Invasive Mold Infections Following Hurricane Harvey-Houston, Texas
- PMID: 36910694
- PMCID: PMC10003735
- DOI: 10.1093/ofid/ofad093
Invasive Mold Infections Following Hurricane Harvey-Houston, Texas
Abstract
Background: Characterizing invasive mold infection (IMI) epidemiology in the context of large flooding events is important for public health planning and clinical decision making.
Methods: We assessed IMI incidence (per 10 000 healthcare encounters) 1 year before and after Hurricane Harvey at 4 hospitals in Houston, Texas. Potential IMI cases were assigned as proven or probable cases using established definitions, and surveillance cases using a novel definition. We used rate ratios to describe IMI incidence and multivariable logistic regression to examine patient characteristics associated with IMI case status.
Results: IMI incidence was significantly higher posthurricane (3.69 cases) than prehurricane (2.50 cases) (rate ratio, 1.48 [95% confidence interval, 1.10-2.00]), largely driven by surveillance IMI cases. Aspergillus was the most common species cultured (33.5% prehurricane and 39.9% posthurricane). About one-quarter (25.8%) of IMI patients lacked classical IMI risk factors such as hematologic malignancy and transplantations. Overall, 45.1% of IMI patients received intensive care, and in-hospital all-cause mortality was 24.2%.
Conclusions: IMI incidence likely increased following Hurricane Harvey and outcomes for IMI patients were severe. Patient and clinician education on IMI prevention and identification is warranted, particularly as the frequency of extreme weather events increases due to climate change.
Keywords: aspergillosis; hurricane; invasive mold infections; surveillance.
© The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America.
Conflict of interest statement
Potential conflicts of interest. S. Wu. is a coinvestigator on an active Astellas-sponsored investigator-initiated research grant, and a coinvestigator on an active Gilead-sponsored investigator-initiated research grant. L. O.-Z. received institutional payments from CDC, institutional grants from Pfizer, Cidara, Scynexis, and Astellas, and consulting fees from Pfizer, Cidara, Merck, F2G, Astellas, Gilead, Octapharma, Viracor, and Appilli. R. L. A. received institutional payments from CDC. M. N. received institutional payments from CDC, grants from the National Institutes of Health and Gilead, and honoraria from University of Fukui, Japan. D. P. K. received institutional payments from CDC. All other authors report no potential conflicts.
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