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Deprecated: Implicit conversion from float 265.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 J+Infect 2021 ; 83 (1): 96-103 Nephropedia Template TP
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Genetic epidemiology of SARS-CoV-2 transmission in renal dialysis units - A high risk community-hospital interface #MMPMID33895226
Li KK; Woo YM; Stirrup O; Hughes J; Ho A; Filipe ADS; Johnson N; Smollett K; Mair D; Carmichael S; Tong L; Nichols J; Aranday-Cortes E; Brunker K; Parr YA; Nomikou K; McDonald SE; Niebel M; Asamaphan P; Sreenu VB; Robertson DL; Taggart A; Jesudason N; Shah R; Shepherd J; Singer J; Taylor AHM; Cousland Z; Price J; Lees JS; Jones TPW; Lopez CV; MacLean A; Starinskij I; Gunson R; Morris STW; Thomson PC; Geddes CC; Traynor JP; Breuer J; Thomson EC; Mark PB
J Infect 2021[Jul]; 83 (1): 96-103 PMID33895226show ga
OBJECTIVES: Patients requiring haemodialysis are at increased risk of serious illness with SARS-CoV-2 infection. To improve the understanding of transmission risks in six Scottish renal dialysis units, we utilised the rapid whole-genome sequencing data generated by the COG-UK consortium. METHODS: We combined geographical, temporal and genomic sequence data from the community and hospital to estimate the probability of infection originating from within the dialysis unit, the hospital or the community using Bayesian statistical modelling and compared these results to the details of epidemiological investigations. RESULTS: Of 671 patients, 60 (8.9%) became infected with SARS-CoV-2, of whom 16 (27%) died. Within-unit and community transmission were both evident and an instance of transmission from the wider hospital setting was also demonstrated. CONCLUSIONS: Near-real-time SARS-CoV-2 sequencing data can facilitate tailored infection prevention and control measures, which can be targeted at reducing risk in these settings.