Search and Contain: Impact of an integrated genomic and epidemiological surveillance and response program for control of carbapenemase-producing Enterobacterales.
AuthorLane, CR; Brett, J; Schultz, M; Gorrie, CL; Stevens, K; Cameron, DRM; St George, S; van Diemen, A; Easton, M; Stuart, RL; ...
Source TitleClinical Infectious Diseases
PublisherOxford University Press (OUP)
University of Melbourne Author/sKwong, Jason; Seemann, Torsten; Lane, Courtney; Brett, Judith; Gorrie, Claire; Schultz, Mark; Stevens, Kerrie; Cameron, Donna; St George, Siobhan; Sait, Michelle; ...
AffiliationMicrobiology and Immunology
Document TypeJournal Article
CitationsLane, C. R., Brett, J., Schultz, M., Gorrie, C. L., Stevens, K., Cameron, D. R. M., St George, S., van Diemen, A., Easton, M., Stuart, R. L., Sait, M., Peleg, A. Y., Stewardson, A. J., Cheng, A. C., Spelman, D. W., Waters, M. J., Ballard, S. A., Sherry, N. L., Williamson, D. A. ,... Howden, B. P. (2020). Search and Contain: Impact of an integrated genomic and epidemiological surveillance and response program for control of carbapenemase-producing Enterobacterales.. Clin Infect Dis, https://doi.org/10.1093/cid/ciaa972.
Access StatusOpen Access
BACKGROUND: Multi-resistant organisms (MROs) pose a critical threat to public health. Population-based programs for control of MROs such as Carbapenemase-producing Enterobacterales (CPE) have emerged and evaluation is needed. We assess the feasibility and impact of a state-wide CPE surveillance and response program deployed in December 2015 across Victoria, Australia (population 6.5 million). METHODS: A prospective multi-modal intervention including active screening, carrier isolation, centralised case investigation and comparative pathogen genomics was implemented. We analyze trend in CPE incidence and clinical presentation, risk factors and local transmission over the program's first three years (January 2016 to December 2018). RESULTS: CPE case ascertainment increased over the study period to 1.42 cases/100,000 population, linked to increased screening without a concomitant rise in active clinical infections (0.45-0.60 infections/100,000 population, p=0.640). KPC-2 infection decreased from 0.29 infections/100,000 population prior to intervention to 0.03 infections/100,000 population in 2018 (p=0.003). Comprehensive case investigation identified putative overseas community acquisition. Median time between isolate referral and initial genomic and epidemiological assessment for local transmission was 11 days (IQR 9-14). Prospective surveillance identified numerous small transmission networks (median 2, range 1-19 cases), predominantly IMP and KPC, with median pairwise distance of 8 (IQR 4-13) single nucleotide polymorphisms; low diversity between clusters of the same sequence type suggested genomic cluster definitions alone are insufficient for targeted response. CONCLUSIONS: We demonstrate the value of centralised CPE control programs to increase case ascertainment, resolve risk factors and identify putative local transmission through prospective genomic and epidemiological surveillance; methodologies are transferable to low-prevalence settings and MROs globally.
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