Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/20276
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dc.contributor.authorChua, Kyra Y L-
dc.contributor.authorStewardson, Andrew J-
dc.date2019-02-12-
dc.date.accessioned2019-03-04T22:04:12Z-
dc.date.available2019-03-04T22:04:12Z-
dc.date.issued2019-02-12-
dc.identifier.citationAntimicrobial resistance and infection control 2019; 8: 36-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/20276-
dc.description.abstractCeftriaxone-resistant Enterobacteriaceae are priority pathogens of critical importance. Escherichia coli is the most commonly isolated Enterobacteriaceae. There are few data regarding non-invasive ceftriaxone-resistant E. coli (CR-EC) isolates in the Australian community. We aimed to describe the prevalence, phenotype, geographic variation, and sociodemographic predictors of ceftriaxone-resistance among E. coli isolates recovered from urine specimens. In August 2017, we prospectively analysed E. coli isolates recovered from urine specimens submitted to Dorevitch Pathology (Victoria, Australia), a laboratory that services patients in the community and hospitals. In addition to patient-level predictors of ceftriaxone resistance, we mapped patient postcodes to community-level indicators including Index of Relative Socioeconomic Deprivation, remoteness, and proportion of residents born overseas. We used Poisson regression with log link and robust standard errors to quantify the association between ceftriaxone resistance and patient- and community-level factors. We included 6732 non-duplicate E. coli isolates. Most (89.2%, 6008/6732) were obtained from female patients. Median age was 56 years (IQR, 32-74). Most patients (90.5%, 5789/6732) were neither referred from a hospital nor residing in a residential aged care facility (RACF). Among the 6732 isolates, 5.7% (382) were CR-EC, ranging from 3.5% (44/1268) in inner regional areas to 6.3% (330/5267) in major cities. Extended spectrum ß-lactamase (ESBL) -production was the most common mechanism for ceftriaxone resistance (89%, 341/382). Nitrofurantoin was the most active oral agent against CR-EC. Eight CR-EC isolates (2.4%) were susceptible only to amikacin, meropenem and nitrofurantoin. None were resistant to meropenem. On multivariable analysis, ceftriaxone resistance was associated with age, residence in a RACF (adjusted relative risk [aRR] 2.94, 95% confidence interval [CI] 2.10-4.13), specimen referral from hospital (aRR 2.05, 95% CI 1.45-2.9), and the proportion of residents born in North Africa and the Middle East (aRR 1.30 for each 5% absolute increase, 95% CI 1.09-1.54), South-East Asia (aRR 1.14, 95% CI 1.02-1.27), and Southern and Central Asia (aRR 1.16, 95% CI 1.04-1.28). These results provide insights into sociodemographic variation in CR-EC in the community. A better understanding of this variation may inform empiric treatment guidelines and strategies to reduce community dissemination of CR-EC.-
dc.language.isoeng-
dc.subject(MeSH)-
dc.subjectAustralia-
dc.subjectCeftriaxone-
dc.subjectCensuses-
dc.subjectDemography-
dc.subjectDrug resistance, bacterial-
dc.subjectEscherichia coli-
dc.subjectUrinary tract infections-
dc.subjectVictoria-
dc.titleIndividual and community predictors of urinary ceftriaxone-resistant Escherichia coli isolates, Victoria, Australia.-
dc.typeJournal Article-
dc.identifier.journaltitleAntimicrobial resistance and infection control-
dc.identifier.affiliationDepartment of Microbiology, Austin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationDepartment of Infectious Diseases, Alfred Hospital and Central Clinical School, Monash University, Melbourne, Victoria Australiaen
dc.identifier.affiliationDepartment of Microbiology, Dorevitch Pathology, Heidelberg, Victoria Australiaen
dc.identifier.affiliationDepartment of Infectious Diseases, Austin Health, Heidelberg, Victoria, Australia-
dc.identifier.doi10.1186/s13756-019-0492-8-
dc.identifier.orcid0000-0001-6805-1224-
dc.identifier.pubmedid30805183-
dc.type.austinJournal Article-
local.name.researcherChua, Kyra Y L
item.languageiso639-1en-
item.openairetypeJournal Article-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptMicrobiology-
crisitem.author.deptInfectious Diseases-
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