TY - JOUR
T1 - Impact of healthcare-associated acquisition on community-onset Gram-negative bloodstream infection
T2 - A population-based study
AU - Al-Hasan, M. N.
AU - Eckel-Passow, J. E.
AU - Baddour, L. M.
N1 - Funding Information:
This work was made possible by research grant R01-AG034676 from the National Institute of Arthritis and Musculoskeletal and Skin Diseases (National Institutes of Health, US Public Health Service).
Funding Information:
Funding The study received funding from the Small Grants Program and the Baddour Family Fund at the Mayo Clinic, Rochester, MN, USA. The funding source had no role in study design.
PY - 2012/6
Y1 - 2012/6
N2 - We performed a population-based study to examine the influence of healthcare-associated acquisition on pathogen distribution, antimicrobial resistance, shortand long-term mortality of community-onset Gramnegative bloodstream infections (BSI). We identified 733 unique patients with community-onset Gram-negative BSI (306 healthcare-associated and 427 community-acquired) among Olmsted County, Minnesota, residents from 1 January 1998 to 31 December 2007. Multivariate logistic regression was used to examine the association between healthcare-associated acquisition and microbiological etiology and antimicrobial resistance. Multivariate Cox proportional hazards regression was used to evaluate the influence of the site of acquisition on mortality. Healthcare-associated acquisition was predictive of Pseudomonas aeruginosa (odds ratio [OR] 3.14, 95% confidence intervals [CI]: 1.59-6.57) and the group of Enterobacter, Citrobacter, and Serratia species (OR 2.23, 95% CI: 1.21-4.21) as causative pathogens of community-onset Gram-negative BSI. Healthcare-associated acquisition was also predictive of fluoroquinolone resistance among community-onset Gramnegative bloodstream isolates (OR 2.27, 95% CI: 1.18-4.53). Healthcare-associated acquisition of BSI was independently associated with higher 28-day (hazard ratio [HR] 3.73, 95%CI: 2.13-6.93) and 1-year mortality (HR 3.60, 95%CI: 2.57-5.15). Because of differences in pathogen distribution, antimicrobial resistance, and outcomes between healthcare-associated and community-acquired Gram-negative BSI, identification of patients with healthcare-associated acquisition of BSI is essential to optimize empiric antimicrobial therapy.
AB - We performed a population-based study to examine the influence of healthcare-associated acquisition on pathogen distribution, antimicrobial resistance, shortand long-term mortality of community-onset Gramnegative bloodstream infections (BSI). We identified 733 unique patients with community-onset Gram-negative BSI (306 healthcare-associated and 427 community-acquired) among Olmsted County, Minnesota, residents from 1 January 1998 to 31 December 2007. Multivariate logistic regression was used to examine the association between healthcare-associated acquisition and microbiological etiology and antimicrobial resistance. Multivariate Cox proportional hazards regression was used to evaluate the influence of the site of acquisition on mortality. Healthcare-associated acquisition was predictive of Pseudomonas aeruginosa (odds ratio [OR] 3.14, 95% confidence intervals [CI]: 1.59-6.57) and the group of Enterobacter, Citrobacter, and Serratia species (OR 2.23, 95% CI: 1.21-4.21) as causative pathogens of community-onset Gram-negative BSI. Healthcare-associated acquisition was also predictive of fluoroquinolone resistance among community-onset Gramnegative bloodstream isolates (OR 2.27, 95% CI: 1.18-4.53). Healthcare-associated acquisition of BSI was independently associated with higher 28-day (hazard ratio [HR] 3.73, 95%CI: 2.13-6.93) and 1-year mortality (HR 3.60, 95%CI: 2.57-5.15). Because of differences in pathogen distribution, antimicrobial resistance, and outcomes between healthcare-associated and community-acquired Gram-negative BSI, identification of patients with healthcare-associated acquisition of BSI is essential to optimize empiric antimicrobial therapy.
UR - http://www.scopus.com/inward/record.url?scp=84863831261&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84863831261&partnerID=8YFLogxK
U2 - 10.1007/s10096-011-1424-6
DO - 10.1007/s10096-011-1424-6
M3 - Article
C2 - 21983895
AN - SCOPUS:84863831261
SN - 0934-9723
VL - 31
SP - 1163
EP - 1171
JO - European Journal of Clinical Microbiology
JF - European Journal of Clinical Microbiology
IS - 6
ER -