Epidemiology, clinical outcomes and risk factors of third-generation cephalosporin-resistant Escherichia coli hospitalized infections in remote Australia—a case–control study

Author:

Camilleri Shayne12ORCID,Tsai Danny345ORCID,Langham Freya16,Ullah Shahid37,Chiong Fabian18

Affiliation:

1. Department of Medicine, Alice Springs Hospital , Alice Springs, NT , Australia

2. Department of Infectious Diseases, Austin Health , Melbourne, VIC , Australia

3. Flinders Health and Medical Research Institute, Flinders University , Adelaide, SA , Australia

4. UQ Centre for Clinical Research, University of Queensland , Brisbane, QLD , Australia

5. Pharmacy Department, Alice Springs Hospital , Alice Springs, NT , Australia

6. Department of Infectious Diseases, Monash Health , Melbourne, VIC , Australia

7. College of Medicine and Public Health, Flinders University , Adelaide, SA , Australia

8. Department of Infectious Diseases, Canberra Hospital , Canberra, ACT , Australia

Abstract

Abstract Background Incidence of third-generation cephalosporin-resistant (3GCR) Escherichia coli infections has increased in remote Australia from 2012 to 2018. Objectives To describe the epidemiology of 3GCR E. coli in Central Australia. Methods A case–control study was conducted in the primary Central Australian hospital. Patient characteristics, antibiotic usage and clinical outcomes were compared between adult hospitalizations with 3GCR and susceptible E. coli isolates in 2018–19. Poisson regression was used to compare the incidence of 3GCR hospitalizations between Indigenous and non-Indigenous individuals. Patient characteristics and antibiotic usage were tested for associations with 3GCR isolates using univariate analysis. Results A total of 889 E. coli isolates were identified, of which 187 (21%) were 3GCR. The incidence of 3GCR E. coli infection was 2.15 per 1000 person-years, with an incidence rate ratio of 6.8 (95% CI 4.6–10.1) between Indigenous and non-Indigenous individuals. When compared with the control group, 3GCR E. coli infections were associated with a higher Charlson comorbidity index (CCI ≥3 in 30.7% versus 15.0%, P < 0.001) and were more commonly healthcare associated (52.4% versus 26.7%, P < 0.001). A higher 1 year mortality was observed in the 3GCR group after adjustment for comorbidity (OR = 4.43, P = 0.002), but not at 30 days (2.4% versus 0.0%, P = 0.2). The 3GCR group used more antibiotics in the past 3 months (OR = 5.75, P < 0.001) and 12 months (OR = 3.65, P < 0.001). Conclusions 3GCR E. coli infections in remote Australia disproportionally affect Indigenous peoples and are associated with a high burden of comorbidities and antibiotic use. Strategies to enhance antimicrobial stewardship should be considered in this remote setting.

Publisher

Oxford University Press (OUP)

Subject

Microbiology (medical),Infectious Diseases,Immunology and Allergy,Microbiology,Immunology

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