reaction assays have been in use for some time, pathology stewardship and optimising diagnostic yield is a continuing exercise. As costs decrease, there is also now increased access and experience with whole genome sequencing, including metagenomic sequencing, which offers unparalleled resolution especially in the investigations of potential outbreaks. However, their role in routine diagnostic use remains uncommon and standardisation of techniques and workflow are required for wider implementation.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.