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Multidrug-resistant Proteus mirabilis bloodstream infections: risk factors and outcomes
Mario Tumbarello1, Enrico Maria Trecarichi, Barbara Fiori
1Faculty of Medicine, Institutes of Infectious Diseases, Catholic University of the Sacred Heart, Rome, Italy. tumbarello@rm.unicatt.it
Abstract:
Our aims were to identify (i) risk factors associated with the acquisition of multidrug-resistant (MDR, to 3 or more classes of antimicrobials) Proteus mirabilis isolates responsible for bloodstream infections (BSIs) and (ii) the impact on mortality of such infections. Risk factors for acquiring MDR P. mirabilis BSIs were investigated in a case-case-control study; those associated with mortality were assessed by comparing survivors and nonsurvivors in a cohort study. The population consisted of 99 adult inpatients with P. mirabilis BSIs identified by our laboratory over an 11-year period (1999 to 2009), 36 (33.3%) of which were caused by MDR strains, and the overall 21-day mortality rate was 30.3%. Acquisition of an MDR strain was independently associated with admission from a long-term care facility (odds ratio [OR], 9.78; 95% confidence interval [CI], 1.94 to 49.16), previous therapy with fluoroquinolones (OR, 5.52; 95% CI, 1.30 to 23.43) or oxyimino-cephalosporins (OR, 4.72; 95% CI, 1.31 to 16.99), urinary catheterization (OR, 3.89; 95% CI, 1.50 to 10.09), and previous hospitalization (OR, 2.68; 95% CI, 10.4 to 6.89). Patients with MDR P. mirabilis BSIs received inadequate initial antimicrobial therapy (IIAT, i.e., treatment with drugs to which the isolate displayed in vitro resistance) more frequently than those with non-MDR infections; they also had increased mortality and (for survivors) longer post-BSI-onset hospital stays. In multivariate regression analysis, 21-day mortality was associated with septic shock at BSI onset (OR, 12.97; 95% CI, 32.2 to 52.23), P. mirabilis isolates that were MDR (OR, 6.62; 95% CI, 16.4 to 26.68), and IIAT (OR, 9.85; 95% CI, 26.7 to 36.25), the only modifiable risk factor of the 3. These findings can potentially improve clinicians' ability to identify P. mirabilis BSIs likely to be MDR, thereby reducing the risk of IIAT--a major risk factor for mortality in these cases--and facilitating the prompt implementation of appropriate infection control measures.
Insights
Multidrug-resistant Proteus mirabilis bloodstream infections (BSIs) are linked to long-term care, prior antibiotic use, and urinary catheters. Inadequate initial antimicrobial therapy for MDR P. mirabilis BSIs significantly increases mortality risk.
Area of Science:
- Infectious Diseases
- Clinical Microbiology
- Epidemiology
Background:
- Proteus mirabilis is a common cause of bloodstream infections (BSIs).
- The emergence of multidrug-resistant (MDR) strains poses a significant clinical challenge.
- Understanding risk factors and mortality impact of MDR P. mirabilis BSIs is crucial for patient outcomes.
Purpose of the Study:
- To identify risk factors associated with acquiring MDR P. mirabilis BSIs.
- To determine the impact of MDR P. mirabilis BSIs on patient mortality.
- To evaluate the association between inadequate initial antimicrobial therapy (IIAT) and mortality.
Main Methods:
- A case-case-control study was used to investigate risk factors for MDR P. mirabilis BSIs.
- A cohort study compared survivors and nonsurvivors to assess mortality risks.
- Data from 99 adult inpatients with P. mirabilis BSIs between 1999 and 2009 were analyzed.
Main Results:
- 33.3% of P. mirabilis BSIs were caused by MDR strains.
- Independent risk factors for MDR P. mirabilis BSIs included long-term care facility admission, prior fluoroquinolone or oxyimino-cephalosporin therapy, urinary catheterization, and previous hospitalization.
- MDR P. mirabilis BSIs were associated with higher mortality, increased likelihood of IIAT, and longer hospital stays for survivors.
- Factors independently associated with 21-day mortality were septic shock, MDR P. mirabilis BSIs, and IIAT.
Conclusions:
- Long-term care facility admission and specific prior antibiotic exposures are key risk factors for MDR P. mirabilis BSIs.
- Inadequate initial antimicrobial therapy (IIAT) is a major modifiable risk factor for mortality in patients with P. mirabilis BSIs.
- Early identification of patients at risk for MDR P. mirabilis BSIs can help reduce IIAT and improve clinical outcomes.
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