Study: Resistant urinary tract infections increase risk of relapse
Researchers with the University of Pennsylvania Perelman School of Medicine have found that community-onset urinary tract infections (UTIs) caused by extended-cephalosporin-resistant Enterobacteriaceae (ESC-R EB) are associated with a sevenfold risk of clinical failure and an increase in inappropriate antibiotic therapy, according to a study today in Infection Control and Hospital Epidemiology.
The retrospective cohort study, conducted at two emergency departments and a network of outpatient practices in the University of Pennsylvania Health System, included all patients who presented with community-onset EB UTIs from December 2010 through April 2013. Exposed patients were identified as those who had an ESC-R EB. They were randomly matched 1:1 with patients who had an ESC-susceptible EB UTI. The primary outcome was clinical failure, defined by repeat clinical visit or phone call for ongoing UTI symptoms.
A total of 302 patients were included in the study, with 151 exposed and 151 unexposed. Within the entire cohort, 86 patients (29%) experienced clinical failure. On multivariable analysis, UTI caused by an ESC-R EB was significantly associated with clinical failure (adjusted odds ratio [aOR], 7.07; 95% confidence interval [CI], 3.16 to 15.82; P < .01). Other independent risk factors for clinical failure included infection with Citrobacter spp and a need for hemodialysis.
The researchers also found that a UTI caused by ESC-R EB was a significant independent risk factor for inappropriate initial antibiotic therapy (IIAT) within 48 hours of UTI evaluation (aOR, 4.40; 95% CI, 2.64 to 7.33; P < .01). They concluded, however, that IIAT was only partially responsible for the worse outcomes associated with ESC-R EB.
"This study adds to the evidence that drug-resistant bacteria are an increasing issue, even in the community and even in patients who have something seemingly uncomplicated, like a urinary tract infection," lead study author and University of Pennsylvania clinical epidemiologist Judith Anesi, MD, said in a press release from the Society for Healthcare Epidemiology of America (SHEA), publisher of the journal. "This is an alarming finding, and interventions to curb antibiotic resistance are urgently needed."
Oct 30 Infect Control Hosp Epidemiol abstract
Oct 30 SHEA press release
UK study finds hospital antifungal stewardship reduces costs
An antifungal stewardship (AFS) program centered around specialist input resulted in significant cost savings at a London hospital, with no adverse effects on microbiologic or clinical outcomes, researchers reported today in the Journal of Antimicrobial Chemotherapy.
The AFS program at St. George's Hospital, instituted in October 2010, involves all patients receiving antifungal therapy with amphotericin B, echinocandins, intravenous fluconazole, flucytosine, or voriconazole. All identified patients are seen on a weekly stewardship ward round by an infectious diseases consultant and antimicrobial pharmacist. To determine the effectiveness of the program, researchers collected clinical, microbiologic, and financial outcome data from October 2010 to September 2016.
A total of 432 patients were reviewed 769 times during the study period. The most common drug initiated was amphotericin B (181 patients, 35%), followed by intravenous fluconazole (142 patients, 29%) and echinocandins (120 patients, 23%). In the case of empirical prescribing, 82% (150/183) of patients were subsequently found to have no evidence of invasive fungal infection (IFI). Advice was offered in 64% of reviews (494/769) and was followed in 84% of evaluable recommendations. Of 138 patients prescribed empirical antifungal therapy who had no IFI, 62% had their prescriptions stopped within a week, compared with 44% in a pre-intervention 2009 audit.
Following implementation of the program, annual antifungal expenditure fell by 30%, then increased to 20% above pre-intervention (2009-10) over a 5-year period. But this was a significantly lower rise compared with national antifungal expenditures, which doubled over the same period. Inpatient mortality, Candida species distribution, and rates of resistance were not adversely affected by the intervention.
"In summary, we demonstrate that an AFS program is readily implementable and sustainable over 6 years, offering a large scope for targeted intervention to prevent unnecessary prescribing, with good clinician acceptance and no compromise of clinical outcomes," the authors of the study write.
Oct 30 J Antimicrob Chemother abstract
Study examines risk factors for carbapenem-resistant Pseudomonas
In a study yesterday in the Journal of Antimicrobial Chemotherapy, French researchers determined that the risk of acquiring carbapenem-resistant Pseudomonas aeruginosa (CRPA) was associated with carbapenem exposure and with exposure to beta-lactams inactive against P aeruginosa.
The multicenter prospective case–case-control study included 1,808 adults hospitalized in 10 French intensive care units in 2009. Cases were patients with CRPA and patients with carbapenem-susceptible P aeruginosa (CSPA), and controls were patients without P aeruginosa. The researchers investigated antibiotics associated with CRPA isolation and with CSPA isolation after adjusting for non-antibiotic exposures and inpatient characteristics.
Fifty-nine CRPA, 83 CSPA, and 142 control patients were compared. In multivariable analysis, after adjustment for confounders and other non-antibiotic exposures, CRPA cases were independently associated with exposure to carbapenems (odds ratio [OR], 1.205; 95% CI, 1.079 to 1.346) and with exposure to a group of beta-lactams inactive against P aeruginosa (OR, 1.101; 95% CI, 1.010 to 1.201). The antibiotics included amoxicillin, amoxicillin-clavulanic acid, oxacillin, cloxacillin, ertapenem, and first- and second-generation cephalosporins. Conversely, exposure to beta-lactams active against P aeruginosa was an independent protective factor for CSPA isolation (OR, 0.868; 95% CI, 0.722 to 0.976).
The authors of the study hypothesize that the increased risk for CRPA associated with beta-lactams inactive against P aeruginosa may be due to antibiotic selection pressure, with the selection of intestinal flora making the host more susceptible to colonization by resistant strains. They conclude that clinicians should weigh the potential benefits of administering these antibiotics against the increased risk of CRPA infection.
Oct 29 J Antimicrob Chemother abstract