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Intensive care unit-acquired Stenotrophomonas maltophilia: incidence, risk factors, and outcome

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Abstract Introduction The aim of this study was to determine incidence, risk factors, and impact on outcome of intensive care unit (ICU)-acquired Stenotrophomonas maltophilia. Methods This prospective observational case-control study, which was a part of a cohort study, was conducted in a 30-bed ICU during a three year period. All immunocompetent patients hospitalised >48 hours were eligible. Patients with non-fermenting Gram-negative bacilli (NF-GNB) at ICU admission were excluded. Patients without ICU-acquired S. maltophilia who developed an ICU-acquired NF-GNB other than S. maltophilia were also excluded. Screening (tracheal aspirate and skin, anal, and nasal swabs) for NF-GNB was performed in all patients at ICU admission and weekly. Univariate and multivariate analyses were performed to determine risk factors for ICU-acquired S. maltophilia and for ICU mortality. Results Thirty-eight (2%) patients developed an S. maltophilia ICU-acquired colonisation and/or infection and were all successfully matched with 76 controls. Chronic obstructive pulmonary disease (COPD) and duration of antibiotic treatment (odds ratio [OR] [95% confidence interval (CI)] = 9.4 [3 to 29], p < 0.001, and 1.4 [1 to 2.3], p = 0.001, respectively) were independently associated with ICU-acquired S. maltophilia. Mortality rate (60% versus 40%, OR [95% CI] = 1.3 [1 to 1.7, p = 0.037]), duration of mechanical ventilation (23 ± 16 versus 7 ± 11 days, p < 0.001), and duration of ICU stay (29 ± 21 versus 15 ± 17 days, p < 0.001) were significantly higher in cases than in controls. In addition, ICU-acquired infection related to S. maltophilia was independently associated with ICU mortality (OR [95% CI] = 2.8 [1 to 7.7], p = 0.044). Conclusion COPD and duration of antibiotic treatment are independent risk factors for ICU-acquired S. maltophilia. ICU-acquired S. maltophilia is associated with increased morbidity and mortality rates. ICU-acquired infection related to S. maltophilia is an independent risk factor for ICU mortality.
Title: Intensive care unit-acquired Stenotrophomonas maltophilia: incidence, risk factors, and outcome
Description:
Abstract Introduction The aim of this study was to determine incidence, risk factors, and impact on outcome of intensive care unit (ICU)-acquired Stenotrophomonas maltophilia.
Methods This prospective observational case-control study, which was a part of a cohort study, was conducted in a 30-bed ICU during a three year period.
All immunocompetent patients hospitalised >48 hours were eligible.
Patients with non-fermenting Gram-negative bacilli (NF-GNB) at ICU admission were excluded.
Patients without ICU-acquired S.
maltophilia who developed an ICU-acquired NF-GNB other than S.
maltophilia were also excluded.
Screening (tracheal aspirate and skin, anal, and nasal swabs) for NF-GNB was performed in all patients at ICU admission and weekly.
Univariate and multivariate analyses were performed to determine risk factors for ICU-acquired S.
maltophilia and for ICU mortality.
Results Thirty-eight (2%) patients developed an S.
maltophilia ICU-acquired colonisation and/or infection and were all successfully matched with 76 controls.
Chronic obstructive pulmonary disease (COPD) and duration of antibiotic treatment (odds ratio [OR] [95% confidence interval (CI)] = 9.
4 [3 to 29], p < 0.
001, and 1.
4 [1 to 2.
3], p = 0.
001, respectively) were independently associated with ICU-acquired S.
maltophilia.
Mortality rate (60% versus 40%, OR [95% CI] = 1.
3 [1 to 1.
7, p = 0.
037]), duration of mechanical ventilation (23 ± 16 versus 7 ± 11 days, p < 0.
001), and duration of ICU stay (29 ± 21 versus 15 ± 17 days, p < 0.
001) were significantly higher in cases than in controls.
In addition, ICU-acquired infection related to S.
maltophilia was independently associated with ICU mortality (OR [95% CI] = 2.
8 [1 to 7.
7], p = 0.
044).
Conclusion COPD and duration of antibiotic treatment are independent risk factors for ICU-acquired S.
maltophilia.
ICU-acquired S.
maltophilia is associated with increased morbidity and mortality rates.
ICU-acquired infection related to S.
maltophilia is an independent risk factor for ICU mortality.

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