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Polymicrobial intensive care unit-acquired pneumonia: prevalence, microbiology and outcome
Miquel Ferrer1,2,3, Leonardo Filippo Difrancesco4,5, Adamantia Liapikou6,7
1Department of Pneumology, Thorax Institute, Hospital Clinic, Villarroel 170, 08036, Barcelona, Spain. miferrer@clinic.ub.es.
Background:
Microbial aetiology of intensive care unit (ICU)-acquired pneumonia (ICUAP) determines antibiotic treatment and outcomes. The impact of polymicrobial ICUAP is not extensively known. We therefore investigated the characteristics and outcomes of polymicrobial aetiology of ICUAP.
Method:
Patients with ICUAP confirmed microbiologically were prospectively compared according to identification of 1 (monomicrobial) or more (polymicrobial) potentially-pathogenic microorganisms. Microbes usually considered as non-pathogenic were not considered for the etiologic diagnosis. We assessed clinical characteristics, microbiology, inflammatory biomarkers and outcome variables.
Results:
Among 441 consecutive patients with ICUAP, 256 (58%) had microbiologic confirmation, and 41 (16%) of them polymicrobial pneumonia. Methicillin-sensitive Staphylococcus aureus, Haemophilus influenzae, and several Enterobacteriaceae were more frequent in polymicrobial pneumonia. Multi-drug and extensive-drug resistance was similarly frequent in both groups. Compared with monomicrobial, patients with polymicrobial pneumonia had less frequently chronic heart disease (6, 15% vs. 71, 33%, p = 0.019), and more frequently pleural effusion (18, 50%, vs. 54, 25%, p = 0.008), without any other significant difference. Appropriate empiric antimicrobial treatment was similarly frequent in the monomicrobial (185, 86%) and the polymicrobial group (39, 95%), as were the initial response to the empiric treatment, length of stay and mortality. Systemic inflammatory response was similar comparing monomicrobial with polymicrobial ICUAP.
Conclusion:
The aetiology of ICUAP confirmed microbiologically was polymicrobial in 16% cases. Pleural effusion and absence of chronic heart disease are associated with polymicrobial pneumonia. When empiric treatment is frequently appropriate, polymicrobial aetiology does not influence the outcome of ICUAP.
Insights
Polymicrobial intensive care unit-acquired pneumonia (ICUAP) occurs in 16% of cases. When treated appropriately, polymicrobial ICUAP does not significantly impact patient outcomes compared to monomicrobial cases.
Area of Science:
- Infectious Diseases
- Critical Care Medicine
- Microbiology
Background:
- Microbial etiology of intensive care unit-acquired pneumonia (ICUAP) is crucial for guiding antibiotic therapy and predicting patient outcomes.
- The clinical characteristics and impact of polymicrobial ICUAP remain incompletely understood.
- This study aimed to investigate the features and outcomes associated with polymicrobial ICUAP.
Purpose of the Study:
- To characterize polymicrobial ICUAP.
- To compare clinical features, microbiology, and outcomes of polymicrobial versus monomicrobial ICUAP.
- To determine if polymicrobial etiology affects ICUAP outcomes.
Main Methods:
- Prospective comparison of ICUAP patients with microbiologically confirmed monomicrobial or polymicrobial infections.
- Exclusion of non-pathogenic microorganisms from etiologic diagnosis.
- Assessment of clinical data, microbial findings, inflammatory markers, and patient outcomes.
Main Results:
- Of 256 microbiologically confirmed ICUAP cases, 16% were polymicrobial.
- Polymicrobial pneumonia was associated with more frequent pleural effusion and less frequent chronic heart disease.
- Appropriate empiric antimicrobial treatment, initial response, length of stay, and mortality were similar between monomicrobial and polymicrobial groups.
Conclusions:
- Polymicrobial infections account for 16% of microbiologically confirmed ICUAP.
- Pleural effusion and absence of chronic heart disease are linked to polymicrobial ICUAP.
- Appropriate empiric treatment ensures that polymicrobial etiology does not negatively influence ICUAP outcomes.
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